Page last updated: 2024-12-07

n-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl)phenyl)methanesulfonamide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

N-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl)phenyl)methanesulfonamide: FP 846 is purified form of sulfentrazone; protoporphyrinogen oxidase inhibitor [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

sulfentrazone : A member of the class of triazoles that is 5-oxo-1,2,4-triazole which is substituted at positions 1, 3, and 4 by 2,4-dichloro-5-[(methylsulfonyl)amino]phenyl, methyl, and difluoromethyl groups, respectively. A protoporphyrinogen oxidase inhibitor, it is used as a herbicide to control broad-leaved weeds in soya and tobacco crops. Not approved for use within the European Union. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID86369
CHEMBL ID1884669
CHEBI ID9339
SCHEMBL ID44683
MeSH IDM0451644

Synonyms (56)

Synonym
f 6285
n-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl)phenyl)methanesulfonamide
sulfentrazone [iso]
authority
hsdb 7014
methanesulfonamide, n-(2,4-dichloro-5-(4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl)phenyl)-
sulfentrazone
f6285
122836-35-5
NCGC00163868-01
n-{2,4-dichloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1h-1,2,4-triazol-1-yl]phenyl}methanesulfonamide
NCGC00163868-02
n-[2,4-dichloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-1,2,4-triazol-1-yl]phenyl]methanesulfonamide
NCGC00163868-03
cas-122836-35-5
tox21_301091
NCGC00254991-01
dtxcid4012645
dtxsid6032645 ,
fp-846
7ty7wt1599 ,
fp 846
unii-7ty7wt1599
AKOS016011234
FT-0631107
2',4'-dichloro-5'-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl)methanesulfonanilide
fmc-97285
f-6285
sulfentrazone [hsdb]
sulfentrazone [mi]
SCHEMBL44683
n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo -1h-1,2,4 -triazol-1-yl] phenyl]methanesulfonamide
n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4 -triazol-1-yl] phenyl]methanesulfonamide
n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl] phenyl]methanesulfonamide
chebi:9339 ,
CHEMBL1884669
fmc 97285
n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl]phenyl]methanesulfonamide
n-(2,4-dichloro-5-(4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1h-1,2,4-triazol-1-yl)phenyl)methanesulfonamide
J-004865
methanesulfonamide, n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl]phenyl]-
sulfentrazone, pestanal(r), analytical standard
AS-75027
bdbm50486212
sulfentrazone 10 microg/ml in acetonitrile
boral
n-[2,4-dichloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1h-1,2,4-triazol-1-yl]phenyl]methanesulfonamide, 9ci
fmc 6285
sulfentrazon
Q7636194
D95628
HY-135745
CS-0113915
U0110
mfcd00869633
capaz

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
") biochars, produced using either fast- or slow-pyrolysis, on the bioavailability of metsulfuron and sulfentrazone herbicides in soil."( Bioavailability of Metsulfuron and Sulfentrazone Herbicides in Soil as Affected by Amendment with Two Contrasting Willow Biochars.
Hangs, RD; Schoenau, JJ; Szmigielski, AM, 2018
)
0.48

Dosage Studied

ExcerptRelevanceReference
" In addition, among six tested crops, wheat exhibited high tolerance to compound 1b even at a dosage of 300 g ai/ha."( Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
Jiang, LL; Tan, Y; Wang, ZF; Wu, QY; Xi, Z; Yang, GF; Zuo, Y, 2011
)
0.37
" Maize exhibits relative tolerance against compound 9F-6 at the dosage of 150 g ai/ha, but it is susceptible to saflufenacil even at 75 g ai/ha."( Synthesis, Herbicidal Activity, and QSAR of Novel N-Benzothiazolyl- pyrimidine-2,4-diones as Protoporphyrinogen Oxidase Inhibitors.
Niu, CW; Su, SW; Wu, Q; Xi, Z; Yang, GF; Zuo, Y, 2016
)
0.43
" Different variables that could influence the sulfentrazone conversion were investigated, such as nitrogen atmosphere, pH and dosage of the nanoparticles and initial concentration of sulfentrazone."( Sulfentrazone dechlorination by iron-nickel bimetallic nanoparticles.
Cruz, JC; Lima, CF; Lopes, RP; Nascimento, MA; Silva, AA, 2016
)
0.43
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitorAn EC 1.3.3.* (oxidoreductase acting on donor CH-CH group with oxygen as acceptor) inhibitor that interferes with the action of protoporphyrinogen oxidase (EC 1.3.3.4).
herbicideA substance used to destroy plant pests.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (4)

ClassDescription
sulfonamideAn amide of a sulfonic acid RS(=O)2NR'2.
dichlorobenzeneAny member of the class of chlorobenzenes carrying two chloro groups at unspecified positions.
organofluorine compoundAn organofluorine compound is a compound containing at least one carbon-fluorine bond.
triazolesAn azole in which the five-membered heterocyclic aromatic skeleton contains three N atoms and two C atoms.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (10)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AR proteinHomo sapiens (human)Potency22.45480.000221.22318,912.5098AID743035; AID743036
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency55.93330.000657.913322,387.1992AID1259377; AID1259378
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency0.89130.000214.376460.0339AID588532
pregnane X nuclear receptorHomo sapiens (human)Potency17.78280.005428.02631,258.9301AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency21.19900.000229.305416,493.5996AID588514; AID743075
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency2.45410.001024.504861.6448AID743215
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency21.87240.001019.414170.9645AID743191
activating transcription factor 6Homo sapiens (human)Potency21.87240.143427.612159.8106AID1159516
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Protoporphyrinogen oxidase, chloroplasticNicotiana tabacum (common tobacco)Ki0.03000.03000.03000.0300AID1107514
Protoporphyrinogen oxidaseHomo sapiens (human)Ki0.72150.72001.36092.9300AID1081027; AID1091968
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (6)

Processvia Protein(s)Taxonomy
porphyrin-containing compound biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
protoporphyrinogen IX biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
heme biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
heme A biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
heme B biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
heme O biosynthetic processProtoporphyrinogen oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (2)

Processvia Protein(s)Taxonomy
oxygen-dependent protoporphyrinogen oxidase activityProtoporphyrinogen oxidaseHomo sapiens (human)
flavin adenine dinucleotide bindingProtoporphyrinogen oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (3)

Processvia Protein(s)Taxonomy
mitochondrial inner membraneProtoporphyrinogen oxidaseHomo sapiens (human)
mitochondrial intermembrane spaceProtoporphyrinogen oxidaseHomo sapiens (human)
mitochondrial membraneProtoporphyrinogen oxidaseHomo sapiens (human)
mitochondrial inner membraneProtoporphyrinogen oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (114)

Assay IDTitleYearJournalArticle
AID1091968Inhibition of Homo sapiens (human) protoporphyrinogen oxidase2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1107510Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107485Phytotoxicity against four-leaf stage Brassica napus (oilseed rape) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090996Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107478Post-emergence herbicidal activity against Symphyotrichum subulatum assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107512Post emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107506Post-emergence herbicidal activity against Setaria faberi (Giant Foxtail) seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082274Inhibition of Homo sapiens (human) recombinant protoporphyrinogen oxidase by UV-vis spectrophotometry2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090990Herbicidal activity against Chenopodium album assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107482Post-emergence herbicidal activity against Cerastium arvense assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090985Herbicidal activity against Brassica juncea assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090983Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090988Herbicidal activity against Senna tora assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107489Phytotoxicity against four-leaf stage Oryza sativa (rice) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090981Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107493Phytotoxicity against 4-leaf stage Glycine max (soybean) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090994Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107479Post-emergence herbicidal activity against Boehmeria nivea assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107484Phytotoxicity against 4-leaf stage Triticum aestivum (wheat) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1081027Inhibition of Homo sapiens (human) recombinant protoporphyrinogen oxidase expressed in Escherichia coli JM109 assessed as oxidation of protoporphyrinogen IX substrate by UV-visible spectrophotometry2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1107514Inhibition of Nicotiana tabacum (tobacco) recombinant PPO assessed as protoporphyrinogen IX formation at room temperature by fluorimetric assay2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082265Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090971Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107504Post-emergence herbicidal activity against Brassica juncea seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090987Herbicidal activity against Senna tora assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082271Herbicidal activity against Setaria faberi (Giant Foxtail) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107508Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1081023Post-emergence herbicidal activity against Brassica juncea assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1090991Herbicidal activity against Chenopodium album assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107491Phytotoxicity against four-leaf stage Brassica napus (oilseed rape) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107499Post emergence herbicidal activity against Amaranthus retroflexus seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090993Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090992Herbicidal activity against Chenopodium album assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090972Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107476Post-emergence herbicidal activity against Solanum nigrum (black nightshade) assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090976Herbicidal activity against Portulaca oleracea assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107495Phytotoxicity against four-leaf stage Oryza sativa (rice) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082257Herbicidal activity against Setaria faberi (Giant Foxtail) assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1091965Herbicidal activity against Setaria viridis assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1107473Post-emergence herbicidal activity against Myosoton aquaticum assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082261Herbicidal activity against Brassica juncea assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090979Herbicidal activity against Cerastium arvense assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082264Herbicidal activity against Setaria faberi (Giant Foxtail) assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107481Post-emergence herbicidal activity against Eleusine indica assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107487Phytotoxicity against four-leaf stage Gossypium hirsutum (cotton) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090978Herbicidal activity against Cerastium arvense assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090982Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082272Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1082262Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1081024Post-emergence herbicidal activity against Poa annua assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1081025Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1091962Herbicidal activity against Chenopodium album assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1090970Herbicidal activity against Setaria viridis (green foxtail) assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107498Post-emergence herbicidal activity against Chenopodium album seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082253Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090977Herbicidal activity against Portulaca oleracea assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107503Post-emergence herbicidal activity against Brassica juncea seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107471Post-emergence herbicidal activity against Ludwigia prostrata assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107474Post-emergence herbicidal activity against Sonchus asper assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107507Post-emergence herbicidal activity against Setaria faberi (Giant Foxtail) seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090995Herbicidal activity against Setaria viridis (green foxtail) assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082269Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1082259Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090986Herbicidal activity against Brassica juncea assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090974Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107467Post-emergence herbicidal activity against Senna tora assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1091963Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1091966Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1107477Post-emergence herbicidal activity against Capsella bursa-pastoris assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107486Phytotoxicity against four-leaf stage Zea mays cv. Anjou (maize) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107472Post-emergence herbicidal activity against Commelina communis (Asiatic dayflower) assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082256Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107502Post-emergence herbicidal activity against Brassica juncea seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090984Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1090975Herbicidal activity against Portulaca oleracea assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082263Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1082270Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107469Post-emergence herbicidal activity against Raddix phytolaccae assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107475Post-emergence herbicidal activity against Polygonum humifusum assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107497Post-emergence herbicidal activity against Chenopodium album seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1081026Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1107494Phytotoxicity against four-leaf stage Gossypium hirsutum (cotton) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082260Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107468Post-emergence herbicidal activity against Physalis alkekengi assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1091967Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1090973Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082268Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107509Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107480Post-emergence herbicidal activity against Amaranthus spinosus assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1081021Post-emergence herbicidal activity against Eclipta prostrata assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1107483Post-emergence herbicidal activity against Veronica polita assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107470Post-emergence herbicidal activity against Ammannia baccifera assessed as plant growth inhibition at 75 g ai/ha2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107492Phytotoxicity against four-leaf stage Zea mays cv. Anjou (maize) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090980Herbicidal activity against Cerastium arvense assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107511Post emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1090989Herbicidal activity against Senna tora assessed as growth inhibition at 37.5 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1107488Phytotoxicity against 4-leaf stage Glycine max (soybean) plants assessed as plant growth inhibition at 150 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1091961Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1107501Post emergence herbicidal activity against Amaranthus retroflexus seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082266Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 37.5 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107496Post-emergence herbicidal activity against Chenopodium album seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107505Post-emergence herbicidal activity against Setaria faberi (Giant Foxtail) seedlings assessed as plant growth inhibition at 75 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1081022Post-emergence herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at emulsified concentrate of 150 g/ai ha after 15 days by greenhouse test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Design, synthesis, and 3D-QSAR analysis of novel 1,3,4-oxadiazol-2(3H)-ones as protoporphyrinogen oxidase inhibitors.
AID1090969Herbicidal activity against Setaria viridis (green foxtail) assessed as growth inhibition at 75 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
AID1082254Herbicidal activity against Brassica juncea assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1107490Phytotoxicity against 4-leaf stage Triticum aestivum (wheat) plants assessed as plant growth inhibition at 75 g ai/ha applied through spraying measured 30 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107513Post emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) seedlings assessed as plant growth inhibition at 150 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1107500Post emergence herbicidal activity against Amaranthus retroflexus seedlings assessed as plant growth inhibition at 37.5 g ai/ha measured 15 days after compound treatment under greenhouse conditions2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
Design and synthesis of 1-(benzothiazol-5-yl)-1H-1,2,4-triazol-5-ones as protoporphyrinogen oxidase inhibitors.
AID1082255Herbicidal activity against Eclipta prostrata assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1091964Herbicidal activity against Brassica juncea assessed as growth inhibition at 150 g ai/ha using post-emergence protocol under greenhouse conditions measured 15 days after compound treatment2010Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22
Design, syntheses and 3D-QSAR studies of novel N-phenyl pyrrolidin-2-ones and N-phenyl-1H-pyrrol-2-ones as protoporphyrinogen oxidase inhibitors.
AID1082273Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1082258Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 75 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1082267Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as growth inhibition at 150 g/ha postemergence treatment measured after 15 days by Greenhouse test2011Journal of agricultural and food chemistry, Jun-08, Volume: 59, Issue:11
Design and syntheses of novel N-(benzothiazol-5-yl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and N-(benzothiazol-5-yl)isoindoline-1,3-dione as potent protoporphyrinogen oxidase inhibitors.
AID1090997Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 150 g of active ingredient/ha administered using post-emergence treatment measured 15 days post treatment protocol under greenhouse conditions2008Journal of agricultural and food chemistry, Mar-26, Volume: 56, Issue:6
Syntheses and herbicidal activities of novel triazolinone derivatives.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (5.88)18.2507
2000's5 (14.71)29.6817
2010's19 (55.88)24.3611
2020's8 (23.53)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.59

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.59 (24.57)
Research Supply Index3.58 (2.92)
Research Growth Index5.17 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.59)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other35 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]