Hexaconazole is a triazole fungicide that acts by inhibiting the biosynthesis of ergosterol, a vital component of fungal cell membranes. Its synthesis involves a multi-step process, starting with the reaction of 1,2,4-triazole with an appropriate alkyl halide followed by a series of reactions to introduce the desired substituents. Hexaconazole is highly effective against a broad spectrum of fungal diseases in a wide range of crops, including wheat, barley, rice, and fruit trees. Its importance lies in its ability to control fungal infections, protect crops from yield losses, and improve food security. Extensive research on hexaconazole focuses on its mode of action, efficacy against different fungal species, environmental fate, and potential risks to non-target organisms. Understanding these aspects is crucial for optimizing its application and minimizing its negative impacts.'
2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol : A member of the class of triazoles that is 1-hexyl-1H-1,2,4-triazole in which the hydrogens at position 2 of the hexyl chain are replaced by hydroxy and 2,4-dichlorophenyl groups.
hexaconazole : A racemate comprising equimolar amounts of (R)- and (S)-hexaconazole. An agricultural fungicide introduced in the 1980s, it is not approved for use within the European Union.
ID Source | ID |
---|---|
PubMed CID | 66461 |
CHEMBL ID | 1898860 |
CHEBI ID | 83711 |
SCHEMBL ID | 21992 |
MeSH ID | M0364690 |
Synonym |
---|
AC-16157 |
LS-14301 |
1h-1,2,4-triazole-1-ethanol, alpha-butyl-alpha-(2,4-dichlorophenyl)- |
NCGC00164270-01 |
1h-1,2,4-triazole-1-ethanol, alpha-butyl-alpha-(2,4-dichlorophenyl)-, (+-)- |
anvil l |
anvil liquid |
anvil |
r 154523 |
pp 523 |
sitara |
alpha-butyl-alpha-(2,4-dichlorophenyl)-1h-1,2,4-triazole-1-ethanol (+-)- |
contaf 5ec |
(rs)-2-(2,4-dichlorophenyl)-1-(1h-1,2,4-triazol-1-yl)hexan-2-ol |
anvil (fungicide) |
contaf |
fd 4053 |
chlortriafol |
hexaconazole [bsi:iso] |
79983-71-4 |
2-(2,4-dichlorophenyl)-1-(1h-1,2,4-triazol-1-yl)hexan-2-ol |
hexaconazole |
NCGC00164270-02 |
2-(2,4-dichlorophenyl)-1-(1,2,4-triazol-1-yl)hexan-2-ol |
FT-0655723 |
A839797 |
NCGC00164270-03 |
C18466 |
ec 413-050-7 |
unii-sx9r3x1fqv |
sx9r3x1fqv , |
tox21_300684 |
cas-79983-71-4 |
NCGC00254592-01 |
dtxcid2014653 |
dtxsid4034653 , |
chebi:83711 , |
CHEMBL1898860 |
rs-2-(2,4-dichlorophenyl)-1-(1h-1,2,4-triazol-1-yl)hexan-2-ol |
hexaconazol |
AKOS015895354 |
SCHEMBL21992 |
(+/-)-hexaconazole |
r-154523 |
pp-523 |
hexaconazole [iso] |
hexaconazole, (+/-)- |
pc-1002 , |
1h-1,2,4-triazole-1-ethanol, .alpha.-butyl-.alpha.-(2,4-dichlorophenyl)- |
planete |
hexaconazole [mi] |
CS-5814 |
HY-A0278 |
.alpha.-butyl-.alpha.-(2,4-dichlorophenyl)-1h-1,2,4-triazole-1-ethanol (.+/-.)- |
2-(2,4-dichlorophenyl)-1-(1h-1,2,4-triazol-1-yl)-2-hexanol # |
1h-1,2,4-triazole-1-ethanol, .alpha.-butyl-.alpha.-(2,4-dichlorophenyl)-, (.+/-.)- |
hexaconazol, pestanal(r), analytical standard |
hexaconazole 100 microg/ml in acetonitrile |
hexaconazole 10 microg/ml in cyclohexane |
Q424794 |
hexaconzole |
hexaconazole 1000 microg/ml in toluene |
(-)-hexaconazol |
F87564 |
(+/-)-2-(2,4-dichlorophenyl)-1-(1h-1,2,4-triazol-1-yl)-2-hexanol |
Hexaconazole (HEZ) is a triazole fungicide registered to prevent and control grey mold disease on tomatoes. Nanohexaconazol is a highly efficient fungicide against Rhizoctonia solani.
Nanohexaconazole was tested in vitro and there were no significant adverse effect in their numbers observed. This proved the safety of the nanofungicide.
Excerpt | Reference | Relevance |
---|---|---|
"Little is known about the bioaccumulation and toxicity of hexaconazole (HEX) in spite of the fact that they are indispensable parts for a comprehensive assessment of its environmental behavior and toxic effects in organisms of freshwater ecosystems." | ( Enantioselective bioaccumulation of hexaconazole and its toxic effects in adult zebrafish (Danio rerio). Li, D; Teng, M; Wang, Y; Xu, L; Zhang, R; Zhou, Z; Zhu, W, 2015) | 0.94 |
" Impact of nanohexaconazole on soil nitrifiers was tested in vitro and there were no significant adverse effect in their numbers observed as compared to conventional registered formulation, proving the safety of the nanofungicide." | ( Development and Quality Control of Nanohexaconazole as an Effective Fungicide and Its Biosafety Studies on Soil Nitifiers. Alam, MI; Gogoi, R; Gopal, M; Goswami, A; Kumar, R; Nair, KK; Singh, PK; Srivastava, C, 2015) | 1.04 |
"The widespread application of triazole fungicides makes people attach great concern over its adverse effects in mammalian." | ( Comparative cytotoxic effects of five commonly used triazole alcohol fungicides on human cells of different tissue types. Huang, Q; Liu, X; Muhayimana, S; Xiong, H; Xu, J; Xue, Y; Zhang, X, 2020) | 0.56 |
"Although fungicides could be the best solution in combating fungal infections in crops, however, the phytotoxic level of fungicides to the crops should be tested first to ensure that it is safe for the crops." | ( Phytotoxicity of chitosan-based agronanofungicides in the vegetative growth of oil palm seedling. Daim, LDJ; Fakurazi, S; Hilmi, NHZ; Hussein, MZ; Idris, AS; Maluin, FN; Yusof, NA, 2020) | 0.56 |
Excerpt | Reference | Relevance |
---|---|---|
" However, it was observed that high accumulation of the fungicide in the stem tissue and leaf after the treatment using the chitosan-hexaconazole nanoparticles, which is good for better bioavailability for the treatment of the fungi, Ganoderma boninense." | ( Residual analysis of chitosan-based agronanofungicides as a sustainable alternative in oil palm disease management. Daim, LDJ; Fakurazi, S; Hilmi, NHZ; Hussein, MZ; Idris, AS; Maluin, FN; Maznah, Z; Yusof, NA, 2020) | 0.76 |
Role | Description |
---|---|
chelator | A ligand with two or more separate binding sites that can bind to a single metallic central atom, forming a chelate. |
[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] |
Class | Description |
---|---|
tertiary alcohol | A tertiary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has three other carbon atoms attached to it. |
triazoles | An azole in which the five-membered heterocyclic aromatic skeleton contains three N atoms and two C atoms. |
dichlorobenzene | Any member of the class of chlorobenzenes carrying two chloro groups at unspecified positions. |
[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 | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 79.6407 | 0.0072 | 15.7588 | 89.3584 | AID1224835 |
pregnane X receptor | Rattus norvegicus (Norway rat) | Potency | 12.5893 | 0.0251 | 27.9203 | 501.1870 | AID651751 |
RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 52.9050 | 0.0060 | 38.0041 | 19,952.5996 | AID1159521; AID1159523 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 18.9480 | 0.0007 | 14.5928 | 83.7951 | AID1259369; AID1259392 |
AR protein | Homo sapiens (human) | Potency | 47.0128 | 0.0002 | 21.2231 | 8,912.5098 | AID1259243; AID1259247; AID743035; AID743042; AID743054; AID743063 |
caspase 7, apoptosis-related cysteine protease | Homo sapiens (human) | Potency | 61.0684 | 0.0133 | 26.9810 | 70.7614 | AID1346978 |
estrogen receptor 2 (ER beta) | Homo sapiens (human) | Potency | 48.5084 | 0.0006 | 57.9133 | 22,387.1992 | AID1259378 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 24.1148 | 0.0010 | 22.6508 | 76.6163 | AID1224838; AID1224839; AID1224893 |
progesterone receptor | Homo sapiens (human) | Potency | 39.1399 | 0.0004 | 17.9460 | 75.1148 | AID1346784; AID1346795 |
glucocorticoid receptor [Homo sapiens] | Homo sapiens (human) | Potency | 35.3655 | 0.0002 | 14.3764 | 60.0339 | AID588532; AID720691; AID720692 |
retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 50.0949 | 0.0030 | 41.6115 | 22,387.1992 | AID1159552; AID1159553; AID1159555 |
retinoid X nuclear receptor alpha | Homo sapiens (human) | Potency | 30.1163 | 0.0008 | 17.5051 | 59.3239 | AID1159527; AID1159531 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 47.6240 | 0.0015 | 30.6073 | 15,848.9004 | AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403 |
farnesoid X nuclear receptor | Homo sapiens (human) | Potency | 54.9141 | 0.3758 | 27.4851 | 61.6524 | AID743217 |
pregnane X nuclear receptor | Homo sapiens (human) | Potency | 34.4901 | 0.0054 | 28.0263 | 1,258.9301 | AID1346982; AID720659 |
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 54.4968 | 0.0002 | 29.3054 | 16,493.5996 | AID1259244; AID1259248; AID588513; AID743069; AID743075; AID743078; AID743079; AID743080; AID743091 |
peroxisome proliferator-activated receptor delta | Homo sapiens (human) | Potency | 49.7913 | 0.0010 | 24.5048 | 61.6448 | AID588534; AID743215 |
peroxisome proliferator activated receptor gamma | Homo sapiens (human) | Potency | 44.3765 | 0.0010 | 19.4141 | 70.9645 | AID588536; AID743140 |
vitamin D (1,25- dihydroxyvitamin D3) receptor | Homo sapiens (human) | Potency | 47.0996 | 0.0237 | 23.2282 | 63.5986 | AID743241 |
caspase-3 | Homo sapiens (human) | Potency | 61.0684 | 0.0133 | 26.9810 | 70.7614 | AID1346978 |
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a | Homo sapiens (human) | Potency | 48.5084 | 0.0017 | 23.8393 | 78.1014 | AID743083 |
thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 31.6825 | 0.0016 | 28.0151 | 77.1139 | AID1224843; AID1224895; AID1259385; AID1259395 |
v-jun sarcoma virus 17 oncogene homolog (avian) | Homo sapiens (human) | Potency | 41.2480 | 0.0578 | 21.1097 | 61.2679 | AID1159526; AID1159528 |
thyroid hormone receptor beta isoform a | Homo sapiens (human) | Potency | 14.0954 | 0.0100 | 39.5371 | 1,122.0200 | AID588545; AID588547 |
thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 59.9188 | 0.0003 | 23.4451 | 159.6830 | AID743065; AID743067 |
heat shock protein beta-1 | Homo sapiens (human) | Potency | 61.6146 | 0.0420 | 27.3789 | 61.6448 | AID743210 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 40.5262 | 0.0006 | 27.2152 | 1,122.0200 | AID651741; AID743202; AID743219 |
Voltage-dependent calcium channel gamma-2 subunit | Mus musculus (house mouse) | Potency | 61.0684 | 0.0015 | 57.7890 | 15,848.9004 | AID1259244 |
Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 76.8806 | 0.0023 | 19.5956 | 74.0614 | AID651631 |
Glutamate receptor 2 | Rattus norvegicus (Norway rat) | Potency | 61.0684 | 0.0015 | 51.7393 | 15,848.9004 | AID1259244 |
ATPase family AAA domain-containing protein 5 | Homo sapiens (human) | Potency | 61.0684 | 0.0119 | 17.9420 | 71.5630 | AID651632 |
Ataxin-2 | Homo sapiens (human) | Potency | 61.0684 | 0.0119 | 12.2221 | 68.7989 | AID651632 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1419497 | Antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2310 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419532 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 1.95 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081953 | Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081952 | Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081945 | Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1090398 | Antifungal activity against Athelia rolfsii assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1419559 | Selectivity index, ratio of EC100 for toxicity in human A549 cells to MIC50 for antifungal activity against Aspergillus flavus ATCC MYA-3631 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419562 | Selectivity index, ratio of EC100 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Aspergillus nidulans ATCC 38163 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419550 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC 1237 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1092232 | Antifungal activity against Alternaria porri by food poison technique | 2012 | European journal of medicinal chemistry, Dec, Volume: 58 | Synthesis of novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects. |
AID1419561 | Selectivity index, ratio of EC100 for toxicity in human A549 cells to MIC50 for antifungal activity against Aspergillus nidulans ATCC 38163 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081385 | Fungicidal activity against Fusarium oxysporum by poisoned food technique | 2010 | Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5 | Synthesis of nalidixic acid based hydrazones as novel pesticides. |
AID1419547 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2310 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419502 | Antifungal activity against Candida parapsilosis ATCC 22019 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1080819 | Fungicidal activity against Athelia rolfsii assessed as fungal growth inhibition at 28 degC by poisoned food technique | 2009 | Journal of agricultural and food chemistry, Sep-23, Volume: 57, Issue:18 | Schiff bases as potential fungicides and nitrification inhibitors. |
AID1419498 | Antifungal activity against ITC and FLC-resistant Candida albicans ATCC 1237 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419494 | Antifungal activity against Candida albicans ATCC 64124 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1110724 | Antifungal activity against Fusarium sp. assessed as fungal growth (Rvb = 77 mm) | 2000 | Farmaco (Societa chimica italiana : 1989), May, Volume: 55, Issue:5 | Studies on arylfuran derivatives. Part XI. Synthesis, characterisation and biological studies on some Mannich bases carrying 2,4-dichlorophenylfurfural moiety. |
AID1419552 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-1003 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1090395 | Antifungal activity against Macrophomina phaseolina assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1081388 | Fungicidal activity against Rhizoctonia bataticola by poisoned food technique | 2010 | Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5 | Synthesis of nalidixic acid based hydrazones as novel pesticides. |
AID1419533 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 3.9 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419499 | Antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-1003 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419503 | Antifungal activity against Aspergillus flavus ATCC MYA-3631 incubated for 48 hrs by CLSI M38-A2 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419534 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 7.8 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419542 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against Candida albicans ATCC 64124 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419545 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-90819 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419518 | Toxicity in human A549 cells assessed as reduction in cell viability at 15.6 ug/ml incubated for 24 hrs by resazurin dye based assay | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419496 | Antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-90819 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419551 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-1003 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1105386 | Antifungal activity against Athelia rolfsii ITCC 6181 by food poisoning method | 2013 | European journal of medicinal chemistry, Jan, Volume: 59 | Microwave synthesis, characterization and bio-efficacy evaluation of novel chalcone based 6-carbethoxy-2-cyclohexen-1-one and 2H-indazol-3-ol derivatives. |
AID1081386 | Fungicidal activity against Alternaria porri by poisoned food technique | 2010 | Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5 | Synthesis of nalidixic acid based hydrazones as novel pesticides. |
AID1419536 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 31.3 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419544 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2876 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081941 | Antifungal activity against Pythium debaryanum assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081387 | Fungicidal activity against Rhizoctonia solani by poisoned food technique | 2010 | Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5 | Synthesis of nalidixic acid based hydrazones as novel pesticides. |
AID1081949 | Antifungal activity against Fusarium udum assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419537 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 62.5 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419538 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 125 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1101069 | Fungicidal activity against Rhizoctonia solani infected Oryza sativa var. Nipponbare assessed per 10 acres applied by submerged-treatment 7 days prior to infection measured after 5 days | 2000 | Chemical & pharmaceutical bulletin, Aug, Volume: 48, Issue:8 | Synthesis and systemic fungicidal activity of silicon-containing azole derivatives. |
AID1419495 | Antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2876 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419539 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC100 for antifungal activity against Candida albicans ATCC 10231 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419553 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against Candida glabrata ATCC 2001 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1092234 | Antifungal activity against Athelia rolfsii by food poison technique | 2012 | European journal of medicinal chemistry, Dec, Volume: 58 | Synthesis of novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects. |
AID1419501 | Antifungal activity against Candida krusei ATCC 6258 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081954 | Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081958 | Antifungal activity against Athelia rolfsii assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419505 | Antifungal activity against Aspergillus terreus ATCC MYA-3633 incubated for 48 hrs by CLSI M38-A2 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081943 | Antifungal activity against Pythium debaryanum assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081971 | Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081967 | Antifungal activity against Fusarium udum assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419556 | Selectivity index, ratio of EC100 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Candida krusei ATCC 6258 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081957 | Antifungal activity against Athelia rolfsii assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081942 | Antifungal activity against Pythium debaryanum assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081947 | Antifungal activity against Fusarium udum assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419543 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2876 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419549 | Selectivity index, ratio of EC50 for toxicity in human A549 cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC 1237 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419541 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC100 for antifungal activity against Candida albicans ATCC 10231 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081959 | Antifungal activity against Pythium debaryanum assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419515 | Toxicity in human BEAS2B cells assessed as reduction in cell viability incubated for 24 hrs by resazurin dye based assay | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081956 | Antifungal activity against Athelia rolfsii assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419493 | Antifungal activity against Candida albicans ATCC 10231 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419557 | Selectivity index, ratio of EC100 for toxicity in human A549 cells to MIC50 for antifungal activity against Candida parapsilosis ATCC 22019 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419554 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Candida glabrata ATCC 2001 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419535 | Hemolytic activity in mouse erythrocytes assessed as hemolysis level at 15.6 ug/ml incubated for 1 hr at 37 degC | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419558 | Selectivity index, ratio of EC100 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Candida parapsilosis ATCC 22019 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419514 | Toxicity in human A549 cells assessed as reduction in cell viability incubated for 24 hrs by resazurin dye based assay | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1080818 | Fungicidal activity against Rhizoctonia bataticola assessed as fungal growth inhibition at 28 degC by poisoned food technique | 2009 | Journal of agricultural and food chemistry, Sep-23, Volume: 57, Issue:18 | Schiff bases as potential fungicides and nitrification inhibitors. |
AID1081963 | Antifungal activity against Pythium aphanidermatum assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1090396 | Antifungal activity against Rhizoctonia bataticola assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1419548 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against ITC and FLC-susceptible Candida albicans ATCC MYA-2310 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1090393 | Antifungal activity against Pythium debaryanum assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1419540 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Candida albicans ATCC 64124 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081955 | Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1105385 | Antifungal activity against Rhizoctonia solani ITCC 5563 by food poisoning method | 2013 | European journal of medicinal chemistry, Jan, Volume: 59 | Microwave synthesis, characterization and bio-efficacy evaluation of novel chalcone based 6-carbethoxy-2-cyclohexen-1-one and 2H-indazol-3-ol derivatives. |
AID1081951 | Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081389 | Fungicidal activity against Athelia rolfsii by poisoned food technique | 2010 | Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5 | Synthesis of nalidixic acid based hydrazones as novel pesticides. |
AID1092233 | Antifungal activity against Fusarium oxysporum by food poison technique | 2012 | European journal of medicinal chemistry, Dec, Volume: 58 | Synthesis of novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects. |
AID1081979 | Antifungal activity against Athelia rolfsii assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1090397 | Antifungal activity against Rhizoctonia solani Nees assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1081944 | Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081950 | Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 7.25 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1081975 | Antifungal activity against Rhizoctonia solani assessed as growth inhibition by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419519 | Toxicity in human BEAS2B cells assessed as reduction in cell viability at 15.6 ug/ml incubated for 24 hrs by resazurin dye based assay | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419504 | Antifungal activity against Aspergillus nidulans ATCC 38163 incubated for 48 hrs by CLSI M38-A2 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419500 | Antifungal activity against Candida glabrata ATCC 2001 incubated for 48 hrs by modified CLSI M27-A3 protocol based method | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1090394 | Antifungal activity against Pythium aphanidermatum assessed as inhibition of fungal growth | 2006 | Journal of agricultural and food chemistry, Mar-22, Volume: 54, Issue:6 | Antifungal activity of 4-methyl-6-alkyl-2H-pyran-2-ones. |
AID1081946 | Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 31 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
AID1419560 | Selectivity index, ratio of EC100 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Aspergillus flavus ATCC MYA-3631 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419555 | Selectivity index, ratio of EC100 for toxicity in human A549 cells to MIC50 for antifungal activity against Candida krusei ATCC 6258 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419564 | Selectivity index, ratio of EC100 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against Aspergillus terreus ATCC MYA-3633 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1419546 | Selectivity index, ratio of EC50 for toxicity in human BEAS2B cells to MIC50 for antifungal activity against ITC and FLC-resistant Candida albicans ATCC MYA-90819 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1092235 | Antifungal activity against Rhizoctonia bataticola by food poison technique | 2012 | European journal of medicinal chemistry, Dec, Volume: 58 | Synthesis of novel 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-thiones and evaluation of their biocidal effects. |
AID1419563 | Selectivity index, ratio of EC100 for toxicity in human A549 cells to MIC50 for antifungal activity against Aspergillus terreus ATCC MYA-3633 | 2017 | European journal of medicinal chemistry, Jun-16, Volume: 133 | Novel alkylated azoles as potent antifungals. |
AID1081948 | Antifungal activity against Fusarium udum assessed as growth inhibition at 15.50 ug/ml by poisoned food technique | 2011 | Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 | Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 23 (25.27) | 29.6817 |
2010's | 51 (56.04) | 24.3611 |
2020's | 17 (18.68) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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 strong demand-to-supply ratio for research on this compound.
| This Compound (40.03) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 1 (1.10%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 90 (98.90%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |