Compounds > thaxtomine a
Page last updated: 2024-11-08

thaxtomine a

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Description

thaxtomine A: a phytotoxin produced by Streptomyces scabies; RN given for (3R-trans)-isomer; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID180098
CHEMBL ID2270642
SCHEMBL ID12381685
MeSH IDM0360825

Synonyms (19)

Synonym
thaxtomine a
phytotoxin 1 (streptomyces scabies)
nsc-630669
nsc630669
thaxtomin a
(3r,6s)-3-hydroxy-3-[(3-hydroxyphenyl)methyl]-1,4-dimethyl-6-[(4-nitro-1h-indol-3-yl)methyl]piperazine-2,5-dione
thaztomin a
2,5-piperazinedione, 3-hydroxy-3-((3-hydroxyphenyl)methyl)-1,4-dimethyl-6-((4-nitro-1h-indol-3-yl)methyl)-, (3r-trans)-
122380-18-1
2,5-piperazinedione, 3-hydroxy-3-((3-hydroxyphenyl)methyl)-1,4-dimethyl-6-((4-nitro-1h-indol-3-yl)methyl)-, (3r,6s)-
CHEMBL2270642
SCHEMBL12381685
HB4107
J-004796
2,5-piperazinedione, 3-hydroxy-3-[(3-hydroxyphenyl)methyl]-1,4-dimethyl-6-[(4-nitro-1h-indol-3-yl)methyl]-, (3r,6s)-
XEA38018
CS-0085883
HY-124212
AKOS040754179

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The four selected compounds show effective herbicidal activities against Brassica campestris, Amaranthus retroflexus, and Abutilon theophrasti, which are comparable or better than dichlobenil, even at a dosage of 187."( Synthesis and biological evaluations of a series of thaxtomin analogues.
Hang, H; Li, Y; Lu, X; Ma, J; Ning, X; Niu, C; Song, H; Wang, PG; Wang, Q; Wang, X; Yang, X; Zhang, H; Zhang, J, 2015)		0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (98)

Assay IDTitleYearJournalArticle
AID1101358Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as stunting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101370Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 0.5 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101408Growth inhibition of Arabidopsis thaliana var. Columbia assessed as stunting after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101406Herbicidal activity against Agrostis stolonifera var. palustris assessed as stunting after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101330Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 100 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101421Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 25 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101392Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 4 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101420Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 1 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101367Pre-emergence growth inhibition of Avena fatua assessed as visual injury at 1 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101323Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 10 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101415Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 0.2 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101411Herbicidal activity against Lemna minor (common duckweed) after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101379Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 2 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101347Pre-emergence growth inhibition of Helianthus annuus (sunflower) after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101390Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 1 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101371Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 2 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101319Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 1 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101374Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 1 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101332Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 10 ug/seedling applied to leaf after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101383Post-emergence growth inhibition of Avena fatua assessed as visual injury at 0.5 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101422Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 5 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101423Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 0.2 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101378Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 0.5 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101360Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as stunting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101414Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 0.04 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101327Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 100 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101404Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 4 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101419Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 0.008 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101410Growth inhibition of Arabidopsis thaliana var. Columbia after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101340Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as meristematic at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101395Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 0.5 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101338Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as meristematic at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101320Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 10 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101324Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 100 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101352Post-emergence growth inhibition of Avena fatua assessed as meristematic at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101350Post-emergence growth inhibition of Avena fatua assessed as wilting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101336Pre-emergence growth inhibition of Avena fatua assessed as meristematic at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101398Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 4 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101349Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as wilting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101322Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 1 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101380Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 4 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101412Herbicidal activity against Agrostis stolonifera var. palustris after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101321Herbicidal activity against Helianthus annuus (sunflower) assessed as visual injury at 100 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101391Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 2 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101407Growth inhibition of Arabidopsis thaliana var. Columbia assessed as root tip puffing after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101384Post-emergence growth inhibition of Avena fatua assessed as visual injury at 1 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101385Post-emergence growth inhibition of Avena fatua assessed as visual injury at 2 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101366Pre-emergence growth inhibition of Avena fatua assessed as visual injury at 2 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101386Post-emergence growth inhibition of Avena fatua assessed as visual injury at 4 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101424Herbicidal activity against Agrostis stolonifera var. palustris assessed as visual injury at 0.04 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101329Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 10 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101402Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 1 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101369Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 1 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101397Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 2 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101335Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 10 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101339Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as meristematic at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101351Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as wilting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101353Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as wilting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101376Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 2 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101333Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 100 ug/seedling applied to leaf after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101403Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 2 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101356Post-emergence growth inhibition of Avena fatua assessed as stunting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101377Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 1 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101359Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as stunting at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101361Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101348Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101343Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as stunting at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101346Pre-emergence growth inhibition of Avena fatua after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101372Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 0.5 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101413Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 0.008 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101405Herbicidal activity against Agrostis stolonifera var. palustris assessed as root tip puffing after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101409Herbicidal activity against Agrostis stolonifera var. palustris after 9 days by agarose-based test2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101345Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101334Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 1 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101342Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as stunting at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101357Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as meristematic at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101365Pre-emergence growth inhibition of Avena fatua assessed as visual injury at 0.5 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101368Pre-emergence growth inhibition of Avena fatua assessed as visual injury at 4 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101363Post-emergence growth inhibition of Helianthus annuus (sunflower) after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101373Pre-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 4 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101355Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as meristematic at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101354Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as meristematic at 0.5 to 4 kg/ha after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101344Pre-emergence growth inhibition of Helianthus annuus (sunflower) assessed as stunting at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101417Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 25 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101416Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 1 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101396Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 1 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101362Post-emergence growth inhibition of Avena fatua after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101337Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 100 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101328Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 1 ug/seedling applied to meristem after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101401Post-emergence growth inhibition of Helianthus annuus (sunflower) assessed as visual injury at 0.5 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101418Herbicidal activity against Lemna minor (common duckweed) assessed as visual injury at 5 ppm after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101325Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 1 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101326Herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 10 ug/seedling applied to cotyledon after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101331Herbicidal activity against Abutilon theophrasti (velvetleaf) assessed as visual injury at 1 ug/seedling applied to leaf after 1 week relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101341Pre-emergence growth inhibition of Avena fatua assessed as stunting at 0.5 to 4 kg/ha after 16 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101375Pre-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) assessed as visual injury at 4 kg/ha after 16 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101364Post-emergence herbicidal activity against Ipomoea hederacea (ivy-leaved morning glory) after 9 days2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
AID1101389Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as visual injury at 0.5 kg/ha after 9 days relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Herbicidal properties of the thaxtomin group of phytotoxins.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (63)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's26 (41.27)29.6817
2010's33 (52.38)24.3611
2020's4 (6.35)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.22

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 Index11.22 (24.57)
Research Supply Index4.16 (2.92)
Research Growth Index5.38 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.22)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (4.76%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other60 (95.24%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
salicylic acid
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).		2.0710monohydroxybenzoic acidalgal metabolite;
antifungal agent;
antiinfective agent;
EC 1.11.1.11 (L-ascorbate peroxidase) inhibitor;
keratolytic drug;
plant hormone;
plant metabolite
hydrogen
Hydrogen: The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas.. dihydrogen : An elemental molecule consisting of two hydrogens joined by a single bond.		2.0210elemental hydrogen;
elemental molecule;
gas molecular entity		antioxidant;
electron donor;
food packaging gas;
fuel;
human metabolite
indoleacetic acid
indoleacetic acid: RN given refers to unlabeled parent cpd; structure in Merck Index, 9th ed, #4841. auxin : Any of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek alphaupsilonxialphanuomega, "to grow").. indole-3-acetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1H-indol-3-yl group.		2.5220indole-3-acetic acids;
monocarboxylic acid		auxin;
human metabolite;
mouse metabolite;
plant hormone;
plant metabolite
pipecolic acid
pipecolic acid: RN given refers to cpd without isomeric designation. pipecolic acid : A piperidinemonocarboxylic acid in which the carboxy group is located at position C-2.. pipecolate : A piperidinecarboxylate that is the conjugate base of pipecolic acid.		2.1710piperidinemonocarboxylic acid
nitrates
Nitrates: Inorganic or organic salts and esters of nitric acid. These compounds contain the NO3- radical.		3.5420monovalent inorganic anion;
nitrogen oxoanion;
reactive nitrogen species
nitrites
Nitrites: Salts of nitrous acid or compounds containing the group NO2-. The inorganic nitrites of the type MNO2 (where M=metal) are all insoluble, except the alkali nitrites. The organic nitrites may be isomeric, but not identical with the corresponding nitro compounds. (Grant & Hackh's Chemical Dictionary, 5th ed)		2.0210monovalent inorganic anion;
nitrogen oxoanion;
reactive nitrogen species		human metabolite
7-nitroindazole
7-nitroindazole: an inhibitor of nitric oxide synthase; exhibits anti-nociceptive activity without increasing blood pressure		2.0210
pimagedine
pimagedine: diamine oxidase & nitric oxide synthase inhibitor; an advanced glycosylation end product inhibitor; used in the treatment of diabetic complications; structure. aminoguanidine : A one-carbon compound whose unique structure renders it capable of acting as a derivative of hydrazine, guanidine or formamide.		2.0210guanidines;
one-carbon compound		EC 1.14.13.39 (nitric oxide synthase) inhibitor;
EC 1.4.3.4 (monoamine oxidase) inhibitor
dichlobanil
2,6-dichlorobenzonitrile : A nitrile that is benzonitrile which is substituted by chlorines at positions 2 and 6. A cellulose synthesis inhibitor, it is used as a pre-emergent and early post-emergent herbicide.		2.4320dichlorobenzene;
nitrile		agrochemical;
cellulose synthesis inhibitor;
environmental contaminant;
herbicide;
xenobiotic
phenylalanine
Phenylalanine: An essential aromatic amino acid that is a precursor of MELANIN; DOPAMINE; noradrenalin (NOREPINEPHRINE), and THYROXINE.. L-phenylalanine : The L-enantiomer of phenylalanine.. phenylalanine : An aromatic amino acid that is alanine in which one of the methyl hydrogens is substituted by a phenyl group.		2.0110amino acid zwitterion;
erythrose 4-phosphate/phosphoenolpyruvate family amino acid;
L-alpha-amino acid;
phenylalanine;
proteinogenic amino acid		algal metabolite;
EC 3.1.3.1 (alkaline phosphatase) inhibitor;
Escherichia coli metabolite;
human xenobiotic metabolite;
micronutrient;
mouse metabolite;
nutraceutical;
plant metabolite;
Saccharomyces cerevisiae metabolite
tryptophan
Tryptophan: An essential amino acid that is necessary for normal growth in infants and for NITROGEN balance in adults. It is a precursor of INDOLE ALKALOIDS in plants. It is a precursor of SEROTONIN (hence its use as an antidepressant and sleep aid). It can be a precursor to NIACIN, albeit inefficiently, in mammals.. tryptophan : An alpha-amino acid that is alanine bearing an indol-3-yl substituent at position 3.		4.2450erythrose 4-phosphate/phosphoenolpyruvate family amino acid;
L-alpha-amino acid zwitterion;
L-alpha-amino acid;
proteinogenic amino acid;
tryptophan zwitterion;
tryptophan		antidepressant;
Escherichia coli metabolite;
human metabolite;
micronutrient;
mouse metabolite;
nutraceutical;
plant metabolite;
Saccharomyces cerevisiae metabolite
arginine
Arginine: An essential amino acid that is physiologically active in the L-form.. arginine : An alpha-amino acid that is glycine in which the alpha-is substituted by a 3-guanidinopropyl group.		2.4220arginine;
glutamine family amino acid;
L-alpha-amino acid;
proteinogenic amino acid		biomarker;
Escherichia coli metabolite;
micronutrient;
mouse metabolite;
nutraceutical
alpha-naphthylphthalamic acid
alpha-naphthylphthalamic acid: RN given refers to parent cpd; structure. naptalam : A dicarboxylic acid monoamide which results from addition of one equivalent of 1-naphthylamine to phthalic anhydride.		2.0810carboxylic acid;
dicarboxylic acid monoamide;
N-(1-naphthyl)carboxamide		herbicide
indazoles
Indazoles: A group of heterocyclic aromatic organic compounds consisting of the fusion of BENZENE and PYRAZOLES.		2.0210indazole
cellobiose
beta-cellobiose : A cellobiose with beta configuration at the reducing-end glucose residue.		3.1950cellobioseepitope
ng-nitroarginine methyl ester
NG-Nitroarginine Methyl Ester: A non-selective inhibitor of nitric oxide synthase. It has been used experimentally to induce hypertension.		2.0210alpha-amino acid ester;
L-arginine derivative;
methyl ester;
N-nitro compound		EC 1.14.13.39 (nitric oxide synthase) inhibitor
glucose, (beta-d)-isomer
beta-D-glucose : D-Glucopyranose with beta configuration at the anomeric centre.. (1->4)-beta-D-glucan : A beta-D-glucan in which the glucose units are connected by (1->4) linkages.. (1->3)-beta-D-glucan : A beta-D-glucan in which the glucose units are connected by (1->3) linkages.		210D-glucopyranoseepitope;
mouse metabolite
isoxaben
isoxaben : A benzamide obtained by formal condensation of the carboxy group of 2,6-dimethoxybenzoic acid and the amino group of 3-(3-methylpentan-3-yl)-1,2-oxazol-5-amine.		3.1650benzamides;
isoxazoles		cellulose synthesis inhibitor;
herbicide
1-phenazinecarboxylic acid
1-phenazinecarboxylic acid: from Streptomyces cinnamonensis; RN given refers to parent cpd; structure given in first source. phenazine-1-carboxylic acid : An aromatic carboxylic acid that is phenazine substituted at C-1 with a carboxy group.		2.4920aromatic carboxylic acid;
monocarboxylic acid;
phenazines		antifungal agent;
antimicrobial agent;
bacterial metabolite
n(omega)-hydroxyarginine
N(omega)-hydroxyarginine: can cause vasorelaxation of bovine intrapulmonary artery; structure given in first source. N(5)-[(Z)-amino(hydroxyimino)methyl]-L-ornithine : An N(5)-[amino(hydroxyimino)methyl]-L-ornithine in which the double bond has Z-configuration.		2.0210amino acid zwitterion;
N(5)-[(E)-amino(hydroxyimino)methyl]ornithine;
N(5)-[(hydroxyamino)(imino)methyl]ornithine;
N(5)-[(Z)-amino(hydroxyimino)methyl]ornithine;
N(5)-[amino(hydroxyimino)methyl]-L-ornithine;
N(5)-[amino(hydroxyimino)methyl]ornithine;
N(omega)-hydroxy-L-arginine
omega-n-methylarginine
omega-N-Methylarginine: A competitive inhibitor of nitric oxide synthetase.. N(omega)-methyl-L-arginine : A L-arginine derivative with a N(omega)-methyl substituent.		2.0210amino acid zwitterion;
arginine derivative;
guanidines;
L-arginine derivative;
non-proteinogenic L-alpha-amino acid
lignin
Lignin: The most abundant natural aromatic organic polymer found in all vascular plants. Lignin together with cellulose and hemicellulose are the major cell wall components of the fibers of all wood and grass species. Lignin is composed of coniferyl, p-coumaryl, and sinapyl alcohols in varying ratios in different plant species. (From Merck Index, 11th ed). lignin : A polyphenylpropanoid derived from three monolignol monomers: trans-p-coumaryl alcohol, coniferol and trans-sinapyl alcohol. There is extensive cross-linking and no defined primary structure.		2.0510
thaxtomine b
thaxtomine B: RN given for (3R-trans)-isomer; a phytotoxin produced by Streptomyces scabies; structure in first source		3.1350
solanine
Solanine: A mixture of alpha-chaconine and alpha-solanine, found in SOLANACEAE plants.. solanine : A glycoalkaloid poison found in species of the nightshade family (Solanaceae), such as the potato (Solanum tuberosum). It is a trisccharide derivative of solanidine [(22beta)-solanid-5-en-3beta-ol].		2.0310
actinorhodin
actinorhodin: structure. actinorhodin : A member of the class of benzoisochromanequinone that is produced by Streptomyces coelicolor A3(2) and exhibits antibiotic activity.		2.0710
alpha-chaconine
alpha-chaconine: glycoside of solanidine; structure in 5th source		2.0310glycoalkaloid;
steroid saponin
pectins
Pectins: High molecular weight polysaccharides present in the cell walls of all plants. Pectins cement cell walls together. They are used as emulsifiers and stabilizers in the food industry. They have been tried for a variety of therapeutic uses including as antidiarrheals, where they are now generally considered ineffective, and in the treatment of hypercholesterolemia.. alpha-D-galacturonic acid : The alpha-anomer of D-galacturonic acid.		2.0510D-galactopyranuronic acid
sesquiterpenes
[no description available]		2.0510
D-fructopyranose
[no description available]		210cyclic hemiketal;
D-fructose;
fructopyranose		sweetening agent
scopoletin
[no description available]		2.0510hydroxycoumarinplant growth regulator;
plant metabolite
concanamycin b
concanamycin B: from Streptomyces diastatochromogenes S-45; structure given in first source		3.1910
concanamycin a
concanamycin A: from Streptomyces diastatochromogenes S-45; inhibits vacuolar H+ ATPase. concanamycin A : A concanamycin in which the lactone ring contains 4 double bonds and is substituted by 4 methyl groups, 2 hydroxy groups, 2 methoxy groups and an ethyl group.		3.1910carbamate ester;
concanamycin		antifungal agent;
EC 3.6.3.14 (H(+)-transporting two-sector ATPase) inhibitor;
metabolite
fd 891
FD 891: an 18-membered macrolide with an epoxide ring at C8 and C9; the epoxide may play an important role in its cytocidal activity; structure given in first source		3.1910
cytochrome c-t
Cytochromes c: Cytochromes of the c type that are found in eukaryotic MITOCHONDRIA. They serve as redox intermediates that accept electrons from MITOCHONDRIAL ELECTRON TRANSPORT COMPLEX III and transfer them to MITOCHONDRIAL ELECTRON TRANSPORT COMPLEX IV.		2.0210
cellulose
DEAE-Cellulose: Cellulose derivative used in chromatography, as ion-exchange material, and for various industrial applications.		3.3160glycoside
ubiquinone
Ubiquinone: A lipid-soluble benzoquinone which is involved in ELECTRON TRANSPORT in mitochondrial preparations. The compound occurs in the majority of aerobic organisms, from bacteria to higher plants and animals.		2.610
borrelidin
treponemycin: isolated from Streptomyces albovinaceous; active against Treponema hyodysenteriae. borrelidin : A macrolide that is isolated from several Streptomyces species and displays antibiotic, antineoplastic and antimalarial properties.		3.1910aliphatic nitrile;
diol;
macrolide;
monocarboxylic acid;
secondary alcohol		antifungal agent;
antimalarial;
antimicrobial agent;
antineoplastic agent;
apoptosis inducer;
bacterial metabolite
heme
Heme: The color-furnishing portion of hemoglobin. It is found free in tissues and as the prosthetic group in many hemeproteins.. ferroheme : Any iron(II)--porphyrin coordination complex.. ferroheme b : Heme b in which the iron has oxidation state +2.. heme : A heme is any tetrapyrrolic chelate of iron.		3.1710
methylnitronitrosoguanidine
Methylnitronitrosoguanidine: A nitrosoguanidine derivative with potent mutagenic and carcinogenic properties.. N-methyl-N'-nitro-N-nitrosoguanidine : An N-nitroguanidine compound having nitroso and methyl substituents at the N'-position		2.0210nitroso compoundalkylating agent
ConditionIndicatedRelationship StrengthStudiesTrials
Disease Resistance
The capacity of an organism to defend itself against pathological processes or the agents of those processes. This most often involves innate immunity whereby the organism responds to pathogens in a generic way. The term disease resistance is used most frequently when referring to plants.		02.3110
Genetic Predisposition
[description not available]		02.0510