baeomycesic acid

Description

baeomycesic acid: structure in first source [MeSH]

Baeomycesic acid : no description available [CHeBI]

Cross-References

ID Source	ID
PubMed CID	5321461
CHEMBL ID	2227773
SCHEMBL ID	18621794
CHEBI ID	144121
MeSH ID	M0480704

Synonyms (8)

Synonym
baeomycesic acid
CHEBI:144121
4-(3-formyl-2-hydroxy-4-methoxy-6-methylbenzoyl)oxy-2-hydroxy-3,6-dimethylbenzoic acid
CHEMBL2227773
baeomycessaure
baeomycesicacid
644-66-6
SCHEMBL18621794

Drug Classes (1)

Class	Description
carbonyl compound	Any compound containing the carbonyl group, C=O. The term is commonly used in the restricted sense of aldehydes and ketones, although it actually includes carboxylic acids and derivatives.

Bioassays (27)

Assay ID	Title	Year	Journal	Article
AID1081962	Antifungal activity against Pythium debaryanum assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081970	Antifungal activity against Fusarium udum assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID977599	Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM	2013	Molecular pharmacology, Jun, Volume: 83, Issue:6 ISSN: 1521-0111	Structure-based identification of OATP1B1/3 inhibitors.
AID977602	Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM	2013	Molecular pharmacology, Jun, Volume: 83, Issue:6 ISSN: 1521-0111	Structure-based identification of OATP1B1/3 inhibitors.
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 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081969	Antifungal activity against Fusarium udum assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081961	Antifungal activity against Pythium debaryanum assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081981	Antifungal activity against Athelia rolfsii assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081982	Antifungal activity against Athelia rolfsii assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081978	Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081980	Antifungal activity against Athelia rolfsii assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081960	Antifungal activity against Pythium debaryanum assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
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 ISSN: 1520-5118	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 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081977	Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081964	Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	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 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081974	Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081965	Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	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 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081972	Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081976	Antifungal activity against Rhizoctonia solani assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081968	Antifungal activity against Fusarium udum assessed as growth inhibition at 62.5 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081973	Antifungal activity against Rhizoctonia bataticola assessed as growth inhibition at 125 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
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 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1081966	Antifungal activity against Pythium aphanidermatum assessed as growth inhibition at 250 ug/ml by poisoned food technique	2011	Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6 ISSN: 1520-5118	Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl.
AID1159550	Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening	2015	Nature cell biology, Nov, Volume: 17, Issue:11 ISSN: 1476-4679	6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.

Research

Studies (6)

Timeframe	Studies, This Drug (%)	All Drugs %
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (16.67)	29.6817
2010's	5 (83.33)	24.3611
2020's	0 (0.00)	2.80

Study Types

Publication Type	This drug (%)	All Drugs (%)
Trials	0 (0.00%)	5.53%
Reviews	1 (16.67%)	6.00%
Case Studies	0 (0.00%)	4.05%
Observational	0 (0.00%)	0.25%
Other	5 (83.33%)	84.16%

Substance	Classes	Roles	Relationship Strength
salophen	carbonyl compound		low
aklomide	carbonyl compound; organohalogen compound		low
ethyl citrate	carbonyl compound		low
tributyl citrate	carbonyl compound		low
benzoyl peroxide	carbonyl compound		low
chelidonic acid	carbonyl compound; pyrans		low
toness	carbonyl compound		low
phenyl 4-aminosalicylate	carbonyl compound		low
2-Methoxybenzaldehyde	carbonyl compound		low
acetylsalicylsalicylic acid	carbonyl compound		low
evernic acid	carbonyl compound		low
2,6-dimethoxybenzoic acid	benzenes; carbonyl compound		low
trimethylolpropane trimethacrylate	carbonyl compound		low
2,4,5-trimethoxybenzaldehyde	carbonyl compound		low
benorilate	carbonyl compound		low
3,4-dimethylbenzaldehyde	carbonyl compound		low
psoromic acid	carbonyl compound		low
trimethylolpropane triacrylate	carbonyl compound		low
flurofamide	carbonyl compound; organohalogen compound		low
Eugenyl benzoate	carbonyl compound		low
simvastatin acid	carbonyl compound		low
magnesium salicylate	benzenes; carbonyl compound		low
physodic acid	carbonyl compound		low
toxoflavin	carbonyl compound; pyrimidotriazine	antibacterial agent; antineoplastic agent; apoptosis inducer; bacterial metabolite; toxin; virulence factor; Wnt signalling inhibitor	low
atranorin	carbonyl compound		low
guacetisal	carbonyl compound		low
alloclamide	carbonyl compound; organohalogen compound		low
lobaric acid	carbonyl compound		low
carbetapentane citrate	carbonyl compound		low
diffractaic acid	carbonyl compound		low
fluorocitrate	carbonyl compound		low
nitroaspirin	carbonyl compound		low
hydroxycitric acid	carbonyl compound		low
4-iodo-n-piperidinoethylbenzamide	carbonyl compound; organohalogen compound		low
gyrophoric acid	carbonyl compound		low
barbatic acid	carbonyl compound		low
perlatolinic acid	carbonyl compound		low
vernodalin	carbonyl compound		low
hydroxycitric acid	carbonyl compound		low
2-[(2-methoxy-2-oxoethyl)thio]benzoic acid methyl ester	carbonyl compound		low
olivetoric acid	carbonyl compound		low
3-butene-1,2,3-tricarboxylic acid	carbonyl compound		low
3-bromo-N-[2-(4-nitroanilino)ethyl]benzamide	carbonyl compound; organohalogen compound		low
4-chloro-N-(2,3-dihydro-1,4-benzodioxin-3-ylmethyl)benzamide	carbonyl compound; organohalogen compound		low
2-(2-methoxyethylthio)-N-(1,3,4-thiadiazol-2-yl)benzamide	carbonyl compound		low
2,4-difluoro-N-[[(5-methyl-1H-pyrazol-3-yl)amino]-oxomethyl]benzamide	carbonyl compound; organohalogen compound		low
3-(4-methylbenzoyl)acrylic acid	carbonyl compound		low
2-chloro-N-(2-phenylethyl)benzamide	carbonyl compound; organohalogen compound		low
N-[2-(1-cyclohexenyl)ethyl]-4-fluorobenzamide	carbonyl compound; organohalogen compound		low
N-[2-(1H-benzimidazol-2-yl)ethyl]-4-chloro-3-nitrobenzamide	carbonyl compound; organohalogen compound		low
N'-[(4-chlorophenyl)-oxomethyl]-2-pyrazinecarbohydrazide	carbonyl compound; organohalogen compound		low
1-azepanyl-[2-methoxy-4-(methylthio)phenyl]methanone	carbonyl compound; thiol		low
4-chloro-N-(4-methyl-2-thiazolyl)-2-nitrobenzamide	carbonyl compound; organohalogen compound		low
3-fluoro-N-(1H-1,2,4-triazol-5-yl)benzamide	carbonyl compound; organohalogen compound		low
3-bromo-N-(2-furanylmethyl)benzamide	carbonyl compound; organohalogen compound		low
N'-[(2-chlorophenyl)-oxomethyl]-2-thiophenecarbohydrazide	carbonyl compound; organohalogen compound		low
n-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide	carbonyl compound; organohalogen compound		low
4-fluoro-N-(5-methyl-2-pyridinyl)benzamide	carbonyl compound; organohalogen compound		low
2-methoxy-4-(methylthio)-N-pyridin-4-ylbenzamide	carbonyl compound; thiol		low
2-chloro-4,5-difluoro-N-(5-methyl-2-pyridinyl)benzamide	carbonyl compound; organohalogen compound		low
3-bromo-N-[(tert-butylamino)-sulfanylidenemethyl]-4-methoxybenzamide	carbonyl compound; organohalogen compound		low
4-chloro-N-[[(4,6-dimethyl-2-pyrimidinyl)thio]methyl]benzamide	carbonyl compound; organohalogen compound		low
N'-(1,3-benzothiazol-2-yl)-4-fluorobenzohydrazide	carbonyl compound; organohalogen compound		low
4-chloro-N-(1,2-dimethyl-5-benzimidazolyl)benzamide	carbonyl compound; organohalogen compound		low
1-[[(2-chlorophenyl)-oxomethyl]amino]-3-(2-methoxy-5-methylphenyl)thiourea	carbonyl compound; organohalogen compound		low
2-bromo-N-[2,3-dihydroindol-1-yl(sulfanylidene)methyl]benzamide	carbonyl compound; organohalogen compound		low
4-bromo-N'-[(4-bromophenyl)-oxomethyl]-1-methyl-3-pyrazolecarbohydrazide	carbonyl compound; organohalogen compound		low
2-fluoro-N-[2-(3-pyridinyl)-3H-benzimidazol-5-yl]benzamide	carbonyl compound; organohalogen compound		low
[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]-[2-(ethylthio)phenyl]methanone	carbonyl compound		low
N'-[2,6-bis(4-morpholinyl)-4-pyrimidinyl]-2,4-dichlorobenzohydrazide	carbonyl compound; organohalogen compound		low
N'-[2,6-bis(4-morpholinyl)-4-pyrimidinyl]-3,4-dichlorobenzohydrazide	carbonyl compound; organohalogen compound		low
4-fluoro-N-(3-pyridinyl)benzamide	carbonyl compound; organohalogen compound		low
4-bromo-N'-(3,4-dihydro-2H-pyrrol-5-yl)benzohydrazide	carbonyl compound; organohalogen compound		low
1-(4-bromophenyl)-4-[1-naphthalenyl(oxo)methyl]-3-pyrazolecarboxylic acid ethyl ester	carbonyl compound; naphthalenes		low
4-methyl-3-(4-morpholinylsulfonyl)benzoic acid [3-[[oxo(thiophen-2-yl)methyl]amino]phenyl] ester	carbonyl compound		low
3-[(2,4-difluorophenoxy)methyl]-4-methoxybenzaldehyde	carbonyl compound		low
4-bromo-3-nitrobenzoic acid [2-[anilino(oxo)methyl]phenyl] ester	carbonyl compound		low
2-bromo-N'-[(3-chlorophenyl)-oxomethyl]benzohydrazide	carbonyl compound; organohalogen compound		low
3-chloro-N-(2-methyl-3-oxo-1,2,4-thiadiazol-5-yl)benzamide	carbonyl compound; organohalogen compound		low
3,4-dichloro-N-(4-chloro-3-methyl-5-isoxazolyl)benzamide	carbonyl compound; organohalogen compound		low
3,4-dichloro-N-(2-thiophen-2-ylethyl)benzamide	carbonyl compound; organohalogen compound		low
3-chloro-N-[3-[[(3-chloro-4-nitrophenyl)-oxomethyl]amino]-2,2-dimethylpropyl]-4-nitrobenzamide	carbonyl compound; organohalogen compound		low
4-chloro-N-[[[oxo-(3,4,5-trimethoxyphenyl)methyl]hydrazo]-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
3-bromo-4-methoxy-N-[(propan-2-ylamino)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
2-(2-methoxyethylthio)-N-(2-thiazolyl)benzamide	carbonyl compound		low
2-(2-methoxyethylthio)-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzamide	carbonyl compound		low
3-bromo-N-[(2-hydroxyethylamino)-sulfanylidenemethyl]-4-methoxybenzamide	carbonyl compound; organohalogen compound		low
N-[[[(2,4-dichlorophenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]-2,2-dimethylpropanamide	carbonyl compound; organohalogen compound		low
4-chloro-N-[(2-methylpropylamino)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
2-chloro-N-[(2-pyrimidinylamino)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
N-[5-(1,3-benzodioxol-5-ylmethyl)-4-methyl-2-thiazolyl]-4-chlorobenzamide	carbonyl compound; organohalogen compound		low
N-(3,5-dichloro-2-pyridinyl)-2-methoxy-4-(methylthio)benzamide	carbonyl compound; thiol		low
2-[[[[(4-fluorophenyl)-oxomethyl]amino]-sulfanylidenemethyl]amino]-4-(5-methyl-2-furanyl)-3-thiophenecarboxylic acid ethyl ester	carbonyl compound; organohalogen compound		low
N-[2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl]-2-fluorobenzamide	carbonyl compound; organohalogen compound		low
2-(1,3,4-oxadiazol-2-yl)phenyl 4-chlorobenzoate	carbonyl compound		low
N'-[(4-chlorophenyl)-oxomethyl]-2-thiophen-2-yl-4-thiazolecarbohydrazide	carbonyl compound; organohalogen compound		low
N'-[(4-chlorophenyl)-oxomethyl]-2-methyl-4-thiazolecarbohydrazide	carbonyl compound; organohalogen compound		low
N-[2-cyano-5-(cyanomethylthio)-4-phenyl-3-thiophenyl]-4-fluorobenzamide	carbonyl compound; organohalogen compound		low
2-chloro-N-[(methylcarbamoylamino)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
t 0070907	carbonyl compound; organohalogen compound		low
4-fluoro-N-(7-methyl-4-oxo-2-thieno[3,2-d][1,3]thiazinyl)benzamide	carbonyl compound; organohalogen compound		low
N'-(4-tert-butyl-2-thiazolyl)-4-chlorobenzohydrazide	carbonyl compound; organohalogen compound		low
N-(4-bromo-2-tert-butyl-5-methyl-3-pyrazolyl)-2,4-dichlorobenzamide	carbonyl compound; organohalogen compound		low
2-[(3-methoxyphenyl)-oxomethyl]-3,3-bis(methylthio)-2-propenenitrile	carbonyl compound		low
4-chloro-N-[2-(4-nitroanilino)ethyl]benzamide	carbonyl compound; organohalogen compound		low
(2-chlorophenyl)-(5-hydroxy-3-methyl-5-phenyl-4H-pyrazol-1-yl)methanone	carbonyl compound; organohalogen compound		low
5-chloro-N-[2-(2-furanyl)-2-(1-pyrrolidinyl)ethyl]-2-methoxybenzamide	carbonyl compound; organohalogen compound		low
(3-bromophenyl)-[5-(4-bromophenyl)-3-ethyl-5-hydroxy-4H-pyrazol-1-yl]methanone	carbonyl compound; organohalogen compound		low
3-chloro-N-(5-chloro-2-pyridinyl)-4-ethoxybenzamide	carbonyl compound; organohalogen compound		low
2-fluoro-N-(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)benzamide	carbonyl compound; organohalogen compound		low
N-[[[(2-chlorophenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]-2-nitrobenzamide	carbonyl compound; organohalogen compound		low
4-chloro-N-[5-(2,3-dihydro-1,4-dioxin-5-yl)-1,3,4-oxadiazol-2-yl]benzamide	carbonyl compound; organohalogen compound		low
2-(2-cyanophenyl)sulfinyl-N-methylbenzamide	carbonyl compound		low
4-fluoro-N-[[2-(3-pyridinyl)-1-piperidinyl]-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
N-[[[(4-fluorophenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]-2-furancarboxamide	carbonyl compound; organohalogen compound		low
3-bromo-4-methyl-N-[(2-oxolanylmethylamino)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
2-chloro-N-[3-[4-[3-[[(2-chloro-5-nitrophenyl)-oxomethyl]amino]propyl]-1-piperazinyl]propyl]-5-nitrobenzamide	carbonyl compound; organohalogen compound		low
2-bromo-N-[[(2-methylcyclohexyl)amino]-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
3-chloro-N-[5-(3-pyridinyl)-1,3,4-oxadiazol-2-yl]benzamide	carbonyl compound; organohalogen compound		low
2-[[2-(cyclohexylamino)-2-oxoethyl]thio]benzoic acid [2-(cyclohexylamino)-2-oxoethyl] ester	carbonyl compound		low
2,4-dichloro-N-[(2,8-dimethyl-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indol-5-yl)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
1-tert-butyl-3-[[(2-chlorophenyl)-oxomethyl]amino]thiourea	carbonyl compound; organohalogen compound		low
4-bromo-N-[(2,8-dimethyl-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indol-5-yl)-sulfanylidenemethyl]benzamide	carbonyl compound; organohalogen compound		low
reductone	carbonyl compound		low
2,5-dichloro-N-[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]benzamide	carbonyl compound; organohalogen compound		low
fulvoplumierin	carbonyl compound; pyrans		low
fumarprotocetraric acid	carbonyl compound		low
Squamatic acid	carbonyl compound		low
reumycin	carbonyl compound; pyrimidotriazine	antimicrobial agent; antineoplastic agent; bacterial metabolite	low
bromebric acid	carbonyl compound		low
3-(dimethylamino)-1-phenylprop-2-en-1-one	carbonyl compound		low
protocetraric acid	carbonyl compound		low
N'1-(6-methylpyridazin-3-yl)-4-chlorobenzene-1-carbohydrazide	carbonyl compound; organohalogen compound		low
pnu-282987	carbonyl compound; organohalogen compound		low
iniparib	carbonyl compound; organohalogen compound		low
mumefural	carbonyl compound		low
3-bromo-N-[5-(4-morpholinylsulfonyl)-1,3,4-thiadiazol-2-yl]benzamide	carbonyl compound; organohalogen compound		low
3-bromo-N-[2-[(3R,6S)-6-[(4-methoxyphenyl)methyl]-3-(phenylmethyl)-2,3,5,6-tetrahydroimidazo[1,2-a]imidazol-7-yl]ethyl]-4-methylbenzamide	carbonyl compound; organohalogen compound		low
(2,6-difluorophenyl)-[4-(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)-1-piperazinyl]methanone	carbonyl compound; organohalogen compound		low
3-[4-[3-(3-fluorophenyl)-3-oxoprop-1-enyl]-1-methyl-2-pyrrolyl]-N-hydroxy-2-propenamide	carbonyl compound		low
N-(1-azabicyclo[2.2.2]octan-3-yl)-6-chloro-7-nitro-1H-benzimidazole-4-carboxamide	carbonyl compound; organohalogen compound		low

Substance	Studies	Classes	Roles	First Year	Last Year	Average Age	Relationship Strength	2010's
hexaconazole	1	dichlorobenzene; tertiary alcohol; triazoles	chelator	2011	2011	13.0	low	1
atranorin	1	carbonyl compound		2011	2011	13.0	low	1
2,4-dihydroxy-6-methylbenzoic acid ethyl ester	1	4-hydroxybenzoate ester		2011	2011	13.0	medium	1
methyl 2,4-dihydroxy-3,6-dimethyl benzoate	1	4-hydroxybenzoate ester		2011	2011	13.0	low	1
Methyl Haematommate	1	4-hydroxybenzoate ester		2011	2011	13.0	medium	1
salazinic acid	1			2011	2011	13.0	low	1
lichexanthone	1	aromatic ether; phenols; xanthones	plant metabolite	2011	2011	13.0	medium	1

Substance	Studies	Classes	Roles	First Year	Last Year	Average Age	Relationship Strength	2000's	2010's
beta-resorcylic acid	1			2011	2011	13.0	low	0	1
emodin	1	trihydroxyanthraquinone	antineoplastic agent; laxative; plant metabolite; tyrosine kinase inhibitor	2004	2004	20.0	low	1	0
usnic acid	1	benzofurans		2004	2004	20.0	low	1	0
4-butyrolactone	1	butan-4-olide	metabolite; neurotoxin	2004	2004	20.0	low	1	0
orcinol	2	5-alkylresorcinol; dihydroxytoluene	Aspergillus metabolite	2011	2013	12.0	medium	0	2
physcione	1	dihydroxyanthraquinone	anti-inflammatory agent; antibacterial agent; antifungal agent; antineoplastic agent; apoptosis inducer; hepatoprotective agent; metabolite	2004	2004	20.0	low	1	0
protolichesterinic acid	1			2004	2004	20.0	low	1	0
atranorin	1	carbonyl compound		2013	2013	11.0	low	0	1
lobaric acid	1	carbonyl compound		2004	2004	20.0	low	1	0
benzofurans	1			2004	2004	20.0	low	1	0
12-hydroxy-5,8,10,14-eicosatetraenoic acid	1			2004	2004	20.0	low	1	0
salicylates	1	monohydroxybenzoate	plant metabolite	2004	2004	20.0	low	1	0

Condition	Studies	First Year	Last Year	Average Age	Relationship Strength	2010's
Benign Neoplasms	1	2015	2015	9.0	high	1
Cancer of Prostate	1	2011	2011	13.0	high	1
Neoplasms	1	2015	2015	9.0	high	1
Prostatic Neoplasms	1	2011	2011	13.0	high	1

Dosage (1)

Article	Year
Anti-proliferative lichen compounds with inhibitory activity on 12(S)-HETE production in human platelets. Phytomedicine : international journal of phytotherapy and phytopharmacology, , Volume: 11, Issue:7-8	2004

baeomycesic acid

Description

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Synonyms (8)

Drug Classes (1)

Bioassays (27)

Research

Studies (6)

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Related Drugs (156)

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