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Details

Stereochemistry ACHIRAL
Molecular Formula C17H16O8
Molecular Weight 348.3041
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ASTERRIC ACID

SMILES

COC(=O)C1=CC(O)=CC(OC)=C1OC2=CC(C)=CC(O)=C2C(O)=O

InChI

InChIKey=XOKVHFNTYHPEHN-UHFFFAOYSA-N
InChI=1S/C17H16O8/c1-8-4-11(19)14(16(20)21)12(5-8)25-15-10(17(22)24-3)6-9(18)7-13(15)23-2/h4-7,18-19H,1-3H3,(H,20,21)

HIDE SMILES / InChI

Molecular Formula C17H16O8
Molecular Weight 348.3041
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.0 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Two new secondary metabolites from the mangrove endophytic fungus Pleosporales sp. SK7.
2020-10
Evaluating the outcomes of submerged co-cultivation: production of lovastatin and other secondary metabolites by Aspergillus terreus in fungal co-cultures.
2019-07
Induction of secondary metabolism of Aspergillus terreus ATCC 20542 in the batch bioreactor cultures.
2016-04
Erratum: Secondary Metabolites from Aspergillus fumigatus, an Endophytic Fungus from the Liverwort Heteroscyphus tener (Steph.) Schiffn.
2015-12
Secondary metabolites from Aspergillus fumigatus, an endophytic fungus from the liverwort Heteroscyphus tener (Steph.) Schiffn.
2015-09
3-Nitroasterric Acid Derivatives from an Antarctic Sponge-Derived Pseudogymnoascus sp. Fungus.
2015-04-24
Bioactive sulfur-containing sulochrin dimers and other metabolites from an Alternaria sp. isolate from a Hawaiian soil sample.
2014-10-24
A new diphenyl ether from Phoma sp. strain, SHZK-2.
2012
New species in Aspergillus section Terrei.
2011-06-30
Metabolites from the endophytic mitosporic Dothideomycete sp. LRUB20.
2009-01
Bioactive asterric acid derivatives from the Antarctic ascomycete fungus Geomyces sp.
2008-09
A new spiroketal from Aspergillus terreus, an endophytic fungus in Opuntia ficusindica Mill.
2008-04
Cyclopentenones, scaffolds for organic syntheses produced by the endophytic fungus mitosporic dothideomycete sp. LRUB20.
2006-09
Fungal metabolites, asterric acid derivatives inhibit vascular endothelial growth factor (VEGF)-induced tube formation of HUVECs.
2002-06
New chlorinated diphenyl ethers from an Aspergillus species.
2002-01
Transformations of Penicillium islandicum and Penicillium frequentans that produce anthraquinone-related compounds.
1995-11
Asterric acid, a new endothelin binding inhibitor.
1992-10
Studies in the biochemistry of micro-organisms. 115. Metabolites of Penicillium frequentans Westling: isolation of sulochrin, asterric acid, (+)-bisdechlorogeodin and two new substituted anthraquinones, questin and questinol.
1964-08
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:09 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:09 GMT 2025
Record UNII
J3Q23XL4KN
Record Status Validated (UNII)
Record Version
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Name Type Language
RES-1214-1
Preferred Name English
ASTERRIC ACID
Common Name English
Benzoic acid, 2-(2-carboxy-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxy-, 1-methyl ester
Systematic Name English
TAN-1415A
Common Name English
2-Hydroxy-6-(4-hydroxy-2-methoxy-6-(methoxycarbonyl)phenoxy)-4-methylbenzoic acid
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID60206405
Created by admin on Mon Mar 31 19:15:09 GMT 2025 , Edited by admin on Mon Mar 31 19:15:09 GMT 2025
PRIMARY
CAS
577-64-0
Created by admin on Mon Mar 31 19:15:09 GMT 2025 , Edited by admin on Mon Mar 31 19:15:09 GMT 2025
PRIMARY
FDA UNII
J3Q23XL4KN
Created by admin on Mon Mar 31 19:15:09 GMT 2025 , Edited by admin on Mon Mar 31 19:15:09 GMT 2025
PRIMARY
PUBCHEM
3080568
Created by admin on Mon Mar 31 19:15:09 GMT 2025 , Edited by admin on Mon Mar 31 19:15:09 GMT 2025
PRIMARY
WIKIPEDIA
Asterric acid
Created by admin on Mon Mar 31 19:15:09 GMT 2025 , Edited by admin on Mon Mar 31 19:15:09 GMT 2025
PRIMARY