SYDOWININ A

COC(=O)C1=CC=CC2=C1C(=O)C3=C(O)C=C(CO)C=C3O2

InChIKey=UBYOEDLUKKPPPN-UHFFFAOYSA-N

InChI=1S/C16H12O6/c1-21-16(20)9-3-2-4-11-13(9)15(19)14-10(18)5-8(7-17)6-12(14)22-11/h2-6,17-18H,7H2,1H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Targets

Primary Target	Pharmacology	Condition	Potency
lymphocyte proliferation 2 Target ID: GO:0046651 Sources: https://www.ncbi.nlm.nih.gov/pubmed/30544794	Inhibitor 8297

PubMed

Title	Date	PubMed
A novel dihydroxanthenone, AGI-B4 with inhibition of VEGF-induced endothelial cell growth.	2002 Jul	12243460
Combined Cytotoxicity of the Phycotoxin Okadaic Acid and Mycotoxins on Intestinal and Neuroblastoma Human Cell Models.	2018 Dec 8	30544794

Substance Class	Chemical Created by `admin` on `Sat Dec 16 12:28:27 GMT 2023` Edited by `admin` on `Sat Dec 16 12:28:27 GMT 2023`
Record UNII	ZS4IVQ1908
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

SYDOWININ A

Common Name

English

METHYL 8-HYDROXY-6-(HYDROXYMETHYL)-9-OXO-XANTHENE-1-CARBOXYLATE

Systematic Name

English

9H-XANTHENE-1-CARBOXYLIC ACID, 8-HYDROXY-6-(HYDROXYMETHYL)-9-OXO-, METHYL ESTER

Systematic Name

English

Code System Code Type Description

CAS

58450-01-4

Created by admin on Sat Dec 16 12:28:27 GMT 2023 , Edited by admin on Sat Dec 16 12:28:27 GMT 2023

PRIMARY

FDA UNII

ZS4IVQ1908

Created by admin on Sat Dec 16 12:28:27 GMT 2023 , Edited by admin on Sat Dec 16 12:28:27 GMT 2023

PRIMARY

EPA CompTox

DTXSID00635917

Created by admin on Sat Dec 16 12:28:27 GMT 2023 , Edited by admin on Sat Dec 16 12:28:27 GMT 2023

PRIMARY

PUBCHEM

23872092

Created by admin on Sat Dec 16 12:28:27 GMT 2023 , Edited by admin on Sat Dec 16 12:28:27 GMT 2023

PRIMARY