RHEOEMODIN

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C14H8O6
Molecular Weight	272.2097
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RHEOEMODIN

Structure Search

SMILES

OC1=CC2=C(C(O)=C1)C(=O)C3=C(O)C=C(O)C=C3C2=O

InChI

InChIKey=NTGIIKCGBNGQAR-UHFFFAOYSA-N

InChI=1S/C14H8O6/c15-5-1-7-11(9(17)3-5)14(20)12-8(13(7)19)2-6(16)4-10(12)18/h1-4,15-18H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

Title	Date	PubMed
High-performance liquid chromatography-off line mass spectrometry analysis of anthraquinones produced by Geosmithia lavendula.	2010-10-01	20801456
Hydroxylated anthraquinones produced by Geosmithia species.	2009	19649732

Name

Type

Language

RHEOEMODIN

Common Name

English

1,3,6,8-TETRAHYDROXY-9,10-ANTHRAQUINONE

Preferred Name

English

1,3,6,8-TETRAHYDROXYANTHRAQUINONE

Systematic Name

English

ANTHRAQUINONE, 1,3,6,8-TETRAHYDROXY-

Systematic Name

English

9,10-ANTHRACENEDIONE, 1,3,6,8-TETRAHYDROXY-

Systematic Name

English

Code System Code Type Description

MESH

C544948

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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CHEBI

68717

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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FDA UNII

701Q96563R

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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CAS

52940-12-2

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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PUBCHEM

3016789

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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EPA CompTox

DTXSID80200980

Created by admin on Mon Mar 31 18:51:23 GMT 2025 , Edited by admin on Mon Mar 31 18:51:23 GMT 2025

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SUBSTANCE RECORD


					701Q96563R