CINNABARINIC ACID

Details

Stereochemistry	ACHIRAL
Molecular Formula	C14H8N2O6
Molecular Weight	300.2231
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

NC1=C(C(O)=O)C2=NC3=C(OC2=CC1=O)C=CC=C3C(O)=O

InChI

InChIKey=FSBKJYLVDRVPTK-UHFFFAOYSA-N

InChI=1S/C14H8N2O6/c15-10-6(17)4-8-12(9(10)14(20)21)16-11-5(13(18)19)2-1-3-7(11)22-8/h1-4H,15H2,(H,18,19)(H,20,21)

HIDE SMILES / InChI

Molecular Formula	C14H8N2O6
Molecular Weight	300.2231
Charge	0
Count

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

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Metabotropic glutamate receptor 4 5 Target ID: P31423 Gene ID: 24417.0 Gene Symbol: Grm4 Target Organism: Rattus norvegicus (Rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/22311707	Agonist 2752

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:59:34 GMT 2025` Edited by `admin` on `Mon Mar 31 18:59:34 GMT 2025`
Record UNII	2XYB6EX2PG
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CINNABARINIC ACID

Common Name

English

2-AMINO-3-OXO-3H-PHENOXAZINE-1,9-DICARBOXYLIC ACID

Preferred Name

English

2-AMINO-3-OXO-3H-PHENOXAZIN-1,9-DICARBOXYLIC ACID

Systematic Name

English

2-AMINO-3H-PHENOXAZIN-ONE-1,9-DICARBOXYLIC ACID

Systematic Name

English

3H-PHENOXAZIN-1,9-DICARBOXYLIC ACID, 2-AMINO-3-OXO-

Systematic Name

English

CYNNABARINNIC ACID

Common Name

English

3H-PHENOXAZINE-1,9-DICARBOXYLIC ACID, 2-AMINO-3-OXO-

Common Name

English

Code System Code Type Description

PUBCHEM

114918

Created by admin on Mon Mar 31 18:59:34 GMT 2025 , Edited by admin on Mon Mar 31 18:59:34 GMT 2025

PRIMARY

CAS

606-59-7

Created by admin on Mon Mar 31 18:59:34 GMT 2025 , Edited by admin on Mon Mar 31 18:59:34 GMT 2025

PRIMARY

FDA UNII

2XYB6EX2PG

Created by admin on Mon Mar 31 18:59:34 GMT 2025 , Edited by admin on Mon Mar 31 18:59:34 GMT 2025

PRIMARY

EPA CompTox

DTXSID30209408

Created by admin on Mon Mar 31 18:59:34 GMT 2025 , Edited by admin on Mon Mar 31 18:59:34 GMT 2025

PRIMARY