NCS-356

Details

Stereochemistry	RACEMIC
Molecular Formula	C10H9ClO3
Molecular Weight	212.63
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC(\C=C\C(O)=O)C1=CC=C(Cl)C=C1

InChI

InChIKey=FPLZDFIDWYDARU-AATRIKPKSA-N

InChI=1S/C10H9ClO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-6,9,12H,(H,13,14)/b6-5+

HIDE SMILES / InChI

Molecular Formula	C10H9ClO3
Molecular Weight	212.63
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	1
Optical Activity	( + / - )

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Solute carrier family 52, riboflavin transporter, member 2 4 Target ID: Q9HAB3 Gene ID: 79581.0 Gene Symbol: SLC52A2 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/10571257	Agonist 2752

PubMed

Title	Date	PubMed
Gamma-butyrolactone (GBL) disruption of passive avoidance learning in the day-old chick appears to be due to its effect on GABAB not gamma-hydroxybutyric [corrected] acid (GHB) receptors.	2009-02-11	18948143
Gamma-hydroxybutyrate receptor function studied by the modulation of nitric oxide synthase activity in rat frontal cortex punches.	1999-12-01	10571257

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:17:16 GMT 2025` Edited by `admin` on `Mon Mar 31 22:17:16 GMT 2025`
Record UNII	535Z468F1A
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(2E)-4-(4-CHLOROPHENYL)-4-HYDROXY-2-BUTENOIC ACID

Preferred Name

English

NCS-356

Common Name

English

2-BUTENOIC ACID, 4-(4-CHLOROPHENYL)-4-HYDROXY-, (2E)-

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID8048448

Created by admin on Mon Mar 31 22:17:16 GMT 2025 , Edited by admin on Mon Mar 31 22:17:16 GMT 2025

PRIMARY

PUBCHEM

5794315

Created by admin on Mon Mar 31 22:17:16 GMT 2025 , Edited by admin on Mon Mar 31 22:17:16 GMT 2025

PRIMARY

CAS

99389-57-8

Created by admin on Mon Mar 31 22:17:16 GMT 2025 , Edited by admin on Mon Mar 31 22:17:16 GMT 2025

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FDA UNII

535Z468F1A

Created by admin on Mon Mar 31 22:17:16 GMT 2025 , Edited by admin on Mon Mar 31 22:17:16 GMT 2025

PRIMARY

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