BECIPARCIL

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C12H13NO3S2
Molecular Weight	283.367
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BECIPARCIL

Structure Search

SMILES

O[C@@H]1CS[C@@H](SC2=CC=C(C=C2)C#N)[C@H](O)[C@H]1O

InChI

InChIKey=LVFZTPIRDLQIGF-KXNHARMFSA-N

InChI=1S/C12H13NO3S2/c13-5-7-1-3-8(4-2-7)18-12-11(16)10(15)9(14)6-17-12/h1-4,9-12,14-16H,6H2/t9-,10+,11-,12+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C12H13NO3S2
Molecular Weight	283.367
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://adisinsight.springer.com/drugs/800004709

Beciparcil, an antithrombotic drug, that was studied against thrombosis, however, further investigations were discontinued in 1997.

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed
Synthesis of the 3-methyl ether and 4-deoxy derivatives of 4-cyanophenyl 1,5-dithio-beta-D-xylopyranoside (Beciparcil).	1999-03-31	10420590
Synthesis of 4-cyanophenyl and 4-nitrophenyl 1,5-dithio-L- and -D-arabinopyranosides possessing antithrombotic activity.	1998-10	9825522
Synthesis of 4-cyanophenyl 1,5-dithio-beta-D-glucopyranoside and its 6-deoxy, as well as 6-deoxy-5-ene derivatives as oral antithrombotic agents.	1997-11-28	9468629

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:17:31 GMT 2025` Edited by `admin` on `Mon Mar 31 18:17:31 GMT 2025`
Record UNII	K90ZOR23P1
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LF 4.0212

Preferred Name

English

BECIPARCIL

Official Name

English

beciparcil [INN]

Common Name

English

P-((5-THIO-B-D-XYLOPYRANOSYL)THIO)BENZONITRILE

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C263

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

Code System Code Type Description

CAS

130782-54-6

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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NCI_THESAURUS

C73225

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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EVMPD

SUB05674MIG

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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SMS_ID

100000086091

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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INN

7061

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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MESH

C116179

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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ChEMBL

CHEMBL2103997

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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PUBCHEM

71788

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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FDA UNII

K90ZOR23P1

Created by admin on Mon Mar 31 18:17:31 GMT 2025 , Edited by admin on Mon Mar 31 18:17:31 GMT 2025

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Related Record Type Details


					K90ZOR23P1

ACTIVE MOIETY

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