ACENOCOUMAROL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H15NO6
Molecular Weight	353.3255
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ACENOCOUMAROL

Structure Search

SMILES

CC(=O)CC(C1=CC=C(C=C1)[N+]([O-])=O)C2=C(O)C3=CC=CC=C3OC2=O

InChI

InChIKey=VABCILAOYCMVPS-UHFFFAOYSA-N

InChI=1S/C19H15NO6/c1-11(21)10-15(12-6-8-13(9-7-12)20(24)25)17-18(22)14-4-2-3-5-16(14)26-19(17)23/h2-9,15,22H,10H2,1H3

HIDE SMILES / InChI

Molecular Formula	C19H15NO6
Molecular Weight	353.3255
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:06:18 UTC 2023` Edited by `admin` on `Fri Dec 15 16:06:18 UTC 2023`
Record UNII	I6WP63U32H
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ACENOCOUMAROL

Official Name

English

MINI-SINTROM

Brand Name

English

NSC-760052

Code

English

2H-1-BENZOPYRAN-2-ONE, 4-HYDROXY-3-(1-(4-NITROPHENYL)-3-OXOBUTYL)-

Systematic Name

English

3-(.ALPHA.-ACETONYL-P-NITROBENZYL)-4-HYDROXYCOUMARIN

Common Name

English

ACENOCOUMAROL [HSDB]

Common Name

English

Acenocoumarol [WHO-DD]

Common Name

English

ACENOCOUMAROL [MART.]

Common Name

English

acenocoumarol [INN]

Common Name

English

ACENOCOUMARIN

Common Name

English

ACENOCOUMAROL [MI]

Common Name

English

NICOUMALONE

Common Name

English

Classification Tree Code System Code

WHO-ATC

B01AA07

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

NCI_THESAURUS

C263

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

WHO-VATC

QB01AA07

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

Code System Code Type Description

WIKIPEDIA

ACENOCOUMAROL

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

PRIMARY

CAS

152-72-7

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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NSC

760052

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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NCI_THESAURUS

C75152

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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FDA UNII

I6WP63U32H

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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ChEMBL

CHEMBL397420

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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DRUG CENTRAL

48

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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MERCK INDEX

m1300

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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Merck Index

PUBCHEM

54676537

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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RXCUI

154

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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RxNorm

HSDB

3201

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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DRUG BANK

DB01418

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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EPA CompTox

DTXSID2022541

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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ECHA (EC/EINECS)

205-807-3

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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LACTMED

Acenocoumarol

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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INN

503

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

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MESH

D000074

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

PRIMARY

SMS_ID

100000091427

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

PRIMARY

EVMPD

SUB05211MIG

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

PRIMARY

CHEBI

53766

Created by admin on Fri Dec 15 16:06:18 UTC 2023 , Edited by admin on Fri Dec 15 16:06:18 UTC 2023

PRIMARY

Related Record Type Details


					JRD7912W79

ACENOCOUMAROL, (R)-

ENANTIOMER -> RACEMATE


					4O90VF03HV

ACENOCOUMAROL, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					I6WP63U32H

ACTIVE MOIETY