MOROCROMEN

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C21H27N3O5
Molecular Weight	401.4562
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MOROCROMEN

Structure Search

SMILES

CC1=C(CCN2CCOCC2)C(=O)OC3=C1C=CC(NC(=O)N4CCOCC4)=C3

InChI

InChIKey=BVXGJMKPMTXSFM-UHFFFAOYSA-N

InChI=1S/C21H27N3O5/c1-15-17-3-2-16(22-21(26)24-8-12-28-13-9-24)14-19(17)29-20(25)18(15)4-5-23-6-10-27-11-7-23/h2-3,14H,4-13H2,1H3,(H,22,26)

HIDE SMILES / InChI

Molecular Formula	C21H27N3O5
Molecular Weight	401.4562
Charge	0
Count

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

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7198446 | https://www.ncbi.nlm.nih.gov/pubmed/7201825 | https://www.ncbi.nlm.nih.gov/pubmed/934347

Morocromen is an oxobenzopyranyl derivative patented by Troponwerke Dinklage und Co. as the coronary dilating agent.

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed

Patents

Patents

Sample Use Guides

In Vivo Use Guide

Dog: 4.0 mg/kg

Route of Administration: Intravenous

Substance Class	Chemical Created by `admin` on `Sat Dec 16 16:30:43 GMT 2023` Edited by `admin` on `Sat Dec 16 16:30:43 GMT 2023`
Record UNII	762D3F7OY3
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MOROCROMEN

Official Name

English

morocromen [INN]

Common Name

English

4-METHYL-7-(4-MORPHOLINECARBOXAMIDO)-3-(2-MORPHOLINOETHYL)COUMARIN

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29707

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

Code System Code Type Description

SMS_ID

100000080370

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

CAS

35843-07-3

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

EVMPD

SUB09069MIG

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

MESH

C012447

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

INN

3665

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

EPA CompTox

DTXSID20189386

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

NCI_THESAURUS

C66199

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

PUBCHEM

65793

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

FDA UNII

762D3F7OY3

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

ChEMBL

CHEMBL2105094

Created by admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023

PRIMARY

Related Record Type Details


					762D3F7OY3

ACTIVE MOIETY