U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H29N5O3
Molecular Weight 387.476
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of URAPIDIL

SMILES

COC1=C(C=CC=C1)N2CCN(CCCNC3=CC(=O)N(C)C(=O)N3C)CC2

InChI

InChIKey=ICMGLRUYEQNHPF-UHFFFAOYSA-N
InChI=1S/C20H29N5O3/c1-22-18(15-19(26)23(2)20(22)27)21-9-6-10-24-11-13-25(14-12-24)16-7-4-5-8-17(16)28-3/h4-5,7-8,15,21H,6,9-14H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C20H29N5O3
Molecular Weight 387.476
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:37:17 UTC 2023
Edited
by admin
on Fri Dec 15 18:37:17 UTC 2023
Record UNII
A78GF17HJS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
URAPIDIL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
6-(3-(4-(O-METHOXYPHENYL)-1-PIPERAZINYL)PROPYLAMINO)-1,3-DIMETHYLURACIL
Common Name English
NSC-310405
Code English
urapidil [INN]
Common Name English
URAPIDIL [MART.]
Common Name English
URAPIDIL [JAN]
Common Name English
Urapidil [WHO-DD]
Common Name English
EBRANTIL
Brand Name English
URAPIDIL [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QC02CA06
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
WHO-ATC C02CA06
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
NCI_THESAURUS C29713
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
NCI_THESAURUS C270
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
Code System Code Type Description
MERCK INDEX
m11320
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY Merck Index
MESH
C015568
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
CAS
34661-75-1
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
DRUG CENTRAL
2796
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
PUBCHEM
5639
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
INN
3169
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
DRUG BANK
DB12661
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
ECHA (EC/EINECS)
252-130-4
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
ChEMBL
CHEMBL279229
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
EPA CompTox
DTXSID9021425
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
WIKIPEDIA
Urapidil
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
SMS_ID
100000076662
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
NSC
310405
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
EVMPD
SUB11384MIG
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
FDA UNII
A78GF17HJS
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
NCI_THESAURUS
C152806
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY
RXCUI
39230
Created by admin on Fri Dec 15 18:37:17 UTC 2023 , Edited by admin on Fri Dec 15 18:37:17 UTC 2023
PRIMARY RxNorm
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY