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Details

Stereochemistry RACEMIC
Molecular Formula C21H32N4O5
Molecular Weight 420.5026
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIREPOLOL

SMILES

CCCCOC1=CC=C(OCC(O)CNCCNC2=CC(=O)N(C)C(=O)N2C)C=C1

InChI

InChIKey=BAPQHWDWPMIUKD-UHFFFAOYSA-N
InChI=1S/C21H32N4O5/c1-4-5-12-29-17-6-8-18(9-7-17)30-15-16(26)14-22-10-11-23-19-13-20(27)25(3)21(28)24(19)2/h6-9,13,16,22-23,26H,4-5,10-12,14-15H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C21H32N4O5
Molecular Weight 420.5026
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:44:18 GMT 2023
Edited
by admin
on Sat Dec 16 16:44:18 GMT 2023
Record UNII
V1J0B4P41O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIREPOLOL
INN  
INN  
Official Name English
pirepolol [INN]
Common Name English
2,4(1H,3H)-PYRIMIDINEDIONE, 6-((2-((3-(4-BUTOXYPHENOXY)-2-HYDROXYPROPYL)AMINO)ETHYL)AMINO)-1,3-DIMETHYL-
Systematic Name English
CAS-434
Code English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
Code System Code Type Description
SMS_ID
100000081644
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
CAS
69479-26-1
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
INN
5246
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID30989415
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL1742416
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
CAS
128182-66-1
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
SUPERSEDED
EVMPD
SUB09905MIG
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
PUBCHEM
68887
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
FDA UNII
V1J0B4P41O
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
NCI_THESAURUS
C66418
Created by admin on Sat Dec 16 16:44:18 GMT 2023 , Edited by admin on Sat Dec 16 16:44:18 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY