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

Details

Stereochemistry ACHIRAL
Molecular Formula C21H25N7
Molecular Weight 375.4701
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ENMD-981693

SMILES

CN1CCN(CC1)C2=CC(NC3=NNC(C)=C3)=NC(\C=C\C4=CC=CC=C4)=N2

InChI

InChIKey=BLQYVHBZHAISJM-CMDGGOBGSA-N
InChI=1S/C21H25N7/c1-16-14-20(26-25-16)23-19-15-21(28-12-10-27(2)11-13-28)24-18(22-19)9-8-17-6-4-3-5-7-17/h3-9,14-15H,10-13H2,1-2H3,(H2,22,23,24,25,26)/b9-8+

HIDE SMILES / InChI

Molecular Formula C21H25N7
Molecular Weight 375.4701
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 20:20:51 UTC 2023
Edited
by admin
on Fri Dec 15 20:20:51 UTC 2023
Record UNII
J6U9WP10T7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ENMD-981693
Common Name English
ENMD-2076 FREE BASE
Common Name English
ENMD 981693
Code English
4-PYRIMIDINAMINE, 6-(4-METHYL-1-PIPERAZINYL)-N-(5-METHYL-1H-PYRAZOL-3-YL)-2-((1E)-2-PHENYLETHENYL)-
Systematic Name English
(E)-N-(5-METHYL-1H-PYRAZOL-3-YL)-6-(4-METHYLPIPERAZIN-1-YL)-2-STYRYLPYRIMIDIN-4-AMINE
Systematic Name English
R-440
Code English
RO-317453
Code English
Code System Code Type Description
FDA UNII
J6U9WP10T7
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
SMS_ID
300000013151
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
ChEMBL
CHEMBL52885
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID60239430
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
PUBCHEM
16041424
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
MESH
C551397
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
CAS
934353-76-1
Created by admin on Fri Dec 15 20:20:52 UTC 2023 , Edited by admin on Fri Dec 15 20:20:52 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY