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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H27N5O2
Molecular Weight 321.4179
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CC-90001

SMILES

C[C@@H]1CC[C@H](C[C@H]1O)NC2=C(C=NC(NC(C)(C)C)=N2)C(N)=O

InChI

InChIKey=QBBRJRLJWXRSHQ-CKYFFXLPSA-N
InChI=1S/C16H27N5O2/c1-9-5-6-10(7-12(9)22)19-14-11(13(17)23)8-18-15(20-14)21-16(2,3)4/h8-10,12,22H,5-7H2,1-4H3,(H2,17,23)(H2,18,19,20,21)/t9-,10-,12-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H27N5O2
Molecular Weight 321.4179
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:47:42 UTC 2023
Edited
by admin
on Sat Dec 16 18:47:42 UTC 2023
Record UNII
JD5ZWE631K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CC-90001
Code English
5-PYRIMIDINECARBOXAMIDE, 2-((1,1-DIMETHYLETHYL)AMINO)-4-(((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYL)AMINO)-
Systematic Name English
2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE
Systematic Name English
CC90001
Code English
2-((1,1-DIMETHYLETHYL)AMINO)-4-(((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYL)AMINO)-5-PYRIMIDINECARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 573116
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
Code System Code Type Description
CAS
1403859-14-2
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
PRIMARY
PUBCHEM
71237511
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
PRIMARY
INN
12099
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
PRIMARY
FDA UNII
JD5ZWE631K
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
PRIMARY
SMS_ID
100000182794
Created by admin on Sat Dec 16 18:47:42 UTC 2023 , Edited by admin on Sat Dec 16 18:47:42 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Blocks LPS-induced c-jun phosphorylation. . CC-90001 was 12.9-fold more 50 potent for JNK1 inhibition than JNK2.
EC50
Related Record Type Details
ACTIVE MOIETY