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Details

Stereochemistry ACHIRAL
Molecular Formula C19H15F3N4O
Molecular Weight 372.3438
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CP-944629

SMILES

CC(C)(C)C1=NN=C2C=CC(=CN12)C3=C(N=CO3)C4=C(F)C=C(F)C(F)=C4

InChI

InChIKey=VNZJNPIWZYMGAO-UHFFFAOYSA-N
InChI=1S/C19H15F3N4O/c1-19(2,3)18-25-24-15-5-4-10(8-26(15)18)17-16(23-9-27-17)11-6-13(21)14(22)7-12(11)20/h4-9H,1-3H3

HIDE SMILES / InChI

Molecular Formula C19H15F3N4O
Molecular Weight 372.3438
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q16539|||Q8TDX0
Gene ID: 1432.0
Gene Symbol: MAPK14
Target Organism: Homo sapiens (Human)
1.8 nM [IC50]
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:30:10 GMT 2023
Edited
by admin
on Sat Dec 16 17:30:10 GMT 2023
Record UNII
KB2ZD36HED
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CP-944629
Code English
3-TERT-BUTYL-6-(4-(2,4,5-TRIFLUOROPHENYL)-1,3-OXAZOL-5-YL)(1,2,4)TRIAZOLO(4,3-A)PYRIDINE
Systematic Name English
3-TERT-BUTYL-6-(4-(2,4,5-TRIFLUOROPHENYL)OXAZOL-5-YL)-(1,2,4)TRIAZOLO(4,3-A)PYRIDINE
Systematic Name English
1,2,4-Triazolo[4,3-a]pyridine, 3-(1,1-dimethylethyl)-6-[4-(2,4,5-trifluorophenyl)-5-oxazolyl]-
Systematic Name English
3-(1,1-DIMETHYLETHYL)-6-(4-(2,4,5-TRIFLUOROPHENYL)-5-OXAZOLYL)-1,2,4-TRIAZOLO(4,3-A)PYRIDINE
Systematic Name English
Code System Code Type Description
CAS
668990-94-1
Created by admin on Sat Dec 16 17:30:10 GMT 2023 , Edited by admin on Sat Dec 16 17:30:10 GMT 2023
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PUBCHEM
9999342
Created by admin on Sat Dec 16 17:30:10 GMT 2023 , Edited by admin on Sat Dec 16 17:30:10 GMT 2023
PRIMARY
FDA UNII
KB2ZD36HED
Created by admin on Sat Dec 16 17:30:10 GMT 2023 , Edited by admin on Sat Dec 16 17:30:10 GMT 2023
PRIMARY
WIKIPEDIA
CP-944629
Created by admin on Sat Dec 16 17:30:10 GMT 2023 , Edited by admin on Sat Dec 16 17:30:10 GMT 2023
PRIMARY