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

Details

Stereochemistry ABSOLUTE
Molecular Formula C24H30N6O4
Molecular Weight 466.5328
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PF-07054894

SMILES

CN(C)C(=O)C1=C(O)C(NC2=C(N[C@@H](C3=NN(C)C=C3C)C4(C)CCCC4)C(=O)C2=O)=CC=N1

InChI

InChIKey=WZBSYWCLIMRAHO-QFIPXVFZSA-N
InChI=1S/C24H30N6O4/c1-13-12-30(5)28-15(13)22(24(2)9-6-7-10-24)27-17-16(20(32)21(17)33)26-14-8-11-25-18(19(14)31)23(34)29(3)4/h8,11-12,22,27,31H,6-7,9-10H2,1-5H3,(H,25,26)/t22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H30N6O4
Molecular Weight 466.5328
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:28:19 UTC 2023
Edited
by admin
on Sat Dec 16 19:28:19 UTC 2023
Record UNII
X88GCV5DSA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PF-07054894
Code English
2-Pyridinecarboxamide, 4-[[2-[[(R)-(1,4-dimethyl-1H-pyrazol-3-yl)(1-methylcyclopentyl)methyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-3-hydroxy-N,N-dimethyl-
Systematic Name English
4-[[2-[[(R)-(1,4-Dimethyl-1H-pyrazol-3-yl)(1-methylcyclopentyl)methyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]-3-hydroxy-N,N-dimethyl-2-pyridinecarboxamide
Systematic Name English
Code System Code Type Description
PUBCHEM
146444831
Created by admin on Sat Dec 16 19:28:19 UTC 2023 , Edited by admin on Sat Dec 16 19:28:19 UTC 2023
PRIMARY
CAS
2413693-96-4
Created by admin on Sat Dec 16 19:28:19 UTC 2023 , Edited by admin on Sat Dec 16 19:28:19 UTC 2023
PRIMARY
FDA UNII
X88GCV5DSA
Created by admin on Sat Dec 16 19:28:19 UTC 2023 , Edited by admin on Sat Dec 16 19:28:19 UTC 2023
PRIMARY
Related Record Type Details
TARGET->WEAK INHIBITOR
Kd
TARGET -> INHIBITOR
Kd
TARGET -> INHIBITOR
Blocked in vitro CCL20-dependent human T cell chemotaxis. slow dissociation rate and consequent prolonged residence time of PF-07054894 on CCR6 is consistent with its insurmountable pattern of chemotaxis inhibition.
IC50
Related Record Type Details
ACTIVE MOIETY