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Details

Stereochemistry ACHIRAL
Molecular Formula C25H21FN2O
Molecular Weight 384.4454
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CP-461 FREE BASE

SMILES

CC1=C(CC(=O)NCC2=CC=CC=C2)C3=C(C=CC(F)=C3)\C1=C/C4=CC=NC=C4

InChI

InChIKey=NVCAMOJXQVJSOM-XKZIYDEJSA-N
InChI=1S/C25H21FN2O/c1-17-22(13-18-9-11-27-12-10-18)21-8-7-20(26)14-24(21)23(17)15-25(29)28-16-19-5-3-2-4-6-19/h2-14H,15-16H2,1H3,(H,28,29)/b22-13-

HIDE SMILES / InChI

Molecular Formula C25H21FN2O
Molecular Weight 384.4454
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

CP-461 is an orally bioavailable second-generation apoptotic antineoplastic drug and analog of the nonsteroidal anti-inflammatory drug sulindac. CP-461 is an inhibitor of monophosphate-phosphodiesterase, an enzyme that inhibits the normal apoptosis signal pathway. Inhibition of cGMP-PDE permits the apoptotic signal pathway to proceed unopposed, resulting in apoptotic cell death. CP-461 was initially developed by OSI Pharmaceuticals, and in the early 2000s, CP-461 was investigated in phase I and phase 2 clinical trials for the treatment of chronic lymphocytic leukemia, Crohn's disease, malignant melanoma, renal cell carcinoma, and prostate cancer, both alone and in combination with other chemotherapeutic agents. The coadministration of CP-461 with other agents, however, did not increase the response rate. CP-461 was licensed to Celek Pharmaceuticals, where the compound was repurposed for the treatment of bladder cancer, but no development was reported.

Approval Year

PubMed

PubMed

TitleDatePubMed
Activation of protein kinase G up-regulates expression of 15-lipoxygenase-1 in human colon cancer cells.
2005-09-15
Synergistic effects of acyclic retinoid and OSI-461 on growth inhibition and gene expression in human hepatoma cells.
2004-10-01
Pro-apoptotic actions of exisulind and CP461 in SW480 colon tumor cells involve beta-catenin and cyclin D1 down-regulation.
2002-11-01
Cyclic GMP-dependent protein kinase activation and induction by exisulind and CP461 in colon tumor cells.
2001-11
Cyclic GMP mediates apoptosis induced by sulindac derivatives via activation of c-Jun NH2-terminal kinase 1.
2000-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:36:23 GMT 2025
Edited
by admin
on Mon Mar 31 21:36:23 GMT 2025
Record UNII
824ZMS3BGL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OSI-461 FREE BASE
Preferred Name English
CP-461 FREE BASE
Common Name English
1H-INDENE-3-ACETAMIDE, 5-FLUORO-2-METHYL-N-(PHENYLMETHYL)-1-(4-PYRIDINYLMETHYLENE)-, (1Z)-
Systematic Name English
Code System Code Type Description
CAS
227619-92-3
Created by admin on Mon Mar 31 21:36:23 GMT 2025 , Edited by admin on Mon Mar 31 21:36:23 GMT 2025
PRIMARY
PUBCHEM
6445782
Created by admin on Mon Mar 31 21:36:23 GMT 2025 , Edited by admin on Mon Mar 31 21:36:23 GMT 2025
PRIMARY
FDA UNII
824ZMS3BGL
Created by admin on Mon Mar 31 21:36:23 GMT 2025 , Edited by admin on Mon Mar 31 21:36:23 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT