BCPA

For research use only. Not for therapeutic Use.

  • CAT Number: I040922
  • CAS Number: 547731-67-9
  • Molecular Formula: C22H22Cl2N2O2
  • Molecular Weight: 417.33
  • Purity: ≥95%
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BCPA is a Pin1 regulator without cytotoxicity. BCPA attenuates the reduction of Pin1 protein to inhibit receptor activator of RANKL-induced osteoclastogenesis. BCPA regulates osteoclast activation, used to osteoporosis research[1].


Catalog Number I040922
CAS Number 547731-67-9
Synonyms

(E)-3-(2-chlorophenyl)-N-[4-[[(E)-3-(2-chlorophenyl)prop-2-enoyl]amino]butyl]prop-2-enamide

Molecular Formula C22H22Cl2N2O2
Purity ≥95%
InChI InChI=1S/C22H22Cl2N2O2/c23-19-9-3-1-7-17(19)11-13-21(27)25-15-5-6-16-26-22(28)14-12-18-8-2-4-10-20(18)24/h1-4,7-14H,5-6,15-16H2,(H,25,27)(H,26,28)/b13-11+,14-12+
InChIKey KHDKYKZKDQMAKP-PHEQNACWSA-N
SMILES C1=CC=C(C(=C1)C=CC(=O)NCCCCNC(=O)C=CC2=CC=CC=C2Cl)Cl
Reference

[1]. Cho E, et al. BCPA {N, N′-1, 4-Butanediylbis [3-(2-chlorophenyl) acrylamide]} Inhibits osteoclast differentiation through increased retention of peptidyl-prolyl cis-trans isomerase never in mitosis A-interacting 1[J]. International Journal of Molecular Sciences, 2018, 19(11): 3436.

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