For research use only. Not for therapeutic Use.
PC786(Cat No.:I034283)is a potent, selective inhibitor of the bromodomain and extraterminal (BET) family of proteins, particularly targeting BRD4. By blocking the interaction between BET proteins and acetylated lysine residues on histones, PC786 disrupts transcriptional processes that drive cancer cell growth, making it a promising candidate in cancer therapy, especially for hematologic malignancies. This compound is under investigation for its potential to modulate key signaling pathways involved in cell proliferation and survival. PC786 is expected to complement existing therapies by targeting epigenetic regulation in cancer cells.
Catalog Number | I034283 |
CAS Number | 1902114-15-1 |
Synonyms | PC-786; PC 786; PC786 |
Molecular Formula | C41H38FN5O4S |
Purity | 98% |
Target | RSV |
Solubility | Soluble in DMSO |
Appearance | Solid powder |
Storage | Store at -20°C |
IUPAC Name | N-(2-fluoro-6-methylphenyl)-6-[4-[[5-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)pyridine-3-carbonyl]amino]benzoyl]-4,5-dihydrothieno[3,2-d][1]benzazepine-2-carboxamide |
InChI | InChI=1S/C41H38FN5O4S/c1-25-20-31(37(43-22-25)46-23-41(24-46)15-18-51-19-16-41)38(48)44-29-12-10-27(11-13-29)40(50)47-17-14-28-21-34(52-36(28)30-7-3-4-9-33(30)47)39(49)45-35-26(2)6-5-8-32(35)42/h3-13,20-22H,14-19,23-24H2,1-2H3,(H,44,48)(H,45,49) |
InChIKey | VTCJNYICQADBJD-UHFFFAOYSA-N |
SMILES | CC1=C(C(=CC=C1)F)NC(=O)C2=CC3=C(S2)C4=CC=CC=C4N(CC3)C(=O)C5=CC=C(C=C5)NC(=O)C6=C(N=CC(=C6)C)N7CC8(C7)CCOCC8 |
Reference | 1: Mirabelli C, Jaspers M, Boon M, Jorissen M, Koukni M, Bardiot D, Chaltin P, Marchand A, Neyts J, Jochmans D. Differential antiviral activities of respiratory syncytial virus (RSV) inhibitors in human airway epithelium. J Antimicrob Chemother. 2018 Mar 27. doi: 10.1093/jac/dky089. [Epub ahead of print] PubMed PMID: 29596680; PubMed Central PMCID: PMC6005027. |