CAS: 2010159-48-3
Formel:C57H70ClN7O10S
InChl:InChI=1S/C57H70ClN7O10S/c1-36-29-48(62-45-18-16-44(58)17-19-45)47-30-43(15-20-49(47)65(36)38(3)66)40-11-13-42(14-12-40)54(69)59-21-22-72-23-24-73-25-26-74-27-28-75-34-51(68)63-53(57(4,5)6)56(71)64-33-46(67)31-50(64)55(70)60-32-39-7-9-41(10-8-39)52-37(2)61-35-76-52/h7-20,30,35-36,46,48,50,53,62,67H,21-29,31-34H2,1-6H3,(H,59,69)(H,60,70)(H,63,68)/t36-,46+,48+,50-,53+/m0/s1
InChI Key:InChIKey=UHWNJFZTYJNBAN-HYXXSBGTSA-N
SMILES:N([C@H]1C=2C(N(C(C)=O)[C@@H](C)C1)=CC=C(C2)C3=CC=C(C(NCCOCCOCCOCCOCC(N[C@H](C(=O)N4[C@H](C(NCC5=CC=C(C=C5)C6=C(C)N=CS6)=O)C[C@@H](O)C4)[C@](C)(C)C)=O)=O)C=C3)C7=CC=C(Cl)C=C7
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3 Produkte.
MZP-55
CAS:MZP-55 is a selective BRD3/4 degrader based on PROTAC technology(Brd4BD2 with Kd of 8 nM)Formel:C57H70ClN7O10SReinheit:98%Farbe und Form:SolidMolekulargewicht:1080.73MZP-55
CAS:MZP-55 is a natural product that inhibits the bromodomain and regulates the acetyltransferase. It has been shown to inhibit the transcriptional activity of the acetyltransferase and block the binding of acetylated proteins to DNA, which may lead to heart disease, cancer, and other diseases. MZP-55 also has anti-viral properties. MZP-55 has been shown to be effective against human immunodeficiency virus (HIV) and malignant cells from patients with neurological disorders or immunodeficiencies. MZP-55 is a promising potential therapeutic agent for renal fibrosis.Formel:C57H70ClN7O10SReinheit:Min. 95%Molekulargewicht:1,080.72 g/mol
