ID: ALA4566111

Max Phase: Preclinical

Molecular Formula: C39H43N9O8

Molecular Weight: 765.83

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCCN(Cc1ccc(C(=O)NO)cc1)C(=O)Nc1ccc(OCCCCn2cc(CNc3ccc4c(c3)C(=O)N(C3CCC(=O)NC3=O)C4=O)nn2)cc1

Standard InChI:  InChI=1S/C39H43N9O8/c1-2-3-18-46(23-25-6-8-26(9-7-25)35(50)44-55)39(54)41-27-10-13-30(14-11-27)56-20-5-4-19-47-24-29(43-45-47)22-40-28-12-15-31-32(21-28)38(53)48(37(31)52)33-16-17-34(49)42-36(33)51/h6-15,21,24,33,40,55H,2-5,16-20,22-23H2,1H3,(H,41,54)(H,44,50)(H,42,49,51)

Standard InChI Key:  WEOZNDRZTWXKJS-UHFFFAOYSA-N

Associated Targets(Human)

Cereblon/Histone deacetylase 6 114 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 765.83Molecular Weight (Monoisotopic): 765.3235AlogP: 4.10#Rotatable Bonds: 17
Polar Surface Area: 217.19Molecular Species: NEUTRALHBA: 12HBD: 5
#RO5 Violations: 2HBA (Lipinski): 17HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.05CX Basic pKa: 1.32CX LogP: 2.81CX LogD: 2.80
Aromatic Rings: 4Heavy Atoms: 56QED Weighted: 0.04Np Likeness Score: -1.35

References

1. Wu H, Yang K, Zhang Z, Leisten ED, Li Z, Xie H, Liu J, Smith KA, Novakova Z, Barinka C, Tang W..  (2019)  Development of Multifunctional Histone Deacetylase 6 Degraders with Potent Antimyeloma Activity.,  62  (15): [PMID:31271281] [10.1021/acs.jmedchem.9b00516]

Source