ID: ALA4876012

Max Phase: Preclinical

Molecular Formula: C34H37N7O7

Molecular Weight: 655.71

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(COc1ccc(CC(=O)Nc2cc(C3CCC3)[nH]n2)cc1)NCCCCNc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O

Standard InChI:  InChI=1S/C34H37N7O7/c42-28-14-13-26(32(45)38-28)41-33(46)23-7-4-8-24(31(23)34(41)47)35-15-1-2-16-36-30(44)19-48-22-11-9-20(10-12-22)17-29(43)37-27-18-25(39-40-27)21-5-3-6-21/h4,7-12,18,21,26,35H,1-3,5-6,13-17,19H2,(H,36,44)(H,38,42,45)(H2,37,39,40,43)

Standard InChI Key:  CVHGRDODKULBHE-UHFFFAOYSA-N

Associated Targets(Human)

Protein cereblon/CDK9 113 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: 655.71Molecular Weight (Monoisotopic): 655.2754AlogP: 2.65#Rotatable Bonds: 14
Polar Surface Area: 191.69Molecular Species: NEUTRALHBA: 9HBD: 5
#RO5 Violations: 1HBA (Lipinski): 14HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.13CX Basic pKa: 2.23CX LogP: 2.29CX LogD: 2.29
Aromatic Rings: 3Heavy Atoms: 48QED Weighted: 0.13Np Likeness Score: -1.06

References

1. King HM, Rana S, Kubica SP, Mallareddy JR, Kizhake S, Ezell EL, Zahid M, Naldrett MJ, Alvarez S, Law HC, Woods NT, Natarajan A..  (2021)  Aminopyrazole based CDK9 PROTAC sensitizes pancreatic cancer cells to venetoclax.,  43  [PMID:33895280] [10.1016/j.bmcl.2021.128061]

Source