ID: ALA4872714

Max Phase: Preclinical

Molecular Formula: C32H39BrN6O3

Molecular Weight: 635.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Oc1cc(N2CCc3c(nc(OCC4(CN5CCOCC5)CC4)nc3N3CC4CCC(C3)N4)C2)c2c(Br)cccc2c1

Standard InChI:  InChI=1S/C32H39BrN6O3/c33-26-3-1-2-21-14-24(40)15-28(29(21)26)38-9-6-25-27(18-38)35-31(36-30(25)39-16-22-4-5-23(17-39)34-22)42-20-32(7-8-32)19-37-10-12-41-13-11-37/h1-3,14-15,22-23,34,40H,4-13,16-20H2

Standard InChI Key:  OUEMNZQTVGHAFW-UHFFFAOYSA-N

Associated Targets(Human)

A-427 643 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

GTPase KRas 1864 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: 635.61Molecular Weight (Monoisotopic): 634.2267AlogP: 4.09#Rotatable Bonds: 7
Polar Surface Area: 86.22Molecular Species: BASEHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.32CX Basic pKa: 9.95CX LogP: 4.29CX LogD: 2.69
Aromatic Rings: 3Heavy Atoms: 42QED Weighted: 0.40Np Likeness Score: -0.27

References

1. Kargbo RB..  (2021)  Targeting the KRAS G12D Mutant as Potential Therapy in Cancer.,  12  (8.0): [PMID:34413947] [10.1021/acsmedchemlett.1c00390]

Source