ID: ALA4290951

Max Phase: Preclinical

Molecular Formula: C42H48F3N3O6

Molecular Weight: 747.86

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(OC(F)(F)F)cc(C(=O)N[C@H](C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)COc2c(C)cccc2C)C(C)C)c1

Standard InChI:  InChI=1S/C42H48F3N3O6/c1-26(2)38(48-40(51)32-19-27(3)20-34(23-32)54-42(43,44)45)41(52)46-33(21-30-15-8-6-9-16-30)24-36(49)35(22-31-17-10-7-11-18-31)47-37(50)25-53-39-28(4)13-12-14-29(39)5/h6-20,23,26,33,35-36,38,49H,21-22,24-25H2,1-5H3,(H,46,52)(H,47,50)(H,48,51)/t33-,35-,36-,38-/m0/s1

Standard InChI Key:  UMAVWAIIPRHXTB-WLVMASMISA-N

Associated Targets(Human)

CAAX prenyl protease 1 homolog 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 747.86Molecular Weight (Monoisotopic): 747.3495AlogP: 6.55#Rotatable Bonds: 17
Polar Surface Area: 125.99Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.48CX Basic pKa: CX LogP: 8.48CX LogD: 8.48
Aromatic Rings: 4Heavy Atoms: 54QED Weighted: 0.10Np Likeness Score: -0.42

References

1. Matralis AN, Xanthopoulos D, Huot G, Lopes-Paciencia S, Cole C, de Vries H, Ferbeyre G, Tsantrizos YS..  (2018)  Molecular tools that block maturation of the nuclear lamin A and decelerate cancer cell migration.,  26  (20): [PMID:30309670] [10.1016/j.bmc.2018.10.001]

Source