ID: ALA594997

Max Phase: Preclinical

Molecular Formula: C30H44N6O8S2

Molecular Weight: 680.85

Molecule Type: Protein

Associated Items:

Representations

Canonical SMILES:  CC(C)C[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](CS)NC(=O)CNS(=O)(=O)c1cccc2c(N(C)C)cccc12)C(C)C)C(=O)O

Standard InChI:  InChI=1S/C30H44N6O8S2/c1-17(2)13-21(30(41)42)33-25(37)14-31-29(40)27(18(3)4)35-28(39)22(16-45)34-26(38)15-32-46(43,44)24-12-8-9-19-20(24)10-7-11-23(19)36(5)6/h7-12,17-18,21-22,27,32,45H,13-16H2,1-6H3,(H,31,40)(H,33,37)(H,34,38)(H,35,39)(H,41,42)/t21-,22-,27-/m0/s1

Standard InChI Key:  QOMZJCAMVYHQBC-BERHBOFZSA-N

Associated Targets(Human)

Protein farnesyltransferase beta subunit 120 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: ProteinTopical: 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: 680.85Molecular Weight (Monoisotopic): 680.2662AlogP: 0.47#Rotatable Bonds: 17
Polar Surface Area: 203.11Molecular Species: ACIDHBA: 9HBD: 7
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 3.71CX Basic pKa: 4.68CX LogP: -0.28CX LogD: -2.42
Aromatic Rings: 2Heavy Atoms: 46QED Weighted: 0.12Np Likeness Score: -0.71

References

1. Krzysiak AJ, Aditya AV, Hougland JL, Fierke CA, Gibbs RA..  (2010)  Synthesis and screening of a CaaL peptide library versus FTase reveals a surprising number of substrates.,  20  (2): [PMID:20005705] [10.1016/j.bmcl.2009.11.011]

Source