ID: ALA2031584

Max Phase: Preclinical

Molecular Formula: C29H33ClF3N5O

Molecular Weight: 560.06

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nc(C2CCN(C(=O)[C@@H]3C[C@@](C)(N(C)C)C[C@H]3c3ccc(F)cc3F)CC2)n(-c2ccc(F)c(Cl)c2)n1

Standard InChI:  InChI=1S/C29H33ClF3N5O/c1-17-34-27(38(35-17)20-6-8-25(32)24(30)14-20)18-9-11-37(12-10-18)28(39)23-16-29(2,36(3)4)15-22(23)21-7-5-19(31)13-26(21)33/h5-8,13-14,18,22-23H,9-12,15-16H2,1-4H3/t22-,23+,29-/m0/s1

Standard InChI Key:  ZVMJQGQCDPKDMY-CTWZREHQSA-N

Associated Targets(Human)

Plasma 7708 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lysosomal Pro-X carboxypeptidase 567 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasma 6361 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lysosomal Pro-X carboxypeptidase 241 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: 560.06Molecular Weight (Monoisotopic): 559.2326AlogP: 5.87#Rotatable Bonds: 5
Polar Surface Area: 54.26Molecular Species: BASEHBA: 5HBD: 0
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 10.00CX LogP: 5.31CX LogD: 2.75
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.39Np Likeness Score: -1.54

References

1. Graham TH, Liu W, Verras A, Reibarkh M, Bleasby K, Bhatt UR, Chen Q, Garcia-Calvo M, Geissler WM, Gorski JN, He H, Lassman ME, Lisnock J, Li X, Shen Z, Tong X, Tung EC, Wiltsie J, Xie D, Xu S, Xiao J, Hale JJ, Pinto S, Shen DM..  (2012)  A new class of prolylcarboxypeptidase inhibitors, part 2: the aminocyclopentanes.,  22  (8): [PMID:22444685] [10.1016/j.bmcl.2012.02.077]

Source