ID: ALA4536592

Max Phase: Preclinical

Molecular Formula: C40H54N4O4

Molecular Weight: 654.90

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cccc(C(C)(C)NC[C@@H](O)[C@H](Cc2ccccc2)NC(=O)c2cc(C(=O)NCC3CCCCC3)cc(N3CCCCC3)c2)c1

Standard InChI:  InChI=1S/C40H54N4O4/c1-40(2,33-18-13-19-35(26-33)48-3)42-28-37(45)36(22-29-14-7-4-8-15-29)43-39(47)32-23-31(24-34(25-32)44-20-11-6-12-21-44)38(46)41-27-30-16-9-5-10-17-30/h4,7-8,13-15,18-19,23-26,30,36-37,42,45H,5-6,9-12,16-17,20-22,27-28H2,1-3H3,(H,41,46)(H,43,47)/t36-,37+/m0/s1

Standard InChI Key:  CPENPHULHCEEFK-PQQNNWGCSA-N

Associated Targets(Human)

Cathepsin D 3201 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmepsin 4 112 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: 654.90Molecular Weight (Monoisotopic): 654.4145AlogP: 6.22#Rotatable Bonds: 14
Polar Surface Area: 102.93Molecular Species: BASEHBA: 6HBD: 4
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.92CX Basic pKa: 8.85CX LogP: 6.54CX LogD: 5.08
Aromatic Rings: 3Heavy Atoms: 48QED Weighted: 0.16Np Likeness Score: -0.64

References

1. Zogota R, Kinena L, Withers-Martinez C, Blackman MJ, Bobrovs R, Pantelejevs T, Kanepe-Lapsa I, Ozola V, Jaudzems K, Suna E, Jirgensons A..  (2019)  Peptidomimetic plasmepsin inhibitors with potent anti-malarial activity and selectivity against cathepsin D.,  163  [PMID:30529637] [10.1016/j.ejmech.2018.11.068]

Source