N-((S)-1-((2S,3S)-5-((R)-1-((S)-1-amino-4-methyl-1-oxopentan-2-ylamino)-3-chloro-1-oxopropan-2-ylamino)-3-hydroxy-5-oxo-1-phenylpentan-2-ylamino)-3-methyl-1-oxobutan-2-yl)picolinamide

ID: ALA1098668

Chembl Id: CHEMBL1098668

PubChem CID: 46236672

Max Phase: Preclinical

Molecular Formula: C31H43ClN6O6

Molecular Weight: 631.17

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)C[C@H](NC(=O)[C@H](CCl)NC(=O)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1ccccn1)C(C)C)C(N)=O

Standard InChI:  InChI=1S/C31H43ClN6O6/c1-18(2)14-23(28(33)41)37-30(43)24(17-32)35-26(40)16-25(39)22(15-20-10-6-5-7-11-20)36-31(44)27(19(3)4)38-29(42)21-12-8-9-13-34-21/h5-13,18-19,22-25,27,39H,14-17H2,1-4H3,(H2,33,41)(H,35,40)(H,36,44)(H,37,43)(H,38,42)/t22-,23-,24-,25-,27-/m0/s1

Standard InChI Key:  AWQGEUFVOMSATO-CPHHOOCTSA-N

Associated Targets(Human)

CTSD Tchem Cathepsin D (3201 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PMII Plasmepsin 2 (774 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHO (4503 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 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

Calculated Properties

Molecular Weight: 631.17Molecular Weight (Monoisotopic): 630.2933AlogP: 1.05#Rotatable Bonds: 17
Polar Surface Area: 192.61Molecular Species: NEUTRALHBA: 7HBD: 6
#RO5 Violations: 2HBA (Lipinski): 12HBD (Lipinski): 7#RO5 Violations (Lipinski): 3
CX Acidic pKa: 11.74CX Basic pKa: 2.10CX LogP: 1.41CX LogD: 1.41
Aromatic Rings: 2Heavy Atoms: 44QED Weighted: 0.14Np Likeness Score: -0.10

References

1. Gupta D, Yedidi RS, Varghese S, Kovari LC, Woster PM..  (2010)  Mechanism-based inhibitors of the aspartyl protease plasmepsin II as potential antimalarial agents.,  53  (10): [PMID:20438064] [10.1021/jm100233b]
2. Cheuka PM, Dziwornu G, Okombo J, Chibale K..  (2020)  Plasmepsin Inhibitors in Antimalarial Drug Discovery: Medicinal Chemistry and Target Validation (2000 to Present).,  63  (9): [PMID:31913032] [10.1021/acs.jmedchem.9b01622]

Source