MMV1802214

ID: ALA5312868

Chembl Id: CHEMBL5312868

Max Phase: Preclinical

Molecular Formula: C25H27N5

Molecular Weight: 397.53

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccn2cc(-c3ccc(N4CCC(NCc5cccnc5)CC4)cc3)nc2c1

Standard InChI:  InChI=1S/C25H27N5/c1-19-8-12-30-18-24(28-25(30)15-19)21-4-6-23(7-5-21)29-13-9-22(10-14-29)27-17-20-3-2-11-26-16-20/h2-8,11-12,15-16,18,22,27H,9-10,13-14,17H2,1H3

Standard InChI Key:  QSYIPIHNJKDQSH-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5312868

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Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 397.53Molecular Weight (Monoisotopic): 397.2266AlogP: 4.46#Rotatable Bonds: 5
Polar Surface Area: 45.46Molecular Species: BASEHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 9.02CX LogP: 3.56CX LogD: 1.94
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.54Np Likeness Score: -1.94

References

1. Bosc N, Felix E, Gardner JMF, Mills J, Timmerman M, Asveld D, Rensen K, Mukherjee P, Das R, Chenu E, Besson D, Burrows JN, Duffy J, Laleu B, Guantai EM, Leach AR..  (2023)  MAIP: An Open-Source Tool to Enrich High-Throughput Screening Output and Identify Novel, Druglike Molecules with Antimalarial Activity.,  14  (12): [PMID:38116432] [10.1021/acsmedchemlett.3c00369]

Source

Source(1):