MMV1802521

ID: ALA5308930

Chembl Id: CHEMBL5308930

Max Phase: Preclinical

Molecular Formula: C24H31FN4O

Molecular Weight: 410.54

Associated Items:

Names and Identifiers

Canonical SMILES:  CN1CCN(CCOc2ccccc2CN(C)Cc2cc3cc(F)ccc3[nH]2)CC1

Standard InChI:  InChI=1S/C24H31FN4O/c1-27-9-11-29(12-10-27)13-14-30-24-6-4-3-5-19(24)17-28(2)18-22-16-20-15-21(25)7-8-23(20)26-22/h3-8,15-16,26H,9-14,17-18H2,1-2H3

Standard InChI Key:  MECZMHQQESPZTR-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5308930

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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: 410.54Molecular Weight (Monoisotopic): 410.2482AlogP: 3.57#Rotatable Bonds: 8
Polar Surface Area: 34.74Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 7.94CX LogP: 3.51CX LogD: 2.68
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.62Np Likeness Score: -1.67

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):