MMV1802468

ID: ALA5312448

Chembl Id: CHEMBL5312448

Max Phase: Preclinical

Molecular Formula: C21H27F3N4O

Molecular Weight: 408.47

Associated Items:

Names and Identifiers

Canonical SMILES:  FC(F)(F)c1ccc(N2CCC[C@H](NC3CCN(Cc4ccco4)CC3)C2)nc1

Standard InChI:  InChI=1S/C21H27F3N4O/c22-21(23,24)16-5-6-20(25-13-16)28-9-1-3-18(14-28)26-17-7-10-27(11-8-17)15-19-4-2-12-29-19/h2,4-6,12-13,17-18,26H,1,3,7-11,14-15H2/t18-/m0/s1

Standard InChI Key:  QKAUJUXFINJHOI-SFHVURJKSA-N

Alternative Forms

  1. Parent:

    ALA5312448

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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: 408.47Molecular Weight (Monoisotopic): 408.2137AlogP: 3.92#Rotatable Bonds: 5
Polar Surface Area: 44.54Molecular Species: BASEHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 9.74CX LogP: 3.25CX LogD: 0.93
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.81Np Likeness Score: -2.14

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):