ID: ALA3325596

Max Phase: Preclinical

Molecular Formula: C23H15F3N4O

Molecular Weight: 420.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C(=O)c1ccc2ncc(-c3ccc(C(F)(F)F)cc3)n2c1)c1ccc(C#N)cc1

Standard InChI:  InChI=1S/C23H15F3N4O/c1-29(19-9-2-15(12-27)3-10-19)22(31)17-6-11-21-28-13-20(30(21)14-17)16-4-7-18(8-5-16)23(24,25)26/h2-11,13-14H,1H3

Standard InChI Key:  WTTOSRDUVSTFGU-UHFFFAOYSA-N

Associated Targets(non-human)

Plasmodium cynomolgi 553 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium yoelii 6656 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

Properties

Molecular Weight: 420.39Molecular Weight (Monoisotopic): 420.1198AlogP: 5.17#Rotatable Bonds: 3
Polar Surface Area: 61.40Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 5.43CX LogP: 4.02CX LogD: 4.01
Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.46Np Likeness Score: -1.94

References

1. Zou B, Nagle A, Chatterjee AK, Leong SY, Tan LJ, Sim WL, Mishra P, Guntapalli P, Tully DC, Lakshminarayana SB, Lim CS, Tan YC, Abas SN, Bodenreider C, Kuhen KL, Gagaring K, Borboa R, Chang J, Li C, Hollenbeck T, Tuntland T, Zeeman AM, Kocken CH, McNamara C, Kato N, Winzeler EA, Yeung BK, Diagana TT, Smith PW, Roland J..  (2014)  Lead optimization of imidazopyrazines: a new class of antimalarial with activity on Plasmodium liver stages.,  (8): [PMID:25147620] [10.1021/ml500244m]

Source