2,6-dimethyl-4-[3-(6-quinolyl)imidazo[1,2-a]pyrazin-6-yl]phenol

ID: ALA3729345

Chembl Id: CHEMBL3729345

PubChem CID: 117769677

Max Phase: Preclinical

Molecular Formula: C23H18N4O

Molecular Weight: 366.42

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cc(-c2cn3c(-c4ccc5ncccc5c4)cnc3cn2)cc(C)c1O

Standard InChI:  InChI=1S/C23H18N4O/c1-14-8-18(9-15(2)23(14)28)20-13-27-21(11-26-22(27)12-25-20)17-5-6-19-16(10-17)4-3-7-24-19/h3-13,28H,1-2H3

Standard InChI Key:  OULBKRIVANEERU-UHFFFAOYSA-N

Associated Targets(Human)

HepG2-CD81 (19978 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Beta-TC6 (562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium berghei (192651 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: 366.42Molecular Weight (Monoisotopic): 366.1481AlogP: 4.93#Rotatable Bonds: 2
Polar Surface Area: 63.31Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 10.24CX Basic pKa: 4.38CX LogP: 4.02CX LogD: 4.02
Aromatic Rings: 5Heavy Atoms: 28QED Weighted: 0.48Np Likeness Score: -0.91

References

1.  (2014)  Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5, 
2. Antonova-Koch Y, Meister S, Abraham M, Luth MR, Ottilie S, Lukens AK, Sakata-Kato T, Vanaerschot M, Owen E, Jado JC, Maher SP, Calla J, Plouffe D, Zhong Y, Chen K, Chaumeau V, Conway AJ, McNamara CW, Ibanez M, Gagaring K, Serrano FN, Eribez K, Taggard CM, Cheung AL, Lincoln C, Ambachew B, Rouillier M, Siegel D, Nosten F, Kyle DE, Gamo FJ, Zhou Y, Llinás M, Fidock DA, Wirth DF, Burrows J, Campo B, Winzeler EA..  (2018)  Open-source discovery of chemical leads for next-generation chemoprotective antimalarials.,  362  (6419): [PMID:30523084] [10.1126/science.aat9446]