1,4-dihydro-3-(1'H-pyrazolo-3'-yl)-8-phenylpyrazolo[5,1-c][1,2,4]triazin-4-one

ID: ALA4228455

Chembl Id: CHEMBL4228455

PubChem CID: 145968900

Max Phase: Preclinical

Molecular Formula: C14H10N6O

Molecular Weight: 278.27

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=c1c(-c2cc[nH]n2)n[nH]c2c(-c3ccccc3)cnn12

Standard InChI:  InChI=1S/C14H10N6O/c21-14-12(11-6-7-15-17-11)18-19-13-10(8-16-20(13)14)9-4-2-1-3-5-9/h1-8,19H,(H,15,17)

Standard InChI Key:  ICYCWACHPRPMAN-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4228455

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Associated Targets(non-human)

Gabrg2 GABA-A receptor; alpha-1/beta-2/gamma-2 (554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gabrg2 GABA A receptor alpha-5/beta-3/gamma-2 (149 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: 278.27Molecular Weight (Monoisotopic): 278.0916AlogP: 1.47#Rotatable Bonds: 2
Polar Surface Area: 91.73Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 9.29CX Basic pKa: 0.91CX LogP: 2.53CX LogD: 2.52
Aromatic Rings: 4Heavy Atoms: 21QED Weighted: 0.58Np Likeness Score: -1.45

References

1. Guerrini G, Ciciani G, Daniele S, Martini C, Costagli C, Guarino C, Selleri S..  (2018)  A new class of pyrazolo[5,1-c][1,2,4]triazines as γ-aminobutyric type A (GABAA) receptor subtype ligand: synthesis and pharmacological evaluation.,  26  (9): [PMID:29650463] [10.1016/j.bmc.2018.04.011]

Source