ID: ALA5195348

Max Phase: Preclinical

Molecular Formula: C16H10F2N4O

Molecular Weight: 312.28

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1nc2ccccc2[nH]1)c1cc2c(F)cc(F)cc2[nH]1

Standard InChI:  InChI=1S/C16H10F2N4O/c17-8-5-10(18)9-7-14(19-13(9)6-8)15(23)22-16-20-11-3-1-2-4-12(11)21-16/h1-7,19H,(H2,20,21,22,23)

Standard InChI Key:  GCKVDJPBBGKETN-UHFFFAOYSA-N

Associated Targets(Human)

KNS-42 217 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Daoy 570 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HFF-1 186 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cannabinoid CB1 receptor 20913 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cannabinoid CB2 receptor 16942 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

Properties

Molecular Weight: 312.28Molecular Weight (Monoisotopic): 312.0823AlogP: 3.57#Rotatable Bonds: 2
Polar Surface Area: 73.57Molecular Species: NEUTRALHBA: 2HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.97CX Basic pKa: 2.50CX LogP: 3.34CX LogD: 3.34
Aromatic Rings: 4Heavy Atoms: 23QED Weighted: 0.53Np Likeness Score: -1.57

References

1. Alsayed SSR, Suri A, Bailey AW, Lane S, Werry EL, Huang CC, Yu LF, Kassiou M, Sredni ST, Gunosewoyo H..  (2021)  Synthesis and antitumour evaluation of indole-2-carboxamides against paediatric brain cancer cells.,  12  (11.0): [PMID:34825187] [10.1039/D1MD00065A]

Source