ID: ALA5276066

Max Phase: Preclinical

Molecular Formula: C21H14ClN3O

Molecular Weight: 359.82

Associated Items:

Representations

Canonical SMILES:  O=c1c2ccccc2nc(-c2ccncc2)n1/C=C/c1ccccc1Cl

Standard InChI:  InChI=1S/C21H14ClN3O/c22-18-7-3-1-5-15(18)11-14-25-20(16-9-12-23-13-10-16)24-19-8-4-2-6-17(19)21(25)26/h1-14H/b14-11+

Standard InChI Key:  SEFCZNFIOOZCLG-SDNWHVSQSA-N

Associated Targets(non-human)

Tobacco mosaic virus 2972 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: 359.82Molecular Weight (Monoisotopic): 359.0825AlogP: 4.74#Rotatable Bonds: 3
Polar Surface Area: 47.78Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.63CX LogP: 4.35CX LogD: 4.35
Aromatic Rings: 4Heavy Atoms: 26QED Weighted: 0.53Np Likeness Score: -0.93

References

1. Alagarsamy V, Chitra K, Saravanan G, Solomon VR, Sulthana MT, Narendhar B..  (2018)  An overview of quinazolines: Pharmacological significance and recent developments.,  151  [PMID:29656203] [10.1016/j.ejmech.2018.03.076]

Source