ID: ALA4848680

Max Phase: Preclinical

Molecular Formula: C14H14N6

Molecular Weight: 266.31

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C/C(=N\Nc1nc2ccccc2n1C)c1ncccn1

Standard InChI:  InChI=1S/C14H14N6/c1-10(13-15-8-5-9-16-13)18-19-14-17-11-6-3-4-7-12(11)20(14)2/h3-9H,1-2H3,(H,17,19)/b18-10+

Standard InChI Key:  WKCUDMVIYHTGCZ-VCHYOVAHSA-N

Associated Targets(Human)

TOV112D 110 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

NCI-H1299 3248 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mu opioid receptor 19785 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serotonin 2a (5-HT2a) receptor 14758 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Norepinephrine transporter 10102 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 266.31Molecular Weight (Monoisotopic): 266.1280AlogP: 2.20#Rotatable Bonds: 3
Polar Surface Area: 67.99Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.94CX Basic pKa: 5.16CX LogP: 2.59CX LogD: 2.50
Aromatic Rings: 3Heavy Atoms: 20QED Weighted: 0.58Np Likeness Score: -1.44

References

1. Gilleran JA, Yu X, Blayney AJ, Bencivenga AF, Na B, Augeri DJ, Blanden AR, Kimball SD, Loh SN, Roberge JY, Carpizo DR..  (2021)  Benzothiazolyl and Benzoxazolyl Hydrazones Function as Zinc Metallochaperones to Reactivate Mutant p53.,  64  (4.0): [PMID:33538587] [10.1021/acs.jmedchem.0c01360]

Source