ID: ALA4866982

Max Phase: Preclinical

Molecular Formula: C11H9N3S

Molecular Weight: 215.28

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  N#Cc1ccccc1Cc1cnc(N)s1

Standard InChI:  InChI=1S/C11H9N3S/c12-6-9-4-2-1-3-8(9)5-10-7-14-11(13)15-10/h1-4,7H,5H2,(H2,13,14)

Standard InChI Key:  OKSWEXUXMSNDEZ-UHFFFAOYSA-N

Associated Targets(Human)

Calcium-activated potassium channel subunit alpha-1 435 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: 215.28Molecular Weight (Monoisotopic): 215.0517AlogP: 2.19#Rotatable Bonds: 2
Polar Surface Area: 62.70Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.29CX LogP: 2.57CX LogD: 2.56
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.83Np Likeness Score: -1.84

References

1. Qi XL, Jo H, Wang XY, Ji TT, Lin HX, Park CS, Cui YM..  (2021)  Synthesis and BK channel-opening activity of 2-amino-1,3-thiazole derivatives.,  43  [PMID:33964448] [10.1016/j.bmcl.2021.128083]

Source