ID: ALA550153

Max Phase: Preclinical

Molecular Formula: C14H13N3O3S

Molecular Weight: 303.34

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)c1cc(N(Cc2ccsc2)Cc2ccco2)[nH]n1

Standard InChI:  InChI=1S/C14H13N3O3S/c18-14(19)12-6-13(16-15-12)17(7-10-3-5-21-9-10)8-11-2-1-4-20-11/h1-6,9H,7-8H2,(H,15,16)(H,18,19)

Standard InChI Key:  GARCZYVSFNZCAR-UHFFFAOYSA-N

Associated Targets(Human)

HM74 nicotinic acid GPCR 353 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hydroxycarboxylic acid receptor 2 1903 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

Properties

Molecular Weight: 303.34Molecular Weight (Monoisotopic): 303.0678AlogP: 2.97#Rotatable Bonds: 6
Polar Surface Area: 82.36Molecular Species: ACIDHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.92CX Basic pKa: 1.29CX LogP: 2.81CX LogD: -0.40
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.73Np Likeness Score: -2.02

References

1. Skinner PJ, Webb PJ, Sage CR, Dang TH, Pride CC, Chen R, Tamura SY, Richman JG, Connolly DT, Semple G..  (2009)  5-N,N-Disubstituted 5-aminopyrazole-3-carboxylic acids are highly potent agonists of GPR109b.,  19  (15): [PMID:19524438] [10.1016/j.bmcl.2009.05.108]

Source