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6-Chloro-3-hydroxybenzo[b]thiophene-2-carboxylic acid ID: ALA2057740
Chembl Id: CHEMBL2057740
Cas Number: 1393803-55-8
PubChem CID: 62706326
Max Phase: Preclinical
Molecular Formula: C9H5ClO3S
Molecular Weight: 228.66
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C(O)c1sc2cc(Cl)ccc2c1O
Standard InChI: InChI=1S/C9H5ClO3S/c10-4-1-2-5-6(3-4)14-8(7(5)11)9(12)13/h1-3,11H,(H,12,13)
Standard InChI Key: HYDDMVANLIFXSD-UHFFFAOYSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 228.66Molecular Weight (Monoisotopic): 227.9648AlogP: 2.96#Rotatable Bonds: 1Polar Surface Area: 57.53Molecular Species: ACIDHBA: 3HBD: 2#RO5 Violations: ┄HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 3.09CX Basic pKa: ┄CX LogP: 3.59CX LogD: 0.27Aromatic Rings: 2Heavy Atoms: 14QED Weighted: 0.79Np Likeness Score: -1.14
References 1. Hansen FK, Khankischpur M, Tolaymat I, Mesaros R, Dannhardt G, Geffken D.. (2012) Efficient synthesis and 5-LOX/COX-inhibitory activity of some 3-hydroxybenzo[b]thiophene-2-carboxylic acid derivatives., 22 (15): [PMID:22749420 ] [10.1016/j.bmcl.2012.06.012 ]