ID: ALA593759

Max Phase: Preclinical

Molecular Formula: C15H10FN

Molecular Weight: 223.25

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Fc1ccc2c(c1)Cc1c-2[nH]c2ccccc12

Standard InChI:  InChI=1S/C15H10FN/c16-10-5-6-11-9(7-10)8-13-12-3-1-2-4-14(12)17-15(11)13/h1-7,17H,8H2

Standard InChI Key:  JWTKADSGXREMMQ-UHFFFAOYSA-N

Associated Targets(Human)

Carbonic anhydrase I 13240 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Carbonic anhydrase II 17698 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Carbonic anhydrase IV 2163 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Carbonic anhydrase VI 993 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Carbonic anhydrase 3 27 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: 223.25Molecular Weight (Monoisotopic): 223.0797AlogP: 3.88#Rotatable Bonds: 0
Polar Surface Area: 15.79Molecular Species: NEUTRALHBA: 0HBD: 1
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.42CX Basic pKa: CX LogP: 3.90CX LogD: 3.90
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.47Np Likeness Score: -0.55

References

1. Talaz O, Gülçin I, Göksu S, Saracoglu N..  (2009)  Antioxidant activity of 5,10-dihydroindeno[1,2-b]indoles containing substituents on dihydroindeno part.,  17  (18): [PMID:19683932] [10.1016/j.bmc.2009.07.077]
2. Ekinci D, Cavdar H, Durdagi S, Talaz O, Sentürk M, Supuran CT..  (2012)  Structure-activity relationships for the interaction of 5,10-dihydroindeno[1,2-b]indole derivatives with human and bovine carbonic anhydrase isoforms I, II, III, IV and VI.,  49  [PMID:22245047] [10.1016/j.ejmech.2011.12.022]

Source