2-((5-fluoro-7-methoxy-1H-benzo[d]imidazol-2-yl)methyl)-1H-benzo[d]imidazole-5-carboxamidine

ID: ALA201843

Chembl Id: CHEMBL201843

PubChem CID: 44407547

Max Phase: Preclinical

Molecular Formula: C17H15FN6O

Molecular Weight: 338.35

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(F)cc2[nH]c(Cc3nc4cc(C(=N)N)ccc4[nH]3)nc12

Standard InChI:  InChI=1S/C17H15FN6O/c1-25-13-6-9(18)5-12-16(13)24-15(23-12)7-14-21-10-3-2-8(17(19)20)4-11(10)22-14/h2-6H,7H2,1H3,(H3,19,20)(H,21,22)(H,23,24)

Standard InChI Key:  GJTQNDNNXOMAJV-UHFFFAOYSA-N

Associated Targets(Human)

F10 Tclin Coagulation factor X (9693 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F2 Tclin Thrombin and coagulation factor X (145 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F10 Tclin Coagulation factor VII and X (116 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

Calculated Properties

Molecular Weight: 338.35Molecular Weight (Monoisotopic): 338.1291AlogP: 2.46#Rotatable Bonds: 4
Polar Surface Area: 116.46Molecular Species: BASEHBA: 4HBD: 4
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 11.43CX Basic pKa: 10.70CX LogP: 1.43CX LogD: -0.59
Aromatic Rings: 4Heavy Atoms: 25QED Weighted: 0.34Np Likeness Score: -1.09

References

1. Young WB, Sprengeler P, Shrader WD, Li Y, Rai R, Verner E, Jenkins T, Fatheree P, Kolesnikov A, Janc JW, Cregar L, Elrod K, Katz B..  (2006)  Generation of potent coagulation protease inhibitors utilizing zinc-mediated chelation.,  16  (3): [PMID:16257204] [10.1016/j.bmcl.2005.10.023]

Source