2-((6-methoxy-1H-benzo[d]imidazol-2-yl)methyl)-1H-benzo[d]imidazole-5-carboxamidine

ID: ALA203989

Chembl Id: CHEMBL203989

PubChem CID: 44407777

Max Phase: Preclinical

Molecular Formula: C17H16N6O

Molecular Weight: 320.36

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc2[nH]c(Cc3nc4cc(C(=N)N)ccc4[nH]3)nc2c1

Standard InChI:  InChI=1S/C17H16N6O/c1-24-10-3-5-12-14(7-10)23-16(21-12)8-15-20-11-4-2-9(17(18)19)6-13(11)22-15/h2-7H,8H2,1H3,(H3,18,19)(H,20,22)(H,21,23)

Standard InChI Key:  SGOHQLWVNHDEHF-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: 320.36Molecular Weight (Monoisotopic): 320.1386AlogP: 2.32#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: 11.58CX Basic pKa: 10.73CX LogP: 1.33CX LogD: -0.75
Aromatic Rings: 4Heavy Atoms: 24QED Weighted: 0.34Np Likeness Score: -0.78

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