ID: ALA2391042

Max Phase: Preclinical

Molecular Formula: C24H28F3N5O7S

Molecular Weight: 473.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1CCCN(c2ccc(N3C[C@H](CNC(=O)c4cnc(N)s4)OC3=O)cc2)C1.O=C(O)C(F)(F)F

Standard InChI:  InChI=1S/C22H27N5O5S.C2HF3O2/c1-2-31-20(29)14-4-3-9-26(12-14)15-5-7-16(8-6-15)27-13-17(32-22(27)30)10-24-19(28)18-11-25-21(23)33-18;3-2(4,5)1(6)7/h5-8,11,14,17H,2-4,9-10,12-13H2,1H3,(H2,23,25)(H,24,28);(H,6,7)/t14?,17-;/m0./s1

Standard InChI Key:  FEILVNBXMTYMBP-UXRSAYELSA-N

Associated Targets(Human)

Integrin alpha-IIb/beta-3 3481 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypsin 2137 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Thrombin 11687 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Coagulation factor X 9693 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: 473.56Molecular Weight (Monoisotopic): 473.1733AlogP: 2.26#Rotatable Bonds: 7
Polar Surface Area: 127.09Molecular Species: NEUTRALHBA: 9HBD: 2
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.57CX Basic pKa: 4.05CX LogP: 1.94CX LogD: 1.94
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.59Np Likeness Score: -1.53

References

1. Trstenjak U, Ilaš J, Kikelj D..  (2013)  Low molecular weight dual inhibitors of factor Xa and fibrinogen binding to GPIIb/IIIa with highly overlapped pharmacophores.,  64  [PMID:23644213] [10.1016/j.ejmech.2013.03.056]

Source