ID: ALA3889895

Max Phase: Preclinical

Molecular Formula: C33H42N6O3

Molecular Weight: 570.74

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)COC(=O)/N=C(\N)c1ccc(CC2NCCn3c2nc2cc(C4(C(=O)N5CCCC5)CCCC4)ccc23)cc1

Standard InChI:  InChI=1S/C33H42N6O3/c1-22(2)21-42-32(41)37-29(34)24-9-7-23(8-10-24)19-27-30-36-26-20-25(11-12-28(26)39(30)18-15-35-27)33(13-3-4-14-33)31(40)38-16-5-6-17-38/h7-12,20,22,27,35H,3-6,13-19,21H2,1-2H3,(H2,34,37,41)

Standard InChI Key:  ZYCXYTNQQMOFHW-UHFFFAOYSA-N

Associated Targets(non-human)

Thrombin 80 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: 570.74Molecular Weight (Monoisotopic): 570.3318AlogP: 4.86#Rotatable Bonds: 7
Polar Surface Area: 114.84Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.55CX LogP: 4.70CX LogD: 4.32
Aromatic Rings: 3Heavy Atoms: 42QED Weighted: 0.31Np Likeness Score: -0.65

References

1. Chen D, Shi J, Liu J, Zhang X, Deng X, Yang Y, Cui S, Zhu Q, Gong G, Xu Y..  (2017)  Design, synthesis and antithrombotic evaluation of novel non-peptide thrombin inhibitors.,  25  (2): [PMID:27884512] [10.1016/j.bmc.2016.11.012]

Source