ID: ALA4292610

Max Phase: Preclinical

Molecular Formula: C37H34N6O6S

Molecular Weight: 690.78

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOc1ccc(OC)cc1C1(N2CCN(c3ccncc3)CC2)C(=O)N(S(=O)(=O)c2ccc(OC)c3cccnc23)c2ccc(C#N)cc21

Standard InChI:  InChI=1S/C37H34N6O6S/c1-4-49-33-10-8-27(47-2)23-30(33)37(42-20-18-41(19-21-42)26-13-16-39-17-14-26)29-22-25(24-38)7-9-31(29)43(36(37)44)50(45,46)34-12-11-32(48-3)28-6-5-15-40-35(28)34/h5-17,22-23H,4,18-21H2,1-3H3

Standard InChI Key:  FKCDNXBPCBYUIK-UHFFFAOYSA-N

Associated Targets(Human)

Vasopressin V1b receptor 1301 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: 690.78Molecular Weight (Monoisotopic): 690.2261AlogP: 4.72#Rotatable Bonds: 9
Polar Surface Area: 138.19Molecular Species: BASEHBA: 11HBD: 0
#RO5 Violations: 2HBA (Lipinski): 12HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 8.70CX LogP: 4.38CX LogD: 3.55
Aromatic Rings: 5Heavy Atoms: 50QED Weighted: 0.21Np Likeness Score: -0.96

References

1. Geneste H, Bhowmik S, van Gaalen MM, Hornberger W, Hutchins CW, Netz A, Oost T, Unger L..  (2018)  Novel, potent, selective and brain penetrant vasopressin 1b receptor antagonists.,  28  (19): [PMID:30098866] [10.1016/j.bmcl.2018.07.043]

Source