ID: ALA2069507

Max Phase: Preclinical

Molecular Formula: C25H26N4O2S

Molecular Weight: 446.58

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=S1(=O)CCC(C2N[C@@H](c3nc(-c4ccccc4)c[nH]3)Cc3c2[nH]c2ccccc32)CC1

Standard InChI:  InChI=1S/C25H26N4O2S/c30-32(31)12-10-17(11-13-32)23-24-19(18-8-4-5-9-20(18)27-24)14-21(28-23)25-26-15-22(29-25)16-6-2-1-3-7-16/h1-9,15,17,21,23,27-28H,10-14H2,(H,26,29)/t21-,23?/m1/s1

Standard InChI Key:  UAWQTTVKSRHYOM-FKHAVUOCSA-N

Associated Targets(Human)

Somatostatin receptor 3 1562 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 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: 446.58Molecular Weight (Monoisotopic): 446.1776AlogP: 4.31#Rotatable Bonds: 3
Polar Surface Area: 90.64Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.87CX Basic pKa: 7.29CX LogP: 2.87CX LogD: 2.62
Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.44Np Likeness Score: -0.47

References

1. Pasternak A, Feng Z, de Jesus R, Ye Z, He S, Dobbelaar P, Bradley SA, Chicchi GG, Tsao KL, Trusca D, Eiermann GJ, Li C, Feng Y, Wu M, Shao Q, Zhang BB, Nargund R, Mills SG, Howard AD, Yang L, Zhou YP..  (2012)  Stimulation of Glucose-Dependent Insulin Secretion by a Potent, Selective sst3 Antagonist.,  (4): [PMID:24900466] [10.1021/ml200272z]

Source