ID: ALA4217961

Max Phase: Preclinical

Molecular Formula: C23H25Cl2N3OS

Molecular Weight: 462.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C([C@@H]1CSCCN1Cc1cc(Cl)ccc1Cl)N1CCN(C2CC2)c2ccccc21

Standard InChI:  InChI=1S/C23H25Cl2N3OS/c24-17-5-8-19(25)16(13-17)14-26-11-12-30-15-22(26)23(29)28-10-9-27(18-6-7-18)20-3-1-2-4-21(20)28/h1-5,8,13,18,22H,6-7,9-12,14-15H2/t22-/m0/s1

Standard InChI Key:  ZYTAIZIRDNQZKZ-QFIPXVFZSA-N

Associated Targets(Human)

G-protein coupled bile acid receptor 1 1723 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

G-protein coupled bile acid receptor 1 577 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: 462.45Molecular Weight (Monoisotopic): 461.1095AlogP: 4.93#Rotatable Bonds: 4
Polar Surface Area: 26.79Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.33CX LogP: 4.87CX LogD: 4.87
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.64Np Likeness Score: -1.50

References

1. Chen T, Reich NW, Bell N, Finn PD, Rodriguez D, Kohler J, Kozuka K, He L, Spencer AG, Charmot D, Navre M, Carreras CW, Koo-McCoy S, Tabora J, Caldwell JS, Jacobs JW, Lewis JG..  (2018)  Design of Gut-Restricted Thiazolidine Agonists of G Protein-Coupled Bile Acid Receptor 1 (GPBAR1, TGR5).,  61  (17): [PMID:30141927] [10.1021/acs.jmedchem.8b00308]

Source