ID: ALA4215038

Max Phase: Preclinical

Molecular Formula: C23H26Cl2N2O2

Molecular Weight: 433.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C(=O)[C@@H]1CCCN1Cc1cc(Cl)ccc1Cl)c1ccccc1OCC1CC1

Standard InChI:  InChI=1S/C23H26Cl2N2O2/c1-26(20-5-2-3-7-22(20)29-15-16-8-9-16)23(28)21-6-4-12-27(21)14-17-13-18(24)10-11-19(17)25/h2-3,5,7,10-11,13,16,21H,4,6,8-9,12,14-15H2,1H3/t21-/m0/s1

Standard InChI Key:  VACNFKXKXUJPNR-NRFANRHFSA-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: 433.38Molecular Weight (Monoisotopic): 432.1371AlogP: 5.41#Rotatable Bonds: 7
Polar Surface Area: 32.78Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 6.02CX LogP: 5.14CX LogD: 5.12
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.59Np Likeness Score: -1.62

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