ID: ALA4102951

Max Phase: Preclinical

Molecular Formula: C24H21N3O2

Molecular Weight: 383.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(-n2nc(C)c3cnc(-c4ccc([C@H]5C[C@@H]5C(=O)O)cc4)cc32)cc1

Standard InChI:  InChI=1S/C24H21N3O2/c1-14-3-9-18(10-4-14)27-23-12-22(25-13-21(23)15(2)26-27)17-7-5-16(6-8-17)19-11-20(19)24(28)29/h3-10,12-13,19-20H,11H2,1-2H3,(H,28,29)/t19-,20+/m1/s1

Standard InChI Key:  NOQAZVKRASANGW-UXHICEINSA-N

Associated Targets(Human)

FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ffar1 Free fatty acid receptor 1 (306 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ffar4 Omega-3 fatty acid receptor 1 (147 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: 383.45Molecular Weight (Monoisotopic): 383.1634AlogP: 4.89#Rotatable Bonds: 4
Polar Surface Area: 68.01Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.55CX Basic pKa: 3.94CX LogP: 3.99CX LogD: 1.58
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.54Np Likeness Score: -1.02

References

1. McCoull W, Bailey A, Barton P, Birch AM, Brown AJ, Butler HS, Boyd S, Butlin RJ, Chappell B, Clarkson P, Collins S, Davies RM, Ertan A, Hammond CD, Holmes JL, Lenaghan C, Midha A, Morentin-Gutierrez P, Moore JE, Raubo P, Robb G..  (2017)  Indazole-6-phenylcyclopropylcarboxylic Acids as Selective GPR120 Agonists with in Vivo Efficacy.,  60  (7): [PMID:28374589] [10.1021/acs.jmedchem.7b00210]

Source