ID: ALA4216735

Max Phase: Preclinical

Molecular Formula: C28H27F5N2O5

Molecular Weight: 566.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)CCC(=O)N(C1CC1)[C@H]1c2cc(C(F)F)ccc2N(C(=O)c2ccc(OC(F)(F)F)cc2)[C@H]2CCC[C@H]21

Standard InChI:  InChI=1S/C28H27F5N2O5/c29-26(30)16-6-11-22-20(14-16)25(34(17-7-8-17)23(36)12-13-24(37)38)19-2-1-3-21(19)35(22)27(39)15-4-9-18(10-5-15)40-28(31,32)33/h4-6,9-11,14,17,19,21,25-26H,1-3,7-8,12-13H2,(H,37,38)/t19-,21+,25-/m1/s1

Standard InChI Key:  WLLHLVHRBAXWRA-FZOAFFARSA-N

Associated Targets(Human)

G protein-coupled receptor 44 4688 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: 566.52Molecular Weight (Monoisotopic): 566.1840AlogP: 6.25#Rotatable Bonds: 8
Polar Surface Area: 87.15Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.15CX Basic pKa: CX LogP: 5.11CX LogD: 2.04
Aromatic Rings: 2Heavy Atoms: 40QED Weighted: 0.38Np Likeness Score: -0.75

References

1. Huang X, Brubaker J, Zhou W, Biju PJ, Xiao L, Shao N, Huang Y, Dong L, Liu Z, Bitar R, Buevich A, Jung J, Peterson SL, Butcher JW, Close J, Martinez M, MacCoss RN, Zhang H, Crawford S, McCormick KD, Aslanian R, Nargund R, Correll C, Gervais F, Qiu H, Yang X, Garlisi C, Rindgen D, Maloney KM, Siliphaivanh P, Palani A..  (2018)  Discovery of MK-8318, a Potent and Selective CRTh2 Receptor Antagonist for the Treatment of Asthma.,  (7): [PMID:30034600] [10.1021/acsmedchemlett.8b00145]

Source