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2-((2R,4R)-1-(4-(((3R,4R)-1-(5-ethoxy-2-fluorophenyl)-3-methylpiperidin-4-yl)oxy)phenyl)-4-(trifluoromethyl)pyrrolidin-2-yl)acetic acid ID: ALA5287383
Max Phase: Preclinical
Molecular Formula: C27H32F4N2O4
Molecular Weight: 524.56
Associated Items:
Names and Identifiers Canonical SMILES: CCOc1ccc(F)c(N2CC[C@@H](Oc3ccc(N4C[C@H](C(F)(F)F)C[C@@H]4CC(=O)O)cc3)[C@H](C)C2)c1
Standard InChI: InChI=1S/C27H32F4N2O4/c1-3-36-22-8-9-23(28)24(14-22)32-11-10-25(17(2)15-32)37-21-6-4-19(5-7-21)33-16-18(27(29,30)31)12-20(33)13-26(34)35/h4-9,14,17-18,20,25H,3,10-13,15-16H2,1-2H3,(H,34,35)/t17-,18-,20-,25-/m1/s1
Standard InChI Key: WGYIJLVIRQSKEY-QSWVLOPZSA-N
Molfile:
RDKit 2D
37 40 0 0 0 0 0 0 0 0999 V2000
0.0070 1.6484 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7216 2.0607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4335 1.6488 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4335 0.8236 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7234 0.4118 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0070 0.8199 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1481 0.4110 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
2.9016 0.7465 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4536 0.1335 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0412 -0.5807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2343 -0.4092 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6512 -0.9923 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8646 -1.7889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2815 -2.3720 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.6612 -2.0023 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.2782 0.1335 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.6906 0.8477 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
4.2782 -0.6926 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
4.9925 -0.2787 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
-0.7070 2.0607 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.4213 1.6484 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4212 0.8237 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1354 0.4114 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.8496 0.8237 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.8496 1.6484 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1354 2.0607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5638 0.4114 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5641 -0.4132 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2765 -0.8237 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9909 -0.4112 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.9925 0.4092 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2810 0.8255 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.2810 1.6502 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
-4.2765 -1.6484 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.5622 -2.0607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1354 2.8854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5622 -2.8854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 1 0
4 3 2 0
5 4 1 0
6 5 2 0
1 6 1 0
7 4 1 0
7 8 1 0
8 9 1 0
9 10 1 0
10 11 1 0
11 7 1 0
11 12 1 6
12 13 1 0
13 14 1 0
13 15 2 0
9 16 1 6
16 17 1 0
16 18 1 0
16 19 1 0
1 20 1 0
21 20 1 6
22 21 1 0
23 22 1 0
24 23 1 0
25 24 1 0
26 25 1 0
21 26 1 0
27 24 1 0
28 27 2 0
29 28 1 0
30 29 2 0
31 30 1 0
32 31 2 0
27 32 1 0
32 33 1 0
29 34 1 0
34 35 1 0
26 36 1 1
35 37 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 524.56Molecular Weight (Monoisotopic): 524.2298AlogP: 5.75#Rotatable Bonds: 8Polar Surface Area: 62.24Molecular Species: ACIDHBA: 5HBD: 1#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 2CX Acidic pKa: 4.36CX Basic pKa: 2.98CX LogP: 5.32CX LogD: 2.59Aromatic Rings: 2Heavy Atoms: 37QED Weighted: 0.44Np Likeness Score: -0.59
References 1. Jurica EA, Wu X, Williams KN, Haque LE, Rampulla RA, Mathur A, Zhou M, Cao G, Cai H, Wang T, Liu H, Xu C, Kunselman LK, Antrilli TM, Hicks MB, Sun Q, Dierks EA, Apedo A, Moore DB, Foster KA, Cvijic ME, Panemangalore R, Khandelwal P, Wilkes JJ, Zinker BA, Robertson DG, Janovitz EB, Galella M, Li YX, Li J, Ramar T, Jalagam PR, Jayaram R, Whaley JM, Barrish JC, Robl JA, Ewing WR, Ellsworth BA.. (2023) Optimization of physicochemical properties of pyrrolidine GPR40 AgoPAMs results in a differentiated profile with improved pharmacokinetics and reduced off-target activities., 85 [PMID:37030194 ] [10.1016/j.bmc.2023.117273 ]