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5-(((2S,3S)-3-((3,5-dichlorobenzyl)oxy)-2-phenylpiperidin-1-yl)methyl)thiophene-2-carboxylic acid ID: ALA4866995
PubChem CID: 164619680
Max Phase: Preclinical
Molecular Formula: C24H23Cl2NO3S
Molecular Weight: 476.43
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: O=C(O)c1ccc(CN2CCC[C@H](OCc3cc(Cl)cc(Cl)c3)[C@@H]2c2ccccc2)s1
Standard InChI: InChI=1S/C24H23Cl2NO3S/c25-18-11-16(12-19(26)13-18)15-30-21-7-4-10-27(23(21)17-5-2-1-3-6-17)14-20-8-9-22(31-20)24(28)29/h1-3,5-6,8-9,11-13,21,23H,4,7,10,14-15H2,(H,28,29)/t21-,23-/m0/s1
Standard InChI Key: GHIYYCUTSNOOKM-GMAHTHKFSA-N
Molfile:
RDKit 2D
31 34 0 0 0 0 0 0 0 0999 V2000
38.3750 -3.3926 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.3750 -4.2098 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.0803 -4.6142 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
39.7855 -4.2098 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.7855 -3.3926 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
39.0803 -2.9799 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.4944 -2.9861 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
40.4926 -4.6194 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.4883 -5.4366 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.1946 -5.8462 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9039 -5.4385 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9024 -4.6171 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.1956 -4.2113 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
40.4968 -2.1689 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.2057 -1.7624 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9120 -2.1755 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.6204 -1.7696 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
42.6233 -0.9516 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9118 -0.5411 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.2063 -0.9493 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
41.9113 0.2769 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
43.3267 -2.1806 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
39.0803 -5.4314 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.3725 -5.8400 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.6259 -5.5126 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.0791 -6.1199 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.4877 -6.8276 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.2870 -6.6576 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
37.1555 -7.5753 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.3428 -7.6608 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
37.6359 -8.2364 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
1 6 1 0
2 3 1 0
3 4 1 0
4 5 1 0
5 6 1 0
5 7 1 6
4 8 1 6
8 9 2 0
9 10 1 0
10 11 2 0
11 12 1 0
12 13 2 0
13 8 1 0
7 14 1 0
14 15 1 0
15 16 2 0
16 17 1 0
17 18 2 0
18 19 1 0
19 20 2 0
20 15 1 0
19 21 1 0
17 22 1 0
3 23 1 0
23 24 1 0
24 25 2 0
25 26 1 0
26 27 2 0
27 28 1 0
28 24 1 0
29 30 1 0
29 31 2 0
27 29 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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: 476.43Molecular Weight (Monoisotopic): 475.0776AlogP: 6.68#Rotatable Bonds: 7Polar Surface Area: 49.77Molecular Species: ACIDHBA: 4HBD: 1#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1CX Acidic pKa: 2.51CX Basic pKa: 8.21CX LogP: 4.02CX LogD: 3.97Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.41Np Likeness Score: -0.80
References 1. Hanisak J, Soriano A, Adam GC, Basso A, Bauman D, Bell D, Frank E, O'Donnell G, Tawa P, Verras A, Yu Y, Zhang L, Seganish WM.. (2021) Discovery of the First Non-cGMP Mimetic Small Molecule Activators of cGMP-Dependent Protein Kinase 1 α (PKG1α)., 12 (8.0): [PMID:34413956 ] [10.1021/acsmedchemlett.1c00264 ]