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(R)-1-[4-(4-Propyl-phenyl)-3,6-dihydro-2H-pyridine-1-sulfonyl]-piperidine-2-carboxylic acid hydroxyamide ID: ALA126563
PubChem CID: 44351324
Max Phase: Preclinical
Molecular Formula: C20H29N3O4S
Molecular Weight: 407.54
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CCCc1ccc(C2=CCN(S(=O)(=O)N3CCCC[C@@H]3C(=O)NO)CC2)cc1
Standard InChI: InChI=1S/C20H29N3O4S/c1-2-5-16-7-9-17(10-8-16)18-11-14-22(15-12-18)28(26,27)23-13-4-3-6-19(23)20(24)21-25/h7-11,19,25H,2-6,12-15H2,1H3,(H,21,24)/t19-/m1/s1
Standard InChI Key: USVRFHGEBWZPCD-LJQANCHMSA-N
Molfile:
RDKit 2D
28 30 0 0 1 0 0 0 0 0999 V2000
1.6625 0.5500 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
1.4500 -0.2500 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
1.0292 -0.9625 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4875 0.5458 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
0.2042 -0.9542 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1375 0.4708 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7542 1.2083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9500 1.2708 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.0750 1.1375 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.9292 1.2458 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9625 0.4375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8667 -0.1792 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.2000 -0.2417 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.6917 -0.2167 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.2083 -1.6667 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.4000 1.1375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3417 -0.2875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2750 -0.2542 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4417 -1.6792 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1667 -0.3250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.2292 1.1083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6125 0.3708 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.0333 -1.6667 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.4375 0.3333 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6792 -0.9750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8167 -0.3917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2542 -1.6875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6417 -0.4292 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0
3 2 1 0
4 1 1 0
3 5 1 6
6 14 1 0
7 10 1 0
8 1 2 0
9 1 2 0
10 4 1 0
11 6 1 0
12 4 1 0
13 5 2 0
14 12 1 0
15 5 1 0
16 11 2 0
17 11 1 0
18 2 1 0
3 19 1 0
20 17 2 0
21 16 1 0
22 20 1 0
23 15 1 0
24 22 1 0
25 18 1 0
26 24 1 0
27 25 1 0
28 26 1 0
7 6 2 0
27 19 1 0
21 22 2 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: 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: 407.54Molecular Weight (Monoisotopic): 407.1879AlogP: 2.33#Rotatable Bonds: 6Polar Surface Area: 89.95Molecular Species: NEUTRALHBA: 4HBD: 2#RO5 Violations: ┄HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 8.71CX Basic pKa: ┄CX LogP: 2.20CX LogD: 2.18Aromatic Rings: 1Heavy Atoms: 28QED Weighted: 0.56Np Likeness Score: -0.85
References 1. Chen JJ, Dewdney N, Lin X, Martin RL, Walker KA, Huang J, Chu F, Eugui E, Mirkovich A, Kim Y, Sarma K, Arzeno H, Van Wart HE.. (2003) Design and synthesis of orally active inhibitors of TNF synthesis as anti-rheumatoid arthritis drugs., 13 (22): [PMID:14592482 ] [10.1016/j.bmcl.2003.08.076 ]