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2-((1-Benzyl-4-fluoropiperidin-4-yl)methyl)-5,6-dimethoxy-2,3-dihydrobenzo[b]thiophene 1,1-dioxide ID: ALA5204649
PubChem CID: 168296690
Max Phase: Preclinical
Molecular Formula: C23H28FNO4S
Molecular Weight: 433.55
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: COc1cc2c(cc1OC)S(=O)(=O)C(CC1(F)CCN(Cc3ccccc3)CC1)C2
Standard InChI: InChI=1S/C23H28FNO4S/c1-28-20-13-18-12-19(30(26,27)22(18)14-21(20)29-2)15-23(24)8-10-25(11-9-23)16-17-6-4-3-5-7-17/h3-7,13-14,19H,8-12,15-16H2,1-2H3
Standard InChI Key: JWPVAICIJAADBU-UHFFFAOYSA-N
Molfile:
RDKit 2D
30 33 0 0 0 0 0 0 0 0999 V2000
-1.0922 2.5129 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.8797 1.7158 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
-0.2952 2.3002 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.4090 1.0623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4159 1.0623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8284 0.3479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4159 -0.3665 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8284 -1.0810 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6534 -1.0810 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
2.0658 -1.7954 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8908 -1.7954 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3051 -2.5129 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1296 -2.5129 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5386 -1.7964 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1260 -1.0818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3035 -1.0818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.0658 -0.3665 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6534 0.3479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2409 1.0623 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
-0.9009 0.3949 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6836 0.6407 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6836 1.4657 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3953 1.8774 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1097 1.4652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1097 0.6370 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3935 0.2290 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8241 0.2245 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.5386 0.6370 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8241 1.8778 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.5386 1.4652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
2 3 2 0
2 4 1 0
4 5 1 0
5 6 1 0
6 7 1 0
7 8 1 0
8 9 1 0
9 10 1 0
10 11 1 0
11 12 1 0
12 13 2 0
13 14 1 0
14 15 2 0
15 16 1 0
16 11 2 0
9 17 1 0
17 18 1 0
18 6 1 0
6 19 1 0
20 4 1 0
21 20 1 0
21 22 2 0
22 2 1 0
22 23 1 0
23 24 2 0
24 25 1 0
25 26 2 0
26 21 1 0
25 27 1 0
27 28 1 0
24 29 1 0
29 30 1 0
M END Associated Targets(non-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: 433.55Molecular Weight (Monoisotopic): 433.1723AlogP: 3.80#Rotatable Bonds: 6Polar Surface Area: 55.84Molecular Species: NEUTRALHBA: 5HBD: ┄#RO5 Violations: ┄HBA (Lipinski): 5HBD (Lipinski): ┄#RO5 Violations (Lipinski): ┄CX Acidic pKa: ┄CX Basic pKa: 6.82CX LogP: 2.84CX LogD: 2.74Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.69Np Likeness Score: -0.46
References 1. Liu Y, Uras G, Onuwaje I, Li W, Yao H, Xu S, Li X, Li X, Phillips J, Allen S, Gong Q, Zhang H, Zhu Z, Liu J, Xu J.. (2022) Novel inhibitors of AChE and Aβ aggregation with neuroprotective properties as lead compounds for the treatment of Alzheimer's disease., 235 [PMID:35339839 ] [10.1016/j.ejmech.2022.114305 ]