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(Z)-(1-(4-chlorobenzyl)-1H-indol-2-yl)(4-(4-(pyridin-4-yl)but-1-enyl)piperidin-1-yl)methanone ID: ALA4852837
PubChem CID: 164616795
Max Phase: Preclinical
Molecular Formula: C30H30ClN3O
Molecular Weight: 484.04
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: O=C(c1cc2ccccc2n1Cc1ccc(Cl)cc1)N1CCC(/C=C\CCc2ccncc2)CC1
Standard InChI: InChI=1S/C30H30ClN3O/c31-27-11-9-25(10-12-27)22-34-28-8-4-3-7-26(28)21-29(34)30(35)33-19-15-24(16-20-33)6-2-1-5-23-13-17-32-18-14-23/h2-4,6-14,17-18,21,24H,1,5,15-16,19-20,22H2/b6-2-
Standard InChI Key: QHXSGGLDCXGHIX-KXFIGUGUSA-N
Molfile:
RDKit 2D
35 39 0 0 0 0 0 0 0 0999 V2000
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28.5166 -11.8309 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.2246 -12.2440 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.9384 -11.8305 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.9356 -11.0037 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.2228 -10.5984 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.6509 -12.2421 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.6522 -13.0634 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
31.0704 -14.3228 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.3216 -13.5411 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.2491 -14.3241 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.9934 -13.5462 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.1950 -13.3785 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.6515 -13.9877 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.9077 -14.7674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.7055 -14.9315 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.8058 -10.5989 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
32.1020 -13.2857 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.2690 -12.4817 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.7154 -13.8344 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
32.5440 -14.6340 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.1494 -15.1776 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.9314 -14.9262 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
34.1005 -14.1216 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.4917 -13.5684 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
34.5428 -15.4772 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.3241 -15.2206 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.4941 -14.4172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.2755 -14.1647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.8868 -14.7157 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.7126 -15.5172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.3190 -16.0638 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.1014 -15.8115 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
38.2738 -15.0034 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.6619 -14.4561 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 2 0
6 1 1 0
4 7 1 0
7 8 1 0
8 12 1 0
11 9 1 0
9 10 2 0
10 8 1 0
11 12 2 0
12 13 1 0
13 14 2 0
14 15 1 0
15 16 2 0
16 11 1 0
1 17 1 0
10 18 1 0
18 19 2 0
18 20 1 0
20 21 1 0
20 25 1 0
21 22 1 0
22 23 1 0
23 24 1 0
24 25 1 0
23 26 1 0
26 27 2 0
27 28 1 0
28 29 1 0
29 30 1 0
30 31 2 0
31 32 1 0
32 33 2 0
33 34 1 0
34 35 2 0
35 30 1 0
M END Associated Targets(non-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: 484.04Molecular Weight (Monoisotopic): 483.2077AlogP: 6.78#Rotatable Bonds: 7Polar Surface Area: 38.13Molecular Species: NEUTRALHBA: 3HBD: ┄#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 5.69CX LogP: 6.31CX LogD: 6.30Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.27Np Likeness Score: -0.68
References 1. Barraza SJ, Sindac JA, Dobry CJ, Delekta PC, Lee PH, Miller DJ, Larsen SD.. (2021) Synthesis and biological activity of conformationally restricted indole-based inhibitors of neurotropic alphavirus replication: Generation of a three-dimensional pharmacophore., 46 [PMID:34098081 ] [10.1016/j.bmcl.2021.128171 ]