N-[5-(2-methylsulfanylphenyl)-1,3,4-oxadiazol-2-yl]cyclohexanecarboxamide
Modify Date: 2026-06-28 16:20:35
![N-[5-(2-methylsulfanylphenyl)-1,3,4-oxadiazol-2-yl]cyclohexanecarboxamide Structure](https://www.chemsrc.com/extcaspic/360/886909-46-2.png)
N-[5-(2-methylsulfanylphenyl)-1,3,4-oxadiazol-2-yl]cyclohexanecarboxamide structure
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Common Name | N-[5-(2-methylsulfanylphenyl)-1,3,4-oxadiazol-2-yl]cyclohexanecarboxamide | ||
|---|---|---|---|---|
| CAS Number | 886909-46-2 | Molecular Weight | 317.4 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H19N3O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | N-[5-(2-methylsulfanylphenyl)-1,3,4-oxadiazol-2-yl]cyclohexanecarboxamide |
|---|
| Molecular Formula | C16H19N3O2S |
|---|---|
| Molecular Weight | 317.4 |
| InChIKey | YQJFRZLSSOILFI-UHFFFAOYSA-N |
| SMILES | CSC1=CC=CC=C1C2=NN=C(O2)NC(=O)C3CCCCC3 |
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Name: Modulation of AMPAR-stargazin complexes
Source: Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters
Target: Stargazin (mouse)
External Id: WaveGuideAssay:441
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|
Name: Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu...
Source: 15621
Target: G protein-activated inward rectifier potassium channel 2
External Id: VANDERBILT_HTS_GIRK2_HPP
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