N-[5-(2-phenylethyl)-1,3,4-thiadiazol-2-yl]furan-2-carboxamide structure
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Common Name | N-[5-(2-phenylethyl)-1,3,4-thiadiazol-2-yl]furan-2-carboxamide | ||
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| CAS Number | 5482-77-9 | Molecular Weight | 299.3 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C15H13N3O2S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | N-[5-(2-phenylethyl)-1,3,4-thiadiazol-2-yl]furan-2-carboxamide |
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| Molecular Formula | C15H13N3O2S |
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| Molecular Weight | 299.3 |
| InChIKey | OWOWSASWQGANHX-UHFFFAOYSA-N |
| SMILES | C1=CC=C(C=C1)CCC2=NN=C(S2)NC(=O)C3=CC=CO3 |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence Cell-Based Secondary Assay to Measure Toxicity of Compounds Not in the P...
Source: Broad Institute
Target: N/A
External Id: 2037-07_INHIBITORS_DOSE-TITRATION_MLPCN-DRYPOWDER
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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Name: Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Calcineurin
Source: Broad Institute
Target: calcineurin A1, putative; calmodulin-binding protein 1, putative; serine/threonine-protein phosphatase 2B catalytic subunit A1, putative [Candida dubliniensis CD36]
External Id: 2037-06_INHIBITORS_DOSE-TITRATION_MLPCN-DRYPOWDER
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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