N-pyridin-2-ylthiophene-2-carboxamide结构式
|
常用名 | N-pyridin-2-ylthiophene-2-carboxamide | 英文名 | N-pyridin-2-ylthiophene-2-carboxamide |
|---|---|---|---|---|
| CAS号 | 62289-80-9 | 分子量 | 204.24800 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C10H8N2OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | N-pyridin-2-ylthiophene-2-carboxamide |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C10H8N2OS |
|---|---|
| 分子量 | 204.24800 |
| 精确质量 | 204.03600 |
| PSA | 70.23000 |
| LogP | 2.46840 |
| InChIKey | GFDOUDIYCCVPDR-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccn1)c1cccs1 |
|
~73%
N-pyridin-2-ylt... 62289-80-9 |
| 文献:Nicolas, Lionel; Angibaud, Patrick; Stansfield, Ian; Meerpoel, Lieven; Reymond, Sebastien; Cossy, Janine RSC Advances, 2013 , vol. 3, # 41 p. 18787 - 18790 |
|
~%
N-pyridin-2-ylt... 62289-80-9 |
| 文献:Kyrides et al. Journal of the American Chemical Society, 1947 , vol. 69, p. 2239 |
|
~%
N-pyridin-2-ylt... 62289-80-9 |
| 文献:Zhang, Jianmin; Pettersson, Hanna I.; Huitema, Carly; Niu, Chunying; Yin, Jiang; James, Michael N. G.; Eltis, Lindsay D.; Vederas, John C. Journal of Medicinal Chemistry, 2007 , vol. 50, # 8 p. 1850 - 1864 |
|
实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
|
|
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
|
|
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
|
|
实验名称:Inhibition of hepatitis A virus 3C proteinase at 1 uM by microplate assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL972295
|
|
实验名称:Inhibition of hepatitis A virus 3C proteinase at 10 uM by microplate assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL972294
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:Inhibition of hepatitis A virus 3C proteinase at 0.25 uM by microplate assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL972296
|
|
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
|
|
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
|
|
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
|
| Thiophen-2-carbonsaeure-[2]pyridylamid |
| HMS2347F15 |
| thiophene-2-carboxylic acid-[2]pyridylamide |
| HMS1692D01 |
| Thiophene-2-carboxylic acid pyridin-2-ylamide |