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N-(5-硝基-1,3-噻唑-2-基)戊酰胺

更新时间:2025-12-02 11:10:23

N-(5-硝基-1,3-噻唑-2-基)戊酰胺结构式
N-(5-硝基-1,3-噻唑-2-基)戊酰胺结构式
委托求购
常用名 N-(5-硝基-1,3-噻唑-2-基)戊酰胺 英文名 Pentanamide,N-(5-nitro-2-thiazolyl)
CAS号 14538-17-1 分子量 229.25600
密度 1.376g/cm3 沸点 N/A
分子式 C8H11N3O3S 熔点 N/A
MSDS N/A 闪点 N/A

 N-(5-硝基-1,3-噻唑-2-基)戊酰胺名称

中文名 N-(5-硝基-1,3-噻唑-2-基)戊酰胺
英文名 N-(5-nitro-1,3-thiazol-2-yl)pentanamide
英文别名 更多

 N-(5-硝基-1,3-噻唑-2-基)戊酰胺物理化学性质

密度 1.376g/cm3
分子式 C8H11N3O3S
分子量 229.25600
精确质量 229.05200
PSA 116.05000
LogP 2.77620
InChIKey HAQCGFVINUGJBS-UHFFFAOYSA-N
SMILES CCCCC(=O)Nc1ncc([N+](=O)[O-])s1
折射率 1.605

 N-(5-硝基-1,3-噻唑-2-基)戊酰胺合成线路

~66%

N-(5-硝基-1,3-噻唑-2-基)戊酰胺结构式

N-(5-硝基-1,3-噻唑-...

14538-17-1

文献:Nava-Zuazo, Carlos; Chavez-Silva, Fabiola; Moo-Puc, Rosa; Chan-Bacab, Manuel Jesus; Ortega-Morales, Benjamin Otto; Moreno-Diaz, Hermenegilda; Diaz-Coutino, Daniel; Hernandez-Nunez, Emanuel; Navarrete-Vazquez, Gabriel Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 5 p. 1626 - 1633

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N-(5-硝基-1,3-噻唑-2-基)戊酰胺结构式

N-(5-硝基-1,3-噻唑-...

14538-17-1

文献:Kravchenya, N. A. Pharmaceutical Chemistry Journal, 1983 , vol. 17, # 11 p. 809 - 810 Khimiko-Farmatsevticheskii Zhurnal, 1983 , vol. 17, # 11 p. 1340 - 1342

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N-(5-硝基-1,3-噻唑-2-基)戊酰胺结构式

N-(5-硝基-1,3-噻唑-...

14538-17-1

文献:Kravchenya, N. A. Pharmaceutical Chemistry Journal, 1983 , vol. 17, # 11 p. 809 - 810 Khimiko-Farmatsevticheskii Zhurnal, 1983 , vol. 17, # 11 p. 1340 - 1342

 N-(5-硝基-1,3-噻唑-2-基)戊酰胺上下游产品

N-(5-硝基-1,3-噻唑-2-基)戊酰胺上游产品  4

N-(5-硝基-1,3-噻唑-2-基)戊酰胺下游产品  0

 N-(5-硝基-1,3-噻唑-2-基)戊酰胺靶点实验

查看更多实验

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: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: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: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.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Selectivity index, ratio of IC50 for human THP1 cells to IC50 for Trypanosoma brucei ...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4310793
实验名称:Selectivity index, ratio of IC50 for human SK-N-SH cells to IC50 for wild type Trypan...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4310791
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 N-(5-硝基-1,3-噻唑-2-基)戊酰胺英文别名

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