雄烯酮

• 常用名: 雄烯酮
• 英文名: (5α)-Androst-16-en-3-one
• CAS号: 18339-16-7
• 分子量: 272.425
• 密度: 1.0±0.1 g/cm3
• 沸点: 371.6±42.0 °C at 760 mmHg
• 分子式: C₁₉H₂₈O
• 熔点: 140-145ºC(lit.)
• 闪点: 157.7±22.8 °C

雄烯酮名称

• 中文名: 雄烯酮
• 英文名: 5α-androst-16-en-3-one
• 中文别名: 男性酯酮

雄烯酮物理化学性质

• 密度: 1.0±0.1 g/cm3
• 沸点: 371.6±42.0 °C at 760 mmHg
• 熔点: 140-145ºC(lit.)
• 分子式: C₁₉H₂₈O
• 分子量: 272.425
• 闪点: 157.7±22.8 °C
• 精确质量: 272.214020
• PSA: 17.07000
• LogP: 5.30
• InChIKey: HFVMLYAGWXSTQI-QYXZOKGRSA-N
• SMILES: CC12C=CCC1C1CCC3CC(=O)CCC3(C)C1CC2
• 外观性状: 白色晶体
• 蒸汽压: 0.0±0.8 mmHg at 25°C
• 折射率: 1.530
• 储存条件: 室温，干燥

雄烯酮安全信息

• 危险品运输编码: NONH for all modes of transport
• WGK德国: -

雄烯酮靶点实验

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：Cytotoxicity counterscreen for inhibitors of SARS-CoV-2 cell entry 来源：NCGC 靶标：N/A External Id：TRND-SARS-CoV-2-cytotox-48hr

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：Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Validation... 来源：NMMLSC 靶标：ATP-binding cassette sub-family B member 6, mitochondrial [Homo sapiens] External Id：UNMCMD_ABCB6_1o_ValidationSet

实验名称：Primary qHTS to identify inhibitors of SARS-CoV-2 cell entry 来源：NCGC External Id：TRND-SARS-CoV-2-PP

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雄烯酮英文别名

• MFCD00010479
• 5α-Androst-16-en-3-one
• 5alpha-Androstenone
• Androst-16-en-3-one
• 5a-androst-16-en-3-one
• (5α)-Androst-16-en-3-one
• 5alpha-androst-16-en-3-one
• androstenone
• (5S,8R,9S,10S,13R,14S)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15-dodecahydrocyclopenta[a]phenanthren-3-one
• EINECS 242-220-1