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Β-雌二醇-6-肟

更新时间:2025-08-21 16:24:21

Β-雌二醇-6-肟结构式
Β-雌二醇-6-肟结构式
品牌特惠专场
常用名 Β-雌二醇-6-肟 英文名 6-Ketoestradiol
CAS号 571-92-6 分子量 286.366
密度 1.3±0.1 g/cm3 沸点 478.9±45.0 °C at 760 mmHg
分子式 C18H22O3 熔点 281-283ºC
MSDS 美版 闪点 257.5±25.2 °C

 Β-雌二醇-6-肟用途


6-Ketoestradiol 可用于合成含 7α-取代的雌二醇复合物。

 Β-雌二醇-6-肟名称

中文名 6-酮雌二醇
英文名 6-Keto 17β-Estradiol
中文别名 Β-雌二醇-6-肟 | Β-雌二醇-6-肟 | (17B)-3,17-二羟基雌甾-1,3,5(10)-三烯-6-酮
英文别名 更多

 Β-雌二醇-6-肟物理化学性质

密度 1.3±0.1 g/cm3
沸点 478.9±45.0 °C at 760 mmHg
熔点 281-283ºC
分子式 C18H22O3
分子量 286.366
闪点 257.5±25.2 °C
精确质量 286.156891
PSA 57.53000
LogP 3.30
InChIKey ZHTDDOWJIRXOMA-YVEZLPLXSA-N
SMILES CC12CCC3c4ccc(O)cc4C(=O)CC3C1CCC2O
蒸汽压 0.0±1.3 mmHg at 25°C
折射率 1.612
储存条件 室温

 Β-雌二醇-6-肟安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危害码 (欧洲) Xn
安全声明 (欧洲) 22-24/25
危险品运输编码 NONH for all modes of transport

 Β-雌二醇-6-肟文献7

更多文献
C6-(N,N-butyl-methyl-heptanamide) derivatives of estrone and estradiol as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Chemical synthesis and biological evaluation.

Bioorg. Med. Chem. 15 , 714-26, (2007)

A series of estrone and estradiol derivatives having an N-butyl,methyl heptanamide side chain at C6-position were synthesized, tested as inhibitors of type 1 17beta-HSD and assessed for their possible...

An efficient stereoselective synthesis of 6-alpha-aminoestradiol: preparation of estradiol fluorescent probes.

Steroids 62 , 462, (1997)

6-Oxoestradiol (2) was protected as its bis[(2-trimethylsilylethoxy)methyl] ether (4) and converted to the corresponding oxime (4). The oxime (4) on reduction with zinc in ethanol afforded the bis-SEM...

RP-HPLC analysis of phenolic acids of selected Central European Carex L. (Cyperaceae) species and its implication for taxonomy.

J. AOAC Int. 94 , 9-16, (2011)

Eighteen species belonging to the Carex genus were checked for the presence and the amount of eight phenolic acids (p-hydroxybenzoic, vanillic, caffeic, syringic, protocatechuic, p-coumaric, sinapic, ...

 Β-雌二醇-6-肟靶点实验

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: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 Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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 Β-雌二醇-6-肟英文别名

6-ketoestradiol
(17β)-3,17-Dihydroxyestra-1,3,5(10)-trien-6-one
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