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11α-Hydroxyprogesterone 11-hemisuccinate | 41238-98-6

中文名称
——
中文别名
——
英文名称
11α-Hydroxyprogesterone 11-hemisuccinate
英文别名
11α-hydroxyprogesterone hemisuccinate;11α-hydroxyprogesterone-hemisuccinate;11α-hemisuccinylprogesterone;11α-Hydroxyprogesteron-11-hemisuccinat;Progesteron-11α-hemisuccinat;Progesterone-11-Alpha-Ol-Hemisuccinate;4-[[(8S,9S,10R,11R,13S,14S,17S)-17-acetyl-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-11-yl]oxy]-4-oxobutanoic acid
11α-Hydroxyprogesterone 11-hemisuccinate化学式
CAS
41238-98-6
化学式
C25H34O6
mdl
——
分子量
430.541
InChiKey
JBBNFGYRYNBDIH-DBGGZKJISA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    603.0±55.0 °C(Predicted)
  • 密度:
    1.22±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    31
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    97.7
  • 氢给体数:
    1
  • 氢受体数:
    6

SDS

SDS:790005ea2f5101b8789c253fd4c98143
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    11α-Hydroxyprogesterone 11-hemisuccinateammonium hydroxideN-羟基丁二酰亚胺碳酸氢钠N,N'-二环己基碳二亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 8.0h, 生成 N-(2-Carbamoyl-ethyl)-succinamic acid (8S,9S,10R,11R,13S,14S,17S)-17-acetyl-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl ester
    参考文献:
    名称:
    Influence of functional groups on homologous antibody affinity of 11α-hydroxyprogesterone derivatives. I. Synthesis and affinity evaluation
    摘要:
    Syntheses and cross-reactivities with progesterone toward the same specific antibody are reported for a series of amides of 11 alpha-hydroxyprogesterone 11-hemisuccinate. Some hypotheses are made regarding the effects of the chemical structure of the substituents on the immunological properties of derivatives.
    DOI:
    10.1016/0039-128x(88)90124-9
  • 作为产物:
    描述:
    丁二酸酐11Alpha-孕酮4-二甲氨基吡啶 作用下, 以 1,4-二氧六环 为溶剂, 反应 5.0h, 以43.3%的产率得到11α-Hydroxyprogesterone 11-hemisuccinate
    参考文献:
    名称:
    A rapid approach to 11α-hemisuccinylprogesterone synthesis
    摘要:
    The synthetic hapten 11 alpha-hemisuccinylprogesterone (11 alpha-hemisuccinyl-pregn-4-ene-3,20-dione), when linked to the appropriate macromolecular carrier, has been used successfully as a solid-phase antigen for progesterone detection in immunoassay. In this study the synthesis of 11 alpha-hemisuccinylprogesterone from 11 alpha-hydroxyprogesterone has been improved by using 4-dimethylaminopyridine (DMAP in refluxing dioxane, a highly nucleophilic polar solvent.
    DOI:
    10.1016/0039-128x(88)90119-5
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文献信息

  • Synthesis of conjugates of 11α-hydroxyprogesterone with β-nicotinamide adenine dinucleotide (β-NAD) and adenosine triphosphate (ATP)
    作者:David N. Kirk、Barry W. Miller
    DOI:10.1039/p19880002983
    日期:——
    Conjugates of 11α-hydroxyprogesterone with adenosine triphosphate and nicotinamide adenine dinucleotide have been prepared in which the steroid is attached to the nucleotides via bridges from C-11 to the terminal phosphate and C-8 positions of ATP, and to the N-6 and C-8 positions on the adenine ring of NAD. Preliminary evaluation of the bioluminescence of these conjugates is reported.
    已经制备了11α-羟基孕酮三磷酸腺苷和烟酰胺腺嘌呤二核苷酸的结合物,其中类固醇通过从C-11到ATP的末端磷酸和C-8位置以及N-6和C的桥连接到核苷酸上。 NAD腺嘌呤环上的-8位。报道了对这些缀合物的生物发光的初步评估。
  • Influence of the site of conjugation on the specificity of antibodies to progesterone
    作者:Gordon D. Niswender
    DOI:10.1016/0039-128x(73)90104-9
    日期:1973.9
  • The use of homologous and hetebologous 125 I-radioligands in the radioimmunoassay of progesterone
    作者:R Allen
    DOI:10.1016/0039-128x(78)90059-4
    日期:1978.11
    Eight homologous and heterologous 125I-radioligand systems for the radioimmunoassay of progesterone were examined. Using an antiserum raised to 11alpha-hydroxyprogesterone 11-succinyl-bovine serum albumin, standard curves were set up with the homologous radioligands, 11alpha-hydroxyprogesterone 11-succinyl-[125I]-iodotyramine, -[125I]-iodohistamine and -[125I]-iodotyrosine methyl ester. Heterologous bridge systems were represented by progesterone-11alpha-oxycarbonyl-[125I]-iodotyrosine methyl ester and 11alpha-hydroxyprogesterone 11-phthalyl-[125I]-iodotyrosine methyl ester, and heterologous site systems by progesterone-3-(O-carboxymethyl)oxime-[125I]-iodotyramine, progesterone-12-(O-carboxymethyl)oxime-[125I]-iodotyramine, and progesterone-20-(O-carboxymethyl)oxime-[125I]-iodohistamine. The preparation of the steroid derivatives and iodination by a two-phase method are described. The curves obtained from the homologous radioligands were relatively insensitive compared with a tritiated system, with the tyrosine methyl ester derivative providing a more sensitive assay than the corresponding tyramine or histamine analogues. The heterologous bridge systems gave more sensitive curves than the homologous tracers whilst the 3- and 12-(O-carboxymethyl)oxime derivatives of progesterone furnished curves as sensitive as the tritiated reference. Progesterone-20-(O-carboxymethyl)oxime-[125I]-iodohistamine was not bound by the antibody.
  • Two new fluorescent derivatives of progesterone to use in fluoro immunoassay
    作者:C. Parini、M.A. Bacigalupo、S. Colombi、L. Ferrara、F. Franceschetti、R. Saita
    DOI:10.1016/0039-128x(85)90038-8
    日期:1985.10
    Synthesis, fluorometric and immunological properties of two new fluorescent derivatives of progesterone are reported. Both compounds were obtained from 11 alpha-hydroxyprogesterone 11-hemisuccinate; the fluorescent molecules were joined to the steroid by bifunctional arms. The first of these is cysteamine whose thiol group was reacted with N-(3-fluoranthenyl) maleimide, and the second is tyramine whose phenolic group was reacted with 1-nitroso-2 naphthol.
  • KIRK, DAVID N.;MILLER, BARRY W., J. CHEM. SOC. PERKIN TRANS. PT 1,(1988) N1, C. 2983-2992
    作者:KIRK, DAVID N.、MILLER, BARRY W.
    DOI:——
    日期:——
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