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lithocholic acid

中文名称
——
中文别名
——
英文名称
lithocholic acid
英文别名
(4S)-4-[(3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid
lithocholic acid化学式
CAS
——
化学式
C24H40O3
mdl
——
分子量
376.58
InChiKey
SMEROWZSTRWXGI-LFYYPNPWSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.3
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    lithocholic acidchromium(VI) oxide2-乙氧基-1-乙氧碳酰基-1,2-二氢喹啉三乙胺 作用下, 以 吡啶乙酸乙酯 为溶剂, 反应 5.25h, 生成 N-(methoxycarbonylmethyl)-3-oxo-5β-cholan-24-oic acid amide 3-(O-carboxymethyl)oxime
    参考文献:
    名称:
    Preparation and antigenic property of 3-dehydrolithocholylglycine 3-(O-carboxymethyl)oxime-bovine serum albumin conjugate
    摘要:
    The preparation and antigenic property of 3-dehydrolithocholyglycine-bovine serum albumin (BSA) conjugate in which the hapten is linked to the carrier protein through an (O-carboxymethyl) oxime bridge at the C-3 position on the steroid nucleus is described. Antibody raised against antigen in the rabbit possessed high titer and specificity to lithocholylglycine, exhibiting no significant cross-reaction with free lithocholic acid or lithocholyltaurine.
    DOI:
    10.1016/0039-128x(83)90005-3
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文献信息

  • Synthesis, in-vitro antiprotozoal activity and molecular docking study of isothiocyanate derivatives
    作者:Kosar Babanezhad Harikandei、Peyman Salehi、Samad Nejad Ebrahimi、Morteza Bararjanian、Marcel Kaiser、Ahmed Al-Harrasi
    DOI:10.1016/j.bmc.2019.115185
    日期:2020.1
    against T. brucei rhodesiense with IC50s below 2.0 μM and SI between 2.7 and 29.3. Four primary amine derivatives of noscapine and five isothiocyanate derivatives exhibited antiplasmodial activity with IC50s in the range of 1.1-2.7 µM and SI values between 1.1 and 14.5. The isothiocyanate derivative 7c showed against T. cruzi with an IC50 value of 1.9 µM and SI 4. Molecular docking and ADMET studies
    从Noscapine,胆汁酸,氨基酸和一些芳香族化合物开始合成了新型异硫氰酸酯衍生物。测试了合成衍生物对四种单细胞原生动物即布鲁氏锥虫,克鲁氏梭菌,杜氏利什曼原虫和恶性疟原虫的抗寄生虫活性。有趣的是,七个异硫氰酸酯类似物表现出对多形利什曼原虫的抗寄生虫活性,其IC50值为0.4至1.0 µM,选择性指数(SI)为7.8至18.4,与标准药物miltefosine相当(IC50 = 0.7μM)。化合物7h表现出最佳的抗菌活性,IC50值为0.4 µM。七种产品表现出对杜氏布鲁氏菌的抑制活性,IC50值低于2.0μM,SI值在2.7至29.3之间。Noscapine的4种伯胺衍生物和5种异硫氰酸酯衍生物表现出抗血浆活性,IC50在1.1-2.7 µM的范围内,SI值在1.1至14.5之间。异硫氰酸酯衍生物7c表现出抗克氏锥虫的IC50值为1.9 µM和SI4。进行了分子对接和ADMET研究,
  • Photocatalytic Cleavage of Trityl Protected Thiols and Alcohols
    作者:Sho Murakami、Cosima Brudy、Bartholomäus Pieber、Moritz Bachmann、Yoshiji Takemoto
    DOI:10.1055/a-1979-5933
    日期:——
    We report the visible light photocatalytic cleavage of trityl thioethers or ethers under pH-neutral conditions. The method results in the formation of the respective symmetrical disulfides and alcohols in moderate to excellent yield. The protocol only requires the addition of a suitable photocatalyst and light rendering it orthogonal to several functionalities, including acid labile protective groups
    我们报告了在 pH 中性条件下三苯甲基硫醚或醚的可见光光催化裂解。该方法导致以中等到极好的收率形成相应的对称二硫化物和醇。该协议只需要添加合适的光催化剂和光使其与多种功能正交,包括酸不稳定保护基团。相同的条件可用于直接将三苯甲基保护的硫醇转化为不对称的二硫化物或硒硫化物,并在固相有机合成中裂解三苯甲基树脂。
  • Nucleophile-Controlled Trapping of Gold Carbene by Nitriles and Water: Synthesis of 5<i>H</i>-Pyrimido[5,4-<i>b</i>]indoles and 2-Benzylidene-3-indolinones
    作者:Yun-Long Zhu、Yi-Fan Dong、Si-Ru Wang、You-Gui Li、Xiang Wu、Long-Wu Ye
    DOI:10.1021/acs.orglett.3c03856
    日期:2024.1.26
    A gold-catalyzed, nucleophile-controlled cascade reaction of N-(2-azidophenyl-ynyl)methanesulfonamides with nitriles and water is described that provides structurally diverse 5H-pyrimido[5,4-b]indoles and 2-benzylidene-3-indolinones in good to excellent yields. Mechanistic studies indicate that the β-sulfonamido-α-imino gold carbene is the key intermediate which is generated through the gold-catalyzed
    描述了N- (2-叠氮苯基-炔基)甲磺酰胺与腈和水的金催化亲核试剂控制级联反应,提供结构多样的 5 H-嘧啶基[5,4 -b ]吲哚和 2-亚苄基-3-二氢吲哚酮的收率良好至极好。机理研究表明,β-磺酰胺基-α-亚氨基金卡宾是金催化N- (2-叠氮苯基-炔基)甲磺酰胺环化生成的关键中间体,并与腈进行正式的[4 + 2]级联成环反应分别与水发生分子内S N 2′型反应。
  • 15β-Hydroxylation of Lithocholic Acid by cunninghamella sp.
    作者:S. Kulprecha、T. Nihira、C. Shimomura、K. Yamada、N. Nilubol、T. Yoshida、H. Taguchi
    DOI:10.1016/s0040-4020(01)91292-x
    日期:1984.1
  • Preparation and antigenic property of 3-dehydrolithocholylglycine 3-(O-carboxymethyl)oxime-bovine serum albumin conjugate
    作者:S. Yamauchi、M. Kojima、F. Nakayama
    DOI:10.1016/0039-128x(83)90005-3
    日期:1983.2
    The preparation and antigenic property of 3-dehydrolithocholyglycine-bovine serum albumin (BSA) conjugate in which the hapten is linked to the carrier protein through an (O-carboxymethyl) oxime bridge at the C-3 position on the steroid nucleus is described. Antibody raised against antigen in the rabbit possessed high titer and specificity to lithocholylglycine, exhibiting no significant cross-reaction with free lithocholic acid or lithocholyltaurine.
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