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5-Methyl-tetrahydrofolsaeure | 39605-23-7

中文名称
——
中文别名
——
英文名称
5-Methyl-tetrahydrofolsaeure
英文别名
2-[[4-[(2-Amino-5-methyl-4-oxo-1,6,7,8-tetrahydropteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid;2-[[4-[(2-amino-5-methyl-4-oxo-3,6,7,8-tetrahydropteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid
5-Methyl-tetrahydrofolsaeure化学式
CAS
39605-23-7
化学式
C20H25N7O6
mdl
——
分子量
459.462
InChiKey
ZNOVTXRBGFNYRX-UHFFFAOYSA-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

  • 密度:
    1.62±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    33
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    199
  • 氢给体数:
    7
  • 氢受体数:
    10

SDS

SDS:d61cd87e1bf25bea6f39e15d0b41c213
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反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Synthesis and Activity of a Tetrahydrofolate Inhibitor of the Enzyme N10-Formyl-H4-folate-Met-tRNAfMet Transformylase
    摘要:
    DOI:
    10.3987/r-1986-11-3079
  • 作为产物:
    描述:
    [4-(2-amino-10-methyl-4-oxo-6,7,8,9-tetrahydro-4a,7-cycloimino-pyrimido[4,5-b] [1,4] diazepine-5(4H)-yl)benzoyl]-glutamate 在 sodium tetrahydroborate 、 sodium hydroxide 作用下, 以 为溶剂, 反应 1.5h, 生成 5-Methyl-tetrahydrofolsaeure
    参考文献:
    名称:
    EP2837632
    摘要:
    公开号:
  • 作为试剂:
    描述:
    4-吡唑硼酸频哪醇酯Dicaesio carbonate 、 在 碳酸氢钠乙酸乙酯5-Methyl-tetrahydrofolsaeure 作用下, 以 1,4-二氧六环 为溶剂, 反应 0.25h, 以to give the title compound (21 mg, 17%)的产率得到
    参考文献:
    名称:
    New Acetyl Coenzyme A Carboxylase (ACC) Inhibitors And Uses In Treatments Of Obesity And Diabetes Mellitus - 087
    摘要:
    本发明涉及Acetyl辅酶A羧化酶(ACC)抑制剂,其按照公式(I)或其对映体或其药学上可接受的盐,其中R1,R2,R3,R4,R5,E,L,Z和n的定义如本文所述,以及制备这种化合物的过程,包含它们的制药组合物,使用这种抑制剂的用途以及它们的治疗用途的方法,特别是在肥胖和糖尿病治疗中的应用。
    公开号:
    US20090306133A1
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文献信息

  • Methods for delivery of nucleic acids
    申请人:Satishchandran C.
    公开号:US20060084617A1
    公开(公告)日:2006-04-20
    This invention features methods and compositions for delivery of nucleic acids (e.g., DNA, RNA, PNA, and hybrids thereof) to cells. The nucleic acid delivery complexes of the invention permit biologically active nucleic acids to be delivered to cells and organisms in vitro and in vivo in a manner and form that allows the nucleic acids to carry out their desired biological function.
    这项发明涉及用于将核酸(例如,DNA、RNA、PNA及其杂合体)递送到细胞中的方法和组合物。本发明的核酸递送复合物使得生物活性的核酸能够以某种方式和形式递送到体外和体内的细胞和生物体中,从而允许核酸执行其所需的生物学功能。
  • [EN] TARGETED BIFUNCTIONAL DEGRADERS<br/>[FR] AGENTS DE DÉGRADATION BIFONCTIONNELS CIBLÉS
    申请人:UNIV YALE
    公开号:WO2021072269A1
    公开(公告)日:2021-04-15
    The present invention provides, in one aspect, bifunctional compounds that can be used to promote or enhance degradation of certain circulating proteins. In another aspect, the present invention provides bifunctional compounds that can be used to promote or enhance degradation of certain autoantibodies. In certain embodiments, treatment or management of a disease and/or disorder requires degradation, removal, or reduction in concentration of the circulating protein or the autoantibody in the subject. Thus, in certain embodiments, administration of a compound of the invention to the subject removes or reduces the circulation concentration of the circulating protein or the autoantibody, thus treating, ameliorating, or preventing the disease and/or disorder. In certain embodiments, the circulating protein is TNF.
    本发明在一个方面提供了可以用来促进或增强降解某些循环蛋白的双功能化合物。在另一个方面,本发明提供了可以用来促进或增强降解某些自身抗体的双功能化合物。在某些实施方式中,治疗或管理疾病和/或疾病需要降解、去除或减少受试者体内循环蛋白或自身抗体的浓度。因此,在某些实施方式中,将本发明的化合物给予受试者可去除或减少循环蛋白或自身抗体的循环浓度,从而治疗、改善或预防疾病和/或疾病。在某些实施方式中,循环蛋白是TNF。
  • [EN] ENGINEERED ANTIBODIES AS MOLECULAR DEGRADERS THROUGH CELLULAR RECEPTORS<br/>[FR] ANTICORPS CONÇUS COMME AGENTS DE DÉGRADATION MOLÉCULAIRE PAR L'INTERMÉDIAIRE DE RÉCEPTEURS CELLULAIRES
    申请人:UNIV YALE
    公开号:WO2021072246A1
    公开(公告)日:2021-04-15
    The present disclosure provides, in one aspect, bifunctional compounds that can be used to promote or enhance degradation of certain circulating proteins. In certain embodiments, the circulating protein mediates a disease and/or disorder in a subject, and treatment or management of the disease and/or disorder requires degradation, removal, or reduction in concentration of the circulating protein in the subject. Thus, in certain embodiments, administration of a compound of the disclosure to the subject removes or reduces the circulation concentration of the circulating protein, thus treating, ameliorating, or preventing the disease and/or disorder.
    本公开提供了一种双功能化合物,可用于促进或增强特定循环蛋白的降解。在某些实施例中,循环蛋白在受试者中介导疾病和/或紊乱,治疗或管理该疾病和/或紊乱需要降解、去除或减少受试者中循环蛋白的浓度。因此,在某些实施例中,将本公开的化合物给予受试者可去除或减少循环蛋白的循环浓度,从而治疗、改善或预防疾病和/或紊乱。
  • [EN] CRYSTALLINE BINARY SODIUM SALTS OF 5-METHYL-(6S)-TETRAHYDROFOLIC ACID WITH ORGANIC BASES<br/>[FR] SELS DE SODIUM BINAIRE CRISTALLINS D'ACIDE 5-MÉTHYL-(6S)-TÉTRAHYDROFOLIQUE AVEC DES BASES ORGANIQUES
    申请人:MERCK PATENT GMBH
    公开号:WO2018178142A1
    公开(公告)日:2018-10-04
    The present invention is directed to crystalline salt of 5-methyl-(6S)-tetrahydrofolic acid comprising (i) 5-methyl-(6S)-tetrahydrofolic acid, (ii) sodium and (iii) an organic base having a pKa value from 6 to 11; wherein the molar ratio of 5-methyl-(6S)-tetrahydrofolic acid to the sodium is from :0.5 to 1:1.5 and the molar ratio of 5-methyl-(6S)-tetrahydrofolic acid to the organic base is 1:0.5 to 1:1.5 and/or hydrates and/or solvates thereof, as well as, a processes of obtaining the same.
    本发明涉及5-甲基-(6S)-四氢叶酸的结晶盐,包括(i) 5-甲基-(6S)-四氢叶酸,(ii) 钠和(iii) 具有pKa值在6到11之间的有机碱;其中5-甲基-(6S)-四氢叶酸与钠的物质摩尔比为:0.5至1:1.5,5-甲基-(6S)-四氢叶酸与有机碱的物质摩尔比为1:0.5至1:1.5,以及它们的水合物和/或溶剂合物,以及获得它们的方法。
  • [EN] CRYSTALLINE SALT COMPRISING 5-METHYL-(6S)-TETRAHYDROFOLIC ACID AND 4-(2-HYDROXYETHYL)-MORPHOLINE<br/>[FR] SEL CRISTALLIN COMPRENANT DE L'ACIDE 5-MÉTHYL-(6S)-TÉTRAHYDROFOLIQUE ET DE LA 4-(2-HYDROXYÉTHYL)-MORPHOLINE
    申请人:MERCK PATENT GMBH
    公开号:WO2020007834A1
    公开(公告)日:2020-01-09
    The present inventionrefers to a crystalline salt comprising5-methyl-(6S)- tetrahydrofolic acid and 4-(2-hydroxyethyl)-morpholine wherein the molar ratio of -methyl-(6S)-tetrahydrofolic acid to 4-(2-hydroxyethyl)-morpholine is from 1:0.3 to :2.0 (in mol/mol) and/or hydrates and/or solvates thereof as well as to a process of obtaining the same.
    本发明涉及一种结晶盐,包括5-甲基-(6S)-四氢叶酸和4-(2-羟乙基)-吗啉,其中-甲基-(6S)-四氢叶酸与4-(2-羟乙基)-吗啉的摩尔比为1:0.3到2.0(以摩尔比计算),以及其水合物和/或溶剂合物,以及获得该结晶盐的方法。
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