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8-(p-Nitrophenyl)theophylline | 1094-63-9

中文名称
——
中文别名
——
英文名称
8-(p-Nitrophenyl)theophylline
英文别名
8-(4-nitrophenyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione;8-(4-nitrophenyl)-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione;N1,N3-dimethyl-8-p-nitrophenylxanthine;1,3-dimethyl-8-(4-nitro-phenyl)-3,7-dihydro-purine-2,6-dione;8-p-Nitrophenyltheophyllin;1,3-dimethyl-8-(4-nitrophenyl)-7H-purine-2,6-dione
8-(p-Nitrophenyl)theophylline化学式
CAS
1094-63-9
化学式
C13H11N5O4
mdl
——
分子量
301.261
InChiKey
GZKNQJOZTRVLIX-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

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    115
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:eecf45f3087ed04d657227ebd91fe5ae
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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
  • 下游产品
    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:
    8-(p-Nitrophenyl)theophylline 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以10%的产率得到8-(p-aminophenyl)theophylline
    参考文献:
    名称:
    1,3-二烷基-8-(对-磺基苯基)黄嘌呤:A1-和A2-腺苷受体的有效水溶性拮抗剂。
    摘要:
    评估了茶碱和其他1,3-二烷基黄嘌呤的一系列8-(取代苯基)衍生物作为脑组织中A1-和A2-腺苷受体拮抗剂的效能和选择性。茶碱对A1和A2受体的功效相似(Ki = 14 microM)。作为腺苷受体拮抗剂,8-苯基茶碱的功效比茶碱高25-35倍,而8-苯基咖啡因的功效仅比咖啡因高2-3倍。对羟基芳基取代基增强了8-苯基茶碱作为腺苷拮抗剂的效力。对-羧基和对-硫芳基取代基降低了8-苯基茶碱的效力,产生了水溶性腺苷拮抗剂,在腺苷受体上,它们的效力比茶碱大2-5倍。8-(取代的苯基)茶碱均没有特别选择性地作为对A1-和A2-腺苷受体的拮抗剂。1,3-二丙基-8-苯基黄嘌呤代表一种有效的和选择性的A1受体拮抗剂,在A1受体上的效力比在A2受体上高约23倍。对羟基芳基取代基进一步增强了1,3-二丙基-8-苯基黄嘌呤在A1和A2受体上的效力。8-(2-氨基-4-氯苯基)-1,3-二丙基黄嘌呤是A1受体
    DOI:
    10.1021/jm00382a018
  • 作为产物:
    描述:
    5,6-二氨基-1,3-二甲基脲嘧啶氯化亚砜溶剂黄146 作用下, 以 甲醇 为溶剂, 反应 0.08h, 生成 8-(p-Nitrophenyl)theophylline
    参考文献:
    名称:
    1,3-二烷基-8-(对-磺基苯基)黄嘌呤:A1-和A2-腺苷受体的有效水溶性拮抗剂。
    摘要:
    评估了茶碱和其他1,3-二烷基黄嘌呤的一系列8-(取代苯基)衍生物作为脑组织中A1-和A2-腺苷受体拮抗剂的效能和选择性。茶碱对A1和A2受体的功效相似(Ki = 14 microM)。作为腺苷受体拮抗剂,8-苯基茶碱的功效比茶碱高25-35倍,而8-苯基咖啡因的功效仅比咖啡因高2-3倍。对羟基芳基取代基增强了8-苯基茶碱作为腺苷拮抗剂的效力。对-羧基和对-硫芳基取代基降低了8-苯基茶碱的效力,产生了水溶性腺苷拮抗剂,在腺苷受体上,它们的效力比茶碱大2-5倍。8-(取代的苯基)茶碱均没有特别选择性地作为对A1-和A2-腺苷受体的拮抗剂。1,3-二丙基-8-苯基黄嘌呤代表一种有效的和选择性的A1受体拮抗剂,在A1受体上的效力比在A2受体上高约23倍。对羟基芳基取代基进一步增强了1,3-二丙基-8-苯基黄嘌呤在A1和A2受体上的效力。8-(2-氨基-4-氯苯基)-1,3-二丙基黄嘌呤是A1受体
    DOI:
    10.1021/jm00382a018
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文献信息

  • Studies on heterocyclic compounds. XXXII. Synthesis of 8-substituted theophyllines from 6-amino-5-benzylideneamino-1,3-dimethyluracils with nickel peroxide.
    作者:SATOSHI MINEO、HARUO OGURA、KUNIO NAKAGAWA
    DOI:10.1248/cpb.28.2835
    日期:——
    Oxidation of 6-amino-5-benzylideneamino-1, 3-dimethyluracils (Ia-e) with nickel peroxide (Ni-PO) in dimethylsulfoxide (DMSO) afforded 8-substituted theophyllines (IIa-e) and dimethylsulfone. Ni-PO oxidation of the Schiff base acetate (V) of 5, 6-diamino-1, 3-dimethyluracil with D-glucose did not give a nucleoside analog ; in stead, 1, 3, 7, 9-tetramethyl-2, 4, 6, 8-(1H, 3H, 7H, 9H)pyrimido[5, 4-g]pteridinetetrone (VI) and penta-O-acetylgluconic acid were obtained. The reaction mechanisms of Ni-PO and the Schiff bases (Ia-e, V) are discussed.
    在二甲基亚砜(DMSO)中,6-氨基-5-苄叉氨基-1,3-二甲基脲(Ia-e)与过氧化镍(Ni-PO)的氧化反应生成了8-取代的茶碱(IIa-e)和二甲基亚砜。5,6-二氨基-1,3-二甲基脲与D-葡萄糖形成的希夫碱乙酸盐(V)在Ni-PO氧化下并未形成核苷类似物;取而代之,得到了1,3,7,9-四甲基-2,4,6,8-(1H,3H,7H,9H)嘧啶[5,4-g]蝶啶四酮(VI)和五-O-乙酰基葡糖酸。本文还讨论了Ni-PO与希夫碱(Ia-e, V)的反应机理。
  • Smooth Metal‐Free Photoinduced Preparation of Valuable 8‐Arylxanthines
    作者:Havall Othman Abdulla、Ahmed A. Amin、Carlotta Raviola、Till Opatz、Stefano Protti、Maurizio Fagnoni
    DOI:10.1002/ejoc.201900638
    日期:2020.3.15
    A set of 8‐arylxanthines was prepared under metal‐free conditions and in aqueous solvents from arylazo sulfones and caffeine or theophylline. Notably, the process took place by simply exposing the reaction vessel to visible or solar light, and unreacted xanthine could be easily recovered during the purification step.
    在无金属条件下和在水性溶剂中由芳基偶氮砜和咖啡因或茶碱制备了一组8-芳基黄嘌呤。值得注意的是,该过程是通过简单地将反应容器暴露于可见光或太阳光下进行的,并且未反应的黄嘌呤可以在纯化步骤中容易地回收。
  • Low glycemic response compositions
    申请人:The Procter & Gamble Co.
    公开号:US20020187219A1
    公开(公告)日:2002-12-12
    The present disclosure is related to compositions useful in the field of foods and beverages. In particular, the present invention relates to those compositions that reduce the postprandial rise in blood glucose (described as low Glycemic Index) that synergistically provide enhanced metabolism in the mammalian system and inhibit the storage of systemic fat. In particular, the present invention relates to compositions comprising: a) one or more flavanols; b) one or more bracers; and c) vitamin B; wherein the composition exhibits a Glycemic Index of about 55 or less. As disclosed, the unique combination of ingredients, which provide the defined, low Glycemic Index, work synergistically together to enhance perception of energy and/or improve physiological energy via metabolism enhancement over a long duration of time, without resulting in sudden peaks of glucose in the mammalian system. Thus, the present compositions effectively modulate glucose in the system, thereby providing energy to the system without resulting in the storage of systemic fat.
    本公开涉及在食品和饮料领域有用的组合物。特别是,本发明涉及那些能够减少餐后血糖上升(描述为低升糖指数)的组合物,这些组合物在哺乳动物系统中协同作用,提供增强的代谢作用并抑制系统性脂肪的储存。特别是,本发明涉及包括:a)一种或多种黄烷醇;b)一种或多种支链氨基酸;和c)维生素B的组合物;其中该组合物表现出约55或更低的升糖指数。如本文所述,这些独特的成分组合,以定义的低升糖指数为特征,协同作用,能够提高能量感知和/或通过代谢增强长时间改善生理能量,而不会导致哺乳动物系统中的血糖突然峰值。因此,本组合物有效地调节系统中的葡萄糖,从而为系统提供能量而不导致系统性脂肪的储存。
  • Compositions, kits, and methods for promoting defined health benefits
    申请人:——
    公开号:US20030069202A1
    公开(公告)日:2003-04-10
    The present invention is directed to compositions comprising: (a) a first component selected from the group consisting of gelatin, cartilage, aminosugars, glycosaminoglycans, methylsulfonylmethane, precursors of methylsulfonylmethane, S-adenosylmethionine, salts thereof, and mixtures thereof; and (b) a second component comprising: (i) a cation source selected from the group consisting of calcium, potassium, magnesium, and mixtures thereof; and (ii) an edible acid source. The present invention is further directed to food, beverage, pharmaceutical, over-the- counter, and dietary supplement products, which comprise the present compositions. The invention also relates to kits comprising the present compositions and information that use of the composition promotes one or more of the presently defined health benefits, including joint health, bone health, cardiac health, and anti-inflammation. The present invention additionally relates to methods of treating joint function, bone function, cardiac function, or inflammation comprising administering to a mammal a composition as defined herein.
    本发明涉及包括以下组分的组合物:(a)从明胶、软骨、氨基糖、糖胶质、甲基磺酰甲烷、甲基磺酰甲烷的前体、S-腺苷甲硫氨酸、其盐和其混合物中选择的第一组分; 和(b)包括:(i)从钙、钾、镁和其混合物中选择的阳离子源; 和(ii)可食用的酸源的第二组分。本发明还涉及包含本组合物的食品、饮料、制药、非处方药和膳食补充剂产品。本发明还涉及包含本组合物和使用该组合物促进当前定义的健康益处之一或多个的信息的套件。本发明还涉及治疗关节功能、骨功能、心脏功能或炎症的方法,包括向哺乳动物投与本文所定义的组合物。
  • Beverage compositions comprising arabinogalactan and defined vitamins
    申请人:The Procter & Gamble Co.
    公开号:US20020110632A1
    公开(公告)日:2002-08-15
    The present invention is directed to compositions comprising: a) a first component which is arabinogalactan; and b) a second component comprising two or more vitamins selected from the group consisting of vitamin A, vitamin C, vitamin D, vitamin E, and B-complex vitamins. In an alternative embodiment of the present invention, the compositions comprise: a) a first component which is arabinogalactan; and b) a second component comprising one or more vitamins selected from the group consisting of vitamin A, vitamin D, and vitamin E. The present compositions are useful to provide beverages which increase the solubility of fat-soluble vitamins, and deliver the benefits of fiber, one or more of the defined vitamins, and/or provide other health benefits, including fighting infection, promoting healthy bacteria, and providing a desired dietary fiber benefit. Additionally, the present invention provides beverage compositions having excellent taste, and other organoleptic properties, despite the inclusion of the fiber and vitamin components. These and other benefits of the present invention are described herein.
    本发明涉及包括:a)阿拉伯半乳糖和b)由维生素A、维生素C、维生素D、维生素E和B族维生素中选择两种或更多种组成的第二组分的组合物。在本发明的另一实施例中,组合物包括:a)阿拉伯半乳糖和b)由维生素A、维生素D和维生素E中选择一种或多种组成的第二组分。本组合物有助于提供增加脂溶性维生素溶解度的饮料,并提供纤维、一个或多个定义的维生素的益处和/或提供其他健康益处,包括抗感染、促进健康细菌和提供所需的膳食纤维益处。此外,本发明提供了具有出色口感和其他感官特性的饮料组合物,尽管包括纤维和维生素成分。本发明的其他优点在此描述。
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