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Arginine butyl ester

中文名称
——
中文别名
——
英文名称
Arginine butyl ester
英文别名
butyl 2-amino-5-(diaminomethylideneamino)pentanoate
Arginine butyl ester化学式
CAS
——
化学式
C10H22N4O2
mdl
——
分子量
230.31
InChiKey
UQTGZDUYNOOQRP-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):
    -0.3
  • 重原子数:
    16
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    117
  • 氢给体数:
    3
  • 氢受体数:
    4

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:
    Arginine butyl ester三氟乙酸酐 生成 butyl 5-[[amino-[(2,2,2-trifluoroacetyl)amino]methylidene]amino]-2-[(2,2,2-trifluoroacetyl)amino]pentanoate
    参考文献:
    名称:
    JHAM, G. N.;CAMPOS, L. G., J. CHROMATOGR., 436,(1988) N 1, 100-102
    摘要:
    DOI:
  • 作为产物:
    参考文献:
    名称:
    JHAM, G. N.;CAMPOS, L. G., J. CHROMATOGR., 436,(1988) N 1, 100-102
    摘要:
    DOI:
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文献信息

  • CATIONIC LIPIDS, METHODS FOR PREPARING THE SAME, AND DELIVERY SYSTEMS HAVING ABILITY TO TRANSITION INTO CELLS COMPRISING THE SAME
    申请人:Park Myung-Ok
    公开号:US20130123485A1
    公开(公告)日:2013-05-16
    The present invention provides cationic lipids, methods for preparing the same, and delivery systems comprising the same. The present invention can provide cationic lipids which enhance the efficiency of intracellular or in vivo delivery of multiple-anionic target compounds such as drugs, anticancer agents, nucleic acids, etc., have no intracellular toxicity, but show increased stability, methods for preparing the same, and delivery systems comprising the same.
    本发明提供了阳离子脂质、其制备方法以及包含该脂质的传递系统。本发明可以提供增强多阴离子靶向化合物(如药物、抗癌剂、核酸等)在细胞内或体内传递效率的阳离子脂质,不具有细胞内毒性,但表现出增加的稳定性,以及其制备方法和包含该脂质的传递系统。
  • METHOD FOR PREPARING POLYMERIC PROTEIN COMPOSED OF MONOMERIC PROTEIN PRODUCED BY FUSING PROTEIN HAVING IMMUNOGLOBULIN FOLD STRUCTURE TO PROTEIN CAPABLE OF SERVING AS SUBUNIT STRUCTURE
    申请人:Ajinomoto Co., Inc.
    公开号:EP2725104A1
    公开(公告)日:2014-04-30
    The present invention provides a method for producing a multimeric protein consisting of a monomeric protein obtained by fusing a protein having an immunoglobulin fold structure to a protein that can serve as a subunit structure, the method including the steps of: (A) preparing the monomeric protein having an insoluble granular form in cells of a microorganism; (B) solubilizing the monomeric protein prepared in step (A) with an aqueous solution containing lauroyl-L-Glu; (C) diluting a solution obtained in step (B) in a buffer containing arginine hydrochloride to lower a concentration of lauroyl-L-Glu; and (D) replacing a solvent of a solution obtained in step (C) with a buffer using gel filtration chromatography or the like.
    本发明提供了一种生产多聚体蛋白质的方法,该多聚体蛋白质由具有免疫球蛋白折叠结构的蛋白质与可作为亚单位结构的蛋白质融合得到的单体蛋白质组成,该方法包括以下步骤: (A) 在微生物细胞中制备具有不溶性颗粒状的单体蛋白; (B) 用含有月桂酰-L-Glu 的水溶液增溶步骤(A)中制备的单体蛋白; (C) 在含有盐酸精氨酸的缓冲液中稀释步骤(B)中得到的溶液,以降低月桂酰-L-谷氨酰的浓度;以及 (D) 使用凝胶过滤色谱法或类似方法将步骤(C)中得到的溶液的溶剂替换为缓冲液。
  • Method for preparing polymeric protein composed of monomeric protein produced by fusing protein having immunoglobulin fold structure to protein capable of serving as subunit structure
    申请人:AJINOMOTO CO., INC.
    公开号:US10308969B2
    公开(公告)日:2019-06-04
    The present invention provides a method for producing a multimeric protein composed of a monomeric protein, wherein the monomeric protein is obtained by fusing a protein having an immunoglobulin fold structure to a protein that can serve as a subunit structure, the method including the steps of: (A) preparing the monomeric protein having an insoluble granular form in cells of a microorganism; (B) solubilizing the monomeric protein prepared in step (A) with an aqueous solution containing lauroyl-L-Glu; (C) diluting a solution obtained in step (B) in a buffer containing arginine hydrochloride to lower a concentration of lauroyl-L-Glu; and (D) replacing a solvent of a solution obtained in step (C) with a buffer using gel filtration chromatography or the like.
    本发明提供了一种生产由单体蛋白质组成的多聚体蛋白质的方法,其中单体蛋白质是通过将具有免疫球蛋白折叠结构的蛋白质与可作为亚单位结构的蛋白质融合而得到的,该方法包括以下步骤: (A) 在微生物细胞中制备具有不溶性颗粒状的单体蛋白; (B) 用含有月桂酰-L-Glu 的水溶液增溶步骤(A)中制备的单体蛋白; (C) 在含有盐酸精氨酸的缓冲液中稀释步骤(B)中得到的溶液,以降低月桂酰-L-谷氨酰的浓度;以及 (D) 使用凝胶过滤色谱法或类似方法将步骤(C)中得到的溶液的溶剂替换为缓冲液。
  • Topical and oral delivery of arginine to cause beneficial effects
    申请人:——
    公开号:US20010002405A1
    公开(公告)日:2001-05-31
    The use of orally administered L-arginine in conjunction with a topical preparation for producing enhanced blood flow in tissue thus causing beneficial effects such as warming cold tissue of the hands and feet, promoting hair growth on bald scalp tissue, promoting healing of superficial ulcers such as leg ulcers in persons with diabetes, and overcoming male erectile failure (impotence) is disclosed. Specifically, use of orally administered L-arginine in conjunction with this is topical preparation provides local delivery of the amino acid L-arginine, an important biological precursor to the main substance which is responsible for relaxation of blood vessels permitting enhancement of blood flow. In the preferred embodiments, the L-arginine is provided so that it can be topically applied to the cold tissue. The preparation also contains an agent which aids in the transfer of L-arginine into the tissue. In the preferred embodiments this agent overcomes the resistance to transfer caused by the high charge density of L-arginine. In the preferred embodiments this means is high ionic strength created by addition of sodium chloride. This preparation, when topically applied to cold tissue, warming begins within 10 to 45 minutes and is sustained for periods as long as 2 to 18 hours. Further this preparation when applied nightly to bald scalp tissue for a period of time causes substantial growth of hair on the bald scalp, causes the healing of superficial ulcers such as leg ulcers and overcomes impotence.
    本发明公开了口服 L-精氨酸与外用制剂配合使用的方法,口服 L-精氨酸与外用制剂配合使用可增强组织中的血流量,从而产生有益的效果,如温暖手脚冰冷的组织、促进秃头组织的毛发生长、促进浅表溃疡(如糖尿病患者的腿部溃疡)愈合以及克服男性勃起功能障碍(阳痿)。具体来说,将口服 L-精氨酸与本局部制剂结合使用,可在局部提供氨基酸 L-精氨酸,这是一种重要的生物前体物质,其主要作用是松弛血管,促进血液流动。在优选的实施方案中,提供的 L-精氨酸可局部应用于冷组织。制剂中还含有一种有助于将 L-精氨酸转移到组织中的制剂。在优选的实施方案中,这种制剂可以克服 L-精氨酸的高电荷密度所造成的转移阻力。在优选的实施方案中,这种手段是通过添加氯化钠产生高离子强度。这种制剂局部用于冷组织时,可在 10 至 45 分钟内开始升温,持续时间长达 2 至 18 小时。此外,这种制剂每晚涂抹在秃头组织上一段时间后,可使秃头上的头发大量生长,使浅表溃疡(如腿部溃疡)愈合,并克服阳痿。
  • Topical and oral arginine to cause beneficial effects
    申请人:——
    公开号:US20030018076A1
    公开(公告)日:2003-01-23
    The use of orally administered L-arginine in conjunction with a topical preparation for producing enhanced blood flow in tissue thus causing beneficial effects such as warming cold tissue of the hands and feet, promoting hair growth on bald scalp tissue, promoting healing of superficial ulcers such as leg ulcers in persons with diabetes, and overcoming male erectile failure (impotence) is disclosed. Specifically, use of orally administered L-arginine in conjunction with this is topical preparation provides local delivery of the amino acid L-arginine, an important biological precursor to the main substance which is responsible for relaxation of blood vessels permitting enhancement of blood flow. In the preferred embodiments, the L-arginine is provided so that it can be topically applied to the cold tissue. The preparation also contains an agent which aids in the transfer of L-arginine into the tissue. In the preferred embodiments this agent overcomes the resistance to transfer caused by the high charge density of L-arginine. In the preferred embodiments this means is high ionic strength created by addition of sodium chloride. This preparation, when topically applied to cold tissue, warming begins within 10 to 45 minutes and is sustained for periods as long as 2 to 18 hours. Further this preparation when applied nightly to bald scalp tissue for a period of time causes substantial growth of hair on the bald scalp, causes the healing of superficial ulcers such as leg ulcers and overcomes impotence.
    本发明公开了口服 L-精氨酸与外用制剂配合使用的方法,口服 L-精氨酸与外用制剂配合使用可增强组织中的血流量,从而产生有益的效果,如温暖手脚冰冷的组织、促进秃头组织的毛发生长、促进浅表溃疡(如糖尿病患者的腿部溃疡)愈合以及克服男性勃起功能障碍(阳痿)。具体来说,将口服 L-精氨酸与本局部制剂结合使用,可在局部提供氨基酸 L-精氨酸,L-精氨酸是一种重要的生物前体物质,其主要作用是松弛血管,促进血液流动。在优选的实施方案中,提供的 L-精氨酸可局部应用于冷组织。制剂中还含有一种有助于将 L-精氨酸转移到组织中的制剂。在优选的实施方案中,这种制剂可以克服 L-精氨酸的高电荷密度造成的转移阻力。在优选的实施方案中,这种手段是通过添加氯化钠产生高离子强度。这种制剂局部用于冷组织时,可在 10 至 45 分钟内开始升温,持续时间长达 2 至 18 小时。此外,这种制剂每晚涂抹在秃头组织上一段时间后,可使秃头上的头发大量生长,使浅表溃疡(如腿部溃疡)愈合,并克服阳痿。
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