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N6-Monomethylarginin | 17072-43-4

中文名称
——
中文别名
——
英文名称
N6-Monomethylarginin
英文别名
L-NMMA;2-azaniumyl-5-[(N'-methylcarbamimidoyl)amino]pentanoate
N<sup>6</sup>-Monomethylarginin化学式
CAS
17072-43-4
化学式
C7H16N4O2
mdl
MFCD20543014
分子量
188.23
InChiKey
NTNWOCRCBQPEKQ-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):
    -4.1
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.714
  • 拓扑面积:
    114
  • 氢给体数:
    4
  • 氢受体数:
    4

文献信息

  • [EN] INHIBITORS OF GROWTH FACTOR ACTIVATION ENZYMES<br/>[FR] INHIBITEURS D'ENZYMES D'ACTIVATION DE FACTEUR DE CROISSANCE
    申请人:UNIV WASHINGTON
    公开号:WO2016144654A1
    公开(公告)日:2016-09-15
    The present invention generally relates to compounds that are useful for inhibiting one or more of hepatocyte growth factor activator, matriptase, hepsin, Factor Xa, or thrombin. The present invention also relates to various methods of using the inhibitor compounds including treating a malignancy, a pre-malignant condition, or cancer by administering an effective amount of the inhibitor to a subject in need thereof.
    本发明通常涉及对抑制肝细胞生长因子激活剂、麦曲丝蛋白、赫普星、Xa因子或凝血酶等的化合物有用的化合物。本发明还涉及使用抑制剂化合物的各种方法,包括通过向需要的受试者施用有效量的抑制剂来治疗恶性肿瘤、癌前病变或癌症。
  • [EN] COMPOUNDS AND METHODS FOR TREATING CANCER, VIRAL INFECTIONS, AND ALLERGIC CONDITIONS<br/>[FR] COMPOSÉS ET MÉTHODES DE TRAITEMENT DU CANCER, D'INFECTIONS VIRALES ET D'AFFECTIONS ALLERGIQUES
    申请人:JANETKA JAMES
    公开号:WO2020264187A1
    公开(公告)日:2020-12-30
    The present invention generally relates to compounds that are useful for inhibiting one or more trypsin-like S1 serine proteases, HGFA, matriptase, hepsin, KLK5 and/or TMPRSS2 as well as cysteine proteases including trypsin-like cysteine proteases (e.g. Cathepsin B). The present invention also relates to various methods of using the inhibitor compounds to treat or prevent viral infections, including those caused by coronaviruses and influenza, conditions associated with KLK5, various malignancies, pre-malignant conditions, and cancer.
    本发明通常涉及一种用于抑制一个或多个类似胰蛋白酶的S1丝氨酸蛋白酶HGFA、matriptase、hepsin、KLK5和/或TMPRSS2以及胱蛋白酶包括类似胰蛋白酶的胱蛋白酶(例如Cathepsin B)的化合物。本发明还涉及使用这些抑制剂化合物治疗或预防病毒感染的各种方法,包括由冠状病毒和流感病毒引起的感染,与KLK5相关的疾病、各种恶性肿瘤、癌前病变和癌症。
  • MODIFIED LIPIDATED RELAXIN B CHAIN PEPTIDES AND THEIR THERAPEUTIC USE
    申请人:Sanofi
    公开号:US20190233494A1
    公开(公告)日:2019-08-01
    The present invention relates to a biologically active single chain Relaxin peptide having the following formula (I) (SEQ ID NO 105): N ter -Ac-X 10 -E-G-R-E-X 15 -V-R-X 18 -X 19 -I-X 21 -X 22 -E-G-X 25 -S-X 27 -X 28 -X 29 -X 30 —X 31 —X 32 —X 33 —NH 2 —C ter or a salt or solvate thereof. It also concerns a pharmaceutical composition comprising at least one peptide of the invention, and the peptide or the pharmaceutical composition for its use as a medicament.
    本发明涉及一种具有以下式子(I)(SEQ ID NO 105)的生物活性单链Relaxin肽:Nter-Ac-X10-E-G-R-E-X15-V-R-X18-X19-I-X21-X22-E-G-X25-S-X27-X28-X29-X30—X31—X32—X33—NH2—Cter或其盐或溶剂。本发明还涉及包含本发明中至少一种肽的制药组合物,以及该肽或制药组合物作为药物的用途。
  • 5,6-DIHYDRO-1H-PYRIDIN-2-ONE COMPOUNDS
    申请人:Tran Chinh V.
    公开号:US20100034773A1
    公开(公告)日:2010-02-11
    The invention is directed to 5,6-dihydro-1H-pyridin-2-one compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.
    该发明涉及5,6-二氢-1H-吡啶-2-酮化合物和含有这种化合物的药物组合物,用于治疗丙型肝炎病毒感染。
  • DEVICE AND METHOD FOR SOLUBILIZING, SEPARATING, REMOVING AND REACTING CARBOXYLIC ACIDS IN OILS, FATS, AQUEOUS OR ORGANIC SOLUTIONS BY MEANS OF MICRO-OR NANOEMULSIFICATION
    申请人:Dietz Ulrich
    公开号:US20130090488A1
    公开(公告)日:2013-04-11
    The present invention is directed to solubilizing compounds, a device and a method for solubilizing and removing carboxylic acids and especially fatty acids from oils, fats, aqueous emulsion, aqueous media and organic solutions. Devices utilizing the inventive method shall be used for separating carboxylic acids from oils, fats, aqueous emulsion, lipophilic media or organic solutions, respectively by preparing an aqueous micro- or nanoemulsion of the carboxylic acids especially the fatty acids and the solubilizing compound which contains at least one amidino and/or gianidino group. Solubilization effects of solubilizing compounds combined with the inventive use of separation methods for carboxylic acids can be used to treat persons in need of removal of fatty acids or analyze carboxylic acids from blood or process other solutions in food, pharmacy, chemistry, bio fuel industry or other industrial processings.
    本发明涉及溶解化合物、用于从油、脂肪、乳液、介质和有机溶液中溶解和去除羧酸,特别是脂肪酸的装置和方法。采用本发明方法的装置将用于通过制备羧酸特别是脂肪酸和含有至少一种基甲酰基和/或基团的溶解化合物的微观或纳米乳液,分离油、脂肪、乳液、亲脂性介质或有机溶液中的羧酸。溶解化合物的溶解效果与本发明所述的羧酸分离方法相结合,可用于治疗需要去除脂肪酸或从血液中分析羧酸或处理食品、药品、化学生物燃料工业或其他工业加工过程中的其他溶液的人员。
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