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(RS)-(4-amino-3,4-dihydro-2H-chromen-7-yl)methanol | 784205-09-0

中文名称
——
中文别名
——
英文名称
(RS)-(4-amino-3,4-dihydro-2H-chromen-7-yl)methanol
英文别名
(4-aminochroman-7-yl)methanol;(4-Aminochroman-7-yl)-methanol;(4-amino-3,4-dihydro-2H-chromen-7-yl)methanol
(RS)-(4-amino-3,4-dihydro-2H-chromen-7-yl)methanol化学式
CAS
784205-09-0
化学式
C10H13NO2
mdl
MFCD18651495
分子量
179.219
InChiKey
DBLPNNSIIBSYMC-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
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    55.5
  • 氢给体数:
    2
  • 氢受体数:
    3

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:
    (RS)-(4-amino-3,4-dihydro-2H-chromen-7-yl)methanolmanganese(IV) oxide 、 silica-supported carbodiimide 、 三乙酰氧基硼氢化钠1-羟基苯并三唑溶剂黄146 作用下, 以 四氢呋喃二氯甲烷1,2-二氯乙烷N,N-二甲基甲酰胺丙酮 为溶剂, 反应 71.0h, 生成 (S)-3-(naphthalene-7-sulfonamido)-3-phenyl-N-((R)-7-(piperidin-1-ylmethyl)chroman-4-yl)propanamide
    参考文献:
    名称:
    Identification of a Nonpeptidic and Conformationally Restricted Bradykinin B1 Receptor Antagonist with Anti-Inflammatory Activity
    摘要:
    We report the discovery of chroman 28, a potent and selective antagonist of human, nonhuman primate, rat, and rabbit bradykinin B1 receptors (0.4-17 nM). At 90 mg/kg s.c., 28 decreased plasma extravasation in two rodent models of inflammation. A novel method to calculate entropy is introduced and ascribed similar to 30% of the gained affinity between "flexible" 4 (K-i = 132 nM) and "rigid" 28 (K-i = 0.77 nM) to decreased conformational entropy.
    DOI:
    10.1021/jm061224g
  • 作为产物:
    描述:
    4-氧代苯并二氢吡喃-7-羧酸甲酯 在 sodium tetrahydroborate 、 lithium aluminium tetrahydride 、 二苯基膦叠氮化物 作用下, 以 四氢呋喃甲醇甲苯 为溶剂, 反应 0.08h, 生成 (RS)-(4-amino-3,4-dihydro-2H-chromen-7-yl)methanol
    参考文献:
    名称:
    Identification of a Nonpeptidic and Conformationally Restricted Bradykinin B1 Receptor Antagonist with Anti-Inflammatory Activity
    摘要:
    We report the discovery of chroman 28, a potent and selective antagonist of human, nonhuman primate, rat, and rabbit bradykinin B1 receptors (0.4-17 nM). At 90 mg/kg s.c., 28 decreased plasma extravasation in two rodent models of inflammation. A novel method to calculate entropy is introduced and ascribed similar to 30% of the gained affinity between "flexible" 4 (K-i = 132 nM) and "rigid" 28 (K-i = 0.77 nM) to decreased conformational entropy.
    DOI:
    10.1021/jm061224g
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文献信息

  • [EN] BICYCLIC COMPOUNDS HAVING BRADYKININ RECEPTORS AFFINITY AND PHARMACEUTICAL COMPOSITIONS THEREOF<br/>[FR] COMPOSES BICYCLIQUES PRESENTANT UNE AFFINITE POUR LES RECEPTEURS DE LA BRADYKININE ET COMPOSITIONS PHARMACEUTIQUES EN CONTENANT
    申请人:AMGEN INC
    公开号:WO2004092116A1
    公开(公告)日:2004-10-28
    Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疼痛和炎症介导的疾病等方面有效。该发明涵盖了新颖的化合物、类似物、前药和其药学上可接受的衍生物,以及用于预防和治疗涉及疼痛、炎症等疾病和其他疾病或病况的药物组合物和方法。该发明还涉及制备这类化合物的方法,以及在这类方法中有用的中间体。
  • Piperazine derivatives and methods of use
    申请人:Chen J. Jian
    公开号:US20050014749A1
    公开(公告)日:2005-01-20
    Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疼痛和炎症介导的疾病等方面有效。该发明涵盖了新颖的化合物、类似物、前药和其药学上可接受的衍生物,以及用于预防和治疗涉及疼痛、炎症等疾病或其他疾病或病况的药物组合物和方法。该发明还涉及制备这类化合物的方法,以及在这类方法中有用的中间体。
  • 1,2,3,4-Tetrahydropyrazin-2-yl acetamides and methods of use
    申请人:Askew C. Benny
    公开号:US20060025400A1
    公开(公告)日:2006-02-02
    Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疼痛和疾病,如炎症介导的疾病,具有有效性。该发明涵盖了新颖的化合物、类似物、前药和其药学上可接受的衍生物,药物组合物以及用于预防和治疗涉及疼痛、炎症等疾病和其他不适或情况的方法。该发明还涉及制备此类化合物的方法,以及在此类过程中有用的中间体。
  • Substituted sulfones and methods of use
    申请人:Askew C. Benny
    公开号:US20060111347A1
    公开(公告)日:2006-05-25
    Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疼痛和炎症介导的疾病有效。本发明涵盖新颖的化合物、类似物、前药和其药学上可接受的衍生物、制备这些化合物的药物组合物以及预防和治疗涉及疼痛、炎症等疾病和其他不适或病况的方法。本发明还涉及制备这些化合物的过程,以及在这些过程中有用的中间体。
  • Compounds and methods of use
    申请人:Groneberg D. Robert
    公开号:US20050124654A1
    公开(公告)日:2005-06-09
    Selected compounds are effective for treatment of pain and diseases, such as inflammation mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving pain, inflammation, and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    所选化合物对于治疗疼痛和炎症介导的疾病等方面有效。该发明包括新颖的化合物、类似物、前药和其药学上可接受的衍生物、制药组合物以及预防和治疗涉及疼痛、炎症等疾病和其他疾病或病况的方法。该发明还涉及制备这种化合物的过程以及在这种过程中有用的中间体。
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