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6-[(R)-4-(4-benzyl-phthalazin-1-yl)-2-methyl-piperazin-1-yl]-nicotinic acid ethyl ester | 1057677-83-4

中文名称
——
中文别名
——
英文名称
6-[(R)-4-(4-benzyl-phthalazin-1-yl)-2-methyl-piperazin-1-yl]-nicotinic acid ethyl ester
英文别名
ethyl 6-[(2R)-4-(4-benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]pyridine-3-carboxylate
6-[(R)-4-(4-benzyl-phthalazin-1-yl)-2-methyl-piperazin-1-yl]-nicotinic acid ethyl ester化学式
CAS
1057677-83-4
化学式
C28H29N5O2
mdl
——
分子量
467.571
InChiKey
AZTPRIPWSNDKNT-HXUWFJFHSA-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):
    5
  • 重原子数:
    35
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    71.4
  • 氢给体数:
    0
  • 氢受体数:
    7

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:
    6-[(R)-4-(4-benzyl-phthalazin-1-yl)-2-methyl-piperazin-1-yl]-nicotinic acid ethyl ester 在 lithium hydroxide monohydrate 作用下, 以 乙醇 为溶剂, 以52%的产率得到(R)-6-(4-(4-benzylphthalazin-1-yl)-2-methylpiperazin-1-yl)nicotinic acid
    参考文献:
    名称:
    Orally Active 7-Substituted (4-Benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]nicotinonitriles as Active-Site Inhibitors of Sphingosine 1-Phosphate Lyase for the Treatment of Multiple Sclerosis
    摘要:
    Sphingosine 1-phosphate (S1P) lyase has recently been implicated as a therapeutic target for the treatment of multiple sclerosis (MS), based on studies in a genetic mouse model. Potent active site directed inhibitors of the enzyme are not known so far. Here we describe the discovery of (4-benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]nicotinonitrile 5 in a high-throughput screen using a biochemical assay, and its further optimization. This class of compounds was found to inhibit catalytic activity of S1PL by binding to the active site of the enzyme, as seen in the cocrystal structure of derivative 31 with the homodimeric human S1P lyase. 31 induces profound reduction of peripheral T cell numbers after oral dosage and confers pronounced protection in a rat model of multiple sclerosis. In conclusion, this novel class of direct S1P lyase inhibitors provides excellent tools to further explore the therapeutic potential of T cell-targeted therapies in multiple sclerosis and other autoimmune and inflammatory diseases.
    DOI:
    10.1021/jm500338n
  • 作为产物:
    参考文献:
    名称:
    Orally Active 7-Substituted (4-Benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]nicotinonitriles as Active-Site Inhibitors of Sphingosine 1-Phosphate Lyase for the Treatment of Multiple Sclerosis
    摘要:
    Sphingosine 1-phosphate (S1P) lyase has recently been implicated as a therapeutic target for the treatment of multiple sclerosis (MS), based on studies in a genetic mouse model. Potent active site directed inhibitors of the enzyme are not known so far. Here we describe the discovery of (4-benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]nicotinonitrile 5 in a high-throughput screen using a biochemical assay, and its further optimization. This class of compounds was found to inhibit catalytic activity of S1PL by binding to the active site of the enzyme, as seen in the cocrystal structure of derivative 31 with the homodimeric human S1P lyase. 31 induces profound reduction of peripheral T cell numbers after oral dosage and confers pronounced protection in a rat model of multiple sclerosis. In conclusion, this novel class of direct S1P lyase inhibitors provides excellent tools to further explore the therapeutic potential of T cell-targeted therapies in multiple sclerosis and other autoimmune and inflammatory diseases.
    DOI:
    10.1021/jm500338n
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文献信息

  • Organic Compounds and Their Uses
    申请人:Dai Miao
    公开号:US20100069368A1
    公开(公告)日:2010-03-18
    The present disclosure relates to compounds relating to the diagnosis and treatment of pathologies relating to the Hedgehog pathway, including but not limited to tumor formation, cancer, neoplasia, and non-malignant hyperproliferative disorders; specifically relating to compounds of formula I:
    本公开涉及与Hedgehog通路相关的病理诊断和治疗相关化合物,包括但不限于肿瘤形成、癌症、肿瘤新生和非恶性增生性疾病;具体涉及式I的化合物。
  • Benzyl and pyridinyl derivatives as modulators of the hedgehog signaling pathway
    申请人:Dai Miao
    公开号:US08536168B2
    公开(公告)日:2013-09-17
    The present disclosure relates to compounds relating to the diagnosis and treatment of pathologies relating to the Hedgehog pathway, including but not limited to tumor formation, cancer, neoplasia, and non-malignant hyperproliferative disorders; specifically relating to compounds of formula I:
    本公开涉及与Hedgehog通路相关的病理诊断和治疗相关的化合物,包括但不限于肿瘤形成、癌症、肿瘤新生和非恶性增生性疾病;具体涉及公式I的化合物。
  • ORGANIC COMPOUNDS AND THEIR USES
    申请人:Novartis AG
    公开号:EP2137162B1
    公开(公告)日:2018-08-01
  • US8536168B2
    申请人:——
    公开号:US8536168B2
    公开(公告)日:2013-09-17
  • [EN] ORGANIC COMPOUNDS AND THEIR USES<br/>[FR] COMPOSÉS ORGANIQUES ET LEURS UTILISATIONS
    申请人:NOVARTIS AG
    公开号:WO2008110611A1
    公开(公告)日:2008-09-18
    [EN] The present disclosure relates to compounds relating to the diagnosis and treatment of pathologies relating to the Hedgehog pathway, including but not limited to tumor formation, cancer, neoplasia, and non-malignant hyperproliferative disorders; specifically relating to compounds of formula (I).
    [FR] La présente invention porte sur des composés se rapportant au diagnostic et au traitement de pathologies concernant la voie de Hedgehog, comprenant mais sans y être limitées, la formation de tumeur, le cancer, la néoplasie, et les troubles hyperprolifératifs non malins. De façon précise, l'invention porte sur les composés représentés par la formule (I).
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