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(E)-甲基4-(N-羟基-4-(4-((萘-1-基-氨基甲酰氧基)甲基)苄氨基)丁氨基)-4-氧代丁-2-烯酸酯 | 1310877-95-2

中文名称
(E)-甲基4-(N-羟基-4-(4-((萘-1-基-氨基甲酰氧基)甲基)苄氨基)丁氨基)-4-氧代丁-2-烯酸酯
中文别名
(2E)-4-[羟基[4-[[[4-[[[((1-萘基氨基)羰基]氧]甲基]苯基]甲基]氨基]丁基]氨基]-4-氧代-2-丁烯酸甲酯
英文名称
methylstat
英文别名
methyl (E)-4-[hydroxy-[4-[[4-(naphthalen-1-ylcarbamoyloxymethyl)phenyl]methylamino]butyl]amino]-4-oxobut-2-enoate
(E)-甲基4-(N-羟基-4-(4-((萘-1-基-氨基甲酰氧基)甲基)苄氨基)丁氨基)-4-氧代丁-2-烯酸酯化学式
CAS
1310877-95-2
化学式
C28H31N3O6
mdl
——
分子量
505.571
InChiKey
MUJOCHRZXRZONW-FOCLMDBBSA-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

物化性质

  • 溶解度:
    二甲基亚砜:>5mg/mL

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    37
  • 可旋转键数:
    14
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    117
  • 氢给体数:
    3
  • 氢受体数:
    7

制备方法与用途

甲基stat是一种有效的组蛋白去甲基化酶抑制剂,显示出低细胞毒性的抗增殖活性。它能够诱导细胞凋亡和G0/G1期的细胞周期阻滞,并增加p53和p21蛋白平的表达。此外,甲基stat还能够抑制各种细胞因子诱导的血管生成。因此,甲基stat可用作化学探针,研究其在血管生成中的作用。[1][2]

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

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文献信息

  • EPIGENETIC INHIBITORS FOR SENSITIZING HEMATOLOGIC OR OTHER MALIGNANCIES TO GLUCOCORTICOID THERAPY
    申请人:UNIVERSITY OF SOUTHERN CALIFORNIA
    公开号:US20200181284A1
    公开(公告)日:2020-06-11
    The present disclosure as disclosed in various embodiments is related to glueocorticoid compositions and glucocorticoid therapies for treating hematologic or other malignancies, methods and compositions for enhancing the chemotherapeutic effect of glucocorticoids, methods for determining early relapse of a hematologic or other malignancy in a subject, and methods for treating relapse of a hematologic or other malignancy in a subject.
  • METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE
    申请人:Design Therapeutics, Inc.
    公开号:US20210238226A1
    公开(公告)日:2021-08-05
    The present disclosure relates to compounds and methods for modulating the expression of dmpk, atxn1, atxn2, atxn3, cacna1a, atxn7, ppp2r2br tbp, htt, jph3r ar, or atn1 and treating diseases and conditions in which dmpk, atxn1, atxn2, atxn3, cacna1a, atxn1, ppp2r2b, tbp, htt, jph3, ar, or atn1 plays an active role. The compound can be a transcription modulator molecule having a first terminus, a second terminus, and oligomeric backbone, wherein: a) the first terminus comprises a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence CAG or CTG; b) the second terminus comprises a protein-binding moiety binding to a regulatory molecule that modulates an expression of a gene comprising the nucleotide repeat sequence CAG or CTG; and c) the oligomeric backbone comprising a linker between the first terminus and the second terminus.
  • METHODS AND COMPOSITIONS FOR TREATING CHRONIC INFLAMMATORY INJURY, METAPLASIA, DYSPLASIA AND CANCERS OF EPITHELIAL TISSUES
    申请人:University of Houston System
    公开号:US20220202792A1
    公开(公告)日:2022-06-30
    The present disclosure provides methods and formulations for treating a patient suffering from one or more of chronic inflammatory injury, metaplasia, dysplasia or cancer of an epithelial tissue, which method comprises administering to the patient an agent that selectively kills or inhibits the proliferation or differentiation of pathogenic epithelial stem cells (PESCs) relative to normal epithelial stem cells in the tissue in which the PESCs are found. Representative epithelial tissues include pulmonary, genitourinary, gastrointestinal/esophageal, pancreatic and hepatic tissues.
  • US8735622B2
    申请人:——
    公开号:US8735622B2
    公开(公告)日:2014-05-27
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