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西罗莫斯 | 57695-04-2

中文名称
西罗莫斯
中文别名
——
英文名称
sitamaquine
英文别名
MMV000063;N,N-diethyl-N'-(6-methoxy-4-methyl-[8]quinolyl)-hexanediyldiamine;N,N-Diaethyl-N'-(6-methoxy-4-methyl-[8]chinolyl)-hexandiyldiamin;8-(6-diethylaminohexylamino)-6-methoxylepidine;N',N'-diethyl-N-(6-methoxy-4-methylquinolin-8-yl)hexane-1,6-diamine
西罗莫斯化学式
CAS
57695-04-2
化学式
C21H33N3O
mdl
——
分子量
343.513
InChiKey
RVAKDGYPIVSYEU-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

物化性质

  • 沸点:
    bp0.05 190-200°
  • 密度:
    1.033±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    25
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    37.4
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:8537c17bf6321d50e410bd8af28406e9
查看

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

点击查看最新优质反应信息

文献信息

  • COMPOUNDS USEFUL AGAINST KINETOPLASTIDEAE PARASITES
    申请人:Davioud-Charvet Elisabeth
    公开号:US20120214996A1
    公开(公告)日:2012-08-23
    Dibenzylidene and heterobenzylideneacetone derivatives, related 4-piperidones, related 4-thiopyranones and the corresponding sulfinyl- and sulfonyl-analogues for their use for prophylaxis or treatment of trypanosomiasis and leishmaniasis.
    二苄基亚烷和杂二苄基亚烷乙酮衍生物,相关的4-哌啶酮,相关的4-噻opyranones以及相应的亚磺酰基和磺酰基类似物,用于预防或治疗锥虫病和利什曼病。
  • QUINOLINE DERIVATIVES AS ANTI-CANCER AGENTS
    申请人:TANG Johnny Cheuk-on
    公开号:US20120165370A1
    公开(公告)日:2012-06-28
    Quinoline derivatives showing anticancer activities against cancer cell lines of hepatocellular carcinoma (Hep3B), lung carcinoma (A549), esophageal squamous cell carcinoma (HKESC-1, HKESC-4 and KYSE150). The quinoline derivatives have a backbone structure of the following formulas:
    喹啉衍生物显示抗癌活性,针对肝细胞癌(Hep3B)、肺癌(A549)、食道鳞状细胞癌(HKESC-1、HKESC-4和KYSE150)细胞系。这些喹啉衍生物具有以下结构的骨架式样:
  • DITERPENOID MEMBRANOLIDE COMPOUNDS HAVING ANTI-LEISHMANIA ACTIVITY AND USES THEREOF
    申请人:BAKER BILL J.
    公开号:US20160030388A1
    公开(公告)日:2016-02-04
    In a screening program, the Antarctic sponge Dendrilla membranosa was found to produce diterpenoid secondary metabolites with activity against the leishmaniasis-causing parasite Leishmania donovani . The present invention concerns compositions useful for control of Leishmania spp. parasites in vitro and in vivo and treatment of leishmaniasis; methods for treatment of leishmaniasis; and methods for controlling Leishmania spp. parasites in vitro and in vivo.
    在筛选程序中,发现南极海绵Dendrilla membranosa产生二萜类次生代谢物,对引起利什曼病的寄生虫Leishmania donovani具有活性。本发明涉及用于控制离子球虫属寄生虫的组成物,包括体外和体内的治疗利什曼病的方法,以及控制离子球虫属寄生虫体内和体外的方法。
  • Method of making and administering quinoline derivatives as anti-cancer agents
    申请人:Chan Albert Sun-chi
    公开号:US20090054482A1
    公开(公告)日:2009-02-26
    The present invention relates methods of preparing quinoline derivative compounds, and administering such compounds in the treatment of solid and non-solid tumors, notably on liver cancer.
    本发明涉及制备喹啉衍生物化合物的方法,并在治疗实体和非实体肿瘤方面,特别是在肝癌方面使用这些化合物的方法。
  • [EN] MULTI- API LOADING PRODRUGS<br/>[FR] PROMÉDICAMENTS CHARGÉS DE MULTIPLES PRINCIPES ACTIFS
    申请人:ALKERMES INC
    公开号:WO2012088441A1
    公开(公告)日:2012-06-28
    The present invention accomplishes this by having multiple molecules of parent drugs attached to carrier moieties and by extending the period during which the parent drug is released and absorbed after administration to the patient and providing a longer duration of action per dose than the parent drug itself. Prodrug conjugates are suitable for sustained delivery of heteroaryl, lactam- amide-, imide-, sulfonamide-, carbamate-, urea-, benzamide-, acylaniline-, cyclic amide- and tertiary amine-containing parent drugs that are substituted at the amide nitrogen or oxygen atom with labile aldehyde-linked prodrug moieties. The carrier groups of the prodrugs can be hydrophobic to reduce the polarity and solubility of the parent drug under physiological conditions.
    本发明通过将多个母药分子附着在载体基团上,并延长母药在患者服用后释放和吸收的时间,从而实现此目的,并提供每剂次比母药本身更长的作用时间。前药偶联物适用于异杂环、内酰胺、酰胺、磺酰胺、氨基甲酸酯、脲、苯甲酰胺、酰基苯胺、环状酰胺和三级胺含有母药,该母药在酰胺氮或氧原子处以不稳定的醛类前药基团取代。前药的载体基团可以是疏水性的,在生理条件下降低母药的极性和溶解度。
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