摩熵化学
数据开放平台 数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[1-(3,4-Dihydroxy-5-methyloxolan-2-yl)-5-fluoro-2-oxopyrimidin-4-yl] carbamate

中文名称
——
中文别名
——
英文名称
[1-(3,4-Dihydroxy-5-methyloxolan-2-yl)-5-fluoro-2-oxopyrimidin-4-yl] carbamate
英文别名
[1-(3,4-dihydroxy-5-methyloxolan-2-yl)-5-fluoro-2-oxopyrimidin-4-yl] carbamate
[1-(3,4-Dihydroxy-5-methyloxolan-2-yl)-5-fluoro-2-oxopyrimidin-4-yl] carbamate化学式
CAS
——
化学式
C10H12FN3O6
mdl
——
分子量
289.22
InChiKey
BESASEJKDQKIPI-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):
    -1.4
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    135
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • THERAPY INVOLVING ANTIBODIES AGAINST CLAUDIN 18.2 FOR TREATMENT OF CANCER
    申请人:Ganymed Pharmaceuticals AG
    公开号:EP2976360A1
    公开(公告)日:2016-01-27
  • [EN] THERAPY INVOLVING ANTIBODIES AGAINST CLAUDIN 18.2 FOR TREATMENT OF CANCER<br/>[FR] THÉRAPIE UTILISANT DES ANTICORPS DIRIGÉS CONTRE LA CLAUDINE-18.2 POUR LE TRAITEMENT DU CANCER
    申请人:GANYMED PHARMACEUTICALS AG
    公开号:WO2014146778A1
    公开(公告)日:2014-09-25
    The present invention generally provides a therapy for effectively treating and/or preventing diseases associated with cells expressing CLDN 18.2, in particular cancer diseases such as gastroesophageal cancer. Data are presented demonstrating that administration of an anti-CLDN18.2 antibody to human patients with gastroesophageal cancer is safe and well-tolerated up to a dose of at least 1000 mg/m2. Furthermore, data are presented demonstrating that the antibody is fully functional in these patients to execute anti-tumor cell effects and evidence for antitumoral activity was obtained.
  • [EN] SYNERGISTIC ENHANCEMENT OF 5-FLUOROURACIL CYTOTOXICITY BY DEOXYURIDINE ANALOGS IN CANCER CELLS<br/>[FR] STIMULATION SYNERGIQUE DE LA CYTOTOXICITÉ DU 5-FLUOROURACILE DANS DES CELLULES CANCÉREUSES PAR DES ANALOGUES DE DÉSOXYURIDINE
    申请人:STC UNM
    公开号:WO2015142867A1
    公开(公告)日:2015-09-24
    In one embodiment, the invention provides a method of treating a subject who suffers from a neoplasm (including a cancer such as a radiotherapeutic-resistant cancer) by administering to the subject a therapeutically effective amount of (a) 5-formyl-2'-deoxyuridine (fdU or foUdR) or a 5-formyl-2'-deoxyuridine derivative, optionally in combination with 5-hydroxy-2'-deoxyuridine (hUdR); and (b) at least one composition selected from the group consisting of either 5-fluorouracil (5-FU), a 5-FU prodrug (e.g. 5- fluoro-2'-deoxyuridine (FdU)) or 5-FU metabolite. In a preferred embodiment, a subject who suffers from colorectal cancer (CRC) or metastatic colorectal cancer (mCRC) is treated with a therapeutically-effective amount of fdU and either 5-FU or the 5-FU prodrug 5-fluoro-2'- deoxyuridine (FdU). Related pharmaceutical compositions are also provided.
  • [EN] DRUG COMBINATIONS WITH SELECTIVE ANDROGEN RECEPTOR MODULATORS (SARMS) AND METHODS OF MAKING AND USING THEM<br/>[FR] COMBINAISONS DE MÉDICAMENTS AVEC DES MODULATEURS DE RÉCEPTEUR D'ANDROGÈNE SÉLECTIFS (SARM), ET LEURS PROCÉDÉS DE FABRICATION ET D'UTILISATION
    申请人:VICUS THERAPEUTICS LLC
    公开号:WO2016061135A1
    公开(公告)日:2016-04-21
    In alternative embodiments, provided are therapeutic combinations, pharmaceutical compositions, formulations, kits and devices comprising drug combinations including a selective androgen receptor modulator (SARM), e.g., such as enobosarm or andarine, with one or more additional drugs or active agents, and methods for making and using them for treating, ameliorating, reversing or preventing a cancer such as a breast cancer, a basal-like carcinoma, a ductal carcinoma or an ovarian cancer, a tumor, a burn or a short stature or related syndrome or condition.
查看更多

同类化合物

阿糖胞苷杂质6 西奈芬净 腺苷硒基蛋氨酸 脱氧腺嘌呤核苷 甲硫腺苷 环西奈芬净 异丙基2-((2R,3S,4R,5R)-5-(6-氨基-9H-嘌呤-9-基)-3,4-二羟基四氢呋喃-2-基)乙酸酯 尿嘧啶多氧菌素 C 多氧菌素 去氧氟尿苷 卡培他滨杂质N 卡培他滨杂质 卡培他滨中间体1 卡培他滨USP杂质 卡培他滨USP杂质 卡培他滨USP杂质 卡培他滨-d11 卡培他滨 化合物55 加洛他滨 [2-(癸酰氨基)-3-羟基-3-苯基丙基]N-[2-[[(2R,3S,4R,5R)-5-(2,4-二氧代嘧啶-1-基)-3,4-二羟基四氢呋喃-2-基]甲基氨基]-2-氧代乙基]氨基甲酸酯 [(3R,4R,5R)-2-(6-氨基-8-叠氮基嘌呤-9-基)-5-甲基-4-(2,4,6-三硝基苯氧基)四氢呋喃-3-基]氧基二氢磷酸酯 S-腺苷蛋氨酸对甲苯磺酸硫酸盐 S-腺苷蛋氨酸丁二磺酸盐 S-腺苷蛋氨酸 S-腺苷甲硫氨酸对甲苯磺酸盐 S-腺苷基-L-蛋氨碘盐 S-腺苷乙硫氨酸 S-腺苷-L-蛋氨酸 S-腺苷-L-半胱氨酸 S-腺苷-3-硫代丙胺 S-腺苷-3-甲硫基丙胺 S-甲基-5'-甲硫基腺苷 S-次黄苷基高半胱氨酸 S-N(6)-甲基腺苷高半胱氨酸 S-(5’-腺苷基)-L-氯化蛋氨酸 S-(5'-腺苷)-L-高半胱氨酸 N-双环[2.2.1]-2-庚基-5-氯-5-脱氧腺苷酸 N-[6-[2-[[(2S,3S,4R,5R)-3,4-二羟基-5-[6-[(4-硝基苯基)甲基氨基]嘌呤-9-基]四氢呋喃-2-基]甲硫基]乙基氨基]-6-氧代己基]-3',6'-二羟基-3-氧代螺[2-苯并呋喃-1,9'-氧杂蒽]-5-甲酰胺 N(4)-腺苷-N(4)-甲基-2,4-二氨基丁酸 9-{5-[(3-氨基-3-羧基丙基)(甲基)-lambda4-硫基]-5-脱氧呋喃戊糖基}-9H-嘌呤-6-胺 9-[(2R,3R,4S,5R)-3,4-二羟基-5-甲基四氢呋喃-2-基]-3H-嘌呤-2,6-二酮 9-(5-脱氧-beta-D-核-呋喃己糖基)-9H-嘌呤-6-胺 9-(5',6'-二脱氧-beta-己-5'-炔呋喃核糖基)腺嘌呤 8-氨基[1”-(N”-丹磺酰)-4”-氨基丁基]-5’-(1-氮丙啶基)-5’-脱氧腺苷 8-叠氮基-S-腺苷蛋氨酸 6-氯-9-(5-脱氧-D-呋喃核糖基)-9H-嘌呤 6-氨基-9-(5-脱氧-alpha-D-呋喃木糖基)-9H-嘌呤 5′-氨基-5′-脱氧腺苷对甲苯磺酸盐 5’-脱氧-5-氟胞嘧啶核苷