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7-O-Methylepinogarol

中文名称
——
中文别名
——
英文名称
7-O-Methylepinogarol
英文别名
23-(dimethylamino)-4,8,12,22,24-pentahydroxy-10-methoxy-1,12-dimethyl-20,25-dioxahexacyclo[19.3.1.02,19.05,18.07,16.09,14]pentacosa-2,4,7(16),8,14,18-hexaene-6,17-dione
7-O-Methylepinogarol化学式
CAS
——
化学式
C28H31NO10
mdl
——
分子量
541.5
InChiKey
LWYJUZBXGAFFLP-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):
    0.8
  • 重原子数:
    39
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    166
  • 氢给体数:
    5
  • 氢受体数:
    11

ADMET

毒理性
  • 毒性数据
毒性数据:大鼠(静脉注射):LD50 77400微克/千克
ToxicityData:Rat(iv): LD50: 77400 µg/kg
来源:NCI Investigational Drugs
毒理性
  • 毒性数据
毒性数据:小鼠(腹腔注射):LD50 83500微克/千克
ToxicityData:Mouse(ip): LD50: 83500 µg/kg
来源:NCI Investigational Drugs

文献信息

  • Methylnogarol compositions and uses thereof
    申请人:——
    公开号:US20020022652A1
    公开(公告)日:2002-02-21
    A method of treatment of a host with a cellular proliferative disease, comprising contacting the host with a methylnogarol and an antiproliferative agent, each in an amount sufficient to modulate said cellular proliferative disease, is described. In some embodiments the methylnogarol comprises menogaril (7-O-Methylnogarol; 7-Con-O-Methylnogarol; U-52047; 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione, 4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13 -dimethyl, -(2alpha,3beta,4alpha,5beta,6alpha, 11 alpha, 13alpha)-, (P)-; 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-; 7(R)-O-Methylnogarol; 7-OMEN). Antiproliferative agents of the invention comprise alkylating agents, intercalating agents, metal coordination complexes, pyrimidine nucleosides, purine nucleosides, inhibitors of nucleic acid associated enzymes and proteins, and agents affecting structural proteins and cytoplasmic enzymes. The invention comprises the described methods as well as compositions comprising a methylnogarol and an antiproliferative agent.
    本文描述了一种治疗患有细胞增殖性疾病的宿主的方法,该方法包括使宿主与一种甲基诺加洛尔和一种抗增殖剂接触,每种物质的量都足以调节所述细胞增殖性疾病。在一些实施方案中,甲基诺卡洛包括 menogaril (7-O-Methylnogarol; 7-Con-O-Methylnogarol; U-52047; 2,6-Epoxy-2H-naphthaceno[1,2-b]肟-9,16-二酮, 4-(二甲基氨基)-3,4,5,6,11,12,13,14-八氢-3,5,8,10,13-五羟基-11-甲氧基-6,13-二甲基, -(2α,3β,4α,5β,6α, 11α, 13α)-, (P)-;2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-; 7(R)-O-Methylnogarol; 7-OMEN).本发明的抗增殖剂包括烷化剂、插层剂、金属配位络合物、嘧啶核苷、嘌呤核苷、核酸相关酶和蛋白质的抑制剂,以及影响结构蛋白和细胞质酶的制剂。本发明包括所述方法以及包含甲基诺卡洛和抗增殖剂的组合物。
  • GENE CLUSTER INVOLVED IN NOGALAMYCIN BIOSYNTHESIS, AND ITS USE IN PRODUCTION OF HYBRID ANTIBIOTICS
    申请人:GALILAEUS OY
    公开号:EP1123310A1
    公开(公告)日:2001-08-16
  • US4086245A
    申请人:——
    公开号:US4086245A
    公开(公告)日:1978-04-25
  • [EN] GENE CLUSTER INVOLVED IN NOGALAMYCIN BIOSYNTHESIS, AND ITS USE IN PRODUCTION OF HYBRID ANTIBIOTICS<br/>[FR] GROUPE DE GENES INTERVENANT DANS LA BIOSYNTHESE DE NOGALMYCINE ET SON UTILISATION DANS LA PRODUCTION D'ANTIBIOTIQUES HYBRIDES
    申请人:GALILAEUS OY
    公开号:WO2000024775A1
    公开(公告)日:2000-05-04
    The present invention relates to the gene cluster for nogalamycin biosynthesis derived from Streptomyces nogalater, and the use of the genes therein to obtain novel hybrid antibiotics for drug screening.
  • [EN] METHYLNOGAROL COMPOSITIONS AND USES THEREOF<br/>[FR] COMPOSITIONS DE METHYLNOGAROL ET UTILISATIONS
    申请人:CHEMGENEX THERAPEUTICS INC
    公开号:WO2001080842A2
    公开(公告)日:2001-11-01
    A method of treatment of a host with a cellular proliferative disease, comprising contacting the host with a methylnogarol and an antiproliferative agent, each in an amount sufficient to modulate said cellular proliferative disease, is described. In some embodiments the methylnogarol comprises menogaril (7-O-Methylnogarol; 7-Con-O-Methylnogarol; U-52047; 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione, 4-(dimethylamino)-3, 4, 5, 6, 11, 12, 13, 14-octahydro-3, 5, 8, 10, 13-pentahydroxy-11-methoxy-6, 13-dimethyl-, (2alpha, 3beta, 4alpha, 5beta, 6alpha, 11alpha, 13alpha)-, (P)-; 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9, 16-dione, 4-(dimethylamino)-3, 4, 5, 6, 11, 12, 13, 14-octahydro-3, 5, 8, 10, 13-pentahydroxy-11-methoxy-6, 13-dimethyl-; 7(R)-O-Methylnogarol; 7-OMEN). Antiproliferative agents of the invention comprise alkylating agents, intercalating agents, metal coordination complexes, pyrimidine nucleosides, purine nucleosides, inhibitors of nucleic acid associated enzymes and proteins, and agents affecting structural proteins and cytoplasmic enzymes. The invention comprises the described methods as well as compositions comprising a methylnogarol and an antiproliferative agent.
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