摩熵化学
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

2-Tert-butyl-5-propylpyrimidine

中文名称
——
中文别名
——
英文名称
2-Tert-butyl-5-propylpyrimidine
英文别名
2-tert-butyl-5-propylpyrimidine
2-Tert-butyl-5-propylpyrimidine化学式
CAS
——
化学式
C11H18N2
mdl
——
分子量
178.27
InChiKey
JZZVORWVSLQVPU-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):
    3.2
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • NOVEL 3-(4(BENZYLOXY)PHENYL)HEX-4-INOIC ACID DERIVATIVE, METHOD OF PREPARING SAME AND PHARMACEUTICAL COMPOSITION FOR PREVENTING AND TREATING METABOLIC DISEASE INCLUDING SAME AS EFFECTIVE INGREDIENT
    申请人:HYUNDAI PHARM CO., LTD
    公开号:US20160024063A1
    公开(公告)日:2016-01-28
    The present invention relates to a novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative, a preparation method thereof, and a pharmaceutical composition comprising the same as an active ingredient for the prevention and treatment of metabolic disease. The novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative, the optical isomer thereof, or the pharmaceutically acceptable salt thereof of the present invention has excellent activities of activating GPR40 protein and promoting insulin secretion accordingly but has no toxicity when co-administered with other drugs. That is, the novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative, the optical isomer thereof, or the pharmaceutically acceptable salt thereof of the present invention can be co-administered with other drugs and can promote the activation of GPR40 protein significantly, so that the composition comprising the same as an active ingredient can be efficiently used as a pharmaceutical composition for the prevention and treatment of metabolic disease such as obesity, type I diabetes, type II diabetes, incompatible glucose tolerance, insulin resistance, hyperglycemia, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, dyslipidemia, and syndrome X, etc.
    本发明涉及一种新型的3-(4-(苄氧基)苯基)己-4-羧酸生物,其制备方法以及包含该衍生物作为活性成分的药物组合物,用于预防和治疗代谢性疾病。本发明的这种新型的3-(4-(苄氧基)苯基)己-4-羧酸生物、其光学异构体或其药用可接受盐,对于激活GPR40蛋白并相应地促进胰岛素分泌具有优良活性,且在与其他药物联合使用时没有毒性。也就是说,本发明的这种新型的3-(4-(苄氧基)苯基)己-4-羧酸生物、其光学异构体或其药用可接受盐,可以与其他药物联合使用,并且能显著促进GPR40蛋白的激活,使得包含其作为活性成分的组合物能有效地用作预防和治疗诸如肥胖、I型糖尿病、II型糖尿病、糖耐量异常、胰岛素抵抗、高血糖、高脂血症、高甘油三酯血症、高胆固醇血症、血脂异常和X综合症等代谢性疾病的药物组合物。
  • TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE
    申请人:NewGen Therapeutics, Inc.
    公开号:US20140221314A1
    公开(公告)日:2014-08-07
    The invention provides for compositions comprising phosphorous containing tricyclic compounds, including phthalazin-1(2H)-one derivatives. The compounds are potent inhibitors of the enzyme poly(ADP-ribose)polymerase (PARP), particularly PARP-1 and potentially PARP-2. The also show good cellular activity in inhibiting poly(ADP-ribose) oligomer formation. The compounds may be useful as mono-therapy or in combination with other therapeutic agents in the treatment conditions where PARP is implicated, such as cancer, inflammatory diseases and ischemic conditions. Thus, also provided are methods for the treatment of a condition where PARP is implicated comprising administering to an effective amount of a compound of the invention to an individual in need thereof.
    本发明提供了包含含三环化合物的组合物,包括邻苯二酮-1(2H)-酮衍生物。这些化合物是聚(ADP-核糖)聚合酶(PARP)的有效抑制剂,特别是PARP-1和潜在的PARP-2。它们还表现出良好的细胞活性,能够抑制聚(ADP-核糖)寡聚体形成。这些化合物可用作单一治疗或与其他治疗药物联合使用,治疗PARP参与的疾病,如癌症、炎症性疾病和缺血性疾病。因此,本发明还提供了一种治疗PARP参与的疾病的方法,包括向需要的个体施用本发明化合物的有效量。
  • COMPOSITE PREPARATION, CONTAINING NOVEL 3-(4-(BENZYLOXY)PHENYL)HEX-4-INOIC ACID DERIVATIVE AND ANOTHER ACTIVE INGREDIENT, FOR PREVENTING OR TREATING METABOLIC DISEASES
    申请人:Hyundai Pharm Co., Ltd.
    公开号:EP3207928A2
    公开(公告)日:2017-08-23
    The present invention relates to a pharmaceutical composition for preventing or treating metabolic diseases, in which a novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative and at least another active ingredient, which is selected from the group consisting of dipeptidyl peptidase-4 (DPPIV) inhibitor-based, sulfonylurea-based, thiazolidinedione (TZD)-based, biguanide-based, and sodium/glucose cotransporter 2 (SGLT2) inhibitor-based drugs, may be administered in combination or in the form of a composite preparation. The use of the composition of the present invention can provide a remarkably excellent blood sugar reducing effect in various animal diabetic disease models, and the composition of the present invention can be favorably used as a pharmaceutical composition for preventing or treating metabolic diseases, such as obesity, diabetes type I, diabetes type II, glucose intolerance symptoms, insulin resistance symptoms, hyperglycemia, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, dyslipidemia, and syndrome X.
    本发明涉及一种用于预防或治疗代谢性疾病的药物组合物,其中含有一种新型 3-(4-(苄氧基)苯基)己-4-氨基酸生物和至少另一种活性成分、其中,一种新型 3-(4-(苄氧基)苯基)己-4-嗪酸衍生物和至少另一种活性成分可以联合给药或以复合制剂的形式给药,这些活性成分选自由二肽基肽酶-4 (DPPIV) 抑制剂、磺酰类、噻唑烷二酮 (TZD)、双胍类和/葡萄糖共转运体 2 (SGLT2) 抑制剂组成的组。使用本发明的组合物可在各种动物糖尿病疾病模型中提供显著优异的降血糖效果,本发明的组合物可作为药物组合物用于预防或治疗代谢性疾病,如肥胖、I 型糖尿病、II 型糖尿病、葡萄糖不耐受症状、胰岛素抵抗症状、高血糖症、高脂血症、高甘油三酯血症、高胆固醇血症、血脂异常和 X 综合征。
  • Composite preparation, containing novel 3-(4--(benzyloxy)phenyl)hex-4-inoic acid derivative and another active ingredient, for preventing or treating metabolic diseases
    申请人:HYUNDAI PHARM CO., LTD.
    公开号:US10821110B2
    公开(公告)日:2020-11-03
    The present invention relates to a pharmaceutical composition for preventing or treating metabolic diseases, in which a novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative and at least another active ingredient, which is selected from the group consisting of dipeptidyl peptidase-4 (DPPIV) inhibitor-based, sulfonylurea-based, thiazolidinedione (TZD)-based, biguanide-based, and sodium/glucose cotransporter 2 (SGLT2) inhibitor-based drugs, may be administered in combination or in the form of a composite preparation. The use of the composition of the present invention can provide a remarkably excellent blood sugar reducing effect in various animal diabetic disease models, and the composition of the present invention can be favorably used as a pharmaceutical composition for preventing or treating metabolic diseases, such as obesity, diabetes type I, diabetes type II, glucose intolerance symptoms, insulin resistance symptoms, hyperglycemia, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, dyslipidemia, and syndrome X.
    本发明涉及一种用于预防或治疗代谢性疾病的药物组合物,其中含有一种新型 3-(4-(苄氧基)苯基)己-4-氨基酸生物和至少另一种活性成分、其中,一种新型 3-(4-(苄氧基)苯基)己-4-嗪酸衍生物和至少另一种活性成分可以联合给药或以复合制剂的形式给药,这些活性成分选自由二肽基肽酶-4 (DPPIV) 抑制剂、磺酰类、噻唑烷二酮 (TZD)、双胍类和/葡萄糖共转运体 2 (SGLT2) 抑制剂组成的组。使用本发明的组合物可在各种动物糖尿病疾病模型中提供显著优异的降血糖效果,本发明的组合物可作为药物组合物用于预防或治疗代谢性疾病,如肥胖、I 型糖尿病、II 型糖尿病、葡萄糖不耐受症状、胰岛素抵抗症状、高血糖症、高脂血症、高甘油三酯血症、高胆固醇血症、血脂异常和 X 综合征。
  • COMPOSITE PREPARATION, CONTAINING NOVEL 3-(4--(BENZYLOXY)PHENYL)HEX-4-INOIC ACID DERIVATIVE AND ANOTHER ACTIVE INGREDIENT, FOR PREVENTING OR TREATING METABOLIC DISEASES
    申请人:HYUNDAI PHARM CO., LTD.
    公开号:US20170296539A1
    公开(公告)日:2017-10-19
    The present invention relates to a pharmaceutical composition for preventing or treating metabolic diseases, in which a novel 3-(4-(benzyloxy)phenyl)hex-4-inoic acid derivative and at least another active ingredient, which is selected from the group consisting of dipeptidyl peptidase-4 (DPPIV) inhibitor-based, sulfonylurea-based, thiazolidinedione (TZD)-based, biguanide-based, and sodium/glucose cotransporter 2 (SGLT2) inhibitor-based drugs, may be administered in combination or in the form of a composite preparation. The use of the composition of the present invention can provide a remarkably excellent blood sugar reducing effect in various animal diabetic disease models, and the composition of the present invention can be favorably used as a pharmaceutical composition for preventing or treating metabolic diseases, such as obesity, diabetes type I, diabetes type II, glucose intolerance symptoms, insulin resistance symptoms, hyperglycemia, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, dyslipidemia, and syndrome X.
查看更多