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2-cyano-4H-thieno[3,2-b]pyrrole-5-carboxylic acid | 332099-48-6

中文名称
——
中文别名
——
英文名称
2-cyano-4H-thieno[3,2-b]pyrrole-5-carboxylic acid
英文别名
——
2-cyano-4H-thieno[3,2-b]pyrrole-5-carboxylic acid化学式
CAS
332099-48-6
化学式
C8H4N2O2S
mdl
——
分子量
192.198
InChiKey
PAUZWINNRRQSPP-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:
    530.1±45.0 °C(Predicted)
  • 密度:
    1.67±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    105
  • 氢给体数:
    2
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    4H-噻吩[3,2-b]吡咯-5-羧酸乙酯甲醇 、 lithium hydroxide monohydrate 、 盐酸羟胺三氯氧磷 作用下, 以 四氢呋喃1,2-二氯乙烷N,N-二甲基甲酰胺 为溶剂, 反应 2.5h, 生成 2-cyano-4H-thieno[3,2-b]pyrrole-5-carboxylic acid
    参考文献:
    名称:
    [EN] SUBSTITUTED TRICYCLIC AMIDES, ANALOGUES THEREOF, AND METHODS USING SAME
    [FR] AMIDES TRICYCLIQUES SUBSTITUÉS, ANALOGUES DE CEUX-CI ET PROCÉDÉS LES METTANT EN OEUVRE
    摘要:
    本公开涵盖了替代三环酰胺,或其类似物的化合物,其化学式为(I),其中X、Y、环A、R1、R5、R6和R7如本文所定义,并包括化合物(I)的组合物,可用于治疗或预防患者体内的乙型肝炎病毒(HBV)和/或丙型肝炎病毒(HDV)感染。
    公开号:
    WO2021229302A1
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文献信息

  • Use of glycogen phosphorylase inhibitors
    申请人:——
    公开号:US20030004162A1
    公开(公告)日:2003-01-02
    The invention provides methods of treating prophylactically an individual in whom Type 2 diabetes mellitus has not yet presented, but in whom there is an increased risk of developing such condition, which methods comprise administering to an individual in need thereof an effective amount of a glycogen phosphorylase inhibitor; effective amounts of a glycogen phosphorylase inhibitor and a non-glycogen phosphorylase inhibiting anti-diabetic agent; or effective amounts of a glycogen phosphorylase inhibitor and an anti-obesity agent. The invention further provides methods of treating prophylactically an individual in whom Type 2 diabetes mellitus has not yet presented, but in whom there is an increased risk of developing such condition, which methods comprise administering to an individual in need thereof a pharmaceutical composition comprising effective amounts of a glycogen phosphorylase inhibitor and a non-glycogen phosphorylase inhibiting anti-diabetic agent; or effective amounts of a glycogen phosphorylase inhibitor and an anti-obesity agent.
    本发明提供了一种预防性地治疗尚未出现2型糖尿病但存在发展为该病风险的个体的方法,该方法包括向需要该方法的个体施用有效量的糖原磷酸化酶抑制剂;有效量的糖原磷酸化酶抑制剂和非糖原磷酸化酶抑制的抗糖尿病剂;或者有效量的糖原磷酸化酶抑制剂和抗肥胖剂。本发明还提供了一种预防性地治疗尚未出现2型糖尿病但存在发展为该病风险的个体的方法,该方法包括向需要该方法的个体施用包含有效量的糖原磷酸化酶抑制剂和非糖原磷酸化酶抑制的抗糖尿病剂的药物组合物;或者有效量的糖原磷酸化酶抑制剂和抗肥胖剂。
  • Bicyclic pyrrolyl amides as glycogen phosphorylase inhibitors
    申请人:Pfizer Inc.
    公开号:US06399601B1
    公开(公告)日:2002-06-04
    This invention relates to compounds of Formula I or stereoisomers, pharmaceutically acceptable salts or prodrugs thereof or a pharmaceutically acceptable salts of the prodrugs. This invention also relates to pharmaceutical compositions comprising a compound of Formula I, and to methods of treatment of diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia.
    本发明涉及式I化合物的化合物或立体异构体、药学上可接受的盐或前药,或前药的药学上可接受的盐。本发明还涉及包含式I化合物的药物组合物,以及治疗糖尿病、胰岛素抵抗、糖尿病性神经病变、糖尿病性肾病变、糖尿病性视网膜病变、白内障、高血糖、高胆固醇血症、高血压、高胰岛素血症、高脂血症、动脉粥样硬化或组织缺血的方法。
  • Tetrazole compounds as thyroid receptor ligands
    申请人:——
    公开号:US20020006946A1
    公开(公告)日:2002-01-17
    The present invention relates to tetrazole compounds of Formula I, stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, and pharmaceutically acceptable salts of the prodrugs. 1 The invention also relates to compositions comprising the tetrazole compounds and to methods of treating obesity, diabetes, atherosclerosis, hypertension, coronary heart disease, hypercholesterolemia, hyperlipidemia, thyroid disease, thyroid cancer, hypothyroidism, depression, glaucoma, cardiac arrhythmias, congestive heart failure, and osteoporosis using the tetrazole compounds.
    本发明涉及公式I的四唑化合物、立体异构体、药用可接受的盐及其前药,以及前药的药用可接受的盐。该发明还涉及包含四唑化合物的组合物,以及使用四唑化合物治疗肥胖、糖尿病、动脉粥样硬化、高血压、冠心病、高胆固醇血症、高脂血症、甲状腺疾病、甲状腺癌、甲状腺功能减退症、抑郁症、青光眼、心律失常、充血性心力衰竭和骨质疏松症的方法。
  • Methods of treating diabetic cardiomyopathy using glycogen phosphorylase inhibitors
    申请人:——
    公开号:US20010046958A1
    公开(公告)日:2001-11-29
    The present invention provides methods of treating diabetic cardiomyopathy, the methods comprising administering to a patient having or at risk of having diabetic cardiomyopathy a therapeutically effective amount of a glycogen phosphorylase inhibitor. The present invention also provides methods of treating diabetic cardiomyopathy, the methods comprising administering to a patient having 1) diabetes and 2) having cardiovascular disease, ischemic heart disease, congestive heart failure, congestive heart failure but not having coronary arteriosclerosis, hypertension, diastolic blood pressure abnormalities, microvascular diabetic complications, abnormal left ventricular function, myocardial fibrosis, abnormal cardiac function, pulmonary congestion, small vessel disease, small vessel disease without atherosclerotic cardiovascular disease or luminal narrowing, coagulopathy, cardiac contusion, or having had or at risk of having a myocardial infarction a therapeutically effective amount of a glycogen phosphorylase inhibitor.
    本发明提供了治疗糖尿病心肌病的方法,该方法包括向患有或有患糖尿病心肌病风险的患者施用治疗有效量的糖原磷酸化酶抑制剂。本发明还提供了治疗糖尿病心肌病的方法,该方法包括向同时患有1)糖尿病和2)心血管疾病、缺血性心脏病、充血性心力衰竭、充血性心力衰竭但不患冠状动脉硬化、高血压、舒张期血压异常、微血管糖尿病并发症、左心室功能异常、心肌纤维化、心脏功能异常、肺充血、小血管病变、无动脉粥样硬化性心血管疾病或腔内狭窄的小血管病变、凝血异常、心脏挫伤或有心肌梗死风险的患者施用治疗有效量的糖原磷酸化酶抑制剂。
  • Methods of treating obesity using a neurotensin receptor ligand
    申请人:——
    公开号:US20010046956A1
    公开(公告)日:2001-11-29
    The present invention relates to methods of treating obesity, diabetes, sexual dysfunction, atherosclerosis, insulin resistance, impaired glucose tolerance, hypercholesterolemia or hypertrigylceridemia using a neurotensin receptor ligand. The present invention also relates to pharmaceutical compositions and kits that comprise a neurotensin receptor ligand.
    本发明涉及使用神经肽T受体配体治疗肥胖症、糖尿病、性功能障碍、动脉粥样硬化、胰岛素抵抗、糖耐量受损、高胆固醇血症或高三酰甘油血症的方法。本发明还涉及包含神经肽T受体配体的制药组合物和工具箱。
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同类化合物

N-甲基-n-[(4-甲基-4H-噻吩并[3,2-b]吡咯-5-基)甲基]胺盐酸盐 6H-噻吩并[2,3-b]吡咯-5-羧酸甲酯 6H-噻吩并[2,3-b]吡咯-5-羧酸乙酯 6H-噻吩并[2,3-b]吡咯-5-羧酸 6-[(3-氨基苯基)甲基]-4,6-二氢-4-甲基-2-(甲基亚磺酰)-5H-噻吩并[2',3':4,5]吡咯并[2,3-D]哒嗪-5-酮 4H-噻唑[3,2-B]吡咯-5-甲酸 4H-噻吩并[3,2-b]吡咯-5-羧酸甲酯 4H-噻吩并[3,2-B]吡咯-5-甲酰肼 4H-噻吩并[3,2-B]吡咯-5-甲酰氯 4H-噻吩并[3,2-B]吡咯-2-羧酸 4H-噻吩[3,2-b]吡咯-5-羧酸乙酯 4H-Dithieno[3,2-b:2',3'-d]吡咯,4-(1-辛基壬基)- 4-辛基-4H-二噻吩并[3,2-b:2,3-d]吡咯 4-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸甲酯 4-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 4-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸 4-甲基-4H-噻[3,2-B]吡咯-5-甲醛 4-R-4H-二噻吩并[3,2-b:2',3'-d]吡咯 3-甲基-4H-噻吩并[3,2-B]吡咯-5-羧酸乙酯 3-溴-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 3-溴-4H-噻吩并[3,2-b]吡咯-5-羧酸 3-溴-4H-噻吩并[3,2-B]吡咯-5-羧酸甲酯 3-氯-4H-噻吩并[3,2-b]吡咯-5-羧酸 2-甲酰基-4H-噻吩并[3,2-B]吡咯-5-羧酸乙酯 2-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 2-甲基-4H-噻吩并[3,2-b]吡咯-5-羧酸 2-溴-6-甲酰基-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 2-溴-6-甲酰基-4-甲基-4H-噻吩并[3,2-B]吡咯-5-羧酸乙酯 2-溴-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 2-溴-4,6-二氢-4-甲基-5H-噻吩并[2,3:4,5]吡咯并[2,3-d]吡嗪-5-酮 2-氯-6H-噻吩并[2,3-b]吡咯-5-羧酸乙酯 2-氯-6H-噻吩并[2,3-B]吡咯-5-羧酸甲酯 2-氯-4H-噻吩并[3,2-b]吡咯-5-羧酸甲酯 2-氯-4H-噻吩并[3,2-b]吡咯-5-羧酸乙酯 2-氯-4H-噻吩并[3,2-b]吡咯-5-羧酸 2-氯-3-甲基-4H-噻吩并[3,2-B]吡咯-5-羧酸乙酯 2,6-二溴-4-正辛基二噻吩并[3,2-b:2',3'-d]吡咯 2,6-二溴-4-(2-乙基己基)-4H-二噻吩并[3,2-b:2,3-d]吡咯 2,3-二氯-4H-噻吩并[3,2-b]吡咯-5-羧酸 (4-甲基-4H-噻吩并[3,2-b]吡咯-5-基)甲醇 (4-(叔丁氧基羰基)-2-氯-4H-噻吩并[3,2-B]吡咯-5-基)硼酸 3-bromo-2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylic acid methyl ester 5-thiophen-3-yl-thieno[3,2-b]pyrrole-4-carboxylic acid tert-butyl ester tert-butyl 5-butyl-4H-thieno[3,2-b]pyrrole-4-carboxylate tert-butyl 4H-thieno[3,2-b]pyrrole-4-carboxylate 2-methyl-4H-thieno[3,2-b]pyrrole-5-carbohydrazide (4-methyl-piperazin-1-yl)-(3-methyl-4H-thieno[3,2-b]pyrrol-5-yl)-methanone 5-methyl-4H-thieno[3,2-b]pyrrole 4-hexyl-2,6-bis(thiophen-2-ylethynyl)-4H-dithieno[3,2-b;2′,3′-d]pyrrole 4-(3-chlorobenzyl)-2,6-bis-phenylethynylthieno[3,2-b]pyrrole-5-carboxylic acid (2-methoxyethyl)amide