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| 1263416-02-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1263416-02-9
化学式
C13H14ClN3O2S
mdl
——
分子量
311.792
InChiKey
VGAHKHDHLLTGPS-SNVBAGLBSA-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

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-β-hydroxylase
    摘要:
    Aldosterone, the final component of the renin-angiotensin-aldosterone system, plays an important role in the pathophysiology of hypertension and congestive heart failure. Aldosterone synthase (CYP11B2) catalyzes the last three steps of aldosterone biosynthesis, and as such appears to be a target for the treatment of these disorders. A sulfonamide-imidazole scaffold has proven to be a potent inhibitor of CYP11B2. Furthermore, this scaffold can achieve high levels of selectivity for CYP11B2 over CYP11B1, a key enzyme in the biosynthesis of cortisol. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.06.086
  • 作为产物:
    描述:
    N,N-二异丙基乙胺 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 生成
    参考文献:
    名称:
    The discovery of potent inhibitors of aldosterone synthase that exhibit selectivity over 11-β-hydroxylase
    摘要:
    Aldosterone, the final component of the renin-angiotensin-aldosterone system, plays an important role in the pathophysiology of hypertension and congestive heart failure. Aldosterone synthase (CYP11B2) catalyzes the last three steps of aldosterone biosynthesis, and as such appears to be a target for the treatment of these disorders. A sulfonamide-imidazole scaffold has proven to be a potent inhibitor of CYP11B2. Furthermore, this scaffold can achieve high levels of selectivity for CYP11B2 over CYP11B1, a key enzyme in the biosynthesis of cortisol. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.06.086
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同类化合物

噻吩并[3,2-d]异噻唑-5-羧酸乙酯 5-苯基-3-(1H-吡唑-1-基)噻吩并[2,3-d]异噻唑1,1-二氧化 4-氯-8-(甲基硫烷基)异噻唑并[4',5':4,5]噻吩并[3,2-d][1,2,3]三嗪 4-氨基-3-甲硫基噻吩并[4,5-d][1,2]噻唑-5-甲酰胺 4-氨基-3-甲基噻吩并[2,3-c]异噻唑-5-羧酸乙酯 4-氨基-3-[(4-氟苯甲基)硫烷基]噻吩并[2,3-c]异噻唑-5-甲酰胺 4-[2-(6-甲氧基萘-2-基)丙基]-N-甲基哌嗪-1-甲酰胺 4,6-二氢噻吩并[3,4-d][1,3]噻唑5,5-二氧化物 3-甲基噻吩并[2,3-c]异噻唑-5-羧酸乙酯 3-(4-氯-3,5-二甲基-1H-吡唑-1-基)噻吩并[3,4-d]异噻唑1,1-二氧化 3-(4-氯-1H-吡唑-1-基)噻吩并[3,4-d]异噻唑1,1-二氧化 3-(3,5-二甲基吡唑-1-基)噻吩并[3,4-d][1,2]噻唑1,1-二氧化物 2-甲基噻吩并噻唑 2-甲基噻吩并[2,3-d]异噻唑-3(2H)-酮 1,1-二氧化物 2-氨基噻吩并[2,3-d]噻唑-6-羧酸 甲酯 2-氨基噻吩并[2,3-D]噻唑 1,1-二氧代噻吩并[2,3-D]异噻唑-3-酮 (9CI)-2-氨基-噻吩并[2,3-d]噻唑-5-羧酸 2-[[1-Oxo-2-[6-(trifluoromethyl)pyridin-3-yl]-1,2-thiazolidin-1-ylidene]amino]-1,3-thiazol-4-one 6-cyano-2-ethyl-5-(trimethylsilyl)thieno[2,3-b]pyridine methyl 5-(1-methoxy-2-methylpropyl)-2,2'-bisthiazole-4-carboxylate 5-(2-methylpropen-1-yl)-2,2'-bisthiazole-4-carboxylic acid N-tert-Butyl-S-(4-chloro-isothiazolo[4,5-d]isothiazol-3-yl)-thiohydroxylamine ethyl 2-oxo-5-chloro-6-phenyl-3-benzothiazolineacetate 2-Hydroxy-5-phenylthieno<2,3-d>thiazol 1,1-dioxo-5-phenyl-1λ6-[1,4,2]dithiazinane-3-thione 1,1-dioxo-5-p-tolyl-1λ6-[1,4,2]dithiazinane-3-thione 5-phenyl-thieno[2,3-d]thiazol-2-ylamine 4-amino-1λ6,2-thiazinane-1,1-dione hydrochloride 4-(2,2-dioxo-2,3,3a,9a-tetrahydro-1H-2λ6-benzo[b]thieno[3,4-e][1,4]thiazin-9-yl)-butylamine 3-Propyl-4,6-dihydro-thieno[3,4-d]isothiazole 5,5-dioxide 4,5-dichloro-N-[3-(2-chloro-6-fluorophenyl)-1,2,4-thiadiazol-5-yl]thiophene-2-sulfonamide ethyl 6-N-formylaminothieno<2,3-d>thiazole-5-carboxylate 3,5-dichloro-thieno[3,2-b]thiophene-2-carboxylic acid 3-morpholin-4-yl-propylamide 7-acetyl-3,4,8-triamino-1H-pyrazolo<3,4-d>thieno<2,3-b>pyridin Methyl2-aminothieno[2,3-d][1,3]thiazole-5-carboxylatehydrochloride (3aR,6aR)-3-Benzyl-5,5-dioxo-hexahydro-5λ6-thieno[3,4-d]thiazol-2-ylideneamine; hydrobromide ethyl 3,5-dimethylthieno[3,2-c]diazepine-1-carboxylate 3,5-dimethyl-2-(4-methyl-thiazol-2-ylmethyl)-2H-[1,2]thiazine 1,1-dioxide 3-Methylthio-7-amino-isothiazolo<3',4':2,3>thieno<2,3-c>pyrimidin 13-Isobutyl-5.11-imino-5H.11H-dipyrido<2.3-b:2'.3'-f><1.5>dithiocin K-(4-Amino-3-methylthio-thieno<2,3-c>isothiazol-5)-carboxylat SN56 ethyl 4-amino-3-methylthiothieno<3,2-d>isothiazole-5-carboxylate 3-methyl-4-(3-methyl-5-phenylthiophen-2-yl)-4H-pyrimidine;hydrochloride 2-(Dimethylamino)thieno[2,3-d][1,3]thiazole-5-carboxylic acid 7-Bromothieno[3,2-c]pyridine-2-carboxylic acid 2,3-Dihydro-2-methyl-3-thioxo-thieno<3,4-d>isothiazol-1,1-dioxid