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N-[(5-Bromo-1,3-thiazol-2-yl)carbamoyl]-6,7-dihydro-4H-thieno[3,2-c]pyran-2-sulfonamide | 1158208-20-8

中文名称
——
中文别名
——
英文名称
N-[(5-Bromo-1,3-thiazol-2-yl)carbamoyl]-6,7-dihydro-4H-thieno[3,2-c]pyran-2-sulfonamide
英文别名
N-(5-bromothiazol-2-ylcarbamoyl)-6,7-dihydro-4H-thieno[3,2-c]pyran-2-sulfonamide;1-(5-bromo-1,3-thiazol-2-yl)-3-(6,7-dihydro-4H-thieno[3,2-c]pyran-2-ylsulfonyl)urea
N-[(5-Bromo-1,3-thiazol-2-yl)carbamoyl]-6,7-dihydro-4H-thieno[3,2-c]pyran-2-sulfonamide化学式
CAS
1158208-20-8
化学式
C11H10BrN3O4S3
mdl
——
分子量
424.32
InChiKey
WGBGKFSPGAVVBQ-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):
    2.7
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    162
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

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文献信息

  • Sulfonylureido thiazoles as fructose-1,6-bisphosphatase inhibitors for the treatment of Type-2 diabetes
    作者:Eric Kitas、Peter Mohr、Bernd Kuhn、Paul Hebeisen、Hans Peter Wessel、Wolfgang Haap、Armin Ruf、Jörg Benz、Catherine Joseph、Walter Huber、Ruben Alvarez Sanchez、Axel Paehler、Agnes Benardeau、Marcel Gubler、Brigitte Schott、Effie Tozzo
    DOI:10.1016/j.bmcl.2009.11.093
    日期:2010.1
    Sulfonylureido thiazoles were identified from a HTS campaign and optimized through a combination of structure-activity studies, X-ray crystallography and molecular modeling to yield potent inhibitors of fructose-1,6-bisphosphatase. Compound 12 showed favorable ADME properties, for example, F=70%, and a robust 32% glucose reduction in the acute db/db mouse model for Type-2 diabetes.
  • AMINOTHIAZOLE DERIVATIVES
    申请人:F. Hoffmann-La Roche AG
    公开号:EP2227468A1
    公开(公告)日:2010-09-15
  • US7973051B2
    申请人:——
    公开号:US7973051B2
    公开(公告)日:2011-07-05
  • [EN] AMINOTHIAZOLE DERIVATIVES<br/>[FR] DÉRIVÉS D'AMINOTHIAZOLE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2009068467A1
    公开(公告)日:2009-06-04
    Compounds of formula (I) as well as pharmaceutically acceptable salts and esters thereof, wherein R1 to R3 have the significance given in claim 1 and which can be used in the form of pharmaceutical compositions.
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同类化合物

化合物SEP-363856HYDROCHLORIDE 6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-甲胺 6,7-二氢-4H-噻吩并[3,2-c]吡喃-2-羧酸乙酯 6,7-二氢-4H-噻吩并[3,2-c]吡喃-2-羧酸 5,7-二氢-4H-噻吩并[2,3-c]吡喃-3-羧酸 5,7-二氢-4H-噻吩并[2,3-C]吡喃-3-羧酸乙酯 4-(2-羟基乙基)-4-甲基-6,7-二氢-4h-噻吩并[3,2-c]吡喃 4,5-二氢螺[哌啶-4,7-噻吩并[2,3-c]吡喃] 4',5'-二氢-螺[哌啶-4,7'-[7H]噻吩并[2,3-c]吡喃]-1-羧酸叔丁酯 2-氯-4,5-二氢螺[哌啶-4,7-噻吩并[2,3-c]吡喃] 2-氨基-5,5-二甲基-4,7-二氢-5H-噻吩并[2,3-C]吡喃-3-羧酸叔丁酯 2-氨基-4,7-二氢-5H-噻吩并[2,3-c]吡喃-3-羧酸乙酯 2-氨基-4,7-二氢-5H-噻吩并[2,3-c]吡喃-3-甲腈 2-[[(苯甲酰基氨基)硫代甲酰]氨基]-4,7-二氢-5,5-二甲基-5H-噻吩并[2,3-C]吡喃-3-羧酸 (4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸 (2-羧基噻吩-3-基)乙酸酐 2-((8-fluoro-5-methylchroman-6-yl)methyl)-N-methylbenzamide 2,4-(2,5,8,11-tetraoxa)dodecano-3-bromo-5-phenylthiophene 2-(cycloheptanecarbonyl-amino)-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid 2-(Cyclopentanecarbonyl-amino)-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid ethyl ester 2-[(hexahydro-2,5-methanopentalen-3a(1H)-ylcarbonyl)amino]-N-[(3R)-tetrahydrofuran-3-yl]-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxamide N-[5-(4-cyanophenyl)methyl-2-thiazolyl]-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxamide 6,7-dihydro-N-methyl-4H-Thieno[3,2-c]pyran-4-methanamine hydrochloride 5-Methyl-7-oxo-4,5-dihydro-7H-thieno<2.3-c>pyran 5,7-dihydro-7-(4-nitrophenyl)-4H-thieno[2,3-c]pyran 1,9-Dimethyl-4,6-dihydrodithieno<3,4-c:3',4'-e>oxepin-4-on N-(3-cyano-5,7-dihydro-4H-thieno[2,3-c]pyran-2-ylcarbamoyl)benzamide {4-methyl-4,6-dihydrothieno[2,3-c]furan-2-yl}hexahydro-2,5-methanopentalene-3a(1H)-carboxylic acid N-benzoyl-N'-(3-cyano-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)thiourea 5,7-dihydro-7,7-dimethyl-4H-thieno[2,3-c]pyran 5,7-dihydro-7-pentyl-4H-thieno[2,3-c]pyran 3-(benzo[d]thiazol-2-yl)-5,7-dihydro-4H-thieno[2,3-c]pyran-2-amine (2-ethyl-6,7-dihydro-4H-thieno[3,2-c]pyran-4-yl)methanamine hydrochloride 2-Bromo-5,5-dimethyl-5H-thieno<3,2-b>pyran