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9,10-dioxa-syn-(methylthiomethyl,methyl)(methyl,methyl)bimane | 76421-82-4

中文名称
——
中文别名
——
英文名称
9,10-dioxa-syn-(methylthiomethyl,methyl)(methyl,methyl)bimane
英文别名
1,2,6-Trimethyl-7-(methylsulfanylmethyl)pyrazolo[1,2-a]pyrazole-3,5-dione
9,10-dioxa-syn-(methylthiomethyl,methyl)(methyl,methyl)bimane化学式
CAS
76421-82-4
化学式
C11H14N2O2S
mdl
——
分子量
238.31
InChiKey
RFINUPUQWVIVIQ-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):
    1.3
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    65.9
  • 氢给体数:
    0
  • 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

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文献信息

  • 4,7-DIHYDROTHIENO[2,3-B]PYRIDINE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS
    申请人:Gamber Gabriel G.
    公开号:US20090306373A1
    公开(公告)日:2009-12-10
    This invention relates generally to compounds and pharmaceutical compositions for the treatment of myosin heavy chain (MyHC)-mediated conditions, and in particular, cardiovascular conditions.
    本发明涉及一般用于治疗肌球蛋白重链(MyHC)介导的疾病,特别是心血管疾病的化合物和制药组合物。
  • Methods For The Treatment Of Myosin Heavy Chain-Mediated Conditions Using 4,7-Dihydrothieno[2,3-B]Pyridine Compounds
    申请人:Gamber Gabriel G.
    公开号:US20110105496A1
    公开(公告)日:2011-05-05
    This invention relates generally to methods for the treatment of myosin heavy chain (MyHC)-mediated conditions, and in particular, cardiovascular conditions.
    本发明涉及治疗肌球蛋白重链(MyHC)介导的疾病的方法,特别是心血管疾病的方法。
  • METHOD AND KIT FOR ASSESSING VIABLE CELLS
    申请人:ChemoMetec A/S
    公开号:US20160131658A1
    公开(公告)日:2016-05-12
    The present invention provides simple, rapid methods and procedures for analyzing cells, hereunder quantitative and qualitative assessment of cells, such as viability. The present invention relates to the use of various optionally substituted reporter compounds particularly detectable upon their reaction with thiol-containing species present in higher concentrations in intact (e.g., living) cells than in non-intact (e.g., dead, stressed and apoptotic) cells. The present invention also relates to the use of various optionally substituted reporter compounds particularly detectable upon their reaction with species present in intact and/or non-intact cells. Moreover, the present invention relates to the use of measuring techniques and/or instruments coupled with the use of various optionally substituted reporter compounds. The invention further relates to compositions used in methods for analyzing cells, such as a composition comprising N-(7-dimethylamino-4-methyl-3-coumarinyl)-maleimide (DACM).
  • US9128097B2
    申请人:——
    公开号:US9128097B2
    公开(公告)日:2015-09-08
  • [EN] USE OF 4, 7-DIHYDROTHIENO [2, 3-B] PYRIDINE COMPOUNDS IN THE TREATMENT OF CARDIOVASCULAR DISEASES<br/>[FR] UTILISATION DE COMPOSES DE 4,7-DIHYDROTHIENO[2,3-B]PYRIDINE DANS LE TRAITEMENT DE MALADIES CARDIOVASCULAIRES
    申请人:GILEAD COLORADO INC
    公开号:WO2007073555A1
    公开(公告)日:2007-06-28
    [EN] This invention relates generally to methods for the treatment of myosin heavy chain (MyHC)-mediated conditions, and in particular, cardiovascular conditions.
    [FR] Cette invention concerne de manière générale des procédés pour le traitement d'états induits par la chaîne lourde de myosine (MyHC), notamment de maladies cardiovasculaires.
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同类化合物

溴代双满 6-硝基-2,4-二氢吡唑并[4,3-c]吡唑-3-羧酸 6-甲基-4-(三氟甲基)-1,6-二氢吡唑并[3,4-c]吡唑-3-基胺 5-(溴甲基)-N,N,N,2,6-五甲基-1,7-二氧代-1H,7H-吡唑并[1,2-A]吡唑-3-甲基溴化铵 3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶 3-硝基-1,4-二氢吡唑并[4,3-c]吡唑 3-(溴甲基)-2,6,7-三甲基-1H,5H-吡唑并[1,2-a]吡唑-1,5-二酮 3,5-双溴甲基-2,6-二甲基吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6-三甲基-5-[(2-吡啶基二硫代)甲基]-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6,7-四甲基-1,5-二氮杂双环[3.3.0]-2,6-辛二烯-4,8-二酮 2,3,5,6-四甲基-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 9,10-dioxa-μ-methylthianio-syn-(methylene,methyl)bimane fluorosulfate 9,10-dioxa-anti-(bromomethyl,methyl)bimane 9,10-dioxa-syn-(hydrogen,bromo)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 4,6-(1,4-tetramethylene)-3,7-dichloro-1,5-diazabicyclo<3.3.0>octa-3,6-diene-2,8-dione 9,10-dioxa-syn-(1-propylthiomethyl,methyl)bimane 9,10-dioxa-μ-tert-butylimino-syn-(methylene,methyl)bimane 9,10-dioxa-anti-(methyl,methyl)(methy,bromo)bimane 9,10-dioxa-syn-(fluoromethyl,methyl)(methyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)(methyl,methyl)bimane bromide 9,10-dioxa-syn-(piperidinomethyl,methyl)bimane 9,10-dioxa-syn-(N-phenyl-N-methylaminomethyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)bimane dibromide 9,10-dioxa-syn-(methylthiomethyl,methyl)bimane 9,10-dioxa-syn-(chloromethyl,methyl)bimane 9,10-dioxa-syn-(dimethylaminomethyl,methyl)bimane 9,10-dioxa-syn-(methoxymethyl,methyl)bimane (E)-1,4-dihydro-4-(nitromethylene)-1,2,5-trimethylpyridine syn-(methyl,hydro)(methyl,iodo)bimane 9,10-dioxa-μ-acetylimino-syn-(methylene,methyl)bimane 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-4-ium-6-yl acetate;bromide 6-Chloro-1,2,5-trimethylpyrazolo[1,2-a]pyrazole-3,7-dione 3-Bromomethyl-5-hydroxymethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione syn-(methyl,iodo)bimane 1,7-bis(ethenyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione 9,10-dioxa-syn-(ethyl,chloro)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 9,10-dioxa-anti-(hydroxymethyl,methyl)(methyl,methyl)bimane dl-9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 1-(4-ethylsulfanyl-4H-pyridin-1-yl)-2,6-dimethylpyridin-4-one 3-Bromomethyl-5-ethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione 9,10-dioxa-anti-(chloromethyl,methyl)bimane 9,10-dioxa-μ-imino-syn-(methylene,methyl)bimane N,N-Dimethyl-2-nitro-2-(2H-tetrazol-5-yl)-1,1-ethenediamine 1-hydroxy-3,5-diiodo-4,6-dimethyl-1H-pyridin-2-one 9,10-dioxa-anti-(ethyl,chloro)bimane 2,6-dichloro-7-ethenyl-1-ethylpyrazolo[1,2-a]pyrazole-3,5-dione 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylic acid ethyl 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylate