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5-ethyl-2H-2,6-methano-3,4,5,6-tetrahydrothieno[3,2-g]-1,2,5-thiadiazocine-8-sulfonamide-1,1-dioxide | 155801-87-9

中文名称
——
中文别名
——
英文名称
5-ethyl-2H-2,6-methano-3,4,5,6-tetrahydrothieno[3,2-g]-1,2,5-thiadiazocine-8-sulfonamide-1,1-dioxide
英文别名
11-Ethyl-7,7-dioxo-5,7lambda6-dithia-8,11-diazatricyclo[6.3.1.02,6]dodeca-2(6),3-diene-4-sulfonamide;11-ethyl-7,7-dioxo-5,7λ6-dithia-8,11-diazatricyclo[6.3.1.02,6]dodeca-2(6),3-diene-4-sulfonamide
5-ethyl-2H-2,6-methano-3,4,5,6-tetrahydrothieno[3,2-g]-1,2,5-thiadiazocine-8-sulfonamide-1,1-dioxide化学式
CAS
155801-87-9
化学式
C10H15N3O4S3
mdl
——
分子量
337.445
InChiKey
GAIVIMMNRYWJBW-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):
    -0.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    146
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

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文献信息

  • TRICYCLIC DERIVATIVES OF THE THIENODIAZOCINE AND THIENOTHIADIAZOCINE CLASSES OF COMPOUNDS
    申请人:MERCK & CO. INC.
    公开号:EP0660836A1
    公开(公告)日:1995-07-05
  • EP0660836A4
    申请人:——
    公开号:EP0660836A4
    公开(公告)日:1995-03-27
  • US5308842A
    申请人:——
    公开号:US5308842A
    公开(公告)日:1994-05-03
  • [EN] TRICYCLIC DERIVATIVES OF THE THIENODIAZOCINE AND THIENOTHIADIAZOCINE CLASSES OF COMPOUNDS<br/>[FR] DERIVES TRICYCLIQUES DES CLASSES DE COMPOSES DE THIENODIAZOCINE ET THIENOTHIADIAZOCINE
    申请人:MERCK & CO., INC.
    公开号:WO1994005674A1
    公开(公告)日:1994-03-17
    (EN) Conformationally constrained tricyclic derivatives of the thienodiazocine and thienothiadiazocine classes of compounds and ring homologs thereof are topically effective carbonic anhydrase inhibitors useful in the treatment of ocular hypertension and glaucoma associated therewith. The compounds are of general structure (I).(FR) L'invention concerne des dérivés tricycliques, contraints par conformation, des classes de composés de la thiénodiazocine et la thiénothiadiazocine et leurs homologues cycliques qui sont des inhibiteurs de l'anhydrase carbonique localement efficaces, utilisés dans le traitement de l'hypertension oculaire et du glaucome associé. Les composés font partie de la structure générale (I).
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同类化合物

布林左胺 布林佐胺盐酸盐 布林佐胺杂质E 布林佐胺杂质C 布林佐胺杂质2 布林佐胺中间体 布林佐胺-d5 布林佐胺 布林佐胺 N-去乙基布林佐胺 6-氯-4-羟基-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪1,1-二氧化物 6-氯-2,3-二氢-4H-噻吩并[3,2-e]-1,2-噻嗪-4-酮1,1-二氧化物 6-乙酰基-1H-噻吩并[2,3-b][1,4]噻嗪-2(3H)-酮 4-羟基-2-甲基-2H-噻吩并[2,3-E]-1,2-噻嗪-3-甲酰胺1,1-二氧化物 3,4-二氢-4-羟基-2H-噻吩并[3,2-e]-1,2-噻嗪-1,1-二氧化物 2-(3-甲氧基丙基)-4-氧代-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪-6-磺酰胺1,1-二氧化物 2,3-二氢-4H-噻吩并[2,3-e][1,2]噻嗪-4-酮1,1-二氧化物 1,5,6-三甲基-1,2,3,4-四氢-2LAMBDA6-噻吩并[2,3-C][1,2]噻嗪-2,2,4-三酮 (S)-6-氯-3,4-二氢-2H-噻吩[3,2-E]-1,2-噻嗪-4-醇 1,1-二氧化氮 (S)-6-氯-2-(3-甲氧基丙基)-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪-4-醇 1,1-二氧化物 (S)-3,4-二氢-4-羟基-2-(3-甲氧丙基)-2H-噻吩并[3,2-E]-1,2-噻嗪-6-磺酰胺 1,1-二氧化物 (4S)-3,4-二氢-2-(3-甲氧基丙基)-2H-噻吩并[3,2-e]-1,2-噻嗪-4-醇 1,1-二氧化物 5,6-Dimethyl-2,3-dihydro-6H-<1,3>thiazin-2-thion (2-Ethyl-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazin-3-yl)-methanol 2-Ethyl-3-hydroxymethyl-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazine-6-sulfonic acid amide 11-benzylidene-2-methyl-5,5-dioxo-8-phenyl-5,6,7,8-tetrahydro-benzo[2,3]thiepino[4,5-d]thiazolo[3,2-a]pyrimidin-10-one 6-Amidino-2,3-dihydro-1-(2-methylthioethyl)-2-oxothieno[2,3-b][1,4]thiazine hydrochloride 6-Amidino-1-butyl-2,3-dihydro-2-oxo-1H-thieno[2,3-b][1,4]thiazine 4,4-dioxide hydrochloride 2-Morpholino-5-phenyl-thieno<2,3-d><1,3>thiazin-4-on 4-Ethylamino-3,4-dihydro-2-[3-(3-methoxypropylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide hydrochloride 3,4-Dihydro-4-[(2-methylpropyl)amino]-2-[(2-methylthio)ethyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[3-(2-methoxyethylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 2-(3-methoxypropyl)-4-oxo-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine, 1,1-dioxide 6'-chloro-2',3'-dihydrospiro[1,3-dioxolan-2,4'-thieno[3,2-e][1,2]thiazine], 1',1'-dioxide 3,4-Dihydro-4-propylamino-2-(3-methylthiopropyl)-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-(3-ethylthiopropyl)-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[(2-methylthio)ethyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 5-Ethyl-3-dimethylaminomethyl-2H-2,6-methano-3,4,5,6-tetrahydrothieno[3,2-g]-1,2,5-thiadiazocine-8-sulfonamide-1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[3-(3-methoxypropylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 3-Methylthio-5-methyl-isothiazolo<3',4':2,3>thieno<3,2-d>oxazin-7-on (R)-3,4-dihydro-4-(d5-ethylamino)-2-(3-3d-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide 2-(2-Morpholin-4-yl-ethyl)-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazine-6-sulfonic acid tert-butylamide 3-hydroxy-2-methyl-4-(2-chlorophenylcarbamoyl)-2H-thieno[3,4-e]-1,2-thiazine 1,1-dioxide [(2R,3R,4R,5S)-2,3,4,5-tetraacetyloxy-6-[[3-[(5R)-3,3-dibutyl-7-(dimethylamino)-1,1-dioxo-4,5-dihydro-2H-1lambda6,4-benzothiazepin-5-yl]phenyl]carbamoylamino]hexyl] acetate N-(1,1-dimethylethyl)-2-[4-(4-morpholinyl)-2-butenyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 6-ethyl-2-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol 3,4-Dihydro-2-methyl-3-oxo-4-(pyridin-2-yl-carbamoyl)-2H-thieno[2,3-e]1,2-thiazin 1,1-dioxide 3,4-Dihydro-4-hydroxy-N-(1,1-dimethylethyl)-2-[4-(4-morpholinyl)-2-butenyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide