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布林佐胺杂质C | 186377-56-0

中文名称
布林佐胺杂质C
中文别名
邻去甲基布林酰胺
英文名称
(R)-4-(ethylamino)-2-(3-hydroxypropyl)-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide1,1-dioxide
英文别名
(4R)-4-(ethylamino)-2-(3-hydroxypropyl)-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide-1,1-dioxide;(R)-4-Ethylamino-3,4-dihydro-2-(3-hydroxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide;O-Desmethyl Brinzolamide;(4R)-4-(ethylamino)-2-(3-hydroxypropyl)-1,1-dioxo-3,4-dihydrothieno[3,2-e]thiazine-6-sulfonamide
布林佐胺杂质C化学式
CAS
186377-56-0
化学式
C11H19N3O5S3
mdl
——
分子量
369.487
InChiKey
WQSYAXSFXFVBTJ-VIFPVBQESA-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

  • 熔点:
    >38°C (dec.)
  • 沸点:
    626.5±65.0 °C(Predicted)
  • 密度:
    1.60±0.1 g/cm3(Predicted)
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.8
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    175
  • 氢给体数:
    3
  • 氢受体数:
    9

SDS

SDS:ee37154fed0d6fbb77dc9f45c958fc3b
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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
  • 下游产品
    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

  • Sulfonamides useful as carbonic anhydrase inhibitors
    申请人:Alcon Laboratories, Inc.
    公开号:US05585377A1
    公开(公告)日:1996-12-17
    Sulfonamides and pharmaceutical compositions containing the compounds useful in controlling intraocular pressure are disclosed. Methods for controlling intraocular pressure through administration of the compositions are also disclosed.
    揭示了含有有益于控制眼内压的化合物的磺胺类药物和制剂。还揭示了通过给药这些制剂来控制眼内压的方法。
  • Design, Synthesis, and Evaluation of NO-Donor Containing Carbonic Anhydrase Inhibitors To Lower Intraocular Pressure
    作者:Qinhua Huang、Eugene Y. Rui、Morena Cobbs、Dac M. Dinh、Hovhannes J. Gukasyan、Jennifer A. Lafontaine、Saurabh Mehta、Brian D. Patterson、David A. Rewolinski、Paul F. Richardson、Martin P. Edwards
    DOI:10.1021/acs.jmedchem.5b00043
    日期:2015.3.26
    The antiglaucoma drugs dorzolamide (1) and brinzolamide (2) lower intraocular pressure (TOP) by inhibiting the carbonic anhydrase (CA) enzyme to reduce aqueous humor production. The introduction of a nitric oxide (NO) donor into the alkyl side chain of dorzolamide (1) and brinzolamide (2) has led to the discovery of NO-dorzolamide 3a and NO-brinzolamide 4a, which could lower TOP through two mechanisms: CA inhibition to decrease aqueous humor secretion (reduce inflow) and NO release to increase aqueous humor drainage (increase outflow). Compounds 3a and 4a have shown improved efficacy of lowering IOP in both rabbits and monkeys compared to brinzolamide (2).
  • US5585377A
    申请人:——
    公开号:US5585377A
    公开(公告)日:1996-12-17
  • [EN] THIENO [3, 2-E] [1, 2] THIAZINE DERIVATIVE AS INHIBITOR OF CARBONIC ANHYDRASE<br/>[FR] DÉRIVÉ DE THIÉNO [3, 2-E] [1, 2] THIAZINE EN TANT QU'INHIBITEUR D'ANHYDRASE CARBONIQUE
    申请人:PFIZER
    公开号:WO2008120099A1
    公开(公告)日:2008-10-09
    [EN] The invention relates to a compound of the formula (I): (I) and to pharmaceutically acceptable salts and solvates thereof. The invention also relates to methods of treating glaucoma, ocular hypertension, age-related macular degeneration, diabetic macular edema, diabetic retinopathy, hypertensive retinopathy, retinal vasculopathies and intraocular pressure in mammals by administering the compound, and to pharmaceutical compositions which contain the compound for such treatments. The invention also relates to methods of preparing the compound.
    [FR] L'invention concerne un composé de formule (I): (I) et des sels et solvates pharmaceutiquement acceptables de celui-ci. L'invention concernent également - des procédés de traitement du glaucome, de l'hypertension oculaire, de la dégénérescence maculaire liée au vieillissement, de l'oedème maculaire diabétique, de la rétinopathie diabétique, de la rétinopathie hypertensive, des vasculopathies rétiniennes et de la tension intraoculaire chez des mammifères par administration du composé, et - des compositions pharmaceutiques qui contiennent le composé pour de tels traitements. L'invention concerne également des procédés de préparation du composé.
  • WO2008/120099
    申请人:——
    公开号:——
    公开(公告)日:——
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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 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 2,3-dihydro-4H-thieno[2,3-e][1,3]thiazine-4-thione 3-(2-isobutylaminoethyl)-2,3-dihydro-4,4-dioxo-6-sulfamoyl-1H-thieno[2,3-b][1,4]thiazine hydrochloride (R)-3,4-dihydro-2-(4-methoxybutyl)-4-propylamino-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide (S)-N-(1,1-dimethylethyl)-3,4-dihydro-4-hydroxy-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide N-(1,1-dimethylethyl)-2-[4-(4-morpholinyl)-2-butenyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 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 6-chloro-3,4-dihydro-2-(4-bromobutyl)-2H-thieno[3,2-e]-1,2-thiazine-4-ol 1,1-dioxide 3,4-dihydro-2,6-dimethyl-3-oxo-2H-thieno[3,2-e]-1,2-thiazine-4-carboxanilide 1,1-dioxide (+)-4-Ethylamino-3,4-dihydro-2-methyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide (+)-4-Hydroxy-2-methyl-2,3-dihydro-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide 3,4-Dihydro-2-methyl-2H-thieno[3,2-e]-1,2-thiazine-4-ol-1,1-dioxide 3,4-Dihydro-4-hydroxy-2-(2-methoxy)ethyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide N-(1,1-Dimethylethyl)-3,4-dihydro-2-(4-methoxybutyl)-4-oxo-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 2,3-Dihydro-N-(1,1-dimethylethyl)-4-oxo-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide N-(2-dimethylaminoethyl)-6-ethyl-2,3-dihydro-1H-thieno[2,3-b][1,4]thiazine-1-carboxamide N-(1,1-Dimethylethyl)-3,4-dihydro-4-hydroxy-2-(4-methoxybutyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide (S)-N-(1,1-Dimethylethyl)-3,4-dihydro-4-hydroxy-2-(4-methoxybutyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 3,4-Dihydro-3-methyl-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide 2-methyl-3,4-dihydro-2H-thieno[2,3-e][1,2]thiazin-4-amine 1,1-dioxide 7-acetyl-1-phenyl-4H-thieno<2,3-b><1,2,4>triazolo<4,3-d><1,4>thiazine T 2097 3-Aethoxycarbonylmethyl-4-hydroxy-2-methyl-2H-thieno<2,3-e>-1,2-thiazin-1,1-dioxid 2-benzylthio-6-ethyl-3H-thieno<2,3-b><1,4>thiazine 2-[(4-methoxyphenyl)methyl]-3-[(4-morpholinyl)methyl]-2H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide 3-[[Bis(2-methoxyethyl)amino]methyl]-2-ethyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 3-Hydroxymethyl-2-(1-methylethyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 3-[[(2-methoxyethyl)(3-methoxypropyl)amino]methyl]-2-methyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 2-(Cyclopropylmethyl)-3-(4-morpholinylmethyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1 dioxide 3-(4-Morpholinylmethyl)-2-propyl-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide