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3-<(methylamino)methyl>-6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide hydrochloride | 126257-71-4

中文名称
——
中文别名
——
英文名称
3-<(methylamino)methyl>-6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide hydrochloride
英文别名
6-chloro-3-(methylaminomethyl)-1,1-dioxo-3,4-dihydro-2H-1lambda6,2,4-benzothiadiazine-7-sulfonamide;hydrochloride;6-chloro-3-(methylaminomethyl)-1,1-dioxo-3,4-dihydro-2H-1λ6,2,4-benzothiadiazine-7-sulfonamide;hydrochloride
3-<(methylamino)methyl>-6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide hydrochloride化学式
CAS
126257-71-4
化学式
C9H13ClN4O4S2*ClH
mdl
——
分子量
377.273
InChiKey
JBRNMOXHLMMCAV-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):
    -0.34
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    147
  • 氢给体数:
    5
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    3-<(methylamino)methyl>-6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide hydrochloride 、 N--L-alanyl>-L-prolin-4-one ethyl ester 在 sodium cyanoborohydride 、 magnesium sulfate 、 N,N-二甲基甲酰胺 作用下, 生成 N--L-alanyl>-(4RS)-4--N-methylamino>-L-proline ethyl ester S,S-dioxide
    参考文献:
    名称:
    Angiotensin converting enzyme inhibitors. 10. Aryl sulfonamide substituted N-[1-carboxy-3-phenylpropyl]-L-alanyl-L-proline derivatives as novel antihypertensives
    摘要:
    Compounds 1a-g consisting of enalaprilat covalently bonded to aryl sulfonamides, including several known thiazide diuretics, were synthesized and tested for ACE inhibitory and diuretic and overall antihypertensive effects. All compounds were potent ACE inhibitors in vitro, with IC50 = 6.5-85 nM. At 10 mg/kg iv or ip in the rat, 1a-g inhibited the AI pressor response by 76-100%; inhibition declined significantly upon oral dosing. Compounds 1a and 1f at 100 mg/kg ip in the sodium-depleted, spontaneously hypertensive rats reduced blood pressure 28-35% and 41-42%, respectively. Compounds 1a and 1f elicited natriuresis and kaliuresis without accompanying volume increases in the rat; 1c at 25 mg/kg iv induced delayed diuresis. Compound 1f has been chosen for further development.
    DOI:
    10.1021/jm00168a013
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文献信息

  • Antihypertensive derivatives
    申请人:RHONE-POULENC RORER PHARMACEUTICALS INC.
    公开号:EP0175266B1
    公开(公告)日:1996-03-20
  • US4749698A
    申请人:——
    公开号:US4749698A
    公开(公告)日:1988-06-07
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