ベナゼプリル塩酸塩

ベナゼプリル塩酸塩 化学構造式
86541-74-4
CAS番号.
86541-74-4
化学名:
ベナゼプリル塩酸塩
别名:
塩酸ベナゼプリル;ベナゼプリル塩酸塩;(3S)-3-[(1S)-1-エトキシカルボニル-3-フェニルプロピル]アミノ-2,3,4,5-テトラヒドロ-2-オキソ-1H-1-ベンゾアゼピン-1-酢酸塩酸塩;ベナゼプリル 塩酸塩;ベナゼプリル塩酸塩 (JAN)
英語名:
Benazepril hydrochloride
英語别名:
Lotensin;Cibace;cgs14824a;Lotension;Cibacen chf;CGS 14824A HCl;Benazepril HCI;3-Cresotic acid;yansuanbeinapuli;Benazepril HCl API
CBNumber:
CB3122020
化学式:
C24H29ClN2O5
分子量:
460.95
MOL File:
86541-74-4.mol
MSDS File:
SDS

ベナゼプリル塩酸塩 物理性質

融点 :
188-190°C
比旋光度 :
D -141.0° (c = 0.9 in ethanol)
貯蔵温度 :
2-8°C
溶解性:
DMSO: ~34 mg/mL、可溶
外見 :
個体
色:
白い
Merck :
14,1031
InChIKey:
VPSRQEHTHIMDQM-FKLPMGAJSA-N
SMILES:
C12=CC=CC=C1CC[C@H](N[C@H](C(=O)OCC)CCC1C=CC=CC=1)C(=O)N2CC(=O)O.Cl |&1:8,10,r|
CAS データベース:
86541-74-4(CAS DataBase Reference)

安全性情報

Sフレーズ  22-24/25
RIDADR  3077
WGK Germany  2
RTECS 番号 CX7065000
HSコード  29337900

ベナゼプリル塩酸塩 価格 もっと(23)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01COBQA-2659
Benazepril HCl
86541-74-4 1g ¥10000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01COBQA-2659
Benazepril HCl
86541-74-4 5g ¥15000 2024-03-01 購入
東京化成工業 B3611 ベナゼプリル塩酸塩 >98.0%(HPLC)(T)
Benazepril Hydrochloride >98.0%(HPLC)(T)
86541-74-4 1g ¥10100 2024-03-01 購入
東京化成工業 B3611 ベナゼプリル塩酸塩 >98.0%(HPLC)(T)
Benazepril Hydrochloride >98.0%(HPLC)(T)
86541-74-4 5g ¥38900 2024-03-01 購入
Sigma-Aldrich Japan B0935 ベナゼプリル 塩酸塩 ≥98% (HPLC), solid
Benazepril hydrochloride ≥98% (HPLC), solid
86541-74-4 250mg ¥99300 2024-03-01 購入

ベナゼプリル塩酸塩 化学特性,用途語,生産方法

外観

白色~ほとんど白色, 結晶性粉末~粉末

溶解性

エタノールに溶け、水にやや溶けにくい。

用途

高血圧の研究。

用途

アンジオテンシン変換酵素 (ACE)阻害剤です。アンジオテンシン変換 酵素を阻害し、アンジオテンシンⅡ生成抑制 作用を示します。

用途

アンジオテンシン変換酵素 (ACE-1)阻害剤です。アンジオテンシン変 換酵素を阻害し、アンジオ

効能

血圧降下薬, アンジオテンシン変換酵素(ACE)阻害薬

商品名

チバセン (サンファーマ)

説明

Benazepril hydrochloride is a long-acting and effective angiotensin-converting enzyme (ACE) inhibitor used to treat essential hypertension. It is the hydrochloride salt form of benazepril, which is a prodrug of benazeprilat. After hepatic cleavage of the ester group, benazepril is converted to benazeprilat. In healthy humans, it was well tolerated and showed no phmacokinetic interactions with furosemide, hydrochlorothiazide, chlorthalidone, digoxin, cimetidine, atenolol, or naproxen.

化学的特性

This substance is a white to off-white crystalline powder. It is highly soluble in water, ethanol, and methanol with a solubility of over 100 mg/mL.

使用

Benazepril HCl is an angiotensin-converting enzyme (ACE) inhibitors that is commonly used as a sedative, hypnotic, and antihypertensive medication. Benazepril is used alone or together with other medicines to treat high blood pressure (hypertension). It works by reducing the levels of certain chemicals that cause blood vessels to constrict, allowing for smoother blood flow.

定義

ChEBI: Benazepril hydrochloride is a hydrochloride salt resulting from the reaction of benazepril with 1 mol eq. of hydrogen chloride. It is used as a prodrug for angiotensin-converting enzyme inhibitor benazeprilat in the treatment of hypertension and heart failure. It has a role as an EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor. It contains a benazepril(1+).

一般的な説明

Benazepril is a prodrug of the angiotensin converting enzyme (ACE) inhibitor benazeprilat . It is metabolized to benazeprilat by hepatic esterases. Benazepril inhibits the in vitro enzymatic activity of partially purified ACE isolated from rabbit lung (IC50 = 2 nM). It decreases the triglyceride and total cholesterol levels in normotensive rats when administered at a dose of 30 mg/kg and decreases aortic atherosclerosis in cholesterol-fed rabbits when administered at a dose of 3 mg/kg per day. Benazepril (0.1-10 mg/kg per day) reduces blood pressure in spontaneously hypertensive rats. It also decreases proteinuria in cats with chronic kidney disease when administered at doses ranging from 0.5 to 1 mg/kg per day. Formulations containing benazepril have been used to treat hypertension, congestive heart failure, and chronic kidney disease in both human and veterinary medicine.

生物活性

Non-peptide angiotensin-converting enzyme (ACE) inhibitor. Reduces blood pressure and myocardial hypertrophy in spontaneous hypertensive rats.

合成

Benazepril hydrochloride is prepared through the following steps:
Step 1: Preparation of (R)-ethyl 2-hydroxy-4-phenylbutyrate using ethyl 2-oxo-4-phenylbutyrate as a raw material and cinchonidine as a chiral ligand through asymmetric catalytic hydrogenation under high pressure.
Step 2: The intermediate obtained from step 1 reacts with p-nitrobenzenesulfonyl chloride or trifluoromethanesulfonic anhydride to obtain the corresponding sulfonate.
Step 3: The sulfonate obtained from step 2 undergoes nucleophilic substitution and salt hydrolysis with (3S)-3-amino-2,3,4,5-tetrahydro-2-oxo-1H-benzazepine-1-tert-butyl acetate to obtain benazepril hydrochloride.
This procedure has been described in detail in documents such as CN110835319A, US4785089, WO02076375, EP206993, and CN105061312.

Mode of action

The mechanism of action of benazepril is to inhibit the activity of the angiotensin-converting enzyme, blocking the conversion of angiotensin I to angiotensin II Label, thereby alleviating a series of symptoms caused by angiotensin (elevated blood pressure, increased excitatory heart rate caused by vasodilation, insufficient cardiac output, etc.).

参考文献

https://www.novartis.com/us-en/sites/novartis_us/files/lotrel.pdf
https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a216253b-27cb-42ef-b5a8-67fb05aafb88
Extrapyramidal side effect of donepezil hydrochloride in an elderly patient DOI: 10.1097/MD.0000000000019443
Use of convertible isocyanides for the synthesis of benazepril hydrochloride DOI: 10.1007/s12039-021-01892-8

ベナゼプリル塩酸塩 上流と下流の製品情報

原材料

準備製品


ベナゼプリル塩酸塩 生産企業

Global( 419)Suppliers
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ベナゼプリル塩酸塩  スペクトルデータ(1HNMR)


86541-74-4(ベナゼプリル塩酸塩)キーワード:


  • 86541-74-4
  • 1h-1-benzazepine-1-aceticacid,2,3,4,5-tetrahydro-3-((1-(ethoxycarbonyl)-3-phe
  • cgs14824a
  • monohydrochloride,(s-(r*,r*))-nylpropyl)amino)-2-oxo
  • BenazeprilHclC24H28N205.HC1
  • 1H-1-Benzazepine-1-acetic acid, 3-(1S)-1-(ethoxycarbonyl)-3-phenylpropylamino-2,3,4,5-tetrahydro-2-oxo-, monohydrochloride, (3S)-
  • 1H-1-Benzazepine-1-acetic acid, 3-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-, monohydrochloride, [S-(R*,R*)]-
  • CGS 14824A HCl
  • Lotension
  • Benazenprilhydrochloride
  • {(3S)-3-[(1S)-1-Ethoxycarbonyl-3-phenylpropylamino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-yl}acetic acid hydrochloride
  • Benazepril hydrochloride
  • Benazepril hydrochloride
  • (3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid hydrochloride
  • Benazepril Hydrochloride, SS-form
  • 1H-1-Benzazepine-1-acetic acid, 2,3,4,5-tetrahydro-3-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-2-oxo-, monohydrochloride, (S-(R*,R*))-
  • Cibace
  • Cibacen chf
  • Benazepril hydrochloride,(3S)-3-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetic acid hydrochloride
  • Benazepril Hydrochloride (125 mg)
  • 2-((S)-3-((S)-1-ethoxy-1-oxo-4-phenylbutan-2-ylamino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)aceticacidhydrochloride
  • Benazepri hydrochloride
  • Benazepril HCl API
  • 1H-1-Benzazepine-1-acetic acid, 3-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]aMino]-2,3,4,5-tetrahydro-2-oxo-, hydrochloride (1:1), (3S)-
  • 2-((S)-3-((S)-1-ethoxy-1-oxo-4-phenylbutan-2-ylamino)-2-oxo-2,3,4,5-tetrahydrobenzo[b]azepin-1-yl)acetic acid hydrochloride
  • Benazepril hydrochloride
  • Benazepril hydrochloride, 98.5%, an angiotensin-converting enzyme (ACE) inhibitor
  • Benazepril Benazepril HCL
  • yansuanbeinapuli
  • 2-[(3S)-3-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]-2-oxo-4,5-dihydro-3H-1-benzazepin-1-yl]acetic acid hydrochloride
  • Benazepril for system suitability CRS
  • 塩酸ベナゼプリル
  • ベナゼプリル塩酸塩
  • (3S)-3-[(1S)-1-エトキシカルボニル-3-フェニルプロピル]アミノ-2,3,4,5-テトラヒドロ-2-オキソ-1H-1-ベンゾアゼピン-1-酢酸塩酸塩
  • ベナゼプリル 塩酸塩
  • ベナゼプリル塩酸塩 (JAN)
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