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MOEXIPRIL HYDROCHLORIDE

CAS No.
82586-52-5
Chemical Name:
MOEXIPRIL HYDROCHLORIDE
Synonyms
CI-925;Perdix;SPM-925;Univasc;Fempress;RS-10085;RS-10085-197;MOEXIPRIL HYDROCHLORIDE;Moexipril HCl (RS-10085);Moexipril hydrochloride, >=99%
CBNumber:
CB6500845
Molecular Formula:
C27H35ClN2O7
Molecular Weight:
535.03
MDL Number:
MFCD00940481
MOL File:
82586-52-5.mol
MSDS File:
SDS
Last updated:2024-04-25 13:42:50

MOEXIPRIL HYDROCHLORIDE Properties

Melting point 141-1610C
alpha D23 +34.2° (c = 1.1 in ethanol)
storage temp. 2-8°C
solubility H2O: soluble32mg/mL
form powder
FDA UNII Q1UMG3UH45

Pharmacokinetic data

Protein binding 50%
Excreted unchanged in urine 1%
Volume of distribution 183 Litres
Biological half-life 12 (of active metabolite) / Increased

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS09
Signal word  Warning
Hazard statements  H400
Precautionary statements  P273-P391-P501
Hazard Codes  N
Risk Statements  50
Safety Statements  60
RIDADR  UN 3077 9/PG 3
WGK Germany  3
RTECS  NW7174500
HS Code  2933492250
NFPA 704
0
3 0

MOEXIPRIL HYDROCHLORIDE price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M0821 Moexipril hydrochloride powder, ≥98% (HPLC) 82586-52-5 50mg $224 2024-03-01 Buy
Sigma-Aldrich 1445426 Moexipril hydrochloride United States Pharmacopeia (USP) Reference Standard 82586-52-5 100mg $436 2024-03-01 Buy
Cayman Chemical 21255 Moexipril (hydrochloride) ≥98% 82586-52-5 10mg $44 2024-03-01 Buy
Cayman Chemical 21255 Moexipril (hydrochloride) ≥98% 82586-52-5 25mg $87 2024-03-01 Buy
Sigma-Aldrich M0821 Moexipril hydrochloride powder, ≥98% (HPLC) 82586-52-5 100mg $424 2024-03-01 Buy
Product number Packaging Price Buy
M0821 50mg $224 Buy
1445426 100mg $436 Buy
21255 10mg $44 Buy
21255 25mg $87 Buy
M0821 100mg $424 Buy

MOEXIPRIL HYDROCHLORIDE Chemical Properties,Uses,Production

Description

Moexipril hydrochloride is a novel ACE inhibitor first marketed in the U.S.A. for the treatment of hypertension as a monotherapy and as a second-line therapy in combination with diuretics or calcium antagonists. Like other ACE inhibitors, moexipril is a prodrug that is converted in the liver to its diacid moexiprilat which is the active agent. Moexipril displays a higher in vitro inhibitory potency to ACE than enalapril although its effectiveness in reduction of blood pressure in hypertensive patients is similar to that seen with enalapril. It is orally active with a rapid onset and prolonged duration of action. Excellent tolerability has been reported. Moexipril is distinguished by its lower cost than other marketed ACE inhibitors.

Chemical Properties

Crystalline Solid

Originator

Warner-Lambert (U.S.A.)

Uses

Moexipril HCl is a potent orally active non-sulfhydryl angiotensin converting enzyme inhibitor (ACE) with IC50 of 0.041 μM, which is used for the treatment of hypertension and congestive heart failure

Uses

Angiotensin converting enzyme (ACE) inhibitor; dimethoxy analog of quinapril

Definition

ChEBI: Moexipril hydrochloride is a dipeptide.

Manufacturing Process

1) A solution of 2.0 g of t-butyl alanine (S-form) and 3.78 g of ethyl 2-bromo- 4-phenylbutanoate in 25 ml of DMF was treated with 1.8 ml of triethylamine and the solution was heated at 70°C for 18 hours. The solvent was removed at reduced pressure and the residue was mixed with water and extracted with ethyl ether. The organic layer was washed with water and dried over magnesium sulfate. Concentration of the solvent at reduced pressure gave the oily ethyl-α-[(1-carboxyethyl)amino]benzene-t-butanoate.
A solution of 143.7 g of this t-butyl ester in 630 ml of trifluoroacetic acid was stirred at room temperature for one hour. The solvent was removed at reduced pressure and the residue was dissolved in ethyl ether and again evaporated. This operation was repeated. Then the ether solution was treated dropwise with a solution of hydrogen chloride gas in ethyl ether until precipitation ceased. The solid, collected by filtration, was a mixture of diastereoisomers of ethyl-α-[(1-carboxyethyl)amino]benzenebutanoate hydrochloride, melting point 153-165°C; [α]D23 = +3.6° (1% MeOH).
The free amino acid (S,S-form) was prepared by treatment of an aqueous solution of the hydrochloride with saturated sodium acetate. The product was filtered, washed efficiently with cold water and recrystallized from ethyl acetate; melting point 149-151°C; [α]D23 = +29.7°.
2) A stirred solution of 0.0158 mole of ethyl-α-[(1-carboxyethyl)amino] benzenebutanoate hydrochloride in 200 ml of methylene chloride was treated successively with 1.60 g (0.0158 mole) of triethylamine, 0.0158 mole of 1- hydroxybenzotriazole, 0.0158 mole of 1,2,3,4-tetrahydro-6,7-dimethoxy-3- isoquinolinecarboxylic acid and then with 0.0158 mole of dicyclohexylcarbodiimide in 10 ml of methylene dichloride. Dicyclohexylurea gradually separated. The mixture was allowed to stand at room temperature overnight. Hexane (300 ml) was added and the urea was filtered. The filtrate was washed with 250 ml of saturated sodium bicarbonate, dried over sodium sulfate and concentrated to remove solvent. The viscous residue was triturated with 50 ml of ether and filtered to remove insolubles. The filtrate was concentrated to give 2-[2-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1- oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid.
After addition of hydrochloric acid was obtained 2-[2-[[1-(ethoxycarbonyl)-3- phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3- isoquinolinecarboxylic acid, hydrochloride.

brand name

Univasc (Schwarz Pharma).

Therapeutic Function

Antihypertensive

Hazard

Moderately toxic by ingestion.

Biological Activity

Angiotensin-converting enzyme (ACE) inhibitor that is hydrolyzed in the liver to the active metabolite moexiprilat (IC 50 values are 2.1 and 2700 nM for moexiprilat and moexipril respectively). Antihypertensive; decreases mean blood pressure in the spontaneous hypertensive rat (SHR). Also blocks degradation of bradykinin into inactive metabolites.

Clinical Use

Angiotensin-converting enzyme inhibitor:
Hypertension

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: antagonism of hypotensive effect and increased risk of renal impairment with NSAIDs; hyperkalaemia with ketorolac and other NSAIDs.
Antihypertensives: increased risk of hyperkalaemia, hypotension and renal failure with ARB’S and aliskiren.
Bee venom extract: possible severe anaphylactoid
reactions when used together. Ciclosporin: increased risk of hyperkalaemia and nephrotoxicity.
Cytotoxics: increased risk of angioedema with everolimus.
Diuretics: enhanced hypotensive effect; hyperkalaemia with potassium-sparing diuretics.
ESAs: increased risk of hyperkalaemia; antagonism of hypotensive effect.
Gold: flushing and hypotension with sodium aurothiomalate.
Lithium: reduced excretion (possibility of enhanced lithium toxicity).
Potassium salts: increased risk of hyperkalaemia.
Tacrolimus: increased risk of hyperkalaemia and nephrotoxicity.

Metabolism

Moexipril is a prodrug that is converted to an active metabolite, moexiprilat in the gastrointestinal mucosa and liver. Moexipril is excreted mainly in the urine as moexiprilat, unchanged drug, and other metabolites; some moexiprilat may also be excreted in the faeces.

MOEXIPRIL HYDROCHLORIDE Preparation Products And Raw materials

Global( 145)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Henan Tengmao Chemical Technology Co. LTD
+8615238638457 salesvip2@hntmhg.com China 415 58
Ouhuang Engineering Materials (Hubei) Co., Ltd
+8617702722807 admin@hbouhuang.com China 2259 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282 alice@crovellbio.com China 8823 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569266 15319487004 1015@dideu.com China 2263 58

View Lastest Price from MOEXIPRIL HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
MOEXIPRIL HYDROCHLORIDE pictures 2024-04-25 MOEXIPRIL HYDROCHLORIDE
82586-52-5
US $50.00 / kg 1kg 99.10% 50000kg Ouhuang Engineering Materials (Hubei) Co., Ltd
Moexipril HCl pictures 2023-12-09 Moexipril HCl
82586-52-5
US $110.00-90.00 / kilogram 1kilogram 99% 10 tons/per week Henan Tengmao Chemical Technology Co. LTD
MOEXIPRIL HYDROCHLORIDE pictures 2023-08-05 MOEXIPRIL HYDROCHLORIDE
82586-52-5
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
  • Moexipril HCl pictures
  • Moexipril HCl
    82586-52-5
  • US $110.00-90.00 / kilogram
  • 99%
  • Henan Tengmao Chemical Technology Co. LTD

MOEXIPRIL HYDROCHLORIDE Spectrum

(3S)-2-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-3-carboxylic acid hydrochloride 2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylicacidhydrochloride 3-Isoquinolinecarboxylicacid,2-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]aMino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-diMethoxy-,hydrochloride (1:1), (3S)- (3S)- 2-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid,hydrochloride (1:1) RS-10085 Moexipril Hydrochloride (100 mg) Moexipril hydrochloride, >=99% (3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenyl-d5-propyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic Acid Hydrochloride CI-925 Fempress Perdix RS-10085-197 SPM-925 Univasc (3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic Acid Hydrochloride (3S)-2-[(2S)-2-[[(1S)-1-carbethoxy-3-phenyl-propyl]amino]propanoyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-3-carboxylic acid hydrochloride (3S)-2-[(2S)-2-[[(2S)-1-ethoxy-1-oxo-4-phenyl-butan-2-yl]amino]propanoyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-3-carboxylic acid hydrochloride MOEXIPRIL HYDROCHLORIDE UNIVASC;RS10085;RS 10085;RS-10085 (3S)-2-[(2S)-2-[[(1S)-1-Ethoxycarbonyl-3-Phenyl-Propyl]Amino]Propanoyl]-6,7-Dimethoxy-3,4-Dihydro-1H-Isoquinoline-3-Carboxylic Acid Hydrochloride 2-[2-[[1-(ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid, hydrochloride MOEXIPRIL HYDROCHLORIDE USP/EP/BP (S)-2-((S)-2-(((S)-1-Ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride Moexipril HCl (RS-10085) (3S)-2-[(2S)-2-{[(2S)-1-ethoxy-1-oxo-4-phenylbutan -2-yl]amino}propanoyl]-6,7-dimethoxy-1,2,3,4-tetr ahydroisoquinoline-3-carboxylic acid hydrochloride Moexipril HydrochlorideQ: What is Moexipril Hydrochloride Q: What is the CAS Number of Moexipril Hydrochloride Q: What is the storage condition of Moexipril Hydrochloride Q: What are the applications of Moexipril Hydrochloride Moexipril Hydrochloride (1445426) orally active,Apoptosis,Ischemic brain injury,inhibit,hepatic disease,RS10085,Angiotensin-converting Enzyme (ACE),hydrochlorothiazide,essential hypertension,Moexipril hydrochloride,antihypertensive,moexiprilat,angiotensin II,cardiovascular disease,RS 10085,Inhibitor,hypertension,Moexipril 82586-52-5 C27H34N2O7HCl C27H35N2O7Cl C27H35ClN2O7 C27H34N2O7ClH Aromatics Inhibitors API Intermediates & Fine Chemicals Pharmaceuticals Chiral Reagents Coronavirus