Perindopril erbumine
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Perindopril erbumine
structure -
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CAS No:
107133-36-8
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Formula:
C19H32N2O5.C4H11N
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Chemical Name:
Perindopril erbumine
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Synonyms:
1H-Indole-2-carboxylic acid,1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-,(2S,3aS,7aS)-,compd. with 2-methyl-2-propanamine (1:1);1H-Indole-2-carboxylic acid,1-[2-[[1-(ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-,[2S-[1[R*(R*)],2α,3aβ,7aβ]]-,compd. with 2-methyl-2-propanamine (1:1);2-Propanamine,2-methyl-,[2S-[1[R*(R*)],2α,3aβ,7aβ]]-1-[2-[[1-(ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylate;2-Propanamine,2-methyl-,(2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylate;S 9490-3;McN-A 2833-109;Perindopril erbumine;Perindopril-tert-butylamine;Butylaminiperindopril;Prestarium;Coversyl;Coversum;Aceon;Perinodpril erbimune;Procaptan;Perindopril tert-butylamine salt;Perinodopril;Perigard;Conversyl;Perindopril tert-butylamine
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Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
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CAS No:
Description
White Solid
Perindopril erbumine is an addition compound. It has a role as an antihypertensive agent and an EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor. It contains a perindopril(1-).|Perindopril Erbumine is the tert-butylamine salt of perindopril, the ethyl ester of a non-sulfhydryl angiotensin converting enzyme (ACE) inhibitor with antihypertensive activity. Upon hydrolysis, perindopril erbumine is converted to its active form perindoprilat, inhibiting ACE and the conversion of angiotensin I to angiotensin II; consequently, angiotensin II-mediated vasoconstriction and angiotensin II-stimulated aldosterone secretion from the adrenal cortex are inhibited and diuresis and natriuresis ensue.|An angiotensin-converting enzyme inhibitor. It is used in patients with hypertension and heart failure.
Perindopril erbumine Basic Attributes
441.609
441.320282
1312995-182-4
1964X464OJ
758929
DTXSID1044198
C47666
2933999552
Characteristics
122
2.6
Solid
1.15 g/cm3
126-128°C
537.4°C at 760 mmHg
278.8ºC
H2O: soluble10mg/mL, clear
-20°C Freezer
188.8 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Safety Information
NONH for all modes of transport
3
36/37/38
26-36
NL5999600
Xi
P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P340, P308+P313, P312, P321, P332+P313, P362, P403+P233, P405, P501
H315
|Danger|H302 (66.67%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P264, P270, P280, P281, P301+P312, P305+P351+P338, P308+P313, P330, P337+P313, P405, and P501|Aggregated GHS information provided by 16 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Prevention of cardiovascular events, Treatment of hypertension, Treatment of lipid metabolism disorders|Treatment of hypertension|Treatment of hypertension, Treatment of stable coronary artery disease|Prevention of heart failure, Prevention of stroke, Treatment of acute myocardial infarction, Treatment of atherosclerotic heart disease, Treatment of heart failure, Treatment of Prinzmetal's angina|Prevention of cardiovascular events
A class of drugs whose main indications are the treatment of hypertension and heart failure. They exert their hemodynamic effect mainly by inhibiting the renin-angiotensin system. They also modulate sympathetic nervous system activity and increase prostaglandin synthesis. They cause mainly vasodilation and mild natriuresis without affecting heart rate and contractility. (See all compounds classified as Angiotensin-Converting Enzyme Inhibitors.)|Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)
Erbumine, Perindopril
Perindopril erbumine Use and Manufacturing
antibacterial
Human Drugs -> EU pediatric investigation plans|Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:441.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:9
Exact Mass:441.32027148
Monoisotopic Mass:441.32027148
Topological Polar Surface Area:122
Heavy Atom Count:31
Complexity:549
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
1. Perindopril is an angiotensin-converting enzyme inhibitor (ACEI) that reduces aldosterone secretion, increases renin activity, and reduces total peripheral arterial resistance in the long term; 2. It inhibits the degradation of bradykinin into inactive peptides; 3. It can lower blood pressure in patients with low or normal renin levels; 4. Its active ingredient, perindoprilat, exerts an antihypertensive effect without producing drug resistance, and there is no blood pressure rebound after drug withdrawal; 5. It has a vasodilatory effect, restores the elasticity of the large arteries and reduces left ventricular hypertrophy; 6. It can be used in combination with thiazide diuretics to synergistically lower blood pressure; 7. It can moderately lower blood pressure, reduce cardiac load, and increase cardiac output and exercise endurance in the treatment of heart failure.
Registered Holders
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APOTEX PHARMACHEM INDIA PVT LTD
Active
United States
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ALIVUS LIFE SCIENCES LTD
Active
United States
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APITORIA PHARMA PRIVATE LTD
Active
United States
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