U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H30N2O5.ClH
Molecular Weight 474.977
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of QUINAPRIL HYDROCHLORIDE

SMILES

Cl.CCOC(=O)[C@H](CCC1=CC=CC=C1)N[C@@H](C)C(=O)N2CC3=CC=CC=C3C[C@H]2C(O)=O

InChI

InChIKey=IBBLRJGOOANPTQ-JKVLGAQCSA-N
InChI=1S/C25H30N2O5.ClH/c1-3-32-25(31)21(14-13-18-9-5-4-6-10-18)26-17(2)23(28)27-16-20-12-8-7-11-19(20)15-22(27)24(29)30;/h4-12,17,21-22,26H,3,13-16H2,1-2H3,(H,29,30);1H/t17-,21-,22-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C25H30N2O5
Molecular Weight 438.5161
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including https://clinicaltrials.gov/ct2/show/NCT00651287 | https://www.ncbi.nlm.nih.gov/pubmed/25922179 | https://www.ncbi.nlm.nih.gov/pubmed/1691409

Quinapril is the hydrochloride salt of quinapril, the ethyl ester of a non-sulfhydryl, angiotensin-converting enzyme (ACE) inhibitor, quinaprilat. Quinapril hydrochloride is a white to off-white amorphous powder that is freely soluble in aqueous solvents. Quinapril is indicated for the treatment of high blood pressure (hypertension) and as adjunctive therapy in the management of heart failure. It may be used for the treatment of hypertension by itself or in combination with thiazide diuretics, and with diuretics and digoxin for heart failure.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
2.8 nM [IC50]
110.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ACCURETIC

Approved Use

INDICATIONS AND USA. Hypertension: ACCURETIC is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including the class to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with ACCURETIC. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. 6 Reference ID: 3818285 Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (for example, patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. This fixed combination is not indicated for the initial therapy of hypertension (see DOSAGE AND ADMINISTRATION). In using ACCURETIC, consideration should be given to the fact that another angiotensinconverting enzyme inhibitor, captopril, has caused agranulocytosis, particularly in patients with renal impairment or collagen-vascular disease. Available data are insufficient to show that quinapril does not have a similar risk (see WARNINGS: Neutropenia/Agranulocytosis). Angioedema in Black Patients: Black patients receiving ACE inhibitor monotherapy have been reported to have a higher incidence of angioedema compared to non-blacks. It should also be noted that in controlled clinical trials, ACE inhibitors have an effect on blood pressure that is less in black patients than in non-blacks.

Launch Date

1999
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
345 ng/mL
2.5 mg single, intravenous
dose: 2.5 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
1526 ng/mL
10 mg single, intravenous
dose: 10 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1706 μg × h/L
10 mg 2 times / day steady-state, oral
dose: 10 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
580 ng × h/mL
2.5 mg single, intravenous
dose: 2.5 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
2670 ng × h/mL
10 mg single, intravenous
dose: 10 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
3.7 h
10 mg 2 times / day steady-state, oral
dose: 10 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
2.26 h
2.5 mg single, intravenous
dose: 2.5 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
2.29 h
10 mg single, intravenous
dose: 10 mg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
QUINAPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Disc. AE: Headache, Dizziness...
AEs leading to
discontinuation/dose reduction:
Headache (0.7%)
Dizziness (0.8%)
Fatigue (0.3%)
Coughing (0.5%)
Nausea and vomiting (0.3%)
Abdominal pain (0.2%)
Sources:
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Disc. AE: Dizziness, Coughing...
AEs leading to
discontinuation/dose reduction:
Dizziness (0.7%)
Coughing (0.3%)
Fatigue (0.2%)
Nausea and vomiting (0.2%)
Hypotension (0.5%)
Dyspnea (0.2%)
Rash (0.2%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Abdominal pain 0.2%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Fatigue 0.3%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Nausea and vomiting 0.3%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Coughing 0.5%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Headache 0.7%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Dizziness 0.8%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Dyspnea 0.2%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Fatigue 0.2%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Nausea and vomiting 0.2%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Rash 0.2%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Coughing 0.3%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Hypotension 0.5%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Dizziness 0.7%
Disc. AE
40 mg 1 times / day multiple, oral
Recommended
Dose: 40 mg, 1 times / day
Route: oral
Route: multiple
Dose: 40 mg, 1 times / day
Sources:
unhealthy, adult
Health Status: unhealthy
Age Group: adult
Sex: M+F
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer




Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
yes [IC50 6.2 uM]
Drug as victim
PubMed

PubMed

TitleDatePubMed
In vitro study on binding interaction of quinapril with bovine serum albumin (BSA) using multi-spectroscopic and molecular docking methods.
2017-08
Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population.
2017-02
Attenuation of heart failure due to coronary stenosis by ACE inhibitor and angiotensin receptor blocker.
2003-07
Usefulness of quinapril and irbesartan to improve the anti-inflammatory response of atorvastatin and aspirin in patients with coronary heart disease.
2003-05-01
Square wave voltammetric determination of the angiotensin-converting enzyme inhibitors cilazapril, quinapril and ramipril in pharmaceutical formulations.
2003-05
Role of PKC in autocrine regulation of rat ventricular K+ currents by angiotensin and endothelin.
2003-04
Improvement of endothelial dysfunction by angiotensin II blockade accompanied by induction of vascular hepatocyte growth factor system in diabetic spontaneously hypertensive rats.
2003-03
Pharmacokinetics of quinapril in children: assessment during substitution for chronic angiotensin-converting enzyme inhibitor treatment.
2003-02
Effect of combination therapy with dipyridamole and quinapril in diabetic nephropathy.
2003-02
Comparative effects of angiotensin II receptor blockade (candesartan) with angiotensin-converting enzyme inhibitor (quinapril) in rats with dilated cardiomyopathy.
2003-01
Moexipril and quinapril inhibition of tissue angiotensin-converting enzyme activity in the rat: evidence for direct effects in heart, lung and kidney and stimulation of prostacyclin generation.
2003-01
Effects of angiotensin-converting enzyme inhibition and calcium channel blockade on cardiac apoptosis in rats with 2K1C (two-kidney/one-clip) renovascular hypertension.
2003-01
[Angiotensin-converting enzyme, quinapril, in treating chronic cardiac failure].
2003
Time-effect profile of antihypertensive agents assessed with trough/peak ratio, smoothness index and dose omission: an ambulatory blood pressure monitoring study with trandolapril vs. quinapril.
2002-12
The ACE inhibitor, quinapril, ameliorates peritoneal fibrosis in an encapsulating peritoneal sclerosis model in mice.
2002-12
Effects of antihypertensive drugs in experimental type 2 diabetes-related nephropathy.
2002-12
Angiotensin II regulates the synthesis of proinflammatory cytokines and chemokines in the kidney.
2002-12
Optimisation by experimental design of a capillary electrophoretic method for the separation of several inhibitors of angiotensin-converting enzyme using alkylsulphonates.
2002-11-29
Ischemia Management with Accupril post bypass Graft via Inhibition of angiotensin coNverting enzyme (IMAGINE): a multicentre randomized trial - design and rationale.
2002-11
Effect of losartan on nocturnal blood pressure in patients with stroke: comparison with angiotensin converting enzyme inhibitor.
2002-11
Captopril and quinapril reduce reactive oxygen species.
2002-10
Effects of a long-term pharmacological interruption of the renin-angiotensin system on the fibrinolytic system in essential hypertension.
2002-09-06
Prevention of vascular damage in scleroderma with angiotensin-converting enzyme (ACE) inhibition.
2002-09
Enalapril and quinapril improve endothelial vasodilator function and aortic eNOS gene expression in L-NAME-treated rats.
2002-08-16
Using ACE inhibitors appropriately.
2002-08-01
[Is mild essential hypertension without obvious organ complications and risk factors associated with increased levels of circulating markers of endothelial dysfunction? Effect of ACE inhibitor therapy].
2002-08
Influence of antihypertensive drugs on renal microcirculation and renal hemodynamics in cyclosporine A-treated rats.
2002-08
AT1 receptor blockade increases cardiac bradykinin via neutral endopeptidase after induction of myocardial infarction in rats.
2002-08
Circulating intercellular cell adhesion molecule-1, endothelin-1 and von Willebrand factor-markers of endothelial dysfunction in uncomplicated essential hypertension: the effect of treatment with ACE inhibitors.
2002-08
Bradykinin as a major endogenous regulator of endothelial function.
2002-06-12
The mechanism of the angiotensin-converting enzyme inhibitor quinapril is not related to bradykinin level in heart tissue.
2002-06
Subacute and chronic effects of quinapril on cardiac cytokine expression, remodeling, and function after myocardial infarction in the rat.
2002-06
Quinapril treatment restores the vasodilator action of insulin in fructose-hypertensive rats.
2002-05-16
Lowering of blood pressure improves endothelial dysfunction by increase of nitric oxide production in hypertensive rats.
2002-05
Pretreatment with angiotensin-converting enzyme inhibitors attenuates ischemia-reperfusion injury.
2002-05
Ventricular remodeling after myocardial infarction and effects of ACE inhibition on hemodynamics and scar formation in SHR.
2002-04-06
Rapid increase in cardiac adrenomedullin gene expression caused by acute pressure overload: effect of the renin-angiotensin system on gene expression.
2002-04
Quinapril prevents restenosis after coronary stenting in patients with angiotensin-converting enzyme D allele.
2002-04
Inhibition of left ventricular fibrosis by tranilast in rats with renovascular hypertension.
2002-04
Blockade of endothelial enzymes: new therapeutic targets.
2002-03
Influence of angiotensinogen M253T gene polymorphism and an angiotensin converting enzyme inhibitor on restenosis after percutaneous coronary intervention.
2002-02
Simultaneous determination of quinapril and its active metabolite quinaprilat in human plasma using high-performance liquid chromatography with ultraviolet detection.
2002-01-25
Angiotensin II as an inflammatory mediator: evolving concepts in the role of the renin angiotensin system in the failing heart.
2002-01
Effects of quinapril on myocardial function, ventricular remodeling and cardiac cytokine expression in congestive heart failure in the rat.
2002-01
Effects of a citrate buffer system on the solid-state chemical stability of lyophilized quinapril preparations.
2002-01
[Some new data concerning effectiveness of amlodipine, atorvastatine and quinaprile for heart diseases].
2002
[Clinical sequelae of tissue angiotensin converting enzyme inhibition: practicability of use in ischemic heart disease].
2002
Clinical pharmacokinetics and selective pharmacodynamics of new angiotensin converting enzyme inhibitors: an update.
2002
Angiotensin II induced inflammation in the kidney and in the heart of double transgenic rats.
2002
The influence of angiotensin-converting enzyme inhibitors on the aorta elastin metabolism in diet-induced hypercholesterolaemia in rabbits.
2001-03
Patents

Sample Use Guides

The recommended initial dosage of ACCUPRIL in patients not on diuretics is 10 or 20 mg once daily. Dosage should be adjusted according to blood pressure response measured at peak (2–6 hours after dosing) and trough (predosing). Generally, dosage adjustments should be made at intervals of at least 2 weeks. Most patients have required dosages of 20, 40, or 80 mg/day, given as a single dose or in two equally divided doses.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:53:10 GMT 2025
Edited
by admin
on Mon Mar 31 17:53:10 GMT 2025
Record UNII
33067B3N2M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACCURETIC COMPONENT QUINAPRIL HYDROCHLORIDE
Preferred Name English
QUINAPRIL HYDROCHLORIDE
HSDB   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
QUINAPRIL HYDROCHLORIDE [ORANGE BOOK]
Common Name English
QUINAPRIL HYDROCHLORIDE [MI]
Common Name English
Quinapril hydrochloride [WHO-DD]
Common Name English
QUINAPRIL HCL
Common Name English
QUINARETIC COMPONENT QUINAPRIL HYDROCHLORIDE
Common Name English
ACCUPRIL
Common Name English
2-(2-((1-ETHOXYCARBONYL-3-PHENYLPROPYL)AMINO)-1-OXOPROPYL)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID MONOHYDROCHLORIDE(3S-(2(R*(R*)),3R*)
Common Name English
QUINAPRIL HYDROCHLORIDE [USP IMPURITY]
Common Name English
QUINAPRIL HYDROCHLORIDE [HSDB]
Common Name English
CI 906
Code English
QUINAPRIL HYDROCHLORIDE [USP-RS]
Common Name English
QUINAPRIL HYDROCHLORIDE [VANDF]
Common Name English
NSC-758222
Code English
QUINAPRIL HYDROCHLORIDE [USP MONOGRAPH]
Common Name English
(S)-2-[(S)-N-[(S)-1-Carboxy-3-phenylpropyl]alanyl]-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, 1-ethyl ester, monohydrochloride
Common Name English
QUINAPRIL HYDROCHLORIDE [USAN]
Common Name English
QUINAPRIL HYDROCHLORIDE [EP MONOGRAPH]
Common Name English
QUINAPRIL HYDROCHLORIDE [MART.]
Common Name English
QUINAPRIL HYDROCHLORIDE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C247
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
Code System Code Type Description
RS_ITEM_NUM
1593401
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
EVMPD
SUB04164MIG
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
CHEBI
8714
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
RXCUI
235759
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY RxNorm
ChEMBL
CHEMBL1592
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
PUBCHEM
54891
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
HSDB
7046
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
MERCK INDEX
m9437
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY Merck Index
USAN
W-125
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
CAS
82586-55-8
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
NCI_THESAURUS
C29398
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
EPA CompTox
DTXSID3021221
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
DRUG BANK
DBSALT000465
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
FDA UNII
33067B3N2M
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
SMS_ID
100000090468
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
DAILYMED
33067B3N2M
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
NSC
758222
Created by admin on Mon Mar 31 17:53:10 GMT 2025 , Edited by admin on Mon Mar 31 17:53:10 GMT 2025
PRIMARY
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IMPURITY -> PARENT
For the calculation of contents, multiply the peak areas by 1.5
CHROMATOGRAPHIC PURITY (HPLC/UV)
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