SPIRAPRIL HYDROCHLORIDE MONOHYDRATE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C22H30N2O5S2.ClH.H2O
Molecular Weight	521.09
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of SPIRAPRIL HYDROCHLORIDE MONOHYDRATE

Structure Search

SMILES

O.Cl.CCOC(=O)[C@H](CCC1=CC=CC=C1)N[C@@H](C)C(=O)N2CC3(C[C@H]2C(O)=O)SCCS3

InChI

InChIKey=YNPQFYHGQPDXFR-GWRZQJEISA-N

InChI=1S/C22H30N2O5S2.ClH.H2O/c1-3-29-21(28)17(10-9-16-7-5-4-6-8-16)23-15(2)19(25)24-14-22(30-11-12-31-22)13-18(24)20(26)27;;/h4-8,15,17-18,23H,3,9-14H2,1-2H3,(H,26,27);1H;1H2/t15-,17-,18-;;/m0../s1

HIDE SMILES / InChI

Description
Sources: https://www.drugs.com/international/spirapril.html
Curator's Comment: description was created based on several sources, including https://www.drugbank.ca/drugs/DB01348 | https://www.ncbi.nlm.nih.gov/pubmed/18154140 | https://www.ncbi.nlm.nih.gov/pubmed/15490771 | https://www.ncbi.nlm.nih.gov/pubmed/15752941

Spirapril (Renormax) is an ACE inhibitor antihypertensive drug used to treat hypertension. Spiraprilat, the active metabolite of spirapril, competes with angiotensin I for binding at the angiotensin-converting enzyme, blocking the conversion of angiotensin I to angiotensin II. Inhibition of ACE results in decreased plasma angiotensin II. As angiotensin II is a vasoconstrictor and a negative-feedback mediator for renin activity, lower concentrations result in a decrease in blood pressure and stimulation of baroreceptor reflex mechanisms, which leads to decreased vasopressor activity and to decreased aldosterone secretion. Spiraprilat may also act on kininase II, an enzyme identical to ACE that degrades the vasodilator bradykinin.

CNS Activity

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Angiotensin-converting enzyme 97 Target ID: CHEMBL1808 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2544729	Inhibitor 8297		67.0 nM [IC50]

Conditions

Condition	Modality	Targets	Highest Phase	Product
Hypertension 567 Sources: https://www.drugs.com/international/spirapril.html	Primary		Approved 8429	RENORMAX Approved Use Unknown Launch Date 1994
Metabolic syndrome 32 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18154140	Primary		Not Provided 504	RENORMAX Approved Use Unknown Launch Date 1994

C_max

Value	Dose	Co-administered	Analyte	Population
81.6 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/7601014/	6 mg 1 times / day multiple, oral dose: 6 mg route of administration: Oral experiment type: MULTIPLE co-administered:		SPIRAPRILAT plasma	Homo sapiens population: UNHEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN
37.85 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/7601014/	6 mg 1 times / day multiple, oral dose: 6 mg route of administration: Oral experiment type: MULTIPLE co-administered:		SPIRAPRILAT plasma	Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN

AUC

Value	Dose	Co-administered	Analyte	Population
846.75 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/7601014/	6 mg 1 times / day multiple, oral dose: 6 mg route of administration: Oral experiment type: MULTIPLE co-administered:		SPIRAPRILAT plasma	Homo sapiens population: UNHEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN
152.5 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/7601014/	6 mg 1 times / day multiple, oral dose: 6 mg route of administration: Oral experiment type: MULTIPLE co-administered:		SPIRAPRILAT plasma	Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN

T_1/2

Value	Dose	Co-administered	Analyte	Population
1.85 h REVIEW https://pubmed.ncbi.nlm.nih.gov/7601014/	6 mg 1 times / day multiple, oral dose: 6 mg route of administration: Oral experiment type: MULTIPLE co-administered:		SPIRAPRILAT plasma	Homo sapiens population: HEALTHY age: UNKNOWN sex: UNKNOWN food status: UNKNOWN

Doses

Dose	Population	Adverse events
24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	Other AEs: Cough, Dizziness... Other AEs: Cough (3.8%) Dizziness (5.3%) Fatigue (6%) Headache (9%) Oedema (3%) Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/

AEs

AE	Significance	Dose	Population
Oedema	3%	24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/
Cough	3.8%	24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/
Dizziness	5.3%	24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/
Fatigue	6%	24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/
Headache	9%	24 mg 1 times / day steady, oral (max) Recommended Dose: 24 mg, 1 times / day Route: oral Route: steady Dose: 24 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/	unhealthy, adult n = 133 Health Status: unhealthy Condition: hypertension Age Group: adult Sex: M+F Population Size: 133 Sources: https://pubmed.ncbi.nlm.nih.gov/7601014/

Sourcing

Vendor/Aggregator	ID	URL
ChEBI	CHEBI:141522	https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:141522
ZINC	ZINC000004217460	http://zinc15.docking.org/substances/ZINC000004217460

PubMed

Title	Date	PubMed
Mechanism and pressor relevance of the short-term cardiovascular and renin excitatory actions of the selective A2A-adenosine receptor agonists.	1997 Sep	9300315
[Effect of angiotensin converting enzyme inhibitor spirapril on dimensions of experimental myocardial infarction, development of ischemic tachyarrhythmias, and ischemic adaptation of the heart].	2002	12494232
[Influence of ACE inhibitor spirapril on left ventricular hypertrophy].	2002 Dec 5	12613273
[Blood pressure control must be effective until the next tablet. Infarct is most frequent in the morning].	2002 Jan 24	11862799
[Open trial using ACE inhibitor. Left ventricular hypertrophy diminishes].	2002 Nov 28	12532545
Antiproteinuric versus antihypertensive effects of high-dose ACE inhibitor therapy.	2002 Sep	12200795
Drug interaction of spirapril hydrochloride monohydrate and hydrochlorothiazide. A clinical study to compare the pharmacokinetics after administration of spirapril hydrochloride monohydrate tablets, hydrochlorothiazide tablets and fixed combination bi-layer tablets.	2003	12872612
Simultaneous determination of spirapril and spiraprilat in plasma by capillary gas chromatography-mass spectrometry.	2003	12854357
[Blood pressure lowering by the ACE-inhibitor spirapril. "24-hour efficacy of real once daily application of spirapril (HERAS study)"].	2003 Oct 9	15490771
[Effect of spirapril on remodeling of the heart in patients with mild and moderate arterial hypertension].	2007	18260839
[A comparative analysis of normodipin and spirapril effects on intravascular activity of platelets in patients with metabolic syndrome].	2007	18154140
The Lipid lowering and Onset of Renal Disease (LORD) Trial: a randomized double blind placebo controlled trial assessing the effect of atorvastatin on the progression of kidney disease.	2008 Mar 18	18366658

Patents

Sample Use Guides

In Vivo Use Guide

The daily dose is 6 mg, the frequency of application is 1 time / day. After 4-6 weeks, in the absence of a satisfactory therapeutic effect, the dose can be increased.

Route of Administration: Oral

In Vitro Use Guide

Pooled human liver microsomes were obtained from Pfizer Global Supply and the tested compounds were acquired from Pfizer Global Material Management. Each incubation contained tested compounds (Spirapril) (1 mkM), microsomes (0.25 lM protein), NADPH regenerating system (1 mM NADP+, 5 mM isocitric acid and 1 unit/ mL isocitric dehydrogenase), MgCl2 (1 mM) and potassium phosphate buffer (100 mM at pH 7.4). This mixture was incubated at 37 _C for 0, 5, 10, 20, 30 and 60 min before quenching with acetonitrile. Control incubations were prepared using the same procedure without adding the catalytic cofactor NADPH. Individual samples were then analyzed in a ‘trap-and-elute’ mode using LC/MS

Name

Type

Language

SPIRAPRIL HYDROCHLORIDE MONOHYDRATE

Common Name

English

(8S)-7-((2S)-2-(((1S)-1-(ETHOXYCARBONYL)-3-PHENYLPROPYL)AMINO)PROPANOYL)-1,4-DITHIA-7-AZASPIRO(4.4)NONANE-8-CARBOXYLIC ACID HYDROCHLORIDE MONOHYDRATE

Systematic Name

English

1,4-DITHIA-7-AZASPIRO(4.4)NONANE-8-CARBOXYLIC ACID, 7-((2S)-2-(((1S)-1-(ETHOXYCARBONYL)-3-PHENYLPROPYL)AMINO)-1-OXOPROPYL)-, HYDROCHLORIDE, HYDRATE (1:1:1), (8S)-

Common Name

English

SPIRAPRIL HYDROCHLORIDE MONOHYDRATE [EP MONOGRAPH]

Common Name

English

Code System Code Type Description

CAS

200872-06-6