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Details

Stereochemistry ABSOLUTE
Molecular Formula C9H15NO3S.C7H8ClN3O4S2
Molecular Weight 515.024
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPOZIDE

SMILES

C[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O.NS(=O)(=O)C2=C(Cl)C=C3NCNS(=O)(=O)C3=C2

InChI

InChIKey=SFIUYASDNWEYDB-HHQFNNIRSA-N
InChI=1S/C9H15NO3S.C7H8ClN3O4S2/c1-6(5-14)8(11)10-4-2-3-7(10)9(12)13;8-4-1-5-7(2-6(4)16(9,12)13)17(14,15)11-3-10-5/h6-7,14H,2-5H2,1H3,(H,12,13);1-2,10-11H,3H2,(H2,9,12,13)/t6-,7+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C9H15NO3S
Molecular Weight 217.285
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C7H8ClN3O4S2
Molecular Weight 297.739
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created based on several sources, including: https://www.drugs.com/cdi/capozide.html http://www.rxlist.com/capozide-drug.htm

CAPOZIDE (captopril and hydrochlorothiazide tablets, USP) for oral administration combines two antihypertensive agents: captopril and hydrochlorothiazide. The mechanism of action of captopril has not yet been fully elucidated. Captopril prevents the conversion of angiotensin I to angiotensin II by inhibition of ACE, a peptidyldipeptide carboxy hydrolase. Hydrochlorothiazide belongs to thiazide class of diuretics. It reduces blood volume by acting on the kidneys to reduce sodium (Na+) reabsorption in the distal convoluted tubule. CAPOZIDE (captopril and hydrochlorothiazide tablets, USP) is indicated for the treatment of hypertension. The blood pressure lowering effects of captopril and thiazides are approximately additive. Major side effects are: Black, tarry stools; chest pain; chills; cough; fever; painful or difficult urination; shortness of breath; sore throat; sores, ulcers, or white spots on lips or in mouth; swollen glands; unusual bleeding or bruising; unusual tiredness or weakness. It has been reported that indomethacin may reduce the antihypertensive effect of captopril, especially in cases of low renin hypertension. Captopril’s effect will be augmented by antihypertensive agents that cause renin release. For example, diuretics (e.g., thiazides) may activate the renin-angiotensin-aldosterone system.

CNS Activity

Originator

Curator's Comment: Captopril: E. R. Squibb & Sons, Inc. https://www.google.com/patents/US4046889 https://www.google.com/patents/US4105776 Hydrochlorothiazide: G. de StevensL. H. WernerA. HalamandarisS. RiccaJr. https://www.ncbi.nlm.nih.gov/pubmed/13619659

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
CAPOZIDE

Approved Use

CAPOZIDE® (captopril and hydrochlorothiazide tablets, USP) is indicated for the treatment of hypertension. The blood pressure lowering effects of captopril and thiazides are approximately additive.

Launch Date

4.66300797E11
PubMed

PubMed

TitleDatePubMed
Captopril and hydrochlorothiazide combined: Acezide/Capozide.
1989 Jul 24
Captopril versus captopril plus hydrochlorothiazide for essential hypertension in Koreans.
1991 Jan 1
Captopril and hydrochlorothiazide (Capozide) combine to enhance the reduction in voluntary alcohol intake in rats.
1993 Oct
[Capozide-50 alone and in combination with melatonin in therapy of hypertension].
2000
Patents

Sample Use Guides

therapy may be instituted with a single tablet of CAPOZIDE (captopril/hydrochlorothiazide) 25 mg/15 mg taken once daily. For patients insufficiently responsive to the initial dose, additional captopril or hydrochlorothiazide may be added as individual components or by using CAPOZIDE (captopril/hydrochlorothiazide) 50 mg/15 mg, 25 mg/25 mg or 50 mg/25 mg, or divided doses may be used. Daily doses of captopril should not exceed 150 mg and of hydrochlorothiazide should not exceed 50 mg.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: The present study shows that 1-100 microM hydrochlorothiazide (HCTZ) dose dependently inhibits bone resorption by isolated rat osteoclasts in the bone slice assay with an IC50 of approximately 20 microM. https://www.ncbi.nlm.nih.gov/pubmed/7820777
In the presence of captopril (2 X 10^4 M), contractile responses to angiotensln I (5 X 10^10 to 5 X 10^8 M) were attenuated significantly.
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:56:35 UTC 2023
Edited
by admin
on Sat Dec 16 01:56:35 UTC 2023
Record UNII
YQ0UGU4SE2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAPOZIDE
Common Name English
CAPTOPRIL MIXTURE WITH HYDROCHLOROTHIAZIDE
Common Name English
DOSTUREL
Brand Name English
CAPTOPRESS
Brand Name English
L-PROLINE, 1-((2S)-3-MERCAPTO-2-METHYL-1-OXOPROPYL)-, MIXT. WITH 6-CHLORO-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE 1,1-DIOXIDE
Systematic Name English
CAPTOPRIL AND HYDROCHLOROTHIAZIDE
Common Name English
1-((2S)-2-METHYL-3-SULFANYLPROPANOYL)-L-PROLINE - 6-CHLORO-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE 1,1-DIOXIDE (1:1)
Systematic Name English
CAPTOPRIL TZ
Brand Name English
L-PROLINE, 1-(3-MERCAPTO-2-METHYL-1-OXOPROPYL)-, (S)-, MIXT. WITH 6-CHLORO-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE 1,1-DIOXIDE
Systematic Name English
CAPTOPRIL-HYDROCHLOROTHIAZIDE MIXT.
Common Name English
Code System Code Type Description
FDA UNII
YQ0UGU4SE2
Created by admin on Sat Dec 16 01:56:35 UTC 2023 , Edited by admin on Sat Dec 16 01:56:35 UTC 2023
PRIMARY
CAS
110075-07-5
Created by admin on Sat Dec 16 01:56:35 UTC 2023 , Edited by admin on Sat Dec 16 01:56:35 UTC 2023
PRIMARY
PUBCHEM
159328
Created by admin on Sat Dec 16 01:56:35 UTC 2023 , Edited by admin on Sat Dec 16 01:56:35 UTC 2023
PRIMARY
EPA CompTox
DTXSID20911487
Created by admin on Sat Dec 16 01:56:35 UTC 2023 , Edited by admin on Sat Dec 16 01:56:35 UTC 2023
PRIMARY
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