Hydrochlorothiazide

Kufotokozera Kwachidule:

Dzina la API Chizindikiro Kufotokozera US DMF EU DMF CEP
Hydrochlorothiazide Ma diuretics USP/EP/CEP 16750 CEP 2006-011


Tsatanetsatane wa Zamalonda

Zolemba Zamalonda

PRODUCT DETAIL

Kufotokozera

Hydrochlorothiazide (HCTZ), mankhwala okodzetsa pakamwa a gulu la thiazide, amalepheretsa kusintha kwa TGF-β/ Njira yolumikizirana ndi Smad.Hydrochlorothiazide imakhala ndi zotsatira zotsitsimula mwachindunji kudzera pakutsegula njira ya calcium-activated potaziyamu (KCA).Hydrochlorothiazide imathandizira kugwira ntchito kwa mtima, imachepetsa fibrosis komanso imakhala ndi antihypertensive effect.

Mbiri

Hydrochlorothiazide ndi mankhwala okodzetsa a gulu la thiazide.

Mu Vitro

Hydrochlorothiazide ndi m'gulu la thiazide diuretics.Amachepetsa kuchuluka kwa magazi pogwiritsa ntchito impso kuti achepetse kuyamwanso kwa sodium (Na) mu distal convoluted tubule.Malo akuluakulu a nephron akuwonekera pa electroneutral Na + -Cl co-transporter popikisana ndi malo a chloride pa transporter.Posokoneza kayendedwe ka Na mu distal convoluted tubule, hydrochlorothiazide imayambitsa natriuresis ndi kutaya madzi kofanana.Thiazides amawonjezera kuyamwanso kwa calcium m'gawoli mosagwirizana ndi kayendedwe ka sodium.Kuphatikiza apo, ndi njira zina, Hydrochlorothiazide amakhulupirira kuti imachepetsa kukana kwa mitsempha.

Hydrochlorothiazide (HCTZ; oral bygavage; 12.5 mg/kg/d; masabata a 8) yathandiza kuti mtima ugwire ntchito bwino, kuchepetsa mtima wa interstitial fibrosis ndi kagawo kakang'ono ka collagen, kutsika kwa AT1, TGF-β ndi Smad2 mu minyewa yamtima mwa makoswe aamuna akulu a Sprague Dawley.Kuphatikiza apo, hydrochlorothiazide imachepetsa plasma angiotensin II ndi aldosterone.Kuphatikiza apo, hydrochlorothiazide imalepheretsa angiotensin II-induced TGF-.β1 ndi Smad2 protein expression mu neonatal rat ventricular fibroblasts.

Kapangidwe ka mankhwala

Hydrochlorothiazide

CERTIFICATE

2018 GMP-2
原料药GMP证书201811(captopril ,thalidomide etc)
GMP-of-PMDA-in-Chanyoo-平成28年08月03日 Nantong-Chanyoo-Pharmatech-Co
FDA-EIR-Letter-201901

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