Sinesalin
Sinesalin Brand names, Sinesalin Analogs
- Aprinox
- BHFT
- Bendrofluazide
- Bendroflumethazide
- Bendroflumethiazide [Inn]
- Bendroflumethiazidum [Inn-Latin]
- Bendroflumetiazida [Inn-Spanish]
- Bendroflumetiazide [Dcit]
- Bendrofumethiazide
- Bentride
- Benuron
- Benzhydroflumethiazide
- Benzy-Rodiuran
- Benzydroflumethiazide
- Benzylhydroflumethiazide
- Benzylrodiuran
- Berkozide
- Bristuric
- Bristuron
- Centyl
- Corzide
- FT 8
- Flumersil
- Flumesil
- Intolex
- Livesan
- Naigaril
- Nateretin
- Naturetin
- Naturetin-2.5
- Naturine
- Neo-Naclex
- Neo-Rontyl
- Niagaril
- Nikion
- Orsile
- Pluryl
- Pluryle
- Plusuril
- Poliuron
- Rautrax N
- Rauzide
- Relan Beta
- Repicin
- Salural
- Salures
- Sinesalin
- Sodiuretic
- Thiazidico
- Urlea
Sinesalin Brand Names Mixture
- Corzide Tab W Nadolol 40mg (Bendroflumethiazide + Nadolol)
- Corzide Tab W Nadolol 80mg (Bendroflumethiazide + Nadolol)
Sinesalin Chemical_Formula
C15H14F3N3O4S2
Sinesalin RX_link
No information avaliable
Sinesalin fda sheet
Sinesalin msds (material safety sheet)
Sinesalin Synthesis Reference
No information avaliable
Sinesalin Molecular Weight
421.417 g/mol
Sinesalin Melting Point
221-223 oC
Sinesalin H2O Solubility
108 mg/L
Sinesalin State
Solid
Sinesalin LogP
2.085
Sinesalin Dosage Forms
Tablet
Sinesalin Indication
For the treatment of high blood pressure and management of edema
Sinesalin Pharmacology
Bendroflumethiazide, a thiazide diuretic, removes excess water from the body by increasing how often you urinate (pass water) and also widens the blood vessels which helps to reduce blood pressure. It inhibits Na+/Cl- reabsorption from the distal convoluted tubules in the kidneys. Thiazides also cause loss of potassium and an increase in serum uric acid. Thiazides are often used to treat hypertension, but their hypotensive effects are not necessarily due to their diuretic activity. Thiazides have been shown to prevent hypertension-related morbidity and mortality although the mechanism is not fully understood. Thiazides cause vasodilation by activating calcium-activated potassium channels (large conductance) in vascular smooth muscles and inhibiting various carbonic anhydrases in vascular tissue.
Sinesalin Absorption
Absorbed relatively rapidly after oral administration
Sinesalin side effects and Toxicity
No information avaliable
Sinesalin Patient Information
No information avaliable
Sinesalin Organisms Affected
Humans and other mammals
