hydroflumethiazide

Trade name: saluron

Small moleculeapproved

Approved

Jul 22, 1959

Hydroflumethiazide is a thiazide diuretic that inhibits water reabsorption in the nephron by inhibiting the sodium-chloride symporter (SLC12A3) in the distal convoluted tubule, which is responsible for 5% of total sodium reabsorption. Normally, the sodium-chloride symporter transports sodium and chloride from the lumen into the epithelial cell lining the distal convoluted tubule. The energy for this is provided by a sodium gradient established by sodium-potassium ATPases on the basolateral membrane. Once sodium has entered the cell, it is transported out into the basolateral interstitium via the sodium-potassium ATPase, causing an increase in the osmolarity of the interstitium, thereby establishing an osmotic gradient for water reabsorption. By blocking the sodium-chloride symporter, Hydroflumethiazide effectively reduces the osmotic gradient and water reabsorption throughout the nephron. Hydroflumethiazide is used as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Also used in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. — NCATS

Clinical trial activity

0 trials · 0 clinical orgs · 6 marketing orgs

Phase 1
0
Phase 2
0
Phase 3
0
Phase 4
0

Timeline

1950s

  1. Jul 22, 1959

    Shire — Earliest FDA Approval

  2. Jul 22, 1959

    Shire — NDA Secondary Org

  3. Jul 22, 1959

    Shire — NDA Organization

1970s

  1. Dec 20, 1973

    American Home Products — Marketing Organization

1980s

  1. Jan 11, 1985

    Ivax — Marketing Organization

  2. May 31, 1985

    Par Pharmaceuticals — Marketing Organization

  3. Jul 2, 1986

    Watson Pharmaceuticals — Marketing Organization

Indications

Mechanism of action

Combination products

  • salutensin-demi

    with reserpine

    Also known as salutensin

Approval history

  • approvedJul 22, 1959

Chemistry & pharmacology

Loading structure…

SMILES

NS(=O)(=O)C1=CC2=C(NCNS2(=O)=O)C=C1C(F)(F)F
Mol. weight
331.292 g/mol
Lipinski Ro5
Pass
Rule of 3
No
Chirality
Achiral Molecule
Inorganic
No
Polymer
No
Delivery
Oral
Availability
Discontinued

Oral

Yes

Parenteral

No

Topical

No

Sources

Also known as

  • dihydroflumethazide
  • dihydroflumethazide
  • diucardin
  • diucardin
  • hidroflumetiazid
  • hidroflumetiazid
  • hidroflumetiazida
  • hidroflumetiazida
  • hydrenox
  • hydrenox
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydroflumethiazide
  • hydrofluméthiazide
  • hydrofluméthiazide
  • hydroflumethiazidum
  • hydroflumethiazidum
  • idroflumetiazide
  • idroflumetiazide
  • metforylthiadiazin
  • metforylthiadiazin
  • saluron
  • saluron
  • trifluoromethylhydrothiazide

Organizations

Marketing (8)

OrganizationOrg typeRelationshipDate
American Home ProductsFor profitMKTGDec 20, 1973
IvaxFor profitMKTGJan 11, 1985
Par PharmaceuticalsFor profitMKTGMay 31, 1985
ShireFor profitNDA2Jul 22, 1959
ShireFor profitSYNJun 20, 1960
ShireFor profitNDAJul 22, 1959
Upsher-Smith LaboratoriesFor profitMKTG
Watson PharmaceuticalsFor profitMKTGJul 2, 1986