A thiazide diuretic
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Hydroflumethiazide

Item No. 23612

Technical Information
Formal Name
3,4-dihydro-6-(trifluoromethyl)-2H-1,2,4-benzothiadiazine-7-sulfonamide, 1,1-dioxide
CAS Number
135-09-1
Synonyms
  • NSC 44627
Molecular Formula
C8H8F3N3O4S2
Formula Weight
Purity
≥98%
Formulation
A solid
DMSO: Slightly SolubleMethanol: Slightly Soluble
SMILES
O=S1(C2=C(C=C(C(F)(F)F)C(S(N)(=O)=O)=C2)NCN1)=O
InChi Code
InChI=1S/C8H8F3N3O4S2/c9-8(10,11)4-1-5-7(2-6(4)19(12,15)16)20(17,18)14-3-13-5/h1-2,13-14H,3H2,(H2,12,15,16)
InChi Key
DMDGGSIALPNSEE-UHFFFAOYSA-N
Shipping & Storage Information
Storage
4°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Hydroflumethiazide is a thiazide diuretic that also inhibits carbonic anhydrase (CA).1 It is selective for CAII, VB, VII, IX, XII, and XIV (Kis = 305-235 nM) over CAI, IV, and VI (Kis = 2,840-8,250 nM) and CAIII, VA, and XIII (Kis = >10 µM). Diuretics of the thiazide class, of which hydroflumethiazide is a member, inhibit the renal Na+/Cl- cotransporter.2 Formulations containing hydroflumethiazide have been used as diuretics.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Temperini, C., Cecchi, A., Scozzafava, A., et alCarbonic anhydrase inhibitors. Interaction of indapamide and related diuretics with 12 mammalian isozymes and X-ray crystallographic studies for the indapamide-isozyme II adduct. Bioorg. Med. Chem. Lett. 18(8), 2567-2573 (2008).

    2. Hughes, A.D. How do thiazide and thiazide-like diuretics lower blood pressure? J. Renin Angiotensin Aldosterone Syst. 5(4), 155-160 (2004).