Brinzolamide
CAS No. 138890-62-7
Brinzolamide( AL 4862 | Azopt )
Catalog No. M11614 CAS No. 138890-62-7
Brinzolamide is a highly specific, non-competitive, reversible carbonic anhydrase inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 31 | In Stock |
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| 10MG | 45 | In Stock |
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| 25MG | 86 | In Stock |
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| 50MG | 133 | In Stock |
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| 100MG | 194 | In Stock |
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| 200MG | 243 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBrinzolamide
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NoteResearch use only, not for human use.
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Brief DescriptionBrinzolamide is a highly specific, non-competitive, reversible carbonic anhydrase inhibitor.
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DescriptionBrinzolamide is a highly specific, non-competitive, reversible carbonic anhydrase inhibitor. Carbonic anhydrase (CA) is an enzyme found in many tissues of the body including the eye. It catalyzes the reversible reaction involving the hydration of carbon dioxide and the dehydration of carbonic acid. In humans, carbonic anhydrase exists as a number of isoenzymes, the most active being carbonic anhydrase II (CA-II). Inhibition of carbonic anhydrase in the ciliary processes of the eye decreases aqueous humor secretion, presumably by slowing the formation of bicarbonate ions with subsequent reduction in sodium and fluid transport. The result is a reduction in intraocular pressure. Brinzolamide is indicated in the treatment of elevated intraocular pressure in patients with ocular hypertension or open-angle glaucoma. (In Vivo):Brinzolamide (7.5 mg or 12 mg) implanted in a silicone matrix is extremely well tolerated and provides sustained release of brinzolamide and significant reduction in intraocular pressure (IOP) for up to 28 days with no adverse effects or signs of toxicity in normotensive NZW rabbits.
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In Vitro——
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In VivoBrinzolamide (7.5 mg or 12 mg) implanted in a silicone matrix is extremely well tolerated and provides sustained release of brinzolamide and significant reduction in intraocular pressure (IOP) for up to 28 days with no adverse effects or signs of toxicity in normotensive NZW rabbits.The pharmacokinetic parameters of Brinzolamide in rabbits.Animal Model:Rabbits Dosage:7.5 mg, 12 mg Administration:Brinzolamide silicone matrix implant placed in the episcleral space Result:Resulted in a significant IOP reduction of 4.6 mmHg on days 10-28, with concentrations of 12 mg.
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SynonymsAL 4862 | Azopt
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PathwayMembrane Transporter/Ion Channel
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TargetCarbonic Anhydrase
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RecptorCarbonic anhydrase II
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number138890-62-7
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Formula Weight383.51
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Molecular FormulaC12H21N3O5S3
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Purity>98% (HPLC)
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SolubilityDMSO: 77 mg/mL (200.77 mM)
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SMILESCCN[C@H]1CN(S(=O)(=O)C2=C1C=C(S2)S(=O)(=O)N)CCCOC
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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EMAC10101d
compound EMAC10101d, bearing a 2,4-dichorophenyl substituent in position 4 of the dihydrothiazole ring, was the most potent and selective toward hCA II with an inhibitory activity in the low nanomolar range.
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Histone acetyltransf...
Histone acetyltransferase p300 Inhibitor 4c is a 2-aminothiazole derivative. Histone acetyltransferase p300 Inhibitor 4c inhibited hCA I, hCA II, AChE and BChE with Ki values of 0.008 ± 0.001, 0.124 ± 0.017, 0.129 ± 0.030 and 0.083 ± 0.041 μM. 0.017, 0.129 ± 0.030 and 0.083 ± 0.041 μM.
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Cyclamic acid sodium
Cyclamic acid sodium (Cyclohexylsulfamicacidsodium) is a carbonic anhydrase inhibitor and one of the most widely used artificial sweeteners in food and pharmaceuticals.
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