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Results for "

zolamide

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    20
    TargetMol | Inhibitors_Agonists
  • Isotope Products
    2
    TargetMol | Isotope_Products
Zolamide
Tio-urasin, CL 5343, 5-Amino-TDSNH2
T2128114949-00-9
Zolamide (CL 5343) may be used to prevent altitude sickness and reduce the symptoms.
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Acetazolamide
Diamox
T081359-66-5
Acetazolamide (Diamox) is a Carbonic Anhydrase Inhibitor. The mechanism of action of acetazolamide is as a Carbonic Anhydrase Inhibitor. The chemical classification of acetazolamide is Sulfonamides.
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Acetazolamide sodium
OT-302 sodium
T603511424-27-7
Acetazolamide sodium (OT-302 sodium) is a potent carbonic anhydrase (CA)IX inhibitor with diuretic, antigonococcal, and antihypertensive activity and may be used for indications such as epilepsy, glaucoma, edema, and altitude sickness.
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6-8 weeks
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Methazolamide
L584601, CL 8490
T0106554-57-4
Methazolamide (CL 8490) is a carbonic anhydrase inhibitor that is used as a diuretic and in the treatment of glaucoma.
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Dorzolamide hydrochloride
MK507 hydrochloride, L671152 hydrochloride, MK-507 (L-671152) HCl, Dorzolamide HCl
T2134130693-82-2
Dorzolamide hydrochloride (MK507 hydrochloride) is the hydrochloride salt form of dorzolamide, an inhibitor of carbonic anhydrase, a zinc-containing enzyme that catalyzes the rapid conversion of carbon dioxide and water into carbonic acid, protons and bicarbonate ions. Distributed throughout many cells and tissues, various carbonic anhydrases play important roles in mineral and metabolic homeostasis.
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Brinzolamide
AL-4862
T0142138890-62-7
Brinzolamide (AL-4862) is a Carbonic Anhydrase Inhibitor. Its mechanism of action involves inhibiting the enzyme Carbonic Anhydrase.
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Ethoxzolamide
PNU-4191, Redupresin, L-643786
T5012452-35-7
Ethoxzolamide (L-643786) is a carbonic anhydrase inhibitor.
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TargetMol | Citations Cited
Benzolamide
CL-11366, W 1803, CL 11366, CL11366, W-1803
T237823368-13-6
Benzolamide (CL 11366) inhibits carbonic anhydrase effectively and low-threshold calcium currents in hippocampal pyramidal neurons.
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O-desmethyl Brinzolamide (hydrochloride)
T37403
O-desmethyl Brinzolamide is an active metabolite of the carbonic anhydrase (CA) inhibitor brinzolamide .1,2It inhibits CAII and CAIV (IC50s = 0.136 and 165 nM, respectively).1 1.Huang, Q., Rui, E.Y., Cobbs, M., et al.Design, synthesis, and evaluation of NO-donor containing carbonic anhydrase inhibitors to lower intraocular pressureJ. Med. Chem.58(6)2821-2833(2015) 2.Lo Faro, A.F., Tini, A., Gottardi, M., et al.Development and validation of a fast ultra-high-performance liquid chromatography tandem mass spectrometry method for determining carbonic anhydrase inhibitors and their metabolites in urine and hairDrug Test Anal.13(8)1552-1560(2021)
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Methazolamide-d6
T701861795142-30-1
Methazolamide-d6 is intended for use as an internal standard for the quantification of methazolamide by GC- or LC-MS. Methazolamide is a carbonic anhydrase inhibitor. It reduces intraocular pressure and cerebrospinal fluid flow in a rat model of glaucoma. Methazolamide reduces electroshock-induced seizures in rats with an ED50 value of 19.2 mg kg. It also inhibits production of reactive oxygen species (ROS) in a primary cortical neuron (PCN) cellular model of subarachnoid hemorrhage (SAH) and reduces cerebral edema in a mouse model of SAH.3 Methazolamide is larvicidal, with a 50% larvicidal concentration (LC50) value of 724 ppm, but has no activity when administered in the diet to adult A. aegypti. Formulations containing methazolamide have been used in the treatment of glaucoma.
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6-8 weeks
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Sezolamide hydrochloride
Sezolamide,MK-417,Sezolamide HCl,MK 417
T28763119271-78-2
Sezolamide hydrochloride is a potent topical carbonic anhydrase inhibitor.
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8-10 weeks
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Aminozolamide
T6826994641-11-9
Aminozolamide is a carbonic anhydrase inhibitor that may be useful in the treatment of ocular hypertension.
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6-8 weeks
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Sezolamide
T71173123291-07-6
Sezolamide is a carbonic anhydrase inhibitor.
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8-10 weeks
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N-desethyl Brinzolamide (oxalate)
T35713
N-desethyl Brinzolamide is an active metabolite of the carbonic anhydrase (CA) inhibitor brinzolamide .1It inhibits CAII and CAIV activities (IC50s = 1.28 and 128 nM, respectively). 1.Kim, C.-Y., Whittington, D.A., Chang, J.S., et al.Structural aspects of isozyme selectivity in the binding of inhibitors to carbonic anhydrases II and IVJ. Med. Chem.45(4)888-893(2002)
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Chlorzolamide
T2019545541-92-4
CHLORZOLAMIDE is a sulfonamide-based inhibitor that exhibits cytotoxic effects on prostate cancer cells.
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O-Desmethyl Brinzolamide hydrochloride
T870552967475-56-3
O-Desmethyl Brinzolamide hydrochloride (compound 6a), a potent metabolite derived from Brinzolamide, serves as a carbonic anhydrase (CA) inhibitor. It exhibits a dissociation constant (Kd) of 0.136 nM for CA II and an inhibitory concentration (IC50) of 165 nM for CA IV [1].
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10-14 weeks
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N-Desethyl Brinzolamide oxalate
AL-8520 oxalate
T849842775292-24-3
N-Desethyl Brinzolamide oxalate functions as a dual inhibitor targeting Carbonic anhydrase II and Carbonic anhydrase IV, exhibiting inhibitory concentrations (IC50) of 1.28 nM and 128 nM, respectively [1].
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8-10 weeks
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Dorzolamide
T22743120279-96-1
Dorzolamide is an anti-glaucoma agent and is a carbonic anhydrase inhibitor.
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Acetazolamide-d3
T102311189904-01-5
Acetazolamide D3 is a deuterium-labeled Acetazolamide. Acetazolamide is a potent carbonic anhydrase inhibitor.
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7-10 days
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brinzolamide hydrochloride
T64241
Brinzolamide (AL-4862) hydrochloride is a selective inhibitor (IC50: 3.2 nM) of carbonic anhydrase II, inhibiting ciliary CA-II, reducing atrial fluid secretion, and thereby lowering intraocular pressure (IOP). It is useful for studying glaucoma disease.
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1-2 weeks
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