Enzyme
Enzyme inhibitors are molecules that bind to enzymes and decrease their activity. These inhibitors are widely used in research to study enzyme kinetics, regulation, and the role of specific enzymes in metabolic pathways. Enzyme inhibitors are also crucial in drug development, as many therapeutic agents function by inhibiting enzymes involved in disease processes. By targeting enzymes, these inhibitors can modulate biochemical pathways and offer potential treatments for various diseases. At CymitQuimica, we provide a comprehensive selection of high-quality enzyme inhibitors to support your research in biochemistry, pharmacology, and drug discovery.
Subcategories of "Enzyme"
- Carbonic Anhydrase(178 products)
- Hydroxylase(30 products)
- MPO(2 products)
- Reductase(52 products)
- Tyrosinase(67 products)
Found 3587 products of "Enzyme"
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Secreted Phospholipase A2-IIA, human, recombinant
<p>The secreted phospholipase A2-IIA (sPLA2-IIA, PLA2, systematic name phosphatidylcholine 2-acylhydrolase; EC 3.1.1.4) is an enzyme that catalyses the hydrolysis of glycerophospholipids at the sn2 position, yielding 1-acylglycerophosphocholine and a fatty acid. One unit of secreted phospholipase A2-IIA will hydrolyze 1.0 μmole of substrate per min under optimal conditions.</p>Purity:Min. 95%Cellulose catalase
<p>Cellulose catalase is an enzyme-based product, designed specifically to act as a catalyst in the oxidative processes associated with cellulose applications. It is derived from a microbial source, where bacilli or fungi are employed to produce robust catalase enzymes in a fermentation process. The mode of action involves the catalase enzyme’s ability to facilitate the decomposition of hydrogen peroxide into water and oxygen, thereby reducing oxidative damage during cellulose processing.</p>Lipase 077, acidic lipase - recombinant
<p>Lipase 77 recombinantly expressed in P. pastoris comes in a spray-dried formulation. It has its pH optimum at 4-5. Lipases belong to the family of esterases and naturally act on triglycerides at lipid-water interfaces catalyzing hydrolytic reactions, esterifications and transesterification reactions in industrial and food applications. Lipase 77 was shown to hydrolyze p-Nitrophenyl esters of butyrate and triglycerides.</p>α-N-Acetylglucosaminidase
CAS:<p>α-N-Acetylglucosaminidase (recombinant Human NAGLU Protein), degrades heparan sulfate by hydrolysis of terminal GlcNAc resides in N-acetyl-alpha-D-glucosaminides of heparan sulfate.Activity is measured by its ability to hydrolyse 4-Nitrophenyl 2-acetamido-2-deoxy-a-D-glucopyranoside EN03208 or EM31027. The specific activity is >900 pmol/min/μg, as measured under the decribed conditions.</p>Purity:(Sds-Page) Min. 95%Phosphorylase B from rabbit muscle
CAS:<p>Phosphorylase B is an enzymatic protein, specifically an isoform of glycogen phosphorylase, derived from rabbit muscle. This enzyme plays a critical role in glycogen metabolism by catalyzing the phosphorolytic cleavage of α(1→4) glycosidic bonds in glycogen, releasing glucose-1-phosphate. The rabbit muscle source provides a well-studied model due to its high enzyme activity and availability, facilitating in-depth biochemical and structural analysis.</p>Purity:Min. 95%Methazolamide-d6
CAS:<p>Methazolamide-d6 is a GC/LC-MS standard for measuring methazolamide, a glaucoma drug that lowers eye pressure and fluid, reduces seizures, and combats ROS.</p>Formula:C5H2D6N4O3S2Color and Shape:SolidMolecular weight:242.31SU 10603
CAS:<p>SU 10603 is a specific inhibitor of 17α-hydroxylase (also known as CYP17A1 and P450c17) used to study steroid hormone synthesis.</p>Formula:C15H12ClNOPurity:99.93% - 99.96%Color and Shape:SolidMolecular weight:257.72QPRTase Protein, Human, Recombinant (His)
<p>Nicotinate-Nucleotide Pyrophosphorylase (QPRT) belongs to the nadC/modD family.</p>Color and Shape:Lyophilized PowderMolecular weight:34 KDa (reducing condition)CK1 δ/CSNK1D Protein, Human, Recombinant (Baculovirus, His)
<p>Expression system: Baculovirus<br>Length: 1-415, Full Length<br>Activity: Not Tested</p>Purity:85%Color and Shape:Odour Lyophilized PowderhCAXII-IN-3
CAS:<p>hCAXII-IN-3 (Compound 6o) is a selective inhibitor of human carbonic anhydrase XII (hCAXII) (Ki: 10.0 nM).</p>Formula:C26H20BrN5O3SColor and Shape:SolidMolecular weight:562.44(R)-Nepicastat HCl
CAS:<p>(R)-Nepicastat HCl (RS-25560-198 HCl), R-enantiomer, inhibits bovine/human dopamine-β-hydroxylase (IC50: 25.1/18.3 nM); not affecting other enzymes/receptors.</p>Formula:C14H15F2N3S·HClPurity:98%Color and Shape:SolidMolecular weight:331.81Telotristat besilate
CAS:<p>Telotristat besilate is an inhibitor of tryptophan hydroxylase.</p>Formula:C31H28ClF3N6O6SPurity:98%Color and Shape:SolidMolecular weight:705.11L 645151
CAS:<p>L 645151 is an inhibitor of lipophilic CA.</p>Formula:C12H14N2O4S2Color and Shape:SolidMolecular weight:314.38L 662583
CAS:<p>L 662583 is a topical inhibitor of carbonic anhydrase.</p>Formula:C13H17ClN2O5S3Purity:98%Color and Shape:SolidMolecular weight:412.93Carbonic anhydrase inhibitor 14
CAS:<p>CA inhibitor 14 blocks hCA I/II/IX/XII (K i of 1203/99.7/9.4/27.7 nM) and CDK2 (IC50: 20.3 μM), showing antitumor effects.</p>Formula:C18H17N7O2SColor and Shape:SolidMolecular weight:395.44L-693612
CAS:<p>L-693612 is an inhibitor of carbonic anhydrase.</p>Formula:C14H24N2O5S3Purity:98%Color and Shape:SolidMolecular weight:396.55GV2-20
CAS:<p>GV2-20 is an effective carbonic anhydrase 2 inhibitors.</p>Formula:C15H13N3O6Purity:98%Color and Shape:SolidMolecular weight:331.28WES-1
CAS:<p>WES-1 (Compound 8g), a carbonic anhydrase IX inhibitor (Ki: 55.9 μM), exhibits broad-spectrum antiproliferative activity against various cancer cell lines,</p>Formula:C20H20N4O3SPurity:98%Color and Shape:SolidMolecular weight:396.46Clofenamide
CAS:<p>Clofenamide is a low-ceiling sulfonamide diuretic.</p>Formula:C6H7ClN2O4S2Color and Shape:SolidMolecular weight:270.71hCAXII-IN-5
CAS:<p>hCAXII-IN-5, or compound 6o, is a potent, selective hCAXII inhibitor with Ki values: hCAI & II >10000, hCAIX 286.1, hCAXII 1.0 nM.</p>Formula:C23H22N2O4Color and Shape:SolidMolecular weight:390.43
