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(177 products)
- Hydroxylase(30 products)
- MPO(2 products)
- Reductase(52 products)
- Tyrosinase(67 products)
Found 3586 products of "Enzyme"
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C. rugosa Lipase 01, CRL 1 from Candida rugosa - ELCR01
<p>Lipases belong to the family of esterases and naturally act on triglycerides at lipid-water interfaces. Lipases/esterases can be used as versatile tools in hydrolytic reactions, esterifications and transesterification reactions in industrial and food applications. The Lipase 01 from the yeast Candida rugosa has a temperature optimum in the 30 - 50 °C range and pH optimum between pH 7 and 8.</p>Protease from Streptomyces griseus
CAS:<p>Protease enzymes break down proteins and are essential for many biological processes, including digestion, cellular regulation and blood clotting. They are also used in many industrial and biotechnological applications for example in food processing and in detergents.</p>Purity:Min. 95%Color and Shape:PowderCarboxypeptidase Y, from S. cerevisiae, recombinant, lyophilized - ECPY001
CAS:<p>Carboxypeptidase Y (EC 3.4.16.1) is an exopeptidase enzyme. It hydrolyzes peptide bonds of C-terminal residues and it remains active in the presence of urea at low to moderate concentrations. One unit of the Carboxypeptidase Y will hydrolyze 1.0 μmole of a chromogenic peptide substrate, releasing C-terminal alanine and generating a light-absorbing product. Carboxypeptidase Y has been obtained from yeast S. cerevisiae, has a broad substrate specificity and can therefore be used in sequence analysis of proteins. Carboxypeptidase Y has a temperature optimum in the 20 – 30 °C range and pH optimum between pH 6 and 7.</p>Ribonuclease T1 from aspergillus oryzae
CAS:<p>Ribonuclease T1 is an endonuclease enzyme, which is derived from the fungus Aspergillus oryzae. It specifically cleaves single-stranded RNA at the 3' end of guanosine residues, which involves hydrolyzing the phosphodiester bond to produce 3′-phosphomononucleotides and 5′-hydroxylated oligonucleotides. This enzyme’s high specificity and catalytic efficiency make it valuable for various applications.</p>Purity:Min. 95%Formaldehyde Dehydrogenase
CAS:<p>Formaldehyde dehydrogenase (EC 1.2.1.46) is an enzyme that catalyzes the following reaction: formaldehyde + NAD+ + H2O ⇌ formate + NADH + H+ One unit of formaldehyde dehydrogenase will convert 1.0 µmole of formaldehyde to formic acid per minute at pH 7.5 and 37°C in the presence of NAD+.NAD+ is available here.</p>Glutathione Reductase, baker's yeast
CAS:<p>Glutathione Reductase, baker's yeast, is an enzyme derived from the yeast species *Saccharomyces cerevisiae*. This enzyme is sourced from baker's yeast, providing a renewable and consistent product for various biochemical applications. Its mode of action involves catalyzing the reduction of glutathione disulfide (GSSG) to the sulfhydryl form glutathione (GSH), using NADPH as an electron donor. This reaction is crucial for maintaining the intracellular redox balance by regenerating GSH, the primary cellular antioxidant.</p>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>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%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%hCA I-IN-2
CAS:<p>hCA I-IN-2 (6d) inhibits hCA I (Ki: 18.8 nM) more selectively over II, IX, XII (Ki: 375.1, 1721, 283.9 nM).</p>Formula:C26H20BrN5O3SColor and Shape:SolidMolecular weight:562.44FC11409B
CAS:<p>FC11409B is a CAIX inhibitor, inhibiting breast cancer invasion and metastasis.</p>Formula:C29H23BF4N2O3SColor and Shape:SolidMolecular weight:566.38(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:331.81hCAI/II-IN-4
CAS:<p>hCAI/II-IN-4 inhibits hCA I & II (Ki: 16.95 & 15.22 nM), hCA IX (Ki: 27.04 nM), has anti-hypoxia benefits and is low-toxic for AMS research.</p>Formula:C15H15N3O5S2Color and Shape:SolidMolecular weight:381.43Methazolamide-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:242.31L 662583
CAS:<p>L 662583 is a topical inhibitor of carbonic anhydrase.</p>Formula:C13H17ClN2O5S3Purity:98%Color and Shape:SolidMolecular weight:412.93L 645151
CAS:<p>L 645151 is an inhibitor of lipophilic CA.</p>Formula:C12H14N2O4S2Color and Shape:SolidMolecular weight:314.38QPRTase 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)hCAIX-IN-5
CAS:<p>hCAIX-IN-5 was a selective hCAIX inhibitor, inhibiting hCAI, hCAII, hCAIV, and hCAIX with Ki values of >10000, >10000, 130.7, and 829.1 nM, respectively.</p>Formula:C18H12FNO3Purity:99.26%Color and Shape:SolidMolecular weight:309.29PGDS Protein, Human, Recombinant
<p>Hematopoietic Prostaglandin D Synthase (HPGDS) belongs to the GST superfamily and Sigma family.</p>Color and Shape:Lyophilized PowderMolecular weight:26 KDa (reducing condition)L-693612
CAS:<p>L-693612 is an inhibitor of carbonic anhydrase.</p>Formula:C14H24N2O5S3Purity:98%Color and Shape:SolidMolecular weight:396.55SU 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:257.72hCAI/II-IN-1
CAS:<p>hCAI/II-IN-1 (Compound 3h) is a human carbonic anhydrase I and II (hCA I/II) inhibitor that acts on hCA I (IC50: 0.047 μM) and hCA II (IC50: 0.024 μM).</p>Formula:C18H29N5O3S3Color and Shape:SolidMolecular weight:459.65WES-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:396.46GV2-20
CAS:<p>GV2-20 is an effective carbonic anhydrase 2 inhibitors.</p>Formula:C15H13N3O6Purity:98%Color and Shape:SolidMolecular weight:331.28Quinethazone
CAS:<p>Quinethazone is a thiazide diuretic used to treat hypertension. Common side effects include dizziness, dry mouth, nausea, and low potassium levels.</p>Formula:C10H12ClN3O3SColor and Shape:Fibrous Crystals From 50% Acetone Physical Description Fibrous Crystals Or White Powder (Ntp 1992)Molecular weight:289.74hCAIX-IN-11
CAS:<p>hCAIX-IN-11 inhibits carbonic anhydrases IX & XII with Ki of 32.7 nM & 623.5 nM, respectively.</p>Formula:C21H15ClN4O3Color and Shape:SolidMolecular weight:406.82Phenylthiazolylthiourea
CAS:<p>Phenylthiazolylthiourea ia a dopamine-beta-hydroxylase inhibitor.</p>Formula:C10H9N3S2Color and Shape:SolidMolecular weight:235.33hCAIX-IN-10
CAS:<p>"hCAIX-IN-10 (6i) selectively inhibits carbonic anhydrase IX/XII (Ki: 61.5/586.8 nM), markers in tumor cells, affecting acid-base balance."</p>Formula:C28H21N3O3SColor and Shape:SolidMolecular weight:479.55HCAIX-IN-2
CAS:<p>HCAIX-IN-2 (compound 9d) is a selective inhibitor of carbonic anhydrase and acts on hCA IX (Ki: 24.6 nM) and hCA XII (Ki: 45.3 nM).</p>Formula:C19H16N8O4SColor and Shape:SolidMolecular weight:452.45hCAI/II-IN-3
CAS:<p>"hCAI/II-IN-3 (compound 5b) is a potent dual hCA I/II inhibitor with Ki: 51.25nM (I), 13.15nM (II), helps treat AMS."</p>Formula:C16H18N4O4S2Color and Shape:SolidMolecular weight:394.47hCAIX-IN-6
CAS:<p>6B and 14g inhibit tumor-associated HCA IX with low nanomolar potency; 6K targets HCA XII. All are potential cancer drug leads.</p>Formula:C18H12N2O4SColor and Shape:SolidMolecular weight:352.36hCAII-IN-1
CAS:<p>hCAII-IN-1 (7f) inhibits CA II/IX with Kis 1.2 nM/113.6 nM, potential for cancer treatment.</p>Formula:C21H21BrN6O4SColor and Shape:SolidMolecular weight:533.4hCAXII-IN-2
CAS:<p>hCAXII-IN-2 is a potent inhibitor of hCA XII (Ki: 84.2 nM) and hCA IX (Ki: 268.5 nM), with low activity on hCA I/II.</p>Formula:C21H18ClN3O4Color and Shape:SolidMolecular weight:411.84DTP348
CAS:<p>DTP348: Oral carbonic anhydrase IX inhibitor & hypoxic cell radiosensitizer with sulfamide & 5-nitroimidazole components.</p>Formula:C6H11N5O4SColor and Shape:SolidMolecular weight:249.25hCAXII-IN-4
CAS:<p>hCAXII-IN-4 is a selective and potent CA XII inhibitor with a Ki value of 6.4 nM for human CA XII.</p>Formula:C22H27N5O6SColor and Shape:SolidMolecular weight:489.54PPIE Protein, Human, Recombinant (His)
<p>Peptidyl-prolyl cis-trans isomerase E, also known as Cyclophilin E, Cyclophilin-33, Rotamase E, CYP33, PPIE, is an enzyme which belongs to the cyclophilin-type</p>Color and Shape:Lyophilized PowderMolecular weight:34 KDa (reducing condition)hCAI/II-IN-2
CAS:<p>hCAI/II-IN-2 (2b) inhibits hCA I/II (Ki: 40.97 nM, 15.15 nM) and IX (61.88 nM), fights AMS with anti-hypoxic effects, but has low cellular activity.</p>Formula:C12H12N4O5S2Color and Shape:SolidMolecular weight:356.38Tyrosinase-IN-7
CAS:<p>Tyrosinase-IN-7 is a small-molecule tyrosinase inhibitor (IC50 1.57 μM) that suppresses melanin activity and cell growth with low cytotoxicity.</p>Formula:C15H10O5Purity:99%Color and Shape:SolidMolecular weight:270.24CDK2-IN-11
CAS:<p>CDK2-IN-11 inhibits CDK2 (IC50: 6.4 μM) and targets hCA II, IX, XII (Ki: 23.4-56.3 nM); suited for cancer research.</p>Formula:C18H14ClN7O2SColor and Shape:SolidMolecular weight:427.87L-693612 HCl
CAS:<p>L-693612 HCl is an inhibitor of carbonic anhydrase.</p>Formula:C14H25ClN2O5S3Purity:98%Color and Shape:SolidMolecular weight:433.01hCA IX-IN-2
<p>hCA IX-IN-2 is a highly potent and selective inhibitor of hCA IX, exhibiting an inhibition constant (K I) value of 32.1 nM and demonstrating anti-proliferative</p>Formula:C23H24N2O4STeColor and Shape:SolidMolecular weight:552.11AHR-15010
CAS:<p>AHR-15010 is a novel anti-arthritic agent.</p>Formula:C10H16N2O8S2Purity:98%Color and Shape:SolidMolecular weight:356.37hCAIX/XII-IN-6
<p>hCAIX/XII-IN-6: Oral carbonic anhydrase inhibitor, targets hCA I/II/IV/IX/XII, aids rheumatoid arthritis research. Ki: 6697/2950/4093/4.1/7.7 nM.</p>Formula:C26H23N3O6S4Color and Shape:SolidMolecular weight:601.74hCAIX/XII-IN-2
CAS:<p>Compound 6a: Selective hCAIX/XII inhibitor; Ki: 30 nM (hCAIX), 3.6 nM (hCAXII); >10,000 nM (hCAI/II).</p>Formula:C19H14N2O4Color and Shape:SolidMolecular weight:334.33hCAIX-IN-8
CAS:<p>hCAIX-IN-8, a selective hCAIX inhibitor, IC50: 0.024 μM. Also affects CAII, CAVA (IC50s: 1.99, 1.10 μM), limits cell migration, and induces apoptosis.</p>Formula:C19H16N4O6Color and Shape:SolidMolecular weight:396.35CDK2-IN-12
CAS:<p>CDK2-IN-12 (10b), potent CDK2 inhibitor, IC50: 11.6 μM; inhibits hCA I/II/IX/XII, KI: 3534/638.4/44.3/48.8 nM; anti-cancer properties.</p>Formula:C20H17N9O2SColor and Shape:SolidMolecular weight:447.47Telotristat besilate
CAS:<p>Telotristat besilate is an inhibitor of tryptophan hydroxylase.</p>Formula:C31H28ClF3N6O6SPurity:98%Color and Shape:SolidMolecular weight:705.11hCA I-IN-1
CAS:<p>hCA I-IN-1 inhibits hCA I (Ki: 38.3 nM), II (Ki: 716.4 nM), IX (Ki: 940.1 nM), XII (Ki: 192.8 nM).</p>Formula:C27H23N5O4SColor and Shape:SolidMolecular weight:513.57
