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| Product | Description | |
|---|---|---|
| Naringin dihydrochalcone | Naringin dihydrochalcone. Group: Biochemicals. Grades: Reagent Grade. CAS No. 18916-17-1. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. |  Worldwide |
| Naringin hydrate | Naringin hydrate is a natural compound derived from citrus fruits and has been found to possess various medicinal properties. This product is primarily used for its anti-inflammatory and antioxidant effects. Synonyms: Naringenin 7-Rhamnoglucoside; 4,5,7-Trihydroxyflavanone 7-rhamnoglucoside. Molecular formula: C27H32O14 H2O. Mole weight: 598.55. |  |
| NaringinHydrate | NaringinHydrate. Group: Molecular Biology. Grades: Highly Purified. CAS No. 10236-47-2. Pack Sizes: 25g. Molecular Formula: C27H32O14. US Biological Life Sciences. | Worldwide |
| Narirutin | Narirutin. Group: Biochemicals. Alternative Names: Naringenin-7-O-rutinoside; Isonaringin. Grades: Plant Grade. CAS No. 14259-46-2. Pack Sizes: 20mg. Molecular Formula: C27H32O14, Molecular Weight: 580.535. US Biological Life Sciences. | Worldwide |
| Narirutin | Anti-inflammatory. The flavonoid narirutin could reduce airway inflammation in ovalbumin (OVA)-sensitized / challenged NC / Nga mice, a model of allergic eosinophilic airway inflammation. Uses: Anti-allergic, antiproliferative and anti-oxidant. Synonyms: 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)-; (2S)-7-[[6-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (S)-; Flavanone, 4',5,7-trihydroxy-, 7β-rutinoside; (2S)-Narirutin; Isonaringenin; Isonaringin; Naringenin 7-O-rutinoside; Naringenin 7-rutinoside; Naringenin 7β-rutinoside. Grades: >98%. CAS No. 14259-46-2. Molecular formula: C27H32O14. Mole weight: 580.53. | |
| Narirutin | Narirutin, one of the active constituents isolated from citrus fruits, has antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tubercular potency [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 14259-46-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N0804. |  |
| Narirutin-5-dehydroxy-2,3-dihydro-hexaacetate | 5-Dehydroxy-4-dihydro-narirutin Hexaacetate, as an intermediate in the synthesis of Isorhoifolin (Diosmin EP Impurity C), is a naturally occurring flavonoid that was shown to exhibit potential antidiabetic, antihyperlipidemic and antioxidant effects. Molecular formula: C39H44O19. Mole weight: 816.76. | |
| Narirutin Hexaacetate | Narirutin Hexaacetate, as an intermediate in the synthesis of Isorhoifolin, is a naturally occurring flavonoid that was shown to exhibit potential antidiabetic, antihyperlipidemic and antioxidant effects. Synonyms: (2R,3S,4R,5S,6S)-2-((5-Hydroxy-2-(4-hydroxyphenyl)-4-oxochroman-7-yl)oxy)-6-((((2S,3S,4S,5R,6R)-3,4,5-triacetoxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl Triacetate. CAS No. 24915-80-8. Molecular formula: C39H44O20. Mole weight: 832.75. | |
| Narirutin Octaacetate | Narirutin Octaacetate can be used as an intermediate in the synthesis of Isorhoifolin (Diosmin EP Impurity C), that is a naturally occuring flavonoid that was shown to exhibit potential antidiabetic, antihyperlipidemic and antioxidant effects. Synonyms: Octaacetylnarirutin; (2S)-5-(Acetyloxy)-2-[4-(acetyloxy)phenyl]-2,3-dihydro-7-[[2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-4H-1-benzopyran-4-one; (S)-5-(Acetyloxy)-2-[4-(acetyloxy)phenyl]-2,3-dihydro-7-[[2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-4H-1-benzopyran-4-one. CAS No. 14259-48-4. Molecular formula: C43H48O22. Mole weight: 916.83. | |
| Narlaprevir | Narlaprevir is a potent, selective, orally bioavailable inhibitor of the hepatitis C virus (HCV) nonstructural protein 3 serine protease that is primarily metabolized by the cytochrome P450-3A4 system. Synonyms: SCH-900518; SCH 900518; SCH900518; Narlaprevir. Grades: >98%. CAS No. 865466-24-6. Molecular formula: C36H61N5O7S. Mole weight: 707.96. | |
| Narnatumab | Narnatumab (IMC-RON8) is a neutralizing human monoclonal antibody that blocks RON binding to its ligand, macrophage-stimulating protein (MSP) , with a K d of 32 pM. Narnatumab can be used for the research of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IMC-RON8; LY3012219; Anti-MSPR/RON/CD136 Reference Antibody (narnatumab). CAS No. 1188275-92-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99375. | |
| Naronapride | Naronapride (ATI-7505) is a potent prokinetic 5-HT 4 receptor agonist. Naronapride can be used for gastrointestinal diseases research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ATI-7505. CAS No. 860174-12-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-121826. | |
| Naronapride | Naronapride is a selective 5-HT(4) receptor agonist for gastrointestinal motility disorders. It can accelerate overall colonic transit and tend to accelerate GE and AC emptying and loose stool consistency. In Nov 2016, Renexxion planed two phase III trials for Constipation in USA. Uses: Constipation. Synonyms: ATI-7505; ATI 7505; ATI7505. Grades: 98%. CAS No. 860174-12-5. Molecular formula: C27H41ClN4O5. Mole weight: 537.1. | |
| Naronapride dihydrochloride | Naronapride is a selective 5-HT(4) receptor agonist for gastrointestinal motility disorders. It can accelerate overall colonic transit and tend to accelerate GE and AC emptying and loose stool consistency. In Nov 2016, Renexxion planed two phase III trials for Constipation in USA. Synonyms: ATI-7505 BIS HCl; ATI 7505 BIS HCl; ATI7505 BIS HCl. CAS No. 860169-57-9. Molecular formula: C27H43Cl3N4O5. Mole weight: 610. | |
| Narsoplimab | Narsoplimab (OMS 721) is a high-affinity fully human immunoglobulin gamma 4 (IgG4) monoclonal antibody that binds MASP-2 and blocks lectin pathway activation. Narsoplimab can be used in research of hematopoietic stem-cell transplantation and SARS-CoV-2 [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: OMS 721; Anti-MASP2 Reference Antibody (narsoplimab). CAS No. 2108782-45-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99376. | |
| NAS-181 | NAS-181 is a 5-HT1B receptor antagonist with Ki value of 47 nM. It can increase synthesis and metabolism of 5-HT in the brain following systemic administration and improve passive avoidance retention performance in vivo. Synonyms: NAS-181; NAS 181; NAS181; (2R)-2-[[[3-(4-Morpholinylmethyl)-2H-1-benzopyran-8-yl]oxy]methyl]morpholine dimethanesulfonate. Grades: ≥97% by HPLC. CAS No. 1217474-40-2. Molecular formula: C19H26N2O4.2CH3SO3H. Mole weight: 538.63. | |
| NAS-181 | NAS-181. Group: Biochemicals. Grades: Purified. CAS No. 1217474-40-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Naspm | Naspm (1-Naphthyl acetyl spermine), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA ( CP-AMPA ) receptors antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 1-Naphthylacetyl spermine. CAS No. 122306-11-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12506. | |
| Naspm | A poliamine amide as potent Spermidine uptake inhibitor. Synonyms: 1-Naphthylacetyl spermine. Grades: >98%. CAS No. 122306-11-0. Molecular formula: C22H34N4O. Mole weight: 370.53. | |
| Naspm trihydrochloride | Naspm 3HCl is a potent and selective Ca2+ permeable AMPA receptor blocker. Synonyms: Naspm trihydrochloride. Grades: >98%. CAS No. 1049731-36-3. Molecular formula: C22H37Cl3N4O. Mole weight: 479.91. | |
| Naspm trihydrochloride | Naspm trihydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1049731-36-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Nasunin | Nasunin, an antioxidant anthocyanin, possesses antiangiogenic activity [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Delphinidin-3-(p-coumaroylrutinoside)-5-glucoside. CAS No. 28463-30-1. Pack Sizes: 500 μg; 1 mg; 5 mg. Product ID: HY-N9396. | |
| Nasunin | Nasunin is an anthocyanin isolated as purple colored crystals from eggplant peels. It possesses antiangiogenic activity. Synonyms: Delphanin; Delphinidin-3-(p-coumaroylrutinoside)-5-glucoside. CAS No. 28463-30-1. Molecular formula: C42H47ClO23. Mole weight: 955.27. | |
| NAT | NAT is an initial hit of NAMPT activator. NAMPT is the rate-limiting enzyme in the NAD salvage pathway, which makes it an attractive target for the research of many diseases associated with NAD exhaustion such as neurodegenerative diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 831243-31-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144776. | |
| Nat-20(S)-yne | Nat-20(S)-yne is a potential agonist of hedgehog signaling. Synonyms: (3alpha, 17beta)-17-(1-Hydroxy-1methylpent-4-ynyl)-androst-5-en-3-ol; (3beta)-26,27-Dinorcholest-5-en-24-yne-3,20-diol. Grades: ≥95%. CAS No. 1397692-46-4. Molecular formula: C25H38O2. Mole weight: 370.6. | |
| NATA | NATA. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,4',4''-Tris(N,N-diphenyl-amino)triphenylamine. Product Category: Organic Light Emitting Diode (OLED). CAS No. 105389-36-4. Molecular formula: C54H42N4. Mole weight: 746.94 g/mol. Purity: 95%+. IUPACName: 1-N,1-N-diphenyl-4-N,4-N-bis[4-(N-phenylanilino)phenyl]benzene-1,4-diamine. Canonical SMILES: C1=CC=C(C=C1)N(C2=CC=CC=C2)C3=CC=C(C=C3)N(C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)C7=CC=C(C=C7)N(C8=CC=CC=C8)C9=CC=CC=C9. Density: 1.216 g/ml. Product ID: ACM105389364. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Nataglinide | N-(Trane-4-iso-propyl cylolohexyl carboxyl)-d-phenyl propylic acid. antibiotic . CAS No. 105816-04-4. Product ID: 8-01808. Molecular formula: C19H27NO3. Mole weight: 317.43. Categories: Nateglinide. |  |
| Natalizumab | Natalizumab is a recombinant, humanized IgG4 monoclonal antibody, binds to α4β1- integrin and blocks its interaction with vascular cell adhesion molecule-1 (VCAM-1). Natalizumab can be used for the treatment of relapsing remitting multiple sclerosis and Crohn's disease. Natalizumab is also the first targeted therapy which blocks an essential mechanism for lymphocyte entry to the CNS and thus prevents acute demyelinating relapses [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 189261-10-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-108831. | |
| Natalizumab (Solution) | Natalizumab (Solution) is a recombinant, humanized IgG4 monoclonal antibody, binds to α4β1- integrin and blocks its interaction with vascular cell adhesion molecule-1 (VCAM-1). Natalizumab can be used for the treatment of relapsing remitting multiple sclerosis and Crohn's disease. Natalizumab is also the first targeted therapy which blocks an essential mechanism for lymphocyte entry to the CNS and thus prevents acute demyelinating relapses [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 189261-10-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108831A. | |
| Natamycin | Natamycin (Pimaricin) is a macrolide antibiotic agent produced by several Streptomyces strains. Natamycin inhibits the growth of fungi via inhibition of amino acid and glucose transport across the plasma membrane. Natamycin is a food preservative, an antifungal agent in agriculture, and is widely used for fungal keratitis research [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Pimaricin. CAS No. 7681-93-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0133. | |
| Natamycin | Natamycin (Pimaricin) is a macrolide antibiotic agent produced by several Streptomyces strains. Natamycin inhibits the growth of fungi via inhibition of amino acid and glucose transport across the plasma membrane. Natamycin is a food preservative, an antifungal agent in agriculture, and is widely used for fungal keratitis research. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Pimarizin. Product Category: Inhibitors. CAS No. 7681-93-8. Molecular formula: C33H47NO13. Mole weight: 665.73. Purity: 0.993. IUPACName: (1R,3S,5R,7R,8E,12R,14E,16E,18E,20E,22R,24S,25R,26S)-22-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-1,3,26-trihydroxy-12-methyl-10-oxo-6,11,28-trioxatricyclo[22.3.1.05,7]octacosa-8,14,16,18,20-pentaene-25-carboxylic acid. Canonical SMILES: C[C@@H]1C/C=C/C=C/C=C/C=C/[C@@H](C[C@H]2[C@@H]([C@H](C[C@](O2)(C[C@H](C[C@@H]3[C@H](O3)/C=C/C(=O)O1)O)O)O)C(=O)O)O[C@H]4[C@H]([C@H]([C@@H]([C@H](O4)C)O)N)O. Density: 1.0 at 20°C(lit.) g/ml. Product ID: ACM7681938-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Natamycin | Pimaricin. cataract treatment. CAS No. 7681-93-8. Product ID: 8-01367. Molecular formula: C33H47NO13. Mole weight: 665.72. | |
| Natamycin | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Natamycin | Natamycin. Group: Food ingredients. Pack Sizes: 25Kgs Bags. |  |
| Natamycin | Pimaricin is a macrocyclic tetraene originally isolated from Streptomyces natalensis in 1957. Pimaricin exhibits broad spectrum antifungal activity against yeast and filamentous fungi by binding specifically to ergosterol to block fungal growth. Unlike the related polyenes, nystatin and filipin, pimaricin does not change the permeability of the plasma membrane. Pimaricin is used in the food industry for surface treatment of cheeses as a mould inhibitor. Group: Biochemicals. Alternative Names: Pimaricin; Antibiotic A 5283; Tennecetin; Cl-12625; Mycophyt; Myprozine; Natacyn; Synogil. Grades: Highly Purified. CAS No. 7681-93-8. Pack Sizes: 100mg. Molecular Formula: C??H??NO??, Molecular Weight: 665.73. US Biological Life Sciences. | Worldwide |
| Natamycin (Pimaricin) | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C33H47NO13. CAS No. 7681-93-8. Prepack ID 10237077-1g. Molecular Weight 665.73. See USA prepack pricing. |  |
| N-a-t-Boc-N-g-trityl-asparagine | N-a-t-Boc-N-g-trityl-asparagine. Group: Biochemicals. Grades: Highly Purified. CAS No. 132388-68-2. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Na-t-Butoxycarbonyl-Ne-(2-picolinoyl)-L-lysine 99+% (TLC) | Na-t-Butoxycarbonyl-Ne-(2-picolinoyl)-L-lysine 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 122532-80-3. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Nateglinide | Nateglinide. Group: Biochemicals. Grades: Purified. CAS No. 105816-04-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Nateglinide | Nateglinide(Starlix) is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas. It achieves this by closing ATP-dependent potassium channels in the membrane of the β cells. Uses: Hypoglycemic agents. Synonyms: DJN 608; DJN-608l; DJN608; Nateglinide; Fastic; Starlix; A-4166; A 4166; A4166. Grades: >98%. CAS No. 105816-04-4. Molecular formula: C19H27NO3. Mole weight: 317.42. | |
| Nateglinide | Nateglinide, a D-phenylalanine derivative, is an orally active and short-acting insulinotropic agent and a DPP IV inhibitor. Nateglinide inhibits ATP-sensitive K + channels in pancreatic β-cells. Nateglinide is used for the treatment of type 2 (non-insulin-dependent) diabetes mellitus [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: A4166; Senaglinide. CAS No. 105816-04-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0422. | |
| Nateglinide | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C19H27NO3. CAS No. 105816-04-4. Prepack ID 61864230-1g. Molecular Weight 317.42. See USA prepack pricing. | |
| Nateglinide acyl-β-D-glucuronide | Nateglinide acyl-β-D-glucuronide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-[[trans-4-(1-Methylethyl)cyclohexyl]carbonyl]-D-phenylalanine β-D-Glucopyranuronic Acid. Product Category: Heterocyclic Organic Compound. Appearance: Off-White Solid. CAS No. 183996-85-2. Molecular formula: C25H35NO9. Mole weight: 493.55. Purity: 0.96. IUPACName: (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(2R)-3-phenyl-2-[(4-propan-2-ylcyclohexanecarbonyl)amino]propanoyl]oxyoxane-2-carboxylic acid. Canonical SMILES: CC(C)C1CCC(CC1)C(=O)NC(CC2=CC=CC=C2)C(=O)OC3C(C(C(C(O3)C(=O)O)O)O)O. Product ID: ACM183996852. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nateglinide acyl glucuronide | An impurity of Nateglinide, which is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas. Synonyms: Nateglinide Acyl-β-D-glucuronide; N-[[trans-4-(1-Methylethyl)cyclohexyl]carbonyl]-D-phenylalanine β-D-Glucopyranuronic Acid. Grades: > 95%. CAS No. 183996-85-2. Molecular formula: C25H35NO9. Mole weight: 493.56. | |
| Nateglinide EP Impurity E | An impurity of Nateglinide, which is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas. Synonyms: Nateglinide Ethyl Analog; 4-Desisopropyl-4-ethyl Nateglinide; trans-N-[(4-Ethylcyclohexyl)carbonyl]-D-phenylalanine. Grades: > 95%. CAS No. 105746-45-0. Molecular formula: C18H25NO3. Mole weight: 303.4. | |
| Nateglinide EP Impurity F | An impurity of Nateglinide, which is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas. Synonyms: D-Phenylalanyl Nateglinide; N-[[trans-4-(1-Methylethyl)cyclohexyl]carbonyl]-D-phenylalanyl-D-phenylalanine; N-[(trans-4-Isopropylcyclohexyl)carbonyl]-D-phenylalanyl-D-phenylalanine. Grades: > 95%. CAS No. 944746-48-9. Molecular formula: C28H36N2O4. Mole weight: 464.61. | |
| Nateglinide EP Impurity G | An impurity of Nateglinide, which is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas. Synonyms: Nateglinide Ethyl Ester; N-[[trans-4-(1-Methylethyl)cyclohexyl]carbonyl]-D-phenylalanine Ethyl Ester. Grades: > 95%. CAS No. 187728-85-4. Molecular formula: C21H31NO3. Mole weight: 345.49. | |
| Nateglinide ethyl ester | Nateglinide ethyl ester. Group: Biochemicals. Alternative Names: N-[[trans-4- (1-Methylethyl) cyclohexyl]carbonyl]-D-phenylalanine ethyl ester. Grades: Highly Purified. CAS No. 187728-85-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C21H31NO3. US Biological Life Sciences. | Worldwide |
| Nateglinide-phenyl-d5 | A labeled version of Nateglinide, an Amino-acid derivative that stimulates insulin secretion which is used as an antidiabetic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Nateglinide Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Nateglinide Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Nateglinide (Starlix, A-4166, N-[[trans-4- (1-methylethyl) cyclohexyl]carbonyl]-D-phenylalanine, ) | An Amino-acid derivative that stimulates insulin secretion. Used as an antidiabetic. Group: Biochemicals. Alternative Names: Starlix, A-4166, N-[[trans-4- (1-methylethyl) cyclohexyl]carbonyl]-D-phenylalanine. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Na-(tert-Butyloxycarbonyl)-Na-benzyl-D-alanine 99+% (HPLC) | Na-(tert-Butyloxycarbonyl)-Na-benzyl-D-alanine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Na-(tert-Butyloxycarbonyl)-Na-benzyl-L-alanine 99+% (HPLC) | Na-(tert-Butyloxycarbonyl)-Na-benzyl-L-alanine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Native 6-phospho-D-gluconate dehydrogenase from E. coli | In enzymology, a phosphogluconate dehydrogenase (decarboxylating) (EC 1.1.1.44) is an enzyme that catalyzes the chemical reaction:6-phospho-D-gluconate + NADP+<-> D-ribulose 5-phosphate + CO2 + NADPH. Thus, the two substRates of this enzyme are 6-phospho-D-gluconate and NADP+, whereas its 3 products are D-ribulose 5-phosphate, CO2, and NADPH. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Applications: Determination of d-gluconate and d-glucono-δ-lactone in foodstaffs. Group: Enzymes. Synonyms: 6-Phosphogluconic Dehydrogenase; phosphogluconic acid dehydrogenase; 6-phosphogluconic dehydrogenase; 6-phosphogluconic carboxylase; 6-phosphogluconate dehydrogenase (decarboxylating); 6-phospho-D-gluconate dehydrogenase; EC 1.1.1.44; p. Enzyme Commission Number: EC 1.1.1.44. CAS No. 9073-95-4. 6-Phosphogluconic Dehydrogenase. Activity: > 150 UI/ml, > 45 U/mg. Storage: 4°C. Form: Suspension in Ammonium Sulphate. Source: E. coli. 6-Phosphogluconic Dehydrogenase; phosphogluconic acid dehydrogenase; 6-phosphogluconic dehydrogenase; 6-phosphogluconic carboxylase; 6-phosphogluconate dehydrogenase (decarboxylating); 6-phospho-D-gluconate dehydrogenase; EC 1.1.1.44; phosphogluconate dehydrogenase; decarboxylating; 9073-95-4. Cat No: NATE-1167. |  |
| Native Abalone β-Glucuronidase | β-glucuronidase catalyzes the breakdown of complex carbohydrates. In humans it converts conjugated bilirubin into the unconjugated form, making bilirubin suitable for reabsorption. Group: Enzymes. Synonyms: β-glucuronide glucuronohydrolase glucuronidase; exo-β-D-glucuronidase; ketodase; EC 3.2.1.31; 9001-45-0; β-D-glucuronoside glucuronosohydrolase; GUSB. Enzyme Commission Number: EC 3.1.2.31. CAS No. 9001-45-0. GUSB. Activity: 1,500,000-3,000,000 units/g solid or > 100,000 units/mL. Form: lyophilized powder, Supplied as a lyophilized powder containing citric acid or aqueous solution, Supplied as an aqueous solution containing 0.85% NaCl and 0.02% sodium azide. Source: Abalone. β-glucuronide glucuronohydrolase glucuronidase; exo-β-D-glucuronidase; ketodase; EC 3.2.1.31; 9001-45-0; β-D-glucuronoside glucuronosohydrolase; GUSB. Cat No: NATE-0328. | |
| Native Abalone Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of sulfa...ne conjugates from hamster embryo fibroblasts. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 20-40 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Abalone entrails. Species: Abalone. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0685. | |
| Native Acetyl esterase from Microbial | Catalyzed reaction: Hydrolysis of acetyl esters. Known substrates: Acetylated xylan, ethyl acetate, cephalosporin C and derivatives. Applications: Desacetylation of β-lactam antibiotics; broad range esterase; desacethylation of other substartes. Group: Enzymes. Synonyms: Acetyl esterase (Lyophilized); Acetyl esterase; EC 3.1.1.72. Enzyme Commission Number: EC 3.1.1.72. Acetylxylan esterase. Activity: > 50 U/mg of powder. Storage: Store at -20°C. Form: Lyophilized. Source: Microbial. Acetyl esterase (Lyophilized); Acetyl esterase; EC 3.1.1.72. Cat No: NATE-1169. | |
| Native Achromobacter lyticus Achromopeptidase | Lysyl endopeptidase (EC 3.4.21.50, Achromobacter proteinase I, Achromobacter lyticus alkaline proteinase I, protease I, achromopeptidase, lysyl bond specific proteinase) is an enzyme. This enzyme catalyses the following chemical reaction:Preferential cleavage:Lys-, including-Lys-Pro-. This enzyme is isolated from Achromobacter lyticus. Group: Enzymes. Synonyms: Achromobacter proteinase I; Achromobacter lyticus alkaline proteinase I; protease I; achromopeptidase; lysyl bond specific proteinase; EC 3.4.21.50; 123175-82-6; Lysyl endopeptidase. Enzyme Commission Number: EC 3.4.21.50. CAS No. 123175-82-6. Achromopeptidase. Storage: -20°C. Form: lyophilized powder, Protein ~5 % by biuret, 300-600 units/mg solid. Source: Achromobacter lyticus. Achromobacter proteinase I; Achromobacter lyticus alkaline proteinase I; protease I; achromopeptidase; lysyl bond specific proteinase; EC 3.4.21.50; 123175-82-6; Lysyl endopeptidase. Cat No: NATE-0021. | |
| Native Acid Phosphatase from Microbial | Acid phosphatases (APase) are a family of enzymes that non-specifically catalyze the hydrolysis of monoesters and anhydrides of phosphoric acid to produce inorganic phosphate at an optimum pH of 4 to 7. Acid phosphatase from potatoes is a 111 kDa diner consisting of two subunits at 41 and 35 kDa. This phosphatase has also been shown to cleave DNA. Applications: Hydrolysis of phosphate monoesters. Group: Enzymes. Synonyms: acid phosphatase; 9001-77-8; acid phosphomonoesterase; phosphomonoesterase; glycerophosphatase; acid monophosphatase; acid phosphohydrolase; acid phosphomonoester hydrolase; uteroferrin; acid nucleoside diphosphate phosphatase; orthophosphoric-monoester phosphohydrolase (acid optimum); EC 3.1.3.2; APase. Enzyme Commission Number: EC 3.1.3.2. CAS No. 9001-77-8. Apase. Activity: > 40 U/mg; > 100 U/ml. Storage: 4°C. Form: Suspension in Ammonium Sulphate. Source: Microbial. acid phosphatase; 9001-77-8; acid phosphomonoesterase; phosphomonoesterase; glycerophosphatase; acid monophosphatase; acid phosphohydrolase; acid phosphomonoester hydrolase; uteroferrin; acid nucleoside diphosphate phosphatase; orthophosphoric-monoester phosphohydrolase (acid optimum); EC 3.1.3.2; APase. Cat No: NATE-1170. | |
| Native Acremonium sp. Ascorbate Oxidase | In enzymology, a L-ascorbate oxidase (EC 1.10.3.3) is an enzyme that catalyzes the chemical reaction:2 L-ascorbate + O2<-> 2 dehydroascorbate + 2 H2O. Thus, the two substRates of this enzyme are L-ascorbate and O2, whereas its two products are dehydroascorbate and H2O. This enzyme belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with oxygen as acceptor. This enzyme participates in ascorbate metabolism. It employs one cofactor, copper. Applications: This enzyme is useful for avoidance from interference of ascorbic acid on diagnostic assay such as blood, uric acid, tg, tc and creatinine. Group: Enzymes. Synonyms: ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate:O2 oxidoreductase;. Enzyme Commission Number: EC 1.10.3.3. CAS No. 9029-44-1. AAO. Mole weight: 80 kDa?gel filtration?. Activity: > 200 U/mg. Appearance: Light blue amorphous powder, lyophilized. Storage: Storage at ?20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Acremonium sp. ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate:O2 oxidoreductase; AA oxidase; EC 1.10.3.3; L-ascorbate oxidase. Cat No: NATE-0864. | |
| Native Actinobacillus sp. Creatinase | In enzymology, a creatinase (EC 3.5.3.3) is an enzyme that catalyzes the chemical reaction:creatine + H2O? sarcosine + urea. Thus, the two substrates of this enzyme are creatine and H2O, whereas its two products are sarcosine and urea. This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amidines. Creatinase accelerates the conversion reaction of creatine and water molecule to sarcosine and urea. It always acts in homodimer state and is induced by choline chloride. Applications: Creatinase mixed with sarcosine oxidase may be used to determine the level of creatine in different ph, temperature, enzyme ratio, and buffer concentration. it may also be used to determine the plasma creatinine level by using a centrifugal analyser. Group: Enzymes. Synonyms: Creatine amidinohydrolase; creatinase; 37340-58-2; EC 3.5.3.3. Enzyme Commission Number: EC 3.5.3.3. CAS No. 37340-58-2. Mole weight: mol wt ~100 kDa. Activity: 6.0 U/mg-solid or more. Storage: -20°C. Form: Lyophilized powder containing sugars and EDTA as stabilizers. Source: Actinobacillus sp. Creatine amidinohydrolase; creatinase; 37340-58-2; EC 3.5.3.3. Cat No: NATE-0160. | |
| Native Aerobacter aerogenes Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage o...17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 2-5 units/mg protein (biuret), 10-20 units/mL. Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol containing 0.01 M Tris, pH 7.5. Source: Aerobacter aerogenes. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0686. | |
| Native Aerococcuss viridans Lactate Oxidase | Native Aerococcuss viridans Lactate Oxidase. Native lactate oxidase (ec 1.13.12.4) was purified from aerococcuss viridans. Group: Enzymes. Synonyms: lactate 2-monooxygenase; EC 1.13.12.4; (S)-lactate: oxygen 2-oxidoreductase (decarboxylating); lactate oxidative decarboxylase; lactate oxidase; lactic oxygenase; lactate oxygenase; lactic oxidase; L-lactate monooxygenase; lactate monooxygenase; L-lactate-2-monooxygenase. Enzyme Commission Number: EC 1.13.12.4. CAS No. 9028-72-2. Lactate oxidase. Activity: > 20 U/mg. Appearance: Yellowish powder. Storage: Store in tightly closed containers, desiccated, protected from light, at-20°C. Form: Freeze dried powder. Source: Aerococcuss viridans. lactate 2-monooxygenase; EC 1.13.12.4; (S)-lactate: oxygen 2-oxidoreductase (decarboxylating); lactate oxidative decarboxylase; lactate oxidase; lactic oxygenase; lactate oxygenase; lactic oxidase; L-lactate monooxygenase; lactate monooxygenase; L-lactate-2-monooxygenase. Cat No: DIA-156. | |
| Native Aerococcuss viridans Pyruvate oxidase | In enzymology, a pyruvate oxidase (EC 1.2.3.3) is an enzyme that catalyzes the chemical reaction: pyruvate + phosphate + O2 <-> acetyl phosphate + CO2 + H2O2. The 3 substrates of this enzyme are pyruvate, phosphate, and O2, whereas its 3 products are acetyl phosphate, CO2, and H2O2. Native pyruvate oxidase (ec 1.2.3.3) was purified from aerococcuss viridans. Applications: Useful for enzymatic determination of ast and alt. Group: Enzymes. Synonyms: pyruvate oxidase; EC 1.2.3.3; pyruvate: oxygen 2-oxidoreductase (phosphorylating); pyruvic oxidase; phosphate-dependent pyruvate oxidase. Enzyme Commission Number: EC 1.2.3.3. CAS No. 9001-96-1. Pyruvate oxidase. Activity: > 25 U/mg. Appearance: Yellowish powder. Storage: Store in tightly closed containers, desiccated, protected from light, at-20°C. Form: Freeze dried powder. Source: Aerococcuss viridans. pyruvate oxidase; EC 1.2.3.3; pyruvate: oxygen 2-oxidoreductase (phosphorylating); pyruvic oxidase; phosphate-dependent pyruvate oxidase. Cat No: DIA-169. | |
| Native Aerococcus viridans Glycerol 3-phosphate Oxidase | In enzymology, a glycerol-3-phosphate oxidase (EC 1.1.3.21) is an enzyme that catalyzes the chemical reaction:sn-glycerol 3-phosphate + O2<-> glycerone phosphate + H2O2. Thus, the two substrates of this enzyme are sn-glycerol 3-phosphate and O2, whereas its two products are glycerone phosphate and H2O2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with oxygen as acceptor. This enzyme participates in glycerophospholipid metabolism. It employs one cofactor, FAD. Group: Enzymes. Synonyms: EC 1.1.3.21; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-α-glycerophosphate oxidase; α-glycerophosphate oxidase; L-α-glycerol-3-phosphate oxidase; Glycerol 3-phosph. Enzyme Commission Number: EC 1.1.3.21. CAS No. 9046-28-0. Glycerol-3-phosphate oxidase. Activity: > 70 units/mg solid. Storage: -20°C. Form: Lyophilized powder containing sucrose. Source: Aerococcus viridans. EC 1.1.3.21; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-α-glycerophosphate oxidase; α-glycerophosphate oxidase; L-α-glycerol-3-phosphate oxidase; Glycerol 3-phosphate Oxidase; 9046-28-0; sn-Glycerol 3-phosphate:oxygen 2-oxidoreductase; L-Glycerol 3-phosphate Oxidase; GPO. Cat No: NATE-0314. | |
| Native Aeromonas proteolytica Aminopeptidase | Aminopeptidase from Aeromonas proteolytica is a metalloenzyme, which contains 2 atoms of Zn2+ in a single polypeptide with an approximate molecular weight of 29.5 kDa as determined by sedimentation. This enzyme has a high degree of stability, being stable even at tempeRatures of 70°C for several hours. Partial inactivation occurs in 8 M urea. Maximum stability and activity are between pH 8.0-8.5. Aminopeptidase from Aeromonas proteolytica can function as an esterase. Applications: Aminopeptidases are a family of widely distributed proteases, which may be used to study many significant biological processes such as protein maturation, hormone production, and peptide digestion. the enzyme has been used to measure the kinetic rate constant for the binding of bestatin, a general protease inhibitor, to aminopeptidase. Group: Enzymes. Synonyms: Aminopeptidase; 37288-67-8; EC 3.4.11.10; Aeromonas proteolytica aminopeptidase. Enzyme Commission Number: EC 3.4.11.10. CAS No. 37288-67-8. Aminopeptidase. Storage: -20°C. Form: lyophilized powder, 50-150 units/mg protein. Source: Aeromonas proteolytica. Aminopeptidase; 37288-67-8; EC 3.4.11.10; Aeromonas proteolytica aminopeptidase. Cat No: NATE-0071. | |
| Native Agaricus bisporus Laccase | Laccase is a blue copper oxidase that reduces molecular oxygen to water. Laccase oxidizes polyphenols, methoxy-substituted phenols and diamines, but not tyrosine. Oxidation by laccase is an one-electron reaction that generates a free radical. Applications: Laccase is polyphenol oxidase found in many plants, fungi and microorganisms. laccases may be useful in enzymatic biofuel systems, teeth whitening, textile dyeing, and in other applications that require the removal of oxygen. Group: Enzymes. Synonyms: Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Enzyme Commission Number: EC 1.10.3.2. CAS No. 80498-15-3. Laccase. Activity: > 4 units/mg. Storage: -20°C. Form: powder; deep brown. Source: Agaricus bisporus. Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Cat No: NATE-0370. | |
| Native Alcaligenes faecalis 3-Hydroxybutyrate Dehydrogenase | In mammalian systems, β-hydroxybutyrate dehydrogenase is localized on the inner mitochondrial membrane and requires phosphatidyl choline for activity. In contrast, the enzyme from Pseudomonas is a soluble cytosolic enzyme that does not require a phospholipid allosteric activator. The enzyme is required for the utilization of ketone bodies as a source of metabolic energy. It catalyzes the oxidation of 3-hydroxybutyrate to acetoacetate, the first step in the conversion of ketone bodies to citric acid, which is then further metabolized via the tricarboxylic acid cycle (Krebs cycle). Is an enzyme produced by microorganisms. this product shall be used for a diag...Enzyme Commission Number: EC 1.1.1.30. CAS No. 9028-38-0. 3-HBDH. Mole weight: 60±5 kDa (TSK G-3000SW); 30±5 kDa (SDS-PAGE). Activity: > 1,500 U/mg. Appearance: White powder. Storage: -20°C. Form: Freeze dried powder. Source: Alcaligenes faecalis. 3-hydroxybutyrate dehydrogenase; 3-HBDH; NAD-β-hydroxybutyRate dehydrogenase; hydroxybutyRate oxidoreductase; β-hydroxybutyRate dehydrogenase; D-β-hydroxybutyRate dehydrogenase; D-3-hydroxybutyRate dehydrogenase; D-(-)-3-hydroxybutyRate dehydrogenase; β-hydroxybutyric acid dehydrogenase; 3-D-hydroxybutyRate dehydrogenase; β-hydroxybutyric dehydrogenase; EC 1.1.1.30; 9028-38-0. Cat No: NATE-0005. | |
| Native Alcaligenes sp. Choline Oxidase | In enzymology, a choline oxidase (EC 1.1.3.17) is an enzyme that catalyzes the chemical reaction: choline + O2<-> betaine aldehyde + H2O2. Thus, the two substrates of this enzyme are choline and O2, whereas its two products are betaine aldehyde and H2O2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with oxygen as acceptor. Applications: This enzyme is useful for enzymatic determination of phospholipids when coupled with phospholipase d and for choline esterase-activity in clinical analysis. Group: Enzymes. Synonyms: choline oxidase; EC 1.1.3.17. Enzyme Commission Number: EC 1.1.3.17. CAS No. 9028-67-5. Choline Oxidase. Mole weight: approx. 95 kDa. Activity: GradeIII 10U/mg-solid or more (containing approx. 20% of stabilizers). Stability: Stable at-20°C for at least 6 months. Appearance: Yellowish amorphous powder, lyophilized. Form: Freeze dried powder. Source: Alcaligenes sp. choline oxidase; EC 1.1.3.17. Cat No: DIA-184. | |
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