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| Product | Description | |
|---|---|---|
| Naquotinib | Naquotinib (ASP8273) is an orally available, mutant-selective and irreversible EGFR inhibitor; with IC50s of 8-33 nM toward EGFR mutants and 230 nM for EGFR. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ASP8273. CAS No. 1448232-80-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19729. |  |
| N-Arachidonoyl-serotonin | N-Arachidonoyl-serotonin. Group: Biochemicals. Grades: Highly Purified. CAS No. 187947-37-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C20H42N2O2. US Biological Life Sciences. |  Worldwide |
| N-Arachidonylglycine | N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endocannabinoid anandamide (AEA), is a GPR18 agonist (EC50 = 44.5 nM). Unlike AEA, N-Arachidonylglycine has no activity at either CB1 or CB2 receptors. N-Arachidonylglycine inhibits GLYT2 (IC50 = 5.1 μM). N-Arachidonylglycine also is an effective activator of endometrial cell migration[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NA-Gly. CAS No. 179113-91-8. Pack Sizes: 5 mg (138.30 mM * 100 μL in Ethanol); 10 mg (138.30 mM * 200 μL in Ethanol); 25 mg (138.30 mM * 500 μL in Ethanol); 50 mg (138.30 mM * 1 mL in Ethanol); 100 mg (138.30 mM * 2 mL in Ethanol). Product ID: HY-103332. | |
| Narasin | Narasin is the main component of a polyether antibiotic complex produced by Streptomyces auriofaciens NRRL 5758 & NRRL 8092. Ionophoric antibiotic which inhibits coccidial infection in poultry and mammals. Coccidiostat; growth stimulant. Group: Biochemicals. Alternative Names: (4S)-4-Methylsalinomycin; A 28086A; Antibiotic A 28086A; Antibiotic C 7819B; C 7819B; Monteban; Narasin A; Narasul. Grades: Highly Purified. CAS No. 55134-13-9. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C??H??O??, Molecular Weight: 765.03. US Biological Life Sciences. | Worldwide |
| Narasin A | Narasin A is a polyether antibiotic produced by Str. aureofaciena NRRL 5758. It has anti-gram-positive bacteria, anaerobic bacteria, mycoplasma and coccidia activity, and also has antiviral effect. Synonyms: Salinomycin, 4-methyl-, (4S)-; (4S)-4-Methylsalinomycin; A 28086A; Antibiotic A 28086A; Antibiotic C 7819B; C 7819B; Monteban; Narasin A; Narasul. Grade: ≥98% by HPLC. CAS No. 55134-13-9. Molecular formula: C43H72O11. Mole weight: 765.02. |  |
| Narasin B | Narasin B is a polyether antibiotic produced by Str. aureofaciena NRRL 5758. It has anti-gram-positive bacteria, anaerobic bacteria, mycoplasma and coccidia activity, and also has antiviral effect. Narasin B has a protective effect on chicken coccidiosis infection. CAS No. 58439-94-4. Molecular formula: C43H70O11. Mole weight: 763.01. | |
| Narasin sodium | It is a polyether antibiotic produced by Str. aureo faciens NRRL 5758. It has broad spectrum activity against gram-positive bacteria, anaerobic bacteria and mycoplasma. It also has antiviral and limited antifungal activity. Synonyms: 4-Methylsalinomycin sodium; 1,6,8-Trioxadispiro[4.1.5.3]pentadecane, Salinomycin deriv.; (4S)-4-Methyl Salinomycin Monosodium Salt; Monteban sodium; Narasin A sodium. Grade: >98% by HPLC. CAS No. 58331-17-2. Molecular formula: C43H71NaO11. Mole weight: 787.01. | |
| Naratriptan-[d3] Hydrochloride | Naratriptan-[d3] Hydrochloride is the labelled salt of Naratriptan, which is a selective 5-HT1 receptor agonist and could be used against migraine headaches. Uses: The hydrochloride salt form of isotope labelled naratriptan. Synonyms: Naratriptan D3 Hydrochloride; N-Methyl-d3-2-[3-(1-methyl-4-piperidyl)-1H-indol-5-yl]-ethanesulfonamide Hydrochloride; Naramig-d3; Amerge-d3; GR-85548A D3. Grade: ≥95%; ≥99% atom D. CAS No. 1190021-64-7. Molecular formula: C17H23D3ClN3O2S. Mole weight: 374.94. | |
| Naratriptan hydrochloride | Naratriptan hydrochloride. Group: Biochemicals. Alternative Names: N-Methyl-2-[3-(1-methyl-4-piperidyl)-1H-indol-5-yl]ethanesulfonamide hydrochloride; Naramig; Amerge. Grades: Highly Purified. CAS No. 143388-64-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C17H26ClN3O2S. US Biological Life Sciences. | Worldwide |
| Naratriptan hydrochloride | Naratriptan (GR-85548A) hydrochloride is a selective 5-HT1B/1D receptor agonist. Naratriptan hydrochloride is peripherally active and has good oral bioavailability, inducing cranial artery vasoconstriction by activating 5-HT1B/1D receptors (EC50=0.11 μM for dog basilar artery). Naratriptan hydrochloride also inhibits trigeminal nerve-mediated dural neurogenic plasma extravasation and reduces sterile inflammation. Naratriptan hydrochloride is mainly used in the research of acute migraine, targeting cranial vascular and neuroinflammatory mechanisms[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GR-85548A hydrochloride. CAS No. 143388-64-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-B0197A. | |
| Naratriptan Hydrochloride | Naratriptan Hydrochloride is the hydrochloride salt of naratriptan, a second-generation triptan and selective serotonin 5-HT1B/1D receptor agonist. Among the triptan class, naratriptan is distinguished by the highest bioavailability and longest elimination half-life, attributed in part to its piperidine ring structure replacing the pyrrolidine or ethylamine groups found in other triptans. Applications: Indicated for the acute treatment of migraine attacks. naratriptan hydrochloride is a second-generation triptan with the highest oral bioavailability and longest elimination half-life among triptans, providing sustained migraine relief with convenient dosing and favorable tolerability. Category: Active pharmaceutical ingredients. Synonyms: N-Methyl-2-[3-(1-methyl-4-piperidyl)-1H-indol-5-yl]-ethanesulfonamide Hydrochloride;Naratriptan HCl. CAS No. 143388-64-1. Product ID: API143388641. Molecular formula: C17H26ClN3O2S. Mole weight: 371.9. InChIKey: AWEZYKMQFAUBTD-UHFFFAOYSA-N. Appearance: White to off-white powder. |  |
| Naratriptan impurity 1 | Naratriptan impurity 1. Uses: For analytical and research use. Molecular formula: C20H31N3O4S2. Mole weight: 441.61. Catalog: APB11527. |  |
| Naratriptan N-Oxide | A potential metabolite of Naratriptan. Group: Biochemicals. Alternative Names: N-Nethyl-3-(1-methyl-1-oxido-4-piperidinyl)-1H-indole-5-ethanesulfonamide. Grades: Highly Purified. CAS No. 1159977-52-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Naratuximab | Naratuximab (Anti-TSPAN26/CD37 Reference Antibody (naratuximab)) is a humanized monoclonal antibody that binds CD37 (TSPAN26). Naratuximab can be used to synthesize an ADC compound, Naratuximab emtansine[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Anti-TSPAN26/CD37 Reference Antibody (naratuximab). CAS No. 1622327-39-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99374. | |
| Naratuximab emtansine | Naratuximab emtansine (IMGN529) is a CD37-targeted ADC consisting of a humanized IgG1 mAb coupled to the microtubule disruptor DM1. Naratuximab emtansine has high affinity and specificity for CD37, allowing ADC internalization, processing and intracellular release of DM1. Due to its ability to disrupt microtubule assembly, DM1 can subsequently induce cell cycle arrest and apoptosis[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: IMGN529; Debio 1562. CAS No. 1607824-64-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-132260. | |
| Narazaciclib | Narazaciclib (ON123300), a strong and brain-penetrant[1] multi-kinase inhibitor, inhibits CDK4 (IC50=3.9 nM), Ark5 (IC50=5 nM), PDGFRβ (IC50=26 nM), FGFR1 (IC50=26 nM), RET (IC50=9.2 nM), and FYN (IC50=11 nM). Single agent Narazaciclib causes a dose-dependent suppression of phosphorylation of Akt as well as activation of Erk in brain tumors[2]. Narazaciclib inhibits CDK6 with an IC50 of 9.82 nM[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: ON123300. CAS No. 1357470-29-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12624. | |
| Narbomycin | Narbomycin is produced by the strain of Str. narbonensis ETH 7346. It has anti-gram-positive bacterial activity and is cross-resistance with amycin. And it has no protective effect on mice infected with Streptococcus pyogenes. Synonyms: 12-Deoxypicromycin; SureCN691770; (3R,5R,6S,7S,9R,11E,13R,14R)-14-ethyl-3,5,7,9,13-pentamethyl-2,4,10-trioxooxacyclotetradec-11-en-6-yl 3,4,6-trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranoside. Grade: >98%. CAS No. 6036-25-5. Molecular formula: C28H47NO7. Mole weight: 509.68. | |
| narbonolide synthase | The product, narbonolide, contains a 14-membered ring and is an intermediate in the biosynthesis of narbonomycin and pikromycin in the bacterium Streptomyces venezuelae. The enzyme also produces 10-deoxymethynolide (see EC 2.3.1.239, 10-deoxymethynolide synthase). The enzyme has 29 active sites arranged in four polypeptides (pikAI - pikAIV) with a loading domain, six extension modules and a terminal thioesterase domain. Each extension module contains a ketosynthase (KS), keto reductase (KR), an acyltransferase (AT) and an acyl-carrier protein (ACP). Not all active sites are used in the biosynthesis. Group: Enzymes. Synonyms: pikromycin PKS. Enzyme Commission Number: EC 2.3.1.240. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2189; narbonolide synthase; EC 2.3.1.240; pikromycin PKS. Cat No: EXWM-2189. |  |
| Narciclasine | Narciclasine is a plant growth modulator. Narciclasine modulates the Rho/Rho kinase/LIM kinase/cofilin signaling pathway, greatly increasing GTPase RhoA activity as well as inducing actin stress fiber formation in a RhoA-dependent manner. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Lycoricidinol. CAS No. 29477-83-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-16563. | |
| Narciclasine | Narciclasine. Group: Biochemicals. Grades: Purified. CAS No. 29477-83-6. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Narcissin | Narcissin. Group: Biochemicals. CAS No. 604-80-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Narcissin | Narcissin (Narcissoside), a flavonol glycoside, exhibits evident scavenging activity against both authentic ONOO- and SIN-1-derived ONOO- with IC50s?of 3.5 and 9.6 μM, respectively[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Narcissoside. CAS No. 604-80-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 20 mg. Product ID: HY-N0649. | |
| Narcissin | Narcissoside is extracted from the bulbus of Narcissus tazettaL. var. chinensis Roem. It could be responsible for stronger protection against mitochondrial induced oxidative stress with synergism of rutin in B.flavum flavonoid. Synonyms: Narcissoside; 604-80-8; Narcissin; Isorhamnetin 3-rutinoside; Narcissin Flavonol; Isorhamnetin-3-O-rutinoside; Isorhamnetin 3-O-rutinoside; Isorhamnetin 3-rhamnoglucoside; Isprhamnetin-3-rutinoside; UNII-N4AX11L1TF; N4AX11L1TF; 3-O-RUTINOSYLISORHAMNETIN; C28H32O16; 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetra. Grade: >98%. CAS No. 604-80-8. Molecular formula: C30H46O3. Mole weight: 454.7. | |
| Narcissoside | Narcissoside. Group: Biochemicals. Alternative Names: Isorhamnetin 3-rutinoside; Narcissin. Grades: Plant Grade. CAS No. 604-80-8. Pack Sizes: 20mg. Molecular Formula: C28H32O16, Molecular Weight: 624.544. US Biological Life Sciences. | Worldwide |
| nardilysin | Enzyme of 133 kDa from rat brain and testis. A homologue of pitrilysin containing the His-Phe-Leu-Glu-His zinc-binding sequence, and a highly acidic stretch of 71 residues. Unusually for a metalloendopeptidase, inhibited by bestatin, amastatin and N-ethylmaleimide. In peptidase family M16 (pitrilysin family). Group: Enzymes. Synonyms: N-arginine dibasic convertase; NRD-convertase. Enzyme Commission Number: EC 3.4.24.61. CAS No. 292850-69-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4344; nardilysin; EC 3.4.24.61; 292850-69-2; N-arginine dibasic convertase; NRD-convertase. Cat No: EXWM-4344. | |
| Nardoeudesmol A | Nardoeudesmol A is a natural compound derived from Nardostachys chinensis. With its potent anti-inflammatory and anti-cancer properties, this molecule holds potential in the biomedical industry for the development of drugs targeting various diseases, such as inflammation-related disorders and certain types of cancers. Grade: 96.5%. CAS No. 1445952-30-6. Molecular formula: C15H24O2. Mole weight: 236.354. | |
| Nardosinone | Nardosinone, coming from the roots of Nardostachys jatamansi DC, enhances staurosporine- or dbcAMP-induced neurite outgrowth from PC12D cells, probably by amplifying both the MAP kinase-dependent and -independent signaling pathways of dbcAMP and staurosporine. It could protect against the neuronal injury exposed to OGD, which may be relevant to the promotion of PKA and ERK signaling pathway. Uses: Antidepressant/sedative. Synonyms: (3aR)-1,3aβ,4,7,8,9,9a,9bβ-Octahydro-1,1,9β,9aβ-tetramethyl-5H-naphtho[2,1-c][1,2]dioxol-5-one; 1,1,9β,9aβ-Tetramethyl-3aβ,7,8,9,9a,9bβ-hexahydro-1H-naphtho[2,1-c][1,2]dioxole-5(4H)-one; (3aR,9R,9aR,9bS)-1,3a,4,7,8,9,9a,9b-Octahydro-1,1,9,9a-tetramethyl-5H-naphtho[2,1-c][1,2]dioxol-5-one; 5H-Naphtho[2,1-c][1,2]dioxol-5-one,1,3a,4,7,8,9,9a,9b-octahydro-1,1,9,9a-tetramethyl-, (3aR,9R,9aR,9bS)-. Grade: >98%. CAS No. 23720-80-1. Molecular formula: C15H22O3. Mole weight: 250.33. | |
| Nardosinone | Nardosinone. Group: Biochemicals. Grades: Plant Grade. CAS No. 23720-80-1. Pack Sizes: 20mg. Molecular Formula: C15H22O3, Molecular Weight: 250.33. US Biological Life Sciences. | Worldwide |
| Nardozeste | Nardozeste. CAS No. MIXTURE. VIGON Item # 503242. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Nargenicin | It is a 10-membered macrocyclic lactone antibiotic produced by Nocardia sp. It exhibits potent activity against gram-positive bacteria. It has been shown to enhance retinoate-induced cell differentiation. Synonyms: Nargenicin B1; CP 51467; Antibiotic CP 51467. Grade: >99% by HPLC. CAS No. 75923-01-2. Molecular formula: C28H37NO8. Mole weight: 515.60. | |
| Nargenicin A1 | Nargenicin A1 is a macrolide antibiotic produced by Nocardia sp. that is effective against Gram-positive bacteria including taphylococcus and Clostridia. It shows more potent efficacy against methicilin resistant S. aureus (MRSA) than erythromycin and vancomycin. Synonyms: Antibiotic 47444; CP 47444; NSC 355066; Nodusmicin 9-(1H-pyrrole-2-carboxylate); 1H-Pyrrole-2-carboxylic acid,(1E,3R,4S,7S,8aS,10aR,11R,12R,13R,14R,14aS,14bS)-3,4,6,7,8,8a,10a,11,12,13,14,14a-dodecahydro-14-hydroxy-4-[(1R)-1-hydroxyethyl]-7-methoxy-1,3,13-trimethyl-6-oxo-11,14b-epoxy-14bH-naphth[2,1-e]oxecin-12-yl ester. Grade: ≥99%. CAS No. 70695-02-2. Molecular formula: C28H37NO8. Mole weight: 515.60. | |
| Nargenicin A1 | Antibiotic against Gram-positive bacteria, particularly Staphylococcus and Clostridia. More effective against multi-resistant strains (MRSA) than erythromycin and vancomycin. Inhibits cell proliferation and induces HL-60 cell differentiation in combination with 1,25-Dihydroxyvitamin-D3 and ATRA. Displays low cytotoxicity compared to erythromycin and spiramycin. Group: Biochemicals. Alternative Names: Antibiotic 47444; CP 47444; NSC 355066; Nargenicin; Nargenicin A1; Stereoisomer of 3, 4, 6, 7, 8, 8a, 10a, 11, 12, 13, 14, 14a-dodecahydro-14-hydroxy-4-(1-hydroxyethyl)-7-methoxy-1, 3, 13-trimethyl-6-oxo-11, 14b-epoxy-14bH-naphth[2, 1-e]oxecin-12-yl 1H-pyrrole-2-carboxylate; [3R-[1E, 3R*, 4S*(R*), 7S*, 8aS*, 10aR*, 11R*, 12R*, 13R*, 14R*, 14aS*, 14bS*]]-1H-Pyrrole-2-carboxylic acid 3, 4, 6, 7, 8, 8a, 10a, 11, 12, 13, 14, 14a-Decahydro-14-hydroxy-4-(1-hydroxyethyl)-7-methoxy-1, 3, 13-trimethyl-6-oxo-11, 14b-epoxy-14bH-naphth[2, 1-e]oxecin-12-yl Ester; 9-(1H-Pyrrole-2-carboxylate) Nodusmicin. Grades: Highly Purified. CAS No. 70695-02-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C??H??NO?. US Biological Life Sciences. | Worldwide |
| Naringenin | The aglucon of naringin. Naringenin is a flavonoid that is considered to have a bioactive effect on human health as antioxidant, free radical scavenger, anti-inflammatory, carbohydrate metabolism promoter, and immune system modulator. It is the predominant flavanone in grapefruit. This substance has also been shown to reduce oxidative damage to DNA in vitro. Scientists exposed cells to 80 micromoles of naringenin per liter, for 24 hours, and found that the amount of hydroxyl damage to the DNA was reduced by 24% in that very short period of time.Naringenin found in grapefruit juice has been shown to have an inhibitory effect on the human cytochrome P450 isoform CYP1A2, which can change pharmacokinetics in a human (or orthologous) host of several popular drugs in an adverse manner, even resulting in carcinogens of otherwise harmless substances.Naringenin has also been shown to reduce hepatitis C virus production by infected hepatocytes (liver cells) in cell culture. This seem to be secondary to Naringenin ability to inhibit the secretion of very-low-density lipoprotein by the cells.Naringenin seems to protect LDLR-deficient mice from the obesity effects of a high-fat diet.Naringenin lowers the plasma and hepatic cholesterol concentrations by suppressing HMG-CoA reductase and ACAT in rats fed a high-cholesterol diet. Group: Biochemicals. Alternative Names: 2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; (R,S) | Worldwide |
| Naringenin | Naringenin is the predominant flavanone in Citrus reticulata Blanco; displays strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity. Uses: Scientific research. Category: Signaling pathways. CAS No. 480-41-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-N0100. | |
| Naringenin (4',5,7-Trihydroxyflavanone) | 5g Pack Size. Group: Aroma Chemicals, Building Blocks, Flavours and Fragrance Materials. Formula: C15H12O5. CAS No. 480-41-1. Prepack ID 36117021-5g. Molecular Weight 272.25. See USA prepack pricing. |  |
| Naringenin-7-O- β-D-glucoside | Naringenin-7-O- β-D-glucoside. Group: Biochemicals. Alternative Names: Prunin. Grades: Plant Grade. CAS No. 21637-25-2. Pack Sizes: 20mg. Molecular Formula: C21H22O10, Molecular Weight: 434.397. US Biological Life Sciences. | Worldwide |
| Naringenin 7-O- β-D-Glucuronide | Naringenin 7-O- β-D-Glucuronide. Group: Biochemicals. Alternative Names: (2S)-3,4-Dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2H-1-benzopyran-7-yl β-D-Glucopyranosiduronic Acid; Naringenin 7-O- β-D-Glucuronide. Grades: Plant Grade. CAS No. 158196-34-0. Pack Sizes: 10mg. Molecular Formula: C21H20O11, Molecular Weight: 448.38. US Biological Life Sciences. | Worldwide |
| naringenin 7-O-methyltransferase | The enzyme is involved in the biosynthesis of the sakuranetin, an inducible defense mechanism of the plant Oryza sativa (Asian rice) against pathogen attack. Group: Enzymes. Synonyms: NOMT. Enzyme Commission Number: EC 2.1.1.232. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1835; naringenin 7-O-methyltransferase; EC 2.1.1.232; NOMT. Cat No: EXWM-1835. | |
| naringenin 8-dimethylallyltransferase | Requires Mg2+. This membrane-bound protein is located in the plastids. In addition to naringenin, the enzyme can prenylate several other flavanones at the C-8 position, but more slowly. Along with EC 1.14.13.103 (8-dimethylallylnaringenin 2'-hydroxylase) and EC 2.5.1.71 (leachianone G 2''-dimethylallyltransferase), this enzyme forms part of the sophoraflavanone-G-biosynthesis pathway. Group: Enzymes. Synonyms: N8DT. Enzyme Commission Number: EC 2.5.1.70. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2808; naringenin 8-dimethylallyltransferase; EC 2.5.1.70; N8DT. Cat No: EXWM-2808. | |
| Naringenin chalcone | Naringenin chalcone is an orally active intermediate in flavonol biosynthesis. Naringenin chalcone induces Apoptosis. Naringenin chalcone inhibits the production of MCP-1 and NO. Naringenin chalcone exhibits anticancer activity against glioblastoma. Naringenin chalcone has anti-inflammatory and anti-allergic properties[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. CAS No. 73692-50-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N3007. | |
| Naringenin Chalcone | Formula: Group: Biochemicals. Grades: Plant Grade. CAS No. 73692-50-9. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| naringenin-chalcone synthase | In the presence of NADH and a reductase, 6'-deoxychalcone is produced. Group: Enzymes. Synonyms: chalcone synthase; flavanone synthase; 6'-deoxychalcone synthase; chalcone synthetase; DOCS; CHS. Enzyme Commission Number: EC 2.3.1.74. CAS No. 56803-04-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2254; naringenin-chalcone synthase; EC 2.3.1.74; 56803-04-4; chalcone synthase; flavanone synthase; 6'-deoxychalcone synthase; chalcone synthetase; DOCS; CHS. Cat No: EXWM-2254. | |
| Naringenin-d4 | Naringenin-d4 is the deuterated version of Naringenin (HY-N0100). Naringenin shows strong anti-inflammatory and antioxidant activities. Naringenin has anti-dengue virus (DENV) activity[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1192260-78-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N0100S. | |
| Naringin | Naringin. Group: Biochemicals. Alternative Names: Naringenin 7-Rhamnoglucoside; Naringoside; Aurantin; Isohesperidin. Grades: Plant Grade. CAS No. 10236-47-2. Pack Sizes: 20mg. Molecular Formula: C27H32O14, Molecular Weight: 580.535. US Biological Life Sciences. | Worldwide |
| Naringin | Naringin. CAS No. 10236-47-2. Product ID: PE-0326. Category: Active Pharmaceutical Ingredient. Product Keywords: Pharmaceutical Excipients; Other Materials; Active Pharmaceutical Ingredient; /; Naringin; PE-0326; 10236-47-2; 10236-47-2. Grade: Pharmaceutical Grade. |  |
| Naringin | 100g Pack Size. Group: Aroma Chemicals, Biochemicals, Carbohydrates. Formula: C27H32O14. CAS No. 10236-47-2. Prepack ID 14376036-100g. Molecular Weight 580.53. See USA prepack pricing. | |
| Naringin | Naringin inhibits hepatic P-glycoprotein (P-gp) and some drug-metabolizing cytochrome P450 enzymes, including CYP3A4 and CYP1A2, which may result in drug-drug interactions. Naringin can be used as an edible additive, mainly for gum, refreshing drinks, etc. It is a plant polyphenol that can inhibit tyrosinase, block melanin synthesis, reduce skin pigment intensity, absorb UV, prevent photoaging, reduce sun damage and age spot formation, and whiten and lighten spots. It also has the anti-glycation and antibacterial effect, can effectively improve skin tone and skin texture, prevent the generation of age spots, remove red bloodlines, and improve skin blood microcirculation. Uses: Antioxidant, anticancer, anti-atherogenic. Synonyms: Aurantiin; AI3-19008; AI319008; AI3 19008; Naringoside; (2S)-Naringin; Naringenin 7-Rhamnoglucoside; Naringenin 7-O-neohesperidoside; 4',5,7-trihydroxyflavanone 7-rhamnoglucoside; Naringenin-7-beta-neohesperidoside; (2S)-7-[[2-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; K-ALL; KTB 30983; Naringenin 7-β-neohesperidoside; NSC 5548; OYL-BLP; Sanfix Naringin. Grade: >98%. CAS No. 10236-47-2. Molecular formula: C27H32O14. Mole weight: 580.53. | |
| Naringin | Naringin. Applications: 1.anti-inflammatory, anti-viral, anti-mutation, anti-carcinogen. 2.hypotensive activity, function as urogastrone, alleviating pain.3.tranquilizing, lowering blood viscosity , reduce the emerge of the thrombus. Group: Others. Synonyms: Naringin; 10236-47-2. CAS No. 10236-47-2. Purity: 98%, HPLC. Mole weight: C27H32O14; 580.53. Appearance: light white powder. Storage: 24 months with original packing under 18°C. Store in cool dry place,avoid sunlight and high temperature. Source: Extracted from the fruit of Citrus paradisi. Naringin; 10236-47-2; plant extract. Pack: 1kg, 5kg, 10kg aluminum foil vacuum bag; or 20kg, 25kg Fiber Drum. Cat No: EXTW-206. | |
| Naringin | Naringin is a major flavanone glycoside obtained from tomatoes, grapefruits, and many other citrus fruits. Naringin exhibits biological properties such as antioxidant, anti-inflammatory, and antiapoptotic activities. Naringin also inhibits proliferation and invasion and induces apoptosis in human osteosarcoma cells by inhibiting zinc finger E-box binding homeobox 1 (Zeb1)[1][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Naringoside. CAS No. 10236-47-2. Pack Sizes: 10 mM * 1 mL in DMSO; 200 mg; 10 g. Product ID: HY-N0153. | |
| Naringin 99% HPLC | Naringin 99% HPLC. |  CA, FL & NJ |
| Naringinase | Naringinase, a hydrolytic enzymatic complex, possesses the activity of both α-L-rhamnosidase and β-D-glucosidase. Naringinase has wide occurrence in nature. Naringinase can be used in the biotransformation of steroids, antibiotics, and mainly on glycosides hydrolysis[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9068-31-9. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-129217. | |
| Naringin dihydrochalcone | Naringin dihydrochalcone. Group: Biochemicals. Grades: Reagent Grade. CAS No. 18916-17-1. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| NaringinHydrate | NaringinHydrate. Group: Molecular Biology. Grades: Highly Purified. CAS No. 10236-47-2. Pack Sizes: 25g. Molecular Formula: C27H32O14. US Biological Life Sciences. | Worldwide |
| Naringin natural | Naringin natural. CAS No. 10236-47-2. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| 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. Category: Signaling pathways. CAS No. 14259-46-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N0804. | |
| Narirutin | The flavonoid narirutin is one of the active constituents isolated from citrus fruits with antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tubercular potency. 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. Grade: 98%. CAS No. 14259-46-2. Molecular formula: C27H32O14. Mole weight: 580.53. | |
| 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 |
| Narlaprevir | Narlaprevir (SCH 900518) is a selective and orally bioavailable NS3 protease inhibitor with a Ki value of 6 nM and an EC90 value of 40 nM[1]. Narlaprevir also inhibits the HCV nonstructural protein 3 serine protease[2]. Narlaprevir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 2.3 μM[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SCH 900518. CAS No. 865466-24-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10300. | |
| Narlumosbart | Narlumosbart (JMT103) is an IgG4κ antibody targeting receptor activator of nuclear factor-κB ligand (RANKL)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2646587-68-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99966. | |
| Narmafotinib | Narmafotinib (AMP-945) is an orally active inhibitor of the enzyme focal adhesion kinase (FAK, KD=0.21 nM). Narmafotinib inhibits autophosphorylation of 397Y-FAK in MDA-MB-231 cells with an IC50=7 nM and exhibits low general cellular toxicity (IC50=2.7 μM, MDA-MB-231 cells). Narmafotinib can be used for anti-cancer study[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AMP-945. CAS No. 1393653-34-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145652. | |
| 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. Category: Signaling pathways. 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. Group: Biochemicals. Grades: Purified. CAS No. 1217474-40-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| NAS-181 dimesylate | NAS181 is a potent and selective antagonist of rat 5-HT1B receptor, with a Ki of 47 nM. NAS181 shows 13-fold selectivity for r5-HT1B over bovine 5-HT1B receptor (Ki=630 nM). NAS181 increases the 5-HT turnover and the synaptic concentration of 5-HT by inhibiting terminal r5-HT1B autoreceptors[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1217474-40-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103156. | |
| 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. Category: Signaling pathways. Alternative Names: 1-Naphthylacetyl spermine. CAS No. 122306-11-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12506. | |
| Naspm trihydrochloride | Naspm trihydrochloride (1-Naphthylacetyl spermine trihydrochloride), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA (CP-AMPA) receptors antagonist. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 1-Naphthylacetyl spermine trihydrochloride. CAS No. 1049731-36-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12506A. | |
| Naspm trihydrochloride | Naspm trihydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1049731-36-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| NAT | NAT is an initial hit of NAMPT activator with an EC50 of 5.7 μM and a KD of 379 nM. 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. Category: Signaling pathways. CAS No. 831243-31-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144776. | |
| Natalizumab | Natalizumab (AN100226; BG00002) is a humanized monoclonal IgG4 antibody inhibitor that selectively targets α4 integrin (CD49d). It blocks the interaction of integrins such as α4β1 (VLA-4) with vascular cell adhesion molecule VCAM-1, intercellular adhesion molecule ICAM-1, and fibronectin by competitively binding to the α4 subunit. Natalizumab inhibits the adhesion, retention, and transendothelial migration of immune cells (such as CD4+ T cells), reducing the infiltration of inflammatory cells into the central nervous system or lesion sites, thus exerting anti-inflammatory and immunomodulatory activity. Natalizumab is used in the study of relapsing-remitting multiple sclerosis (RRMS) and also has applications in the study of autoimmune or inflammation-related diseases such as Crohn's disease, B-cell lymphoma, and non-infectious uveitis. Natalizumab can also prevent lymphocytes from entering the central nervous system, thereby preventing acute demyelinating relapses[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 189261-10-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-108831. | |
| Natalizumab (Anti-CD49d) | Natalizumab (Anti-CD49d) (AN100226; BG00002) Solution is a humanized monoclonal IgG4 antibody inhibitor that selectively targets α4 integrin (CD49d), blocking the interaction of integrins such as α4β1 (VLA-4) with vascular cell adhesion molecule VCAM-1, intercellular adhesion molecule ICAM-1, and fibronectin by competitively binding to the α4 subunit. Natalizumab solution inhibits the adhesion, retention, and transendothelial migration of immune cells (such as CD4+ T cells), reducing the infiltration of inflammatory cells into the central nervous system or lesion sites, thereby exerting anti-inflammatory and immunomodulatory activity. Natalizumab (Anti-CD49d) solution is used in the study of relapsing-remitting multiple sclerosis (RRMS) and is also applied in the research of autoimmune or inflammation-related diseases such as Crohn's disease, B-cell lymphoma, and non-infectious uveitis. Natalizumab (Anti-CD49d) can also prevent lymphocytes from entering the central nervous system, thus preventing acute demyelinating relapses[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AN100226; BG00002. CAS No. 189261-10-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108831A. | |
| Natamycin | Natamycin. Group: Food ingredients. Pack Sizes: 25Kgs Bags. |  |
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