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| Product | Description | |
|---|---|---|
| Sunitinib Maleate (Sutent, Sunitinib Malate, SU-11248, PHA-290940AD, PNU-290940AD) | A multi-kinase inhibitor targeting several receptor tyrosine kinases (RTK). Sunitinib and its active metabolite (SU012662) are selective inhibitors of multiple receptor tyrosine kinases, including platelet-derived growth factor receptor and vascular endothelial growth factor receptor, that are associated with tumor growth and angiogenesis. Group: Biochemicals. Alternative Names: Sutent. Grades: Highly Purified. CAS No. 341031-54-7. Pack Sizes: 100mg, 250mg, 500mg. US Biological Life Sciences. |  Worldwide |
| Sunitinib N-glucuronide | Sunitinib N-glucuronide. Molecular formula: C28H35FN4O8. Mole weight: 574.60. |  |
| Sunitinib N-Oxide | Sunitinib N-Oxide. Group: Biochemicals. Alternative Names: N-[2- (Diethyloxidoamino) ethyl]-5-[ (Z) - (5-fluoro-1, 2-dihydro-2-oxo-3H-indol-3-ylidene) methyl]-2, 4-dimethyl-1H-pyrrole-3-carboxamide; 5-(5-Fluoro-2-oxo-1,2-dihydroindol-(3Z)-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethyl-N-oxoaminoethyl)amide. Grades: Highly Purified. CAS No. 356068-99-0. Pack Sizes: 10mg. Molecular Formula: C22H27FN4O3, Molecular Weight: 414.47. US Biological Life Sciences. | Worldwide |
| Sunitinib N-Oxide-d10 | Sunitinib N-Oxide-d10. Group: Biochemicals. Alternative Names: N-[2- (Diethyloxidoamino) ethyl]-5-[ (Z) - (5-fluoro-1, 2-dihydro-2-oxo-3H-indol-3-ylidene) methyl]-2, 4-dimethyl-1H-pyrrole-3-carboxamide-d10; 5-(5-Fluoro-2-oxo-1,2-dihydroindol-(3Z)-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethyl-N-oxoaminoethyl)amide-d10. Grades: Highly Purified. Pack Sizes: 500ug. Molecular Formula: C22H17D10FN4O3, Molecular Weight: 424.53. US Biological Life Sciences. | Worldwide |
| Sunitinib (SU-11248) | Sunitinib is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM, and also inhibits c-Kit. Sunitinib is also a dose-dependent inhibitor of the autophosphorylation activity of IRE1α. Sunitinib induces autophagy and apoptosis. Group: Inhibitors. Alternative Names: SU11248. CAS No. 557795-19-4. Pack Sizes: 50mg. Product ID: S7781. Formula: C22H27FN4O2. Smiles: CCN(CC)CCNC(=O)C1=C(NC(=C1C)C=C2C3=C(C=CC(=C3)F)NC2=O)C. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| Sunitinib (SU11248) Malate | Sunitinib malate is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM in cell-free assays, and also inhibits c-Kit. Sunitinib Malate effectively inhibits autophosphorylation of Ire1α. Sunitinib Malate increases both death receptor and mitochondrial-dependent apoptosis. Group: Inhibitors. Alternative Names: SU11248 malate. CAS No. 341031-54-7. Pack Sizes: 50mg. Product ID: S1042. Formula: C22H27FN4O2.C4H6O5. Smiles: CCN(CC)CCNC(=O)C1=C(NC(=C1C)C=C2C3=C(C=CC(=C3)F)NC2=O)C.C(C(C(=O)O)O)C(=O)O. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Sunply | Sunply. |  |
| Sunset Yellow FCF | Sunset Yellow FCF (Orange Yellow S) is an orange azo dye with a maximum absorption wavelength of 480 nm. Sunset Yellow FCF can be used in food, cosmetics and pharmaceuticals[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Orange Yellow S; Food Yellow 3; CI 15985. CAS No. 2783-94-0. Pack Sizes: 10 mM * 1 mL in Water; 100 mg. Product ID: HY-D0249. |  |
| Sunset Yellow FCF | Sunset yellow FCF is used as a colorant and food additive in many foods. Alternative Names: 6-Hydroxy-5-[2-(4-sulfophenyl)diazenyl]-2-naphthalenesulfonic Acid Sodium Salt; 1-p-Sulfophenylazo-2-hydroxynaphthalene-6-sulfonate disodium salt; 1351 Yellow; 1899 Yellow; Acid Food Yellow 3; Yellow S; Yellow SY; Yellow Sun; Food yellow 3. Grades: >95%. CAS No. 2783-94-0. Molecular formula: C16H10N2Na2O7S2. Mole weight: 452.37. | |
| Sunset Yellow FCF | Provisionally listed for use in food, drugs and cosmetics. Sunset Yellow is useful in fermented foods which must be heat treated. It may be found in orange sodas, orange jelly, marzipan, Swiss rolls, apricot jam, citrus marmalade, lemon curd, sweets, hot chocolate mix and packet soups, trifle mix, breadcrumbs, snack chips, shelf fresh noodles, cheese sauce mixes. Sunset Yellow is a sulfonated version of Sudan I, a possible carcinogen. Sunset Yellow itself may be responsible for causing an allergic reaction in people with an aspirin intolerance, resulting in various symptoms, including gastric upset, diarrhea, vomiting, nettle rash (urticaria), swelling of the skin (angioedema) and migraines. Group: Biochemicals. Grades: Highly Purified. CAS No. 2783-94-0. Pack Sizes: 1g, 10g. US Biological Life Sciences. | Worldwide |
| Sunset Yellow FCF Impurity 1 | Sunset Yellow FCF Impurity 1. Uses: For analytical and research use. CAS No. 61551-82-4. Molecular formula: C20H12Na2O7S2. Mole weight: 474.41. Catalog: APB61551824. |  |
| Sunset Yellow FCF Impurity 2 | Sunset Yellow FCF Impurity 2. Uses: For analytical and research use. CAS No. 1936-15-8. Molecular formula: C16H10N2Na2O7S2. Mole weight: 452.36. Catalog: APB1936158. | |
| Sunset Yellow FCF Impurity 3 | Sunset Yellow FCF Impurity 3. Uses: For analytical and research use. CAS No. 56120-28-6. Molecular formula: C12H9N3Na2O6S2. Mole weight: 401.32. Catalog: APB56120286. | |
| Sunsoft A 171E | Sunsoft A 171E. CAS No. 86529-98-8. | |
| Sunvozertinib | Sunvozertinib is a tyrosine kinase inhibitor with anti-tumor effects. Grades: >98%. CAS No. 2370013-12-8. Molecular formula: C29H35ClFN7O3. Mole weight: 584.1. | |
| Sunvozertinib | Sunvozertinib (DZD9008) is a potent ErbBs (EGFR, Her2, especially mutant forms) and BTK inhibitor. Sunvozertinib shows IC50s of 20.4, 20.4, 1.1, 7.5, and 80.4 nM for EGFR exon 20 NPH insertion, EGFR exon 20 ASV insertion, EGFR L858R and T790M mutations, and Her2 Exon20 YVMA, and EGFR WT A431, respectively (patent WO2019149164A1, example 52)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DZD9008. CAS No. 2370013-12-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-132842. | |
| SuO-Glu-Val-Cit-PAB-MMAE | SuO-Glu-Val-Cit-PAB-MMAE (NHS-Glutarate-Val-Cit-PAB-MMAE) consists a cleavable ADC linker (SuO-Glu-Val-Cit-PAB) and a potent tubulin inhibitor (MMAE). SuO-Glu-Val-Cit-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NHS-Glutarate-Val-Cit-PAB-MMAE. CAS No. 1895916-24-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-130989. | |
| SuO-Glu-Val-Cit-PAB-MMAE | SuO-Glu-Val-Cit-PAB-MMAE consists a cleavable ADC linker (SuO-Glu-Val-Cit-PAB) and a potent tubulin inhibitor (MMAE). SuO-Glu-Val-Cit-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs). Grades: ≥95%. CAS No. 1895916-24-1. Molecular formula: C67H103N11O17. Mole weight: 1334.60. | |
| Supaglutide | Supaglutide is a glucagon-like peptide-1 (GLP-1) analog developed for the treatment of type 2 diabetes mellitus (T2DM). Supaglutide was shown to regulate blood glucose and lipid homeostasis in diabetic rhesus monkeys. Alternative Names: YN011-301. | |
| Super Absorbent Polymer | Super Absorbent Polymer. Molecular formula: C3H2NNa. Mole weight: 75.04g/mol. IUPAC Name: sodium;prop-2-enenitrile. SMILES: [CH-]=CC#N.[Na+]. InChI: InChI=1S/C3H2N.Na/c1-2-3-4;/h1-2H;/q-1;+1. | |
| Super Activated Carbon Nanoparticles | Super Activated Carbon Nanoparticles. CAS No. 7440-44-0. Molecular formula: C. Purity: 99.9 %. | |
| Super Activated Charcoal Nanopowder | Super Activated Charcoal Nanopowder. CAS No. 7440-44-0. Molecular formula: C. Mole weight: 12.01 g/mol. | |
| Supercinnamaldehyde | Supercinnamaldehyde is a potent transient receptor potential ankyrin 1 (TRPA1) activator with an EC50 value of 0.8 μM. Supercinnamaldehyde activates TRPA1 ion channels through covalent modification of cysteines[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 70351-51-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121539. | |
| Superconfluentic acid | Superconfluentic acid is a depside metabolite of the lichen. CAS No. 108529-22-2. Molecular formula: C32H44O8. Mole weight: 556.69. | |
| Super high polymerization degree floating polyvinyl chloride resin | Super high polymerization degree floating polyvinyl chloride resin. | |
| Super large size Nb2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets, the preparation temperature is low, the oxidation is effectively prevented, and the electrochemical and catalytic properties are excellent. CAS No. 12011-99-3. Purity: 0.99. | |
| Super large size Ti2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets. The preparation temperature is low. The oxidation is effectively prevented. CAS No. 12316-56-2. Purity: 0.99. | |
| Super large size Ti3C2Tx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets. The preparation temperature is low. The oxidation is effectively prevented. CAS No. 12363-89-2. Purity: 0.99. | |
| Super large size V2CTx nanosheet | The freeze-thaw method prepares super-large mxene nanosheets, the preparation temperature is low, the oxidation is effectively prevented, and the electrochemical and catalytic properties are excellent. Purity: 0.99. | |
| Super Lux Foam | Super Lux foam is on the very firmest end of the firm spectrum. Super Lux is not only firmer but has a high density as well. It's primarily used in heavy-duty applications where very firm foams are required. Great for automotive seating, scooter, motorcycle, ATV & other outdoor personal transportation seats. | |
| Super Max Foam | In some cases, feathers are used, but when you need quality support and firmness, foam is the best way to go. Our super max foam was designed to be firm and supportive, yet still comfortable, making it a great choice for seats, massage tables, and exercise pads. | |
| superoxide dismutase | A metalloprotein; also known as erythrocuprein, hemocuprein or cytocuprein. Enzymes from most eukaryotes contain both copper and zinc; those from mitochondria and most prokaryotes contain manganese or iron. Group: Enzymes. Synonyms: superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; superoxide dismutase I; superoxide dismutase II; SOD; Cu,Zn-SOD; Mn-SOD; Fe-SOD; SODF; SODS; SOD-1; SOD-2; SOD-3; SOD-4; hemocuprein; erythrocuprein; cytocuprein; cuprein; hepatocuprein. Enzyme Commission Number: EC 1.15.1.1. CAS No. 9054-89-1. SOD. 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-1063; superoxide dismutase; EC 1.15.1.1; 9054-89-1; superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; superoxide dismutase I; superoxide dismutase II; SOD; Cu,Zn-SOD; Mn-SOD; Fe-SOD; SODF; SODS; SOD-1; SOD-2; SOD-3; SOD-4; hemocuprein; erythrocuprein; cytocuprein; cuprein; hepatocuprein. Cat No: EXWM-1063. |  |
| Superoxide Dismutase 2 from Human, Recombinant | SOD2 is part of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. SOD2 binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in SOD2 gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. SOD2 destroys radicals which are usually produced within the cells and which are toxic to biological systems. Group: Enzymes. Synonyms: Superoxide dismutase [Mn]; mitochondrial; IPOB; MNSOD; MVCD6. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 24.4 kDa (219 aa, 25-222 aa + His Tag). Activity: > 1,200 units/mg. Storage: Can be stored at 4°C short term (1-2 weeks). For long term storage, aliquot and store at - 20°C or -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Human. Superoxide dismutase [Mn]; mitochondrial; IPOB; MNSOD; MVCD6; Superoxide Dismutase 2; SOD-2; Mn-SOD; Mn Superoxide dismutase. Cat No: NATE-1658. | |
| Superoxide Dismutase 8,000u/g (Bovine) (SOD) | Superoxide Dismutase 8,000u/g (Bovine) (SOD). |  CA, FL & NJ |
| Superoxide Dismutase A from Bacterial, Recombinant | Superoxide dismutase, Mn, also known as sodA, is a member of the iron/manganese superoxide dismutase family. SodA destroys radicals which are normally produced within the cells and which are toxic to biological systems. It works by catalyzing the dismutation of the superoxide radical O2- to O2 and H2O2, which are then metabolized to H2O and O2 by catalase and glutathione peroxidase. Group: Enzymes. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 25.2 kDa (226 aa, 1-206 aa + His Tag). Activity: >350 units/mg. Form: Liquid. Source: E. coli. Species: Bacterial. Cat No: NATE-1659. | |
| Superoxide Dismutase from Bovine, Recombinant | Superoxide dismutase (SOD) catalyzes the dismutation of superoxide radicals to hydrogen peroxide and molecular oxygen. SOD plays a critical role in the defense of cells against the toxic effects of oxygen radicals. SOD competes with nitric oxide (NO) for superoxide anion (which reacts with NO to form peroxynitrite), thereby SOD promotes the activity of NO. SOD has also been shown to suppress apoptosis in cultured rat ovarian follicles, neural cell lines, and transgenic mice by preventing the conversion of NO to peroxynitrate, an inducer of apoptosis. Sod from bovine erythr ocytes was the first sod to be found in mammalian tissues. before its enzymatic activity was disc.Superoxide dismutase has been used in a study to investigate where lipoproteins may affect the l-arginine-nitric oxide pathway. superoxide dismutase has also been used in a study to investigate the mass spectral evidence for carbonate-anion-radical-induced posttranslational modification of tryptophan to kynurenine in human cu, zn superoxide dismutase. the product has been used to develop an sod assay. this assay used dismutase-mediated inhibition of nadh-dependent nitroblue tetrazolium reduction. Group: Enzymes. Synonyms: Superoxide dismutases; EC 1.15.1.1; superoxidase dismutase; copper-zinc superoxide dismutase; Cu-Zn superoxide dismutase; ferrisuperoxide dismutase; s. | |
| Superoxide Dismutase from Human, Recombinant | Superoxide dismutase (SOD) catalyzes the dismutation of superoxide radicals to hydrogen peroxide and molecular oxygen. SOD plays a critical role in the defense of cells against the toxic effects of oxygen radicals. SOD competes with nitric oxide (NO) for superoxide anion (which reacts with NO to form peroxynitrite), thereby SOD promotes the activity of NO. SOD has also been shown to suppress apoptosis in cultured rat ovarian follicles, neural cell lines, and transgenic mice by preventing the conversion of NO to peroxynitrate, an inducer of apoptosis. Group: Enzymes. Synonyms: Superoxide dismutase [Cu-Zn]; EC 1.15.1.1; SOD1; SOD; ALS; ALS1; IPOA. Enzyme Commission Number: EC 1.15.1.1. Purity: > 95% by SDS-PAGE. SOD. Mole weight: 16.8 kDa (monomer), 33.6 kDa (homodimer). Activity: ~40,000 U/mg. Storage: Store at -20°C. Form: Lyophilized powder. Source: E. coli. Species: Human. Superoxide dismutase [Cu-Zn]; EC 1.15.1.1; SOD1; SOD; ALS; ALS1; IPOA; Cu-Zn superoxide dismutase; Cu,Zn-SOD. Cat No: NATE-1657. | |
| Superoxide dismutase, Porcine erythrocytes | Superoxide dismutase, Porcine erythrocytes (SOD) is the only antioxidant enzyme that scavenges the superoxide anion by converting this free radical to oxygen and hydrogen peroxide, thus preventing peroxynitrite production and further damage. Superoxide dismutase, Porcine erythrocytes is extensively researched and used in anti-inflammatory, antitumor, radiation protection, and antisenility applications[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SOD. CAS No. 9054-89-1. Pack Sizes: 50 KU; 100 KU. Product ID: HY-129064. | |
| Superoxide Dismutase (SOD) 1IU NBT-mg from Melon | Superoxide Dismutase (SOD) 1IU NBT-mg from Melon. | CA, FL & NJ |
| Superoxide oxidoreductase | Superoxide oxidoreductase. Alternative Names: ORGOTEIN; Superoxide dismutases; SOD. CAS No. 9054-89-1. | |
| superoxide reductase | The enzyme contains non-heme iron. Group: Enzymes. Synonyms: neelaredoxin; desulfoferrodoxin. Enzyme Commission Number: EC 1.15.1.2. CAS No. 250679-67-5. 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-1064; superoxide reductase; EC 1.15.1.2; 250679-67-5; neelaredoxin; desulfoferrodoxin. Cat No: EXWM-1064. | |
| Superplanaic acid | Superplanaic acid is a depside obtained from the lichen lecanora planaica. CAS No. 156372-09-7. Molecular formula: C31H44O7. Mole weight: 528.68. | |
| Super Purified Plasma Nanotubes Powder SPT-220 | Super Purified Plasma Nanotubes Powder SPT-220. CAS No. 7440-44-0. Product ID: ACM7440440-242. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Super Purified Plasma Nanotubes Solution SPT-220 | Super Purified Plasma Nanotubes Solution SPT-220. CAS No. 7440-44-0. Product ID: ACM7440440-8. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Super Soft Foam | When the goal is to increase comfort, super soft foam performs wonderfully as backing for furniture and as extra padding atop mattresses to soften and relieve pressure. Super soft foam works best in comfort applications and is highly compactable. | |
| Super Supplements Activated Charcoal Nanopowder | Super Supplements Activated Charcoal Nanopowder. CAS No. 7440-44-0. Molecular formula: C. Purity: 95%. | |
| Super-TDU | Super-TDU is a specific YAP antagonist targeting YAP-TEADs interaction. Super-TDU suppresses tumor growth in gastric cancer mouse model[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1599441-71-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P1727. | |
| Super-TDU 1-31 | Super-TDU (1-31), the 1-31 amino acid fragment of Super-TDU, is an inhibitor of YAP-TEADs and has a strong anti-tumor activity. Alternative Names: Ser-Val-Asp-Asp-His-Phe-Ala-Lys-Ser-Leu-Gly-Asp-Thr-Trp-Leu-Gln-Ile-Gly-Gly-Ser-Gly-Asn-Pro-Lys-Thr-Ala-Asn-Val-Pro-Gln-Thr. Grades: ≥95%. Molecular formula: C141H218N40O48. Mole weight: 3241.48. | |
| Super yellow light-emitting PPV copolymer | Super yellow light-emitting PPV copolymer. CAS No. 26009-24-5. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Super yellow light-emitting PPV copolymer | Features: · soluble super yellow light-emitting PPV copolymer · excellent reproducibility · broad emission spectrum · very high efficiency · very low operation voltage/for PM 100000 cd/m2 pulsed <10 V · very long DC & AC lifetime Typical performance measured in standard device stack (ITO/PEDOT: PSS 20 nm/PDY-132 80 nm/Ba 6 nm/Ag 150 nm): · max. efficiency: 11 Cd/A · V_on: 2.2 V · V @ 100 cd/m2: 3.0 V · V @ 1000 cd/m2: 4.3 V · max. power eff.: 10 lm/W · external quantum eff.: 5.3% · CIE1931 @ 100 cd/m2: (0.50, 0.49) · DC lifetime @ 100 cd/m2 @ RT:>>220000 · AC lifetime @ 200 cd/m2 @ RT: 11000. Alternative Names: PDY-132. CAS No. 26009-24-5. Mole weight: average >1,300. | |
| Supinoxin | Supinoxin (RX-5902) is an orally active inhibitor of phosphorylated-p68 RNA helicase (P-p68) and a potent first-in-class anti-cancer agent. Supinoxin interacts with Y593 phosphorylated-p68 and attenuates the nuclear shuttling of β-catenin. Supinoxin induces cell apoptosis and inhibits growth of TNBC cancer cell lines with IC50s ranging from 10 nM to 20 nM[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: RX-5902. CAS No. 888478-45-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-123611. | |
| Suplatast tosilate | Suplatast tosilate is the tosylate salt form of suplatast, functioning as the active pharmaceutical ingredient (API) classified as a Th2 cytokine inhibitor. Its primary mechanism involves selectively suppressing the production of interleukin-4 (IL-4) and interleukin-5 (IL-5) by helper T cells, thereby inhibiting immunoglobulin E (IgE) synthesis and eosinophil activation, which are key pathways in the allergic inflammatory response. Grades: Pharmaceutical grade. Product ID: PAP-0122. |  |
| Suplatast Tosylate | Suplatast Tosylate is an antiallergic drug. Suplatast Tosylate inhibits antigen-induced histamine release from mast cells as well as IgE antibody formation. Suplatast Tosylate suppresses interleukin (IL)-4 release from T cells, however in human peripheral basophils, Suplatast Tosylate inhibited the antigen-induced release of IL-13 but not IL-4. Group: Biochemicals. Alternative Names: [3- [ [4- (3-ethoxy-2-hydroxypropoxy) phenyl] amino] -3-oxopropyl] dimethylsulfonium 4-Methyl Benzene sulfonate; (±) - [2- [4- (3-Ethoxy-2-hydroxypropoxy) phenylcarbamoyl] ethyl] dimethylsulfonium p-toluenesulfonate; IPD 1151T; Suplatast tosilate. Grades: Highly Purified. CAS No. 94055-76-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Suplatast Tosylate | Suplatast tosylate is a Th2 cytokine inhibitor that attenuates IL-2, IL-5 and IL-13 production and has no effect on IFN-γ production. Acts as an immunoregulator that suppresses IgE production, eosinophil infiltration and histamine release. Shows antiasthmatic, anti-inflammatory and antifibrotic activity in vivo. Suplatast Tosilate (ST) is an innovative anti-allergic medication that has emerged in recent years. It is a synthetic compound known as the l-tosylate ester of suplatast, which is a novel anti-allergic substance. Suplatast Tosilate can hinder the production of pro-inflammatory cytokines, including interleukin-4 and interleukin-5. Moreover, it has also been found to suppress the activity of enzymes involved in generating inflammatory mediators such as cyclooxygenase-2 and phospholipase A2. Category: Active pharmaceutical ingredients. CAS No. 94055-76-2. Product ID: API94055762. Molecular formula: C23H33NO7S2. Mole weight: 499.641. Appearance: Powder. |  |
| Suplite RB Nanopowder | Suplite RB Nanopowder. Purity: >99%. | |
| Suppository Bases, Hard Fat | Hard fat suppository bases consist mainly of mixtures of the triglyceride esters of the higher saturated fatty acids (C8H17COOH to C18H37COOH) along with varying proportions of mono- and diglycerides. It is as a vehicle for the rectal or vaginal administration of a variety of drugs, either to exert local effects or to achieve systemic absorption. Alternative Names: Adeps neutralis; adeps solidus; Akosoft; Akosol; Cremao CS-34; Cremao CS-36; hydrogenated vegetable glycerides; Massa Estarinum; Massupol; Novata; semisynthetic glycerides; Suppocire; Wecobee; Witepsol. | |
| Suprofen | Suprofen. Group: Biochemicals. Alternative Names: a-Methyl-4- (2-thienylcarbonyl) benzeneacetic acid; p-(2-Thenoyl)hydratropic acid; Sutoprofen. Grades: Highly Purified. CAS No. 40828-46-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C14H12O3S. US Biological Life Sciences. | Worldwide |
| Suprofen-d3 | Prostaglandin biosynthesis inhibitor. Analgesic. Group: Biochemicals. Alternative Names: α - (Methyl-d3) -4- (2-thienylcarbonyl) benzeneacetic Acid; p-(2-Thenoyl)hydratropic-d3 Acid; Sutoprofen-d3; R-25061-d3; Masterfen-d3; Srendam-d3; Sulprotin-d3; Supranol-d3; Suprocil-d3; Suprol-d3; Topalgic-d3. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Suramin | Suramin, also called as Germanin, has been demonstrated to inhibit a large variety of enzymes including urease, hexokinase, succinic dehydrogenase, p-glucuronidase, acid phosphatase, lysozyme, thrombin, plasma kallikrein, (Na'-K')-activated ATPase, plasmi. Uses: Antineoplastic agents. Alternative Names: suramin;Germanin;Naganol;Naphuride;Belganyl;Suramine. Grades: 95%. CAS No. 145-63-1. Molecular formula: C51H40N6O23S6. Mole weight: 1297.29. | |
| Suramin Hexasodium Salt (Germanin, NSC 34936, SK 24728) | Sodium salt of Suramin, a hepatitis C virus NS3 helicase inhibitor. Also used in the treatment of arthritis due to problematic collagen.A P2x and P2y purinergic receptor antagonist that displays antitumor, antiangiogenic and antiparasitic activities. Inhibits sirtuin 1, sirtuin 5 and topoisomerase II. Inhibits the cell surface binding of various growth factors including PDGF, EGF, FGFa and FGFb. Blocks association of G protein alpha and b/g-subunits. Potent competitive inhibitor of reverse transcriptase and protects T lymphocytes against in vitro human immunodeficiency virus infection.Potent ATPase inhibitor. Potent competitive inhibitor of reverse transcriptase.lfonic Acid Hexasodium Salt; 309F; 8,8'-[Ureylenebis[m-phenylene carbonylimino (4-methyl-m-phenylene) carbonylimino]]di (1, 3, 5-naphthalenetrisulfonic Acid) Hexasodium Salt; Antrypol; BAY 205; Bayer 205; CI 1003; Fourneau 309; Germanin; Germanin (pharmaceutical); Hexasodium Sym.-bis(m-aminobenzoyl)-m-amino-p-methylbenzoyl-1-naphthylamino-4,6,8-trisulfonate) Carbamide; Moranyl; NF 060; Naganin; Naganine; Naphuride; Naphuride sodium; Sodium Suramin; Suramin Hexasodium; Suramin Sodium; Suramine Sodium. Grades: Highly Purified. CAS No. 129-46-4. Pack Sizes: 50mg, 100mg, 250mg. Molecular Formula: C??H??N?Na?O??S?, Molecular Weight: 1429.17. US Biological Life Sciences. | Worldwide |
| Suramin Sodium | The sodium salt of Suramin which is a P2 purinergic antagonist and has been also found to have the effect in blocking the G protein binds to GPCRs so that it was studied the activity against sorts of cancer cell lines. Alternative Names: Suramin hexasodium; Suramin sodium salt; Suramine sodium salt; Suramin hexasodium salt. Grades: 98%. CAS No. 129-46-4. Molecular formula: C51H34N6Na6O23S6. Mole weight: 1429.17. | |
| Suramin sodium salt | Suramin sodium salt(Suramin hexasodium salt) is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor[1]. Suramin sodium salt is a potent inhibitor of sirtuins: SirT1 (IC50=297 nM), SirT2 (IC50=1.15 μM), and SirT5 (IC50=22 μM)[2]. Suramin sodium salt is a competitive inhibitor of reverse transcriptase (DNA topoisomerase II: IC50=5 μM)[3][4]. Suramin sodium salt is a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor[5]. Suramin sodium salt efficiently inhibits IP5K and is an antiparasitic, anti-neoplastic and anti-angiogenic agent[6][7][8]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suramin hexasodium salt. CAS No. 129-46-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0879A. | |
| Suramin sodium salt (Standard) | Suramin (sodium salt) (Standard) is the analytical standard of Suramin (sodium salt). This product is intended for research and analytical applications. Suramin sodium salt (Suramin hexasodium salt) is a reversible and competitive protein-tyrosine phosphatases (PTPases) inhibitor[1]. Suramin sodium salt is a potent inhibitor of sirtuins: SirT1 (IC50=297 nM), SirT2 (IC50=1.15 μM), and SirT5 (IC50=22 μM)[2]. Suramin sodium salt is a competitive inhibitor of reverse transcriptase (DNA topoisomerase II: IC50=5 μM)[3][4]. Suramin sodium salt is a potent SARS-CoV-2 RNA-dependent RNA polymerase (RdRp) inhibitor[5]. Suramin sodium salt efficiently inhibits IP5K and is an antiparasitic, anti-neoplastic and anti-angiogenic agent[6][7][8]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suramin hexasodium salt (Standard). CAS No. 129-46-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B0879AR. | |
| Surface IgG (sA20-Ig) of A20 (106-114) | Surface IgG (sA20-Ig) of A20 (106-114) is a peptide corresponding to residues 106-114 of Surface IgG (sA20-Ig) of A20. Inoculation of the Id-peptide in A20-engrafted mice caused apoptosis of tumor cells and resulted in tumor growth inhibition and extended survival of diseased animals. Alternative Names: Surface IgG (sA20-Ig) of A20 B-lymphoma cell line (106-114). | |
| Surface Modification Carbon Nanotubes - OH | Surface Modification Carbon Nanotubes - OH. CAS No. 308068-56-6. Purity: >95% (MWNT). | |
| surfactant free, 30 nm Silver nanoparticles | surfactant free, 30 nm Silver nanoparticles. Purity: > 99.9%. | |
| surfactant free, 5 nm Cobalt nanoparticles | surfactant free, 5 nm Cobalt nanoparticles. Purity: > 99%. | |
| Surfactin | Surfactin Inhibitor. Uses: Scientific use. Product Category: T13041. CAS No. 24730-31-2. |  |
| Surfactin | Surfactin is a potent cyclic lipopeptide biosurfactants consists of four isomers (Surfactin A, B, C and D), which mediates flux of mono-and divalent cations, such as calcium, across lipid bilayer membranes. Surfactin can act as an antimicrobial adjuvant with anti-bacterial, anti-fungal, antimycoplasma and hemolytic effects[1][2]. Surfactin also has antiviral activity against a variety of enveloped viruses[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 252023-70-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129555. | |
| Surfactin | Surfactin is a lipopeptide antibiotic and biosurfactant from Bacillus subtilis. Alternative Names: surfactin C. CAS No. 24730-31-2. Molecular formula: C53H93N7O13. Mole weight: 1036.34. | |
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