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| Product | Description | |
|---|---|---|
| Sunitinib Malate | Sunitinib Malate (SU 11248 Malate) is a multi-targeted receptor tyrosine kinase inhibitor with IC 50 s of 80 nM and 2 nM for VEGFR2 and PDGFRβ , respectively [1]. Sunitinib Malate, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SU 11248 Malate. CAS No. 341031-54-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-10255. |  |
| 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-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 |
| Sunply | Sunply. Group: Polymers. |  |
| 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 | 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. Group: Fluorescent dye. Alternative Names: Orange Yellow S; Food Yellow 3; CI 15985. CAS No. 2783-94-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-D0249. | |
| Sunset Yellow FCF | analytical standard. Group: Colorant standards. |  |
| Sunvozertinib | Sunvozertinib (DZD9008) is a potent ErbBs (EGFR, Her2, especially mutant forms) and BTK inhibitor. Sunvozertinib shows IC 50 s 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. Group: Signaling pathways. Alternative Names: DZD9008. CAS No. 2370013-12-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132842. | |
| Sunvozertinib | Sunvozertinib, also known as DZD9008, is an oral, potent, irreversible, and selective EGFR tyrosine kinase inhibitor. Sunvozertinib shows activity against EGFRexon20ins and other mutations. In both cell lines and xenograft models, sunvozertinib shows potent antitumor activity. In the two ongoing phase I clinical studies, sunvozertinib was tolerated up to 400 mg once daily. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sunvozertinib; DZD 9008; (DZD-9008; DZD9008. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 2370013-12-8. Molecular formula: C29H35ClFN7O3. Mole weight: 584.09. Purity: >98%. IUPACName: N-{5-({4-[5-chloro-4-fluoro-2-(2-hydroxypropan-2-yl)anilino]pyrimidin-2-yl}amino)-2-[(3R)-3-(dimethylamino)pyrrolidin-1-yl]-4-methoxyphenyl}prop-2-enamide. Canonical SMILES: C=CC(NC1=CC(NC2=NC=CC(NC3=CC(Cl)=C(F)C=C3C(C)(O)C)=N2)=C(OC)C=C1N4C[C@H](N(C)C)CC4)=O. Product ID: ACM2370013128. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 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. Group: Signaling pathways. Alternative Names: NHS-Glutarate-Val-Cit-PAB-MMAE. CAS No. 1895916-24-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-130989. | |
| 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. Synonyms: YN011-301. |  |
| Super Absorbent Polymer | Super Absorbent Polymer. Group: Polymers. Product ID: sodium; prop-2-enenitrile. Molecular formula: 75.04g/mol. Mole weight: C3H2NNa. [CH-]=CC#N.[Na+]. InChI=1S/C3H2N.Na/c1-2-3-4;/h1-2H;/q-1;+1. NTOWCTQVNUDKBY-UHFFFAOYSA-N. | |
| Super Activated Carbon Nanoparticles | Super Activated Carbon Nanoparticles. Group: Metal nano dispersion. CAS No. 7440-44-0. Mole weight: C. 99.9 %. | |
| Super Activated Charcoal Nanopowder | Super Activated Charcoal Nanopowder. Group: Metal nano dispersion. CAS No. 7440-44-0. Molecular formula: 12.01 g/mol. Mole weight: C. | |
| Supercinnamaldehyde | Supercinnamaldehyde is a potent transient receptor potential ankyrin 1 (TRPA1) activator with an EC 50 value of 0.8 μM. Supercinnamaldehyde activates TRPA1 ion channels through covalent modification of cysteines [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 70351-51-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-121539. | |
| Supercinnamaldehyde | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Superconfluentic acid | Superconfluentic acid is a depside metabolite of the lichen. CAS No. 108529-22-2. Molecular formula: C32H44O8. Mole weight: 556.69. | |
| Super-DHB | suitable for matrix substance for MALDI-MS, ?99.0%. Group: Fluorescence/luminescence spectroscopy. | |
| Superfibronectin from human plasma | solution, sterile-filtered, BioReagent, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Super high polymerization degree floating polyvinyl chloride resin | Super high polymerization degree floating polyvinyl chloride resin. Group: Polymers. | |
| 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. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12011-99-3. 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. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12316-56-2. 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. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. CAS No. 12363-89-2. 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. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| 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-polyethylene glycol from bovine erythrocytes | lyophilized powder, ?1,350 units/mg protein. Group: Fluorescence/luminescence spectroscopy. | |
| 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. Group: 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 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. Uses: Designed for use in research and industrial production. Product Category: Purified Single-wall Carbon Nanotubes. CAS No. 7440-44-0. Product ID: ACM7440440-242. Alfa Chemistry ISO 9001:2015 Certified. | |
| Super Purified Plasma Nanotubes Solution SPT-220 | Super Purified Plasma Nanotubes Solution SPT-220. Uses: Designed for use in research and industrial production. Product Category: Purified Single-wall Carbon Nanotubes. CAS No. 7440-44-0. Product ID: ACM7440440-8. Alfa Chemistry ISO 9001:2015 Certified. | |
| Super Supplements Activated Charcoal Nanopowder | Super Supplements Activated Charcoal Nanopowder. Group: Metal nano dispersion. CAS No. 7440-44-0. Mole weight: C. 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. Group: Peptides. 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. Synonyms: 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. Grade: ≥95%. Molecular formula: C141H218N40O48. Mole weight: 3241.48. | |
| 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. Group: Organic light-emitting diode (oled) materials. Alternative Names: PDY-132. CAS No. 26009-24-5. | |
| 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 ?-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. Group: Signaling pathways. Alternative Names: RX-5902. CAS No. 888478-45-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-123611. | |
| Suplatast tosylate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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 |
| Suplite RB Nanopowder | Suplite RB Nanopowder. Group: Clay nanopowders. >99%. | |
| SUPRACET BRILLIANT RED BD | SUPRACET BRILLIANT RED BD. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Serinyl Pink WD, Disperse Red 58, Supracet Brilliant Red BD, EINECS 228-923-6, CID80765, S0261, 2,2-((4-((6-Methoxybenzothiazol-2-yl)azo)phenyl)imino)bisethanol, 6373-93-9. Product Category: Disperse Dyes. CAS No. 6373-93-9. Molecular formula: C18H20N4O3S. Mole weight: 372.44. Purity: 0.96. IUPACName: 2-[N-(2-hydroxyethyl)-4-[(6-methoxy-1,3-benzothiazol-2-yl)diazenyl]anilino]ethanol. Canonical SMILES: COC1=CC2=C(C=C1)N=C(S2)N=NC3=CC=C(C=C3)N(CCO)CCO. Density: 1.34g/cm³. ECNumber: 228-923-6. Product ID: ACM6373939. Alfa Chemistry ISO 9001:2015 Certified. | |
| Suprafenacine | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Suprafenacine | Suprafenacine is a cell permeable, tubulin -destabilizing molecule which bind microtubules at the colchicine-binding site and inhibit polymerization. Suprafenacine can induce G2/M cell cycle arrest and apoptosis , and can be used for cancer research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SRF. CAS No. 1477482-50-0. Pack Sizes: 1 mg. Product ID: HY-118748. | |
| Supranol brilliant red g | Supranol brilliant red g. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,7-Naphthalenedisulfonic acid,6-(2-(4-(acetylcyclohexylamino)phenyl)diazenyl)-4-(benzoylamino)-5-hydroxy-,sodium salt (1:2); 1,7-Naphthalenedisulfonic acid,4-benzamido-6-((4-(N-cyclohexylacetamido)phenyl)azo)-5-hydroxy-,disodium salt; 1,7-Naphthalenedisu. Product Category: Heterocyclic Organic Compound. CAS No. 6417-35-2. Molecular formula: C31H28N4Na2O9S2. Mole weight: 710.68. Purity: 0.96. IUPACName: disodium (6Z)-6-[[4-[acetyl(cyclohexyl)amino]phenyl]hydrazinylidene]-4-benzamido-5-oxonaphthalene-1,7-disulfonate. Canonical SMILES: CC(=O)N(C1CCCCC1)C2=CC=C(C=C2)NN=C3C(=CC4=C(C=CC(=C4C3=O)NC(=O)C5=CC=CC=C5)S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+]. ECNumber: 613-495-9. Product ID: ACM6417352. Alfa Chemistry ISO 9001:2015 Certified. | |
| Supristol | Supristol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Supristol, Co-trifamole, cotrifamol, cotrifamole, Nevin (mixture), Sulfamoxole and trimethoprim, Trimethoprim and sulfamoxole, Sulfamoxazole + trimethoprim, Sulfamoxole-trimethoprim mixture, Trimethoprim-sulfamoxole mixture, Sulfamoxole mixture with trimethoprim, CID64937, CN 3123, CN-3123, C14H18N4O3.C11H13N3O3S, LS-31253, Benzenesulfonamide, 4-amino-N-(4,5-dimethyl-2-oxazolyl)-, mixt. with 5-((3,4,5-trimethoxyphenyl)methyl)-2,4-pyrimidinediamine, 57197-43-0. Product Category: Heterocyclic Organic Compound. CAS No. 57197-43-0. Molecular formula: C25H31N7O6S. Mole weight: 557.621940 [g/mol]. Purity: 0.96. IUPACName: 4-amino-N-(4,5-dimethyl-1,3-oxazol-2-yl)benzenesulfonamide; 5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine. Product ID: ACM57197430. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 | Suprofen (TN-762) is a non-steroidal anti-inflammatory drug (NSAID). Uses: Scientific research. Group: Signaling pathways. Alternative Names: TN-762. CAS No. 40828-46-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0270. | |
| 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 |
| Suprofen (µ-Methyl-4- (2-thienylcarbonyl) benzeneacetic Acid, p-(-thenooyl)hydratropic Acid,. Sutoprofen, R-25061, Masterfen, Srendam, Sulprotin, Supranol, Suprocil, Suprol, Topalgic) | Prostaglandin biosynthesis inhibitor. Analgesic. Group: Biochemicals. Alternative Names: µ-Methyl-4- (2-thienylcarbonyl) benzeneacetic Acid; p-(-thenooyl)hydratropic Acid; Sutoprofen; R-25061; Masterfen; Srendam; Sulprotin; Supranol; Suprocil; Suprol; Topalgic. Grades: Highly Purified. CAS No. 40828-46-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Suptavumab | Suptavumab (REGN2222) is a human monoclonal antibody. Suptavumab can bind and block a conserved epitope on RSV A and B subtypes. Suptavumab can be used for the research of RSV infection [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: REGN2222. CAS No. 1629615-23-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99586. | |
| Suptopin-2 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| 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 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 ( IC 50 =297 nM), SirT2 ( IC 50 =1.15 μM), and SirT5 ( IC 50 =22 μM) [2]. Suramin sodium salt is a competitive inhibitor of reverse transcriptase ( DNA topoisomerase II : IC 50 =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. Group: Signaling pathways. Alternative Names: Suramin hexasodium salt. CAS No. 129-46-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0879A. | |
| Suramin sodium salt | ?99% (TLC). Group: Fluorescence/luminescence spectroscopy. | |
| 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. Synonyms: Surface IgG (sA20-Ig) of A20 B-lymphoma cell line (106-114). | |
| Surface Modification Carbon Nanotubes - OH | Surface Modification Carbon Nanotubes - OH. Group: Multi wall cnt. CAS No. 308068-56-6. >95% (MWNT). | |
| surfactant free, 30 nm Silver nanoparticles | surfactant free, 30 nm Silver nanoparticles. Group: Elements nanoparticles. > 99.9%. | |
| surfactant free, 5 nm Cobalt nanoparticles | surfactant free, 5 nm Cobalt nanoparticles. Group: Elements nanoparticles. > 99%. | |
| Surfactant (MBAS) 1000 mg/L Calibration Standard | certified reference material. Group: Certified reference materials (crms). | |
| Surfactant (MBAS) 100 mg/L Calibration Standard | certified reference material. Group: Certified reference materials (crms). | |
| Surfactin | Surfactin Inhibitor. Uses: Scientific use. Product Category: T13041. CAS No. 24730-31-2. |  |
| Surfactin | Surfactin is a lipopeptide antibiotic and biosurfactant from Bacillus subtilis. Synonyms: surfactin C. CAS No. 24730-31-2. Molecular formula: C53H93N7O13. Mole weight: 1036.34. | |
| 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. Group: Natural products. CAS No. 252023-70-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-129555. | |
| Surfactin | Surfactin is a lipopeptide antibiotic and biosurfactant. Group: Biochemicals. Grades: Highly Purified. CAS No. 24730-31-2. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C53H93N7O13. US Biological Life Sciences. | Worldwide |
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