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| Product | Description | |
|---|---|---|
| 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 | Supercinnamaldehyde is an activator of the transient receptor potential ankyrin 1 (TRPA1) channel. Uses: Antimutagenic agents. Synonyms: 1-methyl-3-(2-oxopropylidene)indolin-2-one; (3Z)-1-methyl-3-(2-oxopropylidene)indol-2-one. Grades: ≥95%. CAS No. 70351-51-8. Molecular formula: C12H11NO2. Mole weight: 201.2. |  |
| 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 | EC #232-943-0 EC#1.15.1.1. CAS No. 9054-89-1. Product ID: 2-08484. Mole weight: 32500. Purity: ≥3,000 units/mg protein. Properties: from bovine erythrocytes. |  |
| 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 (SOD) 1IU NBT-mg from Melon | Superoxide Dismutase (SOD) 1IU NBT-mg from Melon. | CA, FL & NJ |
| Superoxide oxidoreductase | Synonyms: 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. 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 an inhibitory peptide targeting YAP-TEADs interaction. Synonyms: Super-TDU; 1599441-71-0; s8554. CAS No. 1599441-71-0. Molecular formula: C237H370N66O69S. Mole weight: 5279.94. | |
| 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 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. | |
| 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 |
| Suplatast Tosylate | Suplatast Tosilate is a novel capsular anti-asthmatic agent that suppresses both IgE production, IL-4 and IL-5 synthesis with IC50 above 100 μM. Synonyms: IPD-1151T. Grades: >98%. CAS No. 94055-76-2. Molecular formula: C23H33NO7S2. Mole weight: 499.64. | |
| 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. | |
| Suprafenacine | Suprafenacine is a destabilizer of microtubules (IC50 value 0.38 μM for microtubule polymerization inhibition) resulting in cell cycle arrest in the G2/M phase and apoptosis of cancer cells. Suprafenacine (SRF) binds to microtubules at the colchicine-binding site and causes the inhibition of cancer cell proliferation. Synonyms: (E)-N'-(4-methylbenzylidene)-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide; SRF. Grades: 99%. CAS No. 1477482-50-0. Molecular formula: C16H18N4O. Mole weight: 282.34. | |
| 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. | |
| Suprasterol II | Suprasterol II is an impurity of vitamin D2, which is commonly used for the prevention and treatment of vitamin D deficiency and associated disease, and also used for hypoparathyroidism. Synonyms: (1R,3'R)-1-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methylspiro[2,3,3a,5,6,7-hexahydro-1H-indene-4,1'-2,3,4,5,6,6a-hexahydro-1aH-cyclopropa[a]indene]-3'-ol. CAS No. 562-71-0. Molecular formula: C28H44O. Mole weight: 396.659. | |
| 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 | para-(2-Thenoyl) hydratropic acid. CAS No. 40828-46-4. Product ID: 8-04327. Molecular formula: C14H12O3S. Mole weight: 260.31. | |
| 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 | 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. Synonyms: suramin; Germanin; Naganol; Naphuride; Belganyl; Suramine. Grades: 95%. CAS No. 145-63-1. Molecular formula: C51H40N6O23S6. Mole weight: 1297.29. | |
| Suramin hexasodium salt | Suramin hexasodium salt. CAS No. 129-46-4. Product ID: 8-01397. Molecular formula: C51H34N6Na6O23S6. Mole weight: 1429.15. | |
| 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. Synonyms: 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 ( 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 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 |
| 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. | |
| Surfen dihydrochloride | Surfen dihydrochloride is a potent HS (heparan sulfate) antagonist. Surfen binds to glycosaminoglycans. Surfen neutralizes the anticoagulant activity of both unfractionated and low molecular weight heparins. Surfen affects sulfation of heparin and inhibits degradation by heparin lyases. Surfen inhibits FGF2 binding and signaling. Surfen inhibits cell attachment, and virus infection [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Aminoquinuride dihydrochloride. CAS No. 5424-37-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122704A. | |
| Surfen hydrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Surfynol 104 | Surfynol 104. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,4,7,9-TETRAMETHYL-5-DECYNE-4,7-DIOL, Surfynol 104, 126-86-3, Surfynol 104A, Surfynol 104E, 2,4,7,9-Tetramethyldec-5-yne-4,7-diol, Syrfynol 104, 2,4,7,9-Tetramethyl-5-decyn-4,7-diol, NSC 5630, SBB008941, 1,4-Diisobutyl-1,4-dimethylbutynediol, 5-decyne-4,7-diol-2,4,7,9-tetramethyl, DSSTox_CID_7041, 5-Decyne-4,7-diol, 2,4,7,9-tetramethyl-, DSSTox_RID_78288, DSSTox_GSID_27041, CAS-126-86-3, Surfynol TG, Acetylenol E 00, Olfine STG-E. Product Category: Heterocyclic Organic Compound. CAS No. 8043-35-4. Molecular formula: C14H26O2. Mole weight: 226.355. Purity: 0.96. IUPACName: 2,4,7,9-tetramethyldec-5-yne-4,7-diol. Canonical SMILES: CC(C)CC(C)(C#CC(C)(CC(C)C)O)O. ECNumber: 204-809-1. Product ID: ACM8043354. Alfa Chemistry ISO 9001:2015 Certified. | |
| Surfynol 104 E (technical grade) | Surfynol 104 E (technical grade). Uses: Designed for use in research and industrial production. Product Category: Promotional Products. CAS No. 8043-35-4. Purity: Tech. Product ID: ACM8043354-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Survivin (18-27) | A peptide fragment of Survivin. Survivin, also called BIRC5 , is a member of the apoptosis inhibitor protein family containing a baculovirus domain. Survivin is overexpressed in most human cancers but rarely expressed in normal differentiated adult tissues. Synonyms: Survivin (18-27)(modK); Sur18K10; Baculoviral IAP repeat-containing protein 5 (18-27). | |
| Survivin-3A (96-104) | Survivin-3A (96-104) is a 9-aa peptide. Survivin is the smallest member of the Inhibitor of apoptosis (IAP) family of proteins, involved in inhibition of apoptosis and regulation of cell cycle. | |
| Survivin (80-88) | A peptide fragment of Survivin. Survivin, also called BIRC5 , is a member of the apoptosis inhibitor protein family containing a baculovirus domain. Survivin is overexpressed in most human cancers but rarely expressed in normal differentiated adult tissues. Synonyms: Baculoviral IAP repeat-containing protein 5 (80-88). | |
| Survivin Antagonist, S12 (Survivin Inhibitor II, 3-(2-(benzo[d][1,3]dioxol-5-yl)-2-oxoethyl)-5-bromo-3-hydroxyindolin-2-one) | A cell-permeable hydroxyindolinone compound that acts as a selective antagonist of survivin. Induces mitotic arrest and blocks cell cycle at G2/M phase (~40uM in HeLA cells) leading to apoptotic cell death. Shown to bind to a specific cavity adjacent to the interface involved in the dimerization of survivin. Binding is specific only to native survivin and does not affect any mutant forms. Inhibits HCT116 cell proliferation independently of their p53 status and reduces tumor volume in xenograft models in a dose-dependent manner (5-15mg/kg). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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