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| Product | Description | |
|---|---|---|
| Sulfathiazole (HRP) | 17α, 19-nortestosterone, commonly known as nandrolone, is an anabolic androgen given by mouth and by injection. It is a natural hormone in some animal species and is illegally used in animal husbandry as an anabolic. Following intramuscular injection of 19-nortestosterone laurate, the main metabolite identified in urine and bile is 17α, 19-nortestosterone. 17a, 19-nortestosterone is reported to be naturally occurring in pregnant cattle, but has not been identified in untreated male cattle. Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. |  Worldwide |
| Sulfathiazole-(phenyl-13C6) | 13C Labeled Compounds. CAS No. 1196157-72-8. Mole weight: 261.27. Catalog: ACM1196157728. |  |
| Sulfathiazole sodium | Sulfathiazole sodium is an organosulfur compound that has been used as a short-acting sulfa drug. Uses: Scientific research. Group: Signaling pathways. CAS No. 144-74-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B0507A. |  |
| Sulfathiazole sodium | Sulfathiazole is a short-acting sulfonamide antibiotic. Sulfathiazole is a short-acting sulfa drug. It was a common oral and topical antibiotic until less toxic alternatives were discovered. It is no longer used in humans. Sulfathiazole is added to the diet of laboratory animals to inhibit folate formation by gut bacteria. This ensures that the animal's only source of available folate is from their diet. Uses: Anti-infective agents. Synonyms: Soluthiazomide; Sodium Norsulfazole; RPR 102341. Grades: >98%. CAS No. 144-74-1. Molecular formula: C9H8N3NaO2S2. Mole weight: 277.30. |  |
| Sulfathiazole Sodium Salt | Sulfathiazole sodium salt is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA). It can also be used in biological study of thermotherapy and sulfonamide antibiotics deciphered Cyanobacteria and Proteobacteria microbiome in huanglongbing-affected Citrus paradise and Citrus limon. Group: Biochemicals. Grades: Highly Purified. CAS No. 144-74-1. Pack Sizes: 100g, 250g. Molecular Formula: C9H8N3NaO2S2, Molecular Weight: 277.3. US Biological Life Sciences. | Worldwide |
| Sulfathiazole sodium salt 99+% | Sulfathiazole sodium salt 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Sulfatide sodium salt,from bovine spinal cord | Heterocyclic Organic Compound. CAS No. 113255-27-9. Purity: 0.96. Catalog: ACM113255279. | |
| Sulfatinib | Sulfatinib, an oral drug candidate, is a small molecule inhibitor of vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, and the fibroblast growth factor receptor type 1 (FGFR1). Sulfatinib exhibited an acceptable safety profile and encouraging antitumor activity in patients with advanced solid tumors, particularly neuroendocrine tumors. Synonyms: N-(2-(dimethylamino)ethyl)-1-(3-((4-((2-methyl-1H-indol-5-yl)oxy)pyrimidin-2-yl)amino)phenyl)methanesulfonamide; HMPL012; HMPL012; HMPL 012; Sulfatinib. CAS No. 1308672-74-3. Molecular formula: C24H28N6O3S. Mole weight: 480.58. | |
| Sulfatinib | Sulfatinib (Surufatinib) is a potent and highly selective tyrosine kinase inhibitor against VEGFR1/2/3 , FGFR1 and CSF1R with IC 50 s of in a range of 1 to 24 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Surufatinib; HMPL-012. CAS No. 1308672-74-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12297. | |
| Sulfatinib | Sulfatinib, also known as surufatinib, is an orally bioavailable, small molecule inhibitor of vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, and the fibroblast growth factor receptor type 1 (FGFR1), with potential antineoplastic and anti-angiogenic activities. Upon oral administration, sulfatinib binds to and inhibits VEGFRs and FGFR1 thereby inhibiting VEGFR- and FGFR1-mediated signal transduction pathways. This leads to a reduction of angiogenesis and tumor cell proliferation in VEGFR/FGFR1-overexpressing tumor cells. Expression of VEGFRs and FGFR1 may be upregulated in a variety of tumor cell types. Group: Inhibitors. Alternative Names: HMPL012; HMPL012; HMPL 012; Sulfatinib. CAS No. 1308672-74-3. Molecular formula: C24H28N6O3S. Mole weight: 480.59. Appearance: Solid powder. Purity: >98%. IUPACName: N-(2-(dimethylamino)ethyl)-1-(3-((4-((2-methyl-1H-indol-5-yl)oxy)pyrimidin-2-yl)amino)phenyl)methanesulfonamide. Canonical SMILES: CC1=CC2=C (N1)C=CC (OC3=NC (NC4=CC (CS (NCCN (C)C) (=O)=O)=CC=C4)=NC=C3)=C2. Catalog: ACM1308672743. | |
| Sulfatolamide | Heterocyclic Organic Compound. Alternative Names: sulfatolamide. CAS No. 1161-88-2. Molecular formula: C7H10N2O2S.C7H9N3O2S2. Mole weight: 417.533. Catalog: ACM1161882. | |
| Sulfatroxazole | Sulfatroxazole. Group: Biochemicals. Alternative Names: N1- (4, 5-imethyl-3-isoxazolyl) sulfanilamide; 4, 5-Di methyl -3-sulfanilamidoisoxazole ; Isosulfafurazole; N1- (4, 5-Dimethyl-3-isoxazolyl) Sulfanilamide; N1- (4, 5-Dimethyl-3-isoxazolyl) Sulfanilamide; 4, 5-Di methyl -3-sulfanilamidoisoxazole ; Isosulfafurazole; N1- (4, 5-Dimethyl-3-isoxazolyl) sulfanilamide. Grades: Highly Purified. CAS No. 23256-23-7. Pack Sizes: 50mg. Molecular Formula: C11H13N3O3S, Molecular Weight: 267.3. US Biological Life Sciences. | Worldwide |
| Sulfatroxazole-d4 | Sulfatroxazole-d4. Group: Biochemicals. Alternative Names: N1- (4, 5-imethyl-3-isoxazolyl) sulfanilamide; 4,5-Dimethyl-3-sulfanilamidoisoxazole-d4; Isosulfafurazole-d4; N1- (4, 5-Dimethyl-3-isoxazolyl) Sulfanilamide-d4; N1- (4, 5-Dimethyl-3-isoxazolyl) Sulfanilamide-d4; 4,5-Dimethyl-3-sulfanilamidoisoxazole-d4; Isosulfafurazole-d4; N1- (4, 5-Dimethyl-3-isoxazolyl) sulfanilamide-d4. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C11H9D4N3O3S, Molecular Weight: 271.33. US Biological Life Sciences. | Worldwide |
| Sulfazecin | Sulfazecin is a water-soluble acidic substance produced by Pseudomonas acidophila G 6302. It has anti-Gram-negative bacteria activity and weak anti-Gram-positive bacteria activity. Grades: >98%. CAS No. 77912-79-9. Molecular formula: C12H20N4O9S. Mole weight: 396.38. | |
| Sulf-DBCO-NHS ester | Sulf-DBCO-NHS ester, a cutting-edge chemical reagent, finds its application in the field of biomedicine, serving as a versatile biomolecule labeling and tracking agent. Featuring a DBCO functional group, it selectively binds to the azide residues on proteins or nucleic acids. The ease of incorporation of the product into various assays and diagnostic tools makes it an ideal candidate for designing probes or conjugates. Its efficacy and efficiency have garnered great interest, and it is widely being adopted for various biomedical explorations. CAS No. 1379761-19-9. Molecular formula: C23H17N2NaO8S. Mole weight: 504.4. | |
| Sulfentrazone | Sulfentrazone is a phenyl triazolinone herbicide used for control of certain broadleaf and grass weed species. Sulfentrazone inhibits protoporphyrinogen oxidase, resulting in the disruption of lipid cell membranes [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 122836-35-5. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-135745. | |
| Sulfentrazone | Sulfentrazone is a herbicide and could control sedges in turfgrass effectively. Synonyms: Sulfentrazone; Authority; N-[2,4-dichloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-1,2,4-triazol-1-yl]phenyl]methanesulfonamide. Grades: > 95%. CAS No. 122836-35-5. Molecular formula: C11H10Cl2F2N4O3S. Mole weight: 387.19. | |
| Sulfentrazone | Sulfentrazone. Group: Biochemicals. Alternative Names: 2', 4'-Dichloro-5'- (4-difluoromethyl-4, 5-dihydro-3-methyl-5-oxo-1H-1, 2, 4-triazol-1-yl) methanesulfonanilide; Authority; Authority 75DF; Blanket; Boral; Capaz; Dismiss; F 6285; N- [2, 4-Dichloro-5- [4- (difluoromethyl) -4, 5-dihydro-3-methyl-5-oxo-1H-1, 2, 4-triazol-1-yl] phenyl] methanesulfonamide; Spartan; N- [2, 4-Dichloro-5- [4- (difluoromethyl) -4, 5-dihydro-3-methyl-5-oxo-1H-1, 2, 4-triazol-1-yl] phenyl] methanesulfonamide. Grades: Highly Purified. CAS No. 122836-35-5. Pack Sizes: 1g. Molecular Formula: C11H10Cl2F2N4O3S, Molecular Weight: 387.19. US Biological Life Sciences. | Worldwide |
| Sulfentrazone Impurity 1 | Sulfentrazone Impurity 1 is an impurity of Sulfentrazone, which is a herbicide and could control sedges in turfgrass effectively. Molecular formula: C11H10Cl2F2N4O5S2. Mole weight: 451.25. | |
| sulfhydrogenase | An iron-sulfur protein. The enzyme from the hyperthermophilic archaeon Pyrococcus furiosus is part of two heterotetrameric complexes where the β and γ subunits function as sulfur reductase and the α and Δ subunits function as hydrogenases (EC 1.12.1.3, hydrogen dehydrogenase [NADP+] and EC 1.12.1.4, hydrogen dehydrogenase [NAD(P)+], respectively). Sulfur can also be used as substrate, but since it is insoluble in aqueous solution and polysulfide is generated abiotically by the reaction of hydrogen sulfide and sulfur, polysulfide is believed to be the true substrate. Group: Enzymes. Synonyms: sulfur reductase. Enzyme Commission Number: EC 1.12.98.4. 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-0527; sulfhydrogenase; EC 1.12.98.4; sulfur reductase. Cat No: EXWM-0527. |  |
| sulfide-cytochrome-c reductase (flavocytochrome c) | The enzyme from Allochromatium vinosum contains covalently bound FAD and covalently-bound c-type hemes. Group: Enzymes. Enzyme Commission Number: EC 1.8.2.3. 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-1656; sulfide-cytochrome-c reductase (flavocytochrome c); EC 1.8.2.3. Cat No: EXWM-1656. | |
| sulfide dehydrogenase | A iron-sulfur flavoprotein. In the archaeon Pyrococcus furiosus the enzyme is involved in the oxidation of NADPH which is produced in peptide degradation. The enzyme also catalyses the reduction of sulfur with lower activity. Group: Enzymes. Synonyms: SuDH. Enzyme Commission Number: EC 1.8.1.19. 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-1645; sulfide dehydrogenase; EC 1.8.1.19; SuDH. Cat No: EXWM-1645. | |
| Sulfide Ion Selective Electrode Solutions | Sulfide Ion Selective Electrode Solutions. Group: Electrolytes. |  |
| sulfide:quinone reductase | Contains FAD. Ubiquinone, plastoquinone or menaquinone can act as acceptor in different species. This enzyme catalyses the formation of sulfur globules. It is also an important step in anoxygenic bacterial photosynthesis. Group: Enzymes. Enzyme Commission Number: EC 1.8.5.4. 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-1679; sulfide:quinone reductase; EC 1.8.5.4. Cat No: EXWM-1679. | |
| Sulfinemycin | Sulfinemycin is an anti-worm antibiotic produced by Str.sp. LL-F35101. It has a weak activity (MIC of 128 g/mL) against a few strains such as Staphylococcus aureus. Molecular formula: C16H31NOS. Mole weight: 285.49. | |
| sulfinoalanine decarboxylase | A pyridoxal-phosphate protein. Also acts on L-cysteate. The 1992 edition of the Enzyme List erroneously gave the name sulfoalanine decarboxylase to this enzyme. Group: Enzymes. Synonyms: cysteine-sulfinate decarboxylase; L-cysteinesulfinic acid decarboxylase; cysteine-sulfinate decarboxylase; CADCase/CSADCase; CSAD; cysteic decarboxylase; cysteinesulfinic acid decarboxylase; cysteinesulfinate decarboxylase; sulfoalanine decarboxylase; 3-sulfino-L-alanine carboxy-lyase. Enzyme Commission Number: EC 4.1.1.29. CAS No. 62213-10-9. 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-4772; sulfinoalanine decarboxylase; EC 4.1.1.29; 62213-10-9; cysteine-sulfinate decarboxylase; L-cysteinesulfinic acid decarboxylase; cysteine-sulfinate decarboxylase; CADCase/CSADCase; CSAD; cysteic decarboxylase; cysteinesulfinic acid decarboxylase; cysteinesulfinate decarboxylase; sulfoalanine decarboxylase; 3-sulfino-L-alanine carboxy-lyase. Cat No: EXWM-4772. | |
| Sulfinosine | Heterocyclic Organic Compound. Alternative Names: Sulfinosine, CID130209, 2-Amino-9-beta-ribofuranosylpurine-6-sulfinamide, 2-amino-9-beta--ribofuranosylpurine-6-sulfinamide, C063871, 9H-Purine-6-sulfinamide, 2-amino-9-beta-D-ribofuranosyl-, 124508-99-2. CAS No. 124508-99-2. Molecular formula: C10H14N6O5S. Mole weight: 330.320360 [g/mol]. Purity: 0.96. IUPACName: 2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purine-6-sulfinamide. Canonical SMILES: C1=NC2=C (N1C3C (C (C (O3)CO)O)O)N=C (N=C2S (=O)N)N. Density: 2.46g/cm³. Catalog: ACM124508992. | |
| Sulfinpyrazone | Sulfinpyrazone (G-28315) is an orally active and potent uricosuric agent for chronic and intermittent gouty arthritis. Sulfinpyrazone has antithrombotic and platelet inhibitory effects [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: G-28315. CAS No. 57-96-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1271. | |
| Sulfinpyrazone | Sulfinpyrazone is used in the treatment of gout acting as a uricosuric medication. Group: Biochemicals. Grades: Highly Purified. CAS No. 57-96-5. Pack Sizes: 2.5g, 10g. Molecular Formula: C23H20N2O3S. US Biological Life Sciences. | Worldwide |
| Sulfinpyrazone | Sulfinpyrazone is a uricosuric medication used to treat gout. It inhibits uric acid reabsorption in kidney proximal tubules. It can also used to reduce platelet aggregation by inhibiting degranulation of platelets which reduces the release of ADP and thromboxane. It was developed by Novartis and has been listed. Uses: Sulfinpyrazone is a uricosuric medication used to treat gout. Synonyms: G-28315; G28315; G 28315; Anturane; Sulfinpyrazon; Anturan; Diphenylpyrazone; Anturanil; 1,2-Diphenyl-4-(2-(phenylsulfinyl)ethyl)pyrazolidine-3,5-dione; NSC 75925. Grades: 98%. CAS No. 57-96-5. Molecular formula: C23H20N2O3S. Mole weight: 404.48. | |
| Sulfinyl ion (8CI,9CI) | Heterocyclic Organic Compound. CAS No. 12439-73-5. Molecular formula: OS. Catalog: ACM12439735. | |
| Sulfiram | Sulfiram, an ectoparasiticide, is a agent applied topically to treat scabies [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 95-05-6. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-121817. | |
| sulfiredoxin | In the course of the reaction of EC 1.11.1.15, peroxiredoxin, its cysteine residue is alternately oxidized to the sulfenic acid, S-hydroxycysteine, and reduced back to cysteine. Occasionally the S-hydroxycysteine residue is further oxidized to the sulfinic acid S-hydroxy-S-oxocysteine, thereby inactivating the enzyme. The reductase provides a mechanism for regenerating the active form of peroxiredoxin, i.e. the peroxiredoxin-(S-hydroxycysteine) form. Apparently the reductase first catalyses the phosphorylation of the -S(O)-OH group by ATP to give -S(O)-O-P, which is attached to the peroxiredoxin by a cysteine residue, forming an -S(O)-S- link between the two enzymes. Attack by a thiol splits this bond, leaving the peroxiredoxin as the sulfenic acid and the reductase as the thiol. Group: Enzymes. Synonyms: Srx1; sulphiredoxin; peroxiredoxin-(S-hydroxy-S-oxocysteine) reductase. Enzyme Commission Number: EC 1.8.98.2. CAS No. 710319-61-2. 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-1683; sulfiredoxin; EC 1.8.98.2; 710319-61-2; Srx1; sulphiredoxin; peroxiredoxin-(S-hydroxy-S-oxocysteine) reductase. Cat No: EXWM-1683. | |
| Sulfisomidin | Sulfisomidin, closely related to sulfadimidine, is a sulfonamide antibacterial. Synonyms: 4-amino-N-(2,6-dimethylpyrimidin-4-yl)benzenesulfonamide; Aristamid Augensalbe; Aristamid Augentropfen; Augensalbe, Aristamid; Augentropfen, Aristamid; Elkosin; Sodium, Sulfisomidine; Sulfaisodimidine; Sulfisomidine; Sulfisomidine Sodium; Sulphasomidine. CAS No. 515-64-0. Molecular formula: C12H14N4O2S. Mole weight: 278.33. | |
| Sulfisomidine, Sodium (4-Amino-N- (2, 6-dimethyl-4-pyimidinyl) benzenesulfonamide Sodium) | Sulfisomidine, Sodium (4-Amino-N- (2, 6-dimethyl-4-pyimidinyl) benzenesulfonamide Sodium). Group: Biochemicals. Alternative Names: 4-Amino-N- (2, 6-dimethyl-4-pyimidinyl) benzenesulfonamide Sodium. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Sulfisoxazol (4-amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide) | 25g Pack Size. Group: Analytical Reagents, Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C11H13N3O3S. CAS No. 127-69-5. Prepack ID 11597791-25g. Molecular Weight 267.3. See USA prepack pricing. |  |
| Sulfisoxazol (4-amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide) | 5g Pack Size. Group: Analytical Reagents, Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C11H13N3O3S. CAS No. 127-69-5. Prepack ID 11597791-5g. Molecular Weight 267.3. See USA prepack pricing. | |
| Sulfisoxazole | Sulfisoxazole is a sulfonamide antibacterial with an oxazole substituent. Synonyms: NU445; NU-445; NU 445; Sulfisoxazole; Neazolin; Neoxazol. Grades: >98%. CAS No. 127-69-5. Molecular formula: C11H13N3O3S. Mole weight: 267.3. | |
| Sulfisoxazole | Sulfisoxazole (Sulfafurazole) is an orally active endothelin receptor antagonist with IC 50 values of 0.60 μM and 22 μM against endothelin receptor A and endothelin receptor B, respectively. Sulfisoxazole is a sulfonamide antibacterial agent with an oxazole substituent. Sulfisoxazole inhibits breast cancer exosome release by targeting endothelin receptor A [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sulfafurazole. CAS No. 127-69-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0323. | |
| Sulfisoxazole | Sulfisoxazole. Group: Biochemicals. Grades: Highly Purified. CAS No. 127-69-5. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C11H13N3O3S. US Biological Life Sciences. | Worldwide |
| Sulfisoxazole acetyl | Sulfisoxazole acetyl (N1-Acetylsulfisoxazole), a Sulfisoxazole derivative, is an orally active dihydropteroate synthase inhibitor. Sulfisoxazole acetyl has an antibacterial action [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N1-Acetylsulfisoxazole. CAS No. 80-74-0. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-107923. | |
| Sulfisoxazole (Standard) | Sulfisoxazole (Standard) is the analytical standard of Sulfisoxazole. This product is intended for research and analytical applications. Sulfisoxazole (Sulfafurazole) is an orally active endothelin receptor antagonist with IC 50 values of 0.60 μM and 22 μM against endothelin receptor A and endothelin receptor B, respectively. Sulfisoxazole is a sulfonamide antibacterial agent with an oxazole substituent. Sulfisoxazole inhibits breast cancer exosome release by targeting endothelin receptor A [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 127-69-5. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0323R. | |
| sulfite dehydrogenase | Associated with cytochrome c-551. Group: Enzymes. Synonyms: sulfite cytochrome c reductase; sulfite-cytochrome c oxidoreductase; sulfite oxidase. Enzyme Commission Number: EC 1.8.2.1. CAS No. 37256-47-6. 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-1654; sulfite dehydrogenase; EC 1.8.2.1; 37256-47-6; sulfite cytochrome c reductase; sulfite-cytochrome c oxidoreductase; sulfite oxidase. Cat No: EXWM-1654. | |
| sulfite oxidase | A molybdohemoprotein. Group: Enzymes. Enzyme Commission Number: EC 1.8.3.1. CAS No. 9029-38-3. Sulfite Oxidase. 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-1658; sulfite oxidase; EC 1.8.3.1; 9029-38-3. Cat No: EXWM-1658. | |
| Sulfite oxidase from H. sapiens, Recombinant | Sulfite oxidase (EC 1.8.3.1) is an enzyme in the mitochondria of all eukaryotes.[citation needed] It oxidizes sulfite to sulfate and, via cytochrome c, transfers the electrons produced to the electron transport chain, allowing generation of ATP in oxidative phosphorylation. This is the last step in the metabolism of sulfur-containing compounds and the sulfate is excreted. Sulfite oxidase is a metallo-enzyme that utilizes a molybdopterin cofactor and a heme group. It is one of the cytochromes b5 and belongs to the enzyme super-family of molybdenum oxotransferases that also includes DMSO reductase, xanthine oxidase, and nitrite reductase. Group: Enzymes. Synonyms: sulfite oxidase; EC 1.8.3.1; 9029-38-3. Enzyme Commission Number: EC 1.8.3.1. CAS No. 9029-38-3. Purity: >95 % as judged by SDS-PAGE. Sulfite Oxidase. Mole weight: approx. 50000 Da. Activity: 0.5 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: E. coli. Species: H. sapiens. sulfite oxidase; EC 1.8.3.1; 9029-38-3; Sulfite:oxygen oxidoreductase. Cat No: NATE-1229. | |
| sulfite reductase (coenzyme F420) | The enzyme, isolated from the archaeon Methanocaldococcus jannaschii, is involved in sulfite detoxification and assimilation. Group: Enzymes. Synonyms: coenzyme F420-dependent sulfite reductase; Fsr. Enzyme Commission Number: EC 1.8.98.3. 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-1684; sulfite reductase (coenzyme F420); EC 1.8.98.3; coenzyme F420-dependent sulfite reductase; Fsr. Cat No: EXWM-1684. | |
| Sulfluramid | Sulfluramid. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| sulfoacetaldehyde acetyltransferase | The reaction occurs in the reverse direction to that shown above. Requires Mg2+. Group: Enzymes. Synonyms: Xsc. Enzyme Commission Number: EC 2.3.3.15. CAS No. 56941-15-2. 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-2316; sulfoacetaldehyde acetyltransferase; EC 2.3.3.15; 56941-15-2; Xsc. Cat No: EXWM-2316. | |
| sulfoacetaldehyde dehydrogenase | This reaction is part of a bacterial pathway that can utilize the amino group of taurine as a sole source of nitrogen for growth. At physiological concentrations, NAD+ cannot be replaced by NADP+. The enzyme is specific for sulfoacetaldehyde, as formaldehyde, acetaldehyde, betaine aldehyde, propanal, glyceraldehyde, phosphonoacetaldehyde, glyoxylate, glycolaldehyde and 2-oxobutyrate are not substrates. Group: Enzymes. Synonyms: SafD. Enzyme Commission Number: EC 1.2.1.73. 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-1175; sulfoacetaldehyde dehydrogenase; EC 1.2.1.73; SafD. Cat No: EXWM-1175. | |
| sulfoacetaldehyde dehydrogenase (acylating) | The enzyme is involved in degradation of sulfoacetate. In this pathway the reaction is catalysed in the reverse direction. The enzyme is specific for sulfoacetaldehyde and NADP+. Group: Enzymes. Synonyms: SauS. Enzyme Commission Number: EC 1.2.1.81. 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-1184; sulfoacetaldehyde dehydrogenase (acylating); EC 1.2.1.81; SauS. Cat No: EXWM-1184. | |
| sulfoacetaldehyde reductase | Catalyses the reaction only in the opposite direction. Involved in taurine degradation. The bacterium Chromohalobacter salexigens strain DSM 3043 possesses two enzymes that catalyse this reaction, a constitutive enzyme (encoded by isfD2) and an inducible enzyme (encoded by isfD). The latter is induced by taurine, and is responsible for most of the activity observed in taurine-grown cells. Group: Enzymes. Synonyms: isfD (gene name). Enzyme Commission Number: EC 1.1.1.313. 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-0225; sulfoacetaldehyde reductase; EC 1.1.1.313; isfD (gene name). Cat No: EXWM-0225. | |
| Sulfobetaine 10 | Zwitterionic Detergents. Alternative Names: N-Decyl-N,N-dimethyl-3-ammonio-1-propanesulfonate. CAS No. 15163-36-7. Molecular formula: C15H33NO3S. Mole weight: 307.5. Appearance: White solid. Purity: >99%. IUPACName: 3-[decyl(dimethyl)azaniumyl]propane-1-sulfonate. | |
| Sulfobetaine 10 | Sulfobetaine 10, is a zwitterionic surfactant commonly used in biochemistry and biophysics. It is commonly used to dissolve membrane proteins and other hydrophobic molecules in aqueous solutions. Sulfobetaine 10 has both positively and negatively charged groups in its structure, which allows it to maintain a neutral charge in solution and reduces its tendency to denature proteins. It is considered a mild, non-denaturing surfactant and is widely used in protein research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 15163-36-7. Pack Sizes: 1 g; 5 g. Product ID: HY-126377. | |
| Sulfobetaine-12 | Zwitterionic Detergents. Alternative Names: N-Dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate. CAS No. 14933-08-05. Molecular formula: C17H37NO3S. Mole weight: 335.5. Appearance: White solid. Purity: >99%. | |
| Sulfobetaine-14 | Zwitterionic Detergents. Alternative Names: N-Tetradecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate. CAS No. 14933-09-06. Molecular formula: C19H41NO3S. Mole weight: 363.6. Appearance: White solid. Purity: >99%. | |
| Sulfobetaine-14 | Zwittergent 3-14 (DMAPS) is a zwitterionic detergent commonly used in biochemistry and molecular biology for the solubilization and purification of membrane-bound proteins and other hydrophobic biomolecules, which have both hydrophilic and hydrophobic moieties , so that it has good detergency properties, making it suitable for stabilizing membrane proteins in aqueous solutions. In addition, DMAPS has been used in various techniques such as electrophoresis and chromatography for the separation and analysis of biomolecules. The long The hydrocarbon chains provide it with good membrane penetration and solubilization capabilities, while the sulfonate and quaternary ammonium groups ensure water solubility and charge neutrality. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: SB3-14; DMAPS. CAS No. 14933-09-6. Pack Sizes: 5 g. Product ID: HY-W099581. | |
| Sulfobetaine-16 | 3-(Hexadecyldimethylammonio)propane-1-sulfonate is an organic compound belonging to the class of sulfonates. It is a quaternary ammonium surfactant commonly used in various industrial and laboratory applications such as the production of detergents, personal care products and pharmaceuticals. 3-(Hexadecyldimethylammonio)propane-1-sulfonate is surface active and can be used as an emulsifier, foaming agent and wetting agent. In addition, it is used as a solubilizer in protein purification and as a surfactant in chromatography. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 2281-11-0. Pack Sizes: 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-W099575. | |
| Sulfobromophthalein sodium | Heterocyclic Organic Compound. Alternative Names: Bromsulfalein sodium, 167207_SIAL, Sulfobromophthalein sodium salt hydrate, Sulfobromophthalein disodium salt hydrate, Bromsulfalein sodium disodium salt hydrate, 123359-42-2. CAS No. 123359-42-2. Molecular formula: C20H8Br4Na2O10S2. Mole weight: 838. Appearance: white crystalline powder. Purity: Purity >98%. IUPACName: disodium;2-hydroxy-5-[4,5,6,7-tetrabromo-1-(4-hydroxy-3-sulfonatophenyl)-3-oxo-2-benzofuran-1-yl]benzenesulfonate;hydrate. Canonical SMILES: C1=CC (=C (C=C1C2 (C3=C (C (=C (C (=C3Br)Br)Br)Br)C (=O)O2)C4=CC (=C (C=C4)O)S (=O) (=O)[O-])S (=O) (=O)[O-])O. O. [Na+]. [Na+]. Catalog: ACM123359422. | |
| Sulfobromophthalein Sodium (BSP) | Sulfobromophthalein disodium salt hydrate has been used as a positive control to study the interaction of 11-keto- β-boswellic acid (KBA) and 3-acetyl-11-keto- β-boswellic acid (AKBA) with organic anion transporter OATP1B3. Sulfobromophthalein (BSP) is a high affinity organic ion substrate for organic anion transporting polypeptides (OATPs) and has been used as a substrate for multidrug resistance associated protein 2 (Mrp2). BSP is transported into hepatocytes by OATPs and, after conjugation to glutathione, is excreted into bile by Mrp2. It was found to inhibit the aldo-keto reductase ARK1C20. Group: Biochemicals. Alternative Names: Bromsulfalein disodium salt hydrate; Bromothalein disodium salt hydrate; Sulfobromophthalein disodium salt hydrate; BSP; disodium 2-hydroxy-5-1z-4-oxo-3-sulfonatocyclohexa-2,5-dien-1-ylidene 2,3,4,5-tetrabromo-6-carboxyphenyl methyl benzenesulfonate tetrahydrate. Grades: Highly Purified. CAS No. 123359-42-2. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C20H8Br4O10S2·2Na, Molecular Weight: 837.99. US Biological Life Sciences. | Worldwide |
| Sulfo BSOCOES | Sulfo BSOCOES. Pack Sizes: Milligram Quantities: 100 mg. Order Number: CL105. |  www.prochemonline.com |
| Sulfo-butanedioic acid 1-[2-[(1-oxododecyl)amino]ethyl]este diammonium salt | Heterocyclic Organic Compound. CAS No. 123776-55-6. Purity: 0.96. Catalog: ACM123776556. | |
| Sulfobutylether β- Cyclodextrin | β-Cyclodextrin is a cyclic oligosaccharide containing seven D-(+)-glucopyranose units attached by a(1→4) glucoside bonds. Sulfobutylether b-cyclodextrin is an anionic β-cyclodextrin derivative with a sodium sulfonate salt separated from the hydrophobic cavity by a butyl spacer group. The substituent is introduced at positions 2, 3, and 6 in at least one of the glucopyranose units in the cyclodextrin structure. Synonyms: β-Cyclodextrin sulfobutylether, sodium salt; Captisol; (SBE)m-betaCD; SBE7-b-CD; SBECD; sulfobutylether-β-cyclodextrin, sodium salt. CAS No. 1824100-00-0. Product ID: PE-0597. Molecular formula: C42H70-nO35·(C4H8SO3Na)n. Mole weight: 2163 (where n = approximately 6.5). Category: Biocompatibility enhancer; Osmotic Agents; Solubilizing Agents; Stabilizing Agents; Tablet and Capsule Diluent; Viscosity-increasing Agents; Water activity reducing Agents. Product Keywords: Stabilizers; Solubilizer Excipients; PE-0597; Sulfobutylether β- Cyclodextrin; Biocompatibility enhancer; Osmotic Agents; Solubilizing Agents; Stabilizing Agents; Tablet and Capsule Diluent; Viscosity-increasing Agents; Water activity reducing Agents; C42H70-nO35·(C4H8SO3Na)n; 1824100-00-0. UNII: NA. Chemical Name: β-Cyclodextrin sulfobutylether, sodium salt. Grade: Pharmceutical Excipients. Administration route: SC, oral, inhalation, nasal and ophthalmic, IV and IM. Dosage Form: SC, ora |  |
| Sulfochlorophenol s | Heterocyclic Organic Compound. CAS No. 108321-09-1. Molecular formula: C22H14Cl2N4O16S4. Mole weight: 789.53. Catalog: ACM108321091. | |
| Sulfociprofloxacin | Ciprofloxacin Piperazinyl-N4-sulfate is a metabolite of the fluorinated quinolone antibacterial Ciprofloxacin. Synonyms: 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-sulfo-1-piperazinyl)-3-quinolinecarboxylic Acid; Sulfociprofloxacin; 4-Sulfociprofloxacin; BAY-s 9435. Grades: > 95%. CAS No. 105093-21-8. Molecular formula: C17H18FN3O6S. Mole weight: 413.43. | |
| Sulfo Cy3.5 Carboxylic acids(ethyl) | Cyanine Fluorophores. CAS No. 1284240-77-2. Molecular formula: C39H43N2O14S4+. Mole weight: 892.01. Appearance: Purple powder. Purity: >97%. Catalog: ACM1284240772. | |
| Sulfo-Cy3 Azide | Sulfo-Cy3 Azide is a water-soluble fluorogenic dye containing an azide group, which enables Click Chemistry. Sulfo-Cy3 Azide can be used for the labeling of sensitive molecules such as proteins [1] [2]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Fluorescent dye. CAS No. 1801695-56-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-151710. | |
| Sulfo Cy3 Carboxylic acids(methyl) | Cyanine Fluorophores. Alternative Names: 2-((E)-3-((Z)-1-(5-carboxypentyl)-3,3-dimethyl-5-(sulfinooxy)indolin-2-ylidene)prop-1-en-1-yl)-1,3,3-trimethyl-3H-indol-1-ium-5-sulfonate. CAS No. 1121756-11-3. Molecular formula: C30H36N2O8S2. Mole weight: 616.74. Appearance: Red powder. Purity: 0.95. IUPACName: 2-[(E)-3-[1-(5-carboxypentyl)-3,3-dimethyl-5-sulfinooxyindol-2-ylidene]prop-1-enyl]-1,3,3-trimethylindol-1-ium-5-sulfonate. Canonical SMILES: CC1 (C2=C (C=CC (=C2)S (=O) (=O)[O-])[N+] (=C1C=CC=C3C (C4=C (N3CCCCCC (=O)O)C=CC (=C4)OS (=O)O) (C)C)C)C. Catalog: ACM1121756113-1. | |
| Sulfo-Cy3-YNE | Cyanine Fluorophores. Alternative Names: (2Z)-2-[(E)-3-[3,3-dimethyl-1-[6-oxo-6-(prop-2-ynylamino)hexyl]-5-sulfoindol-1-ium-2-yl]prop-2-enylidene]-1-ethyl-3,3-dimethylindole-5-sulfonicacid. CAS No. 1010386-62-5. Molecular formula: C34H41N3O7S2. Mole weight: 667.84. Appearance: Darkred powder. Purity: 0.95. IUPACName: 2-[3-[3,3-dimethyl-1-[6-oxo-6-(prop-2-ynylamino)hexyl]-5-sulfoindol-1-ium-2-yl]prop-2-enylidene]-1-ethyl-3,3-dimethylindole-5-sulfonate. Canonical SMILES: CCN1C2=C (C=C (C=C2)S (=O) (=O)[O-])C (C1=CC=CC3=[N+] (C4=C (C3 (C)C)C=C (C=C4)S (=O) (=O)O)CCCCCC (=O)NCC#C) (C)C. Catalog: ACM1010386625-1. | |
| Sulfo-Cy5.5 Azide | Sulfo-Cy5.5 Azide is a click chemistry reagent containing an azide group. Sulfo-Cy5.5 Azide is also a water-soluble dye (Ex=673 nm, Em=707 nm), which designed to label sensitive molecules such as peptides, proteins and oligonucleotides. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Fluorescent dye. CAS No. 1955527-41-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-151711. | |
| Sulfo-Cy5 amine | Sulfo-Cy5 amine is a dye derivative of Cyanine 5 (Cy5) (HY-D0821) bearing an amine group. The sulfonate ion increases the water solubility of the compound, making it suitable for use in aqueous solutions. Cy5 is a near-infrared fluorescent dye commonly used in biolabeling and cell imaging. The amine functionality of Sulfo-Cy5 amine can react with carboxyl groups to form covalent bonds. Sulfo-Cy5 amine can bind to biomolecules such as proteins and antibodies to track their location and dynamic changes in biological samples. Uses: Scientific research. Group: Fluorescent dye. CAS No. 2183440-44-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D1375. | |
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