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| Product | Description | |
|---|---|---|
| Sulfathiazole-(phenyl-13C6) | analytical standard. Group: Application areas. |  |
| 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. Grade: >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 |
| 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. Uses: Designed for use in research and industrial production. Additional or Alternative Names: HMPL012; HMPL012; HMPL 012; Sulfatinib. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 1308672-74-3. Molecular formula: C24H28N6O3S. Mole weight: 480.59. 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. Product ID: ACM1308672743. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 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. | |
| 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. Grade: >98%. CAS No. 77912-79-9. Molecular formula: C12H20N4O9S. Mole weight: 396.38. | |
| 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. 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 |
| 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 - Clay | certified reference material, pkg of 30 g. Group: Certified reference materials (crms). | |
| 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 IC Standard | analytical standard. Group: Certified reference materials (crms). | |
| Sulfide in Seawater - Whole Volume | certified reference material. Group: Waste water matrix crms. | |
| Sulfide in Soil - PT | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| Sulfide Ion Selective Electrode Solutions | We offer the products in two grades: ISA; Fill Solution. Group: Ion selective electrode solutions. Alternative Names: Sulfide electrode solution. | |
| 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. | |
| Sulfide - Sandy Loam | certified reference material, pkg of 30 g. Group: Certified reference materials (crms). | |
| Sulfide (Total and Soluble) - WP | Concentrate for dilution to 1L, Proficiency Testing Material. Group: Waste water. | |
| Sulfide - WP | certified reference material. Group: Certified reference materials (crms). | |
| Sulfinalol | Sulfinalol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SULFINALOL; Sulfinalolum. Product Category: Heterocyclic Organic Compound. CAS No. 66264-77-5. Molecular formula: C20H27NO4S. Mole weight: 377.497680 [g/mol]. Purity: 0.96. IUPACName: 4-[1-hydroxy-2-[4-(4-methoxyphenyl)butan-2-ylamino]ethyl]-2-methylsulfinylphenol. Product ID: ACM66264775. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| 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 (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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Enturan, Anturanil, 1,2-Diphenyl-4-[2-(phenylsulfinyl)ethyl]-3,5-pyrazolidinedione, 4-(Phenylsulfoxyethyl)-1,2-diphenyl-3,5-pyrazolidinedione, Sulfoxyphenylpyrazolidine, Diphenylpyrazone, Sulphinpyrazone, Anturan, NSC 75925, Sulfinpyrazone,3,5-Pyrazolidinedione, 1,2-diphenyl-4-[2-(phenylsulfinyl)ethyl]-, 1,2-Diphenyl-4-(2'-phenylsulfinethyl)-3,5-pyrazolidinedione, G 28315, Anturen, Anturane, Sulfinpyrazon, Anturidin, Enturen. | |
| Sulfiram | Sulfiram. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Kutka; tetraethylthiodicarbonic diamide ([[(C2H5)2N]C(S)]2S); diethylcarbamothioyl N,N-diethylcarbamodithioate; Tetmos; Tetrucid; Sulfirame; Sulfiramum; Bis-(diaethyl-thiocarbamoyl)-sulfan; Sanigal; N1,N1,N3,N3-tetraethyl-1,2,3-trithiodicarbonic diamide; Tetmosol; bis (N,N-diethyl thiocarbamoyl)-sulphide; Bis-diaethylthiocarbamoyl-sulfid; SULFIRAM; tetraethylthiuram monosulfide; Sarcocide B. CAS No. 95-05-6. Molecular formula: C10H20N2S3. Mole weight: 264.47. Purity: 95%+. IUPACName: sulfiram. Density: 1.139g/cm³. Product ID: ACM95056. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 | analytical standard. Group: Application areas. | |
| 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) | 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. |  |
| 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. | |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolites. Alternative Names: NSC 33807, NSC 13120, Isoxamin, Sulfaisoxazole, Unisulf, Gantrosan, NSC 683536, 5-Sulfanilamido-3,4-dimethylisoxazole, Dorsulfan Warthausen, 4-Amino-N-(3,4-dimethylisoxazol-5-yl)benzenesulfonamide, 5-(p-Aminobenzenesulphonamido)-3,4-dimethylisoxazole, Sulfoxol, Amidoxal, Norilgan-S, Soxisol, Neoxazol, Stansin, Soxomide, Sulfisoxazole dialamine, Sulfazin, Sulfafurazole, 5-(p-Aminobenzenesulfonamido)-3,4-dimethylisoxazole, N-(3,4-Dimethylisoxazol-5-yl)-4-aminobenzenesulfonamide, Alphazole, NSC 38588, Sulfisoxazol, Neazolin, Sulfisoxazole, N1-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide, Sulsoxin, Roxosul tablets, Sosol, Thiasin, Sulfadimethylisoxazole, 5-(4-Aminophenylsulfonamido)-3,4-dimethylisoxazole, Sulphafurazole, Sulfalar, Uritrisin, Sulfasol, Pancid, Gantrisin, Sulphisoxazole, Gantrisona, Entusul, Sulfagan, Sulfafurazol, 3,4-Dimethyl-5-sulfonamidoisoxazole, Chemouag, Sulbio,3,4-Dimethyl-5-sulfanilamidoisoxazole, Gantrizin. | |
| Sulfisoxazole | analytical standard. Group: Application areas. | |
| Sulfisoxazole-[13C6] | Sulfisoxazole-[13C6] is the labelled analogue of Sulfisoxazole, which is an antibiotic against both Gram-negative and Gram-positive organisms. Synonyms: Sulfisoxazole-13C6; 4-Amino-N-(3,4-dimethylisoxazol-5-yl)benzene-13C6-sulfonamide; Sulfafurazole-13C6; Sulfisoxazole-(phenyl-13C6); N1-(3,4-dimethyl-5-isoxazolyl)sulfanilamide-13C6; 3,4-Dimethyl-5-sulfanilamidoisoxazole-13C6; 5-(p-Aminobenzenesulphonamido)-3,4-dimethylisoxazole-13C6; Alphazole-13C6. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1334378-46-9. Molecular formula: C5[13C]6H13N3O3S. Mole weight: 273.26. | |
| 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 diolamine | Sulfisoxazole diolamine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: NU-445; N-(3,4-Dimethylisoxazol-5-yl)sulphanilamide,compound with 2,2-iminodiethanol (1:1); Sulfafurazol 2,2-imidodiethanol; Benzenesulfonamide,4-amino-N-(3,4-dimethyl-5-isoxazolyl)-,compd. with 2,2-iminobis(ethanol) (1:1); EINECS 224-308-1; N(sup 1)-(3,4. Product Category: Heterocyclic Organic Compound. CAS No. 4299-60-9. Molecular formula: C15H24N4O5S. Mole weight: 372.439860 [g/mol]. Purity: 0.96. IUPACName: 4-amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide; 2-(2-hydroxyethylamino)ethanol. Product ID: ACM4299609. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulfisoxazole-(phenyl-13C6) | analytical standard. Group: Application areas. | |
| 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 in Water | certified reference material. Group: Certified reference materials (crms). | |
| Sulfite in Water - WS | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). | |
| 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 chicken liver | Sulfite oxidase from chicken liver. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SULFITE OXIDASE FROM CHICKEN LIVER;Sulphite oxidase;Sulfiteoxidase;Sulfite:oxygenoxidoreductase;E.C. 1.8.3.1. Product Category: Heterocyclic Organic Compound. CAS No. 9029-38-3. Mole weight: 0. Product ID: ACM9029383. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| Sulfoacetic acid disodium salt | Sulfoacetic acid disodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SULFOACETIC ACID DISODIUM SALT;sulfo-aceticacidisodiumsalt;disodium sulphonatoacetate;Sulfoacetic acid disodium salt,99%. Product Category: Heterocyclic Organic Compound. CAS No. 5462-60-2. Molecular formula: C2H2Na2O5S. Mole weight: 184.08. Density: 1.875g/cm³. Product ID: ACM5462602. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulfo-ara-F-NMN | Sulfo-ara-F-NMN (CZ-48) is a mimetic of nicotinamide mononucleotide (NMN). Sulfo-ara-F-NMN acts selectively, activating SARM1 but inhibiting CD38 (IC50 around 10 ?M). Sulfo-ara-F-NMN induces intracellular cyclic ADP-ribose (cADPR) production[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CZ-48. CAS No. 1374663-29-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-129522. | |
| 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-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 (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-eicosyl este disodium salt | Sulfo-butanedioic acid 1-eicosyl este disodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Disodium 1-icosyl 2-sulphonatosuccinate, EINECS 287-298-8, CID11970951, 85455-64-7. Product Category: Heterocyclic Organic Compound. CAS No. 85455-64-7. Molecular formula: C24H44Na2O7S. Mole weight: 522.646500 [g/mol]. Purity: 0.96. IUPACName: disodium 4-icosoxy-4-oxo-3-sulfonatobutanoate. Product ID: ACM85455647. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulfo-butanedioic acid c-(2-ethylhexyl)c-methyl este sodium salt | Sulfo-butanedioic acid c-(2-ethylhexyl)c-methyl este sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 300-033-3, Sodium C-(2-ethylhexyl) C-methyl hydrogen 2-sulphonatosuccinate, 93919-49-4. Product Category: Heterocyclic Organic Compound. CAS No. 93919-49-4. Molecular formula: C13H23NaO7S. Mole weight: 346.372289 [g/mol]. Purity: 0.96. IUPACName: sodium;3-carboxy-5-ethyl-1-hydroxy-3-methyl-1-oxononane-2-sulfonate. Product ID: ACM93919494. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 |  |
| Sulfocostunolide B | Sulfocostunolide B can be found in the roots of Saussurea lappa. Synonyms: Sulfocostulide B. Grade: >98%. CAS No. 1059671-65-6. Molecular formula: C15H20O5S. Mole weight: 312.4. | |
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