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| Product | Description | |
|---|---|---|
| Succinimidyl bromoacetate ≥97% (NMR) | Succinimidyl bromoacetate ≥97% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. |  Worldwide |
| Succinimidyl Glutaramide-PEG5K-Succinimidyl Glutaramide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 5000. |  |
| Succinimidyl Glutaramide-PEG5K-Succinimidyl Glutaramide | average Mn 5000. Group: Poly(ethylene glycol) and poly(ethylene oxide). |  |
| Succinimidyl iodoacetate 98+% (HPLC) | Succinimidyl iodoacetate 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Succinimidyl Myristate | Succinimidyl Myristate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Succinimidyl Nervonate | Succinimidyl Nervonate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Succinimidyl oxycarbonyl -b-alanine- hydroxysuccinimide ester 99+% (NMR) | Succinimidyl oxycarbonyl -b-alanine- hydroxysuccinimide ester 99+% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Succinimidyl oxycarbonyl -beta-alanine- hydroxysuccinimide ester | Succinimidyl oxycarbonyl -beta-alanine- hydroxysuccinimide ester. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Succinimidyloxycarbonyl polyethyleneglycol resin | TentaGel resins are grafted copolymers consisting of a low crosslinked polystyrene matrix on which poly(ethylene glycol) (PEG or POE) is grafted. Synonyms: SuOCO-PEG Resin; TentaGel S COOSu. |  |
| Succinimidyl-p-formylbenzoate 98+% (HPLC) | Succinimidyl-p-formylbenzoate 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Succinimidyl Succinamide-PEG5K-Succinimidyl Succinamide | average Mn 5000. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Succinimidyl Succinamide-PEG5K-Succinimidyl Succinamide | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Poly(ethylene glycol) and poly(ethylene oxide). Molecular formula: average Mn 5000. | |
| Succinobucol | Succinobucol. Group: Biochemicals. Alternative Names: Butanedioic acid 1-[4-[[1-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]-1-methylethyl]thio]-2,6-bis(1,1-dimethylethyl)phenyl] ester; Probucol monosuccinate. Grades: Highly Purified. CAS No. 216167-82-7. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C35H52O5S2. US Biological Life Sciences. | Worldwide |
| Succinobucol | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Succinobucol | Succinobucol is a phenolic antioxidant with anti-inflammatory and antiplatelet effects. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AGI-1067; Probucol monosuccinate. CAS No. 216167-82-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14937. |  |
| Succinprotocetraric acid | Succinprotocetraric acid. Synonyms: Butanedioic acid, 1-(7-carboxy-4-formyl-3,8-dihydroxy-1,6-dimethyl-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-9-yl)methyl ester; 4-(3-carboxypropanoyloxymethyl)-10-formyl-3,9-dihydroxy-1,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid. CAS No. 50484-90-7. Molecular formula: C22H18O12. Mole weight: 474.37. | |
| Succinyl-(2-hydroxypropyl)-β-cyclodextrin | Succinyl-(2-hydroxypropyl)-β-cyclodextrin. Group: Polysaccharide. | |
| Succinyl-(2-hydroxypropyl)-?-cyclodextrin | >95%. Group: Polysaccharide. | |
| Succinylacetone | Succinylacetone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,6-Dioxoheptanoic Acid-13C5. Product Category: Heterocyclic Organic Compound. CAS No. 881835-86-5. Molecular formula: C213C5H10O4. Mole weight: 163.12. Purity: 0.96. IUPACName: 4,6-dioxoheptanoic acid. Product ID: ACM881835865. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Succinylacetone | Succinylacetone (SA) is a specific marker for the inherited metabolic disease, hepatorenal tyrosinemia. It was developed a stable-isotope. Group: Biochemicals. Alternative Names: 4,6-Dioxoheptanoic Acid. Grades: Highly Purified. CAS No. 51568-18-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Succinylacetone-13C7 | Succinylacetone-13C7 is a labelled analogue of Succinylacetone. Succinylacetone (SA) is a specific marker for the inherited metabolic disease, hepatorenal tyrosinemia. It was developed a stable-isotope for the determination of SA in dried blood spots (DBS) and liquid urine using a 13C4-SA as internal standard. The method was applied retrospectively and prospectively for the diagnosis of hepatorenal tyrosinemia and for follow-up of patients under treatment. Group: Biochemicals. Alternative Names: 4,6-Dioxoheptanoic Acid-13C7; NSC 174804-13C7; 4,6-Dioxoheptanoic-3,4,5,6,7-13C7 Acid. Grades: Highly Purified. CAS No. 51568-18-4. Pack Sizes: 500ug. Molecular Formula: ¹³C?H??O?, Mol. Weight: 165.1. US Biological Life Sciences. | Worldwide |
| Succinyladenosine | Succinyladenosine, the metabolic product of dephosphorylation of intracellular adenylosuccinic acid (S-AMP) by cytosolic 5-nucleotidase, is a biochemical marker of adenylosuccinase (ASL) deficiency [1]. Uses: Scientific research. Group: Natural products. Alternative Names: N6-Succinyl adenosine. CAS No. 4542-23-8. Pack Sizes: 10 mM * 1 mL; 1 mg. Product ID: HY-113284. | |
| Succinyl-Ala-Ala-Pro-Phe-p-nitroanilide - CAS 70967-97-4 | Sensitive chromogenic substrate for human leukocyte cathepsin G that is not reactive with elastase. Group: Fluorescence/luminescence spectroscopy. | |
| Succinyl-alanine-4-nitroanilide | Succinyl-alanine-4-nitroanilide. Synonyms: Suc-ala-NA; Suc-ala-4-nitroanilide; Butanoic acid, 4-((1-methyl-2-((4-nitrophenyl)amino)-2-oxoethyl)amino)-4-oxo-, (S)-. CAS No. 61043-65-0. Molecular formula: C13H15N3O6. Mole weight: 309.27. | |
| Succinyl-α-cyclodextrin | Succinyl-α-cyclodextrin. Group: Polysaccharide. | |
| Succinyl Bis[(phenylimino)-2,1-ethanediyl]bis(3-maleimidopropanamide) | A non-cleavable bismaleimide linker. Group: Biochemicals. Grades: Highly Purified. CAS No. 1346602-61-6. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Succinyl Carnitine Chloride Salt | Succinyl Carnitine Chloride Salt. Group: Biochemicals. Alternative Names: (2R)-3-carboxy-2-(3-carboxy-1-oxopropoxy)-N,N,N-trimethyl-1-propanaminium Inner Salt. Grades: Highly Purified. CAS No. 256928-74-2. Pack Sizes: 10mg. Molecular Formula: C11H19NO6Cl, Molecular Weight: 297.73. US Biological Life Sciences. | Worldwide |
| Succinyl chloride | Succinyl chloride. Group: Biochemicals. Alternative Names: Succinic acid dichloride. Grades: Highly Purified. CAS No. 543-20-4. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C4H4Cl2O2. US Biological Life Sciences. | Worldwide |
| Succinylcholine Chloride | A neuromuscular blocking agent. Muscle relaxant (skeletal). Group: Biochemicals. Alternative Names: 2, 2'-[ (1, 4-Dioxo-1, 4-butanediyl)bis (oxy)]bis[N, N, N-trimethylethanaminium. Grades: Highly Purified. CAS No. 71-27-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Succinylcholine chloride dihydrate | 98.0-102.0%, solid. Group: Fluorescence/luminescence spectroscopy. | |
| succinyl-CoA:acetate CoA-transferase | In acetic acid bacteria the enzyme, which is highly specific, catalyses the conversion of toxic acetate to acetyl-CoA. In the hydrogenosomes of some trichomonads the enzyme catalyses the production of acetate. Group: Enzymes. Synonyms: aarC (gene name); SCACT. Enzyme Commission Number: EC 2.8.3.18. 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-3413; succinyl-CoA:acetate CoA-transferase; EC 2.8.3.18; aarC (gene name); SCACT. Cat No: EXWM-3413. |  |
| succinyl-CoA-D-citramalate CoA-transferase | The enzyme, purified from the bacterium Clostridium tetanomorphum, can also accept itaconate as acceptor, with lower efficiency. Group: Enzymes. Synonyms: Sct. Enzyme Commission Number: EC 2.8.3.20. 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-3416; succinyl-CoA-D-citramalate CoA-transferase; EC 2.8.3.20; Sct. Cat No: EXWM-3416. | |
| succinyl-CoA hydrolase | This enzyme belongs to the family of hydrolases, specifically those acting on thioester bonds. The systematic name of this enzyme class is succinyl-CoA hydrolase. Other names in common use include succinyl-CoA acylase, succinyl coenzyme A hydrolase, and succinyl coenzyme A deacylase. This enzyme participates in citrate cycle (tca cycle). Group: Enzymes. Synonyms: succinyl-CoA acylase; succinyl coenzyme A hydrolase; succinyl coenzyme A deacylase. Enzyme Commission Number: EC 3.1.2.3. CAS No. 9025-86-9. 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-3563; succinyl-CoA hydrolase; EC 3.1.2.3; 9025-86-9; succinyl-CoA acylase; succinyl coenzyme A hydrolase; succinyl coenzyme A deacylase. Cat No: EXWM-3563. | |
| succinyl-CoA-L-malate CoA-transferase | The enzyme, purified from the bacterium Chloroflexus aurantiacus, can also accept itaconate as acceptor, with lower efficiency. It is part of the 3-hydroxypropanoate cycle for carbon assimilation. Group: Enzymes. Synonyms: SmtAB. Enzyme Commission Number: EC 2.8.3.22. 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-3418; succinyl-CoA-L-malate CoA-transferase; EC 2.8.3.22; SmtAB. Cat No: EXWM-3418. | |
| succinyl-CoA:(R)-benzylsuccinate CoA-transferase | Involved in anaerobic catabolism of toluene and is a strictly toluene-induced enzyme that catalyses the reversible regio- and enantio-selective synthesis of (R)-2-benzylsuccinyl-CoA. The enzyme from Thauera aromatica is inactive when (R)-benzylsuccinate is replaced by (S)-benzylsuccinate. Group: Enzymes. Synonyms: benzylsuccinate CoA-transferase. Enzyme Commission Number: EC 2.8.3.15. CAS No. 260966-56-1. 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-3410; succinyl-CoA:(R)-benzylsuccinate CoA-transferase; EC 2.8.3.15; 260966-56-1; benzylsuccinate CoA-transferase. Cat No: EXWM-3410. | |
| Succinyl-CoA synthetase | Succinyl-CoA synthetase catalyzes the only substrate-level phosphoryl-ation step in the tricarboxylic acid cycle. Succinyl-CoA synthetase is a phosphate target for the activation of mitochondrial metabolism [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9080-33-5. Pack Sizes: 550 U. Product ID: HY-E70121. | |
| Succinyl-Coenzyme A sodium | Succinyl-Coenzyme A (Succinyl-CoA) sodium is an intermediate of the citric acid cycle. Succinyl-Coenzyme A sodium can be converted to succinic acid and can also combines with glycine to form δ-ALA to synthesize porphyrins (heme). Succinyl-Coenzyme A sodium can be used in the study of metabolic, neurological and haematological abnormalities (such as porphyrias) caused by nutritional vitamin B 12 deficiency (resulting in a deficiency in Succinyl-Coenzyme A synthesis) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Succinyl-CoA sodium. CAS No. 108347-97-3. Pack Sizes: 1 mg; 5 mg. Product ID: HY-137808. | |
| Succinyl coenzyme A sodium salt | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| Succinyl-Concanavalin A | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Succinyl-?-cyclodextrin | solid. Group: Polysaccharide. | |
| succinyl-diaminopimelate desuccinylase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase. This enzyme is also called N-succinyl-L-alpha,epsilon-diaminopimelic acid deacylase. This enzyme participates in lysine biosynthesis. Group: Enzymes. Synonyms: N-succinyl-L-α,ε-diaminopimelic acid deacylase. Enzyme Commission Number: EC 3.5.1.18. CAS No. 9024-94-6. 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-4407; succinyl-diaminopimelate desuccinylase; EC 3.5.1.18; 9024-94-6; N-succinyl-L-α,ε-diaminopimelic acid deacylase. Cat No: EXWM-4407. | |
| succinyldiaminopimelate transaminase | A pyridoxal-phosphate protein. Group: Enzymes. Synonyms: succinyldiaminopimelate aminotransferase; N-succinyl-L-diaminopimelic glutamic transaminase. Enzyme Commission Number: EC 2.6.1.17. CAS No. 9030-46-0. 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-2857; succinyldiaminopimelate transaminase; EC 2.6.1.17; 9030-46-0; succinyldiaminopimelate aminotransferase; N-succinyl-L-diaminopimelic glutamic transaminase. Cat No: EXWM-2857. | |
| Succinyl-Doxorubicin Liposome (PEGylated) | This formulation is Doxorubicin Liposome (PEGylated) with the carboxyl group, which can be activated by EDC (1-ethyl-3-[3-dimethylaminopropyl] carbodiimide) and react with sulfo-NHS (N-hydroxysulfosuccinimide) to produce a significantly more stable and more soluble active intermediate (NHS ester). The intermediate can covalently conjugate to the amine group on the proteins, peptides or antibodies through displacement of sulfo-NHS group by amine. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes. |  |
| succinylglutamate desuccinylase | Requires Co2+ for maximal activity. N2-Acetylglutamate is not a substrate. This is the final enzyme in the arginine succinyltransferase (AST) pathway for the catabolism of arginine. This pathway converts the carbon skeleton of arginine into glutamate, with the concomitant production of ammonia and conversion of succinyl-CoA into succinate and CoA. The five enzymes involved in this pathway are EC 2.3.1.109 (arginine N-succinyltransferase), EC 3.5.3.23 (N-succinylarginine dihydrolase), EC 2.6.1.11 (acetylornithine transaminase), EC 1.2.1.71 (succinylglutamate-semialdehyde dehydrogenase) and EC 3.5.1.96 (succinylglutamate desuccinylase). Group: Enzymes. Synonyms: N2-succinylglutamate desuccinylase; SGDS; AstE. Enzyme Commission Number: EC 3.5.1.96. CAS No. 99676-40-1. 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-4488; succinylglutamate desuccinylase; EC 3.5.1.96; 99676-40-1; N2-succinylglutamate desuccinylase; SGDS; AstE. Cat No: EXWM-4488. | |
| succinylglutamate-semialdehyde dehydrogenase | This is the fourth enzyme in the arginine succinyltransferase (AST) pathway for the catabolism of arginine. This pathway converts the carbon skeleton of arginine into glutamate, with the concomitant production of ammonia and conversion of succinyl-CoA into succinate and CoA. The five enzymes involved in this pathway are EC 2.3.1.109 (arginine N-succinyltransferase), EC 3.5.3.23 (N-succinylarginine dihydrolase), EC 2.6.1.11 (acetylornithine transaminase), EC 1.2.1.71 (succinylglutamate-semialdehyde dehydrogenase) and EC 3.5.1.96 (succinylglutamate desuccinylase). Group: Enzymes. Synonyms: succinylglutamic semialdehyde dehydrogenase; N-succinylglutamate 5-semialdehyde dehydrogenase; SGSD; AruD; AstD. Enzyme Commission Number: EC 1.2.1.71. 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-1173; succinylglutamate-semialdehyde dehydrogenase; EC 1.2.1.71; succinylglutamic semialdehyde dehydrogenase; N-succinylglutamate 5-semialdehyde dehydrogenase; SGSD; AruD; AstD. Cat No: EXWM-1173. | |
| Succinyl glycine amide | Succinyl glycine amide. Synonyms: Suc-Gly-NH2; 4-[(2-amino-2-oxoethyl)amino]-4-oxobutanoic acid. Grade: ≥ 99% (TLC). CAS No. 200863-20-3. Molecular formula: C6H10N2O4. Mole weight: 174.16. | |
| Succinyl glycine amide | Succinyl glycine amide. Group: Biochemicals. Alternative Names: Suc-Gly-NH2. Grades: Highly Purified. CAS No. 200863-20-3. Pack Sizes: 500mg, 1g, 2g. US Biological Life Sciences. | Worldwide |
| Succinyl glycine amide 99+% (TLC) | Succinyl glycine amide 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 2.5g. US Biological Life Sciences. | Worldwide |
| Succinyl-L-phenylalanine 4-nitroanilide | A substrate for the determination of chymotrypsin activity. Synonyms: Suc-L-Phe-pNA; 4-({1-Benzyl-2-[(4-Nitrophenyl)Amino]-2-Oxoethyl}Amino)-4-Oxobutanoic Acid; (S)-4-[[2-[(4-Nitrophenyl)Amino]-2-Oxo-1-(Phenylmethyl)Ethyl]Amino]-4-Oxobutyric Acid; 4-((1-Benzyl-2-[(4-Nitrophenyl)Amino]-2-Oxoethyl)Amino)-4-Oxobutanoic Acid. Grade: 95%. CAS No. 2440-62-2. Molecular formula: C19H19N3O6. Mole weight: 385.40. | |
| Succinyl-L-proline | Succinyl-L-proline. Synonyms: Suc-L-Pro-OH; 1-(3-Carboxypropanoyl)-L-Proline. Grade: ≥ 99% (TLC). CAS No. 63250-32-8. Molecular formula: C9H13NO5. Mole weight: 215.21. | |
| Succinylmonocholine Chloride | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsimpurity standardspharmaceutical toxicology. Alternative Names: (3-carboxy-1-oxopropoxy)-N,N,N-trimethyl-ethanaminium chloride (1:1), Succinylmonocholine Chloride, Choline, chloride, hydrogen succinate, Succinic acid, monoester with choline chloride, Succinyl monocholine chloride. | |
| Succinylmonocholine chloride(125 mg) | Succinylmonocholine chloride(125 mg). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Succinylmonocholine Chloride (125 mg);2-(3-Carboxy-1-oxopropoxy)-N,N,N-trimethylethanaminium chloride;Succinylmonocholine chloride. Product Category: Heterocyclic Organic Compound. CAS No. 5297-17-6. Mole weight: 0. Product ID: ACM5297176. Alfa Chemistry ISO 9001:2015 Certified. | |
| Succinylmonocholine chloride,usp standard | Succinylmonocholine chloride,usp standard. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Succinylmonocholine, CBDivE_013158, 5297-17-6 (chloride), STOCK1S-58207, MolPort-002-549-847, MolPort-006-672-083, 14720-92-4 (iodide), CID160784, Ethanaminium, 2-(3-carboxy-1-oxopropoxy)-N,N,N-trimethyl-, 5518-77-4. Product Category: Heterocyclic Organic Compound. CAS No. 5518-77-4. Molecular formula: C9H18NO4+. Mole weight: 204.243520 [g/mol]. Purity: 0.96. IUPACName: 2-(4-hydroxy-4-oxobutanoyl)oxyethyl-trimethylazanium. Product ID: ACM5518774. Alfa Chemistry ISO 9001:2015 Certified. Categories: SCHEMBL2517360. | |
| succinylornithine transaminase | A pyridoxal-phosphate protein. Also acts on N2-acetyl-L-ornithine and L-ornithine, but more slowly. In Pseudomonas aeruginosa, the arginine-inducible succinylornithine transaminase, acetylornithine transaminase (EC 2.6.1.11) and ornithine aminotransferase (EC 2.6.1.13) activities are catalysed by the same enzyme, but this is not the case in all species. This is the third enzyme in the arginine succinyltransferase (AST) pathway for the catabolism of arginine. This pathway converts the carbon skeleton of arginine into glutamate, with the concomitant production of ammonia and conversion of succinyl-CoA into succinate and CoA. The five enzymes involved in this pathway are EC 2.3.1.109 (arginine N-succinyltransferase), EC 3.5.3.23 (N-succinylarginine dihydrolase), EC 2.6.1.81 (succinylornithine transaminase), EC 1.2.1.71 (succinylglutamate-semialdehyde dehydrogenase) and EC 3.5.1.96 (succinylglutamate desuccinylase). Group: Enzymes. Synonyms: succinylornithine aminotr. Enzyme Commission Number: EC 2.6.1.81. 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-2922; succinylornithine transaminase; EC 2.6.1.81; succinylornithine aminotransferase; N2-succinylornithine 5-aminotransferase; AstC; SOAT; 2-N-succinyl-L-ornithine:2-oxoglutarate 5-aminotransferase. Cat No: EXWM-2922. | |
| Succinyl phosphonate trisodium salt | Succinyl phosphonate trisodium salt is an ?-ketoglutarate dehydrogenase (KGDHC) inhibitor, effective inhibits (KGDHC) in muscle, bacterial, brain, and cultured human fibroblasts[1][4]. Succinyl phosphonate trisodium salt is an 2-oxoglutarate dehydrogenase (OGDH) inhibitor, impairs viability of cancer cells in a cell-specific metabolism-dependent manner[2]. Succinyl phosphonate trisodium salt inhibits the glutamate-induced ROS production in glutamate-stimulated hippocampal neurons in situ[3]. Uses: Scientific research. Group: Natural products. CAS No. 864167-45-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-12688A. | |
| Succinylsulfathiazole | Succinylsulfathiazole. Uses: For analytical and research use. Group: Pharma & vet compounds & metabolites; pharma & vet compounds & metabolites. Alternative Names: 2-(N4-Succinylsulfanilamido)thiazole,Succinanilic acid, 4'-(2-thiazolylsulfamoyl)- (7CI,8CI), NSC 163939, Kaoxidine, Sulfasuccidin, Cremosuxidine, Rolsul, Kaoxidin, Succinylsulfathiazole, Sulfasuccinil, Colistatin, Thiacyl, Sulfasuccidine,Butanoic acid, 4-oxo-4-[[4-[(2-thiazolylamino)sulfonyl]phenyl]amino]-, 4'-(2-Thiazolylsulfamoyl)succinanilic acid, Sulfasuccithiazole, NSC 14193, Sulfadigesin, Succinylsulphathiazole, p-2-Thiazolylsulfamylsuccinanilic acid, Sulfenterone, Sulfasuxidine. CAS No. 116-43-8. IUPAC Name: 4-oxo-4-[4-(1,3-thiazol-2-ylsulfamoyl)anilino]butanoic acid. Molecular formula: C13H13N3O5S2. Mole weight: 355.39. Catalog: APS116438. SMILES: OC(=O)CCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2nccs2. Format: Neat. Shipping: Room Temperature. | |
| Succinylsulfathiazole | Succinylsulfathiazole is a sulfonamide, it is an ultra long acting drug. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Succinylsulphathiazole. CAS No. 116-43-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-B0921. | |
| Succinylsulfathiazole | Succinylsulfathiazole. Group: Biochemicals. Alternative Names: 4'- (2-Thiazolylsulfamoyl) succinanilic Acid; 2- (N4-Succinylsulfanilamido) thiazole; 4'- (2-Thiazolylsulfamoyl) succinanilic Acid; Colistatin; Cremosuxidine; Kaoxidin; Kaoxidine; NSC 14193; NSC 163939; Rolsul; Succinylsulfathiazole; Succinyl sulphathiazole; Sulfadigesin; Sulfasuccidin; Sulfasuccidine; Sulfasuccinil; Sulfasuccithiazole; Sulfasuxidine; Sulfenterone; Thiacyl; p-2-Thiazolyl sulfamyl succinanilic Acid. Grades: Highly Purified. CAS No. 116-43-8. Pack Sizes: 1g. Molecular Formula: C13H13N3O5S2, Molecular Weight: 355.39. US Biological Life Sciences. | Worldwide |
| Succistearin | Succistearin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CTK1A6654, AG-E-86654, Stearoyl propylene glycol hydrogen succinate, 27216-62-2. Product Category: Heterocyclic Organic Compound. CAS No. 27216-62-2. Molecular formula: C25H48O7. Mole weight: 460.644420 [g/mol]. Purity: 0.96. IUPACName: butanedioic acid;2,3-dihydroxyhenicosan-4-one. Product ID: ACM27216622. Alfa Chemistry ISO 9001:2015 Certified. | |
| Suc-D-Asp-AMC | Suc-D-Asp-AMC is a selective substrate for D-Aspartyl Endopeptidase. Synonyms: Suc-D-Asp-MCA; Succinyl-D-aspartic acid α-(4-methylcoumaryl-7-amide). CAS No. 676465-82-0. Molecular formula: C18H18N2O8. Mole weight: 390.34. | |
| Suc-e8-(Aop)-PLGC(Me)AG-r9-c-NH2 | Suc-e8-(Aop)-PLGC(Me)AG-r9-c-NH2, an activated cell-penetrating peptide linked to nanoparticles, acts as a dual probe for in vivo fluorescence and MR imaging of proteases. | |
| Suc-Gly-Pro-AMC | Suc-Gly-Pro-AMC is a fluorescent substrate. Suc-Gly-Pro-AMC is a fibroblast activation protein (FAP) specific substrate. Suc-Gly-Pro-AMC reacts with recombinant porcine prolyl oligopeptidase. Suc-Gly-Pro-AMC can be used to study the activity of FAP, prolyl endopeptidase (PREP). Suc-Gly-Pro-AMC is used in glioma research[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 80049-85-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145983. | |
| SUC-GLY-PRO-AMC | Suc-GP-AMC is a highly sensitive, fluorogenic substrate used in the determination of prolyl endopeptidase (postproline cleaving enzyme) activity. Synonyms: 7-succinylglycyl-prolyl-4-methylcoumaryl-7-amide; L-Prolinamide,N-(3-carboxy-1-oxopropyl)glycyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-. Grade: >95%. CAS No. 80049-85-0. Molecular formula: C21H23N3O7. Mole weight: 429.42. | |
| Suc-gly-pro-leu-gly-pro-amc | Suc-gly-pro-leu-gly-pro-amc. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SUCCINYLGLYCYL-L-PROLYL-L-LEUCYLGLYCYL-L-PROLINE 4-METHYLCOUMARYL-7-AMIDE;SUC-GLY-PRO-LEU-GLY-PRO-AMC;SUC-GLY-PRO-LEU-GLY-PRO-MCA;N-succinyl-gly-pro-leu-gly-pro 7-*amido-4-methylc;N-(3-carboxy-1-oxopropyl)glycyl-L-prolyl-L-leucylglycyl-N-(4-methyl-2-oxo-. Product Category: Heterocyclic Organic Compound. CAS No. 72698-36-3. Molecular formula: C34H44N6O10. Mole weight: 696.75. Product ID: ACM72698363. Alfa Chemistry ISO 9001:2015 Certified. | |
| SUC-GLY-PRO-LEU-GLY-PRO-AMC | Suc-GPLGP-AMC is a highly sensitive fluorogenic substrate for thimet oligopeptidase (collagenase-like peptidase, Pz-peptidase, metalloendopeptidase 24.15) as well as for post-proline cleaving enzyme (prolyl endopeptidase). Synonyms: succinyl-Gly-Pro-Leu-Gly-Pro-4-methylcoumaryl-7-amide; N-(3-Carboxy-1-oxopropyl)glycyl-L-prolyl-L-leucylglycyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-prolinamide. Grade: 95%. CAS No. 72698-36-3. Molecular formula: C34H44N6O10. Mole weight: 696.75. | |
| Suc-Gly-Pro-pNA | Suc-Gly-Pro-pNA. Synonyms: SUC-GLY-PRO-PNA. CAS No. 115846-45-2. Molecular formula: C17H20N4O7. Mole weight: 392.36. | |
| Suciraslimab | Suciraslimab is an anti- CD22 human IgG1 κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001). Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: SM03. CAS No. 2415439-63-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990781. | |
| Suc-Leu-Leu-Val-Tyr-AMC | Suc-Leu-Leu-Val-Tyr-AMC is a membrane-permeable calpain-specific fluorogenic substrate (Ex/Em = 390/480 nm)[1]. Uses: Scientific research. Group: Peptides. CAS No. 94367-21-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P1002. | |
| Suc-Leu-Leu-Val-Tyr-AMC | Suc-Leu-Leu-Val-Tyr-AMC is a fluorogenic substrate of calpains and 20S proteasome. Synonyms: Suc-LLVY-AMC; Proteasome substrate (fluorogenic); Calpain substrate (fluorogenic). Grade: >97%. CAS No. 94367-21-2. Molecular formula: C40H53N5O10. Mole weight: 763.89. | |
| Suc-Leu-Leu-Val-Tyr-pNA | Suc-Leu-Leu-Val-Tyr-pNA is a chromogenic substrate analogue to the proteasome substrate Suc-LLVY-AMC. Synonyms: Suc-LLVY-pNA; N-(3-Carboxypropanoyl)-L-leucyl-L-leucyl-L-valyl-N-(4-nitrophenyl)-L-tyrosinamide; L-Tyrosinamide, N-(3-carboxy-1-oxopropyl)-L-leucyl-L-leucyl-L-valyl-N-(4-nitrophenyl)-. Grade: ≥90%. CAS No. 1926163-44-1. Molecular formula: C36H50N6O10. Mole weight: 726.83. | |
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