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| Product | Description | |
|---|---|---|
| Succinyl-(2-hydroxypropyl)-a-cyclodextrin | Succinyl-(2-hydroxypropyl)-a-cyclodextrin is a vital component used in the biomedical industry utilized for drug delivery, particularly for hydrophobic drugs. This product enables an increased solubility and stability of drugs, used in studying various diseases such as cancer, cardiovascular disorders and infectious diseases. Synonyms: SuHPACD. |  |
| Succinyl-(2-hydroxypropyl)-b-cyclodextrin | Succinyl-(2-hydroxypropyl)-b-cyclodextrin is a paradigm-shifting biomedical compound, indispensible in multifarious pharmaceutical formulations. This altered cyclodextrin assumes a pivotal function in augmenting solubility, stability and bioavailability of medicinal concoctions. Synonyms: SuHPBCD. Molecular formula: C70H110O51. Mole weight: 1767.59. | |
| Succinyl-(2-hydroxypropyl)-β-cyclodextrin | Succinyl-(2-hydroxypropyl)-β-cyclodextrin. Group: Polysaccharide. |  |
| Succinylacetone | Succinylacetone is an inhibitor of δ-aminolevulinic acid dehydratase that inhibits heme biosynthesis. It is used as a specific marker for the inherited metabolic disease, hepatorenal tyrosinemia. Uses: Enzyme inhibitors. Synonyms: NSC 174804; NSC174804; NSC-174804; 4,6-Dioxoheptanoic acid; Succinyl acetone; Heptanoic acid, 4,6-dioxo-. CAS No. 51568-18-4. Molecular formula: C7H10O4. Mole weight: 158.153. | |
| 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 |
| Succinyl-a-cyclodextrin | Succinyl-alpha-cyclodextrin (SACD) is a compound product used in the research of drug delivery and solubility enhancement. SACD acts as a carrier for poorly water-soluble drugs, improving their bioavailability. With unique structure, SACD is highly effective in encapsulating hydrophobic drugs, making it a promising solution for targeted drug delivery and research of various diseases. Synonyms: Succinyl-alpha-cyclodextrin; Succinyl-α-cyclodextrin. Molecular formula: C36H60-nO30·(C4H5O3)n. | |
| 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-α-cyclodextrin | Succinyl-α-cyclodextrin. Group: Polysaccharide. | |
| Succinyl-b-cyclodextrin | Succinyl-b-cyclodextrin is a biopharmaceutical compound facilitating targeted therapeutic research across heterogeneous medical conditions. Its multifaceted functionality encompasses enhanced solubility and stability of encapsulated drugs, thus aiding in studying diverse ailments such as neoplasms, cardiac pathologies and infectious afflictions. Synonyms: Succinyl-beta-cyclodextrin; Succinyl-β-cyclodextrin. CAS No. 957494-34-7. Molecular formula: C42H70-nO35·(C4H5O3)n. Mole weight: 1833.5. | |
| 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 | Cas No. 306-40-1. | |
| 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 | Succinylcholine Chloride Dihydrate is a nicotinic AChR agonist and also acts as a depolarizing neuromuscular blocker. Uses: Neuromuscular depolarizing agents. Synonyms: 2,2'-(succinylbis(oxy))bis(N,N,N-trimethylethan-1-aminium) Chloride Dihydrate; Bis(trimethylammonioethyl) succinate chloride. Grades: >98%. CAS No. 6101-15-1. Molecular formula: C14H34Cl2N2O6. Mole weight: 397.34. | |
| 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-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. |  |
| Succinyl-gamma-cyclodextrin | Succinyl-gamma-cyclodextrin is a cyclodextrin derivative, used for amplifying the solubility and fortitude of medicaments, thus rendering it an impeccable contender for advanced drug conveyance mechanisms. Synonyms: Succinyl-gamma-cyclodextrin; 159162-90-0. Molecular formula: C48H80-nO40 (C4H5O3)n. Mole weight: 1297.2 + n(100.1). | |
| 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. | |
| Succinylglutaminyl-valyl-valyl-alanyl-alanine-4-nitroanilide | Heterocyclic Organic Compound. CAS No. 115700-57-7. Catalog: ACM115700577. |  |
| 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 | Synonyms: Suc-Gly-NH2; 4-[(2-amino-2-oxoethyl)amino]-4-oxobutanoic acid. Grades: ≥ 99% (TLC). CAS No. 200863-20-3. Molecular formula: C6H10N2O4. Mole weight: 174.16. | |
| 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. Grades: 95%. CAS No. 2440-62-2. Molecular formula: C19H19N3O6. Mole weight: 385.40. | |
| Succinyl-L-proline | Synonyms: Suc-L-Pro-OH; 1-(3-Carboxypropanoyl)-L-Proline. Grades: ≥ 99% (TLC). CAS No. 63250-32-8. Molecular formula: C9H13NO5. Mole weight: 215.21. | |
| 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 | Succinyl phosphonate was found to be effective inhibitors of alpha-ketoglutarate oxidative decarboxylation, catalyzed by both muscle and bacterial alpha-ketoglutarate dehydrogenase complexes, as well as muscle alpha-ketoglutarate dehydrogenase. Synonyms: Succinyl phosphonate. Grades: >98%. CAS No. 26647-82-5. Molecular formula: C4H7O6P. Mole weight: 182.07. | |
| Succinylsulfathiazole | Succinylsulfathiazole, a sulfonamide derivative, could restrain the bacteria in the intestine to block the production of folic acid. Uses: Succinylsulfathiazole could restrain the bacteria in the intestine to block the production of folic acid. Synonyms: colistatin; cremosuxidine; kaoxidin; KAOXIDINE; 2-(n(4)-succinylsulfanilamido)thiazole; 2-(N-SUCCINYLSULFANILAMIDO)THIAZOLE. Grades: >97.0%(LC)(T). CAS No. 116-43-8. Molecular formula: C13H13N3O5S2. Mole weight: 355.38. | |
| 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 |
| 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. 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. |  |
| 18:1 Succinyl PE | Headgroup Modified Lipids. Alternative Names: 1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine-N-(succinyl) (sodium salt); 1,2-Di-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine-N-(succinyl) (sodium salt). CAS No. 111613-33-3. Molecular formula: C45H81NO11PNa. Mole weight: 866.09. Appearance: Powder. Purity: >99%. Canonical SMILES: CCCCCCCC/C=C\CCCCCCCC (=O)OC[C@H] (COP (=O) (O)OCCNC (=O)CCC (=O)O)OC (=O)CCCCCCC/C=C\CCCCCCCC. [Na]. Catalog: ACM111613333. | |
| 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase | Involved in the biosynthesis of lysine in bacteria (including cyanobacteria) and higher plants. The 1992 edition of the Enzyme List erroneously gave the name 2,3,4,5-tetrahydropyridine-2-carboxylate N-succinyltransferase to this enzyme. Group: Enzymes. Synonyms: tetrahydropicolinate succinylase; tetrahydrodipicolinate N-succinyltransferase; tetrahydrodipicolinate succinyltransferase; succinyl-CoA:tetrahydrodipicolinate N-succinyltransferase; succinyl-CoA:2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. Enzyme Commission Number: EC 2.3.1.117. CAS No. 88086-34-4. 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-2056; 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase; EC 2.3.1.117; 88086-34-4; tetrahydropicolinate succinylase; tetrahydrodipicolinate N-succinyltransferase; tetrahydrodipicolinate succinyltransferase; succinyl-CoA:tetrahydrodipicolinate N-succinyltransferase; succinyl-CoA:2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase. Cat No: EXWM-2056. | |
| 2'-Deoxy-5-O-DMT-guanosine-(DMF)-succinyl-CPG | 2'-Deoxy-5-O-DMT-guanosine-(DMF)-succinyl-CPG, an indispensable asset in the biomedical realm for oligonucleotide synthesis, manifests itself as a paramount instrument. It bestows upon us the capability to fabricate altered DNA sequences with utmost efficacy and prodigious output. These sequences hold great significance in combatting genetic disorders, viral afflictions, and neoplastic conditions. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(DMF)-succinyl CPG, an indispensable asset in the realm of biomedical research. Leveraged for synthesizing oligonucleotides, this remarkable entity plays a pivotal role in nurturing nucleic acid-based therapeutics, anatomizing genetic disorders, and comprehending diseases. It spearheads the realm of drug discovery and personalized medicine by endowing scientists with efficacious and controlled DNA sequence synthesis. Prepare to embark on riveting scientific endeavors with this groundbreaking product. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-3'-succinyl CPG, a pinnacle instrument harnessed within the ever-evolving biomedical realm for the profound synthesis of oligonucleotides. Its unparalleled prowess transcends boundaries, propelling therapeutic advancement towards combating afflictions like cancer, genetic anomalies, and viral onslaughts. | |
| 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-succinyl CPG | 2'-Deoxy-5'-O-DMT-guanosine-(iBu)-succinyl CPG, an indispensable resource within the biomedical sector, holds significant prominence in the realm of oligonucleotide synthesis. Garnering immense importance, it is substantially utilized for the formulation of nucleic acid-centered therapeutics and diagnostics pertaining to an array of ailments encompassing cancer, infectious diseases, and genetic disorders. | |
| 2'-Deoxy-5'-O-DMT-inosine 3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-inosine 3'-succinyl CPG is a crucial tool in biomedical research for the synthesis of modified oligonucleotides. It is extensively utilized as a solid support matrix for automated DNA/RNA synthesis, enabling the efficient incorporation of nucleotide modifications. This product plays a vital role in studying and developing various nucleic acid-based therapies, diagnostics, and drug delivery systems targeting specific diseases like cancer and viral infections. | |
| 2'-Deoxy-5'-O-DMT-N2-iBu-guanosine-3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-N2-iBu-guanosine-3'-succinyl CPG, a paramount instrument in the realm of biomedicine, transcends boundaries as a solid support during the synthesis of altered oligonucleotides, specifically in the domain of drug discovery exploration, with a discerning focus on numerous ailments. An exemplar of efficacious pharmaceutical transportation, it empowers the amelioration of an array of afflictions, spanning genetic disorders to viral infestations. Its multifaceted applications herald its invaluable prowess within the biomedical sector. | |
| 2'-Deoxy-5'-O-DMT-uridine 3'-succinyl CPG | 2'-Deoxy-5'-O-DMT-uridine 3'-succinyl CPG is a crucial tool in the biomedical industry for the development of nucleotide-based therapies. It serves as a solid support matrix for the synthesis of nucleic acids, including antisense oligonucleotides and siRNA, targeting a wide range of diseases such as cancer, genetic disorders, and viral infections. This product facilitates the efficient and controlled synthesis of customized nucleotide sequences, aiding researchers in the discovery and advancement of novel medical interventions. | |
| 2'-Deoxy-5'-O-DMT-uridine succinyl 3'-CPG | | |
| 2'-Methyl-adenosine-(benzoyl)-succinyl-CPG | 2'-Methyl-adenosine-(benzoyl)-succinyl-CPG, a highly versatile and pivotal biomedical entity, finds widespread utilization in the realm of pharmaceutical exploration and advancement. This distinctive compound assumes a critical role as an indispensable cornerstone for the synthesis of oligonucleotides and nucleic acid analogs, fostering a promising avenue for combatting an array of diseases such as cancer and viral infections. | |
| 2'-Methyl-adenosine-(Bz)-succinyl-CPG | 2'-Methyl-adenosine-(Bz)-succinyl-CPG, a prominent compound utilized in the realm of biomedical research, plays a pivotal role in oligonucleotide synthesis. As a modified nucleoside building block, it effectively propels the investigation of RNA structure and function. This product finds extensive utility in unraveling the impact of 2'-Methyl-adenosine on gene regulation, thereby demonstrating potential therapeutic applications in the treatment of multifarious ailments, notably cancer and neurological disorders. | |
| 2'-Methyl-cytidine-(Bz)-succinyl-CPG | 2'-Methyl-cytidine-(Bz)-succinyl-CPG, an essential entity within the biomedicine realm, serves as a pivotal tool in the intricate process of synthesizing nucleic acids and diverse oligonucleotides. Its significance arises from its multifaceted applicability in drug discovery investigations, specifically focusing on the advancement of antiviral and anticancer medications. | |
| 2'-Methyl-guanosine-(iBu)-succinyl-CPG | 2'-Methyl-guanosine-(iBu)-succinyl-CPG is a crucial biomedicine product used for solid-phase synthesis of oligonucleotides. It serves as a key building block for the chemical synthesis of modified nucleic acids. With its unique succinyl modification, this CPG derivative enables efficient incorporation into oligonucleotides for pharmaceutical research and diagnostic applications related to drug screening, target identification, and disease detection. | |
| 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase | Requires Mg2+ for maximal activity. This enzyme is involved in the biosynthesis of vitamin K2 (menaquinone). In most anaerobes and all Gram-positive aerobes, menaquinone is the sole electron transporter in the respiratory chain and is essential for their survival. It had previously been thought that the products of the reaction were (1R,6R)-6-hydroxy-2-succinylcyclohexa-2,4-diene-1-carboxylate (SHCHC), pyruvate and CO2 but it is now known that two separate enzymes are involved: this enzyme and EC 4.2.99.20, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase. Under basic conditions, the product can spontaneously lose pyruvate to form SHCHC. Group: Enzymes. Synonyms: SEPHCHC synthase; MenD. Enzyme Commission Number: EC 2.2.1.9. CAS No. 1112282-73-1. 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-2036; 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase; EC 2.2.1.9; 1112282-73-1; SEPHCHC synthase; MenD. Cat No: EXWM-2036. | |
| 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase | This enzyme is involved in the biosynthesis of vitamin K2 (menaquinone). In most anaerobes and all Gram-positive aerobes, menaquinone is the sole electron transporter in the respiratory chain and is essential for their survival. It had previously been thought that the reactions carried out by this enzyme and EC 2.2.1.9, 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase, were carried out by a single enzyme but this has since been disproved. Group: Enzymes. Synonyms: 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylic acid synthase; 6-hydroxy-2-succinylcyclohexa-2,4-diene-1-carboxylate synthase; SHCHC synthase; MenH; YfbB. Enzyme Commission Number: EC 4.2.99.20. CAS No. 122007-88-9. 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-5266; 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase; EC 4.2.99.20; 122007-88-9; 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylic acid synthase; 6-hydroxy-2-succinylcyclohexa-2,4-diene-1-carboxylate synthase; SHCHC synthase; MenH; YfbB. Cat No: EXWM-5266. | |
| 3'-O-DMT-thymidine 3'-succinyl CPG | The 3'-O-DMT-thymidine 3'-succinyl CPG is a vital tool extensively used in the biomedical industry for the synthesis of oligonucleotides. It enables the modification of DNA strands, facilitating research on drug discovery and development, gene expression analysis, and nucleic acid-based diagnostics. This product plays a crucial role in studying DNA-protein interactions, epigenetics, and investigating diseases such as cancer and genetic disorders. | |
| 4-(Succinylamino)phenylboronic acid pinacol ester | 4-(Succinylamino)phenylboronic acid pinacol ester. Group: Salt. Alternative Names: 578762_ALDRICH, BM066, ST5405616, 4-(Succinylamino)phenylboronic acid pinacol ester, 4-(3-Carboxypropionylamino)phenylboronic acid pinacol ester, N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]succinamic acid, 480424-98-4. CAS No. 480424-98-4. Product ID: 4-oxo-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilino]butanoic acid. Molecular formula: 319.16. Mole weight: C16< / sub>H22< / sub>BNO5< / sub>. B1 (OC (C (O1) (C)C) (C)C)C2=CC=C (C=C2)NC (=O)CCC (=O)O. GZCXOZHMQNWRGM-UHFFFAOYSA-N. 96%. | |
| 5'-O-DMT-guanosine-(dmf) 3'-succinyl CPG | 5'-O-DMT-guanosine-(dmf) 3'-succinyl CPG is a crucial tool used in the biomedical industry for solid-phase synthesis of oligonucleotides. This product facilitates the synthesis of modified oligonucleotides with potential applications in gene therapy, antisense drug development, or gene expression studies. It offers precise control over modifications at the nucleotide level, leading to enhanced therapeutic outcomes for various diseases including cancer, genetic disorders, and viral infections. | |
| 5'-O-DMT-N2-DMF-guanosine-3'-succinyl | 5'-O-DMT-N2-DMF-guanosine-3'-succinyl is a modified form of guanosine used in the biomedical industry. With its unique chemical structure, 5'-O-DMT-N2-DMF-guanosine-3'-succinyl holds promise for targeted drug delivery and as a diagnostic tool in biomedicine. | |
| 5'-O-DMT-thymidine 3'-succinyl | 5'-O-DMT-thymidine 3'-succinyl, an essential biomedicine, exhibits remarkable efficacy in alleviating a wide range of afflictions. Through its potent nucleoside analog properties, it flawlessly impedes viral replication, thereby assuming a pivotal role in the realm of antiviral therapies. Furthermore, this exceptional compound assumes utmost importance in DNA synthesis and repair, offering respite to those grappling with DNA-related maladies. | |
| 5'-O-DMT-thymidine-3'-succinyl CPG | | |
| 5'-O-DMT-uridine 3'-succinyl CPG | 5'-O-DMT-uridine 3'-succinyl CPG, a profoundly significant reagent within the biomedical field, serves as a catalyst for the synthesis of intricate oligonucleotides. Demonstrating its versatility, this compound finds wide-ranging applications in academic research, primarily within nucleic acid chemistry. | |
| arginine N-succinyltransferase | Also acts on L-ornithine. This is the first 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: arginine succinyltransferase; AstA; arginine and ornithine N2-succinyltransferase; AOST; AST; succinyl-CoA:L-arginine 2-N-succinyltransferase. Enzyme Commission Number: EC 2.3.1.109. CAS No. 99676-48-9. 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-2047; arginine N-succinyltransferase; EC 2.3.1.109; 99676-48-9; arginine succinyltransferase; AstA; arginine and ornithine N2-succinyltransferase; AOST; AST; succinyl-CoA:L-arginine 2-N-succinyltransferase. Cat No: EXWM-2047. | |
| dihydrolipoyllysine-residue succinyltransferase | A multimer (24-mer) of this enzyme forms the core of the multienzyme complex, and binds tightly both EC 1.2.4.2, oxoglutarate dehydrogenase (succinyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively succinylated by EC 1.2.4.2, and the only observed direction catalysed by EC 2.3.1.61 is that where this succinyl group is passed to coenzyme A. Group: Enzymes. Synonyms: dihydrolipoamide S-succinyltransferase; dihydrolipoamide succinyltransferase; dihydrolipoic transsuccinylase; dihydrolipolyl transsuccinylase; dihydrolipoyl transsuccinylase; lipoate succinyltrans. Enzyme Commission Number: EC 2.3.1.61. CAS No. 9032-28-4. 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-2241; dihydrolipoyllysine-residue succinyltransferase; EC 2.3.1.61; 9032-28-4; dihydrolipoamide S-succinyltransferase; dihydrolipoamide succinyltransferase; dihydrolipoic transsuccinylase; dihydrolipolyl transsuccinylase; dihydrolipoyl transsuccinylase; lipoate succinyltransferase (Escherichia coli); lipoic transsuccinylase; lipoyl transsuccinylase; succinyl-CoA:dihydrolipoamide S-succinyltransferase; succinyl-CoA:dihydrolipoate S-succinyltransferase; enzyme-dihydrolipoyllysine:succinyl-CoA S-succinyltransferase. Cat No: EXWM-2241. | |
| DSPE-PEG(2000) Succinyl | DSPE-PEG(2000) Succinyl. Group: Others. Purity: >99%. Mole weight: 2890.559 (average MW due to polydispersity of PEG). Stability: 1 Year. Storage: -20°C. DSPE-PEG(2000) Succinyl; 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[succinyl(polyethylene glycol)-2000] (ammonium salt) ; Polymers; Polymerizable Lipids; lipid products; lipid. Cat No: PCNZ-014. | |
| ethyl succinyl chloride | ethyl succinyl chloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 14794-31-1. Molecular Formula: C6H9ClO3. Mole Weight: 164.59. Catalog: APB14794311. | |
| homoserine O-succinyltransferase | This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. This enzyme participates in methionine metabolism and sulfur metabolism. Group: Enzymes. Synonyms: homoserine O-transsuccinylase; homoserine succinyltransferase. Enzyme Commission Number: EC 2.3.1.46. CAS No. 62213-51-8. 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-2225; homoserine O-succinyltransferase; EC 2.3.1.46; 62213-51-8; homoserine O-transsuccinylase; homoserine succinyltransferase. Cat No: EXWM-2225. | |
| Mono-methyl polyethylene glycol 20'000 2-(succinyl-amino)ethyl ether | Mono-methyl polyethylene glycol 20'000 2-(succinyl-amino)ethyl ether. Group: Polymers. Alternative Names: mono-Methyl polyethylene glycol 20,000 2-(succinylamino)ethyl ether, O-[2-(3-Succinylamino)ethyl]-O inverted exclamation marka-methyl-polyethylene glycol, 92450-99-2. CAS No. 92450-99-2. Product ID: 4-[2-(2-hydroxyethoxy)ethylamino]-4-oxobutanoic acid; 2-methoxyethanol. Molecular formula: 281.302820 [g/mol]. Mole weight: C7< / sub>H13< / sub>NO4< / sub> (OC2< / sub>H4< / sub>) n. COCCO.C(CC(=O)O)C(=O)NCCOCCO. QJSMXIRALCRBTK-UHFFFAOYSA-N. 96%. | |
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