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| Product | Description | |
|---|---|---|
| UCT 1072M3 | UCT 1072M3 is a topoisomerase II poison isolated from Aspergillus sp. KY4919, which is toxic to HeLa S3 and Lu-65 cells. UCT 1072M3 is a diastereomer of UCT 1072M2. Synonyms: UCT1072M3; UCT-1072M3. Molecular formula: C20H16O7. Mole weight: 368.34. |  |
| UCT4B | UCT4B is an antitumor antibiotic produced by Streptomyces sp. It exhibits topoisomerase II mediated DNA cleavage activity. It suppresses gram-positive bacteria and Klebsiella pneumoniae with MIC of 4.1 and 2.1 μg/mL, respectively. Synonyms: UCT 4B. CAS No. 143200-52-6. Molecular formula: C20H28O7. Mole weight: 380.4. | |
| UD-014 | UD-014 is a selective and long-acting inhibitor of semicarbazide-sensitive amine oxidase (SSAO; VAP-1) (IC50 = 3.2 nM), which shows a therapeutic effect of diabetic nephropathy in a streptozotocin rat model. Uses: The treatment of diabetic nephropathy. Synonyms: UD 014; UD014. | |
| Udenafil | Udenafil (DA8159) is a potent, selective and orally active phosphodiesterase type 5 (PDE5) inhibitor. Udenafil also inhibits cGMP hydrolysis and can be used for erectile dysfunction research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA8159. CAS No. 268203-93-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18253. |  |
| Udenafil | Udenafil is an oral PDE5 inhibitor. Udenafil significantly increased cAMP and cGMP levels and were more highly distributed in the prostate than plasma. The T/P ratio of udenafil was higher than tadalafil. These findings may help in the assessment of the feasibility of using PDE5 Is to concurrently treat both LUTS and erectile dysfunction. After 12 weeks of treatment, the patients treated with udenafil showed significantly greater change from baseline in the IIEF-EF domain score compared with placebo (placebo, 0.20; 100-mg udenafil, 7.52; and 200-mg udenafil, 9.93, respectively) (P < 0.0001). udenafil significantly enhanced the rates of successful penetration (SEP Q2) and maintenance of erection (SEP Q3) (P < 0.0001). Synonyms: DA-8159, DA 8159, DA8159, Udenafil, Zydena. Grades:>98%. CAS No. 268203-93-6. Molecular formula: C25H36N6O4S. Mole weight: 516.66. | |
| Udenafil | An oral phosphodiesterase 5 inhibitor used for the treatment of erectile dysfunction. Group: Biochemicals. Alternative Names: 3- (6, 7-Dihydro-1-methyl-7-oxo-3-propyl -1H-pyrazolo [4, 3-d] pyrimidin-5-yl) -N- [2- (1-methyl-2-pyrrolidinyl) ethyl] -4-propoxy Benzene sulfonamide; DA 8159; Zydena. Grades: Highly Purified. CAS No. 268203-93-6. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Udenafil-d7 | Heterocyclic Organic Compound. Alternative Names: 3-(6,7-Dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]-4-(propoxy-d7)benzenesulfonamide; DA 8159-d7; Zydena-d7. CAS No. 1175992-76-3. Molecular formula: C25H29D7N6O4S. Mole weight: 523.7. Purity: 0.96. IUPACName: 4-(1,1,2,2,3,3,3-heptadeuteriopropoxy)-3-(1-methyl-7-oxo-3-propyl-4H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-[2-(1-methylpyrrolidin-2-yl)ethyl]benzenesulfonamide. Catalog: ACM1175992763. |  |
| UDM-002555 | UDM-002555 is a small-molecule and selective antagonist of protease-activated receptor-4 (PAR-4). It can suppress the activation of platelet in dose manner. In combination with aspirin, it inhibited arterial thrombosis with limited impact on hemostasis in cynomolgus monkeys. Uses: The potential treatment of arterial thrombosis. Synonyms: UDM-002555; UDM 002555; UDM002555. | |
| Udonitrectag | Udonitrectag (REC 0559), a low molecular weight compound that mimics NGF, aims to address the issue of NGF stability [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: REC 0559. CAS No. 1458063-04-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109194. | |
| UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of the B-band lipopolysaccharide of Pseudomonas aeroginosa serotype O5 and of the band-A trisaccharide of Bordetella pertussis, both important respiratory pathogens. The enzyme is highly specific as UDP-α-D-GlcNAc, UDP-α-D-GlcNAcA (UDP-2-acetamido-2-deoxy-α-D-glucuronic acid) and UDP-α-D-GlcNAc3NAc (UDP-2,3-diacetamido-2,3-dideoxy-α-D-glucose) cannot act as substrates. Group: Enzymes. Synonyms: UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Enzyme Commission Number: EC 5.1.3.23. 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-5409; UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase; EC 5.1.3.23; UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Cat No: EXWM-5409. |  |
| UDP-2,3-diacylglucosamine diphosphatase | The enzyme catalyses a step in the biosynthesis of lipid A. Group: Enzymes. Synonyms: UDP-2,3-diacylglucosamine hydrolase; UDP-2,3-diacylglucosamine pyrophosphatase; ybbF (gene name); lpxH (gene name); UDP-2,3-bis[(3R)-3-hydroxymyristoyl]-α-D-glucosamine 2,3-bis[(3R)-3-hydroxymyristoyl]-β-D-glucosaminyl 1-phosphate phosphohydrolase (incorrect). Enzyme Commission Number: EC 3.6.1.54. 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-4626; UDP-2,3-diacylglucosamine diphosphatase; EC 3.6.1.54; UDP-2,3-diacylglucosamine hydrolase; UDP-2,3-diacylglucosamine pyrophosphatase; ybbF (gene name); lpxH (gene name); UDP-2,3-bis[(3R)-3-hydroxymyristoyl]-α-D-glucosamine 2,3-bis[(3R)-3-hydroxymyristoyl]-β-D-glucosaminyl 1-phosphate phosphohydrolase (incorrect). Cat No: EXWM-4626. | |
| UDP-2,4-diacetamido-2,4,6-trideoxy-β-L-altropyranose hydrolase | The enzyme is involved in biosynthesis of pseudaminic acid. Group: Enzymes. Synonyms: PseG; UDP-6-deoxy-AltdiNAc hydrolase; Cj1312; UDP-2,4-bis(acetamido)-2,4,6-trideoxy-β-L-altropyranose hydrolase. Enzyme Commission Number: EC 3.6.1.57. 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-4629; UDP-2,4-diacetamido-2,4,6-trideoxy-β-L-altropyranose hydrolase; EC 3.6.1.57; PseG; UDP-6-deoxy-AltdiNAc hydrolase; Cj1312; UDP-2,4-bis(acetamido)-2,4,6-trideoxy-β-L-altropyranose hydrolase. Cat No: EXWM-4629. | |
| UDP-2-Acetamido-2,4-dideoxy-4-fluorogalactose | UDP-2-Acetamido-2,4-dideoxy-4-fluorogalactose is an indispensable compound assuming a pivotal status in the intricate domain of glycoconjugate synthesis. By serving as a formidable substrate for a plethora of enzymes actively participating in glycosylation processes, this remarkable compound effectively facilitates the intricate modification of proteins and lipids. Synonyms: Uridine 5'-(2-acetamido-2,4-dideoxy-4-fluoro-a-D-galactopyranosyl)diphosphate; dilithium,[(2R,3R,4R,5R,6R)-3-acetamido-5-fluoro-4-hydroxy-6-(hydroxymethyl)oxan-2-yl][[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate; Uridine 5'-(trihydrogen diphosphate),P'-(2-(acetylamino)-2,4-dideoxy-4-fluoro-alpha-D-galactopyranosyl) ester, dilithium salt; Udp-adfg. CAS No. 120596-20-5. Molecular formula: C17H24FLi2N3O16P2. Mole weight: 621.21. | |
| UDP-2-acetamido-2,6-β-L-arabino-hexul-4-ose reductase | Part of the biosynthesis of UDP-N-acetyl-L-fucosamine. Isolated from the bacteria Pseudomonas aeruginosa and Staphylococcus aureus. Group: Enzymes. Synonyms: WbjC; Cap5F. Enzyme Commission Number: EC 1.1.1.367. 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-0284; UDP-2-acetamido-2,6-β-L-arabino-hexul-4-ose reductase; EC 1.1.1.367; WbjC; Cap5F. Cat No: EXWM-0284. | |
| UDP-2-acetamido-2-deoxy-5-thio-D-glucopyranose | | |
| UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase | A pyridoxal 5'-phosphate protein. This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. The enzymes from Pseudomonas aeruginosa serotype O5 and Thermus thermophilus form a complex with the previous enzyme in the pathway, EC 1.1.1.335 (UDP-N-acetyl-2-amino-2-deoxyglucuronate oxidase). Group: Enzymes. Synonyms: WbpE; WlbC. Enzyme Commission Number: EC 2.6.1.98. 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-2939; UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase; EC 2.6.1.98; WbpE; WlbC. Cat No: EXWM-2939. | |
| UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. Group: Enzymes. Synonyms: WbpD; WlbB. Enzyme Commission Number: EC 2.3.1.201. 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-2146; UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase; EC 2.3.1.201; WbpD; WlbB. Cat No: EXWM-2146. | |
| UDP-2-amino-2-deoxy-D-glucose | UDP-2-amino-2-deoxy-D-glucose is a quintessential biochemical compound with pivotal involvement in the intricate biosynthesis of diverse complex carbohydrates. It assumes a critical function as a precursor governing the synthesis of glycosaminoglycans and proteoglycans, entities intricately entwined in multifarious biological processes. Molecular formula: C15H25N3O16P2. Mole weight: 565.32. | |
| UDP-2-deoxy-2-fluoro-D-galactose | UDP-2-deoxy-2-fluoro-D-galactose is a valuable tool in the biomedical industry known for its ability to mimic natural carbohydrates. It can be utilized to investigate the potential therapeutic applications and drug design targeting specific diseases related to carbohydrate metabolism. Synonyms: UDP-2FGal; Uridine 5-(trihydrogen diphosphate), P-(2-deoxy-2-fluoro-α-D-galactopyranosyl) ester. CAS No. 118694-15-8. Molecular formula: C15H23FN2O16P2. Mole weight: 568.29. | |
| UDP-2-deoxy-2-fluoro-D-glucose | UDP-2-deoxy-2-fluoro-D-glucose is an indispensable compound, serving as a potent tool in positron emission tomography (PET) imaging. By virtue of its radiochemical attributes, this glucose analog enables the non-intrusive observation of in vivo glucose metabolism. Its application extends to the research of multifarious conditions encompassing cancer, neurodegenerative ailments and infectious pathologies. Synonyms: Uridine-2-deoxy-2-fluoro-D-glucose diphosphate ester. CAS No. 67341-43-9. Molecular formula: C15H23FN2O16P2. Mole weight: 568.29. | |
| UDP-2-deoxy-2-fluoro-D-mannose | UDP-2-deoxy-2-fluoro-D-mannose is an antiviral compound in the dynamic biomedical sector used for studying diverse viral infections, notably influenza. Synonyms: Uridine 5-(trihydrogen diphosphate), P-(2-deoxy-2-fluoro-a-D-mannopyranosyl) ester. CAS No. 67341-44-0. Molecular formula: C15H23FN2O16P2. Mole weight: 568.29. | |
| UDP-2-deoxy-2-iodo-D-glucose | UDP-2-deoxy-2-iodo-D-glucose stands as an indispensable compound mainly used for examining the intricate syntheses of glycoproteins and traversing the labyrinth of cellular pathways. By virtue of its distinctive iodine-based modification, UDP-2-deoxy-2-iodo-D-glucose assumes an irreplaceable role in unraveling the enigmatic facets of carbohydrate-driven ailments, prominently including cancer and metabolic disorders. Synonyms: Uridine 5'-(trihydrogen diphosphate),P'-(2-deoxy-2-iodo-a-D-glucopyranosyl)ester. Molecular formula: C15H23N2O16P2I. Mole weight: 676.20. | |
| UDP-2-deoxy-a-D-galactose ammonium salt | UDP-2-deoxy-a-D-galactose ammonium salt, a biochemical product of paramount significance in the biomedical industry, serves predominantly as a substrate in enzymatic reactions, in particular, the biosynthesis of glycoconjugates. This product constitutes an indispensable component of studies pertaining to diseases related to defects in glycosylation, such as congenital disorders of glycosylation and cancer. Furthermore, the compound, with its intrinsic therapeutic value, facilitates the development of potential drugs for the treatment of said diseases. Synonyms: Uridine-5'-diphosphate-2-deoxy-a-D-galactose ammonium salt. Molecular formula: C15H30N4O16P2. Mole weight: 584.36. | |
| UDP-2-ketopropyl-a-D-galactose | | |
| UDP-3-O-(3-hydroxymyristoyl)glucosamine N-acyltransferase | The enzyme catalyses a step of lipid A biosynthesis. LpxD from Escherichia prefers (R,S)-3-hydroxytetradecanoyl-[acyl-carrier protein] over (R,S)-3-hydroxyhexadecanoyl-[acyl-carrier protein]. Escherichia coli lipid A acyltransferases do not have an absolute specificity for 14-carbon hydroxy fatty acids but can transfer fatty acids differing by one carbon unit if the fatty acid substrates are available. When grown on 1% propionic acid, lipid A also contains the odd-chain fatty acids tridecanoic acid, pentadecanoic acid, hydroxytridecanoic acid, and hydroxypentadecanoic acid. Group: Enzymes. Synonyms: UDP-3-O-acyl-glucosamine N-acyltransferase; UDP-3-O-(R-3-hydroxymyristoyl)-glucosamine N-acyltransferase; acyltransfer. Enzyme Commission Number: EC 2.3.1.191. 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-2134; UDP-3-O-(3-hydroxymyristoyl)glucosamine N-acyltransferase; EC 2.3.1.191; UDP-3-O-acyl-glucosamine N-acyltransferase; UDP-3-O-(R-3-hydroxymyristoyl)-glucosamine N-acyltransferase; acyltransferase LpxD; acyl-ACP:UDP-3-O-(3-hydroxyacyl)-GlcN N-acyltransferase; firA (gene name); lpxD (gene name); (3R)-3-hydroxymyristoyl-[acyl-carrier protein]:UDP-3-O-[(3R)-3-hydroxymyristoyl]-α-D-glucosamine N-acetyltransferase. Cat No: EXWM-2134. | |
| UDP-3-O-acyl-N-acetylglucosamine deacetylase | A zinc protein. The enzyme catalyses a committed step in the biosynthesis of lipid A. Group: Enzymes. Synonyms: LpxC protein; LpxC enzyme; LpxC deacetylase; deacetylase LpxC; UDP-3-O-acyl-GlcNAc deacetylase; UDP-3-O-((R)-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-acyl)-N-acetylglucosamine deacetylase; UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase; UDP-3-O-[(3R)-3-hydroxymyristoyl]-N-acetylglucosamine amidohydrolase. Enzyme Commission Number: EC 3.5.1.108. 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-4387; UDP-3-O-acyl-N-acetylglucosamine deacetylase; EC 3.5.1.108; LpxC protein; LpxC enzyme; LpxC deacetylase; deacetylase LpxC; UDP-3-O-acyl-GlcNAc deacetylase; UDP-3-O-((R)-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-acyl)-N-acetylglucosamine deacetylase; UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase; UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase; UDP-3-O-[(3R)-3-hydroxymyristoyl]-N-acetylglucosamine amidohydrolase. Cat No: EXWM-4387. | |
| UDP-(3-O-(R-3-hydroxydecanoyl)) N-acetylglucosamine | UDP-(3-O-(R-3-hydroxydecanoyl)) N-acetylglucosamine is an indispensable compound, assuming a critical function in the synthetic pathway of lipid A, a fundamental constituent of bacterial lipopolysaccharides. Its application within the realm of microbial pathogenesis research is extensive, particularly in elucidating the intricate mechanisms underlying lipopolysaccharide biosynthesis and in identifying prospective drug targets to confront pernicious bacterial infections. Synonyms: Uridine-5'-Diphosphate-3-O-(R-3-Hydroxydecanoyl)-N-Acetyl-D-Glucosamine; (3R)- (2R, 3R, 4R, 5S, 6R)-3-Acetamido-2- ( ( ( ( ( ( (2R, 3S, 4R, 5R)-5- (2, 4-dioxo-3, 4-dihydropyrimidin-1 (2H)-yl)-3, 4-dihydroxytetrahydrofuran-2-yl)methoxy) (hydroxy)phosphoryl)oxy) (hydroxy)phosphoryl)oxy)-5-hydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-4-yl 3-hydroxydecanoate; [(2R,3R,4R,5S,6R)-3-acetamido-2-[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl] (3R)-3-hydroxydecanoate; 953426-26-1; U21; Q27466807; (2R, 3R, 4R, 5S, 6R)-3- (acetylamino)-2-{[ (R)-{[ (S)-{[ (2R, 3S, 4R, 5R)-5- (2, 4-dioxo-3, 4-dihydropyrimidin-1 (2H)-yl)-3, 4-dihydroxytetrahydrofuran-2-yl]methoxy} (hydroxy)phosphoryl]oxy} (hydroxy)phosphoryl]oxy}-5-hydroxy-6- (hydroxymethyl)tetrahydro-2H-pyran-4-yl (3R)-3-hydroxydecanoate (non-preferred name). CAS No. 953426-26-1. Molecular formula: C27H45N3O19P2. Mole weight: 777.60. | |
| UDP-3-O-(R-3-hydroxymyristoyl)-GlcNAc disodium | a substrate for UDP-3-O-acyl-N-acetylglucosamine deacetylase(LpxC). Synonyms: UDP-3-O-(R-3-hydroxymyristoyl)-N-acetyl-D-glucosamine sodium. Molecular formula: C31H51N3O19P2·2Na. Mole weight: 877.67. | |
| UDP-3-O-(R-3-hydroxymyristoyl)-N-acetyl-D-glucosamine | UDP-3-O-(R-3-hydroxymyristoyl)-N-acetyl-D-glucosamine is a fundamental substrate widely utilized in the sweeping realm of biomedical science, holding application in the intricate synthesis of lipid A, which is the cardinal constituent that underpins the remarkable lipopolysaccharide (LPS) architecture within bacteria of the Gram-negative ilk. Molecular formula: C31H53N3O19P2. Mole weight: 833.71. | |
| UDP-3-O[R-3-Hydroxymyristoyl]-N-acetylglucosamine | A lipid A precursor for Escherichia coli. Synonyms: UDP-3-O[R-3-Hydroxymyristoyl]-GlcNAc; P'-[2-(acetylamino)?-2-deoxy-3-O-[(3R)?-3-hydroxy-1-oxotetradecyl]?-α-D-glucopyranosyl] Ester Uridine 5'-(trihydrogen diphosphate)?. CAS No. 108636-29-9. Molecular formula: C31H53N3O19P2. Mole weight: 833.71. | |
| UDP-3-O[R-3-Hydroxymyristoyl]-N-acetylglucosamine | UDP-3-O[R-3-Hydroxymyristoyl]-N-acetylglucosamine is a lipid A precursor for Escherichia coli. Group: Biochemicals. Grades: Highly Purified. CAS No. 108636-29-9. Pack Sizes: 500ug, 1mg. Molecular Formula: C31H53N3O19P2. US Biological Life Sciences. | Worldwide |
| UDP-3-O[R-3-Hydroxymyristoyl]-N-acetylglucosamine Tris Salt | UDP-3-O[R-3-Hydroxymyristoyl]-N-acetylglucosamine Tris Salt is a lipid A precursor for Escherichia coli. Synonyms: 1,3-Propanediol, 2-amino-2-(hydroxymethyl)-P'-[2-(acetylamino)-2-deoxy-3-O-(3-hydroxy-1-oxotetradecyl)-α-D-glucopyranosyl] Ester, Compd. With Uridine 5'-(trihydrogen diphosphate); UDP-3-O[R-3-Hydroxymyristoyl]-GlcNAc Tris Salt. Grades: 90%. CAS No. 112710-84-6. Molecular formula: C35H64N4O22P2. Mole weight: 954.84. | |
| UDP-3-O-[R-3-Hydroxymyristoyl]-N-[R-3-hydroxymyristoyl] Glucosamine Tris Salt | UDP-3-O-[R-3-Hydroxymyristoyl]-N-[R-3-hydroxymyristoyl] Glucosamine Tris Salt, the salt version of [2(R),3(R)]-P'-[2-Deoxy-3-O-(3-hydroxy-1-oxotetradecyl)-2-[(3-hydroxy-1-oxotetradecyl)amino]-α-D-glucopyranosyl] Ester Uridine 5'-(trihydrogen diphosphate) can be used in biological study for reconstruction of metabolic network in bovine mammary gland tissue. And it's potent drug and API metabolite. Synonyms: Uridine 5'-(Trihydrogen Diphosphate) P'-[2-Deoxy-3-O-[(3R)-3-hydroxy-1-oxotetradecyl]-2-[[(3R)-3-hydroxy-1-oxotetradecyl]amino]-α-D-glucopyranosyl] Ester Tris Salt. Molecular formula: C47H88N4O23P2. Mole weight: 1139.17. | |
| UDP-4-amino-4,6-dideoxy-N-acetyl-β-L-altrosamine N-acetyltransferase | Isolated from Helicobacter pylori. The enzyme is involved in the biosynthesis of pseudaminic acid. Group: Enzymes. Synonyms: PseH. Enzyme Commission Number: EC 2.3.1.202. 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-2147; UDP-4-amino-4,6-dideoxy-N-acetyl-β-L-altrosamine N-acetyltransferase; EC 2.3.1.202; PseH. Cat No: EXWM-2147. | |
| UDP-4-amino-4,6-dideoxy-N-acetyl-β-L-altrosamine transaminase | A pyridoxal-phosphate protein. The enzyme is involved in biosynthesis of pseudaminic acid. Group: Enzymes. Synonyms: PseC. Enzyme Commission Number: EC 2.6.1.92. 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-2933; UDP-4-amino-4,6-dideoxy-N-acetyl-β-L-altrosamine transaminase; EC 2.6.1.92; PseC. Cat No: EXWM-2933. | |
| UDP-4-amino-4-deoxy-L-arabinose aminotransferase | A pyridoxal 5'-phosphate enzyme. Group: Enzymes. Synonyms: UDP-(β-L-threo-pentapyranosyl-4''-ulose diphosphate) aminotransferase; UDP-4-amino-4-deoxy-L-arabinose-oxoglutarate aminotransferase; UDP-Ara4O aminotransferase; UDP-L-Ara4N transaminase. Enzyme Commission Number: EC 2.6.1.87. 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-2928; UDP-4-amino-4-deoxy-L-arabinose aminotransferase; EC 2.6.1.87; UDP-(β-L-threo-pentapyranosyl-4''-ulose diphosphate) aminotransferase; UDP-4-amino-4-deoxy-L-arabinose-oxoglutarate aminotransferase; UDP-Ara4O aminotransferase; UDP-L-Ara4N transaminase. Cat No: EXWM-2928. | |
| UDP-4-amino-4-deoxy-L-arabinose formyltransferase | The activity is part of a bifunctional enzyme also performing the reaction of EC 1.1.1.305 [UDP-glucuronic acid dehydrogenase (UDP-4-keto-hexauronic acid decarboxylating)]. Group: Enzymes. Synonyms: UDP-L-Ara4N formyltransferase; ArnAFT. Enzyme Commission Number: EC 2.1.2.13. 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-2003; UDP-4-amino-4-deoxy-L-arabinose formyltransferase; EC 2.1.2.13; UDP-L-Ara4N formyltransferase; ArnAFT. Cat No: EXWM-2003. | |
| UDP-4-azido-4-deoxy-D-glucose | Cas No. 1030832-12-2. | |
| UDP-6-amino-6-deoxy-D-glucose | UDP-6-amino-6-deoxy-D-glucose, a highly significant compound within the biomedicine sector, assumes a vital position in the synthesis of diverse antibiotics and antimicrobial agents. Its multifaceted structure and functional attributes are instrumental in the triumphant treatment of bacterial diseases. Consequently, this product finds substantial application in the realm of drug development aimed at countering bacterial infections and antibiotic-resistant strains, thereby presenting promising resolutions for combating infectious pathogens with utmost efficacy. Synonyms: Uridine 5'-(6-amino-6-deoxy-α-D-glucopyranosyl diphosphate); UDP-6-GlcN; [6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate. CAS No. 345197-39-9. Molecular formula: C15H25N3O16P2. Mole weight: 565.32. | |
| UDP-6-azido-6-deoxy-D-Gal | UDP-6-azido-6-deoxy-D-Gal, a nucleotide analog with great potential for studying glycosylation, has been employed in the synthesis of azido-sugars and labeling experiments to scrutinize the capabilities of glycosyltransferases. Its utility extends to probing the contribution of glycosylation in widespread pathological processes such as cancer and inflammation. This product can greatly benefit scientific research by providing precise and versatile tools to better understand glycosylation. Synonyms: Uridine 5'-(trihydrogen diphosphate), P'-(6-azido-6-deoxy-α-D-galactopyranosyl) ester. CAS No. 868208-96-2. Molecular formula: C15H23N5O16P2. Mole weight: 591.32. | |
| UDP-6-azido-6-deoxy-D-Gal.2Na | Cas No. 868208-96-2. | |
| UDP-6-azido-6-deoxy-D-galactose | UDP-6-azido-6-deoxy-D-galactose is a paramount resource within the biomedical sector for the research of glycosylation investigations, acting as a precursor substance for the creative fabrication of manifold galactose-imbued substances. Its idiosyncratic azide moiety engenders its utility for nutrient labeling metabolic assays, the revolutionary click chemistry methodology and profound bioorthogonal reactions. This diversified compound showcases extensive applicability towards the research of galactose-selective interactions, the fostering of glycoconjugate pioneering endeavors and the insightful exploration of carbohydrate-mediated physiological phenomena. CAS No. 868141-12-2. Molecular formula: C15H21N5O16P2 2(C6H16N). Mole weight: 793.69. | |
| UDP-6-azido-6-deoxy-D-glucose | UDP-6-azido-6-deoxy-D-glucose is a vital compound used in biomedical field as a metabolic precursor for glycobiology research. It is commonly utilized in the synthesis of azidosugars, which are crucial for investigating glycoconjugates and understanding their roles in diseases like cancer and viral infections. Synonyms: [6-(Azidomethyl)-3,4,5-trihydroxyoxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate; uridine 5'-(trihydrogn diphosphate), P'-(6-azido-6-deoxy-?-D-glucopyranosyl) ester. CAS No. 537039-67-1. Molecular formula: C15H21N5O17P2. Mole weight: 605.30. | |
| UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine | UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine is an indispensable compound in the biomedical sector, serving as a paramount instrument for investigating glycosylation's intricacies. As a pivotal tool for studying cancer metastasand immune response modulation, this compound exemplifies its capabilities by enabling precise glycan structure marking and visualization. Synonyms: UDP 6-azido-6-deoxy-GalNAc. CAS No. 1202854-87-2. Molecular formula: C17H26N6O16P2. Mole weight: 632.37. | |
| UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt | UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt is a highly significant substance, serving as an indispensable reactive sugar nucleotide analogue for enzyme-mediated labeling and glycoprotein engineering. This compound intricately interweaves within glycosylation-related processes while facilating researchs for cancer, viral infections and autoimmune disorders. Synonyms: UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine sodium salt; UDP 6-azido-6-deoxy-GalNAc sodium salt; UDP 6-azido-6-deoxy-GalNAc disodium salt. Molecular formula: C17H24N6Na2O16P2. Mole weight: 676.33. | |
| UDP-6-deoxy-6-fluoro-D-galactose | UDP-6-deoxy-6-fluoro-D-galactose is a vital compound predominantly used in drug development for studying various diseases such as cancer, diabetes and viral infections. Synonyms: Uridine 5'-(trihydrogen diphosphate),P'-(6-deoxy-6-fluoro-a-D-galactopyranosyl)ester. CAS No. 736904-78-2. Molecular formula: C15H23FN2O16P2. Mole weight: 568.29. | |
| UDP-6-deoxy-6-fluoro-D-glucose | UDP-6-deoxy-6-fluoro-D-glucose is a vital compound extensively used in the biomedical industry playing a crucial role in the research and development of drugs for various diseases, including certain types of cancers. CAS No. 1186506-89-7. Molecular formula: C15H23FN2O16P2. Mole weight: 568.29. | |
| UDP-acetylglucosamine deacetylase from Escherichia coli, Recombinant | UDP-acetylglucosamine deacetylase is a metal-dependent deacetylase from Escherichia coli that removes the acetyl group from the 2-amino group of UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine (myr-UDP-GlcNAc)3. Group: Enzymes. Synonyms: EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. UDP-acetylglucosamine deacetylase. Mole weight: 36.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Escherichia coli. EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Cat No: NATE-1537. | |
| UDP-acetylglucosamine deacetylase from Pseudomonas aeruginosa, Recombinant | UDP-acetylglucosamine deacetylase is a metal-dependent deacetylase from Escherichia coli that removes the acetyl group from the 2-amino group of UDP-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine (myr-UDP-GlcNAc)3. Group: Enzymes. Synonyms: EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. UDP-acetylglucosamine deacetylase. Mole weight: 35.5 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Pseudomonas aeruginosa. EC 3.5.1.-; metal-dependent deacetylase; UDP-acetylglucosamine deacetylase. Cat No: NATE-1538. | |
| UDP-a-D-apiofuranose | | |
| UDP-a-D-galactose | UDP-a-D-galactose is a pivotal nucleotide sugar molecule crucial for biosynthesizing carbohydrates and galactose-containing polysaccharides. Its active involvement in the biosynthesis of glycosphingolipids, the building blocks of cell membranes, makes it indispensable. Any impairment of this molecule might trigger galactosemia and other ailments, accentuating its contribution to cellular homeostasis. Synonyms: UDP-galactose; uridine diphosphate galactose; UDP-D-galactopyranose; Uridine pyrophosphogalactose; UDP-alpha-D-Galactose; Uridinediphosphogalactose; UDP-Gal; Uridine 5'-diphosphate galactose; Uridine 5'-(alpha-D-galactopyranosyl pyrophosphate); Uridine 5'-(trihydrogen diphosphate), P'-alpha-D-galactopyranosyl ester; Uridine 5'-(trihydrogen pyrophosphate), mono-alpha-D-galactopyranosyl ester. Grades: ≥95%. CAS No. 2956-16-3. Molecular formula: C15H24N2O17P2. Mole weight: 566.30. | |
| UDP-a-D-galactose ammonium salt | UDP-a-D-galactose ammonium salt is a crucial biochemical compound widely used industry. It serves as a key precursor in various biosynthetic pathways, especially in the synthesis of glycoconjugates and glycoproteins. This product plays an essential role in studying certain diseases associated with abnormal galactosylation, such as congenital disorders of glycosylation. Synonyms: UDP-D-galactose ammonium salt; UDP-α-D-Gal ammonium salt; Uridine 5'-(trihydrogen diphosphate)? P'-α-D-galactopyranosyl ester ammonium salt; UDP-galactose ammonium salt. Molecular formula: C15H30N4O17P2. Mole weight: 600.36. | |
| UDP-a-D-galacturonic acid | UDP-a-D-galacturonic acid is a crucial molecule in the biomedical industry that serves as a substrate for enzymes involved in the biosynthesis of glycosaminoglycans. It plays an essential role in the treatment of diseases related to glycosaminoglycan deficiencies, such as Maroteaux-Lamy syndrome and Sly syndrome. This product enables researchers to study the biosynthesis and metabolism of glycosaminoglycans, aiding in the development of potential therapies. Synonyms: α-D-Glucopyranuronic acid, 1?P'-ester with uridine 5'-(trihydrogen diphosphate); Uridine[5]diphospho-a-D-galacturonopyranoside; UDP-GlcUA; Glucopyranuronic acid, 1-ester with uridine 5'-pyrophosphate; α-D-Glucopyranuronic acid, ester with uridine 5'-pyrophosphate; UDP-D-glucuronic acid; UDP-glucuronic acid; UDP-α-D-glucuronic acid; Uridine 5'-diphospho-α-D-glucuronic acid; Uridine 5'-diphosphoglucuronic acid; Uridine diphosphate glucuronic acid; Uridine diphospho-D-glucuronic acid; Uridine diphosphoglucuronic acid; Uridine pyrophosphoglucuronic acid; UDP-g acid. Grades: ≥95%. CAS No. 2616-64-0. Molecular formula: C15H22N2O18P2. Mole weight: 580.29. | |
| UDP-a-D-glucose ammonium salt | UDP-a-D-glucose ammonium salt is an invaluable compound in the biomedical field assuming a pivotal role as an indispensable adjunct in pharmacological formulations for the research of diverse ailments encompassing metabolic dysfunctions and specific neoplastic conditions. This remarkable product exerts its influence on drug stabilization, bioaccessibility and precise drug transportation. Molecular formula: C15H30N4O17P2. Mole weight: 600.36. | |
| UDP-a-D-xylose | UDP-a-D-xylose is an indispensable resource, finding extensive application in investigating the intricate involvement of nucleotide sugars in an assortment of cellular mechanisms. With role as a fundamental substrate for enzymatic processes governing the synthesis of glycoproteins, glycolipids and proteoglycans, this esteemed product holds applications in studying maladies associated with aberrant glycosylation, including congenital disorders of glycosylation and select cancer types. Synonyms: uridine[5]diphospho-a-D-xylopyranoside. Molecular formula: C14H22N2O16P2. Mole weight: 536.28. | |
| UDP-a-D-Xylose disodium | UDP-a-D-Xylose disodium is a remarkable biomedical compound for the research of specific ailments, displaying its functionality as an invaluable precursor for the intricate biosynthesis of glycoconjugates. By actively participating in the convoluted process of polysaccharide and proteoglycan formation within cellular entities, this indispensable compound assumes a fundamental role in the intricate metabolism of Xylose is a vital monosaccharide. Consequently, this extraordinary product finds extensive application within the realm of scientific investigation and therapeutic drug discovery, primarily focusing on the amelioration of intricacies linked to carbohydrate metabolism and glycosylation disorders. Synonyms: Uridine 5'-(trihydrogen diphosphate), P'-α-D-xylopyranosyl ester, disodium salt; UDP-Xyl 2Na. CAS No. 108320-89-4. Molecular formula: C14H22N2O16P2Na2. Mole weight: 582.26. | |
| UDP-a-L-rhamnose | UDP-α-L-rhamnose is a vital biomolecule prevalent in the biomedical sector, holding a noteworthy function in the biosynthesis of glycolipids, polysaccharides and natural products. Displaying its extraordinary aptitude as a sugar donor, this compound becomes indispensable in the enzymatic process of synthesizing multifaceted carbohydrates. Notably, UDP-α-L-rhamnose acts as a precursor for generating glycoconjugates containing rhamnose, used to study infectious ailments. Synonyms: Uridine 5-[3-(6-deoxy-L-mannopyranosyl) dihydrogen diphosphate]; Uridine 5-[3-(L-rhamnopyranosyl) dihydrogen diphosphate]. CAS No. 30174-43-7. Molecular formula: C15H24N2O16P2. Mole weight: 550.30. | |
| UDP-a-L-Rha Sodium Salt | UDP-a-L-Rha Sodium Salt is a derivative of uridine, which is a nucleoside, widely distributed in nature, and it's one of the four basic components of ribonucleic acid (RNA). Synonyms: Uridine 5'-Diphospho-a-L-rhamnose Sodium Salt; Uridine 5'-(trihydrogen diphosphate), P'-(6-deoxy-α-L-mannopyranosyl) ester, sodium salt. CAS No. 1526988-33-9. Molecular formula: C15H22N2Na2O16P2. Mole weight: 594.27. | |
| UDP-a-N-acetyl-D-galactosamine ammonium salt | UDP-a-N-acetyl-D-galactosamine ammonium salt, an activated glycosyl donor frequently employed in the biomedical sector, crucially contributes to glycosylation reactions. Its unparalleled importance in the synthesis of glycoproteins, glycolipids, and proteoglycans has been widely acknowledged. This biomolecule has been identified as an essential chemical in the treatment of various diseases, ranging from cancer to inflammation and autoimmune disorders. Its ubiquitous presence in this field underscores its significance in contributing to the advancement of biomedical breakthroughs. Synonyms: [(2R,3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate ammonium salt; UDP-N-acetyl-D-galactosamine ammonium salt. Molecular formula: C17H33N5O17P2. Mole weight: 641.42. | |
| UDP-apiose | UDP-apiose is an indispensable biochemical compound, aiding in studying a diverse array of afflictions such as malignant neoplasms, inflammatory cascades and prodigious autoimmune maladies. By serving as a foundational blueprint for the research of apiosyl enzymes and glycoproteins, it assumes a pivotal stance in orchestrating vital pathways of cellular communication. Synonyms: Uridine diphospho-D-apiose. CAS No. 36020-60-7. Molecular formula: C14H22N2O16P2. Mole weight: 536.28. | |
| UDP-arabinopyranose mutase | The reaction is reversible and at thermodynamic equilibrium the pyranose form is favored over the furanose form (90:10). Group: Enzymes. Synonyms: Os03g40270 protein; UAM1; UAM3; RGP1; RGP3; OsUAM1; OsUAM2; Os03g0599800 protein; Os07g41360 protein. Enzyme Commission Number: EC 5.4.99.30. 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-5571; UDP-arabinopyranose mutase; EC 5.4.99.30; Os03g40270 protein; UAM1; UAM3; RGP1; RGP3; OsUAM1; OsUAM2; Os03g0599800 protein; Os07g41360 protein. Cat No: EXWM-5571. | |
| UDP-arabinose 4-epimerase | This enzyme belongs to the family of isomerases, specifically those racemases and epimerases acting on carbohydrates and derivatives. This enzyme participates in nucleotide sugars metabolism. Group: Enzymes. Synonyms: uridine diphosphoarabinose epimerase; UDP arabinose epimerase; uridine 5'-diphosphate-D-xylose 4-epimerase; UDP-D-xylose 4-epimerase. Enzyme Commission Number: EC 5.1.3.5. CAS No. 9024-18-4. 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-5428; UDP-arabinose 4-epimerase; EC 5.1.3.5; 9024-18-4; uridine diphosphoarabinose epimerase; UDP arabinose epimerase; uridine 5'-diphosphate-D-xylose 4-epimerase; UDP-D-xylose 4-epimerase. Cat No: EXWM-5428. | |
| Udp-beta-L-rhamnose | UDP-beta-L-rhamnose, an indispensable biomolecule extensively employed in the realm of biomedicine, assumes a pivotal stance in the intricate process of L-rhamnose biosynthesis. This saccharide, prevalent among diverse pharmaceutical agents and natural substances, acquires utmost significance in the advancement of therapeutics that aspire to combat bacterial infections, certain cancerous manifestations, and afflictions stemming from inflammation. Synonyms: UDP-L-rhamnose; Uridine 5'-(trihydrogen diphosphate), mono(6-deoxy-beta-L-mannopyranosyl) ester. Grades: 98%. CAS No. 1955-26-6. Molecular formula: C15H24N2O16P2. Mole weight: 550.30. | |
| UDP-β-L-Rhamnose Disodium Salt | UDP-β-L-Rhamnose Disodium Salt, obtained from Uridine 5'-Monophosphate Disodium Salt, is a nucleotide that is a major component of ribonucleic acid. Uridine 5'-Monophosphate Disodium Salt is found in natural RNA rich foods and has been shown to increase cognitive function in animals. Nucleotide is a widely occurring cellular constituent involved in the glycosylation of the endotoxins of Salmonella. Molecular formula: C15H22N2Na2O16P2. Mole weight: 594.27. | |
| UDPβS | UDPβS is a robust nucleotide analog, represents an essential tool, is acclaimed for its profound comprehension of diverse cellular mechanisms. It serves as an exemplary substrate, facilitating meticulous examination of carbohydrate metabolic enzymes, while also bestowing the ability to either activate or impede distinct proteins. Furthermore, UDPβS assumes a pivotal role in probing drug metabolism, deciphering intricate processes of signal transduction, as well as exploring revolutionary therapeutic modalities for afflictions like cancer and neurological disorders. Synonyms: Uridine-5'-(β-thio)-diphosphate, Sodium salt. Grades: ≥ 90 % by HPLC. Molecular formula: C9H14N2O11P2S (free acid). Mole weight: 420.22 (free acid). | |
| UDP-b-L-arabinofuranose | UDP-b-L-arabinofuranose is a prominent compound assuming a pivotal role in the intricate realm of nucleotide sugar synthesis. Owing to its distinct structure, it manifestly serves as a precursor for drugs teeming with arabinofuranose. CAS No. 331001-44-6. Molecular formula: C14H22N2O16P2. Mole weight: 536.28. | |
| UDP-b-L-arabinose | UDP-b-L-arabinose is an indispensable compound, serving as a pivotal substratum in the intricate process of glycoprotein, glycolipid and proteoglycan biosynthesis. Its overarching role encompasses studying cancer, infectious diseases and autoimmune disorders. Synonyms: uridine[5]diphospho-b-L-arabinopyranoside. CAS No. 15839-78-8. Molecular formula: C14H22N2O16P2. Mole weight: 536.28. | |
| UDP-b-L-fucose diammonium salt | UDP-b-L-fucose diammonium salt is a vital compound extensively used in the biomedical industry. It serves as a precursor for the synthesis of fucosylated biomolecules, such as glycans and glycoproteins. Its exceptional properties is used in studying various drug targets and disease pathways associated with fucosylation. Molecular formula: C15H22N2O16P2 N2H8. Mole weight: 584.37. | |
| UDP-b-L-glucose ammonium salt | UDP-b-L-glucose ammonium salt is a biochemical tool used in research applications to study the metabolic pathways and enzyme catalysis involving UDP-sugar transferases. It is also used in the synthesis of glycans and glycoconjugates, as well as in drug discovery and development for the treatment of certain diseases. Molecular formula: C15H30N4O17P2. Mole weight: 600.36. | |
| UDP-D-galactosamine disodium salt | UDP-D-galactosamine disodium salt is an indispensable compound extensively employed in the realm of in the orchestration of glycosaminoglycans' biosynthesis, thereby significantly influencing the processes of cellular communication, immune response and the architecture of the extracellular matrix. Synonyms: Udp galactosamine; UDP-galactosamine; Uridine diphosphate galactosamine; UDP-alpha-D-galactosamine; 17479-06-0; CHEBI:16846; Uridine 5'-diphosphogalactosamine; [(2R,3R,4R,5R,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate; AC1Q6SAB; UDPgalactosamine; UDP-GalN; Uracil Diphosphate galactosamine; CHEMBL2092918; CYKLRRKFBPBYEI-KBQKSTHMSA-N; DTXSID901316536; C02467; Q27102108; uridine 5'-[3-(2-amino-2-deoxygalactopyranosyl) dihydrogen diphosphate]; [(2R,3R,4R,5R,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] hydrogen phosphate. CAS No. 17479-06-0. Molecular formula: C15H23N3O16P2Na2. Mole weight: 609.28. | |
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