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| Product | Description | |
|---|---|---|
| L-galactonate dehydratase | The enzyme takes part in a D-galacturonate degradation pathway in the fungi Trichoderma reesei (Hypocrea jecorina) and Aspergillus niger. Group: Enzymes. Synonyms: LGD1. Enzyme Commission Number: EC 4.2.1.146. 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-4987; L-galactonate dehydratase; EC 4.2.1.146; LGD1. Cat No: EXWM-4987. |  |
| L-Galactono-1,4-lactone | L-Galactono-1,4-lactone is a kind of biochemical reagent. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 1668-08-2. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-W155493. |  |
| L-Galactono-1,4-lactone | L-Galactono-1,4-lactone is a fundamental compound extensively utilized with sector assuming a pivotal position. Its application encompasses the synthesis of ascorbate, popularly known as vitamin C, within the cellular frameworks of both plants and animals. Synonyms: L-Galactonic acid gamma-lactone. CAS No. 1668-08-2. Molecular formula: C6H10O6. Mole weight: 178.14. |  |
| L-galactonolactone dehydrogenase | This enzyme catalyses the final step in the biosynthesis of L-ascorbic acid in higher plants and in nearly all higher animals with the exception of primates and some birds. The enzyme is very specific for its substrate L-galactono-1,4-lactone as D-galactono-γ-lactone, D-gulono-γ-lactone, L-gulono-γ-lactone, D-erythronic-γ-lactone, D-xylonic-γ-lactone, L-mannono-γ-lactone, D-galactonate, D-glucuronate and D-gluconate are not substrates. FAD, NAD+, NADP+ and O2 (cf. EC 1.3.3.12, L-galactonolactone oxidase) cannot act as electron acceptor. Group: Enzymes. Synonyms: galactonolactone dehydrogenase; L-galactono-γ-lactone dehydrogenase; L-galactono-γ-lactone:ferricytochrome-c oxidoreductase; GLDHase; GLDase. Enzyme Commission Number: EC 1.3.2.3. CAS No. 9029-2-1. 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-1370; L-galactonolactone dehydrogenase; EC 1.3.2.3; 9029-02-1; galactonolactone dehydrogenase; L-galactono-γ-lactone dehydrogenase; L-galactono-γ-lactone:ferricytochrome-c oxidoreductase; GLDHase; GLDase. Cat No: EXWM-1370. | |
| L-galactonolactone oxidase | A flavoprotein. Acts on the 1,4-lactones of L-galactonic, D-altronic, L-fuconic, D-arabinic and D-threonic acids; not identical with EC 1.1.3.8 L-gulonolactone oxidase. (cf. EC 1.3.2.3 galactonolactone dehydrogenase). Group: Enzymes. Synonyms: L-galactono-1,4-lactone oxidase. Enzyme Commission Number: EC 1.3.3.12. CAS No. 69403-13-0. 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-1373; L-galactonolactone oxidase; EC 1.3.3.12; 69403-13-0; L-galactono-1,4-lactone oxidase. Cat No: EXWM-1373. | |
| L-Galactose | L-Galactose is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 15572-79-9. Pack Sizes: 10 mg; 25 mg. Product ID: HY-N6614. | |
| L-Galactose-13C6 | L-Galactose-13C6. Group: Biochemicals. Grades: Highly Purified. CAS No. 478518-66-0. Pack Sizes: 1mg. Molecular Formula: 13C6H12O6, Molecular Weight: 186.11. US Biological Life Sciences. |  Worldwide |
| L-galactose 1-dehydrogenase | The enzyme catalyses a step in the ascorbate biosynthesis in higher plants (Smirnoff-Wheeler pathway). The activity with NADP+ is less than 10% of the activity with NAD+. Group: Enzymes. Synonyms: L-GalDH; L-galactose dehydrogenase. Enzyme Commission Number: EC 1.1.1.316. 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-0228; L-galactose 1-dehydrogenase; EC 1.1.1.316; L-GalDH; L-galactose dehydrogenase. Cat No: EXWM-0228. | |
| L-Galactose-1-phosphate | L-Galactose-1-phosphate is a crucial substrate in the pentose phosphate pathway and a precursor for the synthesis of L-ascorbic acid (vitamin C). It plays a significant role in studying diseases caused by vitamin C deficiency. Synonyms: 1-O-phosphono-L-galactopyranose; L-galactopyranose-1-(dihydrogen phosphate). Molecular formula: C6H13O9P. Mole weight: 260.14. | |
| L-galactose 1-phosphate phosphatase | The enzyme from plants also has the activity of EC 3.1.3.25, inositol-phosphate phosphatase. The enzymes have very low activity with D-galactose 1-phosphate (cf. EC 3.1.3.94, D-galactose 1-phosphate phosphatase). Group: Enzymes. Synonyms: VTC4 (gene name) (ambiguous); IMPL2 (gene name) (ambiguous). Enzyme Commission Number: EC 3.1.3.93. 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-3700; L-galactose 1-phosphate phosphatase; EC 3.1.3.93; VTC4 (gene name) (ambiguous); IMPL2 (gene name) (ambiguous). Cat No: EXWM-3700. | |
| L-Galactose-3-13C | L-Galactose-3-13C. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Galactose-6-O-sulphate sodium salt | L-Galactose-6-O-sulphate sodium salt is a crucial compound used in the research of various diseases, particularly those related to carbohydrate metabolism. With its unique properties, this product aids in studying specific enzymes or chemical pathways involved in certain diseases. Molecular formula: C6H11O9SNa. Mole weight: 282.20. | |
| L-Galacturonic acid | Heterocyclic Organic Compound. Alternative Names: L-GALACTURONIC ACID. CAS No. 108729-78-8. Molecular formula: C6H10O7. Mole weight: 194.1394. Purity: 0.96. IUPACName: (2R,3S,4R,5S)-3,4,5,6-tetrahydroxyoxane-2-carboxylicacid. Canonical SMILES: C1(C(C(OC(C1O)O)C(=O)O)O)O. Catalog: ACM108729788. |  |
| L-Galacturonic acid | L-Galacturonic acid is a vital component widely used in the production of pharmaceutical drugs, serving as a key ingredient in the research of various diseases. CAS No. 108729-78-8. | |
| L-γ-Carboxyglutamic acid | Synonyms: H-L-Glu(γ-COOH)-OHã-Carboxy-L-glutamic acid. Grades: ≥ 99% (TLC). CAS No. 53861-57-7. Molecular formula: C6H9NO6. Mole weight: 191.10. | |
| L-gamma-Glutamyl-3-carboxy-4-nitroanilide | Suitable as substrate for γ-glutamyltranspeptidase test. Group: Biochemicals. Grades: Highly Purified. CAS No. 63699-78-5. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C12H13N3O7·NH3, Molecular Weight: 328.28. US Biological Life Sciences. | Worldwide |
| L-gamma-Glutamyl-L-cysteinyl glutathione | . Uses: Used in the synthesis of disulfides related to glutathione. Synonyms: L-γ-Glutamyl-L-cysteinyl-glycine (2-2')-Disulfide -L-γ-glutamyl-L-cysteine; γ-Glu-Cys GSH. CAS No. 90663-73-3. Molecular formula: C18H29N5O11S2. Mole weight: 555.58. | |
| L-γ-Glutamyl-L-cysteinyl-L-lysine | A bifunctional trapping agent ( γ -Glutamyl cysteinyl lysine) is investigated as an alternative of GSH for simultaneous trapping both hard and soft reactive metabolite. Group: Biochemicals. Alternative Names: N2-(N-L-γ-Glutamyl-L-cysteinyl)-L-lysine. Grades: Highly Purified. CAS No. 128960-73-6. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| L-Gamma-glutamyl-L-cysteinyl-L-lysine | Heterocyclic Organic Compound. Alternative Names: N2-(N-L-γ-Glutamyl-L-cysteinyl)-L-lysine. CAS No. 128960-73-6. Molecular formula: C14H26N4O6S. Mole weight: 378.44. Appearance: Pale Yellow Solid. Catalog: ACM128960736. | |
| L-gamma-Glutamyl-L-valylglycine | Synonyms: gamma-Glutamyl-valyl-glycine; (S)-2-Amino-5-(((S)-1-((carboxymethyl)amino)-3-methyl-1-oxobutan-2-yl)amino)-5-oxopentanoic acid. CAS No. 38837-70-6. Molecular formula: C12H21N3O6. Mole weight: 303.31. | |
| L-γ-Glutamyl-p-nitroanilide hydrate | L-γ-Glutamyl-p-nitroanilide (hydrate) is aglutamic acid derivatives. Uses: Scientific research. Group: Peptides. CAS No. 122864-94-2. Pack Sizes: 1 g; 5 g; 10 g; 25 g. Product ID: HY-W345421. | |
| LGB-321 dihydrochloride | This active molecular is a selective ATP-competitive inhibitor of Pan-PIM kinase. LGB-321 is active in PIM2 dependent cell lines that is quite different to other PIM inhibitors reported before. LGB321 inhibits proliferation of a number of cell lines derived from diverse hematological malignancies which is consistent with its activity on all three PIM kinases. LGB321 is efficient in inhibiting tumor xenografts and is well-tolerated within the therapeutic exposure range in animal models. Uses: Anti-tumor. Synonyms: LGB-321 HCl; LGB 321 HCl; LGB321 HCl; N-(4-((3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl)pyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide dihydrochloride. Grades: 98%. CAS No. 1210416-93-5. Molecular formula: C23H24Cl2F3N5O2. Mole weight: 530.37. | |
| LGB-321 HCl | The hydrochloride salt form of LGB-321, a picolinamide derivative, has been found to be a PIM kinases inhibitor that could influence the proliferation of sorts of cell lines related to some hematological malignancies. Synonyms: LGB321 HCl; LGB 321 HCl. Grades: 98%. CAS No. 1469925-36-7. Molecular formula: C23H24Cl2F3N5O2. Mole weight: 530.37. | |
| L-g-Carboxyglutamic acid 99+% (TLC) | L-g-Carboxyglutamic acid 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 53861-57-7. Pack Sizes: 10mg, 50mg, 250mg. US Biological Life Sciences. | Worldwide |
| LGD-2226 | LGD-2226 is a selective and orally active androgen receptor modulator with an EC 50 of 0.2 nM and a K i of 1.5 nM for human androgen receptor. LGD-2226 shows tissue selectivity in animal models, with reduced effects on prostate compared to muscle. LGD-2226 can be used for muscle wasting, osteoporosis and sexual dysfunction [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 328947-93-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-105318. | |
| LGD-2226 | LGD-2226 is a selective androgen receptor modulator used in the treatment of muscle wasting and osteoporosis, shows to have an anabolic effect on muscle and bone tissue. Uses: A selective androgen receptor modulator used in the treatment of muscle wasting and osteoporosis. Synonyms: LGD 2941; LGD2941; LGD-2941; LGD-2226; LGD2226; LGD 2226.6-[Bis(2,2,2-trifluoroethyl)amino]-4-(trifluoromethyl)-2(1H)-quinolinone. Grades: ≥98%. CAS No. 328947-93-9. Molecular formula: C14H9F9N2O. Mole weight: 392.22. | |
| LGD-3303 | LGD-3303 is a selective androgen receptor modulator ( SARM ). Uses: Scientific research. Group: Signaling pathways. CAS No. 917891-35-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103576. | |
| LGD-4665 | LGD-4665, an oral thromobopoietin receptor agonist, is being developed as a new generation small molecule thrombopoietin (TPO) mimetic. It is a highly selective and potent agonist of the TPO receptor and therefore induces differentiation and proliferation of megakaryocytes. The pharmacologic characteristics indicate potential therapeutic use in thrombocytopenic patients with a variety of clinical etiologies. Research demonstrated that LGD-4665 was well-tolerated with an excellent safety profile. Multiple phase-II studies in thrombocytopenic patients due to ITP, Hep-C and MDS with daily and weekly dosing regimens, as well as additional Phase-I pharmacology studies in healthy volunteers are underway. Synonyms: LGD-4665; LGD 4665; LGD4665. CAS No. 1192571-53-1. | |
| LGD-6972 | LGD-6972 is a glucagon receptor antagonist. Group: Antagonists. Alternative Names: LGD-6972; LGD 6972; LGD6972; MB-11262; MB 11262; MB11262. CAS No. 1207989-09-0. Molecular formula: C43H46N2O5S. Mole weight: 702.91. Appearance: Solid powder. Purity: >98%. IUPACName: (R)-2-(4-(2-(4'-(tert-butyl)-[1, 1'-biphenyl]-4-yl)-3-oxo-3-((2', 4', 6'-trimethyl-[1, 1'-biphenyl]-4-yl)amino)propyl)benzamido)ethane-1-sulfonic acid. Canonical SMILES: O=C (NCCS (=O) (O)=O)C1=CC=C (C[C@H] (C2=CC=C (C3=CC=C (C (C) (C)C)C=C3)C=C2)C (NC4=CC=C (C5=C (C)C=C (C)C=C5C)C=C4)=O)C=C1. Catalog: ACM1207989090. | |
| LGD-6972 | LGD-6972 Inhibitor. Uses: Scientific use. Product Category: T11845. CAS No. 1207989-09-0. |  |
| LGD-6972 | LGD-6972 is an orally bioavailable small molecule glucagon receptor antagonist being developed as an adjunct to diet and exercise to improve glycemic control in adults with T2DM. Synonyms: LGD-6972; LGD 6972; LGD6972; 2- [ [4- [ (2R) -2- [4- (4-tert-butylphenyl) phenyl] -3-oxo-3- [4- (2, 4, 6-trimethylphenyl) anilino] propyl] benzoyl] amino] ethanesulfonic acid. CAS No. 1207989-09-0. Molecular formula: C43H46N2O5S. Mole weight: 702.9. | |
| L-g-Ethylidene glutanic acid | | |
| LGK974 | LGK974 is a selective and orally bioavailable Porcupine inhibitor under development for the treatment of cancers that are driven by the Wnt pathway in a Wnt ligand-dependent manner. LGK974 was shown to induce tumor regression in a Wnt-driven murine tumor model. Synonyms: LGK-974; WNT-974; 2-(2',3-Dimethyl-[2,4'-bipyridin]-5-yl)-N-(5-(pyrazin-2-yl)pyridin-2-yl)acetamide; 2-[5-methyl-6-(2-methylpyridin-4-yl)pyridin-3-yl]-N-(5-pyrazin-2-ylpyridin-2-yl)acetamide. Grades: >98%. CAS No. 1243244-14-5. Molecular formula: C23H20N6O. Mole weight: 396.454. | |
| LGK974 (LGK-974, WNT-974, LGK 974, NVP-LGK974) | LGK974 is a highly potent inhibitor of Porcupine (PORCN), a Wnt-specific acyltransferase. LGK974 is orally bioavailable and inhibits WNT signaling in vitro and in vivo. It is reported to exhibit anti-tumor properties without increasing cytotoxicity. Group: Biochemicals. Alternative Names: 2-[5-methyl-6-(2-methylpyridin-4-yl)pyridin-3-yl]-N-(5-pyrazin-2-ylpyridin-2-yl)acetamide; LGK-974; WNT-974; LGK 974; NVP-LGK974; 2,3-Dimethyl-N-[5-(2-pyrazinyl)-2-pyridinyl]-[2,4-bipyridine]-5-acetamide; 2-(2,3-Dimethyl-[2,4-bipyridin]-5-yl)-N-(5-(pyrazin-2-yl)pyridin-2-yl)acetamide. Grades: Highly Purified. CAS No. 1243244-14-5. Pack Sizes: 1mg, 5mg, 25mg, 100mg. Molecular Formula: C??H??N?O, Molecular Weight: 396.44. US Biological Life Sciences. | Worldwide |
| L-Glucitol | L-Glucitol is L-Isomer of D-Glucitol (S677100), a sugar alcohol obtained from the reduction of glucose and is naturally found in various fruits such as apples, pears and peaches. Group: Biochemicals. Grades: Highly Purified. CAS No. 6706-59-8. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C6H14O6, Molecular Weight: 182.17. US Biological Life Sciences. | Worldwide |
| L-Glucitol-1-13C | L-Glucitol-1-13C. Group: Biochemicals. Alternative Names: D-Gulitol-1-13C; L-Sorbitol-1-13C. Grades: Highly Purified. Pack Sizes: 25mg. Molecular Formula: C513CH14O6, Molecular Weight: 183.17. US Biological Life Sciences. | Worldwide |
| L-Glucitol-2-13C | L-Glucitol-2-13C. Group: Biochemicals. Alternative Names: D-Gulitol-2-13C; L-Sorbitol-2-13C. Grades: Highly Purified. Pack Sizes: 25mg. Molecular Formula: C513CH14O6, Molecular Weight: 183.17. US Biological Life Sciences. | Worldwide |
| L-Gluconic acid calcium salt | L-Gluconic acid calcium salt is a scientifically advanced creation, used for studying insufficient calcium levels and enhance skeletal vitality. It functions as an indispensable calcium adjunct aiding in the research of osteoporosis. Synonyms: Calcium L-gluconate. CAS No. 152772-65-1. Molecular formula: C6H11O7 Ca. Mole weight: 215.19. | |
| L-Gluconic Acid N-Succinimide | L-Gluconic Acid N-Succinimide is an analogue of D-Gluconic Acid N-Succinimide (G417430), an intermediate in the synthesis of a phenylboronica acid polymer as a self-regulating insulin delivery system. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg, 500mg. Molecular Formula: C10H15NO9, Molecular Weight: 293.23. US Biological Life Sciences. | Worldwide |
| L-Glucono-1,4-lactone | L-Glucono-1,4-lactone is renowned for its versatility in biomedical applications, serving as an acidifier in beverages and a pivotal Vitamin C precursor. Remarkably, its application extends to the research of liver diseases, alzheimer's and cancer. Synonyms: L-Glucono-gamma-lactone; 74464-44-1; L-glucono-1,4-lactone; Glucono-gamma-lactone, L-; B127M65W5J; (3S,4S,5S)-5-((S)-1,2-Dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one; (3S,4S,5S)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-one; (3S,4S,5S)-5-((1S)-1,2-Dihydroxyethyl)-3,4-dihydroxy-tetrahydrofuran-2-one; UNII-B127M65W5J; L-Gluconic acid, gamma-lactone; SCHEMBL5919577; L-GLUCONO-.GAMMA.-LACTONE; AKOS040752556; L-GLUCONIC ACID. GAMMA.-LACTONE. Molecular formula: C6H10O6. Mole weight: 178.14. | |
| L-Glucono-1,5-lactone | L-Glucono-1,5-lactone, a fundamental constituent within the biomedical sector, assumes an essential role as a precursor for manufacturing L-ascorbic acid (commonly referred to as Vitamin C). Synonyms: L-Gluconic acid d-lactone. CAS No. 52153-09-0. Molecular formula: C6H10O6. Mole weight: 178.14. | |
| L-Glucosamine hydrochloride | L-Glucosamine hydrochloride is a widely utilized compound within the biomedical sector with research extending to joint-associated ailments, comprising osteoarthritand rheumatoid arthritis. Synonyms: 2-Amino-2-deoxy-L-glucose. CAS No. 69839-78-7. Molecular formula: C6H13NO5. Mole weight: 179.17. | |
| L-Glucose | L-Glucose is a profoundly pivotal bioactive compound, propelling cutting-edge research in the intricate domain of diabetes. Unraveling the intricacies of glucose metabolism and orchestrating the intricate dance of insulin signaling pathways, this resplendent compound bequeaths profound scientific revelations. CAS No. 921-60-8. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| L-Glucose | L-Glucose (L-(-)-Glucose) is a stereoisomer of D-Glucose (HY-B0389), which does not readily enter the brain. L-Glucose can promote food intake. L-glucose is combined with a fluorescence detector to produce a fluorescent probe that can be used to visualize and characterize cancer cells. L-Glucose also can be used in the research to enhance memory in mice [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: L-(-)-Glucose. CAS No. 921-60-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W010042. | |
| L-(-)-Glucose | Cas No. 921-60-8. | |
| L-Glucose-1-13C | L-Glucose-1-13C. Group: Biochemicals. Alternative Names: FM 602-1-13C; L(-)-Glucose-1-13C; Levoglucose-1-13C; l-Glucose-1-13C. Grades: Highly Purified. CAS No. 478519-02-7. Pack Sizes: 25mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Glucose-1,2-13C2 | L-Glucose-1,2-13C2. Group: Biochemicals. Alternative Names: FM 602-1,2-13C2; L(-)-Glucose-1,2-13C2; Levoglucose-1,2-13C2; l-Glucose-1,2-13C2. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C413C2H12O6, Molecular Weight: 182.14. US Biological Life Sciences. | Worldwide |
| L-Glucose-1,2,3-13C3 | L-Glucose-1,2,3-13C3. Group: Biochemicals. Alternative Names: FM 602-1,2,3-13C3; L(-)-Glucose-1,2,3-13C3; Levoglucose-1,2,3-13C3; l-Glucose-1,2,3-13C3. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C313C3H12O6, Molecular Weight: 183.13. US Biological Life Sciences. | Worldwide |
| L-Glucose-2-13C | L-Glucose-2-13C. Group: Biochemicals. Alternative Names: FM 602-2-13C; L(-)-Glucose-2-13C; Levoglucose-2-13C; l-Glucose-2-13C. Grades: Highly Purified. CAS No. 478519-05-0. Pack Sizes: 25mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Glucose-3-13C | L-Glucose-3-13C. Group: Biochemicals. Alternative Names: FM 602-3-13C; L(-)-Glucose-3-13C; Levoglucose-3-13C; l-Glucose-3-13C. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Glucuronic Acid | L-Glucuronic Acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 70332-45-5. Molecular Formula: C6H10O7. Mole Weight: 194.14. Catalog: APB70332455. |  |
| L-Glucuronic acid sodium salt | L-Glucuronic acid sodium salt is an indispensable biomedical substance renowned for its applications in studying liver ailments and expediting detoxification mechanisms. Synonyms: Sodium L-glucuronate. Molecular formula: C6H9NaO7. Mole weight: 216.12. | |
| L-Glucurono-3,6-lactone | L-Glucurono-3,6-lactone, an indispensable constituent within the biomedical sector, serves as an eminent precursor in the assemblage of ascorbic acid (commonly known as vitamin C), while finding extensive utilization in the domain of pharmaceutical formulations. By virtue of its indispensability, this product assumes a pivotal position in the amelioration of diverse hepatic afflictions instigated by drug or chemical agents, wherein it functions as a hepatoprotectant and facilitates detoxification. Synonyms: L-Glucuronic acid gamma-lactone. CAS No. 32449-80-2. Molecular formula: C6H8O6. Mole weight: 176.12. | |
| L-Glufosinate | L-Glufosinate is a glutamine synthetase inhibitor and is used as a herbicide (usually as the corresponding ammonium or sodium salt, known as glufosinate-P-ammonium and glufosinate-P-sodium, respectively) to control annual weeds and grasses. Synonyms: Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-, (2S)-; Glufosinate-P; (S)-Phosphinothricin; L-Phosphinothricin; (S)-Glufosinate; (+)-glufosinate; L-homoalanin-4-yl(methyl)phosphinic acid; 4-[hydroxy(methyl)phosphinoyl]-L-homoalanine; L-2-Amino-4-(hydroxymethylphosphinyl)butanoate-; (S)-2-Amino-4-(hydroxymethylphosphinyl)butyric acid. Grades: ≥95%. CAS No. 35597-44-5. Molecular formula: C5H12NO4P. Mole weight: 181.13. | |
| L-Glutamamide | Synonyms: Glutamamide; L-Glutamine amide. CAS No. 2013-17-4. Molecular formula: C5H11N3O2. Mole weight: 145.16. | |
| L-Glutamamide,N-(cyclohexylacetyl)-L-phenylalanyl-L-arginyl-L-seryl-L-valyl-(9ci) | Heterocyclic Organic Compound. Alternative Names: KKI 7, KKI-7, CID3082667, N-Cyclohexylacetyl-phe-arg-ser-val-gln-NH2, N-(Cyclohexylacetyl)-L-phenylalanyl-L-arginyl-L-seryl-L-valyl-L-glutamamide, L-Glutamamide, N-(cyclohexylacetyl)-L-phenylalanyl-L-arginyl-L-seryl-L-valyl-, 113584-01-3. CAS No. 113584-01-3. Molecular formula: C36H58N10O8. Mole weight: 758.91. Purity: 0.96. IUPACName: (2S) -2-[[ (2S) -2-[[ (2S) -2-[[ (2S) -2-[[ (2S) -2-[ (2-cyclohexylacetyl) amino]-3-phenylpropanoyl]amino]-5- (diaminomethylideneamino) pentanoyl]amino]-3-hydroxypropanoyl]amino]-3-methylbutanoyl]amino]pentanediamide. Canonical SMILES: CC (C)C (C (=O)NC (CCC (=O)N)C (=O)N)NC (=O)C (CO)NC (=O)C (CCCN=C (N)N)NC (=O)C (CC1=CC=CC=C1)NC (=O)CC2CCCCC2. Density: 1.39g/cm³. Catalog: ACM113584013. | |
| L-Glutamate Decarboxylase (Crude Enzyme) | Glutamate decarboxylase or glutamic acid decarboxylase (GAD) is an enzyme that catalyzes the decarboxylation of glutamate to GABA and CO 2. In mammals, GAD exists in two isoforms encoded by two different genes - GAD1 and GAD2. These isoforms are GAD67 and GAD65 with molecular weights of 67 and 65 kDa, respectively. GAD1 and GAD2 are expressed in the brain where GABA is used as a neurotransmitter, GAD2 is also expressed in the pancreas. At least two more forms, GAD25 and GAD44 (embryonic; EGAD) are described in the developing brain. They are coded by the alternative transcripts of GAD1, I-80 and I-86: GAD25 is coded by both, GAD44 - only by I-80.This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Medicine; synthesis; diagnostics; food industry. Group: Enzymes. Synonyms: L-glutamic acid. Enzyme Commission Number: EC 4.1.1.15. CAS No. 9024-58-2. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. L-glutamic acid decarboxylase; L-glutamic decarboxylase; cysteic acid decarboxylase; L-glutamate α-decarboxylase; aspartate 1-decarboxylase; aspartic α-decarboxylase; L-aspartate-α-decarboxylase; γ-glutamate decarboxylase; L-glutamate 1-carboxy-lyase. Pack: 100ml. Cat No: NATE-1846. | |
| L-Glutamate Dehydrogenase (Crude Enzyme) | Glutamate dehydrogenase (GLDH) is an enzyme, present in most microbes and the mitochondria of eukaryotes, as are some of the other enzymes required for urea synthesis, that converts glutamate to α-ketoglutarate, and vice versa. In animals, the produced ammonia is usually used as a substrate in theurea cycle. Typically, the α-ketoglutarate to glutamate reaction does not occur in mammals, as glutamate dehydrogenase equilibrium favours the production of ammonia and α-ketoglutarate. Glutamate dehydrogenase also has a very low affinity for ammonia (high Michaelis constant of about 1 mM), and therefore toxic levels of ammonia would have to be present in the bo...; diagnostics. Group: Enzymes. Synonyms: glutamic dehydrogenase; glutamate dehydrogenase (NAD); glutamate oxidoreductase; glutamic acid dehydrogenase; L-glutamate dehydrogenase; NAD-dependent glutamate dehydrogenase; NAD-dependent glutamic dehydrogenase; NAD-glutamate dehydrogenase; NAD-linked glutamate dehydrogenase; NAD-linked glutamic dehydrogenase; NAD-specific glutamic dehydrogenase; NAD-specific glutamate dehydrogenase; NAD:glutamate oxidoreductase; NADH-linked glutamate dehydrogenase. Enzyme Commission Number: EC 1.4.1.2. CAS No. 9001-46-1. GLDH. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 mo | |
| L-glutamate γ-semialdehyde dehydrogenase | This enzyme catalyses the irreversible oxidation of glutamate-γ-semialdehyde to glutamate as part of the proline degradation pathway. (S)-1-pyrroline-5-carboxylate, the product of the first enzyme of the pathway (EC 1.5.5.2, proline dehydrogenase) is in spontaneous equilibrium with its tautomer L-glutamate γ-semialdehyde. In many bacterial species, both activities are carried out by a single bifunctional enzyme.The enzyme can also oxidize other 1-pyrrolines, e.g. 3-hydroxy-1-pyrroline-5-carboxylate is converted into 4-hydroxyglutamate and (R)-1-pyrroline-5-carboxylate is converted into D-glutamate. NADP+ can also act as acceptor, but with lower activity. Group: Enzymes. Synonyms: 1-pyrroline-5-carbo. Enzyme Commission Number: EC 1.2.1.88. CAS No. 9054-82-4. 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-1191; L-glutamate γ-semialdehyde dehydrogenase; EC 1.2.1.88; 9054-82-4; 1-pyrroline-5-carboxylate dehydrogenase; Δ1-pyrroline-5-carboxylate dehydrogenase; 1-pyrroline dehydrogenase; pyrroline-5-carboxylate dehydrogenase; pyrroline-5-carboxylic acid dehydrogenase; L-pyrroline-5-carboxylate-NAD+ oxidoreductase; 1-pyrroline-5-carboxylate:NAD+ oxidoreductase; Δ1-pyrroline-5-carboxylic acid dehydrogenase. Cat No: EXWM-1191. | |
| L-glutamate oxidase | A flavoprotein (FAD).The enzyme from Azotobacter previously listed under this number, which did not produce H2O2, was a crude cell-free extract that probably contained catalase. Group: Enzymes. Synonyms: glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Enzyme Commission Number: EC 1.4.3.11. CAS No. 39346-34-4. L-Glutamate Oxidase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1467; L-glutamate oxidase; EC 1.4.3.11; 39346-34-4; glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Cat No: EXWM-1467. | |
| L-Glutamate Oxidase (Crude Enzyme) | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH 2 group of donors with oxygen as acceptor. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Analysis; food industry; medicine; biotechnology. Group: Enzymes. Synonyms: glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Enzyme Commission Number: EC 1.4.3.11. CAS No. 39346-34-4. L-Glutamate Oxidase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Pack: 100ml. Cat No: NATE-1806. | |
| L-Glutamate Oxidase from Streptomyces sp., Recombinant | In enzymology, a L-glutamate oxidase is an enzyme that catalyzes the chemical reaction:L-glutamate + O2 + H2O<-> 2-oxoglutarate + NH3 + H2O2. The 3 substrates of this enzyme are L-glutamate, O2, and H2O, whereas its 3 products are 2-oxoglutarate, NH3, and H2O2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH2 group of donors with oxygen as acceptor. It employs one cofactor, FAD. Group: Enzymes. Synonyms: L-glutamate oxidase; EC 1.4.3.11; 39346-34-4; glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Enzyme Commission Number: EC 1.4.3.11. CAS No. 39346-34-4. L-Glutamate Oxidase. Activity: > 5.0 unit/mg solid. Storage: 2-8°C. Form: lyophilized powder. Source: E. coli. Species: Streptomyces sp. L-glutamate oxidase; EC 1.4.3.11; 39346-34-4; glutamate (acceptor) dehydrogenase; glutamate oxidase; glutamic acid oxidase; glutamic dehydrogenase (acceptor); L-glutamic acid oxidase. Cat No: NATE-0393. | |
| L-Glutamic acid | 1kg Pack Size. Group: Amino Acids. Formula: C5H9NO4. CAS No. 56-86-0. Prepack ID 15581871-1kg. Molecular Weight 147.13. See USA prepack pricing. |  |
| L-Glutamic acid | Glutamate gets its name because it was originally made from grains. It is widely distributed and is present in almost all protein components. Synonyms: L-GLUTAMICACIDextrapure;(S)-2-Aminopentanedioicacid, Acidumglutamicum, Glu;(S)-2-Aminopentanedioicacid, Glu;L-Glutamicacid, (S)-2-Aminopentanedioicacid, AChemicalbookcidumglutamicum, Glu;L-Glutamicacid, (S)-2-Aminopentanedioicacid, Glu;L-Glutamicacid, extrapure, PhEur, FCC;GlutamicAcid(200mg);L-GLUTAMICACIDRESEARCHGRADE. CAS No. 56-86-0. Product ID: PAP-0024. Molecular formula: C5H9NO4. Category: Amino acid. Product Keywords: Amino Acid Series; L-Glutamic acid; PAP-0024; Amino acid; C5H9NO4; 56-86-0. Appearance: at 100.00 %. mild yeast baked bread;yeasty. Chemical Name: L-Glutamic acid. Grade: Pharmaceutical Grade. Solubility: 1 M HCl: 100 mg/mL;water 7.5 g/L (20 ºC). Storage: 2-8°C. Applications: L-glutamate is widely used, as a drug itself, can treat hepatic coma, but also can be used in the production of monosodium glutamate (monosodium glutamate), food additives, flavors and used in Chemicalbook biochemistry research. L-glutamic acid was prepared by the method of "isoelectric point extraction" and "ion exchange resin" from sugar by microbial fermentation. Boiling Point: 265.74°C (rough estimate). Melting Point: 205 °C (dec.) (lit.). Product Description: L-glutamic acid is mainly used in the production of monosodium glutamate, flavor, and as a substitute for salt, nutrition |  |
| L-Glutamic acid | L-glutamic acid is a non-essential amino acid that acts as an excitatory neurotransmitter in the CNS. Synonyms: Glutamic acid, L-; (+)-L-Glutamic acid; (2S)-2-Azaniumyl-5-hydroxy-5-oxopentanoate; (S)-(+)-Glutamic acid; (S)-2-Amino-1,5-pentanedioic acid; (S)-2-Aminopentanedioic acid; (S)-Glutamic acid; 2-Aminoglutaric acid; L-(+)-Glutamic acid; L-Glutaminic acid; L-α-Aminoglutaric acid; Aciglut; E 620; Glusate; Glutacid; Glutamic acid; Glutamicol; Glutamidex; Glutaminic acid; Glutaminol; Glutaton; l-Glutaminic acid; NSC 143503; Pentanedioic acid, 2-amino-, (S)-; Sortem; α-Aminoglutaric acid; α-Glutamic acid. Grades: >98%. CAS No. 56-86-0. Molecular formula: C5H9NO4. Mole weight: 147.13. | |
| L-Glutamic acid | L-Glutamic acid is an excitatory amino acid neurotransmitter that acts as an agonist for all subtypes of glutamate receptors (metabolic rhodophylline, NMDA, and AMPA). L-Glutamic acid has an agonist effect on the release of DA from dopaminergic nerve endings. L-Glutamic acid can be used in the study of neurological diseases. L-Glutamic acid acts at ionotropic and metabotropic glutamate receptors [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 56-86-0. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-14608. | |
| L-Glutamic Acid 1-(1,1-Dimethylethyl) 5-(Phenylmethyl) Ester Hydrochloride | L-Glutamic Acid 1-(1,1-Dimethylethyl) 5-(Phenylmethyl) Ester Hydrochloride. Group: Biochemicals. Alternative Names: H-Glu(OBzl)-OtBu Hydrochloride. Grades: Highly Purified. CAS No. 105590-97-4. Pack Sizes: 2.5g. Molecular Formula: C16H24ClNO4, Molecular Weight: 329.82. US Biological Life Sciences. | Worldwide |
| L-Glutamic acid-1-13C | L-Glutamic acid-1- 13 C is the 13 C-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 81201-99-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14608S1. | |
| L-Glutamic acid-[1,2-13C2] | L-Glutamic acid-[1,2-13C2] is a labelled L-Glutamic acid. Glutamic acid is a non-essential amino acid that acts as an excitatory neurotransmitter in the CNS. Synonyms: (2R)-2-aminopentanedioic acid-13C2. Grades: 98% by HPLC; 99% atom 13C. Molecular formula: C3[13C]2H9NO4. Mole weight: 149.11. | |
| L-Glutamic acid-13C5 | L-Glutamic acid- 13 C 5 is the 13 C-labeled L-Glutamic acid. L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). L-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 55443-55-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-14608S5. | |
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