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| Product | Description | |
|---|---|---|
| Valerian Root P.E. 4:1 & 10:1 | Valerian Root P.E. 4:1 & 10:1. |  CA, FL & NJ |
| Valerian Root P.E. (Valeriana officinalis) NLT 0.8% Valerenic acids HPLC | Valerian Root P.E. (Valeriana officinalis) NLT 0.8% Valerenic acids HPLC. | CA, FL & NJ |
| Valerian Root Powder (Valeriana officinalis) | Valerian Root Powder (Valeriana officinalis). | CA, FL & NJ |
| VALERIAN ROOT SOLID EXTRACT | VALERIAN ROOT SOLID EXTRACT. Uses: Designed for use in research and industrial production. Additional or Alternative Names: VALERIAN ROOT SOLID EXTRACT;3,5-Cyclo-27-norcholestane-22,26-diol, 6-methoxy-, (3.beta.,5.alpha.,6.beta.,22R)-. Product Category: Heterocyclic Organic Compound. CAS No. 92927-02-1. Product ID: ACM92927021. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Valeric acid | 500g Pack Size. Group: Analytical Reagents, Aroma Chemicals, Biochemicals, Building Blocks, Flavours and Fragrance Materials, Organics. Formula: C5H10O2. CAS No. 109-52-4. Prepack ID 90027004-500g. Molecular Weight 102.13. See USA prepack pricing. |  |
| Valeric acid | Valeric acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 109-52-4. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. |  Worldwide |
| Valeric Acid Sodium Salt | Valeric Acid Sodium Salt. Group: Biochemicals. Alternative Names: Pentanoic Acid Sodium Salt; Sodium n-Valerate; Sodium Pentanoate; Sodium Valerate. Grades: Highly Purified. CAS No. 6106-41-8. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Valeric Anhydride | Valeric Anhydride is used in the synthesis of non-imadazole histamine H3-antagonists. Also used in the preparation of millepachine derivatives as a new class of tubulin polymerization inhibitors. Group: Biochemicals. Alternative Names: Pentanoic Acid 1,1'-AnhydridePentanoic Acid Anhydride; Valeric Anhydride; Pentanoic Anhydride; Valeric Acid Anhydride; Valeryl Anhydride; n-Valeric Anhydride. Grades: Highly Purified. CAS No. 2082-59-9. Pack Sizes: 10ml. US Biological Life Sciences. | Worldwide |
| Valerolactone Gamma | Valerolactone Gamma. CAS No. 108-29-2. FEMA No. 3103. Kosher: Y. VIGON Item # 500582. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Valerolactone Gamma Natural | Valerolactone Gamma Natural. CAS No. 108-29-2. FEMA No. 3103. Kosher: Y. VIGON Item # 502448. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| Valerophenone | Valerophenone is an aromatic ketone that is often used as a tool in the study of various photochemical processes. Valerophenone is also an inhibitor of the enzyme carbonyl reductase. Group: Biochemicals. Alternative Names: 1-Phenyl-1-pentanone; Butyl Phenyl Ketone; NSC 58959; Pentanophenone; Phenyl Butyl Ketone; n-Butyl Phenyl Ketone; n-Valerophenone. Grades: Highly Purified. CAS No. 1009-14-9. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Valerophenone | Valerophenone is an aromatic ketone that is often used as a tool in the study of various photochemical processes. It is also an inhibitor of the enzyme carbonyl reductase. Uses: Benzylhexahydropyrrolo[3,2-b]pyrrole-1(2h)-carboxylate (cas# 1251009-14-9) is a useful research chemical. Synonyms: 1-phenylpentan-1-one. Grades: > 95 %. CAS No. 1009-14-9. Molecular formula: C11H14O. Mole weight: 162.23. |  |
| Valerophenone p-toluenesulfonylhydrazone | Valerophenone p-toluenesulfonylhydrazone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Valerophenone tosylhydrazone, 69015-74-3, AC1MXFAC, ACMC-20aja5, 4-methyl-N-(1-phenylpentylideneamino)benzenesulfonamide, CTK8C5332, MCULE-9457174840, 4-methyl-N-(1-phenylpentylidene)benzenesulfonohydrazide. Product Category: Heterocyclic Organic Compound. CAS No. 69015-74-3. Molecular formula: C18H22N2O2S. Mole weight: 330.44. Purity: 0.96. IUPACName: 4-methyl-N-(1-phenylpentylideneamino)benzenesulfonamide. Canonical SMILES: CCCCC(=NNS(=O)(=O)C1=CC=C(C=C1)C)C2=CC=CC=C2. Density: 1.12g/cm³. Product ID: ACM69015743. Alfa Chemistry ISO 9001:2015 Certified. | |
| Valeroyl salicylate | Valeroyl salicylate is a selective and irreversible COX-1 inhibitor with IC50 values of 0.8 and 15 mM for ovine COX-1 and -2, respectively. Synonyms: 2-Valeryloxybenzoic acid; 2-pentanoyloxybenzoic acid. Grades: ≥99%. CAS No. 64206-54-8. Molecular formula: C12H14O4. Mole weight: 222.2. | |
| Valery 4-Hydroxy Valsartan | An impurity of Valsartan. Valsartan is an antagonist of angiotensin II receptor mainly used for the treatment of high blood pressure and congestive heart failure. Synonyms: 4-Hydroxy Valsartan (Mixture of Diastereomers); (S)-2-{(4(R,S)-Hydroxypentanoyl)-[2'-(1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]amino}-3-methylbutyric Acid; N-(4-Hydroxy-1-oxopentyl)-N-[[2'-(2H-tetrazol-5-yl) [1,1'-biphenyl]-4-yl]methyl]-L-valine; CGP 71580. CAS No. 188259-69-0. Molecular formula: C24H29N5O4. Mole weight: 451.53. | |
| Valerylcarnitine | Valerylcarnitine is an endogenous metabolite, belonging to the short-chain acylcarnitines. Uses: Scientific research. Group: Natural products. CAS No. 40225-14-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113266. |  |
| Valeryl Chloride | Valeryl Chloride is used in the preparation of potent inhibitors of secretory phospholipase A2. Also used in the synthesis of small-molecule inhibitors of protein geranyl geranyl transferase Type I. Group: Biochemicals. Grades: Highly Purified. CAS No. 638-29-9. Pack Sizes: 10g, 25g, 50g. Molecular Formula: C?H?ClO, Molecular Weight: 120.58. US Biological Life Sciences. | Worldwide |
| Valerylcholine iodide | Valerylcholine iodide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AMMONIUM,(2-HYDROXYETHYL)TRIMETHYL-,IODIDE,VALERATE; Pentanoylcholine iodide; Valerylcholine iodide; Ethanaminium,N,N,N-trimethyl-2-((1-oxopentyl)oxy)-,iodide; Trimethyl-(2-valeryloxy-aethyl)-ammonium,Jodid; (2-Hydroxyethyl)trimethylammonium iodide valera. Product Category: Heterocyclic Organic Compound. CAS No. 2963-75-9. Molecular formula: C10H22INO2. Mole weight: 315.19. Purity: 0.96. IUPACName: trimethyl(2-pentanoyloxyethyl)azanium iodide. Product ID: ACM2963759. Alfa Chemistry ISO 9001:2015 Certified. | |
| Valeryl-L-carnitine chloride | Valeryl-L-carnitine is a short-chain acylcarnitine and a derivative of L-carnitine. Synonyms: L-Valerylcarnitine; [(2R)-3-carboxy-2-pentanoyloxypropyl]-trimethylazanium chloride. Grades: ≥98%. CAS No. 162040-64-4. Molecular formula: C12H24NO4·Cl. Mole weight: 281.776. | |
| Valeryl salicylate | Valeryl salicylate is a potent and irreversible cyclooxygenase-1 (COX-1) inhibitor. Valeryl salicylate shows anti-inflammatory effect [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Valeroyl salicylate. CAS No. 64206-54-8. Pack Sizes: 10 mg. Product ID: HY-128473. | |
| Valeryl Salicylate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Valethamate bromide | Valethamate bromide. Group: Biochemicals. Grades: Highly Purified. CAS No. 90-22-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Valethamate bromide | Valethamate bromide is an ester and is a potent rapidly acting anticholinergic spasmolytic and musculotropic agent which accelerates labor by improving cervical dilation [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 90-22-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B2112. | |
| Valganciclovir | In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(I) values (inhibition constant) of 1.68+/-0.30 and 0.043+/- 0.005 mM, respectively. The inhibition by valganciclovir was competitive in both cases. 37 patients were enrolled; 19 patients received treatment with VGV and 18 patients received treatment with GCV. The VGV was not inferior in efficacy to GCV as pre-emptive therapy, with rates of viral clearance at 28 days of 89.5% and 83%, respectively (P-value for non-inferiority = 0.030). Toxicities were similar between the 2 arms. No patients developed CMV disease. Patients being treated with an alemtuzumab-containing regimen received prophylaxis with either valaciclovir 500 mg orally daily orvalganciclovir 450 mg orally twice daily. None of the 20 patients randomized to valganciclovir experienced CMV reactivation (P =.004). Synonyms: Valganciclovir. Grades: >98%. CAS No. 175865-60-8. Molecular formula: C14H22N6O5. Mole weight: 354.36. | |
| Valganciclovir-d5, Hydrochloride | Labelled Valganciclovir, a pro-drug of ganciclovir. Used in treatment of retro-virus. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Valganciclovir HCl | Valganciclovir hydrochloride hydrate is an antiviral used to treat cytomegalovirus infection. It is the prodrug of ganciclovir, a synthetic analog of 2'-deoxy-guanosine which is phosphorylated to a dGTP analog that competitively inhibits the incorporation of dGTP by viral DNA polymerase. Synonyms: RS 079070-194; Ro 107-9070/194; Valcyte; (S)-Valganciclovir Hydrochloride. Grades: >98%. CAS No. 175865-59-5. Molecular formula: C14H23ClN6O5. Mole weight: 390.82. | |
| Valganciclovir hydrochloride | Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir is an antiviral medication used to treat cytomegalovirus infections.IC50 Value:Target: CMVin vitro: In cell culture model systems using Caco-2 cells for PEPT1 and SKPT cells for PEPT2, valganciclovir inhibited glycylsarcosine transport mediated by PEPT1 and PEPT2 with K(I) values (inhibition constant) of 1.68+/-0.30 and 0.043+/- 0.005 mM, respectively. The inhibition by valganciclovir was competitive in both cases.in vivo: 37 patients were enrolled; 19 patients received treatment with VGV and 18 patients received treatment with GCV. The VGV was not inferior in efficacy to GCV as pre-emptive therapy, with rates of viral clearance at 28 days of 89.5% and 83%, respectively (P-value for non-inferiority = 0.030). Toxicities were similar between the 2 arms. No patients developed CMV disease. Patients being treated with an alemtuzumab-containing regimen received prophylaxis with either valaciclovir 500 mg orally daily orvalganciclovir 450 mg orally twice daily. None of the 20 patients randomized to valganciclovir experienced CMV reactivation (P =.004). Uses: Designed for use in research and industrial production. Additional or Alternative Names: VALGANCICLOVIR HYDROCHLORIDE;L-VALINE, 2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHOXY]-3-HYDROXYPROPYL ESTER, MONOHYDROCHLORIDE;VALGANCICLOVIR HCL;L-V | |
| Valganciclovir hydrochloride | Valganciclovir hydrochloride is an orally active antiviral agent. Valganciclovir hydrochloride can inhibit the growth of adenoviruses and have a protective effect on immunosuppressed hamsters. Valganciclovir hydrochloride can be used for the research of Cytomegalovirus [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 175865-59-5. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0032A. | |
| Valganciclovir Hydrochloride | A pro-drug of ganciclovir. Used in treatment of retro-virus. Group: Biochemicals. Alternative Names: 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]-3-hydroxypropyl Ester L-Valine Hydrochloride; RS 079070-194; Ro 107-9070/194; Valcyte; (S)-Valganciclovir Hydrochloride. Grades: Highly Purified. CAS No. 175865-59-5. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C??H??ClN?O?, Molecular Weight: 390.82. US Biological Life Sciences. | Worldwide |
| Valganciclovir Hydrochloride | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardspharmaceutical toxicology. Alternative Names: Ro 107-9070/194, Valcyte, L-Valine, 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]-3-hydroxypropyl ester, monohydrochloride (9CI), RS 079070-194,L-Valine, 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]-3-hydroxypropyl ester, hydrochloride (1:1), Valganciclovir hydrochloride. | |
| Valganciclovir hydrochloride hydrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Valganciclovir hydrochloride impurities | Valganciclovir hydrochloride impurities. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1393911-57-3. Molecular formula: C14H23ClN6O5. Mole weight: 390.83. Catalog: APB1393911573. | |
| Valganciclovir Impurity C | Valganciclovir Impurity C is a derivative of guanine which is on one of the five nucleobases incorporated into biological nucleic acids. Synonyms: 9-Methoxymethyl Guanine; 2-Amino-1,9-dihydro-9-(methoxymethyl)-6H-purin-6-one. Grades: > 95%. CAS No. 1202645-50-8. Molecular formula: C7H9N5O2. Mole weight: 195.18. | |
| Valganciclovir Impurity D | Grades: > 95%. Molecular formula: C14H23N6O5Cl. Mole weight: 390.83. | |
| Val-glu-pro-ile-pro-tyr | Synonyms: Valyl-glutamyl-prolyl-isoleucyl-prolyl-tyrosine; Vepipy; H-Val-Glu-Pro-Ile-Pro-Tyr-OH. CAS No. 94773-24-7. Molecular formula: C35H52N6O10. Mole weight: 716.82. | |
| Val-Gly-NH2 HCl | Synonyms: H-Val-Gly-NH2 hydrochloride; L-valyl-glycinamide hydrochloride. Grades: ≥ 95%. CAS No. 36920-56-6. Molecular formula: C7H15N3O2·HCl. Mole weight: 209.68. | |
| Val-Gly-NH2·HCl | Val-Gly-NH2·HCl. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Val-Gly-NH2·HCl ≥95% (HPLC) | Val-Gly-NH2·HCl ≥95% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Valibose | Valibose is an α-glucosidase inhibitor potentially for the treatment of diabetes. Valibose significantly decreased postprandial and fasting blood glucose, urine glucose, and reduced the levels of serum fructosamine. Valibose also decreased plasma triglyceride and cholesterol levels. Valibose ameliorated metabolic disturbance of glucose and lipids. In addition, valibose markedly reduced level of serum NAG and BUN, and decreased the weight index of kidney. Synonyms: 1,5,6-Trideoxy-1-[[2-hydroxy-1-(hydroxymethyl)?ethyl]?amino]-5-(hydroxymethyl)-D-chiro-Inositol; N-<2-hydroxy-1-(hydroxymethyl)ethyl>validamine; (1R,2S,3S,4S,6R)-4-(2-Hydroxy-1-hydroxymethyl-ethylamino)-6-hydroxymethyl-cyclohexane-1,2,3-triol. Grades: ≥ 98%. CAS No. 83470-79-5. Molecular formula: C10H21NO6. Mole weight: 251.28. | |
| Validamine | Validamine is a cutting-edge compound, serving as a tool of studying autoimmune diseases, most notably rheumatoid arthritis, owing to its inherent immunosuppressive properties. This compound successfully curbs the synthesis of inflammatory cytokines. Synonyms: 6-Amino-4-(hydroxymethyl)-4-cyclohexane-[4H,5H]-1,2,3-triol; (1R,2S,3S,4S,6R)-4-Amino-6-(hydroxymethyl)cyclohexane-1,2,3-triol. CAS No. 32780-32-8. Molecular formula: C7H15NO4. Mole weight: 177.2. | |
| Validamine Impurity 6 | Validamine Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 124492-65-5. Molecular formula: C9H17NO5. Mole weight: 219.24. Catalog: APB124492655. | |
| Validamycin A | Validamycin A, a fungicidal, is an agricultural antibiotic. Validamycin A is originally isolated from Streptomyces hygroscopicus var. limoneus. Validamycin A inhibits the growth of A. flavus , with a MIC of 1?μg/mL [1]. Validamycin A shows potent inhibitory activity against trehalase of Rhizoctonia solani , with an IC 50 of 72 μM [2]. Validamycin A is a reversible tyrosinase inhibitor, with a K i of 5.893 mM [3]. Uses: Scientific research. Group: Natural products. CAS No. 37248-47-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0856. | |
| Validamycin A | The major analogue of a family of cyclitol disaccharides isolated from streptomyces hygroscopicus var. Limoneus. It is a potent antifungal agent used to control fungi in crop production and acts as a potent inhibitor of trehalase, an important enzyme in carbohydrate storage and ultilisation in fungi. Synonyms: jinggangmycin; Antibiotic T 7545A. Grades: >95% by HPLC. CAS No. 37248-47-8. Molecular formula: C20H35NO13. Mole weight: 497.49. | |
| Validamycin A | An inhibitor of trehalase. Validamycin A is an antifungal agent used to protect rice plants against sheath blight caused by the pathogenic fungus, R. solani, due to its ability to inhibit trehalase, a trehalose-hydrolizing enzyme (Ki = 1.9nM; IC50 = 0.7uM).1 It is also effective against the growth and sporulation of R. cerealis, F. culmorum, and other fungi.2 This compound has also been used to study trehalase activity and trehalose biosynthesis.3. Group: Biochemicals. Alternative Names: 1,5,6-Trideoxy-4-O- β-D-glucopyranosyl-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-chiro-inositol; Cepex 10SL; Jinganmycin A; Jinggang; Jinggangmycin; Jinggangmycin A; Validacin; Validamycin; Validamycin A; [1S-(1α,4α,5 β,6α)]-1,5,6-Trideoxy-4-O- β-D-glucopyranosyl-5-(hydroxymethyl)-1-[[4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-chiro-inositol. Grades: Highly Purified. CAS No. 37248-47-8. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C20H35NO13, Molecular Weight: 497.49. US Biological Life Sciences. | Worldwide |
| validamycin A dioxygenase | The enzyme was characterized from the bacterium Streptomyces hygroscopicus subsp. limoneus. Requires Fe2+. Group: Enzymes. Synonyms: vldW (gene name). Enzyme Commission Number: EC 1.14.11.52. 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-0671; validamycin A dioxygenase; EC 1.14.11.52; vldW (gene name). Cat No: EXWM-0671. |  |
| Validamycin B | Validamycin B is an impurity of Validamycin that is resistant to rice sheath blight disease and Pellicularia sasakii. Synonyms: Antibiotic T-7545-B; Val-B; (1R,2R,3S,4S,5R,6S)-2,3,5-trihydroxy-6-(hydroxymethyl)-4-{[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}cyclohexyl beta-D-glucopyranoside; 1,5-Dideoxy-4-O-β-D-glucopyranosyl-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-chiro-inositol. CAS No. 102583-47-1. Molecular formula: C20H35NO14. Mole weight: 513.49. | |
| Validamycin C | An impurity of Validamycin. Validamycin is an antibiotic and fungicide. Synonyms: BRN 4835203; (3-{[4-(hexopyranosyloxy)-2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]amino}-4,5,6-trihydroxycyclohex-1-en-1-yl)methyl hexopyranoside; 2-(hydroxymethyl)-6-[[3-[[5-(hydroxymethyl)-4-[6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-2,3-bis(oxidanyl)cyclohexyl]amino]-4,5,6-tris(oxidanyl)cyclohexen-1-yl]methoxy]oxane-3,4,5-triol. CAS No. 12650-70-3. Molecular formula: C26H45NO18. Mole weight: 659.63. | |
| Validamycin D | An impurity of Validamycin. Validamycin is an antibiotic and fungicide. Synonyms: BRN 4830813; 1,5,6-Trideoxy-5-[(beta-D-glucopyranosyloxy)methyl]-1-[[(1S)-4beta,5alpha,6beta-trihydroxy-3-hydroxymethyl-2-cyclohexen-1beta-yl]amino]-D-chiro-inositol. CAS No. 12650-67-8. Molecular formula: C20H35NO13. Mole weight: 497.5. | |
| Validamycin E | An impurity of Validamycin. Validamycin is an antibiotic and fungicide. Synonyms: BRN 4631911; D-chiro-Inositol, O-alpha-D-glucopyranosyl-(1-4)-O-beta-D-glucopyranosyl-(1-3)-1,5,6-trideoxy-5-(hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-, (1S-(1-alpha,4-alpha,5-beta,6-alpha))-; AC1L48S1; SCHEMBL5160665. CAS No. 12650-71-4. Molecular formula: C26H45NO18. Mole weight: 659.64. | |
| validoxylamine A 7'-phosphate phosphatase | The enzyme, characterized from the bacterium Streptomyces hygroscopicus subsp. limoneus, is involved in the biosynthesis of the antifungal agent validamycin A. Group: Enzymes. Synonyms: vldH (gene name). Enzyme Commission Number: EC 3.1.3.101. 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-3610; validoxylamine A 7'-phosphate phosphatase; EC 3.1.3.101; vldH (gene name). Cat No: EXWM-3610. | |
| validoxylamine A glucosyltransferase | The enzyme, characterized from the bacterium Streptomyces hygroscopicus subsp. limoneus, catalyses the ultimate step in the biosynthesis of the antifungal agent validamycin A. Group: Enzymes. Synonyms: vldK (gene name); valG (gene name). Enzyme Commission Number: EC 2.4.1.338. 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-2576; validoxylamine A glucosyltransferase; EC 2.4.1.338; vldK (gene name); valG (gene name). Cat No: EXWM-2576. | |
| Valienamine HCl | Valienamine HCl is a potent pharmaceutical compound used in the research of bacterial infections, particularly those caused by resistant strains. It exhibits antimicrobial activity by inhibiting the growth of bacteria. Valienamine HCl serves as a key ingredient in various antimicrobial drugs. Uses: Glycoside hydrolase inhibitors. Synonyms: (1S,2S,3R,6S)-6-Amino-4-(hydroxymethyl)-4-cyclohexene-1,2,3-triol. CAS No. 38231-86-6. Molecular formula: C7H13NO4. Mole weight: 175.18. | |
| valienol-1-phosphate guanylyltransferase | The enzyme, characterized from the bacterium Streptomyces hygroscopicus subsp. limoneus, is involved in the biosynthesis of the antifungal agent validamycin A. Group: Enzymes. Synonyms: vldB (gene name). Enzyme Commission Number: EC 2.7.7.91. 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-3305; valienol-1-phosphate guanylyltransferase; EC 2.7.7.91; vldB (gene name). Cat No: EXWM-3305. | |
| Valifenalate | Valifenalate(IR5885; Valiphenal), which is approved for application on high-value crops such as grapes, tomatoes and other vegetables, is effective against various types of mildew and is currently marketed primarily under the Valis moniker; insecticide agent. Synonyms: IR5885; IR 5885; IR-5885; Valiphenal. Grades: >98%. CAS No. 283159-90-0. Molecular formula: C19H27ClN2O5. Mole weight: 398.88. | |
| Valifenalate | analytical standard, mixture of isomers. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Valilactone | Valilactone is an esterase and fatty acid synthase (FAS) inhibitor produced by a cultured strain of soil actinomycetes. Synonyms: (-)-Valilactone; [(2S)-1-[(2S,3S)-3-hexyl-4-oxooxetan-2-yl]heptan-2-yl] (2S)-2-formamido-3-methylbutanoate. Grades: ≥98%. CAS No. 113276-96-3. Molecular formula: C22H39NO5. Mole weight: 397.6. | |
| Valiltramiprosate | ALZ-801 is a potent and orally available small-molecule β-amyloid (Aβ) anti-oligomer and aggregation inhibitor, valine-conjugated proagent of Tramiprosate with substantially improved PK properties and gastrointestinal tolerability compared with the parent compound [1]. ALZ-801 is an advanced and markedly improved candidate for the treatment of alzheimers disease [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALZ-801. CAS No. 1034190-08-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117259. | |
| valine-3-methyl-2-oxovalerate transaminase | This enzyme belongs to the family of transferases, specifically the transaminases, which transfer nitrogenous groups. Group: Enzymes. Synonyms: valine-isoleucine transaminase; valine-3-methyl-2-oxovalerate aminotransferase; alanine-valine transaminase; valine-2-keto-methylvalerate aminotransferase; valine-isoleucine aminotransferase. Enzyme Commission Number: EC 2.6.1.32. CAS No. 9023-14-7. 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-2872; valine-3-methyl-2-oxovalerate transaminase; EC 2.6.1.32; 9023-14-7; valine-isoleucine transaminase; valine-3-methyl-2-oxovalerate aminotransferase; alanine-valine transaminase; valine-2-keto-methylvalerate aminotransferase; valine-isoleucine aminotransferase. Cat No: EXWM-2872. | |
| Valine,4,4,4-trifluoro- | Valine,4,4,4-trifluoro-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,4,4-TRIFLUORO-DL-VALINE;4,4,4-Trifluoro-DL-valine 97%;4,4,4-Trifluoro-DL-valine97%. Product Category: Heterocyclic Organic Compound. CAS No. 16063-79-9. Molecular formula: C5H8F3NO2. Mole weight: 171.12. Purity: 0.96. IUPACName: 2-amino-4,4,4-trifluoro-3-methylbutanoic acid. Canonical SMILES: CC(C(C(=O)O)N)C(F)(F)F. Density: 1.352 g/cm³. Product ID: ACM16063799. Alfa Chemistry ISO 9001:2015 Certified. | |
| Valine Benzyl Ester | L-Valine Benzyl Ester is a L-Valine derivative useful as intermediate for the preparation of peptides. Group: Biochemicals. Alternative Names: L-Valine Phenylmethyl Ester; Benzyl L-Valinate; Valine Benzyl Ester. Grades: Highly Purified. CAS No. 17645-51-1. Pack Sizes: 1g. Molecular Formula: C??H??NO?, Molecular Weight: 207.27. US Biological Life Sciences. | Worldwide |
| valine decarboxylase | A pyridoxal-phosphate protein. Also acts on L-leucine. Group: Enzymes. Synonyms: leucine decarboxylase; L-valine carboxy-lyase. Enzyme Commission Number: EC 4.1.1.14. CAS No. 9031-16-7. 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-4758; valine decarboxylase; EC 4.1.1.14; 9031-16-7; leucine decarboxylase; L-valine carboxy-lyase. Cat No: EXWM-4758. | |
| Valine Dehydrogenase (Crude Enzyme) | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH 2 group of donors with NAD + or NADP + as acceptor. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Group: Enzymes. Synonyms: valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Enzyme Commission Number: EC 1.4.1.8. CAS No. 37255-39-3. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Pack: 100ml. Cat No: NATE-1804. | |
| valine dehydrogenase (NAD+) | The enzyme from Streptomyces spp. has no activity with NADP+ [cf. EC 1.4.1.8, valine dehydrogenase (NADP+)]. Group: Enzymes. Enzyme Commission Number: EC 1.4.1.23. 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-1456; valine dehydrogenase (NAD+); EC 1.4.1.23. Cat No: EXWM-1456. | |
| valine dehydrogenase (NADP+) | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH2 group of donors with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is L-valine:NADP+ oxidoreductase (deaminating). Other names in common use include valine dehydrogenase (nicotinanide adenine dinucleotide phosphate), and valine dehydrogenase (NADP+). Group: Enzymes. Synonyms: valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Enzyme Commission Number: EC 1.4.1.8. CAS No. 37255-39-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1462; valine dehydrogenase (NADP+); EC 1.4.1.8; 37255-39-3; valine dehydrogenase (nicotinanide adenine dinucleotide phosphate); valine dehydrogenase (NADP). Cat No: EXWM-1462. | |
| Valine Ethyl Ester, Hydrochloride | Valine Ethyl Ester, Hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 17609-47-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| valine N-monooxygenase | A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-valine, the first committed steps in the biosynthesis of the cyanogenic glucoside linamarin in Manihot esculenta (cassava). The product of the two hydroxylations, N,N-dihydroxy-L-valine, is extremely labile and dehydrates spontaneously. The dehydrated product is then subject to a decarboxylation that produces the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The product, (E)-2-methylpropanal oxime, undergoes a spontaneous isomerization to the (Z) form. The enzyme can also accept L-isoleucine as substrate, with a lower activity. It is different from EC 1.14.13.117 (isoleucine N-monooxygenase), which prefers L-isoleucine. Group: Enzymes. Synonyms: CYP79D1; CYP79D2. Enzyme Commission Number: EC 1.14.13.118. 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-0718; valine N-monooxygenase; EC 1.14.13.118; CYP79D1; CYP79D2. Cat No: EXWM-0718. | |
| valine-pyruvate transaminase | Different from EC 2.6.1.42, branched-chain-amino-acid-transaminase. Group: Enzymes. Synonyms: transaminase C; valine-pyruvate aminotransferase; alanine-oxoisovalerate aminotransferase. Enzyme Commission Number: EC 2.6.1.66. CAS No. 73379-50-7. 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-2907; valine-pyruvate transaminase; EC 2.6.1.66; 73379-50-7; transaminase C; valine-pyruvate aminotransferase; alanine-oxoisovalerate aminotransferase. Cat No: EXWM-2907. | |
| valine-tRNA ligase | This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in valine, leucine and isoleucine biosynthesis and aminoacyl-trna biosynthesis. Group: Enzymes. Synonyms: valyl-tRNA synthetase; valyl-transfer ribonucleate synthetase; valyl-transfer RNA synthetase; valyl-transfer ribonucleic acid synthetase; valine transfer ribonucleate ligase; valine translase. Enzyme Commission Number: EC 6.1.1.9. CAS No. 9023-47-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5664; valine-tRNA ligase; EC 6.1.1.9; 9023-47-6; valyl-tRNA synthetase; valyl-transfer ribonucleate synthetase; valyl-transfer RNA synthetase; valyl-transfer ribonucleic acid synthetase; valine transfer ribonucleate ligase; valine translase. Cat No: EXWM-5664. | |
| Valine USP | Valine USP. Grades: USP. CAS No. 72-18-4. Product ID: 2-08294. Molecular formula: C5H11NO2. Mole weight: 117.15. |  |
| Valinol | Valinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DL-2-AMINO-3-METHYL-1-BUTANOL;DL-VALINOL;2-AMINO-3-METHYL-1-BUTANOL;DL-2-amino-3-methylbutan-1-ol;valinol;1-Butanol, 2-amino-3-methyl-. Product Category: Heterocyclic Organic Compound. CAS No. 473-75-6. Molecular formula: C5H13NO. Mole weight: 103.16. Density: 0.936 g/mL at 25 °C(lit.). Product ID: ACM473756. Alfa Chemistry ISO 9001:2015 Certified. | |
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