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| Product | Description | |
|---|---|---|
| Valerate sodium | Valerate (sodium) is an ester product. Uses: Scientific research. Group: Signaling pathways. CAS No. 6106-41-8. Pack Sizes: 1 g; 5 g; 10 g; 25 g. Product ID: HY-W007087. |  |
| valerena-4,7(11)-diene synthase | Isolated from the plant Valeriana officinalis (valerian). Note that due to a different numbering system the product is also known as valerena-1,10-diene. Group: Enzymes. Synonyms: VoTPS2; VoTPS7. Enzyme Commission Number: EC 4.2.3.139. 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-5153; valerena-4,7(11)-diene synthase; EC 4.2.3.139; VoTPS2; VoTPS7. Cat No: EXWM-5153. |  |
| Valerenic acid | Valerenic acid. Group: Biochemicals. Grades: Purified. CAS No. 3569-10-6. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Valerenic acid | Valerenic acid is a positive allosteric modulator of GABAA receptors displaying selectivity for receptors containing β2 or β3 subunits. Valerenic acid exhibits sedative, anticonvulsant and anxiolytic effects in vivo. Valerenic acid also acts as a partial agonist of 5-HT5A receptors. Synonyms: valerinic acid; (-)-valerenic acid. Grades: ≥99% by HPLC. CAS No. 3569-10-6. Molecular formula: C15H22O2. Mole weight: 234.33. |  |
| Valerenic acid | Valerenic acid ((-)-Valerenic Acid), a sesquiterpenoid, is an orally active positive allosteric modulator of GABA A receptors. Valerenic acid is also a partial agonist of the 5-HT 5a receptor. Valerenic acid mediates anxiolytic activity via GABA A receptors containing the β3 subunit. Valerenic acid also exhibits potent antioxidant properties [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (-)-Valerenic Acid. CAS No. 3569-10-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-103524. | |
| Valerenic Acid | Valerenic Acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 84638-55-1. Molecular Formula: C17H24O4. Mole Weight: 292.38. Catalog: APB84638551. |  |
| Valeriana Fauriei Root Extract | Use as antioxidant. Use as antibacterial agent. Group: Natural surfactants. Alternative Names: Valeriana officinalis, ext. CAS No. 94167-13-2. Catalog: ACM94167132. |  |
| Valerian Extract | Valerian root extract is extracted from the valerian root that native to Europe and Asia, valerian root extract works like a sedative helping you to relax, and to sleep deeply and restfully, reducing night awakenings as well as increasing dream recall the next day. Valerica Acid has also been found to be useful for cramping, dysmenorrhea, rheumatic pains, epilepsy, and nerve-related high blood pressure. Group: Others. Mole weight: 102.13. Valerian Extract; Valeriana Officinalis. Cat No: EXTC-054. | |
| Valerian Root Extract | Valerian Root Extract. Applications: Antidepressant;improving microcirculation;antibacterial antiviral and anti-tumor;easing the tension, anxiety and improving the role of sleep. Group: Others. Synonyms: Valerian Root Extract; 8057-49-6; Valeriana officinalis. CAS No. 8057-49-6. Purity: 0.3%, 0.8%Valeric Acids. Appearance: Brown fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Root. Species: Valeriana officinalis. Valerian Root Extract; 8057-49-6; Valeriana officinalis; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-157. | |
| Valerian Root Extract | Extract obtained from Valerian Officinalis (Valerian) roots. Contains 20% extract dissolved in water and glycerin. Has sooting, calming, and toning properties. Uses: Creams, lotions, masks, and bath care products. Group: Skin actives. CAS No. 7732-18-5/56-81-5/8057-49-6/122-99-6. Appearance: Light to medium amber liquid, characteristic odor. Catalog: CI-SC-0797. | |
| 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 |
| 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 | 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 | Acids. Alternative Names: Propylacetic acid. CAS No. 64118-37-2. Mole weight: 102.13. Purity: 95%+. IUPACName: Pentanoic acid. Canonical SMILES: CCCCC(=O)O. Density: 0.939 g/mL at 25 °C(lit.). | |
| Valeric acid-3,4,5-13C3 | 13C Labeled Compounds. CAS No. 1173023-05-6. Catalog: ACM1173023056. | |
| 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. 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 | 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 | Heterocyclic Organic Compound. Alternative Names: Pentanoylbenzene. CAS No. 1009-14-9. Molecular formula: C11H14O. Mole weight: 162.23. Appearance: Liquid. Purity: 0.98. IUPACName: 1-Phenylpentan-1-one. Canonical SMILES: CCCCC(=O)C1=CC=CC=C1. Density: 0.975 g/mL at 20 °C(lit.). Catalog: ACM1009149. | |
| 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 |
| Valerylferrocene | Heterocyclic Organic Compound. CAS No. 1272-29-3. Molecular formula: C15H18FeO. Purity: 0.96. Catalog: ACM1272293. | |
| 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. | |
| Valethamate | Valethamate is a pharmaceutical drug that is administered to women for the treatment of urinary incontinence. It is used in combination with pentobarbital sodium and other drugs, such as fatty acids and depressants, to treat urinary incontinence. Valethamate inhibits spontaneous activity in the detrusor muscle by blocking the action of norepinephrine on alpha-adrenergic receptors. This drug has been shown to be clinically effective for treating urinary incontinence in women who have not responded to other treatments. Valethamate has also been shown to cause vessel occlusion when injected into the femoral vein of experimental animals and may increase blood pressure when given intravenously. Group: Other alkaloids. CAS No. 16376-74-2. Molecular formula: C21H21NO6. Mole weight: 383.39 g/mol. Canonical SMILES: CCC (C)C (C1=CC=CC=C1)C (=O)OCC[N+] (C) (CC)CC. Catalog: ACM16376742. | |
| 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-d8 | 2H Labeled Compounds. CAS No. 1132088-63-1. Molecular formula: C14H14D8N6O5. Mole weight: 362.41. Catalog: ACM1132088631. | |
| 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). Group: Inhibitors. 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-VALINE, 2-[(2-AMINO-1, 6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHO | |
| 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 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 hydrochloride impurities1 | Valganciclovir hydrochloride impurities1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 897937-73-4. Molecular Formula: C19H31N7O6. Mole Weight: 453.5. Catalog: APB897937734. | |
| Valganciclovir Impurity 10 | Valganciclovir Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1654737-32-2. Molecular Formula: C14H21ClN6O4. Mole Weight: 372.81. Catalog: APB1654737322. | |
| 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-glu-ala-glu | Heterocyclic Organic Compound. Alternative Names: VAL-GLU-GLU-ALA-GLU, 100930-17-4. CAS No. 100930-17-4. Molecular formula: C23H40N6O12. Mole weight: 575.6. Purity: 0.96. IUPACName: 2- [2- [ [2- [ [2- [ (2-amino-3-methylbutanoyl) amino] -5-hydroxy-5-oxopentanoyl] amino] -5-hydroxy-5-oxopentanoyl] amino] propanoylamino] pentanedioic acid; azane. Catalog: ACM100930174. | |
| 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 | Validamine. Uses: For analytical and research use. Group: Impurity standards. CAS No. 32780-32-8. Molecular Formula: C7H15NO4. Mole Weight: 177.2. Catalog: APB32780328. | |
| Validamine Impurity 1 | Validamine Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 68108-50-9. Molecular Formula: C17H25NO9. Mole Weight: 387.39. Catalog: APB68108509. | |
| Validamine Impurity 2 | Validamine Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 73651-28-2. Molecular Formula: C17H25NO9. Mole Weight: 387.39. Catalog: APB73651282. | |
| Validamine Impurity 3 | Validamine Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 97380-32-0. Molecular Formula: C13H18N2O6. Mole Weight: 298.3. Catalog: APB97380320. | |
| Validamine Impurity 4 | Validamine Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 73410-97-6. Molecular Formula: C13H25NO9. Mole Weight: 339.34. Catalog: APB73410976. | |
| Validamine Impurity 5 | Validamine Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 85240-26-2. Molecular Formula: C22H27NO8S. Mole Weight: 465.52. Catalog: APB85240262. | |
| 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 | 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 | 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 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. | |
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