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| Product | Description | |
|---|---|---|
| Vitamin K1 (Phytonadione) Cis Isomer | Vitamin K1 (Phytonadione) Cis Isomer. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16033-41-3. Molecular Formula: C31H46O2. Mole Weight: 450.71. Catalog: APB16033413. |  |
| Vitamin K1 (Phytonadione) Impurity 1 | Vitamin K1 (Phytonadione) Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 19274-66-9. Molecular Formula: C31H46O2. Mole Weight: 450.71. Catalog: APB19274669. | |
| Vitamin K1 (Phytonadione) Impurity 3 | Vitamin K1 (Phytonadione) Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 15576-40-6. Molecular Formula: C31H46O3. Mole Weight: 466.71. Catalog: APB15576406. | |
| Vitamin K1 (Phytonadione) Impurity 4 | Vitamin K1 (Phytonadione) Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 128941-84-4. Molecular Formula: C31H46O2. Mole Weight: 450.71. Catalog: APB128941844. | |
| Vitamin K1 (Phytonadione) Impurity 5 | Vitamin K1 (Phytonadione) Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 79082-96-5. Molecular Formula: C31H46O2. Mole Weight: 450.71. Catalog: APB79082965. | |
| Vitamin K1 (Phytonadione) Related Compound 4 | Vitamin K1 (Phytonadione) Related Compound 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 19397-95-6. Molecular Formula: C31H44O2. Mole Weight: 448.69. Catalog: APB19397956. | |
| Vitamin K1 (Phytonadione) Related Compound 5 | Vitamin K1 (Phytonadione) Related Compound 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 50281-47-5. Molecular Formula: C33H50O3. Mole Weight: 494.76. Catalog: APB50281475. | |
| Vitamin K2(20) | 1g Pack Size. Group: Analytical Reagents, Biochemicals. Formula: C31H40O2. CAS No. 863-61-6. Prepack ID 90018932-1g. Molecular Weight 444.65. See USA prepack pricing. |  |
| Vitamin K2(45) | . Uses: Vitamin (prothrombogenic). Synonyms: menaquinone 9; (all-E)-2-Methyl-3-(3,7,11,15,19,23,27,31,35-nonamethyl-2,6,10,14,18,22,26,30,34-hexatriacontanonaenyl)-1,4-naphthalenedione; Menaquinone MK 9; Menlaquinone 9; MK 9; Vitamin MK 9. Grades: 97%. CAS No. 523-39-7. Molecular formula: C56H80O2. Mole weight: 785.25. |  |
| Vitamin K2 Impurity 1 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 1 | Vitamin K2 Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 481-85-6. Molecular Formula: C11H10O2. Mole Weight: 174.2. Catalog: APB481856. | |
| Vitamin K2 Impurity 2 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 2 | Vitamin K2 Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 76916-86-4. Molecular Formula: C11H6O3. Mole Weight: 186.17. Catalog: APB76916864. | |
| Vitamin K2 Impurity 3 | Vitamin K2 Impurity 3. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-methyl-3-((2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl)naphthalene-1,4-dione. CAS No. 523-39-7. Molecular Formula: C56H80O2. Mole Weight: 785.23. Catalog: APB523397. | |
| Vitamin K2 Impurity 3 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 3 | Vitamin K2 Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 20962-84-9. Molecular Formula: C11H6O4. Mole Weight: 202.17. Catalog: APB20962849. | |
| Vitamin K2 Impurity 4 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 5 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 5 | Vitamin K2 Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 97804-51-8. Molecular Formula: C36H52O2. Mole Weight: 516.81. Catalog: APB97804518. | |
| Vitamin K2 Impurity 6 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 Impurity 7 | One of the impurities of Vitamin K2, which has been found to be related to arterial health as well as one strength. Molecular formula: C31H40O2. Mole weight: 444.66. | |
| Vitamin K2 (MK4) 1% Beadlet | Vitamin K2 (MK4) 1% Beadlet. |  CA, FL & NJ |
| Vitamin K2 (MK4) Oil USP | Vitamin K2 (MK4) Oil USP. | CA, FL & NJ |
| Vitamin K2 (MK-4) Pure | Vitamin K2 (MK-4) Pure. | CA, FL & NJ |
| Vitamin K2 (MK-6) | Vitamin K2 (MK-6). Uses: For analytical and research use. Group: Impurity standards. CAS No. 84-81-1. Molecular Formula: C41H56O2. Mole Weight: 580.9. Catalog: APB84811. | |
| Vitamin K2-MK7 1% on DCP | Vitamin K2-MK7 1% on DCP. | CA, FL & NJ |
| Vitamin K2 MK-7 1% on MCC | Vitamin K2 MK-7 1% on MCC. | CA, FL & NJ |
| Vitamin K3-d8 | Precursor to verious types of Vitamin K. Used as a micronutrient for livestock and pet foods. Group: Biochemicals. Alternative Names: 2-Methyl-1,4-naphthoquinone-d8; 1,4-Dihydro-1,4-dioxo-2-methylnaphthalene-d8; 2-Methyl-1,4-naphthalenedione-d8; Aquakay-d8; Aquinone-d8; Hemodal-d8; K-Thrombyl-d8; K-Vitan-d8; Kaergona-d8; Kanone-d8; Kappaxan-d8; Kappaxin-d8; Karcon-d8; Kareon-d8; Kativ-G-d8; Kayklot-d8; Kaykot-d8; Kaynone-d8; Kayquinone-d8; Kipca-d8; Kipca-Oil Soluble-d8; Klottone-d8; Koaxin-d8; Kolklot-d8; MNQ-d8; Menadion-d8; Menadione-d8; Menaphthon-d8; Menaphthone-d8; Menaquinone 0-d8; Mitenon-d8; Mitenone-d8; NSC 4170-d8; Panosine-d8; Prokayvit-d8; Synkay-d8; Thyloquinone-d8. Grades: Highly Purified. CAS No. 478171-80-1. Pack Sizes: 25mg. US Biological Life Sciences. |  Worldwide |
| Vitamin K3 ß-cyclodextrin complex | Vitamin K3 ß-cyclodextrin complex. Product ID: 4-00430. |  |
| Vitamin k5 | Vitamin K5 (Synkamin) is a photosensitizer and a antimicrobial agent. Vitamin K5 is a specific PKM2 inhibitor with IC50 values of 28, 191 and 120 μM for PKM2, PKM1 and PKL. Vitamin K5 induces apoptosis of colon 26 cells. Vitamin K5 can be used for the research of infection and cancer, and it also can be used as a preservative for pharmaceuticals, foods, and beverages. Uses: Designed for use in research and industrial production. Additional or Alternative Names: VITAMIN K5;1-hydroxy-2-methyl-4-aminonaphthalene;2-methyl-4-amino-1-hydroxynaphthalene;2-methyl-4-amino-1-naphthol;3-methyl-4-hydroxy-1-naphthylamine;4-amino-2-methyl-1-naphthaleno;4-amino-2-methyl-1-naphthalenol;4-amino-2-methyl-1-naphtho. Product Category: Inhibitors. CAS No. 83-70-5. Molecular formula: C11H11NO. Mole weight: 173.21. Purity: N/A. Canonical SMILES: OC1=C2C=CC=CC2=C(N)C=C1C. Density: 1.232 g/cm³. Product ID: ACM83705. Alfa Chemistry ISO 9001:2015 Certified. |  |
| vitamin-K-epoxide reductase (warfarin-insensitive) | Vitamin K 2,3-epoxide is reduced to 3-hydroxy- (and 2-hydroxy-) vitamin K by 1,4-dithiothreitol, which is oxidized to a disulfide. Not inhibited by warfarin [cf. EC 1.17.4.4, vitamin-K-epoxide reductase (warfarin-sensitive)]. Group: Enzymes. Enzyme Commission Number: EC 1.17.4.5. CAS No. 97089-80-0. 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-1093; vitamin-K-epoxide reductase (warfarin-insensitive); EC 1.17.4.5; 97089-80-0. Cat No: EXWM-1093. |  |
| vitamin-K-epoxide reductase (warfarin-sensitive) | Vitamin K 2,3-epoxide is reduced to vitamin K and possibly to vitamin K hydroquinone by 1,4-dithiothreitol, which is oxidized to a disulfide; some other dithiols and 4-butanethiol can also act. Inhibited strongly by warfarin [cf. EC 1.17.4.5, vitamin-K-epoxide reductase (warfarin-insensitive)]. Group: Enzymes. Enzyme Commission Number: EC 1.17.4.4. CAS No. 55963-40-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1092; vitamin-K-epoxide reductase (warfarin-sensitive); EC 1.17.4.4; 55963-40-1. Cat No: EXWM-1092. | |
| Vitamin P4 Liposome | Vitamin P4, also known as Troxerutin, inhibits platelet aggregation, prevents thrombus formation, improves blood circulation, increases capillary resistance, treats acute ischemic brain injury, and helps improve certain vascular disorders in the body. This product is a pre-formulated liposome encapsulating Vitamin P4. It is only for research purposes. Group: Drug-loaded liposome. Categories: Niosomes, ethosomes, and transfersomes. |  |
| Vitamin U chloride | Vitamin U (S-Methylmethionine sulfonium) chloride is an orally active anti-ulcer agent with antioxidant activity. Vitamin U inhibits adipocyte differentiation. Vitamin U promotes skin wound healing.Vitamin U can be used in the research of gastrointestinal ulceration [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: S-Methylmethionine sulfonium chloride. CAS No. 1115-84-0. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-N2551. |  |
| Vitexin | Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 3681-93-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0013. | |
| Vitexin | 8-(β-D-Glucopyranosyl)-4,5,7-trihydroxyflavone. CAS No. 3681-93-4. Product ID: 8-05147. Molecular formula: C21H20O10. Mole weight: 432.38. Properties: Apigenin flavone glucoside. | |
| Vitexin | Vitexin. Group: Biochemicals. Alternative Names: 8-Glucopyranosyl apigenin; 8-Glucosylapigenin; Orientoside. Grades: Plant Grade. CAS No. 3681-93-4. Pack Sizes: 20mg. Molecular Formula: C21H20O10, Molecular Weight: 432.377999999999. US Biological Life Sciences. | Worldwide |
| Vitexin 2''-O-p-coumarate | Vitexin 2''-O-p-coumarate. Group: Biochemicals. Grades: Plant Grade. CAS No. 59282-55-2. Pack Sizes: 5mg. Molecular Formula: C30H26O12, Molecular Weight: 578.53. US Biological Life Sciences. | Worldwide |
| Vitexin 2''-O-p-coumarate | Vitexin 2''-O-p-coumarate is a compound of the flavonoid class isolated from the seeds of Trigonella foenum-graecum. Vitexin 2''-O-p-coumarate promotes 2BS cell proliferation induced by H(2)O(2). Synonyms: [(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate. Grades: >98%. CAS No. 59282-55-2. Molecular formula: C30H26O12. Mole weight: 578.526. | |
| Vitexin 2''-O-rhamnoside | Vitexin 2''-O-rhamnoside. Group: Biochemicals. CAS No. 64820-99-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vitexin-2'-O-rhamnoside | Vitexin-2"-O-rhamnoside, a main flavonoid glycoside of the leaves of Cratagus pinnatifida Bge, contributes to the protection against H 2 O 2 -mediated oxidative stress damage and has potential to treat cardiovascular system diseases [1]. Uses: Scientific research. Group: Natural products. CAS No. 64820-99-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N0534. | |
| vitexin 2''-O-rhamnoside 7-O-methyltransferase | The flavonoids vitexin and isovitexin 2''-O-arabinoside do not act as substrates for the enzyme from oats (Avena sativa). Group: Enzymes. Enzyme Commission Number: EC 2.1.1.153. CAS No. 90698-29-6. 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-1749; vitexin 2''-O-rhamnoside 7-O-methyltransferase; EC 2.1.1.153; 90698-29-6. Cat No: EXWM-1749. | |
| Vitexin-2-O-rhamnoside (Rhamnosylvitexin, 2"-Rhamnosylvitexin) | Vitexin-2-O-rhamnoside (Rhamnosylvitexin, 2"-Rhamnosylvitexin). Group: Biochemicals. Alternative Names: Vitexin 2''-o-rhamnoside. Grades: Plant Grade. CAS No. 64820-99-1. Pack Sizes: 20mg. Molecular Formula: C27H30O14, Molecular Weight: 578.519. US Biological Life Sciences. | Worldwide |
| Vitexin 4''-O-glucoside | Vitexin 4''-O-glucoside. Group: Biochemicals. CAS No. 178468-00-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vitexin-4''-O-glucoside | Vitexin-4''-O-glucoside is a flavonoid isolated from Crataegus pinnatifida Bunge. Synonyms: 4''-O-Glucosylvitexin; Vitexin 4''-O-glucoside. Grades: 98%. CAS No. 178468-00-3. Molecular formula: C27H30O15. Mole weight: 594.5. | |
| Vitexin-4''-O-glucoside | Vitexin-4''-O-glucoside is a kind of flavonoid fraction from the leaves of Crataegus pinnatifida [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 4''-O-Glucosylvitexin. CAS No. 178468-00-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N5073. | |
| Vitexin-4-rhamnoside | Vitexin-4-rhamnoside is a potent bioactive compound widely used in the biomedical industry. Derived from natural sources, it has been shown to exhibit strong anti-inflammatory and antioxidant properties. This product is commonly employed in the treatment of various diseases such as cancer, cardiovascular disorders, and neurodegenerative conditions. Its therapeutic potential makes it a valuable asset in drug development and disease management within the field of biomedicine. Synonyms: Vitexin rhamnoside; 32426-34-9; 5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]chromen-4-one; Vitexin-4'-Rhamnoside; EINECS 251-036-0; 8-glycosyl-apigenin-rhamnoside; CHEMBL1685071; DTXSID00186171; CHEBI:189451; 2-(4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)-8-beta-D-glucopyranosyl-5,7-dihydroxy-4H-benzopyran-4-one. CAS No. 32426-34-9. Molecular formula: C27H30O14. Mole weight: 578.5. | |
| Vitexin Argininate | Vitexin Argininate. Group: Biochemicals. Grades: Plant Grade. CAS No. Pack Sizes: 20mg. US Biological Life Sciences. | Worldwide |
| vitexin β-glucosyltransferase | Vitexin is a flavonoid from Cannabis sativa (hemp) and some populations of Silene alba. Group: Enzymes. Synonyms: uridine diphosphoglucose-vitexin 2''-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.105. CAS No. 76828-68-7. 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-2333; vitexin β-glucosyltransferase; EC 2.4.1.105; 76828-68-7; uridine diphosphoglucose-vitexin 2''-glucosyltransferase. Cat No: EXWM-2333. | |
| Viton Powder | Viton Powder. Group: other nano materials. CAS No. 19011-17-0. Molecular formula: 233.04 g/mol. 99.9%. |  |
| Vixarelimab | Vixarelimab (KPL-716) is a human anti-oncostatin M ( OSM ) monoclonal antibody that binds to the beta chain of the OSM receptor and inhibits IL-31 and OSM signalling. Vixarelimab can be used in studies of inflammatory skin diseases such as atopic dermatitis and itchy nodular rash [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: KPL-716. CAS No. 2243320-83-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99519. | |
| VJ115 | VJ115 is a novel chemical entity that inhibits the enzyme ENOX1, a NADH oxidase. Genetic and small molecule inhibition of ENOX1 inhibits endothelial cell tubule formation and tumor-mediated neo-angiogenesis. VJ115 inhibition of ENOX1 can impact expression of proteins involved in cytoskeletal reorganization and support a hypothesis in which ENOX1 activity links elevated cellular NADH concentrations with cytoskeletal reorganization and angiogenesis. Synonyms: VJ 115; VJ-115; (Z)-2-((1-benzyl-1H-indol-3-yl)methylene)quinuclidin-3-ol. CAS No. 929256-79-1. Molecular formula: C23H24N2O. Mole weight: 344.45. | |
| VK-2019 | VK-2019 is an oral active, selective EBNA1 ((Epstein-Barr Nuclear Antigen 1) inhibitor and can be used for study of EBV-associated carcinomas [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2044520-06-9. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-W725179. | |
| VK-28 | VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced mitochondrial membrane lipid peroxidation, with an IC 50 of 12.7 μM. VK-28 exhibits significant neuroprotective effects on ICV-6-OHDA. VK-28 can be used for the research of Parkinsons disease and other neurodegenerative diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 312611-92-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W686216. | |
| VKGILS-NH2 | VKGILS-NH2. Group: Biochemicals. Grades: Purified. CAS No. 942413-05-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| VKGILS-NH2 | VKGILS-NH2 is a reversed control peptide for SLIGKV-NH2, which is a protease-activated receptor 2 (PAR2) agonist. Synonyms: retro-PAR-2 (1-6) amide (human); retro-SLIGKVamide; Thrombin Receptor-Like 1 (6-1) amide (human); Proteinase Activated Receptor 2 (6-1) amide (human); PAR-2 (6-1) amide (human). Grades: 98%. CAS No. 942413-05-0. Molecular formula: C28H54N8O7. Mole weight: 614.79. | |
| VKGILS-NH2 | VKGILS-NH2 is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 has no effect on DNA synthesis in cells [1] [2]. Uses: Scientific research. Group: Peptides. CAS No. 942413-05-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1310. | |
| VKGILS-NH2 acetate | VKGILS-NH2 acetate is a reversed control peptide for SLIGKV-NH2, which is a protease-activated receptor 2 (PAR2) agonist. Synonyms: H-Val-Lys-Gly-Ile-Leu-Ser-NH2.CH3CO2H; L-valyl-L-lysyl-glycyl-L-isoleucyl-L-leucyl-L-serinamide acetic acid. Grades: ≥95%. CAS No. 2763585-10-8. Molecular formula: C28H54N8O7.C2H4O2. Mole weight: 674.83. | |
| VLX600 | VLX600 is an iron-chelating inhibitor of oxidative phosphorylation (OXPHOS). VLX600 causes mitochondrial dysfunction and induces a strong shift to glycolysis. VLX600 displays selective cytotoxic activity against malignant cell and induces autophagy. Anticancer activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 327031-55-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-12406. | |
| VM&P Naptha | VM & P Naptha. Category ALIPHATIC SOLVENTS. Pack Sizes Bulk/ Drums |  |
| VMY-1-103 | VMY-1-103 is a potent CDK inhibitor, is also a novel dansylated analog of purvalanol B, was shown to inhibit cell cycle progression and proliferation in prostate and breast cancer cells more effectively than purvalanol B. VMY-1-103 increased the sub G(1) fraction of apoptotic cells, induced PARP and caspase-3 cleavage and increased the levels of the Death Receptors DR4 and DR5, Bax and Bad while decreasing the number of viable cells, all supporting apoptosis as a mechanism of cell death. VMY-1-103 possesses unique antiproliferative capabilities and that this compound may form the basis of a new candidate drug to treat medulloblastoma. Synonyms: VMY1-103; VMY 1-103. Grades: 98%. CAS No. 1209002-43-6. Molecular formula: C34H42ClN9O4S. Mole weight: 708.28. | |
| VNbAlC (MAX) Phase Ceramic Materials | VNbAlC (MAX) Phase Ceramic Materials. Uses: High temperature coating, mxene precursor, conductive self-lubricating ceramic, lithiumionbattery, super capacitor, electrochemical catalysis. Group: Mxene materials. >90%. | |
| Vne I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. G↑TGCAC CACGT↓G. Activity: 10000-20000u.a./ml. Appearance: 10 X SE-buffer O. Storage: -20°C. Form: Liquid. Source: An E.coli strain, that carries the cloned gene VneI from Vibrio nereis 18. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1186RE. | |
| VNPB | VNPB. Group: Organic light-emitting diode (oled) materials. Alternative Names: N4,N4'-di(Naphthalen-1-yl)-N4,N4'-bis(4- vinylphenyl)biphenyl-4,4'-diamine. CAS No. 1010396-31-2. Product ID: N-[4-[4-(4-ethenyl-N-naphthalen-1-ylanilino)phenyl]phenyl]-N-(4-ethenylphenyl)naphthalen-1-amine. Molecular formula: 640.81. Mole weight: C48H36N2. C=CC (C=C1)=CC=C1N (C2=CC=CC3=C2C=CC=C3)C (C=C4)=CC=C4C5=CC=C (N (C6=CC=C (C=C)C=C6)C7=CC=CC8=C7C=CC=C8)C=C5. 1S/C48H36N2/c1-3-35-19-27-41 (28-20-35) 49 (47-17-9-13-39-11-5-7-15-45 (39) 47) 43-31-23-37 (24-32-43) 38-25-33-44 (34-26-38) 50 (42-29-21-36 (4-2) 22-30-42) 48-18-10-14-40-12-6-8-16-46 (40) 48/h3-34H, 1-2H2, WTEWXIOJLNVYBZ-UHFFFAOYSA-N. WTEWXIOJLNVYBZ-UHFFFAOYSA-N. | |
| Voacamine | Voacamine, an indole alkaloid, exhibits potent cannabinoid CB1 receptor antagonistic activity [1]. Voacamine also inhibits P-glycoprotein ( P-gp ) action in multidrug-resistant tumor cells [1]. Uses: Scientific research. Group: Natural products. CAS No. 3371-85-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N6932. | |
| Voacamine | Voacamine is an alkaloid originally isolated from Voacanga. It is a cannabinoid receptor 1 (CB1) antagonist with IC50 value of 41 nM. It has been approved as an antimalarial drug in several African countries. It is also under investigation for modulating multidrug-resistance in tumor cells. Synonyms: NSC 82591; Voacanginine. Grades: ≥98%. CAS No. 3371-85-5. Molecular formula: C43H52N4O5. Mole weight: 704.90. | |
| Voacamine | Botanical Source: Group: Biochemicals. Alternative Names: Voacanginine. Grades: Plant Grade. CAS No. 3371-85-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Voacangine | Voacangine is a kind of alkaloid and has been found to exhibit anti-addictive properties. Synonyms: (-)-Voacangine; Carbomethoxyibogaine; 12-Methoxyibogamine-18-carboxylic acid methyl ester. CAS No. 510-22-5. Molecular formula: C22H28N2O3. Mole weight: 368.48. | |
| Voacangine | Voacangine is an antagonist for TRPV1 and TRPM8 but as an agonist for TRPA1 ( EC 50 =8 μM). Voacangine competitively blockes capsaicin binding to TRPV1 ( IC 50 =50 μM). Voacangine competitively inhibits the binding of menthol to TRPM8 ( IC 50 =9 μM) and it shows noncompetitive inhibition against icilin ( IC 50 =7 μM). Voacangine selectively abrogates chemical agonist-induced TRPM8 activation and did not affect cold-induced activation. Voacangine is an alkaloid isolated from the root bark of Voacanga africana [1]. Uses: Scientific research. Group: Natural products. CAS No. 510-22-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N7536. | |
| Vobarilizumab | Vobarilizumab (ALX-0061) is a humanized bispecific anti- IL-6R and anti-human serum albumin (ALB) monoclonal antibody (mAb) ( K d : 0.19 pM). Vobarilizumab consists of an anti-IL-6R domain and an anti-human serum albumin domain. Vobarilizumab can be used in the research of inflammatory autoimmune diseases, such as rheumatoid arthritis [1] [2] [3]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ALX-0061. CAS No. 1628814-88-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99385. | |
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