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| Product | Description | |
|---|---|---|
| Vesnarinone | Vesnarinone (OPC-8212) is an orally active phosphodiesterase 3 ( PDE3 ) inhibitor. Vesnarinone can increase in calcium flux and decrease in potassium flux. Vesnarinone shows dose-dependent positive inotropic activity. Vesnarinone can be used in heart failure research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: OPC-8212. CAS No. 81840-15-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15297. |  |
| Vesnarinone | Vesnarinone, a quinolinone derivative, is a cardiotonic agent. It has pharmacodynamic effects include inhibition of phosphodiesterase III (PDE3) activity, increases in calcium flux and decreases in potassium flux. Its IC50 value is 1 μM and 300 μM for inhibition of HERG channels and PDE. It is a novel cytokine inhibitor, for the treatment of lung fibrosis using a murine model of bleomycin (BLM)-induced pulmonary fibrosis. It is a new and novel inotropic drug that has unique and complex mechanisms of action. It inhibits phosphodiesterase, thereby leading to increased intracellular calcium, and also affects numerous myocardial ion channels, resulting in the prolongation of the open...eby leading to increased intracellular calcium, and also affects numerous myocardial ion channels, resulting in the prolongation of the opening time of sodium channels and the decrease in the delayed outward and inward rectifying potassium current. it improves ventricular performance most in patients with the worst degree of heart failure. Synonyms: RG-0210; RG 0210; RG0210; OPC-8212; OPC 8212; OPC8212; Piteranometozine; Vesnarinone; Arkin; Arkin-Z. OPC 8212;6-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinone;3,4-Dihydro-6-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)-2(1h)-quinolinone. Grades: >98%. CAS No. 81840-15-5. Molecular formula: C22H25N3O4. Mole weight: 395.45. |  |
| Vesnarinone | Vesnarinone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: VESNARINONE;0PC-8212;3,4-Dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)-quinolinone;Arkin;Piteranometozine. Product Category: Heterocyclic Organic Compound. CAS No. 81840-15-5. Molecular formula: C22H25N3O4. Mole weight: 395.457. Product ID: ACM81840155. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Vespid chemotactic peptide 5g | Vespid chemotactic peptide 5g is an antibacterial peptide isolated from Vespa magnifica. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: H-Phe-Leu-Ile-Ile-Arg-Arg-Pro-Ile-Val-Leu-Gly-Leu-Leu-OH. Grades: >95%. Molecular formula: C75H131N19O14. Mole weight: 1523. | |
| VESP-VB1 | VESP-VB1 is an antibacterial peptide isolated from Vespa bicolor. Synonyms: Phe-Met-Pro-Ile-Ile-Gly-Arg-Leu-Met-Ser-Gly-Ser-Leu. Molecular formula: C64H108N16O16S2. Mole weight: 1421.78. | |
| Vestipitant | Cas No. 334476-64-1. | |
| Vestitol | Vestitol is the compound isolated from leaves of Trifolium arvense [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-Vestitol. CAS No. 56701-24-7. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N8744. | |
| Vestitol | Vestitol. Group: Biochemicals. Grades: Highly Purified. CAS No. 35878-41-2. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H16O4. US Biological Life Sciences. |  Worldwide |
| vestitone reductase | This plant enzyme catalyses the penultimate step in the biosynthesis of the pterocarpin phytoalexins medicarpin and maackiain. This activity was previously classified as part of EC 1.1.1.246, pterocarpin synthase, which is now known to be catalysed by two enzymes, vestitone reductase and EC 4.2.1.139, medicarpin synthase. Group: Enzymes. Synonyms: pterocarpin synthase (incorrect); pterocarpan synthase (incorrect). Enzyme Commission Number: EC 1.1.1.348. CAS No. 118477-70-6. 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-0263; vestitone reductase; EC 1.1.1.348; 118477-70-6; pterocarpin synthase (incorrect); pterocarpan synthase (incorrect). Cat No: EXWM-0263. |  |
| Vetikolacetate | Vetikolacetate. CAS No. 68083-58-9. VIGON Item # 502546. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Vetikone ® | Vetikone ® (Methyl Phenyl Pentan-2-one). CAS No. 7403-42-1. VIGON Item # 501535. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| vetispiradiene synthase | The initial internal cyclization produces the monocyclic intermediate germacrene A. Group: Enzymes. Synonyms: vetispiradiene-forming farnesyl pyrophosphate cyclase; pemnaspirodiene synthase; HVS; vetispiradiene cyclase. Enzyme Commission Number: EC 4.2.3.21. CAS No. 192465-18-2. 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-5178; vetispiradiene synthase; EC 4.2.3.21; 192465-18-2; vetispiradiene-forming farnesyl pyrophosphate cyclase; pemnaspirodiene synthase; HVS; vetispiradiene cyclase. Cat No: EXWM-5178. | |
| Vetival | Vetival. CAS No. 4927-39-3. VIGON Item # 503100. Categories: Speciality Ingrdients Suppliers, Fragrances, vetiver pentanone, Perfumers. | America & Internationally |
| Vetiver Oil - CO2 | Vetiver is a parennial grass that shares a lot of its characteristics with other fragrant grasses like lemongrass, citronella and palmarosa. However unlike these plants, vetiver oil is extracted from the plant's roots rather than its leaves While Vetiver Oil is mainly used in fine fragrances, the Indonesian Vetiver is widely used for making derivatives such as Vetiverol and Vetiveryl Acetate. Uses: Aromatherapy. Group: Plant Extracts. INCI Names: Vetiveria Zizanioides (Vetiver) Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 84238-29-9. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: VT-006. Olfactive Profile: Woody, earthy, rooty, smokey, nutty, powdery, sweet. EC No: 282-490-8. Origin: Indonesia. |  New Jersey |
| Vetiver Oil Haiti | Vetiver Oil Haiti. CAS No. 8016-96-4. Kosher: Y. VIGON Item # 504190. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Cosmetics. | America & Internationally |
| Vetiver Oil Java Crude | Vetiver is a parennial grass that shares a lot of its characteristics with other fragrant grasses like lemongrass, citronella and palmarosa. However unlike these plants, vetiver oil is extracted from the plant's roots rather than its leaves While Vetiver Oil is mainly used in fine fragrances, the Indonesian Vetiver is widely used for making derivatives such as Vetiverol and Vetiveryl Acetate. Uses: Cosmetic and Care, Essential Oils. Group: Plant Extracts. INCI Names: Vetiveria Zizanioides (Vetiver) Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 84238-29-9 ; 8016-96-4. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: VT-001. Olfactive Profile: Woody, smoky, earthy, herbaceous and spicy, sweet, caramel. EC No: 282-490-8. Origin: Indonesia. | New Jersey |
| Vetiver Oil Java M.D. | Vetiver is a parennial grass that shares a lot of its characteristics with other fragrant grasses like lemongrass, citronella and palmarosa. However unlike these plants, vetiver oil is extracted from the plant's roots rather than its leaves. Uses: Perfumery, Cosmetics. Group: Plant Extracts. INCI Names: Vetiveria Zizanioides (Vetiver) Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 84238-29-9 ; 8016-96-4. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: VT-003. Olfactive Profile: Woody, smoky, earthy, herbaceous and spicy, sweet, caramel. EC No: 282-490-8. Origin: Indonesia. | New Jersey |
| Vetiver Oil Java Rectified | Vetiver is a parennial grass that shares a lot of its characteristics with other fragrant grasses like lemongrass, citronella and palmarosa. However unlike these plants, vetiver oil is extracted from the plant's roots rather than its leaves While Vetiver Oil is mainly used in fine fragrances, the Indonesian Vetiver is widely used for making derivatives such as Vetiverol and Vetiveryl Acetate. Uses: Cosmetic and Care, Essential Oils. Group: Plant Extracts. INCI Names: Vetiveria Zizanioides (Vetiver) Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 84238-29-9 ; 8016-96-4. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: VT-002. Olfactive Profile: Woody, smoky, earthy, herbaceous and spicy, sweet, caramel. EC No: 282-490-8. Origin: Indonesia. | New Jersey |
| Vetivert acetate | Vetivert acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Vetiver acetate, Vetivert acetate, Vetiveryl acetate, Vetiverol, acetate, Vetiver acetate, Java, W524301_ALDRICH, EINECS 263-597-9, EINECS 204-225-7, AI3-24214, LS-3152, Vetiveryl acetate (Vetiveria zizanioides (L.) Nash), 1,2,3,3a,4,5,6,8a-Octahydro-2-isopropylidene-4,8-dimethylazulen-6-yl acetate, 6-AZULENOL, 1,2,3,3a,4,5,6,8a-OCTAHYDRO-2-ISOPROPYLIDENE-4,8-DIMETHYL-, ACETATE, 6-Azulenol, 1,2,3,3a,4,5,6,8a-octahydro-4,8-dimethyl-2-(1-methylethylidene)-, acetate, 117-98-6, 62563-80-8. Product Category: Heterocyclic Organic Compound. CAS No. 62563-80-8. Molecular formula: C17H26O2. Mole weight: 262.3871. Purity: N/A. IUPACName: (4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1H-azulen-6-yl) acetate. Canonical SMILES: CC1CC(C=C(C2C1CC(=C(C)C)C2)C)OC(=O)C. Density: 0.976 g/mL at 25ºC(lit.). ECNumber: 204-225-7. Product ID: ACM62563808. Alfa Chemistry ISO 9001:2015 Certified. | |
| Vetiveryl Acetate | Vetiver is a parennial grass that shares a lot of its characteristics with other fragrant grasses like lemongrass, citronella and palmarosa. However unlike these plants, vetiver oil is extracted from the plant's roots rather than its leaves While Vetiver Oil is mainly used in fine fragrances, the Indonesian Vetiver is widely used for making derivatives such as Vetiverol and Vetiveryl Acetate. Uses: Cosmetic and Care, Fragrance Products. Group: Plant Extracts. INCI Names: Vetiveryl Acetate. Grades: FOOD GRADE. CAS No. 84082-84-8. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: VT-005. Olfactive Profile: Woody, smoky, earthy, herbaceous and spicy, sweet, caramel. EC No: 282-031-1. FEMA No: 4218. Origin: Indonesia. | New Jersey |
| Vetynal Extra | Vetynal Extra. CAS No. 57082-24-3. VIGON Item # 500937. Categories: Speciality Ingrdients Suppliers, Fragrances, beta-caryophyllene alcohol acetate, Perfumers. | America & Internationally |
| VGX-1027 | VGX-1027 is an orally active isoxazole compound that exhibits various immunomodulatory properties. VGX-1027 targets macrophages, reducing the production of the proinflammatory mediators TNF-α, IL-1β, IL-10. VGX-1027 has antidiabetogenic effects by limiting cytokine-mediated immunoinflammatory events [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GIT 27. CAS No. 6501-72-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15507. | |
| VH 032-linker 6 | VH 032-linker 6 is a von-Hippel-Lindau protein ligand (VHL) conjugated to a PEGylated crosslinker with terminal alkyne for PROTAC technology. It has been used as a degrader building block in PROTAC for targeted protein degradation. Synonyms: VH032-PEG3-acetylene; (2S,4R)-1-((S)-2-(tert-Butyl)-4-oxo-6,9,12-trioxa-3-azapentadec-14-yn-1-oyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide. Grades: ≥98%. CAS No. 2098799-80-3. Molecular formula: C31H42N4O7S. Mole weight: 614.75. | |
| VH298 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| VH-298 | VH-298 is a high-affinity inhibitor of E3 ubiquitin ligase VHL (Kd value of 80-90 nM) that could block VHL and HIF-α interactions. VH-298 can be used in PROTAC technology. Uses: Enzyme inhibitors. Synonyms: (2S,4R)-1-((S)-2-(1-cyanocyclopropanecarboxamido)-3,3-dimethylbutanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide; EX-A1505; VH 298; VH298; VH-298. Grades: ≥98% by HPLC. CAS No. 2097381-85-4. Molecular formula: C27H33N5O4S. Mole weight: 523.65. | |
| Vhl-1 | Vhl-1 is a cyclic peptide isolated from Viola hederacea (Australian violet), which has antibacterial and antiviral activities. Synonyms: Leaf cyclotide 1; Ser-Ile-Ser-Cys-Gly-Glu-Ser-Cys-Ala-Met-Ile-Ser-Phe-Cys-Phe-Thr-Glu-Val-Ile-Gly-Cys-Ser-Cys-Lys-Asn-Lys-Val-Cys-Tyr-Leu-Asn. | |
| Vhl-2 | Vhl-2 is a cyclic peptide isolated from Viola hederacea (Australian violet), which has antibacterial and antiviral activities. Synonyms: Leaf cyclotide 2; Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Phe-Thr-Gly-Thr-Cys-Tyr-Thr-Asn-Gly-Cys-Thr-Cys-Asp-Pro-Trp-Pro-Val-Cys-Thr-Arg-Asn. Molecular formula: C33H41N5O5S. Mole weight: 619.8. | |
| VHL human | recombinant, expressed in insect cells, ?70% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Vhr1 | Vhr1 is a cyclic peptide isolated from Viola hederacea (Australian violet), which has antibacterial and antiviral activities. Synonyms: Gly-Ile-Pro-Cys-Ala-Glu-Ser-Cys-Val-Trp-Ile-Pro-Cys-Thr-Val-Thr-Ala-Leu-Leu-Gly-Cys-Ser-Cys-Ser-Asn-Lys-Val-Cys-Tyr-Asn. | |
| Vialinin A | Vialinin A is an inhibitor of ubiquitin-specific peptidase 4 (USP4), USP5/isopeptidase T (IsoT) and UCH-L1 deubiquitinating enzyme (DUB) activity (IC50 = 1.5, 5.9 and 22.3 μM, respectively), displaying no significant inhibitory effects on UCH-L3, USP2, and USP8 activity. Vialinin A has been shown to reduce the release of TNF-α (IC50 = 0.09 nM) from RBL-2H3 mast cells. Synonyms: 1,1'-(4,4'',5',6'-Tetrahydroxy[1,1':4',1''-terphenyl]-2',3'-diyl) benzeneacetic acid ester; Ganbajunin C. Grades: ≥98% by HPLC. CAS No. 858134-23-3. Molecular formula: C34H26O8. Mole weight: 562.57. | |
| Vialinin A | Vialinin A (Terrestrin A) is a p-terphenyl compound with antioxidant properties [1]. Vialinin A is a potent inhibitor of TNF-α, USP4, USP5, and sentrin/SUMO-specific protease 1 (SENP1). Vialinin A (Terrestrin A) can be used for autoimmune diseases and cancer research [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Terrestrin A. CAS No. 858134-23-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-103435. | |
| Vialinin A | Vialinin A. Group: Biochemicals. Grades: Purified. CAS No. 858134-23-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Viba 15 | Viba 15 is a cyclic peptide isolated from Viola hederacea (Australian violet), which has antibacterial activities. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Val-Gly-Gly-Thr-Cys-Asn-Thr-Pro-Gly-Cys-Ala-Cys-Ser-Trp-Pro-Val-Cys-Thr-Arg-Asn. Mole weight: 2860. | |
| Viba17 | Viba17 is a cyclic peptide isolated from Viola hederacea (Australian violet), which has antibacterial activities. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Val-Gly-Gly-Thr-Cys-Asn-Thr-Pro-Gly-Cys-Gly-Cys-Ser-Trp-Pro-Val-Cys-Thr-Arg-Asn. Mole weight: 2846.02. | |
| Vibecotamab | Vibecotamab (XmAb14045) is a potent bispecific antibody against CD123 and CD3 that stimulates T cell-mediated targeted killing of CD123-expressing cells. Vibecotamab has antitumor activity and can be used in acute myeloid leukaemia studies [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: XmAb14045. CAS No. 2138442-13-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99521. | |
| Vibegron | Vibegron (MK-4618) is a potent, highly selective and orally active β 3 -adrenoceptor agonist ( EC 50 =1.1 nM). Vibegron can be used for severe urgency urinary incontinence related to overactive bladder [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-4618. CAS No. 1190389-15-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19933. | |
| VIBEGRON | This active molecular is a selective Beta 3 Adrenergic Receptor Agonist and was developed by Kyorin Pharmaceutical for the treatment of OAB (Overactive Bladder). Now, Vibegron is in Phase 3 human clinical trials for the treatment of OAB. In Jan 2015, Vibegron was discontinued Phase-I for hypertension (Combination therapy) in USA. In Mar 2016, Vibegron licensed to Kissei Pharmaceutical in Japan. Uses: Overactive bladder. Synonyms: (6S)-N-[4-[[(2S,5R)-5-[(R)-hydroxy(phenyl)methyl]pyrrolidin-2-yl]methyl]phenyl]-4-oxo-7,8-dihydro-6H-pyrrolo[1,2-a]pyrimidine-6-carboxamide,MK-4618; MK 4618; MK4618; Vibegron. Grades: 98%. CAS No. 1190389-15-1. Molecular formula: C26H28N4O3. Mole weight: 444.54. | |
| Vibegron Impurity 10 | Vibegron Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1865729-64-1. Molecular formula: C31H36N4O5. Mole weight: 544.65. Catalog: APB1865729641. | |
| Vibegron Impurity 4 | Vibegron Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1009092-91-4. Molecular formula: C17H25NO4. Mole weight: 307.39. Catalog: APB1009092914. | |
| Vibi A | Vibi A is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Phe-Gly-Gly-Thr-Cys-Asn-Thr-Pro-Gly-Cys-Ser-Cys-Ser-Tyr-Pro-Ile-Cys-Thr-Arg-Asn. | |
| Vibi B | Vibi B is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Phe-Gly-Gly-Thr-Cys-Asn-Thr-Pro-Gly-Cys-Thr-Cys-Ser-Tyr-Pro-Ile-Cys-Thr-Arg-Asn. | |
| Vibi C | Vibi C is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Ala-Phe-Gly-Ser-Cys-Tyr-Thr-Pro-Gly-Cys-Ser-Cys-Ser-Trp-Pro-Val-Cys-Thr-Arg-Asn. | |
| Vibi D | Vibi D is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Leu-Pro-Val-Cys-Gly-Glu-Thr-Cys-Phe-Gly-Gly-Arg-Cys-Asn-Thr-Pro-Gly-Cys-Thr-Cys-Ser-Tyr-Pro-Ile-Cys-Thr-Arg-Asn. | |
| Vibi F | Vibi F is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Thr-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Leu-Thr-Ser-Ala-Leu-Gly-Cys-Ser-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Lys-Asn. | |
| Vibi G | Vibi G is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Thr-Phe-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Leu-Thr-Ser-Ala-Ile-Gly-Cys-Ser-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Lys-Asn. | |
| Vibi I | Vibi I is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Trp-Ile-Pro-Cys-Leu-Thr-Ser-Thr-Val-Gly-Cys-Ser-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Arg-Asn. | |
| Vibi J | Vibi J is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Thr-Phe-Pro-Cys-Gly-Glu-Ser-Cys-Val-Trp-Ile-Pro-Cys-Ile-Ser-Lys-Val-Ile-Gly-Cys-Ala-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Lys-Asn. | |
| Vibi K | Vibi K is a plant antimicrobial peptide isolated from Viola hederacea (Australian violet). It has activity against bacteria and cancer cells. Synonyms: Gly-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Trp-Ile-Pro-Cys-Leu-Thr-Ser-Ala-Val-Gly-Cys-Pro-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Arg-Asn. | |
| Vibostolimab | Vibostolimab is an anti-TIGIT ( T cell immunoglobulin and ITIM domain ) monoclonal antibody. Vibostolimab shows antitumor activity, and can be used in non-small cell lung cancer (NSCLC) and melanoma research [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2231305-30-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99202. | |
| Vibostolimab | Vibostolimab is an anti-TIGIT monoclonal antibody with antitumor activity. Vibostolimab has been investigated as a monotherapy for advanced solid tumors such as non-small-cell lung cancer (NSCLC). Synonyms: MK-7684; MK 7684; MK7684. CAS No. 2231305-30-7. | |
| Vibozilimod | Vibozilimodum is an immunomodulator. Synonyms: 4-Piperidinecarboxylic acid, 1-[[4-[5-[3-chloro-4-(2-methylpropyl)phenyl]-1,2,4-oxadiazol-3-yl]phenyl]methyl]-4-[(2-methoxyethoxy)methyl]-. Grades: >98%. CAS No. 1403232-33-6. Molecular formula: C29H36ClN3O5. Mole weight: 542.1. | |
| Vibralactone B | Vibralactone B is an antibacterial compound produced from liquid fermentations of Stereum hirsutum that inhibits the growth of E. coli and Pseudomonas aeruginosa. Synonyms: (1beta)-2alpha-Prenyl-3beta-hydroxy-5beta-(hydroxymethyl)-6-oxabicyclo[3.1.0]hexane-2-carboxylic acid 2,3-lactone; 3,7-Dioxatricyclo[4.2.0.02,4]octan-8-one, 4-(hydroxymethyl)-1-(3-methyl-2-buten-1-yl)-, (1S,2R,4R,6S)-; (1S,2R*,3R*,5S)-2,3-epoxyvibralactone. Grades: ≥98%. CAS No. 1093230-95-5. Molecular formula: C12H16O4. Mole weight: 224.25. | |
| Vibralactone D | Vibralactone D is isolated from Boreostereum vibrans and exhibits weak inhibitory effect against isozymes of 11beta-hydroxysteroid dehydrogenases (HSD). Synonyms: (1S,5R,6S)-6-hydroxy-5-(3-methylbut-2-enyl)-3-oxabicyclo[3.2.1]octan-4-one; 3-Oxabicyclo[3.2.1]octan-2-one, 7-hydroxy-1-(3-methyl-2-buten-1-yl)-, (1R,5S,7S)-. Grades: ≥98%. CAS No. 1251748-32-9. Molecular formula: C12H18O3. Mole weight: 210.27. | |
| Vibralactone K | Vibralactone K is isolated from Boreostereum vibrans and has no cytotoxicity against five human cancer cell lines. Synonyms: 1H-Cyclopenta[c]furan-1-one, hexahydro-6-hydroxy-5-(3-methyl-2-buten-1-yl)-, (3aS,5S,6R,6aR)-. Grades: ≥98%. CAS No. 1623786-66-2. Molecular formula: C12H18O3. Mole weight: 210.27. | |
| Vibralactone L | Vibralactone L is isolated from Boreostereum vibrans and has no cytotoxicity against five human cancer cell lines. Synonyms: 3-Furanpropanoic acid, 2,5-dihydro-α-(3-methyl-2-buten-1-yl)-5-oxo-, ethyl ester, (+)-. Grades: ≥98%. CAS No. 1623786-67-3. Molecular formula: C14H20O4. Mole weight: 252.31. | |
| Vibration Pad | Vibration Pad. Group: Polymers. |  |
| vibriolysin | Thermostable enzyme from Vibrio proteolyticus (formerly Aeromonas proteolytica). Specificity related to, but distinct from, those of thermolysin and bacillolysin. A zinc metallopeptidase in family M4 (thermolysin family). Formerly included in EC 3.4.24.4. Group: Enzymes. Synonyms: Aeromonas proteolytica neutral proteinase; aeromonolysin. Enzyme Commission Number: EC 3.4.24.25. CAS No. 69598-88-5. 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-4306; vibriolysin; EC 3.4.24.25; 69598-88-5; Aeromonas proteolytica neutral proteinase; aeromonolysin. Cat No: EXWM-4306. | |
| Vibunazole | Vibunazole is usually used as an antifungal agent. Uses: Antifungal agent. Synonyms: Bay N 7133; BayN 7133; Bay-N 7133; Vibunazole; α-[(4-Chlorophenoxy)?methyl]?-α-(1,?1-dimethylethyl)?-1H-1,?2,?4-triazole-1-ethanol. Grades: 98%. CAS No. 80456-55-9. Molecular formula: C15H20ClN3O2. Mole weight: 309.79. | |
| Viburgenin | Viburgenin, an extract isolated from Rudgea viburnioides, is a triterpenes that shows an antifungal and anticancer activity. Synonyms: (+)-Viburgenin. CAS No. 211506-71-7. Molecular formula: C30H50O5. Mole weight: 490.73. | |
| Vicagrel | Vicagrel is a prodrug of clopidogrel thiolactone, an oral P2Y12 antiplatelet agent used to prevent blood clots, developed to overcome clopidogrel resistance. Currently, Vicagrel is undergoing a phase I active study by Jiangsu Vcare Pharmatech. Synonyms: CHEMBL2042273; SCHEMBL12438770; ZINC84654546; AJ-126334; methyl (2S)-2-(2-acetyloxy-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)-2-(2-chlorophenyl)acetate. CAS No. 1314081-53-2. Molecular formula: C18H18ClNO4S. Mole weight: 379.87. | |
| Vicagrel | Vicagrel is a potent, safe and orally active antiplatelet agent, which works by irreversibly inhibiting P2Y12 receptor. Vicagrel can be used for the research of blood clots in coronary artery disease, peripheral vascular disease, and cerebrovascular disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1314081-53-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118284. | |
| Vicagrel Carboxylic Acid | An impurity of Vicagrel. Vicagrel is a prodrug of clopidogrel thiolactone, an oral P2Y12 antiplatelet agent used to prevent blood clots, developed to overcome clopidogrel resistance. Currently, Vicagrel is undergoing a phase I active study by Jiangsu Vcare Pharmatech. Molecular formula: C17H16ClNO4S. Mole weight: 365.84. | |
| Vicanicin | Vicanicin is a depsidone isolated from the lichen Teloschistesflavicans (Sw.) Norm. Vicanicin can induce apoptosis of DU-145 and LNCaP cells. Synonyms: 2,7-Dichloro-3-hydroxy-8-methoxy-1,4,6,9-tetramethyl-11H-dibenzo[b,e][1,4]dioxepin-11-one. CAS No. 33211-22-2. Molecular formula: C18H16Cl2O5. Mole weight: 383.22. | |
| Vicenin 2 | Vicenin 2, a flavonoid, is an orally active angiotensin-converting enzyme (ACE) inhibitor ( IC 50 of 43.83 μM) [1]. Vicenin 2 has radioprotective, anti-nociceptive effects, anti-glycation anti-inflammatory, antioxidant, anticancer, antiangiogenic properties [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 23666-13-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N2165. | |
| Vicenin-2 | Vicenin-2. Group: Biochemicals. CAS No. 23666-13-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Vicenin-II (6,8-Di-C-glucosylapigenin) | Vicenin-II (6,8-Di-C-glucosylapigenin). Group: Biochemicals. Alternative Names: 6, 8-Di-C-glucopyranosyl apigenin; 6,8-Di-C-glucosylapigenin. Grades: Plant Grade. CAS No. 23666-13-9. Pack Sizes: 10mg. Molecular Formula: C27H30O15, Molecular Weight: 594.518. US Biological Life Sciences. | Worldwide |
| Vicenin III (6-C-Glucosyl-8-C-xylosylapigenin) | Vicenin III (6-C-Glucosyl-8-C-xylosylapigenin). Group: Biochemicals. Alternative Names: Vicenin 3; 6-C-Glucosyl-8-C-xylosylapigenin; 6-beta-D-Glucopyranosyl-8-beta-D-xylopyranosylapigenin. Grades: Plant Grade. CAS No. 59914-91-9. Pack Sizes: 10mg. Molecular Formula: C26H28O14, Molecular Weight: 564.491999999999. US Biological Life Sciences. | Worldwide |
| Vicenistatin | It is a macrocyclic lipid antibiotic produced by the strain of Str. sp. HC34. In vitro it is cytotoxic to human leukemia HL-60 cells and human colon cancer Co-LO205 cells with IC50 (μg/mL) of 0.12 and 0.19, respectively. Synonyms: Azacycloeicosa-3,5,10,13,15-pentaen-2-one, 7,11,13,19-tetramethyl-8-[[2,4,6-trideoxy-4-(methylamino)-β-D-ribo-hexopyranosyl]oxy]-, (3E,5E,7S,8S,10E,13E,15E,19S)-; Antibiotic HC34; NSC 641691; Vicenistatine. CAS No. 150999-05-6. Molecular formula: C30H48N2O4. Mole weight: 500.71. | |
| Vicenistatin M | It is produced by the strain of Streptomyces sp. HC-34. It is a homologue of Mycarose replacing amino sugars in the Vicenstatin molecule, and it loses the cytotoxicity of Vicenstatin. Synonyms: (6S,7S,18S)-20-aza-6,10,12,18-tetramethyl-7-O-(2',6'-dideoxy-3'-C-methyl-β-D-ribo-hexopyranosyl)-cycloicosa-2,4,9,12,14-pentaen-1-one; (3E,5E,10E,13E,15E)-(7S,8S,19S)-8-((2R,4S,5R,6R)-4,5-Dihydroxy-4,6-dimethyl-tetrahydro-pyran-2-yloxy)-7,11,13,19-tetramethyl-azacycloicosa-3,5,10,13,15-pentaen-2-one; Vicenistatine M. CAS No. 312532-50-6. Molecular formula: C30H47NO5. Mole weight: 501.70. | |
| vicianin β-glucosidase | Also hydrolyses, more slowly, (R)-amygdalin and (R)-prunasin, but not gentiobiose, linamarin or cellobiose. Group: Enzymes. Synonyms: vicianin hydrolase. Enzyme Commission Number: EC 3.2.1.119. CAS No. 91608-93-4. 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-3802; vicianin β-glucosidase; EC 3.2.1.119; 91608-93-4; vicianin hydrolase. Cat No: EXWM-3802. | |
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