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| Product | Description | |
|---|---|---|
| Verticillin A | Verticillin A is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: [10b,10'b(11H,11'H)-Bi-3,11a-epidithio-11aH-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole]-1,1',4,4'-tetrone, 2,2',3,3',5a,5'a,6,6'-octahydro-11,11'-dihydroxy-2,2',3,3'-tetramethyl-, (3S,3'S,5aR,5'aR,10bS,10'bS,11S,11'S,11aS,11'aS)-; [10b,10'b(11H,11'H)-Bi-3,11a-epidithio-11aH-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole]-1,1',4,4'-tetrone, 2,2',3,3',5a,5'a,6,6'-octahydro-11,11'-dihydroxy-2,2',3,3'-tetramethyl-, [3S-[3α,5aβ,10bβ(3'R*,5'aS*,10'bR*,11'R*,11'aR*),11β,11aα]]-; Verticillin A, (+)-; (6S,6'S)-19,19'-Dideoxy-6,6'-dihydroxychetocin. CAS No. 889640-30-6. Molecular formula: C30H28N6O6S4. Mole weight: 696.84. |  |
| Verticillin B | Verticillin B is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: (6S,6'S)-19-Deoxy-6,6'-dihydroxychetocin. CAS No. 52212-86-9. Molecular formula: C30H28N6O7S4. Mole weight: 712.84. | |
| Verticillin C | Verticillin C is originally isolated from Verticillium sp. Tm-759. It has the effect of anti-gram-positive bacteria, mycobacterium and protozoa, and has the inhibitory effect on the cancer of Ascites. Synonyms: Verticillin C. Grade: 95%. CAS No. 51798-48-2. Molecular formula: C30H28N6O7S5. Mole weight: 744.90. | |
| Vertimycin | It is a cyclopentane derivative of antibiotic produced by the strain of Streptoverticillium sp. JA 4498. It has anti-gram-positive bacteria and fungal effects. It has weak effect on Ehrlich ascites cancer cells in vitro. Synonyms: Cyclopentanone, 2-(2-hydroxyethoxy)-5-(hydroxymethyl)-; 1-Ethylenodiolo-3-methylolo-cyclopentanone-2; 1-(Aethylendiol-1,2)-methylol-3-cyclopentanon-2. CAS No. 14477-60-2. Molecular formula: C8H14O4. Mole weight: 174.19. | |
| Vertisporin | It is an antibiotic produced by the strain of Verticimonosporium diffractum TM-2098 and TM-2492. It has the effect against a few fungal. It is cytotoxic to HeLa cells with ED50 of 0.001 μg/mL. Synonyms: Spiro[4H-3a,22-(epoxyethano)-10,12-methano-17H,18H-furo[2',3':10,11][1,6]dioxacyclohexadecino[3,4-d][1]benzopyran-11(12H),2'-oxirane]-8,20(5H,22aH)-dione,2,3,10,10a,13a,16-hexahydro-2,3-dihydroxy-10a,15-dimethyl-, (2R,2'S,3R,3aR,6Z,10R,10aS,12R,13aR,17aR,21E,21bR)-. CAS No. 57100-32-0. Molecular formula: C29H36O10. Mole weight: 544.59. | |
| Verubecestat | Verubecestat (MK-8931) is an orally active, high-affinity BACE1 and BACE2 inhibitor with K i values of 2.2 nM and 0.38 nM. Verubecestat effectively reduces Aβ40 and has the potential for Alzheimer's Disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-8931. CAS No. 1286770-55-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16759. |  |
| Verubecestat TFA | Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-secretase inhibitor, and BACE1 protein inhibitor or Beta-site APP-cleaving enzyme 1 inhibitor. Verubecestat is a promising novel therapeutic drug candidate in Alzheimer's disease. Verubecestat reduced Aβ cerebral spinal fluids (CSF) levels up to 92% and was well tolerated by patients. Uses: Designed for use in research and industrial production. Additional or Alternative Names: MK-8931; MK 8931; MK8931; MK-8931-009; SCH 900931; SCH-900931; SCH900931; Verubecestat TFA. Product Category: Inhibitors. Appearance: White to off-white solid powder. CAS No. 2095432-65-6. Molecular formula: C19H18F5N5O5S. Mole weight: 523.44. Purity: >98%. IUPACName: (R)-N-(3-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2H-1,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5-fluoropicolinamide trifluoroacetic acid. Canonical SMILES: O=C(NC1=CC=C(F)C([C@@](C2)(C)N=C(N)N(C)S2(=O)=O)=C1)C3=NC=C(F)C=C3.O=C(O)C(F)(F)F. Product ID: ACM2095432656. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Verucopeptin | It is an antibiotic produced by the strain of Actinomadura verrucosospora Q886-2. It has weak antimicrobial effect and can prolong the survival time of mice transplanted with melanoma. Verucopeptin strongly inhibits v-ATPase activity by directly targeting the v-ATPase ATP6V1G subunit but not ATP1V1B2 or ATP6V1D. Synonyms: 2-hydroxy-N-(17-hydroxy-8,14-dimethyl-2,6,9,12,15,18-hexaoxo-4-propan-2-yl-5-oxa-1,8,11,14,17,23-hexazabicyclo[17.4.0]tricosan-3-yl)-2-[2-hydroxy-5-methoxy-6-[(E)-4,6,8-trimethyldec-2-en-2-yl]oxan-2-yl]propanamide. Grade: 98%. CAS No. 138067-14-8. Molecular formula: C43H73N7O13. Mole weight: 896.08. | |
| very-long-chain 3-oxoacyl-CoA reductase | The second component of the elongase, a microsomal protein complex responsible for extending palmitoyl-CoA and stearoyl-CoA (and modified forms thereof) to very-long-chain acyl CoAs. The enzyme is active with substrates with chain length of C16 to C34, depending on the species. cf. EC 2.3.1.199, very-long-chain 3-oxoacyl-CoA synthase, EC 4.2.1.134, very-long-chain (3R)-3-hydroxyacyl-[acyl-carrier protein] dehydratase, and EC 1.3.1.93, very-long-chain enoyl-CoA reductase. Group: Enzymes. Synonyms: very-long-chain 3-ketoacyl-CoA reductase; very-long-chain β-ketoacyl-CoA reductase; KCR (gene name); IFA38 (gene name). Enzyme Commission Number: EC 1.1.1.330. 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-0244; very-long-chain 3-oxoacyl-CoA reductase; EC 1.1.1.330; very-long-chain 3-ketoacyl-CoA reductase; very-long-chain β-ketoacyl-CoA reductase; KCR (gene name); IFA38 (gene name). Cat No: EXWM-0244. |  |
| very-long-chain 3-oxoacyl-CoA synthase | This is the first component of the elongase, a microsomal protein complex responsible for extending palmitoyl-CoA and stearoyl-CoA (and modified forms thereof) to very-long-chain acyl CoAs. Multiple forms exist with differing preferences for the substrate, and thus the specific form expressed determines the local composition of very-long-chain fatty acids. For example, the FAE1 form from the plant Arabidopsis thaliana accepts only 16 and 18 carbon substrates, with oleoyl-CoA (18:1) being the preferred substrate, while CER6 from the same plant prefers substrates with chain length of C22 to C32. cf. EC 1.1.1.330, very-long-chain 3-oxoacyl-CoA reductase, EC 4.2.1.134, very-long-chain (3R)-3-hydroxyacyl-[acyl-carrier protein] dehydratase, and EC 1.3.1.93, very-long-chain enoyl-CoA reductase. Group: Enzymes. Synonyms: very-long-chain 3-ketoacyl-CoA synthase; very-long-chain β-ketoacyl-CoA. Enzyme Commission Number: EC 2.3.1.199. 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-2142; very-long-chain 3-oxoacyl-CoA synthase; EC 2.3.1.199; very-long-chain 3-ketoacyl-CoA synthase; very-long-chain β-ketoacyl-CoA synthase; condensing enzyme (ambiguous); CUT1 (gene name); CER6 (gene name); FAE1 (gene name); KCS (gene name); ELO (gene name). Cat No: EXWM-2142. | |
| very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase | This is the third component of the elongase, a microsomal protein complex responsible for extending palmitoyl-CoA and stearoyl-CoA (and modified forms thereof) to very-long chain acyl CoAs. cf. EC 2.3.1.199, very-long-chain 3-oxoacyl-CoA synthase, EC 1.1.1.330, very-long-chain 3-oxoacyl-CoA reductase, and EC 1.3.1.93, very-long-chain enoyl-CoA reductase. Group: Enzymes. Synonyms: PHS1 (gene name); PAS2 (gene name). Enzyme Commission Number: EC 4.2.1.134. 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-4975; very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase; EC 4.2.1.134; PHS1 (gene name); PAS2 (gene name). Cat No: EXWM-4975. | |
| very-long-chain acyl-CoA dehydrogenase | Contains FAD as prosthetic group. One of several enzymes that catalyse the first step in fatty acids β-oxidation. The enzyme is most active toward long-chain acyl-CoAs such as C14, C16 and C18, but is also active with very-long-chain acyl-CoAs up to 24 carbons. It shows no activity for substrates of less than 12 carbons. Its specific activity towards palmitoyl-CoA is more than 10-fold that of the long-chain acyl-CoA dehydrogenase. cf. EC 1.3.8.1, short-chain acyl-CoA dehydrogenase, EC 1.3.8.7, medium-chain acyl-CoA dehydrogenase, and EC 1.3.8.8, long-chain acyl-CoA dehydrogenase. Group: Enzymes. Synonyms: ACADVL (gene name). Enzyme Commission Number: EC 1.3.8.9. 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-1416; very-long-chain acyl-CoA dehydrogenase; EC 1.3.8.9; ACADVL (gene name). Cat No: EXWM-1416. | |
| very-long-chain enoyl-CoA reductase | This is the fourth component of the elongase, a microsomal protein complex responsible for extending palmitoyl-CoA and stearoyl-CoA (and modified forms thereof) to very-long-chain acyl CoAs. cf. EC 2.3.1.199, very-long-chain 3-oxoacyl-CoA synthase, EC 1.1.1.330, very-long-chain 3-oxoacyl-CoA reductase, and EC 4.2.1.134, very-long-chain (3R)-3-hydroxyacyl-[acyl-carrier protein] dehydratase. Group: Enzymes. Synonyms: TSC13 (gene name); CER10 (gene name). Enzyme Commission Number: EC 1.3.1.93. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1363; very-long-chain enoyl-CoA reductase; EC 1.3.1.93; TSC13 (gene name); CER10 (gene name). Cat No: EXWM-1363. | |
| Vesatolimod | Vesatolimod (GS-9620) is a potent, selective and orally active agonist of Toll-Like Receptor (TLR7) with an EC 50 of 291 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-9620. CAS No. 1228585-88-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15601. | |
| Vesencumab | Vesencumab (MNRP-1685A) is IG1 antibody against neuropilin-1 (NRP-1). Vesencumab binds to NRP-1 and prevents the subsequent coupling of NRP-1 to VEGFR-2. Vesencumab has anti-angiogenic and anti-neoplastic activities. Vesencumab can be used in the research of metastatic solid tumors, including ovarian cancer[1][2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: MNRP-1685A. CAS No. 1205533-60-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99386. | |
| vesicle-fusing ATPase | A large family of ATP-hydrolysing enzymes involved in the heterotypic fusion of membrane vesicles with target membranes and the homotypic fusion of various membrane compartments. They belong to the AAA-type (ATPase associated with a variety of cell activities) ATPase superfamily. They include peroxin, which apparently is involved in Zellweger's syndrome. Group: Enzymes. Enzyme Commission Number: EC 3.6.4.6. 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-4708; vesicle-fusing ATPase; EC 3.6.4.6. Cat No: EXWM-4708. | |
| Vesicular Stomatitis Virus Nucleoprotein (52-59) | Vesicular Stomatitis Virus Nucleoprotein (52-59) (VSV-8), corresponding to positions 52 to 59 of the vesicular stomatitis virus (VSV) nuclear protein, is expressed in the cytosol of VSV-infected cells. CTL response to VSV in H-2Kb mice is directed against this immunodominant peptide. VSV-8 forms a complex with the mouse MHC Class I molecule H-2Kb, similar to the human HLA Class I. Synonyms: VSV-8; H-Arg-Gly-Tyr-Val-Tyr-Gln-Gly-Leu-OH; L-Leucine, L-arginylglycyl-L-tyrosyl-L-valyl-L-tyrosyl-L-glutaminylglycyl-; N5-(Diaminomethylene)-L-ornithylglycyl-L-tyrosyl-L-valyl-L-tyrosyl-L-glutaminylglycyl-L-leucine. Grade: ≥95%. CAS No. 132326-74-0. Molecular formula: C44H66N12O12. Mole weight: 955.08. | |
| 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. | |
| 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. | |
| Vespid chemotactic peptide 5e | Vespid chemotactic peptide 5e is an antibacterial peptide isolated from Vespa magnifica. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: Phe-Leu-Pro-Ile-Ile-Ala-Lys-Leu-Leu-Gly-Gly-Leu-Leu. Grade: >95%. Molecular formula: C69H118N14O14. Mole weight: 1367.79. | |
| Vespid chemotactic peptide 5f | Vespid chemotactic peptide 5f is an antibacterial peptide isolated from Vespa magnifica. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Synonyms: H-Phe-Leu-Pro-Ile-Pro-Arg-Pro-Ile-Leu-Leu-Gly-Leu-Leu-OH. Grade: >95%. Molecular formula: C74H124N16O14. Mole weight: 1461.9. | |
| 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. Grade: >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. | |
| 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 |
| Vestitol | Vestitol isolated from the herb of Lotus corniculatus L. It has phytoalexin activity. Uses: Antimicrobial activity; anti-inflammatory activity. Synonyms: (3R)-3β-(2-Hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol. Grade: 98.5%. CAS No. 35878-41-2. Molecular formula: C16H16O4. Mole weight: 272.3. | |
| 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. | |
| 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 |
| VGluT1 Antibody [E6H10] | Vesicular Glutamate Transporter 1,VGluT1. Group: Antibodies. Alternative Names: BNPI, VGLUT1, SLC17A7, Vesicular glutamate transporter 1, VGluT1, Brain-specific Na(+)-dependent inorganic phosphate cotransporter, Solute carrier family 17 member 7. CAS No. Pack Sizes: 20uL. Product ID: F3458. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. |  United States; Europe |
| 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. | |
| VH032 | VH032 is a VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. VH032 is a VHL/HIF-1? interaction inhibitor with a Kd | |
| VH285-PEG4-C4-Cl | VH285-PEG4-C4-Cl (HaloPROTAC 3) is a conjugate of ligands for E3 and 16-atom-length linker. The connector of linker is Halogen group. VH285-PEG4-C4-Cl incorporates the VH285 based VHL ligand and an alkyl/ether-based linker. VH285-PEG4-C4-Cl is a highly potent and efficacious degrader of GFP-HaloTag7 with a DC50 of 19 nM. VH285-PEG4-C4-Cl is able to induce 90 % degradation of GFP-Halotag at 625 nM. VH285-PEG4-C4-Cl binds to VHL with an IC50 of 0.54 ?M[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HaloPROTAC 3. CAS No. 1799506-07-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111997. | |
| VH298 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| VH-298 | VH-298 is a highly potent inhibitor of the VHL:HIF-? interaction with a Kd value of 80 to 90 nM. VH-298 leads to HIF-? accumulation inside HeLa cells. VH-298 is an E3 ligase Ligand, and can be used for synthesis of PROTACs[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2097381-85-4. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-100947. | |
| 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. Group: Biochemicals. Grades: Purified. CAS No. 858134-23-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 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. | |
| 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 | Vibegron is a potent, highly selective β3-adrenoceptor agonist (EC50=1.1 nM). Vibegron can be used for severe urgency urinary incontinence related to overactive bladder. CAS No. 1190389-15-1. Product ID: API1190389151. SMILES: C1C[C@@H](N[C@@H]1CC2=CC=C(C=C2)NC(=O)[C@@H]3CCC4=NC=CC(=O)N34)[C@@H](C5=CC=CC=C5)O. Category: Active Pharmaceutical Ingredients. |  |
| 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. | |
| 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. Grade: ≥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)-. Grade: ≥98%. CAS No. 1251748-32-9. Molecular formula: C12H18O3. Mole weight: 210.27. | |
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