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| Product | Description | |
|---|---|---|
| Veratric acid (Standard) | Veratric acid (Standard) is the analytical standard of Veratric acid. This product is intended for research and analytical applications. Veratric acid (3,4-Dimethoxybenzoic acid) is an orally active phenolic compound derived from vegetables and fruits, has antioxidant [1] and anti-inflammatory activities [3]. Veratric acid also acts as a protective agent against hypertension-associated cardiovascular remodelling [2]. Veratric acid reduces upregulated COX-2 expression, and levels of PGE2, IL-6 after UVB irradiation [3]. Uses: Scientific research. Group: Natural products. CAS No. 93-07-2. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N2007R. |  |
| Veratridine | Veratridine. Group: Biochemicals. Grades: Purified. CAS No. 71-62-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| Veratridine | Veratridine (3-Veratroylveracevine) is a plant neurotoxin, a voltage-gated sodium channels ( VGSCs ) agonist. Veratridine inhibits the peak current of Nav1.7, with an IC 50 of 18.39?μM. Veratridine regulates sodium ion channels mainly by activating sodium ion channels, preventing channel inactivation and increasing sodium ion flow [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 3-Veratroylveracevine. CAS No. 71-62-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N6691. | |
| VERATRIDINE | Veratridine, a pentacyclic triterpene acid compound, has been found to be a steroid-derived alkaloid neurotoxin and could be used as a voltage-gated Na+ channel opener. Synonyms: Veratrin (Amorphous); (3β,4α,16β)-4,12,14,16,17,20-Hexahydroxy-4,9-epoxycevan-3-yl 3,4-dimethoxybenzoate. Grade: ≥90% by HPLC. CAS No. 71-62-5. Molecular formula: C36H51NO11. Mole weight: 673.79. |  |
| Veratrole | Veratrole is a key compound found widely in plants that attracts pollinators. Veratrole can be used as a safe fragrance ingredient with low acute and administration toxicity [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 91-16-7. Pack Sizes: 10 mM * 1 mL; 100 g. Product ID: HY-B1812. | |
| Veratrole | Veratrole is common reagent in organic synthesis such as the synthesis of arizonins B1 and C1. Also used in the synthesis of pharmacophores of salmeterol and roflumilast as dual β2-adrenoreceptor agonists-PDE4 inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 91-16-7. Pack Sizes: 10g, 25 g. Molecular Formula: C8H10O2. US Biological Life Sciences. | Worldwide |
| Veratrole (1,2-Dimethoxybenzene) | 100g Pack Size. Group: Building Blocks, Organics. Formula: C6H4(OCH3)2. CAS No. 91-16-7. Prepack ID 10581564-100g. Molecular Weight 138.16. See USA prepack pricing. |  |
| Veratrole (1,2-Dimethoxybenzene) | 500g Pack Size. Group: Building Blocks, Organics. Formula: C6H4(OCH3)2. CAS No. 91-16-7. Prepack ID 10581564-500g. Molecular Weight 138.16. See USA prepack pricing. | |
| Veratryl Aldehyde | Veratryl Aldehyde (3,4 Dimethoxy Benzaldehyde). CAS No. 120-14-9. FEMA No. 3109. Kosher: Y. VIGON Item # 500562. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Veratryl Aldehyde Natural | Veratryl Aldehyde Natural. CAS No. 120-14-9. FEMA No. 3109. Kosher: Y. VIGON Item # 507959. Categories: Speciality Ingrdients Suppliers. | America & Internationally |
| Veratryl Aldehyde Powder | Veratryl Aldehyde Powder. CAS No. 120-14-9. FEMA No. 3109. Kosher: Y. VIGON Item # 503586. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Verbascose | analytical standard. Group: Carbohydrate standards. |  |
| Verbascoside | primary reference standard. Group: Herbal medicinal products standardsphytochemicals. Alternative Names: Acteoside, Stereospermin, trans-Verbascoside, NSC 603831, TJC 160, trans-Acteoside, Kusaginin, (3,4-Dihydroxyphenyl)ethyl O-?-rhamnopyranosyl(1?3)-4-O-caffeoyl-?-D glucopyranoside, Distinctive Phytostem Lilac, O'''-Desarabinosyllavandulifolioside A, Distinctive Active Powder SL Special, Russetinol, ?-D-Glucopyranoside, 2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-?-L-mannopyranosyl)-, 4-[3-(3,4-dihydroxyphenyl)-2-propenoate], (E)-, Verbascoside,?-D-Glucopyranoside, 2-(3,4-dihydroxyphenyl)ethyl 3-O-(6-deoxy-?-L-mannopyranosyl)-, 4-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoate]. | |
| Verbascoside | Verbascoside is isolated from Acanthus mollis, acts as an ATP-competitive inhibitor of PKC, with an IC50 of 25 μM, and has antitumor, anti-inflammatory and antineuropathic pain activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Acteoside. Product Category: Inhibitors. CAS No. 61276-17-3. Molecular formula: C29H36O15. Mole weight: 624.59. Purity: 98%+. IUPACName: Verbascoside. Density: 1.6 g/cm³. Product ID: ACM61276173. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Verbascoside | Verbascoside is isolated from Acanthus mollis , acts as an ATP-competitive inhibitor of PKC , with an IC 50 of 25 μM, and has antitumor, anti-inflammatory and antineuropathic pain activity. Uses: Scientific research. Group: Natural products. Alternative Names: Acteoside; Kusaginin; TJC160. CAS No. 61276-17-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0021. | |
| Verbenalin | Verbenalin is Verbena glycoside, with anti-inflammatory, anti-fungal anti-virus activities. Verbenalin can be used for the research of prostatitis. Verbenalin can reduce cerebral ischemia-reperfusion injury [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 548-37-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N2014. | |
| Verbenalin | Cornin has protective potential against cerebral ischemia injury and its protective effects may be due to amelioration of cerebral mitochondrial function and its antioxidant property. Synonyms: cornin; methyl (1S,4aS,7S,7aR)-1-(beta-D-glucopyranosyloxy)-7-methyl-5-oxo-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate. Grade: >98%. CAS No. 548-37-8. Molecular formula: C17H24O10. Mole weight: 388.37. | |
| Verbenalin (Verbenaloside, Cornin) | Verbenalin (Verbenaloside, Cornin). Group: Biochemicals. Alternative Names: Verbenaloside; Cornin. Grades: Plant Grade. CAS No. 548-37-8. Pack Sizes: 10mg. Molecular Formula: C17H24O10, Molecular Weight: 388.365999999999. US Biological Life Sciences. | Worldwide |
| Verbenone | Verbenone ((-)-Verbenone) is a natural terpene in leaves of the tree, Verbena officinalis [1]. Verbenone has anti-aggregation pheromone and interrupts the attraction of bark beetles to their aggregation pheromones [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (-)-Verbenone. CAS No. 1196-01-6. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-N6661. | |
| Vercirnon | Vercirnon (GSK1605786A) is an orally bioavailable, selective, and potent antagonist of CCR9. Vercirnon inhibits CCR9-mediated Ca2+ mobilization and chemotaxis on Molt-4 cells with IC50 values of 5.4 and 3.4 nM, respectively. Vercirnon is selective for CCR9 over CCR1-12 and CX3CR1-7 (IC50s>10 ?M for all). Vercirnon is an equipotent inhibitor of CCL25-directed chemotaxis of both splice forms of CCR9 (CCR9A and CCR9B) with IC50 values of 2.8 and 2.6 nM, respectively[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GSK-1605786; CCX282-B; Traficet-EN. CAS No. 698394-73-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15724. | |
| Verdalia A | Verdalia A. CAS No. 53018-24-9. VIGON Item # 503255. Categories: Speciality Ingrdients Suppliers, tropical indene, Fragrances, Perfumers. | America & Internationally |
| Verdamycin | It is produced by the strain of Micromonospora grisea. Verdamycin has anti-bacterial effect. In in vivo test of mice, it has protective effect on the infection of Escherichia coli, Pseudomonas aeruginosa and Staphylococcus. Synonyms: Verdamicin; O-3-Deoxy-4-C-methyl-3-(methylamino)-beta-L-arabinopyranosyl-(1-6-)-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-beta-L-threo-hept-4-enopyranosyl-(1-4))-2-deoxy-D-streptamine. Grade: 98%. CAS No. 49863-48-1. Molecular formula: C20H39N5O7. Mole weight: 461.55. | |
| Verdinexor | Verdinexor(KPT-335) is a novel, orally bioavailable selective inhibitor of nuclear export (SINE), inhibits nuclear export protein Exportin 1(XPO1/CRM1) against canine tumor cell lines; also reduce influenza virus replication in vitro and in vivo. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KPT-335. CAS No. 1392136-43-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15970. | |
| Verdiperstat | Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase (MPO) inhibitor, with an IC 50 of 630 nM, and can be used in the research of neurodegenerative brain disorders. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD3241. CAS No. 890655-80-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-17646. | |
| Verdoracine | Verdoracine. CAS No. 14374-92-6. VIGON Item # 503256. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, 2-propenyl-para-cymene. | America & Internationally |
| Verdox | Verdox (Ortho Butyl Cyclohexyl Acetate). CAS No. 88-41-5. VIGON Item # 500867. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Verekitug | Verekitug is an anti- CRLF2 human IgG1 κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2768386-15-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990774. | |
| Vericiguat | Vericiguat (BAY1021189) is a potent, orally available and soluble guanylate cyclase stimulator. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY1021189. CAS No. 1350653-20-1. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16774. | |
| Verinurad | Verinurad (RDEA3170) is a highly potent and specific URAT1 inhibitor with an IC 50 of 25 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RDEA3170. CAS No. 1352792-74-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16733. | |
| Verinurad Impurity4 | Verinurad Impurity4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 125305-75-1. Molecular formula: C9H11NO2S. Mole weight: 197.25. Catalog: APB125305751. | |
| Verinurad Impurity5 | Verinurad Impurity5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1016858-18-6. Molecular formula: C8H6N2O2S. Mole weight: 194.21. Catalog: APB1016858186. | |
| Verinurad Impurity9 | Verinurad Impurity9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1019535-82-0. Molecular formula: C10H9NO2S. Mole weight: 207.25. Catalog: APB1019535820. | |
| Verlamelin | It is a depsipeptide antibiotic produced by the strain of Fungi MF 4683. It has anti-fungal activity against plant pathogens. Synonyms: MSD-A-43F; Verlamelin; A-43F; Antibiotic MSD-A-43F; Antibiotic A-43F; Cyclo[D-Tyr-5-L-Val-oxytetradecanoyl-D-aThr-D-Ala-L-Pro-L-Glu(NH2)-]. CAS No. 74758-64-8. Molecular formula: C45H71N7O11. Mole weight: 886.09. | |
| Verlukast | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (dimethylamino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019; MK 679; R-(-)-MK 571. Grades: Highly Purified. CAS No. 120443-16-5. Pack Sizes: 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Verlukast-d6 | A receptor antagonist for the treatment of respiratory diseases. Group: Biochemicals. Alternative Names: 3- [ [ (R) - [3- [ (1E) -2- (7-Chloro-2-quinolinyl) ethenyl] phenyl] [ [3- (di (methyl-d3) amino) -3-oxopropyl] thio] methyl] thio] -propanoic Acid; L 668019-d6; MK 679-d6; R-(-)-MK 571-d6. Grades: Highly Purified. CAS No. 153698-86-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Verlukast-[d6] | Verlukast-[d6]. Uses: A receptor antagonist for the treatment of respiratory diseases. Synonyms: Verlukast D6. Grade: 95% atom D. CAS No. 153698-86-3. Molecular formula: C26H21D6ClN2O3S2. Mole weight: 521.12. | |
| Vermiculine | Vermiculine is produced by the strain of Pen. vermiculatum CCM-F-2. It has anti-protozoal and anti-tumor effects, and it also has a less potent effect against gram-positive bacteria. Synonyms: Vermiculin; NSC657321; (-)-Vermiculine; 1,11-diene-2,5,10,13-tetrone,8,16-bis(2-oxopropyl)-, (3E,8S,11E,16S)-. CAS No. 37244-00-1. Molecular formula: C20H24O8. Mole weight: 392.40. | |
| Vermistatin | It is a new metabolite from mine-dwelling Penicillium vermiculatum. It is an antibiotic with cytotoxic effects. Synonyms: (R,E)-4,6-dimethoxy-3-(4-oxo-6-(prop-1-en-1-yl)-4H-pyran-3-yl)isobenzofuran-1(3H)-one; Fijiensin; (-)-Fijiensin; NSC 656107; 1(3H)-Isobenzofuranone, 4,6-dimethoxy-3-(4-oxo-6-(1-propenyl)-4H-pyran-3-yl)-, (R)-; 5-(4,6-Dimethoxy-3R-phthalidy)-2-(1E)-propenyl-4H-pyran-4-one. CAS No. 72669-21-7. Molecular formula: C18H16O6. Mole weight: 328.32. | |
| Vernakalant Hydrochloride | Vernakalant hydrochloride is a mixed voltage- and frequency-dependent Na + and atria-preferred K + channel blocker. IC 50 for block by Vernakalant of wild-type and mutant Kv1.5 channels Fractional block is 13.35±0.93 μM, 0.61±0.03 μM, and 1.63±0.09 μM for Kv1.5 channel wt , Kv1.5 channel I508F , Kv1.5 channel T479A , respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RSD1235 hydrochloride. CAS No. 748810-28-8. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14183. | |
| Vernaldehyde ® | Vernaldehyde ®. CAS No. 66327-54-6. Kosher: Y. VIGON Item # 500415. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Vernamycin B | Vernamycin B is originally isolated from Str. loidensis. Vernamycin B has an antimicrobial effect, but is less effective against gram-negative bacteria and mycobacteria. CAS No. 9040-14-6. Molecular formula: C62H85N7O16S. Mole weight: 1216.44. | |
| Verosudil | Verosudil (AR-12286) is a ROCK inhibitor. Verosudil has equal inhibitory activity against ROCK1 and ROCK2 (Ki: 2 nM). Verosudil is less selective for PKA, PKCT, MRCKA, and CAM2A (Ki: 69 nM, 9322 nM, 28 nM, 5855 nM, respectively). Verosudil increases trabecular outflow capacity to reduce intraocular pressure. Verosudil is useful in the study of glaucoma and ocular hypertension[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AR-12286. CAS No. 1414854-42-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-16758. | |
| Verrucarin A | Verrucarin A (Muconomycin A), a Type D macrocyclic mycotoxin derived from the pathogen fungus Myrothecium verrucaria , is an inhibitor of protein synthesis. Verrucarin A inhibits growth of leukemia cell lines and activates caspases and apoptosis and inflammatory signaling in macrophages. Verrucarin A effectively increased the phosphorylation of p38 MAPK and diminished the phosphorylation of ERK/Akt. Verrucarin A caused cell cycle deregulation through the induction of p21 and p53 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Muconomycin A. CAS No. 3148-9-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-107426. | |
| Verrucarin A | It is produced by the strain of Myrothecium verrucaria NRRL 3003. Verrucarin A has the effect of anti-Gram-negative bacteria and fungi, inhibiting Newcastle disease virus, tobacco Mosaic virus, and S-37 sarcoma and Yoshida sarcoma in animals. Synonyms: Muconomycin A; Antibiotic 379Y; VER A; (4S,5R,10E,12Z,16R,16aS,17S,18R,19aR,23aR)-4-hydroxy-5,16a,21-trimethyl-4,5,6,7,16,16a,22,23-octahydro-3H,18H,19aH-spiro[16,18-methano[1,6,12]trioxacyclooctadecino[3,4-d]chromene-17,2'-oxirane]-3,9,14-trione; NSC 126728. Grade: 95%. CAS No. 3148-9-2. Molecular formula: C27H34O9. Mole weight: 502.55. | |
| Verrucarin A from Myrothecium sp. | ?85.0% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Verrucarin B | It is produced by the strain of Myrothecium verrucaria NRRL 3003. Verrucarin B has an effect on Ascites carcinoma, also has a weak inhibitory effect on fungi. Synonyms: (2'S,3'R)-2'-Deoxy-2',3'-oxyverrucarin A. CAS No. 2290-11-1. Molecular formula: C27H32O9. Mole weight: 500.54. | |
| Verrucarin J | Verrucarin J (Muconomycin B) is a metabolite of the Myrothecium fungus family. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Muconomycin B. Product Category: Inhibitors. Appearance: Solid. CAS No. 4643-58-7. Molecular formula: C27H32O8. Mole weight: 484.5. Purity: 95%+. IUPACName: (1R,3R,8R,12E,18E,20Z,24R,25S,26S)-5,13,25-Trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,17,22-trione. Canonical SMILES: CC1=C[C@@H]2[C@]3(COC(/C=C(C)/CCOC(/C=C/C=C\C(OC4[C@]3(C)[C@@]5([C@H](O2)C4)CO5)=O)=O)=O)CC1. Product ID: ACM4643587-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Verrucarin A. | |
| Verrucarin J | Verrucarin J is produced by the strain of Myrothecium verrucaria NRRL 3003. The ED50 of Verrucarin J on giant cell tumor P-815 cells was about 0.001 μg/mL. Uses: For research used only. Synonyms: Muconomycin B; 2',3'-Didehydro-2'-deoxyverrucarin A; Verrucarin A, 2',?3'-didehydro-2'-deoxy-, (2'E)?-; Verrucrin J; Verrucosporin J. Grade: ≥98%. CAS No. 4643-58-7. Molecular formula: C27H32O8. Mole weight: 484.54. | |
| Verrucarin K | Verrucarin K is produced by the strain of Myrothecium verrucaria NRRL 3003. The ED50 of Verrucarin K on giant cell tumor P-815 cells was about 0.001 μg/mL. Synonyms: BRN 1276841; Verrucarin A, 12,13-deepoxy-12,13-didehydro-. CAS No. 63739-93-5. Molecular formula: C27H34O8. Mole weight: 486.55. | |
| Verrucofortine | A diketopiperazine alkaloid derived from tryptophan and leucine. It is a fungal metabolite isolated from penicillium verrucosum. It exhibits no apparent toxicity in mice even at high doses in vivo. Synonyms: Fructigenine B; Verrucosine; Verrucozine; (-)-Verrucofortine; (3S-(3alpha,5aalpha,10balpha,11abeta))-6-Acetyl-10b-(1,1-dimethyl-2-propenyl)-6,10b,11,11a-tetrahydro-3-(2-methylpropyl)-2H-pyrazino(1',2':1,5)pyrrolo(2,3-b)indole-1,4-(3H,5aH)-dione; (3S,5aR,10bR,11aS)-6-acetyl-10b-(1,1-dimethyl-2-propen-1-yl)-6,10b,11,11a-tetrahydro-3-(2-methylpropyl)-2H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione. Grade: >99% by HPLC. CAS No. 113706-21-1. Molecular formula: C24H31N3O3. Mole weight: 409.52. | |
| Verrucofortine (Fructigenine B, Verrucosine, Verrucozine) | Verrucofortine is an alkaloidal diketopiperazine derived from tryptophan and leucine isolated from Penicillium species. There are no reports of intensive investigation of verrucofortine. In vivo, mice showed no apparent toxic effects at high doses. Group: Biochemicals. Alternative Names: Fructigenine B, Verrucosine, Verrucozine. Grades: Highly Purified. CAS No. 113706-21-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Verruculogen | Verruculogen is a tremorgenic mycotoxin isolated from penicillium verruculosu. It can inhibit the K+ channel activated by ca2+, and is a cell cycle inhibitor that prevents M phase division. Synonyms: TR 1 toxin. Grade: >95% by HPLC. CAS No. 12771-72-1. Molecular formula: C27H33N3O7. Mole weight: 511.57. | |
| Verruculogen | Verruculogen is a tremorgenic mycotoxin first isolated from Penicillium verruculosum in 1972 and the structure resolved as an indole alkaloid in 1974. Subsequent investigations have shown that verruculogen is produced by several species of Penicillium and Aspergillus and its presence is a useful taxonomic phenotypic marker. The tremorgenic action of verruculogen is complex but is associated with increases in spontaneous glutamate and aspartate release, decreases in GABA levels and, at toxic doses, an increase in the number and decrease in the affinity of DHP receptors in rat cortex. In in vitro guinea pig ileum preparations, verruculogen causes an increase in contractile responses due to electrical field stimulation, attributed to enhancement of acetylcholine from presynaptic nerve terminals. Verruculogen also inhibits Ca2+-activated K+ channels and is a cell cycle inhibitor blocking division at the M phase. Group: Biochemicals. Grades: Highly Purified. CAS No. 12771-72-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Verruculogen (NA 209A, TR 1) | Fumitremorgin-type alkaloid. Tremorgenic neurotoxic mycotoxin. Selective blocker of KCa1.1 (high-conductance Ca2+-activated K+; BK; maxi-K) channels. Decreases GABA levels in CNS. Increases spontaneous glutamate and aspartate release. At toxic doses, increases the number and decreases the affinity of DHP receptors in rat cortex. Cell cycle inhibitor at the M phase. Inhibits calmodulin and PKC activity. Has apoptotic effects on human T lymphocytes. Stimulates the growth of seedling roots of buckwheat. Group: Biochemicals. Alternative Names: (5R, 10S, 10aR) -1, 10, 10a, 14, 14aS, 15bS-hexahydro-10, 10a-dihydroxy-7-methoxy-2, 2-dimethyl-5- (2-methyl-1-propen-1-yl) -5H, 12H-3, 4-dioxa-5a, 11a, 15a-triazacyclooct [lm]indeno [5, 6-b]fluorene-11, 15 (2H, 13H) -dione. Grades: Highly Purified. CAS No. 12771-72-1. Pack Sizes: 1mg, 5mg. Molecular Formula: C27H33N3O7. US Biological Life Sciences. | Worldwide |
| verruculogen prenyltransferase | Found in a number of fungi. Catalyses the last step in the biosynthetic pathway of the indole alkaloid fumitremorgin A. The enzyme from the fungus Neosartorya fischeri is also active with fumitremorgin B and 12α,13α-dihydroxyfumitremorgin C. Group: Enzymes. Synonyms: FtmPT3. Enzyme Commission Number: EC 2.5.1.107. 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-2723; verruculogen prenyltransferase; EC 2.5.1.107; FtmPT3. Cat No: EXWM-2723. |  |
| verruculogen synthase | Requires Fe2+ and ascorbate. Found in the fungus Aspergillus fumigatus. Both atoms of a dioxygen molecule are incorporated into verruculogen. Involved in the biosynthetic pathways of several indole alkaloids such as fumitremorgin A. Group: Enzymes. Synonyms: fmtF (gene name); FmtOx1. Enzyme Commission Number: EC 1.14.11.38. 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-0656; verruculogen synthase; EC 1.14.11.38; fmtF (gene name); FmtOx1. Cat No: EXWM-0656. | |
| versatile peroxidase | A hemoprotein. This ligninolytic peroxidase combines the substrate-specificity characteristics of the two other ligninolytic peroxidases, EC 1.11.1.13, manganese peroxidase and EC 1.11.1.14, lignin peroxidase. Unlike these two enzymes, it is also able to oxidize phenols, hydroquinones and both low- and high-redox-potential dyes, due to a hybrid molecular architecture that involves multiple binding sites for substrates. Group: Enzymes. Synonyms: VP; hybrid peroxidase; polyvalent peroxidase; reactive-black-5:hydrogen-peroxide oxidoreductase. Enzyme Commission Number: EC 1.11.1.16. CAS No. 42613-30-9, 114995-15-2. Versatile Peroxidase. 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-0497; versatile peroxidase; EC 1.11.1.16; 42613-30-9, 114995-15-2; VP; hybrid peroxidase; polyvalent peroxidase; reactive-black-5:hydrogen-peroxide oxidoreductase. Cat No: EXWM-0497. | |
| Versicolin | Versicolin is originally isolated from Asp. versicolor. It only has antibacterial effect on filamentous fungi, and has no inhibitory effect on yeast-like fungi and bacteria. Synonyms: 2,3,6-Trihydroxytoluene; Toluene-2,3,6-triol; BRN 2249549; 1-methyl-2,3,6-trihydroxybenzene. CAS No. 4389-44-0. Molecular formula: C7H8O3. Mole weight: 140.14. | |
| Versicolorin A | Versicolorin A is a quinone antibiotic produced by the strain of Asp. versicolor. It has the effect of anti-tuberculosis Mycobacterium H37RV and other mycobacteria. Synonyms: Z-(-)-4,6,8-Trihydroxy-3a,12a-dihydroanthra(2,3-b)furo(3,2-d)furan-5,10-dione; NSC 274542; (3aS,12aR)-4,6,8-trihydroxy-3a,12a-dihydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione. Grade: 98%. CAS No. 6807-96-1. Molecular formula: C18H10O7. Mole weight: 338.27. | |
| Versicolorin B | Versicolorin B is a quinone antibiotic produced by the strain of Asp. versicolor. It has the effect of anti-tuberculosis Mycobacterium H37RV and other mycobacteria. Synonyms: (3aS,12aR)-4,6,8-trihydroxy-2,3,3a,12a-tetrahydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione; Anthra(2,3-b)furo(3,2-d)furan-5,10-dione, 2,3,3a,12a-tetrahydro-4,6,8-trihydroxy-, cis-(+-)-. CAS No. 4331-22-0. Molecular formula: C18H12O7. Mole weight: 340.28. | |
| versicolorin B synthase | Isolated from the aflatoxin-producing mold Aspergillus parasiticus. Involved in aflatoxin biosynthesis. Group: Enzymes. Synonyms: versiconal cyclase; VBS. Enzyme Commission Number: EC 4.2.1.143. 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-4984; versicolorin B synthase; EC 4.2.1.143; versiconal cyclase; VBS. Cat No: EXWM-4984. | |
| versiconal hemiacetal acetate esterase | Isolated from the mold Aspergillus parasiticus. Involved in a metabolic grid that leads to aflatoxin biosynthesis. Group: Enzymes. Synonyms: VHA esterase. Enzyme Commission Number: EC 3.1.1.94. 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-3523; versiconal hemiacetal acetate esterase; EC 3.1.1.94; VHA esterase. Cat No: EXWM-3523. | |
| versiconal hemiacetal acetate reductase | Isolated from the mold Aspergillus parasiticus. Involved in a metabolic grid that leads to aflatoxin biosynthesis. Group: Enzymes. Synonyms: VHA reductase; VHA reductase I; VHA reductase II; vrdA (gene name). Enzyme Commission Number: EC 1.1.1.353. 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-0269; versiconal hemiacetal acetate reductase; EC 1.1.1.353; VHA reductase; VHA reductase I; VHA reductase II; vrdA (gene name). Cat No: EXWM-0269. | |
| Vertenex | Vertenex (Para Butyl Cyclohexyl Acetate). CAS No. 32210-23-4. VIGON Item # 501612. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. | America & Internationally |
| Verteporfin | Verteporfin is a small molecule that inhibits TEAD-YAP association and YAP-induced liver overgrowth. It is also a potent second-generation photosensitizing agent derived from porphyrin. Verteporfin is an autophagy inhibitor. Verteporfin inhibits cell proliferation and induces apoptosis. Group: Inhibitors. Alternative Names: CL 318952. CAS No. 129497-78-5. Pack Sizes: 10mg. Product ID: S1786. Formula: C41H42N4O8. Smiles: COC(=O)CCC1=C(C)C2=CC3=NC(=CC4=C(C)C(=C([NH]4)C=C5N=C(C=C1[NH]2)C(=C5C)CCC(O)=O)C=C)C6=CC=C(C(C(=O)OC)C36C)C(=O)OC. Storage Conditions: 3 years-20°C powder. |  United States; Europe |
| Verteporfin | Verteporfin (CL 318952) is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as age-related macular degeneration. Verteporfin is a YAP inhibitor which disrupts YAP-TEAD interactions. Verteporfin induces cell apoptosis. Verteporfinis an autophagy inhibitor that blocks autophagy at an early stage by inhibiting autophagosome formation. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Verteprofin; Verteporphin; trans-3,4-Dicarboxy-4,4a-dihydro-4a,8,14,19-tetramethyl-18-vinyl-23H,25H-benzo(b)porphine-9,13-dipropionic acid 3,4,9-trimethyl ester; Visudyne; VERTEPORFIN (200 MG). Product Category: Inhibitors. Appearance: Powder. CAS No. 129497-78-5. Molecular formula: C41H42N4O8. Mole weight: 1437.61. Purity: 0.95. IUPACName: Verteporfin. Canonical SMILES: C[C@]1(/C2=C/C(N3)=C4C)C(C(/C=C(C(C)=C/5C=C)\NC5=C/C6=N/C(C(CCC(OC)=O)=C6C)=C\C3=C4CCC(O)=O)=N2)=CC=C(C(OC)=O)[C@H]1C(OC)=O.C[C@]7(/C8=C/C(N9)=C%10C)C(C(/C=C(C(C)=C/%11C=C)\NC%11=C/C%12=N/C(C(CCC(O)=O)=C%12C)=C\C9=C%10CCC(OC)=O)=N8)=CC=C(C(OC)=O)[C@H]7C(OC)=O. Product ID: ACM129497785-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Verteporfin | Verteporfin (CL 318952) is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as age-related macular degeneration. Verteporfin is a YAP inhibitor which disrupts YAP-TEAD interactions. Verteporfin induces cell apoptosis [1]. Verteporfinis an autophagy inhibitor that blocks autophagy at an early stage by inhibiting autophagosome formation [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CL 318952. CAS No. 129497-78-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0146. | |
| Verteporfin | Verteporfin. Group: Biochemicals. Alternative Names: CL 318952; Visudyne; (4R,4aS)-rel-24H,26H-Benzo[b]porphine-9,13-dipropanoic acid, 18-ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-monomethyl Ester. Grades: Highly Purified. CAS No. 129497-78-5. Pack Sizes: 10mg. Molecular Formula: C41H44N4O9, Molecular Weight: 736.81. US Biological Life Sciences. | Worldwide |
| Verteporfin | Verteporfin Inhibitor. Uses: Scientific use. Product Category: T3112. CAS No. 129497-78-5. |  |
| Verteporfin Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
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