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| Product | Description | |
|---|---|---|
| Vegetable Oil, Hydrogenated | Hydrogenated vegetable oil is a mixture of triglycerides of fatty acids. The two types that are defined in the USP are characterized by their physical properties. Hydrogenated vegetable oil type I occurs in various forms, e.g.fine powder, flakes, or pellets. The color of the material depends on the manufacturing process and the form. In general, the material is white to yellowish-white with the powder grades appearing more white-colored than the coarser grades. Synonyms: Hydrogenated cottonseed oil: Akofine; Lubritab; Sterotex. CAS No. 68334-00-9. Product ID: PE-0444. Category: Dispersants. Product Keywords: Pharmaceutical Excipients; Excipients for Liquid Dosage Form; Vegetable Oil, Hydrogenated; Dispersion Excipients; Dispersants; 68334-00-9; 68334-00-9. UNII: NA. Chemical Name: Hydrogenated vegetable oil [68334-00-9]. Hydrogenated soybean oil [8016-70-4]. Grade: Pharmceutical Excipients. Administration route: Oral; rectal and vaginal and topical. Dosage Form: Oral capsules and tablets; rectal and vaginal suppositories and topical preparations. Stability and Storage Conditions: Hydrogenated vegetable oil type I is a stable material; typically it is assigned a 2-year shelf-life. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Hydrogenated vegetable oil type I is prepared from refined vegetable oils, which are hydrogenated using a catalyst. App |  |
| VEGF165 from mouse | recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy. |  |
| VEGF165 from rat | recombinant, expressed in E. coli, ?98% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| VEGF165 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| VEGFA Antibody [G24N11] | VEGFA Antibody [G24N11]. Group: Antibodies. Pack Sizes: 20uL. Product ID: F2527. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. |  United States; Europe |
| VEGF-C from mouse | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| VEGF-C from rat | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| VEGF-C human | recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| VEGF-C human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE), ?95% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF-D human | recombinant, expressed in HEK 293 cells, ?95% (SDS-PAGE), ?95% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF human | Animal-component free, recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Inhibitor, CBO-P11 | The VEGF Inhibitor, CBO-P11 controls the biological activity of VEGF. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Inhibitor, Flt???? | The VEGF Inhibitor, Flt2-11 controls the biological activity of VEGF. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Inhibitor, V1 | The VEGF Inhibitor, V1 controls the biological activity of VEGF. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR2/Flt3/c-Kit Inhibitor - CAS 796967-10-7 | The VEGFR2/Flt3/c-Kit Inhibitor, also referenced under CAS 796967-10-7, controls the biological activity of VEGFR2/Flt3/c-Kit. This small molecule/inhibitor is primarily used for Activators/Inducers applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR2-IN-2 | VEGFR2-IN-2 (compound 6e) is a potent and selective VEGFR2 inhibitor with an IC 50 of 19.32 nM. VEGFR2-IN-2 can be used for researching. Uses: Scientific research. Group: Signaling pathways. CAS No. 737818-56-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147133. |  |
| VEGFR-2-IN-29 | VEGFR-2-IN-29 (Compound 5) is a VEGFR-2 inhibitor with an IC 50 of 16.5 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 62802-77-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148040. | |
| VEGFR-2-IN-39 | VEGFR-2-IN-39 (PROTAC-5) is a PROTAC targeting VEGFR-2 ( IC 50 : 208.6 nM). VEGFR-2-IN-39 has low toxicity.VEGFR-2-IN-39 inhibits the proliferation of EA.hy926, one of HUVECs, in a concentration-dependent manner, with an IC 50 of 38.65 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2353417-86-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-160259. | |
| VEGFR-2-IN-5 hydrochloride | VEGFR-2-IN-5 hydrochloride is a VEGFR2 inhibitor extracted from patent WO2013055780A1, Page 69 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2700435-52-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18625A. | |
| VEGFR2/KDR Antagonist | VEGFR2/KDR Antagonist is a VEGFR2/KDR heptapeptide antagonist that inhibits VEGF binding to KDR and prevents VEGF-induced angiogenesis in vivo. Synonyms: H-Ala-Thr-Trp-Leu-Pro-Pro-Arg-OH. Molecular formula: C40H61N11O9. Mole weight: 840.0. |  |
| VEGFR2/KDR fragment 1 (614-624) | VEGFR2/KDR fragment 1 (614-624). | |
| VEGFR2 Kinase Inhibitor I - CAS 15966-93-5 | The VEGFR2 Kinase Inhibitor I, also referenced under CAS 15966-93-5, controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR2 Kinase Inhibitor II - CAS 288144-20-7 | The VEGFR2 Kinase Inhibitor II, also referenced under CAS 288144-20-7, controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR2 Kinase Inhibitor VII, SKLB1002 | The VEGFR2 Kinase Inhibitor VII, SKLB1002 controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR2 Kinase Inhibitor VII, SKLB1002 (VEGFR Tyrosine Kinase Inhibitor XXXV, 6,7-Dimethoxy-4-(5-methyl-1,3,4-thiadiazol-2-ylthio)quinazoline, Vascular Endothelial Growth Factor Receptor 2 Kinase Inhibitor VII) | A cell-permeable quinazoline that acts as a potent, ATP-binding site-targeting, VEGFR2-selective inhibitor (IC50=32nM), while exhibiting much reduced or little activity against 16 other kinases. An effective antiangiogenesis agent (98% inhibition of HUVEC tube formation at 10uM; 80% inhibition of zebrafish embryos intersegmental vessel growth at 2.5uM) that significantly suppresses SW620- and HepG2-derived tumor growth in mice (by 72% and 63%, respectively, in 18 days; 100mg/kg/day; i.p.) in vivo. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| VEGFR2 Kinase Inhibitor VI, Ki8751 - CAS 228559-41-9 | The VEGFR2 Kinase Inhibitor VI, Ki8751, also referenced under CAS 228559-41-9, controls the biological activity of VEGFR2 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR3 Kinase Inhibitor, MAZ51 - CAS 163655-37-6 | The VEGFR3 Kinase Inhibitor, MAZ51, also referenced under CAS 163655-37-6, controls the biological activity of VEGFR3 Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Receptor-1 (Flt-1)/Fc Chimera from mouse | ?90% (SDS-PAGE), recombinant, expressed in NSO cells, lyophilized powder, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Receptor-1 (Flt-1)/Fc Chimera human | >90% (SDS-PAGE), recombinant, expressed in baculovirus infected Sf21 cells, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| VEGF Receptor 2 Antibody [J9N19] | CD309 (FLK1),Flk-1,VEGF Receptor 2,VEGFR-2. Group: Antibodies. Alternative Names: CD309,Flk-1,VEGF Receptor 2,VEGFR-2. Pack Sizes: 20uL. Product ID: F3049. Storage Conditions: -20°C (avoid freeze-thaw cycles), 2 years. | United States; Europe |
| VEGF Receptor-2 (Flk-1, KDR)/Fc Chimera human | >90% (SDS-PAGE), recombinant, expressed in NSO cells, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR-IN-1 | VEGFR-IN-1 (compound 3) is a potent angiogenesis inhibitor with IC 50 s of 0.02, 0.18, 0.24 7.3, and 7 μM for KDR , Flt-1 , c-Kit, EGF-R, and c-Src, respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 269390-69-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101219. | |
| VEGFR/Tie-2/PDGFR Tyrosine Kinase Inhibitor | The VEGFR/Tie-2/PDGFR Tyrosine Kinase Inhibitor controls the biological activity of VEGFR/Tie-2/PDGFR. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR Tyrosine Kinase Inhibitor II - CAS 269390-69-4 | The VEGFR Tyrosine Kinase Inhibitor II, also referenced under CAS 269390-69-4, controls the biological activity of VEGFR Tyrosine Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR Tyrosine Kinase Inhibitor V | The VEGFR Tyrosine Kinase Inhibitor V controls the biological activity of VEGFR Tyrosine Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| VEGFR Tyrosine Kinase Inhibitor VI, AAL-993 - CAS 269390-77-4 | The VEGFR Tyrosine Kinse Inhibitor VI, ALL-993, also referenced under CAS 269390-77-4, controls the biological activity of VEGFR Tyrosine Kinase. This small molecule/inhibitor is primarily used for Cancer applications. Group: Fluorescence/luminescence spectroscopy. | |
| Vejovine (23-82) | Vejovine (23-82) is a new type of antibiotic peptide derived from scorpion venom, which shows significant and effective antibacterial activity against clinical isolates of Gram-negative multi-drug resistant strains of Escherichia coli, Pseudomonas aerμginosa and Acinetobacter baumannii. Synonyms: Gly-Ile-Trp-Ser-Ser-Ile-Lys-Asn-Leu-Ala-Ser-Lys-Ala-Trp-Asn-Ser-Asp-Ile-Gly-Gln-Ser-Leu-Arg-Asn-Lys-Ala-Ala-Gly-Ala-Ile-Asn-Lys-Phe-Val-Ala-Asp-Lys-Ile-Gly-Val-Thr-Pro-Ser-Gln-Ala-Ala-Ser-Met-Thr-Leu-Asp-Glu-Ile-Val-Asp-Ala-Met-Tyr-Tyr-Asp. | |
| Velagliflozin | Velagliflozin is an orally available sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor, with anti-diabetic activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 946525-65-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018. | |
| Velagliflozin proline | Velagliflozin proline is an oral sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor with antidiabetic activity. Velagliflozin proline reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1539295-26-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018A. | |
| Veldoreotide TFA | Veldoreotide (DG3173) TFA a somatostatin analogue, binds to and activate the somatostatin receptors (SSTR) 2, 4, and 5. Veldoreotide TFA inhibits growth hormone (GH) secretion in adenomas compared with Octreotide (HY-P0036). Veldoreotide has the potential to be used as pain modulating agent [1]. Uses: Scientific research. Group: Peptides. Alternative Names: DG3173 TFA; PTR-3173 TFA. CAS No. 2126831-23-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0024A. | |
| Veligrotug | Veligrotug is an IgG1-kappa, anti- IGF1R (insulin-like growth factor 1 receptor, CD221) chimeric monoclonal antibody [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2728655-31-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990084. | |
| Velimogene aliplasmid | Velimogene aliplasmid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: velimogene;Velimogene aliplasmid. Product Category: Heterocyclic Organic Compound. CAS No. 296251-72-4. Product ID: ACM296251724. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Veliparib | ABT-888 is a potent, orally bioavailable PARP-1/-2 inhibitor shown to potentiate DNA damaging agents. The ability to potentiate temozolomide (TMZ) and develop a biological marker for PARP inhibition was evaluated in vivo. Group: Biochemicals. Alternative Names: 2-[(2R)-2-Methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide; A 861695; ABT 888. Grades: Purified. CAS No. 912444-00-9. Pack Sizes: 10mg, 25mg, 50mg. US Biological Life Sciences. | Worldwide |
| Veliparib | Veliparib (ABT-888) is a potent PARP inhibitor, inhibiting PARP1 and PARP2 with K i s of 5.2 and 2.9 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888. CAS No. 912444-00-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10129. | |
| Veliparib (ABT-888) | Veliparib (ABT-888, NSC 737664) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM in cell-free assays, respectively. It is inactive to SIRT2. Veliparib increases autophagy and apoptosis. Phase 3. Group: Inhibitors. Alternative Names: NSC 737664. CAS No. 912444-00-9. Pack Sizes: 1g. Product ID: S1004. Formula: C13H16N4O. Smiles: CC1(CCCN1)C2=NC3=C(C=CC=C3N2)C(=O)N. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| Veliparib dihydrochloride | Veliparib (dihydrochloride) is a potent inhibitor of PARP1 and PARP2 with K i s of 5.2 nM and 2.9 nM in cell-free assays, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888 dihydrochloride. CAS No. 912445-05-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10130. | |
| Vellosimine | Vellosimine is a natural alkaloid found in the herbs of Rauvolfia verticillata. Synonyms: 4-ethyl-4-phenyl-piperidine-2,6-dione; 2,6-Piperidinedione,4-ethyl-4-phenyl. Grade: >95%. CAS No. 6874-98-2. Molecular formula: C19H20N2O. Mole weight: 292.4. | |
| vellosimine dehydrogenase | Also acts on related alkaloids with an endo-aldehyde group as vellosimine (same stereochemistry at C-16) but only slight activity with exo-aldehydes. Detected in many cell suspension cultures of plants from the family Apocynaceae. Group: Enzymes. Enzyme Commission Number: EC 1.1.1.273. CAS No. 86777-26-6. 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-0180; vellosimine dehydrogenase; EC 1.1.1.273; 86777-26-6. Cat No: EXWM-0180. |  |
| Velnacrine maleate | Velnacrine maleate (HP 029) is an orally active cholinesterase inhibitor that can be used for the research of Alzheimer's disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HP 029; Hydroxytacrine maleate. CAS No. 118909-22-1. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W011246. | |
| Velneperit | Velneperit (S-2367) is a novel neuropeptide Y (NPY) Y5 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S2367. CAS No. 342577-38-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14423. | |
| Veloutone | Veloutone. CAS No. 65443-14-3. VIGON Item # 502847. Categories: Speciality Ingrdients Suppliers, Fragrances, fruity cyclopentanone, Perfumers. |  America & Internationally |
| Velpatasvir | Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstructural protein 5A (NS5A) inhibitor with activity against genotype 1 (GT1) to GT6 HCV replicons. Velpatasvir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 2.16 μM [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-5816. CAS No. 1377049-84-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12530. | |
| Velpatasvir | Velpatasvir. Alternative Names: (2S,4S)-TERT-BUTYL 2-(5-(2-((2S,5S)-1-((S)-2-((METHOXYCARBONYL)AMINO)-3-METHYLBUTANOYL)-5-METHYLPYRROLIDIN-2-YL)-1,11-DIHYDROISOCHROMENO[4',3':6,7]NAPHTHO[1,2-D]IMIDAZOL-9-YL)-1H-IMIDAZOL-2-YL)-4-(METHOXYMETHYL)PYRROLIDINE-1-CARBOXYLATE. tert-butyl (2S,4S)-2-[5-[6-[(2S,5S)-1-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]-5-methylpyrrolidin-2-yl]-21-oxa-5,7-. CAS No. 1378391-45-7. Product ID: INT1378391457. Molecular formula: C44H53N7O7. Mole weight: 791.9. EINECS: 807-100-0. SMILES: C[C@H]1CC[C@H](N1C(=O)[C@H](C(C)C)NC(=O)OC)C2=NC3=C(N2)C=CC4=CC5=C(C=C43)OCC6=C5C=CC(=C6)C7=CN=C(N7)[C@@H]8C[C@@H](CN8C(=O)OC(C)(C)C)COC. Category: Intermediates. |  |
| Veltuzumab | Veltuzumab (IMMU-106) is a humanized anti-CD20 monoclonal antibody. Veltuzumab has low EC 50 value of 0.08-0.09 μg/mL in the Daudi cell line. Veltuzumab can be used for the research of cancer including non-Hodgkin lymphoma (NHL) [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IMMU-106; hA20. CAS No. 728917-18-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99224. | |
| Velufenacin | Velufenacin is a muscarinic receptor antagonist [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA-8010. CAS No. 1648737-78-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109196. | |
| Velusetrag | Velusetrag (TD-5108) is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT4R) , with a pK i of 7.7. Velusetrag exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108. CAS No. 866933-46-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457. | |
| Velusetrag hydrochloride | Velusetrag (TD-5108) hydrochloride is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT 4 R) , with a pK i of 7.7. Velusetrag hydrochloride exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag hydrochloride can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108 hydrochloride. CAS No. 866933-51-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457A. | |
| Velutin. | Velutin. Group: Biochemicals. Grades: Plant Grade. CAS No. 25739-41-7. Pack Sizes: 20mg. Molecular Formula: C17H14O6, Molecular Weight: 314.29. US Biological Life Sciences. | Worldwide |
| Velvione ® | Velvione ®. CAS No. 37609-25-9. VIGON Item # 501388. Categories: Speciality Ingrdients Suppliers, Fragrances, musk amberol, Perfumers. | America & Internationally |
| Velzatinib | Velzatinib (M4205) is a multi-target inhibitor for PDGFRB, PDGFRA, CSF1R, c-Kit, FLT3, and LCK, with an IC50s of 2.6, 50, 5.5, 44, 141 and 141 nM, respectively. Velzatinib exhibits antitumor efficacy in xenograft mouse models[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: M4205; IDRX-42. CAS No. 2590556-80-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132166. | |
| Vemircopan | Vemircopan (ALXN2050) is an orally active complement factor D inhibitor. Vemircopan is promising for research of paroxysmal nocturnal hemoglobinuria [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALXN2050; ACH 0145228; ACH-5228. CAS No. 2086178-00-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139588. | |
| Vemurafenib | Vemurafenib (PLX4032) is a first-in-class, selective, potent inhibitor of B-RAF kinase, with IC 50 s of 31 and 48 nM for RAF V600E and c-RAF-1, respectively [1] [4]. Vemurafenib induces cell autophagy [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PLX4032; RG7204; RO5185426. CAS No. 918504-65-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-12057. | |
| Vemurafenib-[d7] | Vemurafenib-[d7] is the labelled analogue of Vemurafenib, which is a B-Raf enzyme inhibitor used for the treatment of late-stage melanoma. Synonyms: Vemurafenib D7. CAS No. 1365986-73-7. Molecular formula: C23H11D7ClF2N3O3S. Mole weight: 496.97. | |
| Vemurafenib, Free Base (PLX4032) | Vemurafenib selective BRAFV600E kinase inhibitor; an antitumor agent. Vemurafenib functions by inhibiting the proliferation and mitogen-activated protein/extracellular signal-regulated kinase (ERK) kinase and ERK phosphorylation in a panel of tumor cell lines, including melanoma cell lines expressing BRAFV600E or other mutant BRAF proteins altered at codon 600. Group: Biochemicals. Alternative Names: N-[3-[[5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]-2,4-difluorophenyl]-1-propanesulfonamide; PLX4032; RG7204; RO51-85426; Zelboraf. Grades: Highly Purified. CAS No. 918504-65-1. Pack Sizes: 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Venadaparib Impurity 33 | Venadaparib Impurity 33. Uses: For analytical and research use. Group: Impurity standards. CAS No. 18584-75-3. Molecular formula: C10H10N4O2. Mole weight: 218.22. Catalog: APB18584753. | |
| Venadaparib Impurity 40 | Venadaparib Impurity 40. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1681017-95-7. Molecular formula: C24H25FN4O2. Mole weight: 420.49. Catalog: APB1681017957. | |
| Venadaparib Impurity 6 | Venadaparib Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 107558-48-5. Molecular formula: C14H11N3O. Mole weight: 237.26. Catalog: APB107558485. | |
| Venetoclax | Venetoclax. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-4-(4-((4'-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)methyl)piperazin-1-yl)-N-((3-nitro-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)phenyl)sulfonyl)benzamide. CAS No. 1257044-40-8. Molecular formula: C45H50ClN7O7S. Mole weight: 868.44. Catalog: APB1257044408. | |
| Venetoclax | Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with a K i of less than 0.01 nM. Venetoclax induces autophagy [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-199; GDC-0199; RG7601. CAS No. 1257044-40-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-15531. | |
| Venetoclax | Venetoclax. Alternative Names: 3-Nitro-4-(((tetrahydro-2H-pyran-4-yl)methyl)amino)benzenesulfonamide. 3-nitro-4-((tetrahydro-2H-pyran-4-yl)methylamino)benzenesulfonamide. 3-nitro-4-[(oxan-4-ylmethyl)amino]benzene-1-sulfonamide. 3-nitro-4-[[(tetrahydro-2H-pyran-4-yl)methyl]amino]Benzenesulfonamide. CAS No. 1228779-96-1. Product ID: INT1228779961. Molecular formula: C12H17N3O5S. Mole weight: 315.35. EINECS: 833-813-1. SMILES: C1COCCC1CNC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]. Category: Intermediates. | |
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