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| Product | Description | |
|---|---|---|
| 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 (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 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. 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. |  |
| 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. | |
| 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 (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. | |
| 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 Inhibitor. Uses: Scientific use. Product Category: T2119. CAS No. 1257044-40-8. |  |
| Venetoclax-[d8] | An isotope labelled Venetoclax. Venetoclax can be used to treat chronic lymphocytic leukemia. Synonyms: 4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-N-[3-nitro-4-({[(2,2,3,3,5,5,6,6-D8)oxan-4-yl]methyl}amino)benzenesulfonyl]-2-{1H-pyrrolo[2,3-b]pyridin-5-yloxy}benzamide. Grade: 95% by HPLC; 98% atom D. CAS No. 1257051-06-1. Molecular formula: C45H42D8ClN7O7S. Mole weight: 876.50. | |
| Venetoclax Impurity 10 | Venetoclax Impurity 10. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: tert-butyl 4-((4'-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)methyl)piperazine-1-carboxylate. CAS No. 1228780-71-9. Molecular formula: C24H35ClN2O2. Mole weight: 419.00. Catalog: APB1228780719. | |
| Venetoclax Impurity 17 | Venetoclax Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: methyl 2-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-4-fluorobenzoate. CAS No. 1235865-75-4. Molecular formula: C15H11FN2O3. Mole weight: 286.26. Catalog: APB1235865754. | |
| Venetoclax Impurity 6 | Venetoclax Impurity 6. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: methyl 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)benzoate. CAS No. 1235865-76-5. Molecular formula: C34H37ClN4O3. Mole weight: 585.14. Catalog: APB1235865765. | |
| Venetoclax Impurity 7 | Venetoclax Impurity 7. 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)benzoic acid. CAS No. 1235865-77-6. Molecular formula: C33H35ClN4O3. Mole weight: 571.11. Catalog: APB1235865776. | |
| Venetoclax Impurity 8 | Venetoclax Impurity 8. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 4'-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-carbaldehyde. CAS No. 1228837-05-5. Molecular formula: C15H17ClO. Mole weight: 248.75. Catalog: APB1228837055. | |
| Venetoclax Impurity 9 | Venetoclax Impurity 9. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (4'-chloro-5,5-dimethyl-3,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)methanol. CAS No. 1228780-51-5. Molecular formula: C15H19ClO. Mole weight: 250.76. Catalog: APB1228780515. | |
| Venlafaxine | Venlafaxine is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class, but it has been referred to as a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI). It is licensed for the treatment of major depressive disorder (MDD), as the treatment for generalized anxiety disorder, and comorbid indications in certain anxiety disorders with depression. It works by blocking the transporter reuptake proteins for key neurotransmitters affecting mood, thereby leaving more active neurotransmitters in the synapse. It can increase dopamine neurotransmission in this part of the brain. It has seemingly superior efficacy in severe depression as a narcotic and is increasingly used as a measure of last resort for refractory cases. Synonyms: Wy 45030; Wy45030; Wy-45030; Effexor; Elafax. Grade: >98%. CAS No. 93413-69-5. Molecular formula: C17H27NO2. Mole weight: 277.4. | |
| Venlafaxine | Venlafaxine (Wy 45030) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy 45030. CAS No. 93413-69-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0196. | |
| Venlafaxine cyclic impurity | Venlafaxine cyclic impurity. Group: Biochemicals. Alternative Names: 5-(4-Methoxyphenyl)-3-methyl-1-oxa-3-azaspiro[5.5]undecane. Grades: Highly Purified. CAS No. 93413-70-8. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C17H25NO2. US Biological Life Sciences. | Worldwide |
| Venlafaxine-[d10] Hydrochloride | One of the isotopic labelled form of Venlafaxine HCl, which is a serotonin-norepinephrine reuptake inhibitor (SNRI) that is used as an antidepressant. Venlafaxine is commonly used to treat depression, general anxiety disorder, social phobia, panic disorder, and vasomotor symptoms. Synonyms: D,L-Venlafaxine-d10 Hydrochloride; 1-[2-(Dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexanol Hydrochloride-d10. CAS No. 1216539-56-8. Molecular formula: C17H18D10ClNO2. Mole weight: 323.92. | |
| Venlafaxine-d6 | Venlafaxine-d 6 is the deuterium labeled Venlafaxine. Venlafaxine (Wy 45030) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant[1]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1020720-02-8. Pack Sizes: 5 mg. Product ID: HY-B0196S. | |
| Venlafaxine-[d6] hydrochloride | An isotope labelled derivative of Venlafaxine. Venlafaxine is a selective serotonin-norepinephrine reuptake inhibitor as an antidepressant. Grade: 95% by HPLC; 98% atom D. CAS No. 1062606-12-5. Molecular formula: C17H22D6ClNO2. Mole weight: 319.90. | |
| Venlafaxine-d6 hydrochloride | Venlafaxine-d 6 (hydrochloride) is the deuterium labeled Venlafaxine hydrochloride. Venlafaxine hydrochloride (Wy 45030 hydrochloride) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant[1]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Wy 45030-d6 hydrochloride. CAS No. 1062606-12-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-B0196AS1. | |
| Venlafaxine EP Impurity G | Venlafaxine EP Impurity G. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1076199-92-2. Molecular formula: C17H27NO. Mole weight: 261.41. Catalog: APB1076199922. | |
| Venlafaxine EP Impurity H | Venlafaxine EP Impurity H. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1329795-88-1. Molecular formula: C24H33NO3. Mole weight: 383.53. Catalog: APB1329795881. | |
| Venlafaxine hydrochloride | Venlafaxine hydrochloride (Wy 45030 hydrochloride) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy 45030 hydrochloride. CAS No. 99300-78-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0196A. | |
| Venlafaxine hydrochloride | Venlafaxine hydrochloride is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class, but it has been referred to as a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI). It is licensed for the treatment of major depressive disorder (MDD), as a treatment for generalized anxiety disorder, and comorbid indications in certain anxiety disorders with depression. It works by blocking the transporter reuptake proteins for key neurotransmitters affecting mood, thereby leaving more active neurotransmitters in the synapse. It can increase dopamine neurotransmission in this part of the brain. It is seemingly superior efficacy in severe depression as narcotics become increasingly used as a measure of last resort for refractory cases. Uses: Antidepressant. Synonyms: Wy-45030; Wy45030; Wy 45030; Effexor hydrochloride; Effexor; VENLAFAXINE HCl; Effexor XR; Trevilor. Grade: >98%. CAS No. 99300-78-4. Molecular formula: C17H28ClNO2. Mole weight: 313.86. | |
| Venlafaxine hydrochloride | Venlafaxine hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 99300-78-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Venlafaxine Hydrochloride | Venlafaxine Hydrochloride is an inhibitor of ST and SLC6A2. CAS No. 99300-78-4. Product ID: API99300784. SMILES: CN(C)CC(C1=CC=C(C=C1)OC)C2(CCCCC2)O.Cl. Category: Active Pharmaceutical Ingredients. | |
| Venlafaxine hydrochloride (Standard) | Venlafaxine (hydrochloride) (Standard) is the analytical standard of Venlafaxine (hydrochloride). This product is intended for research and analytical applications. Venlafaxine hydrochloride (Wy 45030 hydrochloride) is an orally active, potent serotonin (5-HT)/norepinephrine (NE) reuptake dual inhibitor. Venlafaxine is an antidepressant [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Wy 45030 hydrochloride (Standard). CAS No. 99300-78-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0196AR. | |
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