Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 192154 | Vecabrutinib | 1510829-06-7 | >98% |  |
| Vecabrutinib, also known as SNS-062; FP-182, BSK-4841 and BIIB-062; is a potent, nonc | ||||
| 192141 | Valemetostat | 1809336-39-7 | >98% |  |
| Valemetostat is an antineoplastic drug candidate. | ||||
| 1812285 | Verdiperstat | 890655-80-8 | >98% |  |
| erdiperstat, also known as AZD-3241, is a selective and irreversible inhibitor of mye | ||||
| 181253 | Vaborbactam | 1360457-46-0 | >98% |  |
| Vaborbactam, also known as RPX7009, is a potent and selective beta-lactamase inhibito | ||||
| 1810151 | VU0463271 | 1391737-01-1 | >98% |  |
| VU0463271 inhibits co-transporter KCC2. | ||||
| 18891 | Vafidemstat | 1357362-02-7 | >98% |  |
| Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1) | ||||
| 187201 | Verteporfin | 129497-78-5 | >98% |  |
| Verteporfin, also known as Benzoporphyrin derivative monoacid ring A or BPD-MA, is a | ||||
| 185214 | Vicriviroc maleate | 599179-03-0 | >98% |  |
| Vicriviroc, also known as SCH 417690 and SCH-D, is a potent, orally active and select | ||||
| 18583 | Verinurad | 1352792-74-5 | >98% |  |
| Verinurad, also known as RDEA3170, is an organic anion transporter URAT1 (SLC22A12) i | ||||
| 18582 | VcMMAE | 646502-53-6 | >98% |  |
| VcMMAE is a MMAE derivative with valine-citrulline (Vc) linker. VcMMAE can be used to | ||||
| 18581 | VH298 | 2097381-85-4 | >98% |  |
| VH-298 is a potent VHL inhibitor that stabilizes HIF-α and elicits a hypoxic respons | ||||
| 18576 | VU0467154 | 1451993-15-9 | ≧98.0% |  |
| VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept | ||||
| 18572 | Voxilaprevir | 1535212-07-7 | >98% |  |
| Voxilaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease in | ||||
| 18417 | Verubecestat TFA | 2095432-65-6 | >98% |  |
| Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-sec | ||||
| 1783010 | Valbenazine | 1025504-45-3 | 98.0% |  |
| Valbenazine, also known as NBI-98854 and MT-5199, is a potent and selective VMAT2 inh | ||||
| 178307 | Vorapaxar sulfate | 705260-08-8 | 98.0% |  |
| Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep | ||||
| 178306 | Voruciclib | 1000023-04-0 | 98.0% |  |
| Voruciclib, also known as P1446A-05, is a protein kinase inhibitor specific for the c | ||||
| 178916 | Voxelotor(GBT440, GTX011) | 1446321-46-5 | 98.0% | -cas-1446321-46-5.png) |
| Voxelotor (GBT440, GTX011) is a new small molecule compound that increases hemoglobin | ||||
| 2017886 | Vericiguat | 1350653-20-1 | 98.0% |  |
| Vericiguat, also known as BAY1021189 or BAY10-21189, is a potent and orally active sG | ||||
| 2017885 | Varlitinib | 845272-21-1 | 98.0% |  |
| ARRY334543 is a potent selective ErbB-1 and ErbB-2 inhibitor (IC50=7and 2 nM, respect | ||||
| 2017879 | VX-984 (M9831) | 1562396-65-9 | 98.0% | -cas-1562396-65-9.png) |
| VX-984, also known as M9831, is an ATP-competitive inhibitor of the catalytic subunit | ||||
| 20178219 | Volasertib | 755038-65-4 | 98.0% |  |
| Volasertib, also known as BI-6727, is a dihydropteridinone Polo-like kinase 1 (Plk1) | ||||
| 17031001 | VPS34 inhibitor 1 | 1383716-46-8 | 98% | |
| VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor | ||||
| 17022808 | Velpatasvir | 1377049-84-7 | 98% | |
| Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstruct | ||||
| 17022704 | Vorinostat | 149647-78-9 | 98% |  |
| Vorinostat (SAHA) is an HDAC1/3 inhibitor with IC50 of ~10 nM.Vorinostat inhibits the | ||||
| 17011903 | Vigabatrin | 60643-86-9 | 98% |  |
| Vigabatrin, also known as gamma-vinyl-GABA, is an antiepileptic drug that inhibits th | ||||
| 6121401 | Vadadustat ( AKB-6548 ) | 1000025-07-9 | 98% |  |
| Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr | ||||
| 611932 | VLX1570 | 1431280-51-1 | 98% |  |
| VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from | ||||
| 160926001 | Voxtalisib ( XL-765) | 934493-76-2 | 98% by HPLC | -cas-934493-76-2.png) |
| PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic | ||||
| 16070916 | Vorapaxar(free base) | 618385-01-6 | 98% by HPLC | -cas-618385-01-6.png) |
| Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep | ||||