Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
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% | ![]() |
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% | ![]() |
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 | ![]() |
PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic | ||||
16070916 | Vorapaxar(free base) | 618385-01-6 | 98% by HPLC | ![]() |
Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep | ||||
16070804 | VX-702 | 745833-23-2 | 98% by HPLC | ![]() |
VX-702, one of a series of second-generation, is an orally active p38 MAP kinase inhi | ||||
011115 | Vsp34-IN-1 | 1523404-29-6 | 98% | ![]() |
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