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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
185214Vicriviroc maleate599179-03-0>98%
Vicriviroc, also known as SCH 417690 and SCH-D, is a potent, orally active and select
18583Verinurad1352792-74-5>98%
Verinurad, also known as RDEA3170, is an organic anion transporter URAT1 (SLC22A12) i
18582VcMMAE 646502-53-6>98%
VcMMAE is a MMAE derivative with valine-citrulline (Vc) linker. VcMMAE can be used to
18581VH2982097381-85-4>98%
VH-298 is a potent VHL inhibitor that stabilizes HIF-α and elicits a hypoxic respons
18576VU04671541451993-15-9≧98.0%
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept
18572Voxilaprevir 1535212-07-7>98%
Voxilaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease in
18417Verubecestat TFA2095432-65-6>98%
Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-sec
1783010Valbenazine1025504-45-398.0%
Valbenazine, also known as NBI-98854 and MT-5199, is a potent and selective VMAT2 inh
178307Vorapaxar sulfate705260-08-898.0%
Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep
178306Voruciclib1000023-04-098.0%
Voruciclib, also known as P1446A-05, is a protein kinase inhibitor specific for the c
178916Voxelotor(GBT440, GTX011)1446321-46-598.0% 
Voxelotor (GBT440, GTX011) is a new small molecule compound that increases hemoglobin
2017886Vericiguat1350653-20-198.0% 
Vericiguat, also known as BAY1021189 or BAY10-21189, is a potent and orally active sG
2017885Varlitinib845272-21-198.0% 
ARRY334543 is a potent selective ErbB-1 and ErbB-2 inhibitor (IC50=7and 2 nM, respect
2017879VX-984 (M9831)1562396-65-998.0% 
VX-984, also known as M9831, is an ATP-competitive inhibitor of the catalytic subunit
20178219Volasertib755038-65-498.0% 
Volasertib, also known as BI-6727, is a dihydropteridinone Polo-like kinase 1 (Plk1)
17031001VPS34 inhibitor 11383716-46-898% 
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor
17022808Velpatasvir1377049-84-798% 
Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstruct
17022704Vorinostat149647-78-998% 
Vorinostat (SAHA) is an HDAC1/3 inhibitor with IC50 of ~10 nM.Vorinostat inhibits the
17011903Vigabatrin60643-86-998% 
Vigabatrin, also known as gamma-vinyl-GABA, is an antiepileptic drug that inhibits th
6121401Vadadustat ( AKB-6548 )1000025-07-998% 
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
611932VLX15701431280-51-198% 
VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from
160926001Voxtalisib ( XL-765)934493-76-298% by HPLC
PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic
16070916Vorapaxar(free base)618385-01-698% by HPLC 
Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep
16070804VX-702745833-23-298% by HPLC 
VX-702, one of a series of second-generation, is an orally active p38 MAP kinase inhi
011115Vsp34-IN-11523404-29-698% 
Coming soon!
011112VP 14637235106-62-498% 
Coming soon!
010436Vipadenant442908-10-398% 
Vipadenant is an adenosine A2a antagonist with Ki of 1.3 nM; less potent for A1(Ki=69
010434Vatalanib212141-54-398% 
Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
122817VE-8211232410-49-998% 
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13
122401VU 03644391246086-78-198% 
VU 0364439 is a mGlu4 positive allosteric modulator, with EC50 of 19.8 nM.