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Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
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others
PROTAC
Building Blocks
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
Piperidines
Pyridines
Pyrimidines
Quinolines
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
Building Blocks
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
Piperidines
Pyridines
Pyrimidines
Quinolines
Sulfonamides
Thiazoles
Trifluoroborates
Other Azoles
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On Sale
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Custom Synthesis
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Name Index V
Verteporfin
(Catalog# : 187201, Cas# :
129497-78-5
)
Verteporfin, also known as Benzoporphyrin derivative monoacid ring A or BPD-MA, is a
Vicriviroc maleate
(Catalog# : 185214, Cas# :
599179-03-0
)
Vicriviroc, also known as SCH 417690 and SCH-D, is a potent, orally active and select
Verinurad
(Catalog# : 18583, Cas# :
1352792-74-5
)
Verinurad, also known as RDEA3170, is an organic anion transporter URAT1 (SLC22A12) i
VcMMAE
(Catalog# : 18582, Cas# :
646502-53-6
)
VcMMAE is a MMAE derivative with valine-citrulline (Vc) linker. VcMMAE can be used to
VH298
(Catalog# : 18581, Cas# :
2097381-85-4
)
VH-298 is a potent VHL inhibitor that stabilizes HIF-α and elicits a hypoxic respons
VU0467154
(Catalog# : 18576, Cas# :
1451993-15-9
)
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept
Voxilaprevir
(Catalog# : 18572, Cas# :
1535212-07-7
)
Voxilaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease in
Verubecestat TFA
(Catalog# : 18417, Cas# :
2095432-65-6
)
Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-sec
Valbenazine
(Catalog# : 1783010, Cas# :
1025504-45-3
)
Valbenazine, also known as NBI-98854 and MT-5199, is a potent and selective VMAT2 inh
Vorapaxar sulfate
(Catalog# : 178307, Cas# :
705260-08-8
)
Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep
Voruciclib
(Catalog# : 178306, Cas# :
1000023-04-0
)
Voruciclib, also known as P1446A-05, is a protein kinase inhibitor specific for the c
Voxelotor(GBT440, GTX011)
(Catalog# : 178916, Cas# :
1446321-46-5
)
Voxelotor (GBT440, GTX011) is a new small molecule compound that increases hemoglobin
Vericiguat
(Catalog# : 2017886, Cas# :
1350653-20-1
)
Vericiguat, also known as BAY1021189 or BAY10-21189, is a potent and orally active sG
Varlitinib
(Catalog# : 2017885, Cas# :
845272-21-1
)
ARRY334543 is a potent selective ErbB-1 and ErbB-2 inhibitor (IC50=7and 2 nM, respect
VX-984 (M9831)
(Catalog# : 2017879, Cas# :
1562396-65-9
)
VX-984, also known as M9831, is an ATP-competitive inhibitor of the catalytic subunit
Volasertib
(Catalog# : 20178219, Cas# :
755038-65-4
)
Volasertib, also known as BI-6727, is a dihydropteridinone Polo-like kinase 1 (Plk1)
VPS34 inhibitor 1
(Catalog# : 17031001, Cas# :
1383716-46-8
)
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor
Velpatasvir
(Catalog# : 17022808, Cas# :
1377049-84-7
)
Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstruct
Vorinostat
(Catalog# : 17022704, Cas# :
149647-78-9
)
Vorinostat (SAHA) is an HDAC1/3 inhibitor with IC50 of ~10 nM.Vorinostat inhibits the
Vigabatrin
(Catalog# : 17011903, Cas# :
60643-86-9
)
Vigabatrin, also known as gamma-vinyl-GABA, is an antiepileptic drug that inhibits th
Vadadustat ( AKB-6548 )
(Catalog# : 6121401, Cas# :
1000025-07-9
)
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
VLX1570
(Catalog# : 611932, Cas# :
1431280-51-1
)
VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from
Voxtalisib ( XL-765)
(Catalog# : 160926001, Cas# :
934493-76-2
)
PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic
Vorapaxar(free base)
(Catalog# : 16070916, Cas# :
618385-01-6
)
Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep
VX-702
(Catalog# : 16070804, Cas# :
745833-23-2
)
VX-702, one of a series of second-generation, is an orally active p38 MAP kinase inhi
Vsp34-IN-1
(Catalog# : 011115, Cas# :
1523404-29-6
)
Coming soon!
VP 14637
(Catalog# : 011112, Cas# :
235106-62-4
)
Coming soon!
Vipadenant
(Catalog# : 010436, Cas# :
442908-10-3
)
Vipadenant is an adenosine A2a antagonist with Ki of 1.3 nM; less potent for A1(Ki=69
Vatalanib
(Catalog# : 010434, Cas# :
212141-54-3
)
Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
VE-821
(Catalog# : 122817, Cas# :
1232410-49-9
)
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13
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Products Catalog
Signaling Pathway
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- Metabolism
----
PPAR
----
P450
----
HSP
----
PDE
----
Factor Xa
----
Phospholipase
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
NADPH-oxidase
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
-- Vitamin D Related
----
VD/VDR
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
Inhibitors & Agonists
Intermediates
Building Blocks
--
Aldehydes
--
Amines
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
New Products
Natural Compounds
Latest Products
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag