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Autophagy
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DNA Damage
Epigenetics
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
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Cas Index 1
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Cas Index 1
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1)
129497-78-5 | Verteporfin
(Catalog# : 187201)
Verteporfin, also known as Benzoporphyrin derivative monoacid ring A or BPD-MA, is a
1352792-74-5 | Verinurad
(Catalog# : 18583)
Verinurad, also known as RDEA3170, is an organic anion transporter URAT1 (SLC22A12) i
1451993-15-9 | VU0467154
(Catalog# : 18576)
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept
1535212-07-7 | Voxilaprevir
(Catalog# : 18572)
Voxilaprevir is a hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease in
1025504-45-3 | Valbenazine
(Catalog# : 1783010)
Valbenazine, also known as NBI-98854 and MT-5199, is a potent and selective VMAT2 inh
1000023-04-0 | Voruciclib
(Catalog# : 178306)
Voruciclib, also known as P1446A-05, is a protein kinase inhibitor specific for the c
1446321-46-5 | Voxelotor(GBT440, GTX011)
(Catalog# : 178916)
Voxelotor (GBT440, GTX011) is a new small molecule compound that increases hemoglobin
1350653-20-1 | Vericiguat
(Catalog# : 2017886)
Vericiguat, also known as BAY1021189 or BAY10-21189, is a potent and orally active sG
1562396-65-9 | VX-984 (M9831)
(Catalog# : 2017879)
VX-984, also known as M9831, is an ATP-competitive inhibitor of the catalytic subunit
1383716-46-8 | VPS34 inhibitor 1
(Catalog# : 17031001)
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor
1377049-84-7 | Velpatasvir
(Catalog# : 17022808)
Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstruct
149647-78-9 | Vorinostat
(Catalog# : 17022704)
Vorinostat (SAHA) is an HDAC1/3 inhibitor with IC50 of ~10 nM.Vorinostat inhibits the
1000025-07-9 | Vadadustat ( AKB-6548 )
(Catalog# : 6121401)
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
1431280-51-1 | VLX1570
(Catalog# : 611932)
VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from
1523404-29-6 | Vsp34-IN-1
(Catalog# : 011115)
Coming soon!
1232410-49-9 | VE-821
(Catalog# : 122817)
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13
1246086-78-1 | VU 0364439
(Catalog# : 122401)
VU 0364439 is a mGlu4 positive allosteric modulator, with EC50 of 19.8 nM.
163521-12-8 | Vilazodone
(Catalog# : 122208)
Vilazodone is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A rece
163521-08-2 | Vilazodone Hydrochloride
(Catalog# : 121808)
Vilazodone Hcl is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A
1624602-30-7 | VR23
(Catalog# : 120423)
VR23 is a small molecule that potently inhibited the activities of trypsin-like prote
1383716-33-3 | VPS34-IN1
(Catalog# : 111016)
VPS34-IN1 is a selective inhibitor of Vps34.
1616113-45-1 | VRT-1353385
(Catalog# : 101912)
Coming soon!
1257044-40-8 | Venetoclax(ABT-199)
(Catalog# : 60101)
Venetoclax, formerly known as ABT-199(GDC-0199), is a Bcl-2-selective inhibitor with
1246560-33-7 | VS-5584
(Catalog# : 52530)
VS-5584 (SB2343) is a potent and selective dual PI3K/mTOR inhibitor for mTOR, PI3K///
1232416-25-9 | VE-822 ( Berzosertib )
(Catalog# : 51607)
VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga
107355-45-3 | WIN54954
(Catalog# : 20280)
WIN54954 is a broad-spectrum antipicornavirus drug.
1214265-56-1 | WZ-3146
(Catalog# : 19191)
WZ-3146 is a covalent or irreversible pyrimidine-based EGFR inhibitor against EGFR T7
1350752-07-6 | 5WKS
(Catalog# : 1812252)
5WKS, also known as ZINC97756584, is a biochemical.
1206731-57-8 | WT161
(Catalog# : 184315)
WT161 is a novel potent, selective, and bioavailable HDAC6 inhibitor.
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Products Catalog
Signaling Pathway
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
----
Methionine Adenosyltransferase (MAT)
-- 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
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- 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
----
Proton Pump
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
----
CGRP-Receptor
----
TRP-Channel
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- 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
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
1429882-07-4 | MRX-2843
(Catalog# : 26A087)
MRX-2843 is an orally bioavailable inhibitor of two receptor tyrosine kinases (RTKs),
1637394-01-4 | GDC-0134
(Catalog# : 20432)
GDC-0134 is a MAP3K12 (DLK) Inhibitor.
2128698-24-6 | BI-847325
(Catalog# : 25046)
BI-847325 is a novel, ATP-competitive, orally available inhibitor of Aurora kinases a
3137699-54-5 | GDD-261
(Catalog# : 26A084)
GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase (
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
877176-23-3 | Aderamastat ( Synonyms: FP-025 )
(Catalog# : 26A086)
Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in
1857296-22-0 | 5-Formyl-4-methyl-1H-indole-2-carbonitrile
(Catalog# : 25095)
2923986-48-3 | MAT2A inhibitor-[Compound 1]
(Catalog# : 26A083)
Compound 1 is a new MAT2A inhibitor.