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MAPK
Membrane Transporter/Ion Channel
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Proteases
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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
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
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Cas Index 1
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Cas Index 1
154598-52-4 | Efavirenz
(Catalog# : 16122763)
Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with ant
134381-21-8 | Epoxomicin
(Catalog# : 16122762)
Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhib
1942114-09-1 | EAI045
(Catalog# : 16122734)
EAI045 is an allosteric inhibitor that targets selected drug-resistant EGFR mutants b
1234479-76-5 | ERK5-IN-1
(Catalog# : 6111502)
ERK5-IN-1 exhibits potent inhibition of ERK5 with cellular EC50 values of 0.19 M and
1352608-82-2 | EW-7197
(Catalog# : 6111007)
EW-7197 is a highly potent, selective, and orally bioavailable TGF- receptor ALK4/ALK
1252594-99-2 | ETP-46321
(Catalog# : 611825)
ETP-46321 is a potent and orally bioavailable PI3K / inhibitor with IC50 of 2.3/14.2
1345675-02-6 | ETP-46464
(Catalog# : 161009015)
ATR,Bioactive Small Molecule Alphabetical Index,Bioactive Small Molecules,Cell Biolog
1700663-41-7 | EPZ020411
(Catalog# : 16090201)
EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has 10 fol
1808011-22-4 | EPZ031686
(Catalog# : 16071015)
EPZ031686
1334237-71-6 | Etelcalcetide
(Catalog# : 16071011)
Etelcalcetide, also known as AMG 416 and KAI-4169, is a D-amino peptide calcimimetic
1229208-44-9 | Entospletinib (GS-9973)
(Catalog# : 16062803)
Entospletinib, also known as GS-9973, is a highly selective and orally efficacious Sy
1233948-61-2 | EL-102(EL102)
(Catalog# : 1661901)
EL102 is a novel toluidine sulphonamide.EL102 has showedthe potential efficacy in pre
1005-93-2 | Etbicyphat
(Catalog# : 16061502)
Etbicyphat,1,3-Propanediol, 2-ethyl-2-(hydroxymethyl)-, cyclic phosphate
179756-58-2 | eptapirone
(Catalog# : 16060602)
eptapirone
1638250-96-0 | ETC-159
(Catalog# : 16060301)
ETC-159, also known as ETC-1922159, is a potent, selective and orally available PORCN
165800-04-4 | Eperezolid
(Catalog# : 011910)
Eperezolid is a oxazolidinone antibacterial agent.
170364-57-5 | Enzastaurin
(Catalog# : 011122)
Enzastaurin is a potent PKC selective inhibitor with IC50 of 6 nM, 6- to 20-fold sele
1338466-77-5 | EPZ004777
(Catalog# : 010608)
EPZ004777 is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.
1444832-51-2 | Elbasvir
(Catalog# : 010411)
Elbasvir is a HCV NS5A inhibitor, which is currently in phase 2b clinical trials as
113559-13-0 | E-4031
(Catalog# : 122940)
E-4031 is a benzenesulfonamide antiarrhythmic agent; blocks the ATP-sensitive potassi
1150114-62-7 | (2-(Ethoxycarbonyl)furan-3-yl)boronic acid
(Catalog# : 122935)
Coming soon!
188627-80-7 | Eptifibatide
(Catalog# : 122932)
Eptifibatide is an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class.
176644-21-6 | Eniporide
(Catalog# : 122841)
Coming soon!
1446502-11-9 | Enasidenib
(Catalog# : 122811)
Enasidenib is a oral potent, selective, reversible inhibitor of mutant IDH2.
1598383-40-4 | EPZ011989
(Catalog# : 120112)
EPZ011989 is a potent, selective orally bioavailable EZH2 inhibitor with Ki < 3 nM
119431-25-3 | Eliprodil
(Catalog# : 111004)
Eliprodil is a non-competitive NR2B-NMDA receptor antagonist(IC50=1 uM), less potent
1380432-32-5 | EHop-016
(Catalog# : 102615)
EHop-016 is a novel potent and selective inhibitor of Rac GTPase; inhibits Rac1 activ
1108743-60-7 | Entrectinib(RXDX-101)
(Catalog# : 100504)
Entrectinib (RXDX-101) is a selective inhibitor for all three TRK receptor tyrosine k
1257213-52-7 | Ethyl 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxylate
(Catalog# : 91807)
Coming soon!
1516887-33-4 | (E)-3α-hydroxy-6-ethylidene-7-keto-5β-cholan-24-oic acid
(Catalog# : 82729)
Coming soon!
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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)
-- 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
-- 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
-- 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
----
Kallikrein
----
IRAK
-- 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
----
Potassium Channel
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- 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)
-- 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)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- 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
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
1820812-16-5 | TAK-071
(Catalog# : 186269)
TAK-071 is a muscarinic M1 receptor positive allosteric modulator.
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566 is a potent selective SCD-1 inhibitor.
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.