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MAPK
Membrane Transporter/Ion Channel
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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
PI3K/Akt/mTOR
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Ubiquitin
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Cas Index 5
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Cas Index 5
501692-44-0 | Odevixibat
(Catalog# : 20600)
Odevixibat, also known as AZD 8294, is a potent, once-daily, non-systemic ileal bile
502887-71-0 | OUN87710
(Catalog# : 2051503)
OUN87710, also known as MMP-9-IN-1 is a specific matrix metalloproteinase-9 (MMP-9) i
579-13-5 | Oligomycin A
(Catalog# : 186154)
Oligomycin A, also known as MCH 32, is an inhibitor of ATP synthase.
50-56-6 | Oxytocin
(Catalog# : 17030805)
Oxytocin is a medication and hormone. As a medication, it is used to cause contractio
50743-32-3 | 4-oxo-6-propan-2-ylchromene-3-carbonitrile
(Catalog# : 91412)
The related API: AmoxanoxThe related intermediates: ethyl 2-amino-5-oxo-7-propan-2-yl
56461-20-2 | 1-oxo-2,3-dihydroindene-4-carboxylic acid
(Catalog# : 81937)
Coming soon!
5431-44-7 | 2,6-Pyridinedicarboxaldehyde
(Catalog# : S-204148)
58-60-6 | Puromycin Aminonucleoside
(Catalog# : 1791310)
Puromycin Aminonucleoside, also known as PAN, NSC3056, is useful in the study of huma
586379-66-0 | PH-797804
(Catalog# : 17030914)
PH-797804 is a potent and selectiove inhibitor of p38 mitogen-activated protein (MAP)
5608-24-2 | PRIMA-1
(Catalog# : 16122770)
PRIMA-1 is a mutant p53 reactivator. It induces apoptosis and inhibits growth of huma
593960-11-3 | PIK-93
(Catalog# : 160926009)
PIK-93 is a potent PI3K inhibitor. PIK93 selectively inhibits the type III PI 4-kinas
59566-45-9 | 2-Pyrimidineacetonitrile (9CI)
(Catalog# : 101903)
Coming soon!
571190-30-2 | Palbociclib
(Catalog# : 52001)
Palbociclib (PD-0332991) is an orally available pyridopyrimidine-derived cyclin-depen
57452-98-9 | (R)-Praziquantel
(Catalog# : 20655)
(R)-Praziquantel is an active enantiomer of praziquantel that acts as a potent anthel
592542-59-1 | Rigosertib
(Catalog# : 690120)
Rigosertib(ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, w
5552292-08-7 | Rolapitant free base
(Catalog# : 185152)
Rolapitant, also known as SCH-619734, is an orally bioavailable, centrally-acting, se
575474-82-7 | R112
(Catalog# : 031003)
R112 is an ATP-competitive inhibitor of Syk kinase with a Ki of 96 nM. R112 inhibits
518048-05-0 | Raltegravir
(Catalog# : 010412)
Raltegravir is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in
572924-54-0 | Ridaforolimus
(Catalog# : 123018)
Ridaforolimus is a selective mTOR inhibitor with IC50 of 0.2 nM; while not classified
552292-08-7 | Rolapitant
(Catalog# : 122804)
Rolapitant is a potent, highly selective, long-acting Neurokinin-1 (NK-1) receptor an
500287-72-9 | Rilpivirine
(Catalog# : 111904)
Rilpivirine is a pharmaceutical drug, developed by Tibotec, for the treatment of HIV
57233-86-0 | (R)-alpha-Methyl-4-nitrobenzylamine hydrochloride
(Catalog# : 80320)
Coming soon!
528587-70-4 | (1S,5R)-1-(3-fluorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one
(Catalog# : 2091205)
52029-86-4 | STO-609
(Catalog# : 17021319)
STO-609 is a specific inhibitor of the Ca2+/Calmodulin-dependent protein kinase kina
522650-83-5 | SW044248
(Catalog# : 17011714)
SW044248 is a potent and selective Topoisomerase I inhibitor. SW044248 killed approxi
555-66-8 | Shogaol (6-Shogaol)
(Catalog# : 17011703)
Shogaol, also known as (6)-shogaol, is a pungent constituent of ginger similar in che
521984-48-5 | SIS3
(Catalog# : 16122721)
SIS3, a novel specific inhibitor of Smad3, inhibits TGF- and activin signaling by sup
53123-88-9 | Sirolimus (Rapamycin)
(Catalog# : 161009003)
In cells, sirolimus binds to the immunophilin FK Binding Protein-12 (FKBP-12) to gene
501951-42-4 | SB-705498
(Catalog# : 011921)
SB-705498 is a potent, selective and orally bioavailable transient receptor potential
502632-66-8 | Sonolisib
(Catalog# : 122944)
Sonolisib is a small-molecule wortmannin analogue inhibitor of the alpha, gamma, and
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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.