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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
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Protein Tyrosine Kinase
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Cas Index 1
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Cas Index 1
164658-13-3 | CGP60474
(Catalog# : 185171)
CGP60474 is a potent dual cdk1/cdk2 inhibitor (IC50 values are 20 and 50 nM, respecti
1190932-38-7 | COH29
(Catalog# : 184127)
COH29 is an orally available, aromatically substituted thiazole and inhibitor of the
1039455-84-9 | COTI-2
(Catalog# : 184320)
COTI-2 is an P53 gene modulator and AKT2 inhibitor. OTI-2 is active against multiple
1202402-40-1 | CPI-444
(Catalog# : 18439)
CPI-444, also known as V81444, is an orally administered antagonist of the adenosine
1443437-74-8 | CCG-203971
(Catalog# : 18437)
CCG-203971 is an inhibitor of SRE activation in the prostate cancer cell line PC-3 (I
175140-00-8 | CP-376395游离
(Catalog# : 184213)
CP-376395是一种CRF1的选择性拮抗剂。
1402152-13-9 | Copanlisib HCI
(Catalog# : 18351)
Copanlisib also known as BAY 80-6946, is a potent phosphoinositide 3-kinase (PI3K) in
19608-29-8 | CB-03-01
(Catalog# : 1712153)
CB-03-01,也被称为cortexolone 17alpha -丙酸,是一种局部和外围选择性
1797989-42-4 | CHIR99021 HCl
(Catalog# : 179825)
CHIR99021, also known as CT99021, is a glycogen synthase kinase 3β (GSK3β) inhibito
1005334-57-5 | CVT-10216
(Catalog# : 179818)
CVT-10216 is a Potent and selective, reversible inhibitor of aldehyde dehydrogenase 2
14513-15-6 | Cambinol
(Catalog# : 178313)
Cambinol is a SIRT inhibitor. It inhibits expression of pro-inflammatory cytokines, i
119671-47-5 | 2-Chloro-6-morpholinopyran-4-one
(Catalog# : 1781504)
2-Chloro-6-morpholinopyran-4-one
1163719-56-9 | CCT196969
(Catalog# : 178913)
CCT196969, a pan-RAF/SFK inhibitor is active against treatment-naive BRAF and NRAS mu
1846570-40-8 | CM-579
(Catalog# : 2017874)
CM-579 is a bioactive chemical.
1072946-52-1 | (5-Chloro-2-cyanophenyl)boronic acid
(Catalog# : 20178120)
(5-Chloro-2-cyanophenyl)boronic acid
113359-04-9 | Cefozopran
(Catalog# : 17032402)
Cefozopran(SCE 2787) is a fourth-generation cephalosporin.
122841-10-5 | Cefoselis
(Catalog# : 17032401)
Cefoselis is a widely used beta-lactam antibiotic.
1015474-32-4 | CC-122
(Catalog# : 17030313)
CC-122 is an orally available pleiotropic pathway modulator with potential antineopla
125314-13-8 | CP21R7
(Catalog# : 17022715)
CP21R7, also known CP21, is a potent and selective GSK-3 inhibitor.
1316215-12-9 | Citarinostat
(Catalog# : 17022701)
Citarinostat is a HDAC6 specific inhibitor, with IC50 of 4 nM and 76 nM for HDAC6 and
147859-80-1 | CA-074 methyl ester (CA-074 Me)
(Catalog# : 17011104)
CA-074 Me is a membrane-permeable derivative of CA-074 and acts as an irreversible c
1429639-50-8 | CZ415
(Catalog# : 17011101)
CZ415, a potent ATP-competitivemTORinhibitor with very good cell permeability.
1628208-23-0 | CPI-455
(Catalog# : 17109005)
CPI-455 is a specific KDM5 inhibitor, elevating global levels of H3K4 trimethylation
199986-75-9 | CVT-313
(Catalog# : 16122923)
CVT-313 is a potent and selective inhibitor of CDK2 that prevents neointimal prolifer
1213669-91-0 | CTP354
(Catalog# : 16122922)
CTP354, also known as C-21191, a novel deuterated subtype-selective GABA(A) modulator
1198300-79-6 | Cerdulatinib (PRT062070)
(Catalog# : 16122917)
Cerdulatinib, also known as PRT2070 and PRT062070, is a n ovel, oral, dual spleen tyr
178946-89-9 | C-DIM12
(Catalog# : 16122915)
C-DIM12 is a novel synthetic activator of Nurr1. C-DIM12 induces dopaminergic gene ex
1813527-81-9 | CCG215022
(Catalog# : 16122914)
CCG215022 is a potent GRK2 and GRK5 inhibitor. CCG215022 exhibited nanomolar IC50 val
1439399-58-2 | CB-839
(Catalog# : 16122913)
CB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplas
1477949-42-0 | CAY10683
(Catalog# : 16122912)
CAY10683, also known as Santacruzamate A, is a potent and selective histone deacetyla
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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
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
Flurpiridaz-Precursor in stock.
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
2460722-04-5 | Oveporexton ( TAK-861 )
(Catalog# : 25194)
Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
2506273-81-8 | VT-3989
(Catalog# : 25200)
VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran
729-46-4 | JX06
(Catalog# : 25199)
JX06 is an effective, selective, covalent PDK inhibitor.
1616385-51-3 | Bezuclastinib
(Catalog# : 25198)
Bezuclastinib is an oral, small-molecule inhibitor of the kinase activity of the KIT