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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 3
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Cas Index 3
30544-47-9 | Etofenamate
(Catalog# : 52556)
Etofenamate is a non-steroidal anti-inflammatory drug used for the treatment joint an
329932-55-0 | FM19G11
(Catalog# : 192211)
FM19G11 is an inhibitor of Hypoxia Inducible Factors α (HIFα), reported to affect s
347174-05-4 | Ferrostatin-1
(Catalog# : 184210)
Ferrostatin-1 (fe -1)是一种亲脂的抗氧化剂,有效地阻断了铁蛋白的形
38398-32-2 | Ganaxolone
(Catalog# : 20630)
Ganaxolone, also known as CCD 1042 and C1042, is a CNS-selective GABAA modulator that
3459-20-9 | Glymidine sodium
(Catalog# : 20295)
Glymidine sodium is a sulfonamide hypoglycemic agent which stimulates insulin secreti
306974-70-9 | GW1100
(Catalog# : 1811231)
GW1100 is a a selective antagonist of GPR40.
317318-84-6 | GW0742
(Catalog# : 1791110)
GW0742, also known as GW610742 and GW0742X is a PPARδ/β agonist. GW0742 Induces Ear
307983-31-9 | GRA Ex-25
(Catalog# : 17030701)
GRA Ex-25 is an inhibitor of glucagon receptor. Inhibiting the interaction between gl
349085-82-1 | GSK137647A
(Catalog# : 16123010)
GSK137647A is an agonist of the free fatty acid receptor 4 (FFA4/GPR120) with pEC50s
328541-79-3 | GlyH-101
(Catalog# : 16123006)
GlyH-101 is a CFTR inhibitor (cystic fibrosis transmembrane conductance regulator). G
317318-70-0 | GW501516
(Catalog# : 030905)
Coming soon!
379270-37-8 | GS-7340
(Catalog# : 52611)
GS-7340(Tenofovir alafenamide) is a prodrug of tenofovir (TFV) that more efficiently
3034479-99-4 | HC-5404-FU
(Catalog# : 24112)
HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
34604-60-9 | 5-hydroxypyrazine-2-carboxylic acid
(Catalog# : 17021403)
5-hydroxypyrazine-2-carboxylic acid , a metabolite of anti-tuberculosis drug pyrazina
35354-74-6 | Honokiol
(Catalog# : 161009024)
Houpu has traditionally been used in Eastern medicine as analgesic and to treat anxie
338454-14-1 | 1H-Indazole-5-boronic acid
(Catalog# : 032503)
Coming soon!
3007670-38-1 | 5-Iodo-4-methyl-1H-indole-2-carbonitrile
(Catalog# : 25096)
388116-27-6 | indole-4-boronic acid pinacol ester
(Catalog# : 21253)
indole-4-boronic acid pinacol ester, CAS 388116-27-6, is an important intermeidate.
331862-41-0 | IMR-1A
(Catalog# : 6111507)
IMR-1A is the metabolite of IMR-1. IMR-1 is a novel class of Notch inhibitors targeti
371242-69-2 | IC-87114
(Catalog# : 160926004)
It Inhibits p110, p110 and p110 only at much higher concentrations. It does not inhib
325715-02-4 | Indiplon
(Catalog# : 102701)
Indiplon is a pyrazolopyrimidine that acts as a high-affinity positive allosteric mod
313553-47-8 | INH1
(Catalog# : 102606)
INH1 is a small molecule targeting the Hec1/Nek2 mitotic pathway suppresses tumor cel
336113-53-2 | Ispinesib
(Catalog# : 52747)
Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) w
36945-98-9 | Icilin
(Catalog# : 52561)
Icilin(AG 3-5) is a synthetic super-agonist of TRPM8 ion channel.
309271-94-1 | Inauhzin
(Catalog# : 52543)
Inauhzin(INZ) is a novel small molecule that effectively reactivates p53 by inhibitin
314245-33-5 | IU1
(Catalog# : 51637)
IU1 is a reversible and specific inhibitor of proteasome-associating Usp14. It does n
315705-75-0 | JNJ0966
(Catalog# : 193201)
JNJ0966 is a highly selective allosteric inhibitor of matrix metalloproteinase-9 (MMP
383150-41-2 | JTE-013
(Catalog# : 184313)
TE-013 is a potent, selective sphingosine-1-phosphate 2 (S1P2) receptor antagonist th
363571-83-9 | Kinesore
(Catalog# : 193203)
Kinesore is an activator of the function of kinesin-1 in controlling microtubule dyna
330676-02-3 | KH7
(Catalog# : 19362)
KH7 is a novel Inhibitor of Soluble Adenylyl Cyclase (Sac).
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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
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
N/A | AF710B
(Catalog# : 25205)
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
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