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PI3K/Akt/mTOR
Epigenetics
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Angiogenesis
Apoptosis
Autophagy
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MAPK
Cytoskeletal Signaling
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
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Membrane Transporter/Ion Channel
others
PROTAC
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Cas Index 3
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Cas Index 3
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
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!
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).
342639-96-7 | KRIBB11
(Catalog# : 17031014)
KRIBB11 abolishes the heat shock-induced luciferase activity with an IC50 of 1.2 M. I
355025-24-0 | Ki16425
(Catalog# : 61121)
Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 wit
342777-54-2 | LM22B-10
(Catalog# : 187165)
LM22B-10 is a TrkB and TrkC agonist. LM22B-10 exhibits neurotrophic activity (EC50 =
333745-53-2 | LX-2343
(Catalog# : 184131)
LX-2343 is a neuroprotective agent for the treatment of Alzheimer's disease.
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Products Catalog
Signaling Pathway
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
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
2883540-92-7 | STX-478
(Catalog# : 20633)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
1990504-34-1 | Bomedemstat
(Catalog# : 24001)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
2892065-45-9 | PLX-4545
(Catalog# : 24111)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
681159-27-3 | CBR-5884
(Catalog# : 24109)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
1998725-11-3 | JHU-083
(Catalog# : 24108)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
2251753-65-6 | LXH-3-71
(Catalog# : 24107)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
2394874-66-7 | Adrixetinib ( Q-702 )
(Catalog# : 20617)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag