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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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Cas Index 9
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Cas Index 9
97519-39-6 | Ceftibuten
(Catalog# : 17032405)
Ceftibuten(Sch39720) is a third-generation cephalosporin antibiotic.
944808-88-2 | CAY10566
(Catalog# : 010403)
Coming soon!
934240-30-9 | CNV1014802
(Catalog# : 122812)
CNV1014802 is a novel small molecule state-dependent sodium channel blocker; Nav1.7 s
934660-93-2 | Cobimetinib
(Catalog# : 102203)
Cobimetinib is an orally bioavailable small-molecule inhibitor of mitogen-activated p
910232-84-7 | CGI-1746
(Catalog# : 73103)
CGI1746 is a potent and highly selective small-molecule inhibitor of the Btk with IC5
905973-89-9 | CGK 733
(Catalog# : 51917)
CGK 733 is a potent and selective inhibitor ofATM/ATRwithIC50of ~200 nM.
95809-78-2 | CPI-613(Devimistat )
(Catalog# : 51905)
CPI-613( Devimistat ) is an E1 pyruvate dehydrogenase (PDH) modulator that prevents c
911115-16-7 | Decoglurant
(Catalog# : 2071542)
Decoglurant, also known as Ro 4995819, is a negative allosteric modulator of the mGlu
93701-32-7 | 1,3-Dibromo-2-(bromomethyl)benzene
(Catalog# : 2062308)
960539-70-2 | Daprodustat (Synonyms: GSK1278863)
(Catalog# : 112596)
Daprodustat (Synonyms: GSK1278863) is an orally active hypoxia-inducible factor proly
934246-14-7 | Degarelix acetate
(Catalog# : 192262)
Degarelix, also known as FE-200486 and ASP-3550, is a long-acting, synthetic peptide
915769-50-5 | Dovitinib lactate
(Catalog# : 18575)
Dovitinib, also known as TKI-258 or CHIR-258, is an orally bioavailable FGFR3 inhibit
954126-98-8 | Danirixin
(Catalog# : 16111111)
Danirixin is a small molecule, non-peptide, high affinity (IC50 for CXCL8 binding = 1
90332-63-1 | 10-Deacetyl-7-xylosyl paclitaxel
(Catalog# : 611946)
10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxel derivative with improved pharmacolog
924296-17-3 | DUBs-IN-3
(Catalog# : 611929)
DUBs-IN-3 is a potent deubiquitinase enzyme inhibitor with IC50s of 3.1 uM for USP8;
924296-18-4 | DUBs-IN-1
(Catalog# : 611928)
DUBs-IN-1 is a potent deubiquitinase enzyme inhibitor with IC50s of 18 uM/0.71 uM for
917918-79-7 | 4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine,hydrochloride
(Catalog# : 92214)
Coming soon!
944842-54-0 | Decernotinib(VX-509)
(Catalog# : 90733)
Decernotinib(VX-509) may potently inhibits JAK3 in enzyme assays (Ki = 2.5 nM + 0.7 n
90604-02-7 | 1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride
(Catalog# : 83116)
Coming soon!
929046-33-3 | Elinzanetant ( NT-814 )
(Catalog# : 20259)
Elinzanetant, previously known as NT-814 (45), is a dual NK1,3R antagonist and theref
945531-77-1 | Ezutromid
(Catalog# : 16122944)
Ezutromid, also known as BMN-195 and SMTC-1100, is a first orally bioavailable utroph
91119-27-6 | ethyl 5-chloro-7-nitro-1H-indole-2-carboxylate
(Catalog# : 5121008)
ethyl 5-chloro-7-nitro-1H-indole-2-carboxylate,CAS#91119-27-6
923978-27-2 | Elafibranor (GFT505)
(Catalog# : 5112801)
Elafibranor, also known as GFT-505, is a dual PPARα/δ agonist. Elafibranoris curren
934353-76-1 | ENMD-2076
(Catalog# : 111909)
ENMD-2076 has selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.8
90176-80-0 | 4-Fluoro-2-(trifluoromethyl)benzaldehyde
(Catalog# : 20405)
932737-65-0 | FITM
(Catalog# : 17989)
FITM is a potent mGlu1 inhibitor.
945714-67-0 | FPS-ZM1
(Catalog# : 16123002)
FPS-ZM1 is a high-affinity RAGE-specific blocker that inhibits amyloid- binding to RA
957485-64-2 | FPH2
(Catalog# : 032513)
Coming soon!
936091-26-8 | Fedratinib ( TG-101348 )
(Catalog# : 122306)
Fedratinib ( TG-101348 ) is a selective inhibitor of JAK2 with IC50 of 3 nM, 35- and
938435-69-9 | Flobetair
(Catalog# : 102904)
Coming soon!
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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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
1393466-87-9 | PLX8394
(Catalog# : 20613)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
2365193-22-0 | Zelasudil
(Catalog# : 24014)
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho-
2134675-36-6 | Ziftomenib ( KO-539 )
(Catalog# : 24013)
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
2728667-27-2 | Zongertinib
(Catalog# : 24011)
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
2272904-53-5 | Zasocitinib
(Catalog# : 24010)
Zasocitinib is under development for the treatment of moderate to severe plaque psori
2503036-46-0 | RNK-05047
(Catalog# : 24008)
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
1001288-58-9 | Asengeprast (FT011)
(Catalog# : 24009)
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).