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Immunology & Inflammation
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MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
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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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
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Cas Index 3
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Cas Index 3
332012-40-5 | Telatinib
(Catalog# : 121432)
Telatinib is a potent inhibitor of VEGFR2/3, c-Kit and PDGFR with IC50 of 6 nM/4 nM,
300801-52-9 | TG003
(Catalog# : 110226)
TG003 is a novel benzothiazole compound that demonstrates potent inhibition of Clk1/S
323578-37-6 | tert-butyl N-(6-methylpyridin-3-yl)carbamate
(Catalog# : 110202)
Coming soon!
324769-06-4 | tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate
(Catalog# : 91832)
Coming soon!
33545-98-1 | tert-butyl N-(4-aminobutyl)carbamate,hydrochloride
(Catalog# : 90105)
Coming soon!
301673-16-5 | tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate
(Catalog# : 81824)
Coming soon!
313657-42-0 | tert-butyl 3-methylpiperazine-1-carboxylate,hydrochloride
(Catalog# : 81730)
Coming soon!
393781-71-0 | Tert-butyl 2-ethylpiperazine-1-carboxylate
(Catalog# : 81708)
Coming soon!
359629-16-6 | tert-butyl 4-(aminomethyl)piperidine-1-carboxylate,hydrochloride
(Catalog# : 81029)
Coming soon!
312917-14-9 | TCS JNK 5a
(Catalog# : 60202)
TCS JNK 5a(JNK Inhibitor IX) is a selective inhibitor of JNK2 and JNK3 (pIC50 values
380315-80-0 | Tenovin-1
(Catalog# : 52529)
Tenovin-1 is a inhibitor of SIRT1 and SIRT2; activator of p21 and p53.
393105-53-8 | Tiplaxtinin
(Catalog# : 52218)
Tiplaxtinin(PAI-039) is a selective and orally efficacious inhibitor of plasminogen a
329907-28-0 | TTP 22
(Catalog# : 52244)
TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/
3039-71-2 | U-18666A
(Catalog# : 20110401)
U-18666A is an inhibitor of cholesterol synthesis. It acts by inhibiting desmosterol
314241-44-5 | UNC-669
(Catalog# : 178312)
UNC-669 is a L3MBTL domain inhibitor. UNC669 specifically targets lethal 3 malignant
383392-66-3 | UC-112
(Catalog# : 6111407)
UC-112 is a novel potent IAP(Inhibitor of apoptosis) inhibitor; potently inhibit cell
312611-92-0 | VK-28
(Catalog# : 24154)
VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
3008290-92-1 | XJTU-L453
(Catalog# : 24074)
XJTU-L453 is a PI3Kα inhibitor with an IC50 value of 0.4 nM. XJTU-L453 can inhibit t
355406-09-6 | YM-155 hydrochloride
(Catalog# : 6111414)
YM155 is a potent survivin suppressant by inhibiting Survivin promoter activity with
371942-69-7 | YM-201636
(Catalog# : 121426)
YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p110.
36341-25-0 | YL-109
(Catalog# : 110219)
YL-109 has ability to inhibit breast cancer cell growth and invasiveness in vitro and
324077-30-7 | ZM 323881 hydrochloride
(Catalog# : 122214)
 ZM323881 is a potent and selective inhibitor of VEGF-R2 tyrosine kinase in vitr
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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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
GLP Receptor
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
----
URAT1
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
3069891-91-1 | MRT-8102
(Catalog# : 26A101)
MRT-6160 (DDY391) is a potent, highly selective, and orally bioavailable investigatio
3050683-38-7 | MRT-6160
(Catalog# : 26A100)
MRT-6160 is a highly selective first-in-class oral VAV1-targeting molecular glue degr
2803881-11-8 | MRT-2359
(Catalog# : 26A099)
MRT-2359 is a potent, highly selective, and orally bioavailable investigational molec
2417352-91-9 | Emvistegrast (Synonyms: GS-1427)
(Catalog# : 26A097)
Emvistegrast (GS-1427) is an investigational oral α4β7 integrin inhibitor.
2122780-15-6 | EA1080 (Synonyms: NSHO-101)
(Catalog# : 26A098)
Emvistegrast (GS-1427) is an investigational oral α4β7 integrin inhibitor.
1541170-75-5 | Sonlicromanol (Synonyms: KH176)
(Catalog# : 26A094)
Sonlicromanol is a reductive and oxidative distress modulator with anti-inflammatory
1313439-71-2 | Engasertib (Synonyms: ALM301)
(Catalog# : 26A093)
Engasertib (previously known as ALM 301) is a small molecule, selective allosteric AK
2647949-48-0 | Ontunisertib (Synonyms: AGMB-129)
(Catalog# : 26A096)
Ontunisertib (also known as AGMB-129) is an investigational, oral, gastrointestinal-r
2869090-93-5 | VRN110755
(Catalog# : 26A095)
VRN110755 is an orally available, highly selective EGFR inhibitor.
1015787-98-0 | Gefapixant
(Catalog# : 187126)
Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist. Gefapixan