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+86-17702719238
sales@sun-shinechem.com
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
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Cas Index 2
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Cas Index 2
2070015-13-1 | ML241 HCl
(Catalog# : 179111)
ML241 is a potent and selective inhibitors of p97 ATPase. ML241 inhibit p97 ATPase wi
210110-90-0 | Miglustat hydrochloride
(Catalog# : 2017824)
Miglustat, also known as OGT 918, is a drug developed by Actelion and is used prima
21516-68-7 | MONASCIN
(Catalog# : 201708015)
It is a potent inhibitor of car inogenesis measured against chemical- or UV-initiated
23007-85-4 | MPTP hydrochloride
(Catalog# : 16122796)
MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of do
2029049-79-2 | ML390
(Catalog# : 16122749)
ML390 is a human DHODH inhibitor that induces differentiation in acute myeloid leukem
219832-49-2 | MP-A08
(Catalog# : 6111524)
MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S
292057-76-2 | Mcl1-IN-2
(Catalog# : 6111404)
Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value.
256373-96-3 | MCC950 sodium
(Catalog# : 6111014)
MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w
29906-67-0 | 1-METHYL-5-NITRO-1H-INDOLE
(Catalog# : 169701)
1-METHYL-5-NITRO-1H-INDOLE CAS#29906-67-0
210826-40-7 | MCC950
(Catalog# : 030101)
MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM
208538-73-2 | Micafungin sodium
(Catalog# : 120712)
Micafungin is an antifungal drug that belongs to the antifungal class of compounds kn
23012-17-1 | 2-Methyl-1,3-oxazole-4-carboxylic acid
(Catalog# : 91828)
Coming soon!
24623-20-9 | 6-methyl-2,3-dihydroinden-1-one
(Catalog# : 81929)
Coming soon!
24644-78-8 | 4-methyl-2,3-dihydroinden-1-one
(Catalog# : 81923)
Coming soon!
29415-97-2 | Methyl 3-bromo-4-hydroxybenzoate
(Catalog# : 80319)
Coming soon!
2794195-73-4 | Nomelcitinib ( D-2570 )
(Catalog# : 26A036)
Nomelcitinib (D-2570) is a novel TYK2 allosteric inhibitor.
2351225-46-0 | NSD1 inhibitor BT5
(Catalog# : 25207)
BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev
2272917-13-0 | NT-0796
(Catalog# : 25153)
NT-0796 is an oral small molecule which inhibits NLRP3 inflammasome.
2443487-67-8 | Nivegacetor ( Synonyms: RG-6289, RO-7269162)
(Catalog# : 25151)
Nivegacetor (RG-6289, RO-7269162) is an oral gamma-secretase modulator.
2375840-87-0 | NDI-091143
(Catalog# : 24057)
NDI-091143 is a novel potent inhibitor of human ATP-citrate lyase, indirectly disrupt
2354321-33-6 | NMD670
(Catalog# : 24050)
NMD670 is an orally bioavailable skeletal muscle-specific chloride ion channel (ClC-1
2739866-40-9 | NVL-655 ( ALK-IN-27 )
(Catalog# : 24003)
NVL-655 is a novel, brain-penetrant, ALK-selective inhibitor that was designed to add
2244614-14-8 | Navacaprant ( BTRX-335140 )
(Catalog# : 23122601)
Navacaprant (NMRA-335140, BTRX-140) is an oral, selective, reversible, small-molecule
2254741-41-6 | Ninerafaxstat
(Catalog# : 20608)
Ninerafaxstat is a biochemical that decreases fatty acid oxidation and improves mitoc
2154406-04-7 | NBI-921352
(Catalog# : 20602)
NBI-921352 is a potent, highly selective Nav1.6 sodium channel inhibitor being develo
2143096-93-7 | Navitoclax-piperazine
(Catalog# : 20559)
Navitoclax-piperazine, also known as ABT-263-piperazine, is a Navitoclax derative and
2411819-82-2 | NBD-14270
(Catalog# : 20448)
2055599-51-2 | NTP42
(Catalog# : 2051509)
NTP42 is a novel antagonist of the thromboxane prostanoid receptor (TP), currently in
2349367-89-9 (free base) | NVS-ZP7-4
(Catalog# : 204506)
NVS-ZP7-4 is a potent ZIP7 Inhibitor, which inhibits Notch signaling with IC50 of 0.1
2231098-99-8 | NCT-506
(Catalog# : 19354)
NCT-506 is an orally bioavailable aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors wit
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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
-- 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
-- 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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
-- 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
----
Vps34
-- 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
2712741-60-9 | Abdenoflast
(Catalog# : 26A037)
Abdenoflast (VTX2735) is a small-molecule, non-steroidal inhibitor of the NLRP3 infla
2794195-73-4 | Nomelcitinib ( D-2570 )
(Catalog# : 26A036)
Nomelcitinib (D-2570) is a novel TYK2 allosteric inhibitor.
| AMX-883
(Catalog# : 26A035)
Amx-883 is a potent and selective degrader of BRD9 drives differentiation in acute my
3064485-16-8 | CID-078
(Catalog# : 26A034)
CID-078 is a novel, orally bioavailable, passively cell-permeable, potent and selecti
3117940-39-0 | TRI-611
(Catalog# : 26A033)
TRI-611 is an Oral ALK Molecular Glue Degrader.
3054692-62-2 | ECI830
(Catalog# : 26A031)
ECI830 is an experimental CDK2 inhibitor.
3084635-78-6 | NEO-811
(Catalog# : 26A030)
NEO-811 is an investigational molecular glue degrader designed to induce targeted deg
1383716-40-2 | Vps34-PIK-III
(Catalog# : 26A029)
Vps34-PIK-III is a selective inhibitor of VPS34 that binds a unique hydrophobic pocke
13116-77-3 | NSC624206
(Catalog# : 26A028)
NSC624206 is a Ub E1 inhibitor that specifically inhibits thioester bond formation be
2254706-21-1 | CVN-424 ( Solangepras )
(Catalog# : 26A025)
CVN-424 (Solengepras) is a first-in-class, small molecule GPR6 inverse agonist.