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Epigenetics
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Angiogenesis
Apoptosis
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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
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.
333963-40-9 | Lubiprostone
(Catalog# : 16123037)
Lubiprostone, also known as RU-0211, is a medication used in the management of chroni
325970-71-6 | L67
(Catalog# : 16122828)
L67 is a DNA Ligase Inhibitor. L67 inhibited DNA ligases I and III. L67 is a simple c
344897-95-6 | Leukadherin-1
(Catalog# : 161227107)
Leukadherin-1 (LA1) is a small molecule agonist that enhances CD11b/CD18-dependent ce
313368-91-1 | Lumateperone(ITI-007)
(Catalog# : 632801)
ITI-007 is an investigational atypical antipsychotic which is currently under develop
303727-31-3 | L-779450
(Catalog# : 122835)
L-779450 is a potent, selective and ATP-competitive Raf kinase inhibitor (IC50 = 10 n
367514-87-2 | Lurasidone hydrochloride
(Catalog# : 81313)
Lurasidone is an atypical antipsychotic developed by Dainippon Sumitomo Pharma, which
396129-53-6 | LY-364947
(Catalog# : 52509)
LY364947 is a potent ATP-competitive inhibitor of TGFR-I with IC50 of 59 nM, exhibits
352356-71-9 | Methyl 3-methyl-1,2,4-thiadiazole-5-carboxylate
(Catalog# : 20459)
35134-07-7 | 3-Methoxythiophene-2-carbaldehyde
(Catalog# : 2062019)
313254-94-3 | MMG-11
(Catalog# : 1932010)
MMG-11 is a potent and selective dual inhibitor of TLR2/1 and TLR2/6 signaling with l
380449-51-4 | Melphalan flufenamide
(Catalog# : 192279)
Melphalan flufenamide, also known as Melflufen, J-1, or Prodrug J-1, is a melphalan p
35891-70-4 | Myriocin
(Catalog# : 191283)
Myriocin, also known as antibiotic ISP-1 and thermozymocidin, is an atypical amino ac
305335-31-3 | MLN-4760
(Catalog# : 1812295)
MLN-4760 is an angiotensin-converting (ACE2) inhibitor. In huMNCs, MLN-4760-B detecte
315698-17-0 | ML311
(Catalog# : 179826)
ML311, also known as EU-5346, is a potent and selective inhibitor of the Protein-Prot
3659-97-0 | 1-Methylimidazolidine-2,4,5-trione
(Catalog# : 1781501)
1-MethyliMidazolidine-2,4,5-Trione
376348-65-1 | Maraviroc
(Catalog# : 17022804)
Maraviroc (UK-427857; Selzentry; Celsentri) is a selective CCR5 antagonist (IC50= 6.4
329689-23-8 | Monastrol
(Catalog# : 17021322)
Monastrol is a cell-permeable small molecule inhibitor of kinesin-5(KIF11) which is
374913-63-0 | Madrasin
(Catalog# : 16122830)
Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the e
312271-03-7 | M2I-1
(Catalog# : 16122829)
M2I-1, also known as Mad2 Inhibitor-1, is Protein-Protein Interaction Inhibitor Targe
366017-09-6 | Mubritinib
(Catalog# : 16071022)
Mubritinib, also known as TAK-165, is a protein kinase inhibitor which was under deve
3751-48-2 | 3-(3-Methylphenyl)propionic acid
(Catalog# : 90606)
Coming soon!
32249-35-7 | Methyl 3-cyclopropyl-3-oxopropanoate
(Catalog# : 81303)
Related API & intermediates:Cas#147526-32-7 Pitavastatin CalciumCas# 24922-02-9 E
39503-51-0 | Methyl 5-bromo-2,4-dimethoxybenzoate
(Catalog# : 80308)
Coming soon!
338967-87-6 | Mdivi-1
(Catalog# : 52510)
Mdivi-1 is a selective cell-permeable inhibitor of mitochondrial division DRP1 (dynam
326914-06-1 | MHY1485
(Catalog# : 52219)
MHY1485 is a mTOR activator; inhibits the autophagic process by inhibition of fusion
3032452-90-4 | NPD-3519
(Catalog# : 24089)
357400-13-6 | NNC-55-0396
(Catalog# : 24038)
NNC-55-0396 is a highly selective T-type calcium channel blocker which can be used fo
376348-67-3 | N-(8-Benzyl-8-azabicyclo[3.2.1]oct-3-yl-exo)-2-methylpropanamide
(Catalog# : 2071632)
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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
921193-28-4 | BTA-EG4 hydrate
(Catalog# : 24157)
BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
2415281-52-4 | CYD19
(Catalog# : 24156)
CYD19 is a potent Snail/HDAC dual target inhibitor.
98570-83-3 | Phylloflavan
(Catalog# : 24155)
Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW
312611-92-0 | VK-28
(Catalog# : 24154)
VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
160162-42-5 | SR-11302
(Catalog# : 24153)
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
2171065-77-1 | AKOS037652256
(Catalog# : 24152)
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat
2990506-75-5 | ML353
(Catalog# : 24151)
ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM).
1208448-95-6 | MIF098
(Catalog# : 24150)
MIF098 is a macrophage migration inhibitory factor (MIF) antagonist.
2319722-53-5 | TM5441sodium
(Catalog# : 24149)
TM-5441, also known as EBP 883 and BMS-790052, is a potent plasminogen activator inhi
2794934-49-7 | RGT-018
(Catalog# : 24148)
RGT-018 is a potent and orally active SOS1 inhibitor with anti-tumor effects.