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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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Cas Index 1
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Cas Index 1
168079-32-1 | Lixivaptan
(Catalog# : 2071524)
Lixivaptan, laso known as CRTX-080; VPA-985; WAY-VPA-985, is a potent, orally active,
170632-47-0 | Lificiguat
(Catalog# : 2071502)
Lificiguat, also known as YC-1, is a inhibitor of Hypoxia-inducible factor-1alpha (HI
1800046-95-0 | Lanraplenib
(Catalog# : 20732)
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor in develo
1702816-75-8 | Linperlisib free base
(Catalog# : 2061309)
Linperlisib, also known as YY-20394 and PI3Kδ-IN-2, is a potent and selective PI3Kδ
1542135-76-1 | LML-134
(Catalog# : 2051510)
LML134 is an orally active and high selective Histamine 3 receptor (H3R) inverse agon
1848242-58-9 | LUN42589
(Catalog# : 204502)
LUN42589, also known as PI3K/mTOR Inhibitor-2, is a potent dual pan-PI3K/mTOR inhibit
1628256-23-4 (free base) | Lerociclib
(Catalog# : 204302)
Lerociclib , also known as G1T38, is an oral, potent and selective CDK4/6 inhibitor f
1369764-02-2 | Lemborexant (E-2006)
(Catalog# : 6111904)
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib
1226851-11-1 | LCL521
(Catalog# : 19357)
LCL521 is an acid ceramidase (ACDase) inhibitor. LCL521 also inhibits the lysosomal a
156294-36-9 | Larotaxel
(Catalog# : 1922710)
Larotaxel is a semi-synthetic derivative of the taxane 10-deacetylbaccatin III with p
1354690-24-6 | Leniolisib
(Catalog# : 192271)
Leniolisib, also known CDZ173, is a potent phosphatidylinositol 3-kinase inhibitor (P
1052147-86-0 | LP-211
(Catalog# : 1811302)
LP-211 is a a selective agonist of the serotonin 5-HT7 receptor.
1800398-38-2 | LXH254 free base
(Catalog# : 1811213)
LXH254 is an orally available inhibitor of all members of the serine/threonine protei
1231220-79-3 | LY2828360
(Catalog# : 181172)
LY2828360 is a novel potent, selective, and efficacious CB2 agonist.
1040526-12-2 | LP-533401 HCl
(Catalog# : 1810262)
LP-533401 HCl is an inhibitor of tryptophan hydroxylase-1 (Tph-1), the initial enzyme
1454808-95-7 | LP-922761
(Catalog# : 188101)
LP-922761 is a potent and selective AAK1 inhibitor with an in vitro IC50 value of 4.8
1898283-02-7 | LY-3200882
(Catalog# : 186278)
LY-3200882 is an orally active TGFbeta inhibitor. LY3200882 targets transforming grow
1610954-97-6 | LX2761
(Catalog# : 186275)
LX2761 is a locally acting SGLT1 inhibitor that is highly potent in vitro and delays
120408-07-3 | Lometrexol disodium
(Catalog# : 186151)
Lometrexol is a folate analog antimetabolite with antineoplastic activity.
1632032-53-1 | LB-100
(Catalog# : 185312)
LB-100 is a protein phosphatase 2A(PP2A)inhibitor.
1292290-38-0 | LY2881835
(Catalog# : 185252)
LY2881835 is a potent and selective GPR40 agonist potentially for treatment of type 2
1903008-80-9 | Lazertinib
(Catalog# : 512194)
Description:Lazertinib is a an orally available third-generation, selective inhibi
183499-57-2 | L-778123
(Catalog# : 1711249)
L-778,123 is an inhibitor of FPTase and GGPTase-I.
1879887-96-3 | LTURM-34
(Catalog# : 1710138)
LTURM-34 is a novel potent and selective DNA-PK inhibitor, attenuating proliferation
1234015-54-3 | LY2606368 dihydrochloride
(Catalog# : 1710137)
Prexasertib (LY2606368) is an ATP-competitive CHK1 inhibitor with a Ki value of 0.9 n
1361030-48-9 | LDC1267
(Catalog# : 179301)
LDC1267 markedly reduced murine mammary cancer and melanoma metastases dependent on N
125697-93-0 | Lavendustin C
(Catalog# : 1791119)
Lavendustin C, also known as HDBA and NSC 666251, is a potent inhibitor of epidermal
1874276-76-2 | LXS-196
(Catalog# : 1781108)
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1453834-21-3 | LDC4297(LDC044297)
(Catalog# : 178902)
LDC4297,also known as LCD044297,is a potent and selective CDK7 inhibitor.
1951483-29-6 | LY3214996
(Catalog# : 2017887)
LY-3214996 is a potent and selective, orally available inhibitor of extracellular sig
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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)
-- 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
-- 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
-- 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)
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- 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
-- 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
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
2242751-53-5 | Acoramidis hydrochloride
(Catalog# : 24068)
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
2439277-80-0 | MAT2A-IN-9
(Catalog# : 25147)
MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
2446928-30-7 | Gridegalutamide
(Catalog# : 25138)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-
1581714-49-9 | Atuzabrutinib
(Catalog# : 25145)
Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
2254145-43-0 | Andamertinib
(Catalog# : 25144)
Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
2769008-22-0 | MEN-1703
(Catalog# : 25143)