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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
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Aldehydes
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Anilines
Boronic Acids
Bromides
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Catalysts
Chiral Compounds
Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
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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
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
Antibody-drug Conjugate/ADC Related
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Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
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Pyridines
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Cas Index 1
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Cas Index 1
1373422-53-7 | GSKJ1
(Catalog# : 191255)
GSKJ1 is a selective and potent histone demethylase inhibitor (GSK-J1) that has signi
1150701-66-8 | GSK1940029
(Catalog# : 1812102)
GSK1940029, also known as SCD Inhibitor 1, is a SCD Inhibitor. GSK1940029 is a potent
1420367-28-7 | GSK2814338
(Catalog# : 181241)
GSK2814338, also known as Lp-PLA2 -IN-1, is a Lp-PLA2 inhibitor.
1642297-01-5 | GDC-0927
(Catalog# : 1811301)
GDC-0927, also known as SRN-927, is a next-generation oral SERD which appears to have
1923851-49-3 | GSK9311
(Catalog# : 1811233)
GSK9311 is a potent and highly selective inhibitor of the BRPF bromodomain (BRPDF1 pI
1404456-53-6 | GSK-2830371
(Catalog# : 1810292)
GSK 2830371 is a WiP1 inhibitor. It inhibits cell growth and tumor growth in lymphoma
1196541-47-5 | GDC-0575
(Catalog# : 189272)
GDC-0575 (ARRY-575, RG7741) is a potent and selective CHK1 inhibitor with an IC50 of
1025821-33-3 | GSK-626616
(Catalog# : 188241)
GSK 626616 is a YAK3/DYRK3 kinase inhibitor. It is a chemoprotective agent for the po
1373423-53-0 | GSK-J4 free base
(Catalog# : 187163)
GSK-J4 is a cell permeable, potent and selective histone demethylase.
1015787-98-0 | Gefapixant
(Catalog# : 187122)
Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist. Gefapixan
1365970-03-1 | Glecaprevir
(Catalog# : 185311)
Glecaprevir, also known as ABT-493 and A-1282576, is a NS 3/4A inhibitor potentially
1351761-44-8 | GNE-7915
(Catalog# : 18595)
GNE-7915 is a potent LRRK2 kinase inhibitor.
1654725-02-6 | GLPG1837
(Catalog# : 1842811)
GLPG-1837, also known as ABBV-974, is a novel cystic fibrosis transmembrane conductan
1416992-39-6 | GC376 sodium
(Catalog# : 184175)
GC376 is a 3CLpro inhibitor (3C-like protease inhibitor).
1243245-18-2 | GNF-6231
(Catalog# : 18494)
GNF-6231 is a potent, selective, and orally bioavailable Porcupine inhibitor that blo
1616392-22-3 | GSK-3326595
(Catalog# : 184316)
GSK-3326595, also known as EPZ015938, is an orally active, potent and selective inhib
1252608-59-5 | GIBH-130
(Catalog# : 18428)
GIBH-130是一种神经炎症抑制剂。
1346546-69-7 | GSK872
(Catalog# : 17101621)
GSK872 is a a receptor interacting protein kinase-3 (RIP3) inhibitor. GSK872 inhibits
1539314-06-1 | GSK2881078
(Catalog# : 1791316)
GSK-2881078 is a selective androgen receptor modulator potentially for the treatment
1459687-96-7 | GJ-103 sodium
(Catalog# : 1791116)
GJ103 sodium salt is an active analog of the read-through compound GJ072.
1459687-89-8 | GJ-103 free acid
(Catalog# : 1791115)
GJ-103 is an active analog of the read-through compound GJ072. Chemical-induced read
199657-29-9 | Givinostat HCl
(Catalog# : 17919)
Givinostat or gavinostat, aslo known as ITF2357, is a potent and orally active histon
1350462-55-3 | Grazoprevir hydrate
(Catalog# : 1783018)
Grazoprevir, also known as MK5172, is a drug approved for the treatment of hepatitis
1496581-76-0 | GNE-3511
(Catalog# : 1781006)
GNE-3511 is a potent and selective dual leucine zipper kinase (DLK, MAP3K12) inhibito
1336960-13-4 | GSK2193874
(Catalog# : 178914)
GSK2193874 was identified as a selective, orally active TRPV4 blocker that inhibits C
1622848-92-3 | GSK2982772
(Catalog# : 178911)
GSK2982772 is an ATP competitive eceptor-interacting protein-1 (RIP1) kinase inhibit
1254036-77-5 | GSK2269557
(Catalog# : 2017883)
GSK2269557,also known as GSK-2269557, is a potent and selective PI3K inhibitor.
1282514-88-8 | GDC-0326
(Catalog# : 2017881)
GDC-0326 is a potent and selective inhibitor of α-Isoform of Phosphoinositide 3-Kina
1007573-18-3 | GSK-1521498
(Catalog# : 20178215)
GSK-1521498 is a novel -Opioid receptor antagonist. It has been shown to attenuate re
1816331-63-1 | GSK321
(Catalog# : 2017821)
GSK321 is a potent and selective IDH1 mutant inhibitor. GSK321 potently inhibited int
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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
--
Antibody-drug Conjugate/ADC Related
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
266359-83-5 | Reparixin
(Catalog# : 25050)
Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
229005-80-5 | TAK-779
(Catalog# : 25049)
TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
1402608-02-9 | BAY-1125976
(Catalog# : 25048)
BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
1628606-05-2 | Vimseltinib free base
(Catalog# : 25047)
Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
2128698-24-6 | 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl-
(Catalog# : 25046)
1371587-51-7 | Cavosonstat
(Catalog# : 25045)
Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
259657-09-5 | Ivospemin Hydrochloride
(Catalog# : 25044)
Ivospemin is an antineoplastic spermine analogue.
2805997-46-8 | Survodutide
(Catalog# : 25043)
2595308-10-2 | XRD-0394
(Catalog# : 25042)
XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
1621999-82-3 | CC-90003
(Catalog# : 25041)
CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E