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抑制剂/受体激动剂
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
分子砌块
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
中间体
Services
Custom Synthesis
Process Development
Ordering
Contact Us
About Us
Contact Us
+86-17702719238
sales@sun-shinechem.com
Home
抑制剂/受体激动剂
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
分子砌块
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
中间体
Services
Custom Synthesis
Process Development
Ordering
Contact Us
About Us
Contact Us
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Name Index G
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Name Index G
GSK2894631A
(Catalog# : 2071528, Cas# :
2101626-26-8
)
GSK2894631A is a hematopoietic PGD synthase (HPGDS) inhibitor.
GSK8612
(Catalog# : 2071527, Cas# :
2361659-62-1
)
GSK8612 is a potent and highly selective TBK1 inhibitor. GSK8612 inhibited recombinan
GSK547
(Catalog# : 2071522)
GSK547 is a highly selective and potent inhibitor of RIP1 kinase that targets RIP1 in
GSK1016790A
(Catalog# : 2071511, Cas# :
942206-85-1
)
GSK1016790A, also known as GSK101, is a TRPV4 agonist that elicits calcium influx in
GNE-131
(Catalog# : 2071509, Cas# :
1629063-81-5
)
GNE-131 is a Potent and Selective hNaV1.7 Inhibitor (Na V1.7 IC50 = 3 nM) for the Tre
GW284543
(Catalog# : 2061310, Cas# :
790186-68-4
)
GW284543, also known as UNC10225170;, is a potent and selective MEK5 inhibitor with t
G-1
(Catalog# : 206103, Cas# :
881639-98-1
)
G-1 is a selective agonist for GPER. It acts by blocking tubulin polymerization.
Glumetinib
(Catalog# : 203401, Cas# :
1642581-63-2
)
Glumetinib, also known as SCC244, is a novel, potent and highly selective inhibitor o
GNE-2861
(Catalog# : 111892, Cas# :
1394121-05-1
)
GNE-2861 is a potent and exquisitely kinase-selective Group II PAK inhibitor (PAK4 Ki
GSK-199
(Catalog# : 193293, Cas# :
1549811-53-1
)
GSK199 is a selective PAD4 inhibitor with half-maximum inhibitory concentration (IC50
GS-626510
(Catalog# : 193221, Cas# :
1637770-13-8
)
GS-626510 is a potent BET family bromodomains inhibitor. It acts by targeting BRD2/3/
GSK2837808A
(Catalog# : 193194, Cas# :
1445879-21-9
)
GSK2837808A is a potent, selective lactate dehydrogenase A (LDHA) inhibitor (IC50 val
GSK-963
(Catalog# : 193185, Cas# :
2049868-46-2
)
GSK-963, also known as GSK'963 or GSK963, is a potent and selective inhibitor of
GNE-9605
(Catalog# : 192284, Cas# :
1536200-31-3
)
GNE-9605 is a highly potent, selective, and brain-penetrant aminopyrazole leucine-ric
GSK3004774
(Catalog# : 192281, Cas# :
2138814-32-9
)
GSK3004774 is a potent, nonabsorbable agonist of CaSR, with an pEC50 of 7.3, 6.6 and
GW-3965 HCl
(Catalog# : 192251, Cas# :
405911-17-3
)
GW-3965 is a liver X receptor agonist. GW3965 represses the production of pro-inflamm
GSK2334470
(Catalog# : 192224, Cas# :
1227911-45-6
)
GSK2334470 is a potent 3-phosphoinositide-dependent protein kinase (PDK1) inhibitor (
GSK269962 HCl
(Catalog# : 192201, Cas# :
2095432-71-4
)
GSK269962 is a selective ROCK inhibitor with IC50 values of 1.6 and 6 nM for ROCK-I a
GW-803430
(Catalog# : 192194, Cas# :
515141-51-2
)
GW-803430 is a potent, orally active and selective melanin-concentrating hormone rece
GNE-477
(Catalog# : 192181, Cas# :
1032754-81-6
)
GNE-477, a potent and efficacious dual PI3K/mTOR inhibitor.
GSKJ1
(Catalog# : 191255, Cas# :
1373422-53-7
)
GSKJ1 is a selective and potent histone demethylase inhibitor (GSK-J1) that has signi
GSK2643943A
(Catalog# : 191144, Cas# :
//
)
GSK2643943A is a potent USP20 inhibitor with IC50 = 160 nM.
GSK-2807
(Catalog# : 19185, Cas# :
2245255-65-4
)
GSK-2807 is a potent and selective, SAM-competitive inhibitor of SMYD3.
GNE-6640
(Catalog# : 1812291, Cas# :
2009273-67-8
)
GNE-6640 is a novel selective USP7 inhibitor, inducing tumor cell death. GNE-6640 enh
GSK1940029
(Catalog# : 1812102, Cas# :
1150701-66-8
)
GSK1940029, also known as SCD Inhibitor 1, is a SCD Inhibitor. GSK1940029 is a potent
GSK2814338
(Catalog# : 181241, Cas# :
1420367-28-7
)
GSK2814338, also known as Lp-PLA2 -IN-1, is a Lp-PLA2 inhibitor.
GDC-0927
(Catalog# : 1811301, Cas# :
1642297-01-5
)
GDC-0927, also known as SRN-927, is a next-generation oral SERD which appears to have
GSK-5959
(Catalog# : 1811266, Cas# :
901245-65-6
)
GSK-5959 is a potent and selective BRPF1 bromodomain inhibitor (IC50 = 80 nM).
GW-870086
(Catalog# : 1811263, Cas# :
827319-43-7
)
GW-870086 is a glucocorticoid receptor agonist potentially for the treatment of asthm
GSK9311
(Catalog# : 1811233, Cas# :
1923851-49-3
)
GSK9311 is a potent and highly selective inhibitor of the BRPF bromodomain (BRPDF1 pI
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Products Catalog
信号通路
-- 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
抑制剂/受体激动剂
中间体
分子砌块
--
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
新产品
天然化合物
Latest Products
Soquelitinib ( CPI-818 )
(Catalog# : 20671, Cas# :
2226636-04-8
)
Soquelitinib(CPI-818)是一种高度选择性的共价白细胞介素-2诱导的T
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast
LLL12
(Catalog# : 25075, Cas# :
1260247-42-4
)
LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration
RMC-6236
(Catalog# : 25074, Cas# :
2765081-21-6
)
Daraxonrasib, also known as RMC-6236 and RAS-IN-2, is a potent and selective RAS(ON)
MGD-28
(Catalog# : 25073, Cas# :
2991818-13-2
)
MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
TG101209 analog 1
(Catalog# : 25072)
TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
AT-007
(Catalog# : 25071, Cas# :
2170729-29-8
)
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
TAK-653
(Catalog# : 25070, Cas# :
1358751-06-0
)
TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
Emavusertib
(Catalog# : 25069, Cas# :
1801344-14-8
)
Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
Roginolisib
(Catalog# : 25068, Cas# :
1305267-37-1
)
Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel