武汉永璨生物科技有限公司
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抑制剂/受体激动剂
Angiogenesis
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Immunology & Inflammation
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MAPK
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NF-κB
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Stem Cells & Wnt
TGF-beta/Smad
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
Others
Nuclear Receptor
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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
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定制合成
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订购信息
联系我们
公司简介
联系我们
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产品名字索引 G
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产品名字索引 G
Go6976
(Catalog# : 16122723, Cas# :
136194-77-9
)
Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat
GSK2292767
(Catalog# : 16122702, Cas# :
1254036-66-2
)
GSK2292767 is a potent and selective PI3K inhibitor.GSK2292767 is highly selective fo
GSK2981278
(Catalog# : 6111521, Cas# :
1474110-21-8
)
ROR modulator 1 is a retinoid-related orphan receptor gamma (RORy) modulator, extract
GSK163090
(Catalog# : 6111015, Cas# :
844903-58-8
)
GSK163090 is a potent, selective, and orally active 5-HT1A/B/D receptor antagonist wi
GSK-591
(Catalog# : 6111009, Cas# :
1616391-87-7
)
EPZ015866 (GSK591) is a potent selective inhibitor of the arginine methyltransferase
GSK2269557 free base
(Catalog# : 611826, Cas# :
1254036-71-9
)
GSK-2269557 (free base) is a potent and selective PI3Kδ inhibitor over the closely r
GSK2141795 (hydrochloride)
(Catalog# : 611807, Cas# :
1047635-80-2
)
GSK2141795 Hcl is a potent and selective pan-Akt inhibitor with IC50 values of 180 nM
GSK-690693
(Catalog# : 161009019, Cas# :
937174-76-0
)
Pan-AKT kinase inhibitor GSK-690693 binds to and inhibits Akt kinases 1, 2, and 3, wh
GX-674
(Catalog# : 1681201, Cas# :
1432913-36-4
)
GX-674 is an aryl sulfonamide class of antagonists that inhibits Nav1.7.Nav (voltage-
GDC-0084
(Catalog# : 16071405, Cas# :
1382979-44-3
)
GDC-0084, also known as RG7666, is a phosphatidylinositol 3-kinase (PI3K) inhibitor w
Gilteritinib
(Catalog# : 16071108, Cas# :
1254053-43-4
)
Gilteritinib, also known as (ASP2215, is a potent FLT3/AXL inhibitor, which showed po
GDC-0152
(Catalog# : 16071101, Cas# :
873652-48-3
)
GDC-0152 is a second mitochondrial activator of caspases (Smac) mimetic inhibitor of
GSK-461364
(Catalog# : 16071032, Cas# :
929095-18-1
)
GSK-461364 is a Polo-like kinase 1 inhibitor, is also a small molecule Polo-like kina
GPI-1046
(Catalog# : 16071027, Cas# :
186452-09-5
)
GPI-1046
GBR 12783
(Catalog# : 16071019, Cas# :
67469-57-2
)
GBR 12783
GW4064
(Catalog# : 16071018, Cas# :
278779-30-9
)
GW-4064 is a selective agonist of FXR (EC50 = 15 nM).2 It displays no activity at oth
GSK621
(Catalog# : 16070905, Cas# :
1346607-05-3
)
GSK621 is a specific and potentAMPKactivator.
GSK1210151A
(Catalog# : 16070808, Cas# :
1300031-49-5
)
GSK1210151A, also known as I-BET151, is a BET bromodomain inhibitor, which blocks rec
GDC-0994
(Catalog# : 16062801, Cas# :
1453848-26-4
)
GDC-0994, also known as RG7842, is an orally available inhibitor of extracellular sig
GNF-7
(Catalog# : 16060604, Cas# :
839706-07-9
)
BenzaMide
GR148672X
(Catalog# : 032404, Cas# :
263890-70-6
)
Coming soon!
GW501516
(Catalog# : 030905, Cas# :
317318-70-0
)
Coming soon!
Glesatinib(MGCD-265)
(Catalog# : 012001, Cas# :
936694-12-1
)
Glesatinib is a potent tyrosine kinase inhibitor with potential antineoplastic activi
Gamma-Secretase Modulators
(Catalog# : 011909, Cas# :
937812-80-1
)
Coming soon!
GLYX 13
(Catalog# : 011809, Cas# :
117928-94-6
)
Coming soon!
GDC-0623
(Catalog# : 010811, Cas# :
1168091-68-6
)
GDC-0623 is a potent, ATP-uncompetitive inhibitors of MEK1(Ki=0.13 nM, +ATP); 6-fold
Gepotidacin
(Catalog# : 010610, Cas# :
1075236-89-3
)
Gepotidacin is a potent Type II DNA topoisomerase inhibitor. Gepotidacin is a novel a
GGTI-298
(Catalog# : 010609, Cas# :
1217457-86-7
)
GGTI-298 is a potent geranylgeranyltransferase-I (GGTase-I) inhibitor with potential
Givinostat
(Catalog# : 123008, Cas# :
497833-27-9
)
Givinostat is an orally bioavailable hydroxymate inhibitor of histone deacetylase (HD
GSK2838232
(Catalog# : 122924, Cas# :
1443461-21-9
)
GSK2838232 is a novel human immune virus (HIV) maturation inhibitor being developed f
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产品分类
信号通路
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- 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
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
最新产品
Linafexor (别名: CS-0159)
(Catalog# : 26A089, Cas# :
2765593-43-7
)
Linafexor(同义词:CS-0159)是法尼醇X受体(FXR)的强效非胆汁酸激
Prifetrastat (Synonyms: PF-07248144)
(Catalog# : 26A088, Cas# :
2569008-99-5
)
Prifetrastat (Synonyms: PF-07248144) 是一款首创、选择性、口服活性的
Camonsertib
(Catalog# : 24052, Cas# :
2417489-10-0
)
Camonsertib,也称为RP 3500,是一种新型、强效和选择性的ATR抑制剂,
MRX-2843
(Catalog# : 26A087, Cas# :
1429882-07-4
)
MRX-2843 是一种口服可用的双受体酪氨酸激酶(RTKs)抑制剂,作用
GDC-0134
(Catalog# : 20432, Cas# :
1637394-01-4
)
GDC-0134是一种MAP3K12(DLK)抑制剂。
BI-847325
(Catalog# : 25046, Cas# :
2128698-24-6
)
BI-847325是一种新型的、可口服的、竞争ATP结合位点的Aurora激酶和M
GDD-261
(Catalog# : 26A084, Cas# :
3137699-54-5
)
GDD-261是一种口服活性的磷酸甘油酸脱氢酶变构抑制剂(IC50=61nM)
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
Atebimetinib(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制剂
BH-30643
(Catalog# : 26A047, Cas# :
3062177-59-4
)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制
ERAS-801 ( JGK-068S )
(Catalog# : 20635, Cas# :
2490431-16-6
)
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。