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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
分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
Nitro Compounds
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Peg Linkers
Phenols
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Pyridines
Pyrimidines
Quinolines
Sulfonamides
Thiazoles
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联系我们
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
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
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
技术服务
定制合成
工艺研发
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
G-5758
(Catalog# : 24076, Cas# :
2413455-99-7
)
GW-280264 ( GW-280264X )
(Catalog# : 24031, Cas# :
866924-39-2
)
GW-280264 ( GW-280264X ) 是混合 ADAM10/TACE (ADAM17) 金属蛋白酶抑制剂。
Golidocitinib ( AZD-4205 )
(Catalog# : 24028, Cas# :
2091134-68-6
)
Golidocitinib (AZD-4205) 是一种口服 JAK1 选择性激酶抑制剂。
Glecirasib
(Catalog# : 20672, Cas# :
2657613-87-9
)
Ganaxolone
(Catalog# : 20630, Cas# :
38398-32-2
)
Ganaxolone, also known as CCD 1042 and C1042, is a CNS-selective GABAA modulator that
GNE-7883
(Catalog# : 20589, Cas# :
2648450-42-2
)
GNE-7883 is a pan-TEAD inhibitor.
GLPG3667
(Catalog# : 20509, Cas# :
2308520-97-8
)
GLPG3667 是一种口服强效选择性小分子 TYK2 抑制剂,正在开发用于治
苯丁酸甘油酯
(Catalog# : 230401, Cas# :
611168-24-2
)
Glycerol phenylbutyrate 是 sigma-2 (σ2) 受体的一个配体,其 pKi 值
GSK 525762A
(Catalog# : 171459, Cas# :
1260907-17-2
)
GSK5182
(Catalog# : 20375, Cas# :
877387-37-6 (free base)
)
GSK5182 is a specific inverse agonist for estrogen-related receptor γ.
GF-109203X
(Catalog# : L20356, Cas# :
133052-90-1
)
GF-109203X is a potent and highly selective PCK inhibitor, which inhibits PKC isozyme
GDC-046
(Catalog# : L20342, Cas# :
1258292-64-6
)
GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor for TYK2, JAK1
GDC-0214
(Catalog# : c20341, Cas# :
1831144-46-7
)
iJak-381 is a highly potent, selective, and inhalable Janus kinase-1 (JAK-1) inhibito
GYY4137
(Catalog# : L20339, Cas# :
106740-09-4
)
GYY4137 is a novel water-soluble and slow releasing H2S donor. Hydrogen sulfide (H2S)
GDC-0077
(Catalog# : L20335, Cas# :
2060571-02-8
)
Inavolisib, also known as GDC-0077, is a potent and selective PI3K inhibitor. GDC-007
Gloxazone
(Catalog# : 20304, Cas# :
2507-91-7
)
Gloxazone is an effective but toxic anaplasmacide.
Glymidine sodium
(Catalog# : 20295, Cas# :
3459-20-9
)
Glymidine sodium is a sulfonamide hypoglycemic agent which stimulates insulin secreti
Golgicide A
(Catalog# : 20292, Cas# :
1139889-93-2
)
Golgicide A is a Potent, selective and reversible inhibitor of GBF1 ArfGEF. Golgicide
GDC-0077
(Catalog# : 20283)
GDC-0077 is a potent and selective PI3K inhibitor. GDC-0077 blocks an enzyme involved
GS 0573 ( PMEDAP )
(Catalog# : 20275, Cas# :
113852-41-8
)
GS 0573 is an antiviral compound that has been studied for potential treatment of Fel
Giredestrant tartrate
(Catalog# : 20263, Cas# :
2407529-33-1
)
Giredestrant tartrate (GDC-9545 tartrate), a non-steroidal ER ligand, is an orally ac
Giredestrant
(Catalog# : 21248, Cas# :
1953133-47-5
)
Giredestrant, also known as GDC-9545 and RG6171, is a SERD. GDC-9545 is an orally ava
GNF-PF-3777
(Catalog# : 21226, Cas# :
77603-42-0
)
GNF-PF-3777 is a derivative of tryptanthrin.
GSK484 HCl
(Catalog# : 20111801, Cas# :
1652591-81-5
)
GSK484 is a potent PAD-4 inhibitor (Protein-arginine deiminase type-4). GSK484 potent
GCN2iB
(Catalog# : 2071802, Cas# :
2183470-12-2
)
GCN2iB is an ATP-competitive GCN2 inhibitory compound with a better pharmacokinetic p
GRL0617
(Catalog# : 2071625, Cas# :
1093070-16-6
)
GRL0617 is a potent, selective and competitive noncovalent inhibitor of SARS PLPro. G
GS-441524
(Catalog# : 2071546, Cas# :
1191237-69-0
)
GS-441524 is a potent inhibitor of feline infectious peritonitis (FIP) virus with an
GSK3145095
(Catalog# : 2071533, Cas# :
1622849-43-7
)
GSK3145095 is a potent and orally active RIPK1 inhibitor (IC50 = 5 nM) with potential
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
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产品分类
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
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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag