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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Autophagy
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分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
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Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
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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
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
Others
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
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订购信息
联系我们
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产品名字索引 G
GDC-0927
(Catalog# : 1811301, Cas# :
1642297-01-5
)
GDC-0927, 也称为SRN-927,是下一代口服SERD,其作为一类SERD分子的潜
GSK-5959
(Catalog# : 1811266, Cas# :
901245-65-6
)
GSK-5959是一种有效的选择性BRPF1溴域抑制剂(IC50 = 80 nM)。
GW-870086
(Catalog# : 1811263, Cas# :
827319-43-7
)
GW-870086是一种糖皮质激素受体激动剂,有望用于哮喘和特应性皮炎
GSK9311
(Catalog# : 1811233, Cas# :
1923851-49-3
)
GSK9311是BRPF溴域高效高选择性抑制剂(BRPDF1 pIC50 = 6.0;BRPDF2 pIC50 = 4.3
GW1100
(Catalog# : 1811231, Cas# :
306974-70-9
)
GW1100是一种具有选择性的GPR40拮抗剂。
GW6471
(Catalog# : 181151, Cas# :
880635-03-0
)
GW6471是一种PPARα拮抗剂(IC50 = 0.24μM)。GW6471提高SMRT和NCoR的蛋白质亲
GSK-2830371
(Catalog# : 1810292, Cas# :
1404456-53-6
)
GSK 2830371是WiP1抑制剂。它能抑制淋巴瘤和神经母细胞瘤模型中的细
GENZ-882706
(Catalog# : 1810176, Cas# :
2070864-35-4
)
GENZ-882706是一种有效的集落刺激因子-1受体(CSF-1R)抑制剂。
GDC-0575
(Catalog# : 189272, Cas# :
1196541-47-5
)
GDC-0575 (ARRY-575, RG7741)是一种有效的选择性CHK1抑制剂,IC50为1.2 nM。
GSK-626616
(Catalog# : 188241, Cas# :
1025821-33-3
)
GSK 626616是一种YAK3/DYRK3激酶抑制剂。它是一种潜在治疗化疗性贫血
GT 949
(Catalog# : 187182, Cas# :
460330-27-2
)
GT 949是一种选择EAAT2阳性变构调制器(EC50 = 0.26 nM)。提高谷氨酸的易
GSK-J4游离
(Catalog# : 187163, Cas# :
1373423-53-0
)
GSK-J4是一种可渗透的、有效的选择性组蛋白去甲基化酶。
Gefapixant
(Catalog# : 187122, Cas# :
1015787-98-0
)
Gefapixant (MK-7264) 是一个口服的、P2X3 受体活性拮抗剂,其对人同源
GLL398
(Catalog# : 185313, Cas# :
2077980-83-5
)
GLL398是口服选择性雌激素受体下调物。
Glecaprevir
(Catalog# : 185311, Cas# :
1365970-03-1
)
Glecaprevir,也称为ABT-493和A-1282576, 是一种有效治疗HCV的NS 3/4A抑制剂
GW843682X
(Catalog# : 185292, Cas# :
660868-91-7
)
GW843682X是一种选择性抑制剂,具有polo-样激酶1 (PLK1)和polo-样激酶3
GNE-7915
(Catalog# : 18595, Cas# :
1351761-44-8
)
GNE-7915是一种有效的LRRK2激酶抑制剂。
GLPG1837
(Catalog# : 1842811, Cas# :
1654725-02-6
)
GLPG-1837,又名ABBV-974,是一种新型的关于囊性纤维化跨膜电导校准
GC376钠
(Catalog# : 184175, Cas# :
1416992-39-6
)
GC376是一种3CLpro抑制剂(3C-样蛋白酶抑制剂)。
GNF-6231
(Catalog# : 18494, Cas# :
1243245-18-2
)
GNF-6231是一种有效的、具有口服活性的、选择性的Porcupine抑制剂,
GSK-3326595
(Catalog# : 184316, Cas# :
1616392-22-3
)
GSK-3326595,也被称为EPZ015938,是一种具有口服活性的、强效的、选
GIBH-130
(Catalog# : 18428, Cas# :
1252608-59-5
)
GIBH-130 is a neuroinflammation inhibitor.
GSK872
(Catalog# : 17101621, Cas# :
1346546-69-7
)
GSK872是一个受体相互作用蛋白激酶抑制剂(RIP3)。GSK872抑制TNF-α
GSK2881078
(Catalog# : 1791316, Cas# :
1539314-06-1
)
GSK-2881078是一种潜在的对癌症恶病质的治疗选择性雄激素受体调节
GJ-103钠
(Catalog# : 1791116, Cas# :
1459687-96-7
)
GJ103氯化钠是通过自动模拟通读复合物GJ072。
GJ-103 游离酸
(Catalog# : 1791115, Cas# :
1459687-89-8
)
GJ103游离酸是通过自动模拟通读复合物GJ072。化学诱导通读提前终
10074-G5
(Catalog# : 1791112, Cas# :
413611-93-5
)
10074-G5是一种c-Myc/Max互动抑制剂。10074-G5类似于10058-F4,具体抑制c
GW0742
(Catalog# : 1791110, Cas# :
317318-84-6
)
GW0742也称为GW610742和GW0742X 是PPARδ/β激动剂。GW0742诱导有丝分裂后
Givinostat HCl
(Catalog# : 17919, Cas# :
199657-29-9
)
Givinostat或gavinostat,又名ITF2357,是一个强有力的和口服活性的组蛋
阿那匹韦
(Catalog# : 1783018, Cas# :
1350462-55-3
)
阿那匹韦,也称为MK5172,是一种被批准用于治疗丙型肝炎的药物。
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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)
-- 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
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
AZD0095
(Catalog# : 237072, Cas# :
2750001-23-9
)
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
2-MNG
(Catalog# : 24129, Cas# :
2101538-28-5
)
2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂,具有独特的作
MAT2A-IN-9
(Catalog# : 25147, Cas# :
2439277-80-0
)
MAT2A-IN-9(化合物167)是一种2-氧代喹唑啉衍生物,是一种强效的M
Safusidenib
(Catalog# : 25149, Cas# :
1898206-17-1
)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
阿替美替尼(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制
Acoramidis hydrochloride
(Catalog# : 24068, Cas# :
2242751-53-5
)
Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白(TTR
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib ( [LY3410738)是一种有效的选择性的具有口服活性的突变
LOXO-435
(Catalog# : 25080, Cas# :
2833703-74-3
)
LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
Gridegalutamide
(Catalog# : 25138, Cas# :
2446928-30-7
)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
Chiauranib
(Catalog# : 25146, Cas# :
1256349-48-0
)
Chiauranib also known as orally available, small molecule inhibitor of select serine-