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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
- Epigenetics
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- MAPK
- Cytoskeletal Signaling
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- Neuronal Signaling
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Cas号索引 1
- 1404456-53-6 | GSK-2830371 (Catalog# : 1810292)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
- 1196541-47-5 | GDC-0575 (Catalog# : 189272)GDC-0575 (ARRY-575, RG7741)是一种有效的选择性CHK1抑制剂，IC50为1.2 nM。
- 1025821-33-3 | GSK-626616 (Catalog# : 188241)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
- 1373423-53-0 | GSK-J4游离 (Catalog# : 187163)GSK-J4是一种可渗透的、有效的选择性组蛋白去甲基化酶。
- 1015787-98-0 | Gefapixant (Catalog# : 187122)Gefapixant (MK-7264) 是一个口服的、P2X3 受体活性拮抗剂，其对人同源
- 1365970-03-1 | Glecaprevir (Catalog# : 185311)Glecaprevir，也称为ABT-493和A-1282576, 是一种有效治疗HCV的NS 3/4A抑制剂
- 1351761-44-8 | GNE-7915 (Catalog# : 18595)GNE-7915是一种有效的LRRK2激酶抑制剂。
- 1654725-02-6 | GLPG1837 (Catalog# : 1842811)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
- 1416992-39-6 | GC376钠 (Catalog# : 184175)GC376是一种3CLpro抑制剂(3C-样蛋白酶抑制剂)。
- 1243245-18-2 | GNF-6231 (Catalog# : 18494)GNF-6231是一种有效的、具有口服活性的、选择性的Porcupine抑制剂，
- 1616392-22-3 | GSK-3326595 (Catalog# : 184316)GSK-3326595，也被称为EPZ015938，是一种具有口服活性的、强效的、选
- 1252608-59-5 | GIBH-130 (Catalog# : 18428)GIBH-130 is a neuroinflammation inhibitor.
- 1346546-69-7 | GSK872 (Catalog# : 17101621)GSK872是一个受体相互作用蛋白激酶抑制剂（RIP3）。GSK872抑制TNF-α
- 1539314-06-1 | GSK2881078 (Catalog# : 1791316)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
- 1459687-96-7 | GJ-103钠 (Catalog# : 1791116)GJ103氯化钠是通过自动模拟通读复合物GJ072。
- 1459687-89-8 | GJ-103 游离酸 (Catalog# : 1791115)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
- 199657-29-9 | Givinostat HCl (Catalog# : 17919)Givinostat或gavinostat，又名ITF2357，是一个强有力的和口服活性的组蛋
- 1350462-55-3 | 阿那匹韦 (Catalog# : 1783018)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。
- 1496581-76-0 | GNE-3511 (Catalog# : 1781006)GNE-3511是一种具有选择性的双亮氨酸激酶(DLK,MAP3K12)抑制剂，在神经
- 1336960-13-4 | GSK2193874 (Catalog# : 178914)GSK2193874被认定为一种选择性的、口服的TRPV4阻断剂。
- 1622848-92-3 | GSK2982772 (Catalog# : 178911)GSK2982772是一种ATP竞争性的受体- 1(激酶)抑制剂，IC50值为1 nM。它有
- 1254036-77-5 | GSK2269557 (Catalog# : 2017883)GSK2269557,也称为GSK-2269557, 是一种有效且选择性的PI3K抑制剂.。
- 1282514-88-8 | GDC-0326 (Catalog# : 2017881)GDC-0326是一种有效且选择性的磷酸肌醇的α-同种型3-激酶抑制剂(PI
- 1007573-18-3 | GSK-1521498 (Catalog# : 20178215)GSK-1521498是一种新型阿片受体拮抗剂。它已经被证明可以减弱奖励
- 1816331-63-1 | GSK321 (Catalog# : 2017821)GSK321是一种有效的、选择性的IDH1突变抑制剂。GSK321对HT- 1080细胞内
- 1936428-93-1 | GNE-272 (Catalog# : 20178121)GNE-272对CBP / EP300的溴域具有很强的选择性(CBP IC50 = 0.02 μM, EP300 IC5
- 156223-05-1 | GTS-21 (Catalog# : 16123016)GTS-21, also known as DMBX-A, is a derivative of the natural product anabaseine that
- 1910124-24-1 | GSK6853 (GSK-6853) (Catalog# : 16123015)GSK6853 is a potent (300 pM), soluble, cell active (20 nM), and highly selective inhi
- 1346547-00-9 | GSK583 (Catalog# : 16123014)GSK583 is a Highly Potent and Selective Inhibitor of RIP2 Kinase (RIP2K bing IC50=5 n
- 1010411-21-8 | GSK369796 Dihydrochloride (Catalog# : 16123013)GSK369796, also known as N-tert-butylisoquine, is an anti-malaria drug candidate. GSK
产品分类
- ---- 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
- -- 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
最新产品
- 667411-04-3 | TRPM4-IN-2 (Catalog# : 24147)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- 1534-35-6 | Isolithocholic Acid (Catalog# : 24146)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- 877768-84-8 | H2-Gamendazole (Catalog# : 24145)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- 2095432-28-1 | CPI-455 HCl (Catalog# : 24144)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- 1215115-03-9 | KH-3 (Catalog# : 24143)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- 2097938-74-2 | Stafib-2 (Catalog# : 24142)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- 2032123-28-5 | TCRS-417 (Catalog# : 24141)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- 1096144-06-7 | PST3 1a (Catalog# : 24140)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- 2225824-53-1 | YTX-465 (Catalog# : 24139)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
- 944808-88-2 | CAY10566 (Catalog# : 10403)Coming soon!