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- PI3K/Akt/mTOR
- Epigenetics
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Cas号索引 2
- 2365193-22-0 | Zelasudil (Catalog# : 24014)Zelasudil 是一种有效的、高选择性的口服活性抑制剂，针对 Rho 相关
- 2134675-36-6 | Ziftomenib ( KO-539 ) (Catalog# : 24013)Ziftomenib 是一种口服、有效、选择性的小分子抑制剂，针对 menin 和
- 2728667-27-2 | Zongertinib ( BI 1810631 ) (Catalog# : 24011)Zongertinib [BI 1810631] 是一种人表皮生长因子受体 2 （HER2） 抑制剂。
- 2272904-53-5 | Zasocitinib (Catalog# : 24010)Zasocitinib是一种作用于非受体酪氨酸蛋白激酶 （TYK2）靶点的抑制
- 2173389-57-4 | Zilurgisertib (Catalog# : 20657)Zilurgisertib（之前称为 INCB 00928）是一种激活素受体样激酶 2（ALK2，
- 2201048-82-8 | Zagociguat (Catalog# : 20628)Zagociguat is a guanylate cyclase activator.
- 2739829-00-4 | Zidesamtinib ( NVL-520 ) (Catalog# : 20524)Zidesamtinib ( NVL-520 ) 是一种新型脑渗透性 ROS1 选择性酪氨酸激酶抑
- 2648641-36-3 | Zotizalkib ( TPX-0131 ) (Catalog# : 20318)TPX-0131是下一代 ALK 抑制剂候选药物，目前正在我们针对 ALK+ 晚期
- 2254001-81-3 | ZK824859 (Catalog# : 2071513)ZK824859 is a potent uPA inhibitor as a potential treatment for multiple sclerosis. Z
- 2229042-77-5 | ZL0454 (Catalog# : 193281)ZL0454是一种有效的选择性BRD4抑制剂。ZL0454减少气道炎症,抑制TLR3-
- 2031177-48-5 | ZM223 (Catalog# : 19352)ZM223是一种新型非磺胺NEDD8激活酶抑制剂，对HCT116结肠癌细胞具有
- 210344-98-2 | Z-IETD-FMK (Catalog# : 16122771)Z-IETD-FMK is a specific Caspase-8 inhibitor.Z-IETD-FMK, which inhibits the cleavage
- 221877-54-9 | Zotarolimus (Catalog# : 161009018)It is a semi-synthetic derivative of rapamycin. It was designed for use in stents wit
- 210344-95-9 | Z-DEVD-FMK (Catalog# : 16062112)Z-DEVD-FMK(Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and
- 25775-90-0 | Zucapsaicin (Catalog# : 121415)Comig soon!
- 208260-29-1 | ZM 336372 (Catalog# : 52239)ZM 336372 is a potent and selective c-Raf inhibitor with IC50 of 70 nM, 10-fold selec
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
- 2883540-92-7 | STX-478 (Catalog# : 20633)STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
- 1421936-85-7 | Iclepertin (BI-425809) (Catalog# : 24084)Iclepertin（BI-425809）是一种口服的GlyT-1小分子抑制剂，用于治疗与
- 1990504-34-1 | Bomedemstat (Catalog# : 24001)Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
- 2892065-45-9 | PLX-4545 (Catalog# : 24111)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
- 3034880-93-5 | VVD-130037 ( BAY-3605349 ) (Catalog# : 24110)VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
- 681159-27-3 | CBR-5884 (Catalog# : 24109)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
- 1998725-11-3 | JHU-083 (Catalog# : 24108)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
- 2251753-65-6 | LXH-3-71 (Catalog# : 24107)LXH-3-71是一种新型“分子胶”，可诱导PHGDH和DDB1-CUL4泛素连接酶之
- 2259648-80-9 | CC-92480 ( Mezigdomide ) (Catalog# : 20510)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
- 2394874-66-7 | Adrixetinib ( Q-702 ) (Catalog# : 20617)Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag