武汉永璨生物科技有限公司
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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
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产品名字索引 E
- Emraclidine (Catalog# : 24118, Cas# : 2170722-84-4)Emraclidine, also known as CVL-231 and PF-06852231, is a novel, brain-penetrant, high
- EG-2184 (Catalog# : 24075, Cas# : 2770297-66-8)
- E7046 (Catalog# : 24055, Cas# : 1369489-71-3)E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
- EPZ-719 (Catalog# : 24032 , Cas# : 2697176-16-0)
- ERAS-801 ( JGK-068S ) (Catalog# : 20635, Cas# : 2490431-16-6)ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。
- Edecesertib (Catalog# : 20636, Cas# : 2408839-73-4)Edecesertib is a serine/threonine kinase inhibitor and anti-inflammatory. Edecesertib
- Ezurpimtrostat HCl (Catalog# : 20607, Cas# : 1914148-73-4)Ezurpimtrostat is a palmitoyl protein thioesterase 1 (PPT-1) inhibitor.
- EN460 (Catalog# : 20603, Cas# : 496807-64-8)EN460 is an endoplasmic reticulum oxidoreductase (ERO1) inhibitor. EN460 showed a dos
- (E)-4-吗啉酮-2-烯酸盐酸盐 (Catalog# : 20546, Cas# : 1419865-05-6)
- 1-乙基-1H-吡唑-4-甲醛 (Catalog# : 20523, Cas# : 304903-10-4)
- ethyl 5-chloro-6-fluoropyrazolo[1,5-a]pyrimidine-3-carboxylate (Catalog# : 20480, Cas# : 2359650-50-1)
- Ervogastat (PF-06865571) (Catalog# : 20449, Cas# : 2186700-33-2)Ervogastat (PF-06865571) 是一种具有全身作用的二酰基甘油酰基转移酶
- ELQ300 (Catalog# : 20447, Cas# : 1354745-52-0)ELQ300 is a novel inhibitor of the mitochondrial cytochrome bc1 complex (complex III
- Etrumadenant (Catalog# : 20443, Cas# : 2239273- 34-6)Etrumadenant, also known as AB928, is a dual antagonist of the A2aR and A2bR adenosin
- E6446 (Catalog# : 20436, Cas# : 1219925-73-1)E6446 is a TLR inhibitor. E6446 inhibits Toll-like receptor (TLR)7 and 9 signaling. E
- Etrumadenant (Catalog# : 171455, Cas# : 2239273-34-6)Etrumadenant, also known as AB928, is a dual antagonist of the A2aR and A2bR adenosin
- EZM0414 (Catalog# : 171652, Cas# : 2411748-50-8)EZM0414 是一种有效的、选择性的、具有口服生物利用度的 SETD2 抑制
- 4,6-二羟基哒嗪-3-甲酸乙酯 (Catalog# : 20390, Cas# : 1352925-63-3)
- 5-(Ethoxycarbonyl)-2-formyl-4-methyl-1H-pyrrole-3-propanoic Acid Methyl Ester (Catalog# : G20384, Cas# : 54278-05-6)
- 3-甲酰基-4-羟基苯甲酸乙酯 (Catalog# : 20366, Cas# : 82304-99-2)
- ethyl 3-bromo-4-ethoxy-5-formylbenzoate (Catalog# : 20365, Cas# : 2701520-23-0)
- 乙基 4-羟基-6-甲基吡唑并[1,5-A]吡嗪-2-甲酸基酯 (Catalog# : 20360, Cas# : 1443978-76-4)
- 4-氯-6-甲基吡唑并[1,5-A]吡嗪-2-甲酸乙酯 (Catalog# : 20359, Cas# : 1449598-75-7)
- 乙基 4,6-二甲基吡唑并[1,5-A]吡嗪-2-甲酸基酯 (Catalog# : 20358, Cas# : 1449598-76-8)
- Eribulin Mesylate (Catalog# : 20354, Cas# : 441045-17-6)Eribulin is an anticancer drug marketed by Eisai Co. under the trade name Halaven. Er
- 2-氧代-4-乙氧基-1,2-二氢吡啶-3-甲酸乙酯 (Catalog# : 20327, Cas# : 1174046-84-4)
- Ecopipam hydrochloride ( SCH-39166 ) (Catalog# : 20296, Cas# : 190133-94-9)Ecopipam HCl is a Selective Dopamine Receptor D1/D5 Antagonist used in the treatment
- Elinzanetant ( NT-814 ) (Catalog# : 20259, Cas# : 929046-33-3)Elinzanetant，以前称为 NT-814 (45)，是一种双重 NK1,3R 拮抗剂，因此有
- 依拉司群 (Catalog# : 16122809, Cas# : 722533-56-4)依拉司群(Elacestrant), also known as RAD1901, is an orally available, selective e
- E6446 (Catalog# : 21240, Cas# : 1219925-73-1)
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
- TRPM4-IN-2 (Catalog# : 24147, Cas# : 667411-04-3)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- Isolithocholic Acid (Catalog# : 24146, Cas# : 1534-35-6)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- CPI-455 HCl (Catalog# : 24144, Cas# : 2095432-28-1)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- KH-3 (Catalog# : 24143, Cas# : 1215115-03-9)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- Stafib-2 (Catalog# : 24142, Cas# : 2097938-74-2)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- TCRS-417 (Catalog# : 24141, Cas# : 2032123-28-5)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- PST3 1a (Catalog# : 24140, Cas# : 1096144-06-7)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- YTX-465 (Catalog# : 24139, Cas# : 2225824-53-1)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
- CAY10566 (Catalog# : 10403, Cas# : 944808-88-2)Coming soon!