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- Inhibitors&Agonists
- 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
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Name Index E
- Ethyl 3-bromo-4-ethylbenzoate (Catalog# : 81010, Cas# : 1131615-08-1)Coming soon!
- Endoxifen (Catalog# : 81002, Cas# : 112093-28-4)Endoxifen is a novel active metabolite of the anti-cancer drug, Tamoxifen, and it con
- Ethyl 3-iodo-4-methylbenzoate (Catalog# : 80314, Cas# : 859212-59-2)Coming soon!
- 4-ethyl-3-iodanyl-benzoic acid (Catalog# : 80312, Cas# : 103441-03-8)Coming soon!
- Ethyl 5-bromo-2-(trifluoromethoxy)benzoate (Catalog# : 80307, Cas# : 773135-66-3)Coming soon!
- E3330 (Catalog# : 62909, Cas# : 136164-66-4)E3330 is a Ape-1/Ref-1 redox antagonist. it may inhibit the growth of tumor endotheli
- Etoposide (Catalog# : 52801, Cas# : 33419-42-0)Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA.
- EPZ-5676 (Catalog# : 52787, Cas# : 1380288-87-8)EPZ-5676 is a potent and selective aminonucleoside inhibitor of DOT1L histone methylt
- Encorafenib(LGX-818) (Catalog# : 179308, Cas# : 1269440-17-6)Encorafenib, also known as LGX818 is a drug candidate for the treatment of melanoma w
- Eletriptan hydrobromide (Catalog# : 52784, Cas# : 177834-92-3)This product is no information for the time being
- Evacetrapib (Catalog# : 52758, Cas# : 1186486-62-3)Evacetrapib (LY2484595) is a potent and selective inhibitor of CETP with IC50 of 5.5
- Empagliflozin (Catalog# : 52720, Cas# : 864070-44-0)Empagliflozin (BI-10773) is a potent and selective SGLT-2 inhibitor with IC50 of 3.1
- ENMD-2076 Tartrate (Catalog# : 52637, Cas# : 1291074-87-7)ENMD-2076 tartrate has selective activity against Aurora A and Flt3 with IC50 of 14 n
- Entinostat (Catalog# : 52607, Cas# : 209783-80-2)Entinostat (MS-275; SNDX 275) strongly inhibits HDAC1 and HDAC3 with IC50 of 0.51 M a
- EPZ005687 (Catalog# : 52303, Cas# : 1396772-26-1)EPZ-005687 is a potent and selective inhibitor of EZH2 with Ki of 24 nM, 50-fold sele
- Etofenamate (Catalog# : 52556, Cas# : 30544-47-9)Etofenamate is a non-steroidal anti-inflammatory drug used for the treatment joint an
- ELR510444 (Catalog# : 52503, Cas# : 1233948-35-0)ELR510444 is a novel microtubule disruptor; inhibits MDA-MB-231 cell proliferation wi
- EPZ-6438 (Catalog# : 52302, Cas# : 1403254-99-8)EPZ-6438 is a potent, and selectiveEZH2inhibitor withKiandIC50of 2.5 nM and 11 nM, ex
- Elvitegravir(GS-9137) (Catalog# : 52022, Cas# : 697761-98-1)Elvitegravir (EVG, formerly GS-9137) is an integrase inhibitor used to treat HIV infe
Products Catalog
- ---- 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
Latest Products
- STX-478 (Catalog# : 20633, Cas# : 2883540-92-7)STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
- Iclepertin (BI-425809) (Catalog# : 24084, Cas# : 1421936-85-7)Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
- Bomedemstat (Catalog# : 24001, Cas# : 1990504-34-1)Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
- PLX-4545 (Catalog# : 24111, Cas# : 2892065-45-9)PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
- VVD-130037 ( BAY-3605349 ) (Catalog# : 24110, Cas# : 3034880-93-5)VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
- CBR-5884 (Catalog# : 24109, Cas# : 681159-27-3)CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
- JHU-083 (Catalog# : 24108, Cas# : 1998725-11-3)JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
- LXH-3-71 (Catalog# : 24107, Cas# : 2251753-65-6)LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
- CC-92480 ( Mezigdomide ) (Catalog# : 20510, Cas# : 2259648-80-9)CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
- Adrixetinib ( Q-702 ) (Catalog# : 20617, Cas# : 2394874-66-7)Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag