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- Inhibitors & Agonists
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- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
- Metabolic Enzyme/Protease
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- PI3K/Akt/mTOR
- Stem Cells & Wnt
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Name Index G
- GNE-3511 (Catalog# : 1781006, Cas# : 1496581-76-0)GNE-3511 is a potent and selective dual leucine zipper kinase (DLK, MAP3K12) inhibito
- GSK2193874 (Catalog# : 178914, Cas# : 1336960-13-4)GSK2193874 was identified as a selective, orally active TRPV4 blocker that inhibits C
- GW4869 (Catalog# : 178912, Cas# : 6823-69-4)GW4869 (dihydrochloride hydrate) is a cell permeable, selective inhibitor of N-SMase
- GSK2982772 (Catalog# : 178911, Cas# : 1622848-92-3)GSK2982772 is an ATP competitive eceptor-interacting protein-1 (RIP1) kinase inhibit
- GSK180736A (GSK180736) (Catalog# : 178901, Cas# : 817194-38-0)GSK180736A is potent and selective inhibitor of GRK2 with an IC50 of 0.77 M25 and >10
- GSK2269557 (Catalog# : 2017883, Cas# : 1254036-77-5)GSK2269557,also known as GSK-2269557, is a potent and selective PI3K inhibitor.
- GDC-0326 (Catalog# : 2017881, Cas# : 1282514-88-8)GDC-0326 is a potent and selective inhibitor of α-Isoform of Phosphoinositide 3-Kina
- GSK-1521498 (Catalog# : 20178215, Cas# : 1007573-18-3)GSK-1521498 is a novel -Opioid receptor antagonist. It has been shown to attenuate re
- GSK321 (Catalog# : 2017821, Cas# : 1816331-63-1)GSK321 is a potent and selective IDH1 mutant inhibitor. GSK321 potently inhibited int
- GNE-272 (Catalog# : 20178121, Cas# : 1936428-93-1)GNE-272 is a potent and selective in Vivo Probe for the Bromodomains of CBP/EP300 (CB
- Guanoclor (Catalog# : 17030702, Cas# : 5001-32-1)Guanoclor is an antihypertensive drug.
- GRA Ex-25 (Catalog# : 17030701, Cas# : 307983-31-9)GRA Ex-25 is an inhibitor of glucagon receptor. Inhibiting the interaction between gl
- GTS-21 (Catalog# : 16123016, Cas# : 156223-05-1)GTS-21, also known as DMBX-A, is a derivative of the natural product anabaseine that
- GSK6853 (GSK-6853) (Catalog# : 16123015, Cas# : 1910124-24-1)GSK6853 is a potent (300 pM), soluble, cell active (20 nM), and highly selective inhi
- GSK583 (Catalog# : 16123014, Cas# : 1346547-00-9)GSK583 is a Highly Potent and Selective Inhibitor of RIP2 Kinase (RIP2K bing IC50=5 n
- GSK369796 Dihydrochloride (Catalog# : 16123013, Cas# : 1010411-21-8)GSK369796, also known as N-tert-butylisoquine, is an anti-malaria drug candidate. GSK
- GSK2801 (Catalog# : 16123012, Cas# : 1619994-68-1)GSK2801 is a A Selective Chemical Probe for BAZ2B/A bromodomains. BAZ2A/B belong to a
- GSK-2256098 (Catalog# : 16123011, Cas# : 1224887-10-8)GSK2256098, also known as GTPL7939, is a focal adhesion kinase-1 (FAK) inhibitor with
- GSK137647A (Catalog# : 16123010, Cas# : 349085-82-1)GSK137647A is an agonist of the free fatty acid receptor 4 (FFA4/GPR120) with pEC50s
- GSK0660 (Catalog# : 16123009, Cas# : 1014691-61-2)GSK0660 is a selective PPAR antagonist. GSK0660 differentially regulated 273 transcri
- Go6983 (Catalog# : 16123008, Cas# : 133053-19-7)GO6983 is a potent protein kinase C (PKC) inhibitor. GO6893 displays cardioprotective
- GNE-617 (Catalog# : 16123007, Cas# : 1362154-70-8)GNE-617 is a potent nicotinamide phosphoribosyltransferase (NAMPT) inhibitor with IC5
- GlyH-101 (Catalog# : 16123006, Cas# : 328541-79-3)GlyH-101 is a CFTR inhibitor (cystic fibrosis transmembrane conductance regulator). G
- GLPG-1690(ziritaxestat) (Catalog# : 16123005, Cas# : 1628260-79-6)GLPG1690 is a selective autotaxin inhibitor discovered by Galapagos, with potential a
- GDC-0853 (Catalog# : 16123004, Cas# : 1434048-34-6)GDC-0853 is orally available inhibitor of Bruton's tyrosine kinase (BTK) with potenti
- GABOB (beta-hydroxy-GABA) (Catalog# : 16122815, Cas# : 7013-05-0)GABOB, also known as -Amino--hydroxybutyric acid, -hydroxy--aminobutyric acid, -hydro
- Gabexate mesylate (Catalog# : 16122814, Cas# : 56974-61-9)Gabexate is a serine protease inhibitor which is used therapeutically (as gabexate me
- Glasdegib (PF-04449913) (Catalog# : 16122787, Cas# : 1095173-27-5)Glasdegib (PF-04449913) is a potent, and orally bioavailable Smoothened (Smo) inhibit
- Go6976 (Catalog# : 16122723, Cas# : 136194-77-9)Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat
- GSK2292767 (Catalog# : 16122702, Cas# : 1254036-66-2)GSK2292767 is a potent and selective PI3K inhibitor.GSK2292767 is highly selective fo
Products Catalog
- ---- 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)
- ---- NEKs
- -- 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
- ---- Methionine Adenosyltransferase (MAT)
- -- 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
- ---- Bradykinin Receptor
- ---- GLP Receptor
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- ---- Kallikrein
- ---- IRAK
- ---- Reactive Oxygen Species(ROS)
- ---- SOD
- -- 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
- -- Metabolic Enzyme/Protease
- ---- PPAR
- ---- Proteasome
- ---- P450
- ---- Caspase
- ---- HSP
- ---- HIV Protease
- ---- PDE
- ---- MMP
- ---- Factor Xa
- ---- γ-secretase
- ---- Phospholipase
- ---- DPP4
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- NADPH-oxidase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- FPTase
- ---- RAR/RXR
- ---- Acetyl-CoA Carboxylase
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Glutaminase
- ---- Ketohexokinase(KHK)
- ---- Lipase
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- ---- Phosphoglycerate Dehydrogenase (PHGDH)
- -- 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
- ---- Glucosylceramide Synthase (GCS)
- ---- CGRP-Receptor
- ---- TRP-Channel
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- ---- Keap1-Nrf2
- -- 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
- ---- RET
- ---- Phosphoglycerate Kinase (PGK)
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- ---- Vps34
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- ---- Notch
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- ---- DUB
- -- 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
- -- Nuclear Receptor
- ---- Androgen Receptor(AR)
- -- 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
- DPTX-3186 (Catalog# : 26A010, Cas# : 3118994-80-9)DPTX3186, an orally administered small molecule condensate modulator (c-mod) inhibiti
- Avasopasem manganese (GC-4419; M-40419) (Catalog# : 25108, Cas# : 435327-40-5)Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is amimetic of th
- Iclepertin (BI-425809) (Catalog# : 24084, Cas# : 1421936-85-7)Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
- Kartogenin ( KGN ) (Catalog# : 52215, Cas# : 4727-31-5)Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular
- Imisopasem manganese ( M40403; GC4403 ) (Catalog# : 72602, Cas# : 218791-21-0)Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha
- Apecotrep (BI 764198) (Catalog# : 26A048, Cas# : 2311863-36-0)Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor.
- Pantothenate kinase-IN-2 (Catalog# : 26A038, Cas# : 902614-04-4)Pantothenate kinase-IN-2 is a pantothenate kinase inhibitor with IC50 values of 92 nM
- BH-30643 (Catalog# : 26A047, Cas# : 3062177-59-4)BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
- Gridegalutamide (Catalog# : 26A044, Cas# : 2446929-86-6)gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten
- BMS-986365 (Synonyms: CC-94676 ) (Catalog# : 25138, Cas# : 2446928-30-7)BMS-986365, also known as CC-94676, is an orally bioavailable androgen receptor (AR)