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- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
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- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- Proteases
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Name Index H
- HDM-2006 ( Synonyms: DD205-291) (Catalog# : 25163)HDM-2006 (DD-205-291) is a a novel PROTAC-based HPK1 degrader with High Potency and S
- HQ461 (Catalog# : 25162, Cas# : 1226443-41-9)HQ461 is a Molecular-glue degrader. HQ461 acts by promoting an interaction between CD
- HC-7366 (Catalog# : 25076, Cas# : 2803470-63-3)HC-7366 is a potent and selective activator of the general control nonderepressible 2
- 1H-Indazole, 6-bromo-1,3-dimethyl- (Catalog# : 25036, Cas# : 1095539-84-6)
- HC-5404 (Catalog# : 25001, Cas# : 2247396-91-2)HC-5404 is a novel, highly selective and potent PERK inhibitor.
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- HTL14242 (Catalog# : 24115, Cas# : 1644645-32-8)HTL14242 is a mGlu5 Negative Allosteric Modulator. Metabotropic glutamate receptors (
- HC-5404-FU (Catalog# : 24112, Cas# : 3034479-99-4)HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
- HH-0043 (Catalog# : 24077, Cas# : 2922069-42-7)
- HFY-4A (Catalog# : 20661, Cas# : 2094810-82-7)HFY-4A is a HDAC inhibitor. HFY-4A inhibits breast cancer cell proliferation, migrati
- Hynic-TOC (Catalog# : 20658, Cas# : 257943-19-4)Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnosti
- HDAC-IN-58 (Catalog# : 20568, Cas# : 2071224-39-8)HDAC-IN-58 is a HDAC inhibitor.
- 1H-1,2,3-triazole, 4,5-diiodo- (Catalog# : 20521, Cas# : 28194-09-4)
- HM43239 (Catalog# : 20517, Cas# : 2569527-64-4)HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
- 4(3H)-Pyrimidinone, 5-bromo-6-cyclopropyl- (Catalog# : 20482, Cas# : 27192-20-7)
- 2(1H)-Pyridinone, 5,6-dihydro-4-(4-methylphenyl)-3-(2H-tetrazol-5-yl)-6-[4-(4,4,4-trifluorobutoxy)phenyl]-6-(trifluoromethyl)-, (6S)- (Catalog# : 20430, Cas# : 1441057-15-3)
- 1H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester (Catalog# : 20422, Cas# : 2086183-72-2)
- 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-1-[tris(1-methylethyl)silyl]- (Catalog# : 20410, Cas# : 651744-48-8)
- 4-hydroxybiphenyl-4-carboxamide (Catalog# : 20404, Cas# : 182318-78-1)
- 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester (Catalog# : 20388, Cas# : 221675-35-0)
- 6-Hydroxyl-2-tetralone (Catalog# : 20371, Cas# : 52727-28-3)
- HISPOLON(P) (Catalog# : 210201, Cas# : 173933-40-9)
- 5-Hydroxymethyldeoxyuridine (Catalog# : 2091910, Cas# : 5116-24-5)5-Hydroxymethyldeoxyuridine is a nucleoside analog with anticancer and antiviral acti
- 5-hydroxy-2,4-dimethylpyrimidine (Catalog# : 2091204, Cas# : 412003-95-3)2,4-dimethylpyrimidin-5-ol is a key intermidiate ofLemborexant. Kg scale may be provi
- H-BETA-ALA-AMC TFA (Catalog# : 2071633, Cas# : 201847-54-3)
- HC-070 (Catalog# : 206104, Cas# : 1628291-95-1)HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepres
- Hydroxyfasudil HCl (Catalog# : 204610, Cas# : 155558-32-0 (HCl))Hydroxyfasudil, aslo known as HA1100, is a cell-permeable hydroxylated metabolite of
- HBX-41108 (Catalog# : 19317, Cas# : 924296-39-9)HBX 41108 is an inhibitor of ubiquitin-specific protease (USP) 7. HBX 41108 inhibits
- HS-1371 (Catalog# : 192223, Cas# : 2158197-70-5)HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis. HS-1371 directly bi
- HZ-1157 (Catalog# : 19182, Cas# : 1009734-33-1)HZ-1157 is a hepatitis C virus (HCV) inhibitor with inhibitory activities toward HCV
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)
- -- 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
- -- 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
- -- 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
- ---- Kallikrein
- ---- IRAK
- -- 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
- ---- Potassium Channel
- -- 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
- ---- Mitochondrial Metabolism
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
- -- 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)
- -- 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)
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- ---- Lipase
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- 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
- -- 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
- MTX115325 (Catalog# : 186264, Cas# : 2750895-97-5)MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
- LY-3381916 (Catalog# : 193123, Cas# : 2166616-75-5)LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
- Opakalim (Catalog# : 25193, Cas# : 2376397-93-0)Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
- DS68591889 (Catalog# : 25158, Cas# : 2488609-21-6)DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
- CAY 10566 (Catalog# : 10403, Cas# : 944808-88-2)CAY 10566 is a potent selective SCD-1 inhibitor.
- Cadefrecitinib (GLPG-3667) (Catalog# : 20509, Cas# : 2308520-97-8)Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
- QBS10072S (Catalog# : 25190, Cas# : 1802735-28-9)QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
- Dencatistat (Catalog# : 25177, Cas# : 2377000-84-3)Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
- DS-1001b (Catalog# : 25178, Cas# : 1898207-64-1)DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.
- Z57346765 (Catalog# : 25191, Cas# : 1016340-64-9)Z57346765 is a PGK1-specific inhibitor that reduces the activity of metabolic enzymes