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Cas Index 1
- 1001917-37-8 | MK-8033 (Catalog# : 011801)MK8033 is a novel and specific dual ATP competitive c-Met/Ron inhibitor (IC50=1 nM Wt
- 1222800-79-4 | ML324 (Catalog# : 011301)ML324 is a potent JMJD2 demethylase inhibitor with demonstrated antiviral activity.
- 1227923-29-6 | MK7622 (Catalog# : 51627)MK-7622isused as adjunctive therapy to acetylcholinesterase inhibitors (AChEIs) for t
- 1038915-60-4 | MK-4827 (Catalog# : 123007)MK-4827 is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8 nM/2.1 nM; with grea
- 118414-82-7 | MK 886 (Catalog# : 122217)MK 886 is a leukotriene antagonist. It may perform this by blocking the 5-lipoxygenas
- 1430213-30-1 | ML216 (Catalog# : 122101)ML216 is a potent inhibitor of the DNA unwinding activity of BLM helicase; showing si
- 1010085-13-8 | MK-5108 (Catalog# : 121504)MK-5108 is a highly selective Aurora A inhibitor with IC50 of 0.064 nM; 220- and 190-
- 115550-35-1 | Marbofloxacin (Catalog# : 121425)Marbofloxacin is a potent antibiotic of which depends upon its inhibition of DNA-gyra
- 1162656-22-5 | MCB-613 (Catalog# : 111305)Coming soon!
- 133407-82-6 | MG-132 (Catalog# : 111303)MG-132 is an inhibitor of proteasome with IC50 of 100 nM, and also inhibits calpain w
- 1303607-60-4 | MI-773 (Catalog# : 102207)MI-773 is an orally available spiro-oxindole HDM2 (human double minute 2) antagonist
- 1265905-21-2 | methyl 2-((1R,3S)-3-amino-1-hydroxy-4-methylpentyl)thiazole-4-carboxylate (Catalog# : 91809)Coming soon!
- 1206524-85-7 | MK-5172 intermediate (Catalog# : 91802)MK-5172(Grazoprevir) intermediate
- 1206524-84-6 | Methyl (1aR,5S,8S,10R,22aR)-5-tert-butyl-14-methoxy-3,6-dioxo- (Catalog# : 91801)MK-5172(Grazoprevir) intermediate
- 183429-63-2 | METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE (Catalog# : 83111)Coming soon!
- 13623-25-1 | 6-Methoxy-1-indanone (Catalog# : 81924)Coming soon!
- 18372-22-0 | methyl 2-(1H-indol-3-yl)-2-oxoacetate (Catalog# : 81921)Coming soon!
- 196929-78-9 | 2-methylpropane-2-sulfinamide (Catalog# : 81914)Coming soon!
- 129799-08-2 | Methyl 4-Boc-Piperazine-2-Carboxylate (Catalog# : 81704)Coming soon!
- 1131594-45-0 | Methyl 3-bromo-4-(trifluoromethoxy)benzoate (Catalog# : 81018)Coming soon!
- 14034-08-3 | Methyl 3-bromo-4-(tert-butyl)benzoate (Catalog# : 81013)Coming soon!
- 113642-05-0 | Methyl 3-bromo-4-ethylbenzoate (Catalog# : 81007)Coming soon!
- 1131587-97-7 | Methyl 5-bromo-2-methoxy-4-(trifluoromethyl)benzoate (Catalog# : 80310)Coming soon!
- 152849-72-4 | Methyl 5-bromo-2,4-dimethylbenzoate (Catalog# : 80309)Coming soon!
- 121917-57-5 | (-)-MK801(maleate) (Catalog# : 71902)(-)-MK801 is a elective and non-competitive NMDA receptor antagonist. Less active ena
- 1246529-32-7 | MPI-0479605 (Catalog# : 62907)MPI-0479605, a small-molecule inhibitor of the mitotic kinase Mps1.Cells treated with
- 151767-02-1 | Montelukast sodium (Catalog# : 52809)Montelukast Sodium(Singulair) is a potent, selective, anti-inflammatory CysLT1 recept
- 1201902-80-8 | MLN9708 (Catalog# : 52749)MLN9708 immediately hydrolyzed to MLN2238, which is an N-capped dipeptidyl leucine bo
- 1062368-49-3 | ML347 (Catalog# : 52742)ML347(DN193719) is a highly selective ALK1/ALK2 inhibitor with IC50s of 46/32 nM; sho
- 1228960-69-7 | MLN0905 (Catalog# : 52827)MLN0905 is a small-molecule and potent inhibitor of PLK1 with IC50 of 2 nM.
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
- -- 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
- ---- 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)
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- -- 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
- 2243882-74-6 | Zedoresertib (Catalog# : 26A023)Zedoresertib (Debio 0123) is a brain-penetrant, highly selective WEE1 kinase inhibito
- 3033961-38-2 | BEN-28010 (Catalog# : 26A022)BEN-28010 is a freely brain-penetrant, potent, and selective CHK1 inhibitor.
- 3107291-07-3 | Tert-butyl 4-((2-(methylamino)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate (Catalog# : 26B007)
- 2565656-70-2 | Muvalaplin (Catalog# : 20528)Muvalaplin is a small molecule that inhibits formation of Lp(a) by interfering with t
- 2925330-18-1 | MAT2A-IN-22 (Catalog# : 26A021)MAT2A-IN-22 (Compound 29-1) is a blood-brain barrier-penetrant and orally active MAT2
- 1497439-74-3 | AD-8007 (Catalog# : 26A018)AD-8007 is a selective and brain-penetrant inhibitor of acetyl CoA synthase 2 (ACSS2).
- 1802650-31-2 | ZY-444 (Catalog# : 26A020)ZY-444 is an anti-cancer agent by inhibiting PC ( pyruvate carboxylase ) activity.
- 2306525-79-9 | AD-5584 (Catalog# : 26A019)AD-5584 is a novel brain-permeable ACSS2 inhibitors.
- 3079716-11-0 | IDB-003 (Catalog# : 26A017)IDB-003 inhibits MDA-MB-231 tumor growth in vivo.
- 1357362-02-7 | Vafidemstat (Catalog# : 18891)Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1)