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Cas Index 2
- 2756-85-6 | 1-aminocyclohexane-1-carboxylic acid (Catalog# : 83110)Coming soon!
- 2566-29-2 | 2-amino-2-ethylbutanoic acid (Catalog# : 83109)Coming soon!
- 20776-67-4 | 2-Amino-5-chloro-3-methylbenzoic acid (Catalog# : 81720)Coming soon!
- 2122-63-6 | 4-Amino-3-iodobenzoic acid (Catalog# : 80311)Coming soon!
- 219793-45-0 | AHAS inhibitor (Catalog# : 52739)AHAS inhibitor is a novel acetohydroxyacid synthase(AHAS) inhibitor, a promising drug
- 2627-69-2 | AICAR (Catalog# : 52702)AICAR (Acadesine), is an AMP-activated protein kinase activator, which is used for th
- 2770961-85-6 | BIIB-129 (Catalog# : 24086)
- 2770960-52-4 | BIIB-129 (Catalog# : 24025)BIIB129 is a covalent, selective, small molecule inhibitor of Bruton's tyrosine k
- 2769954-39-2 | BLU-451 (Catalog# : 20668)BLU-451, also known as LNG-451, orally bioavailable, central nervous system (CNS) pen
- 2513289-74-0 | BSJ-04-122 (Catalog# : 20550)
- 2095116-40-6 | brigimadlin (Catalog# : 20533)Brigimadlin is an E3 ubiquitin-protein ligase Mdm2 inhibitor with potential as an ant
- 2607829-38-7 | BDTX-1535 (Catalog# : 20512)BDTX-1535 is a brain-penetrant and potent MasterKey inhibitor of oncogenic mutations
- 2140301-96-6 | Brepocitinib Tosylate (Catalog# : 232252)Brepocitinib ( PF-06700841 ) is an orally available, selective inhibitor of non-recep
- 2098836-45-2 | BRD4 degrader AT1 (Catalog# : 20496)BRD4 degrader AT1 is an analogue of MZ1. It shows improved selectivity for BRD4 degra
- 2531244-56-9 | BJJF078 (Catalog# : 20492)BJJF078 is a potent inhibitor of recombinant human and mouse Transglutaminase enzyme
- 2760881-74-9 | BRD0639 (Catalog# : 20485)BRD0639 is a potent PRMT5 inhibitor. BRD0639 engages the target in cells, disrupts PR
- 2114324-48-8 | BMS-986251 (Catalog# : 20445)
- 2376257-44-0 | Bexotegrast ( PLN-74809 ) (Catalog# : 171680)Bexotegrast (Synonyms: PLN-74809) is a small-molecule, dual selective inhibitor of α
- 2766481-17-6 | BGB-15025 (Catalog# : 171452)BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag
- 2477812-42-1 | Benzeneacetamide, N-ethyl-4-formyl- (Catalog# : 20419)
- 2097334-15-9 | Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester (Catalog# : 20391)
- 2230836-55-0 | BI-3406 (Catalog# : 21234)BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
- 2056261-41-5 | BRD0705 (Catalog# : 202112701)BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
- 2141955-96-4 | BLU-782 (Catalog# : 20121701)
- 2242464-44-2 | BAY-2416964 (Catalog# : 2091906)BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
- 279262-28-1 | 4-(2-Butoxyethoxy)phenylboronic acid (Catalog# : 2091203)
- 2225819-06-5 | BAY-2402234 (Catalog# : 2071553)BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
- 273404-37-8 | Belnacasan (Catalog# : 52004)Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver
- 2113650-03-4 | BMS-1001 (Catalog# : 2062901)
- 202865-80-3 | 4-bromo-2-fluoro-1-propan-2-yloxybenzene (Catalog# : 2062316)
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
- 2883540-92-7 | STX-478 (Catalog# : 20633)STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
- 1421936-85-7 | Iclepertin (BI-425809) (Catalog# : 24084)Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
- 1990504-34-1 | Bomedemstat (Catalog# : 24001)Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
- 2892065-45-9 | PLX-4545 (Catalog# : 24111)PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
- 3034880-93-5 | VVD-130037 ( BAY-3605349 ) (Catalog# : 24110)VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
- 681159-27-3 | CBR-5884 (Catalog# : 24109)CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
- 1998725-11-3 | JHU-083 (Catalog# : 24108)JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
- 2251753-65-6 | LXH-3-71 (Catalog# : 24107)LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
- 2259648-80-9 | CC-92480 ( Mezigdomide ) (Catalog# : 20510)CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
- 2394874-66-7 | Adrixetinib ( Q-702 ) (Catalog# : 20617)Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag