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Cas Index 7
- 728865-23-4 | CHIR-090 (Catalog# : SSC65304)CHIR-090 is a potent LpxC inhibitor, displays two-step time-dependent inhibition and
- 743420-02-2 | Chidamide (Catalog# : 52506)Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM
- 741233-61-4 | 2,5-Dichloro-6-Methoxy-4-Methylquinoline (Catalog# : 2062012)
- 76822-21-4 | Danshensu (Catalog# : 17021315)Danshensu, a herbal preparation used in traditional Chinese medicine, possesses poten
- 74588-78-6 | D-64131 (Catalog# : 16122925)D-64131 is a potent and selective tubulin inhibitor. D-64131 inhibits tumor cell prol
- 749234-11-5 | DMAT (Catalog# : 611913)DMAT is a potent and specific CK2 inhibitor with an IC50 of 0.13 uM.
- 7081-53-0 | Doxapram hydrochloride hydrate (Catalog# : 010607)Doxapram hydrochloride hydrate inhibits TASK-1, TASK-3, TASK-1/TASK-3 heterodimeric c
- 77086-21-6 | Dizocilpine (MK-801) (Catalog# : 110901)Dizocilpine is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30
- 717-94-2 | 3-(3,5-Dimethoxyphenyl)propionic acid (Catalog# : 90703)Coming soon!
- 779353-01-4 | Dinaciclib(SCH-727965) (Catalog# : 63010)Dinaciclib is a novel potent small molecule inhibitor of cyclin-dependent kinases (CD
- 747414-17-1 | 1-(2,4-Dihydroxy-5-isopropylphenyl)ethanone (Catalog# : 62801)1-(2,4-Dihydroxy-5-isopropylphenyl)ethanone, CAS#747414-17-1, Off-white solid
- 722533-56-4 | Elacestrant (Catalog# : 16122809)Elacestrant, also known as RAD1901, is an orally available, selective estrogen recept
- 736992-21-5 | Elamipretide (Catalog# : 20178210)Elamipretide, also known as MTP-131 or D-Arg-Dmt-Lys-Phe-NH2,is a cardiolipin peroxid
- 738606-46-7 | ETC-1002 (Catalog# : 16122703)ETC-1002,also known as Bempedoic acid, is an orally available, once-daily LDL-C lower
- 74011-58-8 | Enoxacin (Catalog# : 120411)Coming soon!
- 754240-09-0 | EHT 1864 (Catalog# : 102602)EHT 1864 is a small molecule inhibitor of Rac1 signaling; modulate _gamma_-Secretase-
- 787548-29-2 | ethyl 1-amino-2-ethenylcyclopropane-1-carboxylate (Catalog# : 92209)Coming soon!
- 7149-65-7 | Ethyl L-pyroglutamate (Catalog# : 90104)Coming soon!
- 773135-66-3 | Ethyl 5-bromo-2-(trifluoromethoxy)benzoate (Catalog# : 80307)Coming soon!
- 71079-09-9 | FOY-251 mesylate (Catalog# : 2091911)FOY-251 is a metabolite of Camostat that acts as a pollen protease inhibitor for prev
- 78538-74-6 | FG-7142 (Catalog# : 2091909)FG-7142 is a benzodiazepine receptor ligand with anxiogenic and proconvulsant propert
- 753924-48-0 | 2-fluoro-4-methyl-5-nitrobenzoic acid methyl ester (Catalog# : 2062015)
- 75607-67-9 | Fludarabine Phosphate (Catalog# : 120705)Coming soon!
- 72411-52-0 | 5-(4-FLUOROPHENYL)-2H-PYRAZOL-3-YLAMINE (Catalog# : 92208)Coming soon!
- 700-84-5 | 5-Fluoro-1-indanone (Catalog# : 81925)Coming soon!
- 72216-06-9 | 2-(4-Fluorophenyl)pyrrolidine (Catalog# : 81917)Coming soon!
- 732302-99-7 | Givinostat HCl hydrate (Catalog# : 25118)Givinostat hydrochloride is a novel histone deacetylase inhibitor with potential anti
- 77603-42-0 | GNF-PF-3777 (Catalog# : 21226)GNF-PF-3777 is a derivative of tryptanthrin.
- 790186-68-4 | GW284543 (Catalog# : 2061310)GW284543, also known as UNC10225170;, is a potent and selective MEK5 inhibitor with t
- 7013-05-0 | GABOB (beta-hydroxy-GABA) (Catalog# : 16122815)GABOB, also known as -Amino--hydroxybutyric acid, -hydroxy--aminobutyric acid, -hydro
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
- 2800223-30-5 | Dabogratinib ( TYRA-300 ) (Catalog# : 24073)Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
- N/A | AF710B (Catalog# : 25205)AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
- 2957874-18-7 | MAT2A inhibitor 5 (Catalog# : 25204)MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
- 1235733-73-9 | (Rac)-AF710B (Catalog# : 24083)AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
- 863888-33-9 | Flurpiridaz-nonradiolabeled (Catalog# : 25203)Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
- 863888-32-8 | Flurpiridaz-Precursor (Catalog# : 25202)Flurpiridaz-Precursor in stock.
- 1800405-30-4 | KL1333 (Catalog# : 25201)KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
- 1369489-71-3 | Palupiprant ( E7046 ) (Catalog# : 24055)E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
- 2460722-04-5 | Oveporexton ( TAK-861 ) (Catalog# : 25194)Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
- 2506273-81-8 | VT-3989 (Catalog# : 25200)VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran