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Cas Index 9
- 934369-14-9 | TY-52156 (Catalog# : 61118)TY-52156 is a potent S1P3 receptor antagonist in a competitive manner, and the Ki val
- 925705-73-3 | TG100713 (Catalog# : 160926017)TG100713 is an inhibitor of PI3-kinase (IC50 values are 24, 50, 165 and 215 nM for PI
- 905854-02-6 | Tivantinib (Catalog# : 16070802)Tivantinib (ARQ-197) is an orally bioavailable small molecule inhibitor of c-Met with
- 918633-87-1 | TH-302 (Catalog# : 011812)TH-302 is selective hypoxia-activated prodrug targeting hypoxic regions of solid tumo
- 916141-36-1 | TCS 1102 (Catalog# : 121408)TCS 1102 is a potent, dual orexin receptor antagonist (Ki values are 0.2 and 3 nM for
- 941685-27-4 | trimethyl-[2-[[4-(1H-pyrazol-4-yl)pyrrolo[2,3-d]pyrimidin-7-yl]methoxy]ethyl]silane (Catalog# : 91701)Coming soon!
- 928025-61-0 | tert-butyl (3R)-3-(2-methylpropyl)piperazine-1-carboxylate (Catalog# : 81907)Coming soon!
- 928025-57-4 | tert-butyl (3R)-3-propylpiperazine-1-carboxylate (Catalog# : 81906)Coming soon!
- 928025-58-5 | tert-butyl (3S)-3-propylpiperazine-1-carboxylate (Catalog# : 81905)Coming soon!
- 960283-58-3 | tert-butyl (2S)-2-methylpiperazine-1-carboxylate,hydrochloride (Catalog# : 81034)Coming soon!
- 91131-72-5 | 4-tert-butyl-3-iodobenzoic acid (Catalog# : 80315)Coming soon!
- 937270-47-8 | TG02 ( SB1317 ) (Catalog# : 62502)SB1317 (TG02) is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. SB1317 was so
- 948304-40-3 | UC-1728 (Catalog# : 1812292)UC-1728, also known as t-TUCB, is a Soluble epoxide hydrolase inhibitor.
- 903564-48-7 | UM-164 (Catalog# : 186282)UM-164 is a anticancer inhibitor.CAS 903564-48-7.
- 956590-23-1 | UNBS-5162 (Catalog# : 101907)UNBS5162 is a novel naphthalimide that binds to DNA by intercalation and suppresses C
- 934826-68-3 | Visomitin (Synonyms: SKQ1) (Catalog# : 171423)Visomitin (Synonyms: SKQ1) is mitochondria-targeted antioxidant.
- 934493-76-2 | Voxtalisib ( XL-765) (Catalog# : 160926001)PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic
- 936727-05-8 | VX-809(Lumacaftor) (Catalog# : 92219)From Wikipedia, the free encyclopediaLumacaftor (USAN, codenamed VX-809) is an experi
- 960203-27-4 | Vortioxetine hydrobromide (Catalog# : 52716)Vortioxetine Hcl (Lu AA21004 Hcl) is a multimodal serotonergic agent, inhibits 5-HT1A
- 918504-65-1 | Vemurafenib (PLX4032, RG7204) (Catalog# : 52589)Vemurafenib (PLX4032, RG7204) is a novel and potent inhibitor ofB-RafV600EwithIC50of
- 947669-91-2 | WWL70 (Catalog# : 16122847)WWL70 is selective ABHD6 inhibitor, and it has shown anti-inflammatory and neuroprote
- 90332-66-4 | 7-xylosyltaxol (Catalog# : 611947)7-xylosyltaxol(Taxol-7-xyloside) is a taxol (Paclitaxel) derivative; Paclitaxel binds
- 912656-34-9 | XEN907 (Catalog# : 112006)XEN907 is a spirooxindole blocker of NaV1.7 for the treatment of pain.
- 956958-53-5 | XL147 (Catalog# : 51506)XL147 (SAR245408) is a potent and highly selective inhibitor of class I PI3Ks (, , ,
- 912287-56-0 | YHO-13177 (Catalog# : 6111511)YHO-13177 is a potent and specific inhibitor of BCRP; potentiated the cytotoxicity of
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
- -- Antibody-drug Conjugate/ADC Related
- -- 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
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- 2230263-60-0 | Crelosidenib (Catalog# : 24101)Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast
- 1260247-42-4 | LLL12 (Catalog# : 25075)LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration
- 2765081-21-6 | RMC-6236 (Catalog# : 25074)Daraxonrasib, also known as RMC-6236 and RAS-IN-2, is a potent and selective RAS(ON)
- 2991818-13-2 | MGD-28 (Catalog# : 25073)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
- | TG101209 analog 1 (Catalog# : 25072)TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
- 2170729-29-8 | AT-007 (Catalog# : 25071)AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
- 1358751-06-0 | TAK-653 (Catalog# : 25070)TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
- 1801344-14-8 | Emavusertib (Catalog# : 25069)Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
- 1305267-37-1 | Roginolisib (Catalog# : 25068)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel