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Cas Index 1
- 1170108-38-9 | 3-Boc-Aminomethyl-Azetidine Hydrochloride (Catalog# : 81722)Coming soon!
- 172603-05-3 | 3-(Boc-amino)piperidine (Catalog# : 81702)Coming soon!
- 154057-56-4 | 3-(Bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline (Catalog# : 81306)Related API & intermediates:Cas#147526-32-7 Pitavastatin CalciumCas# 24922-02-9 E
- 162167-97-7 | 1-Boc-3-(aminomethyl)piperidine (Catalog# : 81032)Coming soon!
- 141774-61-0 | 2-(Boc-Aminomethyl)-Piperidine (Catalog# : 81027)Coming soon!
- 135632-53-0 | 4-(Boc-aminomethyl)piperidine (Catalog# : 81026)Coming soon!
- 143238-38-4 | 1-Boc-piperazine (Catalog# : 81025)Coming soon!
- 112275-50-0 | 1-Boc-hexahydro-1,4-diazepine (Catalog# : 81024)Coming soon!
- 13343-63-0 | Benzyl-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside (Catalog# : 80301)Coming Soon
- 1009817-63-3 | b-AP15 (Catalog# : 73106)b-AP15 is a specific inhibitor of the deubiquitinating enzymes Uch37 and Usp14 of the
- 188011-69-0 | Bikinin (Catalog# : 61002)Bikinin(Abrasin) is a potent inhibitor of plant GSK-3/Shaggy-like kinase; activates B
- 1538604-68-0 | BLU9931 (Catalog# : 60303)BLU9931 is a potent and irreversible small-molecule inhibitor of FGFR4, as a targeted
- 1092443-52-1 | BS-181 (Catalog# : 52755)BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selecti
- 19542-67-7 | BAY 11-7082 (Catalog# : 52713)BAY 11-7082 is aNF-Binhibitor, inhibits TNF-inducedIBphosphorylation withIC50of 10 M
- 196309-76-9 | Bay 11-7085 (Catalog# : 52712)BAY 11-7085 is an irreversible inhibitor of TNF-inducedIBphosphorylation withIC50of 1
- 153559-49-0 | Bexarotene (Catalog# : 52601)Bexarotene (Targretin) is a selective RXR agonist approved for the treatment of CTCL.
- 1397219-81-6 | BS-181 HCl (Catalog# : 52578)BS-181 HCl is a highly selectiveCDK7inhibitor withIC50of 21 nM. It is more than 40-fo
- 1174046-72-0 | BMS-794833 (Catalog# : 52205)BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2 with IC50 of 1.7/15 nM
- 1187594-09-7 | Baricitinib (Catalog# : 51908)Baricitinib (also known as LY3009104 or INCB028050) is a novel and potent small molec
- 1256349-48-0 | Chiauranib (Catalog# : 25146)Chiauranib also known as orally available, small molecule inhibitor of select serine-
- 1371587-51-7 | Cavosonstat (Catalog# : 25045)Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
- 1621999-82-3 | CC-90003 (Catalog# : 25041)CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E
- 1403859-14-2 | CC90001 free base (Catalog# : 24095)CC-90001 is a potent and selective JNK inhibitor, which is 12.9-fold more potent for
- 1261451-92-6 | 5-chloro-2-methoxypyridine-3-sulfonyl chloride (Catalog# : 24022)5-chloro-2-methoxypyridine-3-sulfonyl chloride, CAS 1261451-92-6.
- 1370032-20-4 | CUR5g (Catalog# : 20678)CUR5g is a potent autophagy inhibitor.
- 1112968-42-9 | Contezolid free base (Catalog# : 20653)Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i
- 1610759-22-2 | CFI-402257 free base (Catalog# : 20626)CFI-402257 was discontinued for commercial reason.
- 1345858-76-5 | CYM-50308 (Catalog# : 20488)CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity
- 1623747-97-6 | CRANAD-28 (Catalog# : 20478)CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts
- 1621164-74-6 | Camlipixant ( BLU-5937 ) (Catalog# : 20455)Camlipixant is an investigational, twice-daily oral P2X3 receptor antagonist for the
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
- -- 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
- -- 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
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- -- 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
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- -- 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
- -- 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
- 2669009-92-9 | Atebimetinib (Catalog# : 25148)Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
- 2242751-53-5 | Acoramidis hydrochloride (Catalog# : 24068)Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
- 2230263-60-0 | Crelosidenib (Catalog# : 24101)Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
- 2833703-74-3 | LOXO-435 (Catalog# : 25080)LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
- 2439277-80-0 | MAT2A-IN-9 (Catalog# : 25147)MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
- 2446928-30-7 | Gridegalutamide (Catalog# : 25138)Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
- 1256349-48-0 | Chiauranib (Catalog# : 25146)Chiauranib also known as orally available, small molecule inhibitor of select serine-
- 1581714-49-9 | Atuzabrutinib (Catalog# : 25145)Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
- 2254145-43-0 | Andamertinib (Catalog# : 25144)Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
- 2769008-22-0 | MEN-1703 (Catalog# : 25143)