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- Cell Cycle
- TGF-beta/Smad
- DNA Damage
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- Ubiquitin
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Cas Index 1
- 154540-49-5 | Fluoroclebopride (Catalog# : 120811)Coming soon!
- 167933-07-5 | Flibanserin (Catalog# : 101906)Flibanserin is a full agonist of the 5-HT1A receptor (Ki = 1 nM) and, with lower affi
- 146137-76-0 | 2-Fluoro-5-iodobenzaldehyde (Catalog# : 91818)Coming soon!
- 1250921-20-0 | 3-Fluoro-2-(methylamino)benzoic acid (Catalog# : 91805)Coming soon!
- 1194506-26-7 | Fruquintinib (Catalog# : 91711)Fruquintinib is an orally available, small molecule inhibitor of vascular endothelial
- 1643-26-1 | 3-(2-Fluorophenyl)propionic acid (Catalog# : 90609)Coming soon!
- 138423-98-0 | 3-Formylindol-1-yl-Acetic Acid (Catalog# : 81944)Coming soon!
- 1481-32-9 | 6-Fluoro-1-indanone (Catalog# : 81933)Coming soon!
- 1286739-19-2 | FRAX597 (Catalog# : 72803)FRAX597 inhibits the proliferation of NF2-deficient schwannoma cells in culture and d
- 116686-15-8 | FK 3311 (Catalog# : 60203)FK 3311 is a selective inhibitor of COX-2; antiinflammatory agent.
- 131740-09-5 | Flavopiridol(Alvocidib) (Catalog# : 52310)Flavopiridol HCl competes with ATP to inhibit CDKs includingCDK1,CDK2,CDK4andCDK6with
- 1206161-97-8 | Filgotinib (Catalog# : 51612)Filgotinib (GLPG0634) is a selective JAK1 inhibitor with IC50 of 10 nM, 28 nM, 810 nM
- 1191044-58-2 | GSK1059865 (Catalog# : 24131)GSK1059865 is a potent orexin 1 receptor antagonist.
- 1260907-17-2 | GSK 525762A (Catalog# : 171459)
- 133052-90-1 | GF-109203X (Catalog# : L20356)GF-109203X is a potent and highly selective PCK inhibitor, which inhibits PKC isozyme
- 1258292-64-6 | GDC-046 (Catalog# : L20342)GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor for TYK2, JAK1
- 1831144-46-7 | GDC-0214 (Catalog# : c20341)iJak-381 is a highly potent, selective, and inhalable Janus kinase-1 (JAK-1) inhibito
- 106740-09-4 | GYY4137 (Catalog# : L20339)GYY4137 is a novel water-soluble and slow releasing H2S donor. Hydrogen sulfide (H2S)
- 1139889-93-2 | Golgicide A (Catalog# : 20292)Golgicide A is a Potent, selective and reversible inhibitor of GBF1 ArfGEF. Golgicide
- 113852-41-8 | GS 0573 ( PMEDAP ) (Catalog# : 20275)GS 0573 is an antiviral compound that has been studied for potential treatment of Fel
- 1953133-47-5 | Giredestrant (Catalog# : 21248)Giredestrant, also known as GDC-9545 and RG6171, is a SERD. GDC-9545 is an orally ava
- 1652591-81-5 | GSK484 HCl (Catalog# : 20111801)GSK484 is a potent PAD-4 inhibitor (Protein-arginine deiminase type-4). GSK484 potent
- 1093070-16-6 | GRL0617 (Catalog# : 2071625)GRL0617 is a potent, selective and competitive noncovalent inhibitor of SARS PLPro. G
- 1191237-69-0 | GS-441524 (Catalog# : 2071546)GS-441524 is a potent inhibitor of feline infectious peritonitis (FIP) virus with an
- 1622849-43-7 | GSK3145095 (Catalog# : 2071533)GSK3145095 is a potent and orally active RIPK1 inhibitor (IC50 = 5 nM) with potential
- 1629063-81-5 | GNE-131 (Catalog# : 2071509)GNE-131 is a Potent and Selective hNaV1.7 Inhibitor (Na V1.7 IC50 = 3 nM) for the Tre
- 1642581-63-2 | Glumetinib (Catalog# : 203401)Glumetinib, also known as SCC244, is a novel, potent and highly selective inhibitor o
- 1394121-05-1 | GNE-2861 (Catalog# : 111892)GNE-2861 is a potent and exquisitely kinase-selective Group II PAK inhibitor (PAK4 Ki
- 1549811-53-1 | GSK-199 (Catalog# : 193293)GSK199 is a selective PAD4 inhibitor with half-maximum inhibitory concentration (IC50
- 1637770-13-8 | GS-626510 (Catalog# : 193221)GS-626510 is a potent BET family bromodomains inhibitor. It acts by targeting BRD2/3/
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
- 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.
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- 1305267-37-1 | Roginolisib (Catalog# : 25068)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel
- 1198078-60-2 | NT219 (Catalog# : 25067)NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
- 858128-57-1 | SPB linker (Catalog# : 25066)SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
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