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- Inhibitors&Agonists
- PI3K/Akt/mTOR
- Epigenetics
- Protein Tyrosine Kinase
- Angiogenesis
- Apoptosis
- Autophagy
- JAK/STAT
- MAPK
- Cytoskeletal Signaling
- Cell Cycle
- TGF-beta/Smad
- DNA Damage
- Stem Cells & Wnt
- Ubiquitin
- Neuronal Signaling
- NF-κB
- GPCR & G Protein
- Metabolism
- Anti-infection
- Proteases
- Immunology & Inflammation
- Vitamin D Related
- Membrane Transporter/Ion Channel
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- Pyrimidines
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Name Index D
- Dovitinib (Catalog# : 122943, Cas# : 1447274-99-8)Dovitinib is a benzimidazole-quinolinone compound and receptor tyrosine kinase (RTK)
- Doravirine (Catalog# : 122813, Cas# : 1338225-97-0)Coming soon!
- Diethylstilbestrol (Catalog# : 122511, Cas# : 6898-97-1)Diethylstilbestrol is used in the treatment of menopausal and postmenopausal disorder
- Dalcetrapib (Catalog# : 122203, Cas# : 211513-37-0)Dalcetrapib is a rhCETP inhibitor with IC50 of 0.2 M that increases the plasma HDL ch
- Dapoxetine (Catalog# : 121806, Cas# : 119356-77-3)Coming soon
- Dibutylboron trifluoromethanesulfonate (Catalog# : 121501, Cas# : 60669-69-4)Coming soon!
- Deferasirox (Catalog# : 120711, Cas# : 201530-41-8)Deferasirox is an oral iron chelator, which is mainly used to reduce chronic iron ove
- DIGLYCEROL (Catalog# : 120416, Cas# : 59113-36-9)Coming soon!
- Delanzomib (Catalog# : 111302, Cas# : 847499-27-8)Delanzomib is a novel orally-active inhibitor of the chymotrypsin-like activity of th
- Dizocilpine (MK-801) (Catalog# : 110901, Cas# : 77086-21-6)Dizocilpine is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30
- DBeQ (Catalog# : 110221, Cas# : 177355-84-9)DBeQ is a selective, potent, reversible, and ATP-competitive p97 inhibitor with IC50
- 3,5-Dimethyl-2-cyclohexen-1-one (Catalog# : 110210, Cas# : 1123-09-7)Coming soon!
- 2,6-dichloropyridin-4-amine (Catalog# : 110205, Cas# : 2587-02-2)Coming soon!
- D4476 (Catalog# : 102611, Cas# : 301836-43-1)D4476, a cell-permeant inhibitor of CK1_delta_ (IC90 <10 uM), suppresses the site-
- D-Luciferin (Catalog# : 101210, Cas# : 2591-17-5)D-Luciferin is a substrate for firefly luciferase with a Km of approx 2 _mu_M.
- 4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridine,hydrochloride (Catalog# : 92214, Cas# : 917918-79-7)Coming soon!
- 1-(2,2-Difluorobenzo[1,3]dioxol-5-yl)-cyclopropanecarboxylic acid (Catalog# : 92211, Cas# : 862574-88-7)Coming soon!
- 2-(Dicyclohexylphosphino)-2,4,6-Triisopropylbiphenyl (Catalog# : 92204, Cas# : 564483-18-7)Coming soon!
- 2-(2,2-diMethylpyrrolidin-1-yl)ethanaMine (Catalog# : 92201, Cas# : 35018-16-7)Coming soon!
- 3,5-dichloro-6-ethylpyrazine-2-carboxamide (Catalog# : 91830, Cas# : 313340-08-8)Coming soon!
- 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indazole (Catalog# : 91814, Cas# : 1421252-90-5)Coming soon!
- Decernotinib(VX-509) (Catalog# : 90733, Cas# : 944842-54-0)Decernotinib(VX-509) may potently inhibits JAK3 in enzyme assays (Ki = 2.5 nM + 0.7 n
- DDR1-IN-1 (Catalog# : 90801, Cas# : 1449685-96-4)DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50
- 3-(3,5-Dimethoxyphenyl)propionic acid (Catalog# : 90703, Cas# : 717-94-2)Coming soon!
- 3-(3,5-Difluorophenyl)propionic acid (Catalog# : 90616, Cas# : 84315-24-2)Coming soon!
- 3-(2,4-Dihydroxyphenyl)propanoic acid (Catalog# : 90613, Cas# : 5631-68-5)Coming soon!
- D-Serine (Catalog# : 90604, Cas# : 312-84-5)Coming soon!
- 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate (Catalog# : 83117, Cas# : 33301-41-6)Coming soon!
- 1-(Diphenylmethyl)-3-Hydroxyazetidine Hydrochloride (Catalog# : 83116, Cas# : 90604-02-7)Coming soon!
- 1-(Diphenylmethyl)azetidine-3-carbonitrile (Catalog# : 83112, Cas# : 36476-86-5)Coming soon!
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
- TRPM4-IN-2 (Catalog# : 24147, Cas# : 667411-04-3)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- Isolithocholic Acid (Catalog# : 24146, Cas# : 1534-35-6)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- CPI-455 HCl (Catalog# : 24144, Cas# : 2095432-28-1)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- KH-3 (Catalog# : 24143, Cas# : 1215115-03-9)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- Stafib-2 (Catalog# : 24142, Cas# : 2097938-74-2)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- TCRS-417 (Catalog# : 24141, Cas# : 2032123-28-5)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- PST3 1a (Catalog# : 24140, Cas# : 1096144-06-7)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- YTX-465 (Catalog# : 24139, Cas# : 2225824-53-1)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
- CAY10566 (Catalog# : 10403, Cas# : 944808-88-2)Coming soon!