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- Inhibitors & Agonists
- Angiogenesis
- Anti-infection
- Apoptosis
- Autophagy
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- Immunology & Inflammation
- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
- Metabolism
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- Proteases
- PI3K/Akt/mTOR
- Stem Cells & Wnt
- TGF-beta/Smad
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Name Index D
- 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!
- 4,7-Difluoroindan-1-one (Catalog# : 83107, Cas# : 130408-16-1)Coming soon!
- 5,6-difluoro-2,3-dihydroinden-1-one (Catalog# : 83106, Cas# : 161712-77-2)Coming soon!
- 4,5-Difluoro-2,3-dihydro-1H-inden-1-one (Catalog# : 83105, Cas# : 628732-11-6)Coming soon!
- 4,6-difluoro-2,3-dihydroinden-1-one (Catalog# : 81938, Cas# : 162548-73-4)Coming soon!
- 2,4-Dichloro-6-phenyl-1,3,5-triazine (Catalog# : 81719, Cas# : 1700-02-3)Coming soon!
- 5,6-Dichloropyridazin-4-amine (Catalog# : 81006, Cas# : 89180-50-7)Coming soon!
- Dinaciclib(SCH-727965) (Catalog# : 63010, Cas# : 779353-01-4)Dinaciclib is a novel potent small molecule inhibitor of cyclin-dependent kinases (CD
- 1-(2,4-Dihydroxy-5-isopropylphenyl)ethanone (Catalog# : 62801, Cas# : 747414-17-1)1-(2,4-Dihydroxy-5-isopropylphenyl)ethanone, CAS#747414-17-1, Off-white solid
- Daclatasvir (Catalog# : 52776, Cas# : 69304-47-8)Daclatasvir (BMS-790052; EBP 883) is a first-in-class, highly-selective oral HCV NS5A
- Dorsomorphin (Catalog# : 52744, Cas# : 866405-64-3)Dorsomorphin(Compound C; BML-275) has been shown to act as a potent and selective inh
- Dabrafenib (Catalog# : 52731, Cas# : 1195765-45-7)Dabrafenib (GSK2118436) is a mutant BRAFV600 specific inhibitor with IC50 of 0.8 nM,
- DMH-1 (Catalog# : 52730, Cas# : 1206711-16-1)DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/107.9/<5 nM for ALK
- Dorsomorphin dihydrochloride (Catalog# : 52704, Cas# : 1219168-18-9)Dorsomorphin 2Hcl (Compound C; BML-275) has been shown to act as a potent and selecti
- Dapivirine (Catalog# : 52549, Cas# : 244767-67-7)Dapivirine(TMC 120, TMC 120 R147681) is a NNRTI for HIV reverse transcriptase with IC
- Dynasore (Catalog# : 52514, Cas# : 304448-55-3)Dynasore is a cell-permeable small molecule that inhibits the GTPase activity of dyna
- DMOG (Catalog# : 52236, Cas# : 89464-63-1)Dimethyloxallyl Glycine(DMOG) is a cell permeable, competitive inhibitor of HIF-PH(HI
- Doxercalciferol (Catalog# : 52313, Cas# : 54573-75-0)Doxercalciferol is a synthetic analog of vitamin D.
- DAPT(GSI-IX) (Catalog# : 52202, Cas# : 208255-80-5)DAPT (GSI-IX) is a novel-secretaseinhibitor, which inhibits A production withIC50of 2
- DCC-2036(Rebastinib) (Catalog# : 52023, Cas# : 1020172-07-9)Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast
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
- -- 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
- -- 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
- -- 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
- -- 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
- Safusidenib (Catalog# : 25149, Cas# : 1898206-17-1)Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
- HC-7366 (Catalog# : 25076, Cas# : 2803470-63-3)HC-7366 is a potent and selective activator of the general control nonderepressible 2
- Dencatistat (Catalog# : 25177, Cas# : 2377000-84-3)Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
- Flavopiridol ( Alvocidib ) (Catalog# : 237071, Cas# : 146426-40-6)Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
- AG-270 (Catalog# : 25176, Cas# : 2201056-66-6)MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
- AZD-5904 (Catalog# : 181121, Cas# : 618913-30-7)AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
- ALT-007 (Catalog# : 25157, Cas# : 2035010-37-6)ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
- Nizubaglustat ( Synonyms: AZ-3102 ) (Catalog# : 25175, Cas# : 1633666-49-5)Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn
- Catadegbrutinib (Synonyms: BGB-16673; BTK-IN-29) (Catalog# : 25174, Cas# : 2736508-60-2)
- Anatibant (Synonyms: LF 16-0687; XY-2405) (Catalog# : 25173, Cas# : 209733-45-9)