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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
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- Membrane Transporter/Ion Channel
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Name Index T
- Teclozan (Catalog# : 20279, Cas# : 5560-78-1)Teclozan is an antiprotozoal agent. It is a dichloroacetamide.
- TOVINONTRINE ( IMR-687 ) (Catalog# : 218701, Cas# : 2062661-53-2)TOVINONTRINE ( IMR-687 ) is a highly selective and potent small molecule inhibitor of
- 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1-(TRIISOPROPYLSILYL)-1H-INDOLE (Catalog# : 21254, Cas# : 690632-17-8)
- Targocil (Catalog# : 21239, Cas# : 1200443-21-5)Targocil is a antibiotic, inhibiting a late step in wall teichoic acid biosynthesis a
- Tasisulam (Catalog# : 2121222, Cas# : 519055-62-0)Tasisulam, also known as LY573636, is an acyl-sulfonamide with potential antineoplast
- trans-ISRIB (Catalog# : 2112801, Cas# : 1597403-47-8)trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2
- Tolebrutinib (Catalog# : 20736, Cas# : 1971920-73-6)Tolebrutinib, also known as SAR442168, is a Bruton tyrosine kinase inhibitor.
- THAL-SNS-032 (Catalog# : 2091903, Cas# : 2139287-33-3)THAL-SNS-032 is a selective CDK9 degrader. THAL-SNS-032 consists of a CDK-binding SNS
- Trilaciclib hydrochloride (G1T28 hydrochloride) (Catalog# : 2073107, Cas# : 1977495-97-8)TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
- Triazavirin ( Riamilovir ) (Catalog# : 2071631, Cas# : 928659-17-0)Triazavirin (TZV, Riamilovir) is a broad-spectrum antiviral drug that is a nucleoside
- T-3775440 HCl (Catalog# : 2071541, Cas# : 1422535-52-1)T-3775440 HCl is a potent, selecitve, irreversible LSD1 inhibitor.
- 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyridine-3-carboxylic acid (Catalog# : 262322, Cas# : 1476799-74-2)
- tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylate (Catalog# : 2062321, Cas# : 130546-33-7)
- tert-butyl 3-bromo-5-chloro-2-fluorophenyl-carbamate (Catalog# : 2062318, Cas# : 1269232-94-1)
- tert-butyl N-(4-bromo-2-methoxyphenyl)carbamate (Catalog# : 2062310, Cas# : 262433-01-2)
- Thiazole-5-carboxylic acid (Catalog# : 2062302, Cas# : 14527-41-4)
- tert-butyl N-[[4-[(Z)-C-chloro-N-hydroxycarbonimidoyl]phenyl]methyl]-N-methylcarbamate (Catalog# : 2062301, Cas# : 1402390-77-5)
- tert-butyl 4-[[6-[2-(quinoxaline-2-carbonylamino)phenyl]imidazo[2,1-b][1,3]thiazol-3-yl]methyl]piperazine-1-carboxylate (Catalog# : 2062035, Cas# : 925436-46-0)
- tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate (Catalog# : 2062034, Cas# : 359629-19-9)
- 4,4,5,5-tetramethyl-2-(4-propan-2-ylsulfonylphenyl)-1,3,2-dioxaborolane (Catalog# : 2062024, Cas# : 1256359-13-3)
- Tafenoquine-d3 succinate (Catalog# : 2061704, Cas# : 1133378-83-2)Tafenoquine-d3 is a trideuerium-labeled Tafenoquine derivative. Tafenoquine, also kno
- TLR4-C34 (Catalog# : 2061501, Cas# : 40592-88-9)TLR4-C34 is a TLR4 inhibitor that inhibits TLR4 signaling in enterocytes and macropha
- TH257 (Catalog# : 2061311, Cas# : 2244678-29-1)TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor.
- TH-263 (Catalog# : 2061303, Cas# : 313520-94-4)TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
- 2,4,6-tris(4-phenylphenyl)-1,3,5-triazine (Catalog# : S-204158, Cas# : 31274-51-8)
- [4-(2,2,2-trifluoroethoxy)phenyl]boronic acid (Catalog# : S-203041, Cas# : 886536-37-4)g scale to Kg scale may be provided.
- TVB-3664 (Catalog# : 2041503)TVB-3664 is a FASN inhibitor which significantly reduces tubulin palmitoylation and m
- TD-106 (Catalog# : 193184, Cas# : 2250288-69-6)TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degrada
- Tafamidis meglumine (Catalog# : 193183, Cas# : 951395-08-7)Tafamidis meglumine , also known as Fx-1006 or PF-06291826, is a drug for the amelior
- Tafamidis (Catalog# : 193182, Cas# : 594839-88-0)Tafamidis, Tafamidis, also known as Fx-1006 or PF-06291826, is a drug for the amelior
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
- BTA-EG4 hydrate (Catalog# : 24157, Cas# : 921193-28-4)BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
- CYD19 (Catalog# : 24156, Cas# : 2415281-52-4)CYD19 is a potent Snail/HDAC dual target inhibitor.
- Phylloflavan (Catalog# : 24155, Cas# : 98570-83-3)Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW
- VK-28 (Catalog# : 24154, Cas# : 312611-92-0)VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
- SR-11302 (Catalog# : 24153, Cas# : 160162-42-5)SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
- AKOS037652256 (Catalog# : 24152, Cas# : 2171065-77-1)AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat
- ML353 (Catalog# : 24151, Cas# : 2990506-75-5)ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM).
- MIF098 (Catalog# : 24150, Cas# : 1208448-95-6)MIF098 is a macrophage migration inhibitory factor (MIF) antagonist.
- TM5441sodium (Catalog# : 24149, Cas# : 2319722-53-5)TM-5441, also known as EBP 883 and BMS-790052, is a potent plasminogen activator inhi
- RGT-018 (Catalog# : 24148, Cas# : 2794934-49-7)RGT-018 is a potent and orally active SOS1 inhibitor with anti-tumor effects.