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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
- Epigenetics
- Protein Tyrosine Kinase
- Angiogenesis
- Apoptosis
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- JAK/STAT
- MAPK
- Cytoskeletal Signaling
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Cas号索引 1
- 1207283-85-9 | TP-434 (Catalog# : 92216)Coming soon!
- 108605-62-5 | Teriflunomide (Catalog# : 91833)Teriflunomide is the active metabolite of leflunomide which is an immunomodulatory dr
- 192057-12-8 | TsDACH RuCl(p-cymene) (Catalog# : 91825)Coming soon!
- 1282512-48-4 | Taselisib(GDC-0032) (Catalog# : 90732)GDC-0032 (RG7604) is a small molecule PI3 kinase inhibitor. PI3 Kinase is an oncogene
- 1208-64-6 | 3-(4-(tert-Butyl)phenyl)propanoic acid (Catalog# : 90701)Coming soon!
- 1217680-19-7 | tert-butyl ((3S,5S)-5-(hydroxymethyl)pyrrolidin-3-yl)carbamate hydrochloride (Catalog# : 90115)Coming soon!
- 1188263-77-5 | tert-butyl N-[4-(methylamino)butyl]carbamate,hydrochloride (Catalog# : 90106)Coming soon!
- 132945-78-9 | tert-butyl (3S)-3-cyanopyrrolidine-1-carboxylate (Catalog# : 83129)Coming soon!
- 183207-64-9 | tert-butyl 3-(benzylamino)piperidine-1-carboxylate (Catalog# : 83115)Coming soon!
- 1226781-82-3 | tert-butyl 2-(methylsulfonyl)-4,6-dihydropyrrolo[3,4-c]pyrazole-5(2H)-carboxylate (Catalog# : 82721)Coming soon!
- 1280210-79-8 | tert-Butyl 4,6-dihydropyrrolo[3,4-c]pyrazole-5(2H)-carboxylate (Catalog# : 82720)Coming soon!
- 1172623-98-1 | tert-butyl [(2R,3S)-2-(2,5-difluorophenyl)-3,4-dihydro-2H-pyran-3-yl]carbaMate (Catalog# : 82719)Coming soon!
- 1000413-72-8 (free base); 1374598-80-7 (0.5 H2O) | TAK-875 (Catalog# : 82601)TAK-875 is a potent, selective, and orally bioavailable GPR40 agonist, with a pharmac
- 143621-35-6 | Triapine (Catalog# : 82402)Triapine(NSC663249; OCX191; PAN-811) is a ribonucleotide reductase inhibitor, has bee
- 1188263-68-4 | tert-butyl N-(4-aminobutyl)-N-methylcarbamate,hydrochloride (Catalog# : 81918)Coming soon!
- 1188263-67-3 | tert-butyl N-(3-aminopropyl)-N-methylcarbamate,hydrochloride (Catalog# : 81910)Coming soon!
- 169448-87-7 | tert-butyl (2R)-2-(hydroxymethyl)piperazine-1-carboxylate (Catalog# : 81827)Coming soon!
- 1173206-71-7 | tert-Butyl 3-(aminomethyl)azetidine-1-carboxylate hydrochloride (Catalog# : 81723)Coming soon!
- 1188263-72-0 | Tert-Butyl pyrrolidin-3-ylcarbamate hydrochloride (Catalog# : 81714)Coming soon!
- 127346-48-9 | tert-Butyl (3-aminopropyl)carbamate hydrochloride (Catalog# : 81711)Coming soon!
- 189819-75-8 | Tert-butyl 4-aminopiperidine-1-carboxylate,hydrochloride (Catalog# : 81710)Coming soon!
- 1188264-09-6 | tert-butyl 3-(aminomethyl)pyrrolidine-1-carboxylate,hydrochloride (Catalog# : 81706)Coming soon!
- 1188263-74-2 | tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride (Catalog# : 81703)Coming soon!
- 1000853-53-1 | Tert-butyl (2R)-2-methylpiperazine-1-carboxylate,hydrochloride (Catalog# : 81701)Coming soon!
- 1188263-69-5 | tert-Butyl (pyrrolidin-3-ylmethyl)carbamate hydrochloride (Catalog# : 81031)Coming soon!
- 1159826-67-1 | tert-Butyl (piperidin-3-ylmethyl)carbamate hydrochloride (Catalog# : 81028)Coming soon!
- 1222998-36-8 | Torin 1 (Catalog# : 52820)Torin 1 is a potent inhibitor of mTORC1/2 with IC50 of 2 nM/10 nM; exhibits 1000-fold
- 1100598-32-0 | Tepotinib (EMD 1214063) (Catalog# : 52785)Tepotinib (EMD 1214063) is a potent and selective c-Met inhibit
- 1228591-30-7 | TAK-632 (Catalog# : 52562)TAK-632 is a selective pan-RAF kinase inhibitor with IC50 values of 2.4/1.4 nM for BR
- 1197300-24-5 | TGR5 Receptor Agonist (Catalog# : 52557)TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the
产品分类
- ---- 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
- ---- Ketohexokinase
- -- 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
最新产品
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- 2521285-05-0 | Sevabertinib ( 别名：BAY-2927088 ) (Catalog# : 25079)Sevabertinib ( BAY-2927088 )是一种口服非共价酪氨酸激酶受体抑制剂（
- 2387898-69-1 | ATH434 mesylate (Catalog# : 20638)ATH434 是一种口服药物，旨在抑制与神经变性有关的病理蛋白的聚
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- 2671128-05-3 | FHD-286 (Catalog# : 20471)FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i
- 3002056-30-3 | NST-628 (Catalog# : 24058)NST-628 是具有血脑屏障渗透性的 MAPK 通路分子胶，能够抑制 RAF 磷
- 2893778-31-7 | PHGDH-IN-3 (Catalog# : 25077)PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
- 2882165-79-7 | CFT1946 (Catalog# : 25078)CFT1946 是一种口服生物可利用的小分子降解剂，可降解实体瘤中的