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- 抑制剂/受体激动剂
- 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
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- Proteases
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- Vitamin D Related
- Membrane Transporter/Ion Channel
- others
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- Iodos
- Nitro Compounds
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- Piperidines
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Cas号索引 3
- 313348-27-5 | Regadenoson (Catalog# : 1810224)Regadenoson是一种A2A腺苷受体激动剂，是一种冠状血管舒张剂，通常
- 359625-79-9 | Roluperidone ( CYR-101 ) (Catalog# : 2017889)Roluperidone, also known as MIN-101, CYR-101, and MT-210, is a 5-HT2A and sigma 2 rec
- 334969-03-8 | Recilisib钠盐 (Catalog# : 17022712)Recilisib，也被称为 ON 01210钠，是一种放射性保护剂，它可以在接受
- 37854-59-4 | Ro 08-2750 (Catalog# : 17011602)Ro 08-2750是一个强有力的和选择性的神经生长因子(神经生长因子)抑
- 328023-11-6 | Rbin-1 (Catalog# : 1710902)Rbin-1(ribozinoindole-1)是真核核糖体的一种有效的化学抑制剂。它抑制
- 390362-78-4 | RHPS4 (Catalog# : 6111024)RHPS4 is a potent inhibitor of Telomerase at submicromolar.
- 312756-74-4 | RS-1 (Catalog# : 16061501)4-BroMo-N-(4-broMophenyl)-3-[[(phenylMethyl)aMino]sulfonyl]benzaMide;RAD51-stimulator
- 321429-49-6 | (R)-1-(3-Fluorophenyl)ethylamine Hydrochloride (Catalog# : 90725)Coming soon!
- 334618-23-4 | (3R)-piperidin-3-amine,dihydrochloride (Catalog# : 83126)Coming soon!
- 33375-06-3 | (R)-(+)-1-Phenylethyl isocyanate (Catalog# : 82717)Coming soon!
- 3029695-07-3 | SMU-L11 (Catalog# : 24090)
- 303126-97-8 | SR-0987 (Catalog# : 1810263)SR-0987是一个T细胞-特异性RORγ(RORγt)受体激动剂。SR-0987诱导IL-17的
- 307543-71-1 | STF-083010 (Catalog# : 185151)STF-083010,也称为IRE1抑制剂I, 是IRE1/XBP1通路的抑制剂。
- 343306-79-6 | 舒更葡糖钠 (Catalog# : 17011713)舒更葡糖钠是治疗神经肌肉阻滞的药物。
- 307538-42-7 | SMER28 (Catalog# : 17011709)SMER28是一种自噬的小分子调制器，在哺乳动物细胞中独立于雷帕霉
- 312636-16-1 | SKI II (Catalog# : 6111526)SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
- 305834-79-1 | SC79 (Catalog# : 161009025)Akt Activator II, SC79, CAS 305834-79-1, is a cell-permeable compound that interacts
- 380899-24-1 | SB-649868 (Catalog# : 011815)Coming soon!
- 379231-04-6 | Saracatinib (Catalog# : 122913)Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv
- 356559-20-1 | SB 525334 (Catalog# : 102205)SB 525334 is a potent and selective inhibitor of TGF_beta_ receptor I (ALK5) with IC5
- 321429-48-5 | (1S)-1-(3-fluorophenyl)ethanamine,hydrochloride (Catalog# : 90726)Coming soon!
- 325145-35-5 | (S)-1-Boc-2-Ethylpiperazine (Catalog# : 81901)Coming soon!
- 314741-40-7 | (S)-1-Boc-3-(Hydroxymethyl)piperazine (Catalog# : 81825)Coming soon!
- 330161-87-0 | SU6656 (Catalog# : 52754)SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
- 377090-84-1 | SU9516 (Catalog# : 52579)SU-9516 is a selective CDK2 inhibtor with IC50 of 22 nM; less potent for CDK1/CDK4(IC
- 301836-41-9 | SB431542 (Catalog# : 52312)SB431542 is a potent and selective inhibitor ofALK5withIC50of 94 nM, 100-fold more se
- 345627-80-7 | SNS-032 ( BMS-387032 ) (Catalog# : 52105)SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
- 3024657-88-0 | 6,11-二氧代-6,11-二氢-5H-苯并[b]咔唑-2-甲酸叔丁酯 (Catalog# : 24002)Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate, CAS 3024657-88
- 359629-19-9 | tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate (Catalog# : 2062034)
- 313520-94-4 | TH-263 (Catalog# : 2061303)TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
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
- -- 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
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- 1534-35-6 | Isolithocholic Acid (Catalog# : 24146)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- 877768-84-8 | H2-Gamendazole (Catalog# : 24145)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- 2095432-28-1 | CPI-455 HCl (Catalog# : 24144)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- 1215115-03-9 | KH-3 (Catalog# : 24143)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- 2097938-74-2 | Stafib-2 (Catalog# : 24142)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- 2032123-28-5 | TCRS-417 (Catalog# : 24141)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- 1096144-06-7 | PST3 1a (Catalog# : 24140)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- 2225824-53-1 | YTX-465 (Catalog# : 24139)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
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