武汉永璨生物科技有限公司
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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
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- Stem Cells & Wnt
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Cas号索引 1
- 14892-97-8 | SCR7 pyrazine (Catalog# : 1712261)SCR7吡嗪是DNA连接酶IV的小分子抑制剂,防止非同源端连接通过干扰
- 1333207-63-8 | SAR-7334盐酸 (Catalog# : 17101610)SAR-7334是一种新颖的、高效的、生物可利用的TRPC6通道，打开了新
- 1160833-51-1 | SEN-826 (Catalog# : 1710168)SEN-826是一种潜在抗癌剂。
- 1366002-50-7 | Senexin A (Catalog# : 1710136)Senexin A是一种强效的选择性与抑制剂（IC50 = 280 nm）。Senexin A结合
- 1799633-27-4 | S63845 (Catalog# : 171071)s63845是专门结合MCL1的BH3结合槽高亲和力的小分子。s63845有效杀死
- 1105698-15-4 | Salermide (Catalog# : 1791511)salermide是一个强大的肿瘤特异性凋亡的影响长寿基因蛋白质抑制剂
- 1308672-74-3 | Sulfatinib (Catalog# : 179135)Sulfatinib是一种口服的血管内皮生长因子受体（VEGFR）1, 2，3，和成
- 101526-62-9 | 司美利特盐酸盐 (Catalog# : 179830)司美利特，也称为CK-1752，是III类抗心律失常药。它是一种选择性
- 168835-82-3 | SU-1498 (Catalog# : 17984)SU-1498是一种选择性的受体酪氨酸激酶抑制剂，血管内皮生长因子
- 1174428-47-7 | SF2523 (Catalog# : 17918)SF2523是一种高效、选择行的日常pan-PI3K/BRD4抑制剂。具有明显的选
- 1450881-55-6 | SAR-20347 (Catalog# : 1781101)SAR-20347是一种强力JAK1和酪氨酸激酶2的双抑制剂 (TYK2).
- 1523406-39-4 | SAR-405 (Catalog# : 2017882)SAR-405是一种有效且选择性的PIK3C3/Vps34抑制剂，防止自噬和协同MTO
- 148554-65-8 | 雷帕霉素(钠盐) (Catalog# : 20177313)雷帕霉素是第一个体内open-ring代谢物,不影响mTOR的雷帕霉素抑制Ch
- 1184843-57-9 | SAR-020106 (Catalog# : 17031004)SAR-020106是一种 ATP -竞争性、强效和选择性的CHK1抑制剂，其IC50为1
- 1456632-41-9 | SH5-07 (Catalog# : 17031002)SH5-07是一种健壮的氧肟抗酸的STAT3抑制剂，它能在体外诱导抗肿瘤
- 138794-73-7 | Sardomozide HCl (Catalog# : 17030306)Sardomozide，又名SAM486A或CGP48664，是第二代多胺合成抑制剂，它抑制
- 149690-05-1 | 钠盐沙库必曲 (Catalog# : 17030108)沙库必曲，也被称为AHU377，是血管紧张素受体神经内肽酶抑制剂被
- 1801747-42-1 | SHP099游离 (Catalog# : 17030107)<SHP099是强有力的,选择性,具有口服生物利用率,是一种IC50 = 0.07μM的
- 1431699-67-0 | 泰地唑胺杂质 A (Catalog# : 17021402)泰地唑胺杂质 A是磷酸四唑磷酸酯活跃的一部分，对革兰氏阳性菌
- 1265965-22-7 | S49076 (Catalog# : 17021309)S49076是一种新型的、能有效抑制IC50值低于20 nmol/ L的MET、AXL / MER和
- 1001908-89-9 | SRT2183 (Catalog# : 17021306)SRT2183是sirtuin子型SIRT1的小分子激活剂，目前由Sirtris制药公司开发
- 18883-66-4 | 链脲菌素 (Catalog# : 17011712)链脲菌素是一种从链球菌中分离出来的甲基亚硝基脲类抗肿瘤抗生
- 1018899-04-1 | Sotagliflozin (Catalog# : 17011711)Sotagliflozin,也称为LX4211,是一种口服活性和双SGLT1 / SGLT2抑制剂，在
- 127254-12-0 | 西他沙星 (Catalog# : 17011706)西他沙星是一种新型的广谱口服氟喹诺酮，它对许多革兰氏阳性、
- 1801747-11-4 | SHP099盐酸盐 (Catalog# : 17011704)SHP099是一个强有力的、选择性、口服生物利用率和有效的IC50 = 0.0
- 1687736-54-4 | SGC707 (Catalog# : 17011702)SGC707是一种强效、选择性和细胞活性的蛋白质精氨酸甲基转移酶3
- 1884220-36-3 | SBI0206965 (Catalog# : 71161)SBI0206965是一种有效的选择性自噬激酶ULK1抑制剂。许多肿瘤变得沉
- 149400-88-4 | Sardomozide (Catalog# : 17011607)Sardomozide，也叫SAM486A或CGP48664,是一种第二代聚胺合成抑制剂，抑制
- 1092539-44-0 | SAR131675 (Catalog# : 17011605)SAR131675是一种有效的选择性vegfr - 3抑制剂。
- 127373-66-4 | Sivelestat (ONO-5046) (Catalog# : 16122760)Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44
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
最新产品
- 667411-04-3 | TRPM4-IN-2 (Catalog# : 24147)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- 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
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