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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
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- Apoptosis
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Cas号索引 1
- 1263373-43-8 | NVP-2 (Catalog# : 193205)NVP-2是细胞周期蛋白依赖性激酶CDK9的抑制剂。
- 1566-81-0 | NS-1652 (Catalog# : 19361)NS-1652是一种阴离子电导抑制剂。
- 1434639-57-2 | ND-646 (Catalog# : 191102)ND-646是ACC酶ACC1和ACC2的变构抑制剂，可阻止ACC亚基二聚化，在体内
- 1434635-54-7 | ND-630 (Catalog# : 19133)ND-630，也称为GS-0976, NDI-010976和firsocostat, 是一种有效的ACC抑制剂。
- 1448232-80-1 | Naquotinib游离 (Catalog# : 1812297)Naquotinib，又称ASP8273，是一种口服、不可逆、第三代、突变选择、
- 1208315-24-5 | N6022 (Catalog# : 1811304)N6022是一种有效、选择性、可逆性和有效性的s -亚硝基谷胱甘肽还
- 1253584-84-7 | NMS-E973 (Catalog# : 1810293)NMS-E973是一种新型、选择性和强效的热休克蛋白90 (Hsp90)抑制剂。
- 153587-01-0 | NS1619 (Catalog# : 1810227)NS1619是一种Bkca开启工具或大电导Ca2+活化钾(Bkca, KCa1.1)通道激活器
- 1452458-86-4 | Nacubactam (Catalog# : 185169)Nacubactam, 也称为RG-6080, FPI-1459, 和OP-0595, 是一种β-内酰胺酶抑制剂
- 108852-90-0 | Nemorubicin (Catalog# : 185167)Nemorubicin，又名PNU152243A，是一种不同于其母体药物的doxorubicin衍生
- 152946-68-4 | Nolatrexed盐酸盐 (Catalog# : 185166)Nolatrexed，也叫AG337，是一种具有潜在抗癌活性的胸腺嘧啶合成酶抑
- 1773489-72-7 | Nidufexor (Catalog# : 184288)Nidufexor是一个法呢醇X受体(FXR)激动剂。
- 1422144-42-0 | Netarsudil(Mesylate) (Catalog# : 712181)Netarsudil( AR-11324) is a Rho-associated protein kinase inhibitor. Netarsudil is pot
- 1140844-63-8 | nor-NOHA醋酸盐 (Catalog# : 1710169)nor-NOHA是一种强效、选择性、竞争性、以及精氨酸酶的高亲和力抑
- 1262417-51-5 | NMS-P118 (Catalog# : 17101311)NMS-P118是一种有效的、可口服、高选择性PARP-1抑制剂具有优良的AD
- 1508250-71-2 | Nazartinib (EGF816) (Catalog# : 1781004)Nazartinib，也被称为EGF816，是一种口服可用,不可逆转的、第三代、
- 1254032-66-0 | Netarsudil (Catalog# : 1781001)<span style="color:#34495E;font-family:" font-size:14px;background-color
- 1676893-24-5 | NSC781406 (Catalog# : 20178810)NSC781406是一种高效针对PI3K的IC50为2 nM的PI3K和mTOR抑制剂。
- 1916571-90-8 | NCT-503 (Catalog# : 2017888)NCT-503是一种3 -磷酸甘油酸脱氢酶(PHGDH)抑制剂,抑制丝氨酸合成3 -磷
- 1304630-27-0 | NGP-555 (Catalog# : 2017875)NGP 555正在被作为一种预防疾病老年痴呆症的治疗。
- 147149-76-6 | 诺拉曲特 (Catalog# : 17030908)诺拉曲特，也叫AG337，是一种具有潜在抗癌活性的百里香酶抑制剂
- 1221713-92-3 | NPS-1034 (Catalog# : 17030907)NPS-1034是一种新型的MET抑制剂，它能抑制活化的MET受体及其具有结
- 1400-61-9 | 制霉菌素 (Catalog# : 17030905)制霉菌素是一种多烯抗真菌药物，含有三种生物活性成分的抗生素
- 1354744-91-4 | 聚乙二醇纳诺醇 (Catalog# : 17030202)Naloxegol,也称为NKTR-118和AZ-13337019,是一种选择性的阿片拮抗剂，用于
- 1038915-64-8 | 尼拉帕尼盐酸盐 (Catalog# : 17030114)尼拉帕尼, 也称为MK-4827, 是一种具有潜在抗肿瘤活性的聚(ADP-核糖
- 1698878-14-6 | Nampt-IN-1 (Catalog# : 17022705)Nampt-IN-1是NAMPT的一种新型抑制剂，IC50分别为18 nM(NCI- H1155细胞)，4
- 102586-30-1 | NSC12 (Catalog# : 17021317)NSC12是一种可用于抑制FGF2 / FGFR相互作用并具有良好的抗肿瘤活性
- 123653-11-2 | NS-398 (NS398) (Catalog# : 17011106)NS-398是一种cyclooxygenase-2 (COX-2)的选择性抑制剂。
- 1253952-02-1 | Netarsudil (AR-13324) 2HCl (Catalog# : 1710901)Netarsudil (a.k.a. AR-13324)是一种ROCK抑制剂，Ki值为 0.2-10.3 nM。它目前
- 1313363-54-0 | NVP-CGM097 (Catalog# : 16122789)NVP-CGM097 is a highly potent and selective MDM2 inhibitor. It binds to the p53 bindi
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
- 2102501-84-6 | PF-06835919 ( MDK-1846 ) (Catalog# : 193264)MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
- 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
- 68238-36-8 | 异硫蓝 (Catalog# : 178017)Isosulfan blue 是一种用于淋巴管造影中淋巴管识别的蓝色染料。Isos
- 2803470-63-3 | HC-7366 (Catalog# : 25076)HC-7366 is a potent and selective activator of the general control nonderepressible 2
- 2226636-04-8 | Soquelitinib ( CPI-818 ) (Catalog# : 20671)Soquelitinib（CPI-818）是一种高度选择性的共价白细胞介素-2诱导的T
- 2230263-60-0 | Crelosidenib (Catalog# : 24101)Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast
- 1260247-42-4 | LLL12 (Catalog# : 25075)LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration