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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
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Cas号索引 1
- 1399715-48-0 | Setafrastat (Catalog# : 192146)Setafrastat是一种转胺酶抑制剂和血管内皮生长因子(VEGF)促进剂。
- 1037210-93-7 | Saridegib (Catalog# : 1812251)Saridegib，又称IPI-926，是一种口服生物利用的环帕胺衍生物，是Hed
- 1260612-13-2 | SAR260301 (Catalog# : 1812134)SAR260301是强有力的和选择性组 I 磷脂酰肌醇-3-激酶(PI3K)β特定抑制
- 1613695-14-9 | SGC-CBP30 (Catalog# : 1810244)SGC-CBP30是CREBBP (CBP)和EP300的有效选择性抑制剂;它们是一般的转录共
- 1362850-20-1 | Seletalisib (Catalog# : 1810221)Seletalisib，也被称为UCB-5857，是一种有效的选择性PI3激酶抑制剂，
- 188817-13-2 | SC-560 (Catalog# : 185113)SC-560是一种有效的具有口服活性和选择性的COX-1抑制剂。
- 1609452-30-3 | SEL120-34A盐酸盐 (Catalog# : 18574)SEL120-34A是一种高效、选择性的CDK8抑制剂，活跃于AML细胞中，具有
- 1816294-67-3 | SR-4370 (Catalog# : 1842814)SR-4370是一种HDAC抑制剂。
- 1821908-49-9 | SGC2085盐酸盐 (Catalog# : 184287)SGC2085是一种强效的选择性共激活剂，它可以使精氨酸甲基转移酶
- 1222097-72-4 | S38093盐酸盐 (Catalog# : 184176)S38093是组胺H3受体的反向激动剂。
- 1173022-21-3 | STO-609醋酸盐 (Catalog# : 184123)STO-609是一种细胞渗透性抑制剂，钙/钙调蛋白依赖性激酶激酶(CaMK
- 1599441-71-0 | Super-TDU (Catalog# : 18495)Super-TDU是靶向YAP-TEADs interaction的抑制性多肽。
- 1253955-19-9 | (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)methyl 2,4-dimethylbenzoate (Catalog# : 183219)(S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)met
- 132513-51-0 | (S)-2-羟基丁酸正丁酯 (Catalog# : 1712291)(S)-2-羟基丁酸正丁酯是一种分子砌块。
- 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
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
- -- 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
- 2375779-31-8 | GP130 modulator-1 (Catalog# : 25062)GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
- 877459-36-4 | TGN 073 (Catalog# : 25061)TGN 073 is a facilitator of aquaporin-4 (AQP4), an astroglial water channel. The rats
- 2257492-95-6 | OPN expression inhibitor 1 (Catalog# : 25060)OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
- 3036109-10-8 | SDU-071 (Catalog# : 25059)SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
- 2644662-83-7 | BBC0403 (Catalog# : 25058)BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
- 694488-83-0 | MFI8 (Catalog# : 25057)MFI8 is a Mitochondrial Fusion Inhibitor
- 146255-66-5 | DHPG (Catalog# : 25056)DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
- 2413020-56-9 | BAY-593 free base (Catalog# : 25055)BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
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