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
- DNA Damage
- Stem Cells & Wnt
- Ubiquitin
- Neuronal Signaling
- NF-κB
- GPCR & G Protein
- Metabolism
- Anti-infection
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Cas号索引 2
- 288847-34-7 | OXi-4503钠 (Catalog# : 178308)OXi-4503是一种二磷酸酯类药物，开始是从植物纤维中分离出来的，
- 216227-54-2 | ONT-093 (Catalog# : 17030901)ONT-093, 也称为OC-144-093，是一种口服的P-糖蛋白泵抑制剂，用于治疗
- 29700-22-9 | 氧化白藜芦醇 (Catalog# : 17021324)氧化白藜芦醇，一种天然存在的化合物，尤其在Morus alba L中发现。
- 202590-98-5 | OTX015 (Catalog# : 111012)OTX-015 is a new potent BRD2/3/4 inhibitor with evident anti-proliferative activity i
- 270065-52-6 | 1-O-benzyl 2-O-ethyl (2S)-5-oxopyrrolidine-1,2-dicarboxylate (Catalog# : 90103)Coming soon!
- 252990-05-9 | 1-O-tert-butyl 2-O-methyl (2R)-piperazine-1,2-dicarboxylate (Catalog# : 81726)Coming soon!
- 2128698-24-6 | 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl- (Catalog# : 25046)
- 2892065-45-9 | PLX-4545 (Catalog# : 24111)PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂，旨在破坏高
- 2416875-06-2 | 7-氯-5-(3-戊基)吡唑并[1,5-A]嘧啶 (Catalog# : 24081)
- 2893778-31-7 | PHGDH-IN-3 (Catalog# : 24058)PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
- 2101700-15-4 | Pirtobrutinib (Catalog# : 20618)
- 2904682-19-3 | PDS-0330 (Catalog# : 231106)PDS-0330 是一种特异性、有效的Claudin-1抑制剂。PDS-0330 干扰 claudin-1
- 2253123-16-7 | Pimicotinib (Catalog# : 20548)Pimicotinib是一种新型的 CSF-1R 小分子抑制剂，可口服、高选择性、
- 260415-63-2 | PD-173955 (Catalog# : 20499)PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce
- 217171-01-2 | PD-173212 (Catalog# : 20468)PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced
- 2172870-89-0 | Paltusotine ( CRN-00808 ) (Catalog# : 20294)Paltusotine 是一类新型的、口服、选择性、非肽类2型生长抑素受体
- 2230198-02-2 | PF-06882961 (Catalog# : 21251)PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptide-1 r
- 26305-03-3 | Pepstatin (Catalog# : 2071607)Pepstatin inhibits the aspartic protease endothiapepsin.
- 2227425-05-8 | PF-06869206 (Catalog# : 2071506)PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
- 26033-20-5 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE (Catalog# : 2062020)
- 248282-01-1 | Paquinimod (Catalog# : 2061706)Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
- 2170608-82-7 | PZ-2891 (Catalog# : 193282)PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂，
- 2185857-97-8 | PF-06873600 (Catalog# : 191145)PF-06873600是一种口服生物利用的细胞周期蛋白依赖性激酶(CDK)抑制
- 2070014-93-4 | PF-CBP1盐酸 (Catalog# : 179112)PF-CBP1，也称为 PF06670910，是强效、高选择性的CREB结合蛋白布罗莫
- 25606-41-1 | 霜霉威盐酸盐 (Catalog# : 2017080115)霜霉威盐酸盐是一种高效、广谱、氨基甲酸酯类杀菌剂。
- 257933-82-7 | 培利替尼 (Catalog# : 17022702)培利替尼(EKB-569; WAY-EKB 569)是一种有效且不可逆转的IC50为38.5 nM的E
- 202350-68-3 | PNU-159682 (Catalog# : 16071409)PNU-159682 is a major active metabolite of nemorubicin (MMDX) in human liver microsom
- 269718-84-5 | Pardoprunox (Catalog# : 122523)Pardoprunox is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT
- 219580-11-7 | PD173074 (Catalog# : 122212)PD173074 is a small-molecule FGFR3-selective tyrosine kinase inhibitor (TKI), as a th
- 269718-83-4 | Pardoprunox hydrochloride (Catalog# : 111010)Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and
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
- 2991818-13-2 | MGD-28 (Catalog# : 25073)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
- | TG101209 analog 1 (Catalog# : 25072)TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
- 2170729-29-8 | AT-007 (Catalog# : 25071)AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
- 1358751-06-0 | TAK-653 (Catalog# : 25070)TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
- 1801344-14-8 | Emavusertib (Catalog# : 25069)Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
- 1305267-37-1 | Roginolisib (Catalog# : 25068)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel
- 1198078-60-2 | NT219 (Catalog# : 25067)NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
- 858128-57-1 | SPB linker (Catalog# : 25066)SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
- 1404380-58-0 | JTE-151 (Catalog# : 20594)JTE-151 是一种 RORγ 抑制剂，可通过抑制与 Th17 细胞活化相关的 ROR
- 112108-01-7 | Ecopipam ( SCH 39166 ) (Catalog# : 25065)Ecopipam (SCH 39166) 是一种有效的、选择性、具有口服活性的多巴胺