武汉永璨生物科技有限公司
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- 抑制剂/受体激动剂
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- MAPK
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- Ubiquitin
- Neuronal Signaling
- NF-κB
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Cas号索引 1
- 1995889-48-9 | Parsaclisib HCl (Catalog# : L20333)Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
- 1426698-88-5 | Parsaclisib free base (Catalog# : L20332)Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes w
- 1221962-86-2 | PS210 (Catalog# : 20282)PS210 is a substrate-selective inhibitor of protein kinase PDK1. It acts by binding t
- 171744-42-6 | PD-159206 (Catalog# : 20278)PD-159206 is a nucleocapsid inhibitor. It exhibits good antiviral activity against HI
- 18550-98-6 | 3PO (Catalog# : 21227)3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO
- 1034189-82-6 | PF-06802861 ( ARRY 371797 ; ARRY-797 ) (Catalog# : 2073108)ARRY 797（也称为ARRY 371797或PF 06802861）是一种具有口服活性，选择性
- 1917294-46-2 | PF-04745637 (Catalog# : 2071623)PF-04745637 is a TRPV1 antagonist.
- 1629869-44-8 | Pimodivir ( VX-787 ) (Catalog# : 2071401)Pimodivir (VX-787) 是一种可口服的甲型流感病毒聚合酶抑制剂，通过
- 1454619-14-7 | PU-WS13 (Catalog# : 206701)PU-WS13 is a potent, Grp94-specific Hsp90 inhibitor of the purine scaffold class. PU-
- 1953130-87-4 | PTI-428(PTI428) (Catalog# : 31619)PTI-428是一种研究性CFTR放大器，开发用于治疗CFTR基因中发生F508del
- 1415637-72-7 | PF-05085727 (Catalog# : 1932011)PF-05085727是一种强效、选择性和脑穿透性磷酸二酯酶2A抑制剂。
- 1252637-35-6 | Petesicatib (Catalog# : 193206)Petesicatib是一种组织蛋白酶抑制剂的候选药物。
- 187235-37-6 | Pretomanid (Catalog# : 193110)Pretomanid，也被称为PA-824，一种生物还原药物。PA-824具有较强的体
- 1341224-83-6 | PF-4136309 (Catalog# : 192282)PF-4136309，又称INCB8761，是一种口服的人趋化因子受体2 (CCR2)拮抗剂
- 1078166-57-0 | PF04418948 (Catalog# : 191141)PF-04418948是一种新型高效选择性前列腺素EP2受体拮抗剂。
- 1352879-65-2 | PF74 (Catalog# : 1812253)PF-3450074，又称PF74，是一种针对HIV衣壳蛋白的HIV-1抑制剂。PF74与HI
- 1672665-49-4 | PT2385 (Catalog# : 1812135)PT2385是一种口服活性小分子缺氧诱导因子(HIF)-2alpha抑制剂，具有潜
- 133413-70-4 | PF 1022A (Catalog# : 1811232)PF1022A是一种新型的驱虫药，与嗜乳激素样跨膜受体结合，对线虫
- 146464-95-1 | 普拉曲沙 (Catalog# : 1811221)普拉曲沙是二氢叶酸还原酶(DHFR)的一种叶酸模拟抑制剂，对叶酸还
- 1037589-69-7 | PF-05231023 (Catalog# : 1811162)PF-05231023是一种长效FGF21仿生产品。PF-05231023可以减轻非人类灵长类
- 1311174-68-1 | PH-002 (Catalog# : 1810234)PH-002是一种新型的载脂蛋白(apo) E4分子内区域相互作用的神经细胞
- 1513857-77-6 | Pemigatinib (INCB054828) (Catalog# : 1810164)Pemigatinib是一种酪氨酸激酶抑制剂，也是一种抗肿瘤药物候选药物
- 1022899-36-0 | PCI-33380 (Catalog# : 18943)PCI-33380是基于ibrutinib支架设计的，已被用于细胞和体内研究，证实
- 1613373-33-3 | PCO371 (Catalog# : 187125)PCO371是一种有效的、选择性的PTHR1激动剂，用于治疗低甲状旁腺功
- 1927857-61-1 | PQR530 (Catalog# : 18756)PQR530是一种高效的日常pan-PI3K/mTORC1/2抑制剂。
- 1269662-73-8 | Pyrotinib (Catalog# : 18731)Pyrotinib，又称SHR -1258，是一种口服生物利用的双激酶抑制剂，是表
- 1268244-85-4 | PX20606反式消旋体 (Catalog# : 186274)PX20606, 也称为PX-102, 是一种FXR激动剂。
- 1394033-54-5 | PF-05180999 (Catalog# : 186153)PF-05180999是一个强有力的和选择性PDE2a抑制剂(PDE2a的IC50 = 0.001μM，
- 1428333-96-3 | Pritelivir甲磺酸盐 (Catalog# : 186152)Pritelivir，又名AIC-316和BAY 57-1293，是一种有效的螺旋酶抑制剂。
- 1446261-44-4 | Pamiparib (Catalog# : 185233)Pamiparib是高选择性PARP-1/2抑制剂。临床试验中表现出良好的抗肿瘤
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