武汉永璨生物科技有限公司
+86-17702719238
sales@sun-shinechem.com
- 首页
- 抑制剂/受体激动剂
- Angiogenesis
- Anti-infection
- Apoptosis
- Autophagy
- Cell Cycle
- Cytoskeleton
- DNA Damage
- Epigenetics
- GPCR & G Protein
- Immunology & Inflammation
- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
- Metabolism
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- Proteases
- PI3K/Akt/mTOR
- Stem Cells & Wnt
- TGF-beta/Smad
- Ubiquitin
- Vitamin D Related
- PROTAC
- Antibody-drug Conjugate/ADC Related
- Microbiology
- Others
- 分子砌块
- 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
- 中间体
- 技术服务
- 订购信息
- 联系我们
产品名字索引 P
- PF-05085727 (Catalog# : 1932011, Cas# : 1415637-72-7)PF-05085727是一种强效、选择性和脑穿透性磷酸二酯酶2A抑制剂。
- Petesicatib (Catalog# : 193206, Cas# : 1252637-35-6)Petesicatib是一种组织蛋白酶抑制剂的候选药物。
- Pyridone 6 (Catalog# : 193204, Cas# : 457081-03-7)吡啶酮6，也被称为CMP 6或JAK抑制剂I，是一种pan-janus-激活的激酶抑
- Pretomanid (Catalog# : 193110, Cas# : 187235-37-6)Pretomanid，也被称为PA-824，一种生物还原药物。PA-824具有较强的体
- PF-4136309 (Catalog# : 192282, Cas# : 1341224-83-6)PF-4136309，又称INCB8761，是一种口服的人趋化因子受体2 (CCR2)拮抗剂
- 帕利伐米 (Catalog# : 192272, Cas# : 31645-39-3)帕利伐米，又名ZIO201，是一种具有潜在抗肿瘤活性的合成芥菜化合
- PF-06873600 (Catalog# : 191145, Cas# : 2185857-97-8)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
- PF04418948 (Catalog# : 191141, Cas# : 1078166-57-0)PF-04418948是一种新型高效选择性前列腺素EP2受体拮抗剂。
- PF74 (Catalog# : 1812253, Cas# : 1352879-65-2)PF-3450074，又称PF74，是一种针对HIV衣壳蛋白的HIV-1抑制剂。PF74与HI
- PT2385 (Catalog# : 1812135, Cas# : 1672665-49-4)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
- PF 1022A (Catalog# : 1811232, Cas# : 133413-70-4)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
- 普拉曲沙 (Catalog# : 1811221, Cas# : 146464-95-1)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
- PF-05231023 (Catalog# : 1811162, Cas# : 1037589-69-7)PF-05231023是一种长效FGF21仿生产品。PF-05231023可以减轻非人类灵长类
- PA-8 (Catalog# : 1810254, Cas# : 878437-15-1)PA-8是PAC1受体的小分子拮抗剂。
- Pyronaridine Tetraphosphate (Catalog# : 1810242, Cas# : 76748-86-2)Pyronaridine Tetraphosphate是一种抗疟药，能阻断b -血凝素的形成，抑制
- PH-002 (Catalog# : 1810234, Cas# : 1311174-68-1)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
- Pemigatinib (INCB054828) (Catalog# : 1810164, Cas# : 1513857-77-6)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
- Pelitrexol (Catalog# : 189131, Cas# : 446022-33-9)Pelitrexol是GARFT抑制剂，也是具有抗增殖活性的水溶性抗叶酸。
- PCI-33380 (Catalog# : 18943, Cas# : 1022899-36-0)PCI-33380是基于ibrutinib支架设计的，已被用于细胞和体内研究，证实
- Perastine (Catalog# : 187164, Cas# : 4960-10-5)Perastine是一种生物化学药。
- PCO371 (Catalog# : 187125, Cas# : 1613373-33-3)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
- PQR530 (Catalog# : 18756, Cas# : 1927857-61-1)PQR530是一种高效的日常pan-PI3K/mTORC1/2抑制剂。
- Pyrotinib (Catalog# : 18731, Cas# : 1269662-73-8)Pyrotinib，又称SHR -1258，是一种口服生物利用的双激酶抑制剂，是表
- PX20606反式消旋体 (Catalog# : 186274, Cas# : 1268244-85-4)PX20606, 也称为PX-102, 是一种FXR激动剂。
- PF-05180999 (Catalog# : 186153, Cas# : 1394033-54-5)PF-05180999是一个强有力的和选择性PDE2a抑制剂(PDE2a的IC50 = 0.001μM，
- Pritelivir甲磺酸盐 (Catalog# : 186152, Cas# : 1428333-96-3)Pritelivir，又名AIC-316和BAY 57-1293，是一种有效的螺旋酶抑制剂。
- Pridopidine (Catalog# : 18673, Cas# : 346688-38-8)Pridopidine也被称为ACR16，是一种多巴胺稳定剂，它可以改善运动表
- Pamiparib (Catalog# : 185233, Cas# : 1446261-44-4)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
- PAC 14028 (Catalog# : 185223, Cas# : 1005168-10-4)PAC-14028是高效的选择性的瞬时受体电位香草酸亚型1 (TRPV1) 拮抗剂
- PE859 (Catalog# : 185157, Cas# : 1402727-29-0)PE859是一个强有力的IC50值分别为0.66和1.2μM的tau和Aβ聚合抑制剂。
产品分类
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Src
- ---- ALK
- ---- Syk
- ---- HIF
- -- Anti-infection
- ---- CMV
- ---- Filovirus
- ---- HBV
- ---- HCV
- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- Antibacterial
- ---- Antifungal
- ---- Parasite
- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
- ---- TNF-alpha
- ---- Survivin
- ---- IAP
- ---- PERK
- ---- p53
- ---- Mdm2
- ---- E1/E2/E3 Enzyme
- -- Autophagy
- ---- LRRK2
- ---- CXCR
- ---- Autophagy
- -- Cell Cycle
- ---- CDK
- ---- PD-1
- ---- PD-L1
- ---- Chk
- ---- ROCK
- ---- PLK
- ---- APC
- ---- Wee1
- ---- DYRK
- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- ---- Eukaryotic Initiation Factor (eIF)
- ---- NEKs
- -- Cytoskeleton
- ---- HSP
- ---- Kinesin
- ---- Integrin
- ---- Dynamin
- ---- Wnt
- ---- β-catenin
- ---- Gap Junction Protein
- -- DNA Damage
- ---- PARP
- ---- DNA/RNA Synthesis
- ---- Sirtuin
- ---- Topoisomerase
- ---- DNA-PK
- ---- Telomerase
- ---- RAD51
- ---- HDAC
- ---- ATM
- ---- DNA alkylator
- ---- Mps1
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
- ---- HIF-PH
- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- ---- Methionine Adenosyltransferase (MAT)
- -- 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
- ---- Ras
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- ---- Bradykinin Receptor
- ---- GLP Receptor
- -- 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
- ---- Kallikrein
- ---- IRAK
- ---- Reactive-Oxygen-Species-ROS
- -- JAK/STAT
- ---- JAK
- ---- STAT
- ---- Pim
- ---- EGFR
- -- MAPK
- ---- MEK
- ---- Raf
- ---- p38 MAPK
- ---- ERK
- ---- MNK
- ---- Mixed Lineage Kinase
- ---- JNK
- ---- MAP4K
- -- 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
- ---- Proton Pump
- -- 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
- ---- Mitochondrial Metabolism
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- -- 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
- ---- Sigma Receptor
- ---- mAChR
- ---- α-Synuclein
- ---- Tau Protein
- ---- Cannabinoid Receptor
- ---- Transthyretin (TTR)
- ---- Melanocortin Receptor
- ---- Glucosylceramide Synthase (GCS)
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- ---- Keap1-Nrf2
- -- 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
- ---- Bcr-Abl
- ---- FAK
- ---- RET
- ---- Phosphoglycerate Kinase (PGK)
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Lipase
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- ---- Vps34
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- ---- Notch
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- ---- DUB
- -- Vitamin D Related
- ---- VD/VDR
- -- PROTAC
- ---- Molecular Glues
- ---- PROTACs
- -- Antibody-drug Conjugate/ADC Related
- -- Microbiology
- -- Others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- ---- Newest added products
- -- 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
- Mitoquinol mesylate (MitoQ) (Catalog# : 26A042, Cas# : 845959-55-9)Mitoquinol mesylate (MitoQ) 是一种线粒体靶向抗氧化剂，具体而言，它
- SPG-601 ( VSN-16R ) (Catalog# : 24042, Cas# : 1246960-09-7)SPG-601（原名VSN-16R）是一种口服给药、同类首创的小分子药物，是
- LY3039478 ( Crenigacestat ) (Catalog# : 17021601, Cas# : 1421438-81-4)LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂，通过阻断 VEGFA/
- PF-9366 (Catalog# : 184107, Cas# : 72882-78-1)PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A)，肝外同种型。
- MAT2A-IN-22 (Catalog# : 26A021, Cas# : 2925330-18-1)MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
- Pantothenate kinase-IN-3 (Catalog# : 26A041)泛酸激酶-IN-3（亦称化合物21，https://doi.org/10.1021/acs.jmedchem.5c03452）
- Claziprotamidum ( Claziprotamide ; BBP-671 ) (Catalog# : 26A040, Cas# : 2361124-03-8)Claziprotamidum（Claziprotamide；BBP-671）是一种强效、口服有效且能透过
- PZ-3022 (Catalog# : 26A039, Cas# : 2170608-85-0)PZ-3022是一种别构型的PanK激活剂，能够抵消C3-CoA的抑制作用。
- PZ-2891 (Catalog# : 193282, Cas# : 2170608-82-7)PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂，
- Pantothenate kinase-IN-2 (Catalog# : 26A038, Cas# : 902614-04-4)Pantothenate kinase-IN-2是一种泛酸激酶抑制剂，对PanK2的IC50值为92 nM，