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Cas号索引 1
- 1627929-55-8 | PLX51107 (Catalog# : 184285)PLX51107是一种高效、选择性的BRD4抑制剂或BET抑制剂，其体外和体内
- 171179-06-9 | PD 158780 (Catalog# : 184284)PD 158780是表皮生长因子受体(EGFR) (IC50为0.08 nM)的酪氨酸激酶活性的
- 1997387-43-5 | PZM21 (Catalog# : 184162)PZM21是强有力Gi活化剂，对μOR和最小β-arrestin-2具有特殊选择性的补
- 1627607-87-7 | PFI-2盐酸盐 (Catalog# : 184106)在其他甲基转移酶和其他非表观遗传靶点上，PFI-2是一种具有IC50为
- 198474-05-4 | PF-0684000 (Catalog# : 184318)PF-0684000，也称为EOS200271，是强有力的IDO-1抑制剂(IC50 0.15μM)。PF-06
- 1467057-23-3 | PF-06409577 (Catalog# : 18434)PF-06409577是一种有效和具有选择的5腺苷酸活化蛋白激酶(AMPK)激活剂
- 1802929-43-6 | PRN-1371 (Catalog# : 17101614)PRN-1371是一种共价键，不可逆的，高选择性的纤维母细胞生长因子
- 1293395-67-1 | PF-5006739 (Catalog# : 17101612)PF-5006739是一种有效的CK1δ/ε抑制剂。PF-5006739对阿片类药物具有药
- 1383719-97-8 | PF-04628935 (Catalog# : 17101611)PF-04628935是一种有效的关于胃肽感受器的拮抗激动剂，生长激素促
- 1210608-43-7 | PIM447 (Catalog# : 1710134)PIM447，也称为lgh447，是一种有效的Moloney小鼠白血病（PIM）1, 2，和
- 179474-81-8 | Pyridostatin TFA盐 (Catalog# : 1791517)Pyridostatin稳定G-四链体（G4S）在细胞和诱导引起的DNA双链断裂形成
- 179474-85-2 | 琥珀酸普卡比利 (Catalog# : 1791516)琥珀酸普卡比利，也称为r-108512，是一种选择性、高亲和力的5-羟
- 104632-25-9 | 盐酸普拉克索 (Catalog# : 1791510)普拉克索是一个GαI-联多巴胺受体D2、D3和D4受体激动剂。它是相对
- 1435467-38-1 | PF-06281355 (Catalog# : 1791312)PF-06281355，也称为PF-1355，是一种口服有效的、选择性的,有效的机
- 1235481-43-2 | P7C3-OMe (Catalog# : 179116)P7C3-OMe，也称为（R）- P7C3-OMe，是P3C3-A20和P7C3的模拟。减轻C57BL/6J小
- 1962928-21-7 | PF-CBP1 游离 (Catalog# : 179113)PF-CBP1，也称为 PF06670910，是强效、高选择性的CREB结合蛋白布罗莫
- 1817626-54-2 | PF-06650833 (Catalog# : 17988)PF-06650833是一种白细胞介素-1受体相关激酶4 (IRAK4)抑制剂。IRAK4位于
- 1234015-55-4 | Prexasertib 甲磺酸 (Catalog# : 17986)Prexasertib也称为LY2606368，是一种有效，具有选择性的Chk1/Chk2抑制剂
- 192705-79-6 | PD166866 (Catalog# : 178814)PD166866有明显的抗增殖作用。
- 135729-61-2 | 帕洛诺司琼 (Catalog# : 2017080119)帕洛诺司琼是一种5-HT3拮抗剂，用于预防和治疗化疗引起的恶心和
- 1776112-90-3 | PF-06747775 (Catalog# : 175161)PF-06747775(PF06747775;CAS 1776112-90- 3)是表皮生长因子受体(EGFR)突变体T7
- 1331782-27-4 | PF-04995274 (Catalog# : 17031017)PF-04995274是一个5 - HT4受体部分激动剂。它被认为是作为一种治疗阿
- 113906-27-7 | PNU-74654 (Catalog# : 17031011)PNU-75654扰乱通过抑制Wnt信号通路β-catenin与Tcf4之间的交互(KD50 = 450
- 127317-03-7 | 垂体腺苷酸环酶激活多肽 (Catalog# : 17031005)垂体腺苷酸环酶激活多肽(PACAP 1- 27)是一种有效的PACAP受体拮抗剂。
- 1462249-75-7 | PFK-158 (Catalog# : 17030915)PFK-158, 也称为ACT-PFK-158,是一种6 -磷酸果糖- 2激酶/果糖- 2,6 -双磷酸
- 1235403-62-9 | PF-05089771 (Catalog# : 17030912)PF-05089771是一种选择性的Nav1.7抑制剂(IC50 = 1nm)，它与域四的电压传
- 135-87-5 | Piperoxan HCl (Catalog# : 17030708)Piperoxan，也叫benodaine，是一种药物，它是最先被发现的抗组胺剂。
- 1403764-72-6 | PFI-1 (Catalog# : 17030704)PFI-1是一种有效、选择性高的蛋白质相互作用抑制剂，它的目标为
- 1114544-31-8 | 帕纳替尼盐酸盐 (Catalog# : 17030607)帕纳替尼，又名AP24534，是一种口服药物，用于治疗慢性粒细胞白
- 192705-80-9 | PD-161570 (Catalog# : 17030304)PD - 161570是一种选择性FGFR抑制剂(FGFR、PDGFR和EGFR的IC50值分别为40,2
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)
- -- 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
- -- 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
- -- 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
- -- 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)
- -- 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
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- -- 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
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- -- 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
- 2750001-23-9 | AZD0095 (Catalog# : 237072)AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
- 2101538-28-5 | 2-MNG (Catalog# : 24129)2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂，具有独特的作
- 2439277-80-0 | MAT2A-IN-9 (Catalog# : 25147)MAT2A-IN-9（化合物167）是一种2-氧代喹唑啉衍生物，是一种强效的M
- 1898206-17-1 | Safusidenib (Catalog# : 25149)Safusidenib，也称为DS-1001，是一种口服异柠檬酸脱氢酶[NADP]细胞质（
- 2669009-92-9 | Atebimetinib (Catalog# : 25148)阿替美替尼（IMM-1-104）是一种口服的小分子MEK1和MEK2激酶变构抑制
- 2242751-53-5 | Acoramidis hydrochloride (Catalog# : 24068)Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白（TTR
- 2230263-60-0 | Crelosidenib (Catalog# : 24101)Crelosidenib （ [LY3410738）是一种有效的选择性的具有口服活性的突变
- 2833703-74-3 | LOXO-435 (Catalog# : 25080)LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
- 2446928-30-7 | Gridegalutamide (Catalog# : 25138)Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
- 1256349-48-0 | Chiauranib (Catalog# : 25146)Chiauranib also known as orally available, small molecule inhibitor of select serine-