武汉永璨生物科技有限公司
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Cas号索引 1
- 1314890-29-3 | TMP269 (Catalog# : 185254)TMP269是一种具有高强度、选择性和可渗透性的IIa型HDAC抑制剂，其
- 1374743-00-6 | Trilaciclib (G1T28) (Catalog# : 185235)Trilaciclib是一种小分子竞争性细胞周期蛋白依赖性激酶4和6（CDK4 /
- 171235-71-5 | TAPI-1 (Catalog# : 185181)TAPI-1是TACE的抑制剂。它抑制TNF-a、TNFRI(p60)和TNFRII(p80)的裂解。
- 158899-10-6 | TLN-232 (Catalog# : 18594)TLN-232, 也称为CAP-232，是一种具有潜在抗肿瘤活性的合成环七肽。
- 140194-24-7 | 醋酸曲普瑞林 (Catalog# : 18592)醋酸曲普瑞林是一种促性腺激素释放激素激动剂(GnRH激动剂)，用作
- 1383816-29-2 | Tropifexor (Catalog# : 18591)Tropifexor, 也称为LJN452, 是一种用于治疗胆静性肝病和非酒精性脂肪
- 1702809-17-3 | THZ531 (Catalog# : 184172)THZ531是一种共价CDK12和CDK13共价抑制剂。环素依赖性激酶12和13 (CDK
- 1802220-02-5 | TPX-0005 (Catalog# : 18423)TPX-0005是一种Src/FAK/Janus激酶2 (JAK2)抑制剂。TPX-0005 + EGFR TKI抑制RTKs
- 1402601-82-4 | TUG-770 (Catalog# : 1791519)TUG-770是高度有效的游离脂肪酸受体1(FFA1/GPR40)治疗2型糖尿病的激动
- 1429749-41-6 | Thiomyristoyl (Catalog# : 1791113)Thiomyristoyl是一种强效和特异性的IC50为28nM的SIRT2抑制剂。IC50与目标
- 1029877-94-8 | 琥珀酸曲格列汀 (Catalog# : 179811)曲格列汀，也称为SYR472，是一种武田制药正在开发的治疗2型糖尿
- 1374516-07-0 | TUG-891 (Catalog# : 1783014)TUG-891是一种有效且选择性的游离脂肪酸受体4(FFA4 / GPR120)，它既显
- 1361951-15-6 | TP-3654 (Catalog# : 178303)TP-3654是一种Pim-1和Pim-3激酶抑制剂，可用于治疗前列腺癌、急性髓
- 1326712-16-6 | TAK1抑制剂 (Catalog# : 1791412)TAK1 inhibitor isis discontinued.TAK1抑制剂是一种有效的、相对选择性的
- 1351636-18-4 | Tirabrutinib游离 ( ONO-4059 ) (Catalog# : 17031303)Tirabrutinib，也被称为ONO- 4059，是在抑制剂中，一种强大的、具有口
- 1610882-30-8 | TCS-OX2-29盐酸盐 (Catalog# : 17031302)TCS-OX2- 29或TCS OX2 29，也被称为TCSOX229和TCS - OX229，是一种选择性的
- 1603845-32-4 | TX1-85-1 (Catalog# : 17030713)TX1-85-1是一种ErbB3抑制剂. TX2-121-1可能通过异位机制发挥Her3依赖性
- 183204-72-0 | Tipiracil HCl (Catalog# : 17030710)Tipiralacil，又称TPI，是胸腺嘧啶磷酸化酶抑制剂(TPI)。Tipiracil是TAS
- 1234365-97-9 | Tenapanor HCl (Catalog# : 17030113)Tenapanor, 也称为AZD-1722和RDX 5791, 是钠-质子(Na(+)/ H(+))交换器NHE3的抑
- 150915-40-5 | 盐酸替罗非班 (Catalog# : 17030103)替罗非班是一种抗血小板药物。它属于一种名为糖蛋白IIb / IIIa抑
- 135598-68-4 | TAS-109 (Catalog# : 17022810)TAS-109, 也称为DFP-10917和CNDAC,是一种具有潜在抗肿瘤活性的核苷酸脱
- 1256037-58-7 | TRX818 (Catalog# : 17022401)TRX-818是一种可口服的生物制剂，具有潜在的抗肿瘤活性和抗血管
- 15421-84-8 | 乐可安 (Catalog# : 17021310)乐可安是一种PDGF拮抗剂，可抑制PDGF生成胶质瘤细胞的增殖。
- 1439901-97-9 | ONO-4059盐酸盐 (Catalog# : 17012103)ONO-4059是BTK的选择性和新型抑制剂，IC50为2.2 nm，ONO-4059与B细胞内的
- 113942-30-6 | 替莫唑胺酸 (Catalog# : 17011905)替莫唑胺酸, 也称为TMZA, 是一种具有明显抗癌活性的替奥米特(TMZ)
- 1609960-31-7 | TH588 (Catalog# : 17011728)TH588是NUDT1的一种有效抑制剂，其IC50值为5nm，具有良好的代谢稳定
- 1415716-58-3 | TG6-10-1 (Catalog# : 17011727)TG6-10-1是前列腺素E2受体亚型EP2的有效和选择性拮抗剂。
- 1033805-22-9 | 特罗司他乙酯 (Catalog# : 17011722)特罗司他乙酯, 也称为LX 1032或LX 1606, 是一种口服血清素合成抑制剂
- 161715-24-8 | 泰比培南酯 (Catalog# : 17011721)泰比培南酯,也被称为ME1211和TBM-PI, 是一种新型口腔卡宾枪抗生素。
- 193620-69-8 | TAS-301 (Catalog# : 17011719)TAS-301是一种有效的、选择性的球囊冠状动脉过度拉伸损伤后的收
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
- 2763252-25-9 | M3554 (Catalog# : 25017)M3554，一种新型抗GD2抗体药物偶联物。
- | MD-43 (Catalog# : 25016)MD-43是MCT4的强效选择性降解剂。
- 3034880-93-5 | VVD-130037 ( BAY-3605349 ) (Catalog# : 24110)VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
- 2247396-91-2 | HC-5404 抑制剂 (Catalog# : 25001)HC-5404 是一种新型、高选择性、有效的PERK抑制剂。
- 3034479-99-4 | HC-5404-FU (Catalog# : 24112)HC-5404-FU 是一种新型、高选择性、有效的PERK抑制剂。
- 2309409-79-6 | CMP-5 2HCl (Catalog# : 24161)CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
- 2630378-05-9 | Wu-5 (Catalog# : 24160)Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
- 890764-36-0 | VU-29 (Catalog# : 24159)VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin
- 1221186-52-2 | ML-202 (Catalog# : 24158)ML-202 is an activator of pyruvate kinase M2 (PKM2).
- 921193-28-4 | BTA-EG4 hydrate (Catalog# : 24157)BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance