武汉永璨生物科技有限公司
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- MAPK
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产品名字索引 T
- TLN-232 (Catalog# : 18594, Cas# : 158899-10-6)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。
- TRC051384 (Catalog# : 18593, Cas# : 867164-40-7)TRC051384是热休克蛋白Hsp70的诱导物。
- 醋酸曲普瑞林 (Catalog# : 18592, Cas# : 140194-24-7)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
- Tropifexor (Catalog# : 18591, Cas# : 1383816-29-2)Tropifexor, 也称为LJN452, 是一种用于治疗胆静性肝病和非酒精性脂肪
- THZ531 (Catalog# : 184172, Cas# : 1702809-17-3)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
- 托格列净 (Catalog# : 184311, Cas# : 903565-83-3)托格列净，也称为CSG452，是一种高效、高选择性的SGLT2抑制剂，在
- TPX-0005 (Catalog# : 18423, Cas# : 1802220-02-5)TPX-0005是一种Src/FAK/Janus激酶2 (JAK2)抑制剂。TPX-0005 + EGFR TKI抑制RTKs
- tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate (Catalog# : 183214, Cas# : 305860-41-7)tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate is a drug intermediate.
- Timapiprant (Catalog# : 1712152, Cas# : 851723-84-7)Timapiprant, also known as OC000459, is a potent, selective and orally active CRTH2 a
- TUG-770 (Catalog# : 1791519, Cas# : 1402601-82-4)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
- TH-2120 (Catalog# : 179157, Cas# : 81686-22-8)TH-2120，也称为钠离子载体III是一个载体。离子载体适用于血钠活
- Thiomyristoyl (Catalog# : 1791113, Cas# : 1429749-41-6)Thiomyristoyl是一种强效和特异性的IC50为28nM的SIRT2抑制剂。IC50与目标
- TC-O9311 (Catalog# : 179828, Cas# : 444932-31-4)TC-O9311是一种强效的GPR139激动剂（GPR139 在人体细胞CHO-K1表达中EC50
- 琥珀酸曲格列汀 (Catalog# : 179811, Cas# : 1029877-94-8)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
- TUG-891 (Catalog# : 1783014, Cas# : 1374516-07-0)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
- TP-3654 (Catalog# : 178303, Cas# : 1361951-15-6)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
- TAK1抑制剂 (Catalog# : 1791412, Cas# : 1326712-16-6)TAK1 inhibitor isis discontinued.TAK1抑制剂是一种有效的、相对选择性的
- TPCA-1 (Catalog# : 17031308, Cas# : 507475-17-4)TPCA-1是一种有效的IKK-2抑制剂。TPCA-1也是种STAT3磷酸化的高效抑制
- 曲古柳菌素A (Catalog# : 17031306, Cas# : 58880-19-6)曲古柳菌素A, 也称为TSA,是一种HDAC抑制剂. 在生长阶段开始时，TSA
- 噻替派 (Catalog# : 17031304, Cas# : 52-24-4)噻替派是一种多功能型、有机磷烷基化剂，是一种稳定的N,N',N'' -
- Tirabrutinib游离 ( ONO-4059 ) (Catalog# : 17031303, Cas# : 1351636-18-4)Tirabrutinib，也被称为ONO- 4059，是在抑制剂中，一种强大的、具有口
- TCS-OX2-29盐酸盐 (Catalog# : 17031302, Cas# : 1610882-30-8)TCS-OX2- 29或TCS OX2 29，也被称为TCSOX229和TCS - OX229，是一种选择性的
- TX1-85-1 (Catalog# : 17030713, Cas# : 1603845-32-4)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
- Tipiracil HCl (Catalog# : 17030710, Cas# : 183204-72-0)Tipiralacil，又称TPI，是胸腺嘧啶磷酸化酶抑制剂(TPI)。Tipiracil是TAS
- Turofexorate isopropyl (Catalog# : 17030707, Cas# : 629664-81-9)Turofexorate isopropyl，也被称为WAY- 362450和XL335，是一种高效、选择性
- TWS-119 (Catalog# : 17030204, Cas# : 601514-19-6)TWS-119 是一种强有力的和糖原合酶选择性抑制剂激酶-3β(IC50 = 30 nM
- Tenapanor HCl (Catalog# : 17030113, Cas# : 1234365-97-9)Tenapanor, 也称为AZD-1722和RDX 5791, 是钠-质子(Na(+)/ H(+))交换器NHE3的抑
- 盐酸替罗非班 (Catalog# : 17030103, Cas# : 150915-40-5)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
- TAS-109 (Catalog# : 17022810, Cas# : 135598-68-4)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
- TRX818 (Catalog# : 17022401, Cas# : 1256037-58-7)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
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
- -- 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
- TRPM4-IN-2 (Catalog# : 24147, Cas# : 667411-04-3)TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
- Isolithocholic Acid (Catalog# : 24146, Cas# : 1534-35-6)Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- CPI-455 HCl (Catalog# : 24144, Cas# : 2095432-28-1)CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
- KH-3 (Catalog# : 24143, Cas# : 1215115-03-9)KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
- Stafib-2 (Catalog# : 24142, Cas# : 2097938-74-2)Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
- TCRS-417 (Catalog# : 24141, Cas# : 2032123-28-5)TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
- PST3 1a (Catalog# : 24140, Cas# : 1096144-06-7)PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
- YTX-465 (Catalog# : 24139, Cas# : 2225824-53-1)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
- CAY10566 (Catalog# : 10403, Cas# : 944808-88-2)Coming soon!