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产品名字索引 T
- TAK-715 (Catalog# : 187202, Cas# : 303162-79-0)TAK-715是一种有效的p38 MAPK抑制剂。它表现出有效的抑制活性，对主
- TAK-960 (Catalog# : 18762, Cas# : 1137868-52-0)TAK-960是一种可口服的PLK1抑制剂，具有潜在的抗肿瘤活性。
- Theliatinib (Catalog# : 186235, Cas# : 1353644-70-8)Theliatinib又称HMPL-309，是一种新型的小分子、表皮生长因子受体酪
- Tucidinostat (Catalog# : 186233, Cas# : 1616493-44-7)Tucidinostat是组蛋白去乙酰化酶(HDAC) 1、2、3和10的一种苯甲酰胺类抑
- Takinib (Catalog# : 18672, Cas# : 1111556-37-6)Takinib选择性TAK1抑制剂,TNF-α刺激后细胞凋亡模型,类风湿性关节炎
- TMP269 (Catalog# : 185254, Cas# : 1314890-29-3)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
- Trilaciclib (G1T28) (Catalog# : 185235, Cas# : 1374743-00-6)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 /
- TAPI-1 (Catalog# : 185181, Cas# : 171235-71-5)TAPI-1是TACE的抑制剂。它抑制TNF-a、TNFRI(p60)和TNFRII(p80)的裂解。
- TG100572盐酸盐 (Catalog# : 185175, Cas# : 867331-64-4)TG-100572是一种有效且具有选择性的VEGFR2/Src激酶抑制剂。
- 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
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
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- -- 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
- AZD0095 (Catalog# : 237072, Cas# : 2750001-23-9)AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
- 2-MNG (Catalog# : 24129, Cas# : 2101538-28-5)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
- MAT2A-IN-9 (Catalog# : 25147, Cas# : 2439277-80-0)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
- Safusidenib (Catalog# : 25149, Cas# : 1898206-17-1)Safusidenib，也称为DS-1001，是一种口服异柠檬酸脱氢酶[NADP]细胞质（
- Atebimetinib (Catalog# : 25148, Cas# : 2669009-92-9)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
- Acoramidis hydrochloride (Catalog# : 24068, Cas# : 2242751-53-5)Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白（TTR
- Crelosidenib (Catalog# : 24101, Cas# : 2230263-60-0)Crelosidenib （ [LY3410738）是一种有效的选择性的具有口服活性的突变
- LOXO-435 (Catalog# : 25080, Cas# : 2833703-74-3)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
- Gridegalutamide (Catalog# : 25138, Cas# : 2446928-30-7)Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
- Chiauranib (Catalog# : 25146, Cas# : 1256349-48-0)Chiauranib also known as orally available, small molecule inhibitor of select serine-