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T40532MS-PEG10-THP；MS-PEG10-THPMS-PEG10-THP；MS-PEG10-THP
MS-PEG10-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T40532产 地：中国大陆
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T40531THP-PEG10-OH；THP-PEG10-OHTHP-PEG10-OH；THP-PEG10-OH
THP-PEG10-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T40531产 地：中国大陆
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T40494Bis-isopropyl-PEG1；Bis-isopropyl-PEG1Bis-isopropyl-PEG1；Bis-isopropyl-PEG1
Bis-isopropyl-PEG1 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T40494产 地：中国大陆
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T4041Ziritaxestat；化合物GLPG1690GLPG1690；GLPG1690
Ziritaxestat (GLPG1690), an autotaxin inhibitor, currently being evaluated in an exploratory phase 2 study in idiopathic pulmonary fibrosis patients.
价 格：￥电议型 号：T4041产 地：中国大陆
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T40343CC-885-CH2-PEG1-NH-CH3；CC-885-CH2-PEG1-NH-CH3CC-885-CH2-PEG1-NH-CH3；CC-885-CH2-PEG1-NH-CH3
CC-885-CH2-PEG1-NH-CH3 is a neoDegrader compound employed for the production of Antibody neoDegrader Conjugate (AnDC) during synthesis.
价 格：￥电议型 号：T40343产 地：中国大陆
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T40342MC-VC-PABC-amide-PEG1-CH2-CC-885；MC-VC-PABC-amide-PEG1-CH2-CC-885MC-VC-PABC-amide-PEG1-CH2-CC-885；MC
MC-VC-PABC-amide-PEG1-CH2-CC-885 is an Antibody-Drug Conjugate (ADC) utilizing a protein-degrading agent (protac molecular glue, etc.).
价 格：￥电议型 号：T40342产 地：中国大陆
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T40286KRAS G12C inhibitor 19；KRAS G12C抑制剂19KRAS G12C inhibitor 19
KRAS G12C inhibitor 19 is a potent KRAS G12C inhibitor that shows anti-tumor activity in cellular assays, and the family inhibits tumor growth.
价 格：￥电议型 号：T40286产 地：中国大陆
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T40285KRAS G12C inhibitor 18；KRAS G12C inhibitor 18KRAS G12C inhibitor 18
KRAS G12C inhibitor 18 is a potent, orally active compound that inhibits KRAS G12C and exhibits anti-tumor activities.
价 格：￥电议型 号：T40285产 地：中国大陆
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T40282KRAS G12D inhibitor 7；KRAS G12D inhibitor 7KRAS G12D inhibitor 7
KRAS G12D inhibitor 7, is a highly potent inhibitor specifically targeting KRAS G12D.
价 格：￥电议型 号：T40282产 地：中国大陆
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T40281KRAS G12D inhibitor 6；KRAS G12D inhibitor 6KRAS G12D inhibitor 6
KRAS G12D inhibitor 6 is an efficacious compound that effectively inhibits KRAS G12D.
价 格：￥电议型 号：T40281产 地：中国大陆
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T40246KRAS G12D inhibitor 5；KRAS G12D inhibitor 5KRAS G12D inhibitor 5
KRAS G12D inhibitor 5 is a KRAS G12D inhibitor for the potential treatment of pancreatic cancer.
价 格：￥电议型 号：T40246产 地：中国大陆
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T40198Azido-PEG11-CH2COOH；Azido-PEG11-CH2COOHAzido-PEG11-CH2COOH；Azido-PEG11-CH2COOH
Azido-PEG11-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T40198产 地：中国大陆
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T40024Pomalidomide-PEG1-CO2H；化合物T40024Pomalidomide-PEG1-C2-COOH；Pomalidomide-PEG1-C2-COOH
Pomalidomide-PEG1-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker.
价 格：￥电议型 号：T40024产 地：中国大陆
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T39970TLR7/8 agonist 4 hydroxy-PEG10-acid hydrochloride；TLR7/8 agonist 4 hydroxy-PEG10-acid hydrochlorideT
TLR7/8 agonist 4 hydroxy-PEG10-acid hydrochloride (compound 9) is a drug-linker conjugate used in antibody-drug conjugates (ADCs) with high efficacy against tumors. It consists of TLR7/8 agonist 4, a potent TLR7/8 agonist, linked to the ADC linker hydroxy-PEG10-acid which can be cleaved.
价 格：￥电议型 号：T39970产 地：中国大陆
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T39968TLR7/8 agonist 4 hydroxy-PEG10-acid；TLR7/8 agonist 4 hydroxy-PEG10-acidTLR7/8 agonist 4 hydroxy-PEG1
TLR7/8 agonist 4 hydroxy-PEG10-acid (compound 9) is a drug-linker conjugate employed in antibody-drug conjugates (ADC). This compound exhibits remarkable antitumor activity by utilizing TLR7/8 agonist 4, which acts as a potent activator of TLR7/8. The TLR7/8 agonist 4 is linked to hydroxy-PEG10-acid, the ADC linker, via a cleavable bond. Overall, it demonstrates promising pharmaceutical potential in the context of ADC-based therapeutics.
价 格：￥电议型 号：T39968产 地：中国大陆
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T39939Propargyl-PEG10-alcohol；Propargyl-PEG10-alcoholPropargyl-PEG10-alcohol；Propargyl-PEG10-alcohol
Propargyl-PEG10-alcohol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T39939产 地：中国大陆
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T39932ARG1-IN-1ARG1-IN-1ARG1-IN-1
ARG1-IN-1 is a human arginase 1 inhibitor with an IC 50 of 29 nM.
价 格：￥电议型 号：T39932产 地：中国大陆
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T39814Bromo-PEG1-NH2 hydrobromide；Bromo-PEG1-NH2 hydrobromideBromo-PEG1-NH2 hydrobromide；Bromo-PEG1-NH2 hy
Bromo-PEG1-NH2 hydrobromide is a polyethylene glycol (PEG)-based linker compound employed in the synthesis of proteolysis-targeting chimeras (PROTACs).
价 格：￥电议型 号：T39814产 地：中国大陆
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T39801Azido-PEG12-propargyl；Azido-PEG12-propargylAzido-PEG12-propargyl；Azido-PEG12-propargyl
Azido-PEG12-propargyl is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T39801产 地：中国大陆
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T39765Mal-PEG1-Val-Cit-PAB-PNP；Mal-PEG1-Val-Cit-PAB-PNPMal-PEG1-Val-Cit-PAB-PNP；Mal-PEG1-Val-Cit-PAB-PNP
Mal-PEG1-Val-Cit-PAB-PNP is an ADC linker employed in the synthesis of ADCs, enabling cleavage.
价 格：￥电议型 号：T39765产 地：中国大陆
