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T19355Heparan Sulfate硫酸乙酰肝素硫酸乙酰肝素|||硫酸类肝素
Heparan Sulfate, a complex and linear polysaccharide, forms a component of glycoproteins called heparan sulfate proteoglycans, abundantly expressed on the cell surface and within the extracellular matrix.
价 格：￥电议型 号：T19355产 地：中国大陆
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T18963Dabcyl acid；4-二甲胺偶氮苯-4’-羧酸DABCYL|||Para-methyl red；DABCYL|||4-二甲胺偶氮苯-4’-羧酸|||Para-methyl red
Dabcyl acid (DABCYL) is the original dark fluorescence quencher.
价 格：￥电议型 号：T18963产 地：中国大陆
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T1893Parmodulin 2；化合物ML 161ML 161；ML 161
Parmodulin 2 (ML 161) is the inhibitor of protease-activated receptor 1 (PAR1)-mediated platelet activation (IC50: 0.26 μM for the inhibition of platelet P-selectin expression on human platelets). It also inhibits thrombin-induced platelet activation.
价 格：￥电议型 号：T1893产 地：中国大陆
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T18831Thalidomide-propargyl；化合物Thalidomide-propargylThalidomide-propargyl
Thalidomide-propargyl, a Thalidomide-derived Cereblon ligand, facilitates the recruitment of Cereblon. It can be attached to the protein ligand via a linker, producing IMiD-containing PROTACs.
价 格：￥电议型 号：T18831产 地：中国大陆
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T18826Thalidomide-O-PEG2-propargyl；化合物 T18826E3 ligase Ligand-Linker Conjugates 32；E3 ligase Ligand-Linker
Thalidomide-O-PEG2-propargyl (E3 Ligase Ligand-Linker Conjugates 32) is a chemical compound that has been synthesized as a conjugate of an E3 ligase ligand and a linker. It incorporates the cereblon ligand based on Thalidomide, along with a 2-unit PEG linker. This compound is specifically designed for use in PROTAC technology, which utilizes ligand-induced protein degradation [1].
价 格：￥电议型 号：T18826产 地：中国大陆
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T18823Thalidomide-O-amido-PEG4-propargyl；化合物 T18823Thalidomide-O-amido-PEG4-propargyl
Thalidomide-O-amido-PEG4-propargyl is a polyethylene glycol (PEG)-based linker employed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T18823产 地：中国大陆
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T18647Pyrene-PEG5-propargyl；化合物 T18647Pyrene-PEG5-propargyl
Pyrene-PEG5-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：T18647产 地：中国大陆
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T18641SirReal1-O-propargyl；化合物 T18641PROTAC Sirt2-binding moiety 1；PROTAC Sirt2-binding moiety 1
SirReal1-O-propargyl, a moiety based on SirReal1, is a selective and highly potent inhibitor of Sirtuin 2 (Sirt2), demonstrating an IC50 of 2.4 μM. It operates by binding to the cereblon ligand through a linker, facilitating the formation of PROTAC for the degradation of Sirt2[1].
价 格：￥电议型 号：T18641产 地：中国大陆
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T18591Propargyl-PEG8-SH；化合物 T18591Propargyl-PEG8-SH
Propargyl-PEG8-SH 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：T18591产 地：中国大陆
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T18590Propargyl-PEG7-methane；化合物 T18590Propargyl-PEG7-methane
Propargyl-PEG7-methane 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：T18590产 地：中国大陆
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T18589Propargyl-PEG6-SH；化合物 T18589Propargyl-PEG6-SH
Propargyl-PEG6-SH 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：T18589产 地：中国大陆
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T18588Propargyl-PEG5-Ms；化合物Propargyl-PEG5-MsPropargyl-PEG6-Ms；Propargyl-PEG6-Ms
Propargyl-PEG5-Ms (Propargyl-PEG6-Ms) is a PEG-based PROTAC linker. Propargyl-PEG5-Ms can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T18588产 地：中国大陆
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T18587Propargyl-PEG4-Sulfone-PEG4-Boc；化合物 T18587Propargyl-PEG4-Sulfone-PEG4-Boc
Propargyl-PEG4-Sulfone-PEG4-Boc is a polyethylene glycol (PEG)-based linker molecule for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T18587产 地：中国大陆
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T18586Propargyl-PEG4-Sulfone-PEG4-acid；化合物 T18586Propargyl-PEG4-Sulfone-PEG4-acid
Propargyl-PEG4-Sulfone-PEG4-acid serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1].
价 格：￥电议型 号：T18586产 地：中国大陆
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T18585Propargyl-PEG4-S-PEG4-propargyl；化合物 T18585Propargyl-PEG4-S-PEG4-propargyl
Propargyl-PEG4-S-PEG4-propargyl is a PEG-based PROTAC linker employed for PROTAC synthesis [1].
价 格：￥电议型 号：T18585产 地：中国大陆
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T18584Propargyl-PEG4-S-PEG4-Boc；化合物 T18584Propargyl-PEG4-S-PEG4-Boc
Propargyl-PEG4-S-PEG4-Boc is a polyethylene glycol (PEG) based linker, specifically designed for the synthesis of PROTACs [1].
价 格：￥电议型 号：T18584产 地：中国大陆
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T18583Propargyl-PEG4-S-PEG4-acid；化合物 T18583Propargyl-PEG4-S-PEG4-acid
Propargyl-PEG4-S-PEG4-acid is a polyethylene glycol (PEG)-based PROTAC linker, suitable for the synthesis of Proteolysis Targeting Chimera (PROTACs)[1].
价 格：￥电议型 号：T18583产 地：中国大陆
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T18582Propargyl-PEG4-hydrazide；化合物 T18582Propargyl-PEG4-hydrazide
Propargyl-PEG4-hydrazide is a non-cleavable 4-unit polyethylene glycol (PEG) linker specifically designed for antibody-drug conjugate (ADC) synthesis [1].
价 格：￥电议型 号：T18582产 地：中国大陆
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T18581Propargyl-peg3-sulfone-peg3-propargyl；化合物 T18581Propargyl-peg3-sulfone-peg3-propargyl
Propargyl-PEG3-sulfone-PEG3-propargyl is a polyethylene glycol (PEG)-based linker specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T18581产 地：中国大陆
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T18580Propargyl-PEG3-SH；化合物 T18580Propargyl-PEG3-SH
Propargyl-PEG3-SH 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：T18580产 地：中国大陆
