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T14180Alisporivir；化合物 T14180DEB-025|||Debio-025；DEB-025|||Debio-025
Alisporivir (Debio-025) is a cyclophilin inhibitor molecule.It has potent anti-hepatitis C virus (HCV) activity.
价 格：￥电议型 号：T14180产 地：中国大陆
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T1418Bucladesine sodium；布拉地新钠盐dbcAMP|||Dibutyryl-cAMP sodium salt|||Dibutyryl-cAMP|||DC2797|||Sodium dibu
Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a phosphodiester (PDE) inhibitor. Bucladesine sodium has anti-inflammatory activity.
价 格：￥电议型 号：T1418产 地：中国大陆
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T14179Aliconazole；阿利康唑Aliconazole
Aliconazole is an imidazole derivative with antifungal activity for the study of skin infections.
价 格：￥电议型 号：T14179产 地：中国大陆
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T14178Alicapistat；化合物 T14178ABT-957；ABT-957
Alicapistat (ABT-957) is a human calpains 1 and 2 inhibitor. It can potentially be used to treat Alzheimer´s disease (AD).
价 格：￥电议型 号：T14178产 地：中国大陆
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T14177Alexidine dihydrochloride；己联双辛胍二盐酸盐Alexidine dihydrochloride
Alexidine dihydrochloride has antifungal and antibiofilm activity against a diverse range of fungal pathogens. Alexidine dihydrochloride is an anticancer agent that targets a mitochondrial tyrosine phosphatase, PTPMT1, in mammalian cells and causes mitochondrial apoptosis. Thus, Alexidine dihydrochloride has the potential to be developed as a pan-antifungal, antibiofilm drug.
价 格：￥电议型 号：T14177产 地：中国大陆
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T14176Aleglitazar；阿格列扎RO0728804|||R1439；RO0728804|||R1439
Aleglitazar (R1439) (R1439) is a potent dual PPARα/γ agonist, with IC50s of 38 nM and 19 nM for human PPARa and PPARγ, respectively. Aleglitazar can be used for the research of type II diabetes.
价 格：￥电议型 号：T14176产 地：中国大陆
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T14175Aldose reductase-IN-1；化合物Aldose reductase-IN-1AT-001|||Caficrestat；AT-001|||Caficrestat
Aldose reductase-IN-1 (AT-001) is a aldose reductase inhibitor (IC50: 28.9 pM).
价 格：￥电议型 号：T14175产 地：中国大陆
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T14174Ald-Ph-amido-PEG4-C2-acid；化合物 T14174Ald-Ph-amido-PEG4-C2-acid
Ald-Ph-amido-PEG4-C2-acid is a noncleavable linker utilized in the development of antibody-drug conjugates (ADC).
价 格：￥电议型 号：T14174产 地：中国大陆
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T14173Ald-Ph-amido-PEG3-C2-NH2；化合物 T14173Ald-Ph-amido-PEG3-C2-NH2
Ald-Ph-amido-PEG3-C2-NH2 is a PEG-based PROTAC linker employed in PROTACs synthesis[1].
价 格：￥电议型 号：T14173产 地：中国大陆
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T14172Ald-Ph-amido-PEG2-C2-NHS ester；化合物 T14172Ald-Ph-amido-PEG2-C2-NHS ester
Ald-Ph-amido-PEG2-C2-NHS ester is a non-cleavable 2-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs.
价 格：￥电议型 号：T14172产 地：中国大陆
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T14171Ald-Ph-amido-PEG2-C2-acid；化合物 T14171Ald-Ph-amido-PEG2-C2-acid
Ald-Ph-amido-PEG2-C2-acid is a PEG-based PROTAC linker utilized for synthesizing PROTACs[1].
价 格：￥电议型 号：T14171产 地：中国大陆
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T14170Ald-Ph-PEG6-Boc；化合物 T14170Ald-Ph-PEG6-Boc
Ald-Ph-PEG6-Boc 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：T14170产 地：中国大陆
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T14169Ald-Ph-PEG6-acid；化合物 T14169Ald-Ph-PEG6-acid
Ald-Ph-PEG6-acid 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：T14169产 地：中国大陆
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T14168Ald-Ph-PEG4-NH-Boc；化合物 T14168Ald-Ph-PEG4-NH-Boc
Ald-Ph-PEG4-NH-Boc 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：T14168产 地：中国大陆
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T14167Ald-Ph-PEG4-Boc；化合物 T14167Ald-Ph-PEG4-Boc
Ald-Ph-PEG4-Boc 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：T14167产 地：中国大陆
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T14166Ald-Ph-PEG2-NH-Boc；化合物 T14166Ald-Ph-PEG2-NH-Boc
Ald-Ph-PEG2-NH-Boc 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：T14166产 地：中国大陆
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T14165Ald-Ph-amido-PEG4-C2-NHS ester；化合物 T14165Ald-Ph-amido-PEG4-C2-NHS ester
Ald-Ph-amido-PEG4-C2-NHS ester is a non-cleavable 4-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs.
价 格：￥电议型 号：T14165产 地：中国大陆
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T14164Ald-Ph-amido-PEG2-C2-Boc；化合物 T14164Ald-Ph-amido-PEG2-C2-Boc
Ald-Ph-amido-PEG2-C2-Boc is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T14164产 地：中国大陆
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T14163Ald-Ph-amido-C2-PEG3-NH-Boc；化合物 T14163Ald-Ph-amido-C2-PEG3-NH-Boc
Ald-Ph-amido-C2-PEG3-NH-Boc is a polyethylene glycol (PEG)-based bifunctional linker utilized for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T14163产 地：中国大陆
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T14162Ald-Ph-amido-C2-PEG2-amine；化合物 T14162Ald-Ph-amido-C2-PEG2-amine
Ald-Ph-amido-C2-PEG2-amine is a polyethylene glycol (PEG)-based linker utilized for the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T14162产 地：中国大陆
