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T15318Fmoc-NH-PEG4-CH2COOH；化合物 T15318Fmoc-NH-PEG4-CH2COOH
Fmoc-NH-PEG4-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15318产 地：中国大陆
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T15317Fmoc-NH-PEG4-CH2CH2COOH；化合物 T15317Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid；Fmoc-15-amino-4
Fmoc-NH-PEG4-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15317产 地：中国大陆
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T15316Fmoc-NH-PEG3-CH2CH2COOH；化合物 T15316Fmoc-NH-PEG3-CH2CH2COOH
Fmoc-NH-PEG3-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15316产 地：中国大陆
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T15315Fmoc-NH-PEG2-CH2CH2COOH；化合物 T15315Fmoc-NH-PEG2-CH2CH2COOH
Fmoc-NH-PEG2-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15315产 地：中国大陆
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T15314Fmoc-NH-PEG1-CH2COOH；化合物 T15314Fmoc-NH-PEG1-CH2COOH
Fmoc-NH-PEG1-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15314产 地：中国大陆
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T15313Fmoc-NH-PEG1-C2-acid；化合物 T15313Fmoc-NH-PEG1-C2-acid
Fmoc-NH-PEG1-C2-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：T15313产 地：中国大陆
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T15312Fmoc-NH-ethyl-SS-propionic NHS ester；化合物 T15312Fmoc-NH-ethyl-SS-propionic NHS ester
Fmoc-NH-ethyl-SS-propionic NHS ester is a cleavable linker for antibody-drug conjugates (ADCs)[1]. It is employed in the synthesis of ADCs, facilitating the covalent attachment of drugs to antibodies through the formation of stable amide bonds.
价 格：￥电议型 号：T15312产 地：中国大陆
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T15311Fmoc-NH-ethyl-SS-propionic acid；化合物 T15311Fmoc-NH-ethyl-SS-propionic acid
Fmoc-NH-ethyl-SS-propionic acid is a cleavable linker compound utilized for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15311产 地：中国大陆
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T15310Fmoc-N-PEG3-CH2-NHS ester；化合物 T15310Fmoc-N-PEG3-CH2-NHS ester
Fmoc-N-PEG3-CH2-NHS ester serves as a PEG-based PROTAC linker, facilitating the synthesis of PROTACs[1].
价 格：￥电议型 号：T15310产 地：中国大陆
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T1531Mometasone furoate；糠酸莫米松Sch32088；糠酸莫美他松|||糠酸莫米松|||Sch32088
Mometasone furoate (Sch32088) is a pregnadienediol derivative ANTI-ALLERGIC AGENT and ANTI-INFLAMMATORY AGENT that is used in the management of ASTHMA and ALLERGIC RHINITIS. It is also used as a topical treatment for skin disorders.
价 格：￥电议型 号：T1531产 地：中国大陆
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T15309Fmoc-N-methyl-PEG3-CH2CH2COOH；化合物 T15309Fmoc-N-methyl-PEG3-CH2CH2COOH
Fmoc-N-methyl-PEG3-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15309产 地：中国大陆
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T15308Fmoc-Lys (biotin-PEG4)-OH；化合物 T15308Fmoc-Lys (biotin-PEG4)-OH
Fmoc-Lys (biotin-PEG4)-OH is a biotinylated and PEG-modified PROTAC linker utilized for PROTAC synthesis[1].
价 格：￥电议型 号：T15308产 地：中国大陆
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T15307Fmoc-aminooxy-PEG4-acid；化合物 T15307Fmoc-aminooxy-PEG4-acid
Fmoc-aminooxy-PEG4-acid is a PEG-based linker compound employed in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15307产 地：中国大陆
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T15306Fmoc-amino-PEG5-acid；化合物 T15306Fmoc-amino-PEG5-acid
Fmoc-amino-PEG5-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：T15306产 地：中国大陆
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T15305Fmoc-amino-PEG3-CH2COOH；化合物 T15305Fmoc amino PEG3 CH2COOH|||FmocaminoPEG3CH2COOH|||Fmoc-amino-PEG-3-
Fmoc-amino-PEG3-CH2COOH is a polyethylene glycol (PEG)-based linker, primarily employed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T15305产 地：中国大陆
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T15304Fmoc-8-amino-3,6-dioxaoctanoic acid；[2-[2-(Fmoc-氨基)乙氧基]乙氧基]乙酸Fmoc-NH-PEG2-CH2COOH；Fmoc-NH-PEG2-CH2CO
Fmoc-8-amino-3,6-dioxaoctanoic acid (Fmoc-NH-PEG2-CH2COOH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T15304产 地：中国大陆
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T15303FMK 9a；化合物FMK 9aFMK 9a
FMK 9a is an irreversible inhibitor of ATG4B with IC50 values of 80 and 73 nM in the TR-FRET and cellular-based LRA assays.
价 格：￥电议型 号：T15303产 地：中国大陆
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T15302Fluzinamide；氟泽酰胺AHR-8559；AHR-8559
Fluzinamide (AHR-8559) has anticonvulsant effects on ignited amygdala seizures.
价 格：￥电议型 号：T15302产 地：中国大陆
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T15301Fluspirilene；氟司必林Redeptin|||R 6218；Redeptin|||R 6218
Fluspirilene (R 6218) is a non-competitive L-type calcium channel antagonist (IC50: 0.03 μM).Fluspirilene is a long-acting antipsychotic compound used in the treatment of schizophrenia.
价 格：￥电议型 号：T15301产 地：中国大陆
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T15300Fluorofenidone；化合物FluorofenidoneAKF-PD；AKF-PD
Fluorofenidone (AKF-PD) attenuates the progression of renal interstitial fibrosis partly by suppressing NADPH oxidase and extracellular matrix (ECM) deposition via the PI3K/Akt signalling pathway. Fluorofenidone is an analogue of AMR69. Which displays equivalent lower toxicity, antifibrotic activity, and longer half-life.
价 格：￥电议型 号：T15300产 地：中国大陆
