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T15925m-PEG7-NHS ester；化合物 T15925m-PEG7-NHS ester
m-PEG7-NHS ester 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：T15925产 地：中国大陆
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T15924m-PEG7-Ms；化合物 T15924m-PEG7-Ms
m-PEG7-Ms is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15924产 地：中国大陆
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T15923m-PEG7-CH2CH2COOH；化合物 T15923m-PEG7-CH2COOH；m-PEG7-CH2COOH
m-PEG7-CH2COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15923产 地：中国大陆
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T15922m-PEG7-CH2CH2CHO；化合物 T15922m-PEG7-CH2CH2CHO
m-PEG7-CH2CH2CHO is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15922产 地：中国大陆
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T15921m-PEG7-azide；化合物 T15921m-PEG7-azide
m-PEG7-azide 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：T15921产 地：中国大陆
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T15920m-PEG7-Amine；化合物 T15920m-PEG7-Amine
m-PEG7-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15920产 地：中国大陆
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T1592Acetohydroxamic acid乙酰氧肟酸Methylhydroxamic acid|||Acetic acid|||Lithostat|||AHA|||oxime|||N-Hydroxyac
Acetohydroxamic acid (N-Hydroxyacetamide) is an antagonist of the bacterial enzyme urease.
价 格：￥电议型 号：T1592产 地：中国大陆
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T1591LCytidine；胞苷Cytosine-1-β-D-ribofuranoside|||Cytosine β-D-riboside；Cytosine-1-β-D-ribofuranoside|||胞苷|
Cytidine (Cytosine-1-β-D-ribofuranoside) is a pyrimidine nucleoside comprised of a cytosine bound to ribose via a beta-N1-glycosidic bond. Cytidine is a precursor for uridine. Both cytidine and uridine are utilized in RNA synthesis.
价 格：￥电议型 号：T1591L产 地：中国大陆
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T15919m-PEG7-4-nitrophenyl carbonate；化合物m-PEG7-4-nitrophenyl carbonatem-PEG7-4-nitrophenyl carbonate
m-PEG7-4-nitrophenyl carbonate is a PEG-based PROTAC linker that can be used in PROTAC synthesis[1].
价 格：￥电议型 号：T15919产 地：中国大陆
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T15918m-PEG6-Tos；化合物 T15918m-PEG6-Tos
m-PEG6-Tos 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：T15918产 地：中国大陆
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T15917m-PEG6-thiol；化合物 T15917m-PEG6-thiol
m-PEG6-thiol 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：T15917产 地：中国大陆
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T15916m-PEG6-O-CH2COOH；化合物 T15916m-PEG6-O-CH2COOH
m-PEG6-O-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：T15916产 地：中国大陆
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T15915m-PEG6-NHS ester；化合物 T15915m-PEG6-NHS ester
m-PEG6-NHS ester is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15915产 地：中国大陆
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T15914m-PEG6-CH2CH2COOH；化合物 T15914m-PEG6-CH2CH2COOH
m-PEG6-CH2CH2COOH 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：T15914产 地：中国大陆
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T15913m-PEG6-CH2CH2CHO；化合物 T15913m-PEG6-CH2CH2CHO
m-PEG6-CH2CH2CHO is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15913产 地：中国大陆
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T15911m-PEG7-CH2-OH；化合物 T15911m-PEG7-CH2-OH
m-PEG7-CH2-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：T15911产 地：中国大陆
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T1591Ancitabine hydrochloride盐酸环胞苷NSC 145668 HCl|||盐酸环胞苷|||Cyclocytidine hydrochloride|||Cyclo-CMP hydroc
Ancitabine hydrochloride (NSC 145668 HCl) is the hydrochloride salt of a cytarabine congener prodrug with antineoplastic activity. Upon administration, ancitabine is slowly hydrolyzed into cytarabine. Subsequently, cytarabine is converted to the triphosphate form within the cell and then competes with cytidine for incorporation into DNA. Because the arabinose sugar sterically hinders the rotation of the molecule within DNA, DNA replication ceases, specifically during the S phase of the cell cycl
价 格：￥电议型 号：T1591产 地：中国大陆
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T15909m-PEG6-Br；化合物 T15909m-PEG6-Br
m-PEG6-Br 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：T15909产 地：中国大陆
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T15908m-PEG7-Boc；化合物 T15908m-PEG6-Boc；m-PEG6-Boc
m-PEG6-Boc is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15908产 地：中国大陆
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T15907m-PEG6-azide；化合物 T15907m-PEG6-azide
m-PEG6-azide is a six-unit polyethylene glycol linker functionalized with an azide moiety, serving as a non-cleavable linker for the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15907产 地：中国大陆
