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T16065Methyltetrazine-propylamine；化合物 T16065Methyltetrazine-propylamine
Methyltetrazine-propylamine is an alkyl chain-based PROTAC linker utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16065产 地：中国大陆
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T16064Methyltetrazine-Ph-PEG4-azide；化合物 T16064Methyltetrazine-Ph-PEG4-azide
Methyltetrazine-Ph-PEG4-azide is a PEG-based azide linker for PROTAC synthesis[1].
价 格：￥电议型 号：T16064产 地：中国大陆
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T16063Methyltetrazine-Ph-NHS ester；化合物 T16063Methyltetrazine-Ph-NHS ester
Methyltetrazine-Ph-NHS ester is an alkyl/ether-based linker utilized for the synthesis of PROTACs, an abbreviation for proteolysis-targeting chimeras[1].
价 格：￥电议型 号：T16063产 地：中国大陆
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T16062Methyltetrazine-PEG8-NHS ester；化合物 T16062Methyltetrazine-PEG8-NHS ester
Methyltetrazine-PEG8-NHS ester is a polyethylene glycol (PEG) derivative, specifically designed as a PROTAC linker for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T16062产 地：中国大陆
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T16061Methyltetrazine-PEG8-acid；化合物 T16061Methyltetrazine-PEG8-acid
Methyltetrazine-PEG8-acid is a polyethylene glycol (PEG) derivative commonly employed as a linker in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16061产 地：中国大陆
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T16060Methyltetrazine-PEG5-NHS ester；化合物 T16060Methyltetrazine-PEG5-NHS ester
Methyltetrazine-PEG5-NHS ester, a PEG-linked PROTAC linker, enables the synthesis of PROTACs[1].
价 格：￥电议型 号：T16060产 地：中国大陆
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T16059Methyltetrazine-PEG5-alkyne；化合物 T16059Methyltetrazine-PEG5-alkyne
Methyltetrazine-PEG5-alkyne, a PEG-based PROTAC linker, is utilized in synthesizing PROTACs[1].
价 格：￥电议型 号：T16059产 地：中国大陆
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T16058Methyltetrazine-PEG4-maleimide；化合物 T16058Methyltetrazine-PEG4-maleimide
Methyltetrazine-PEG4-maleimide is a PEG-based linker that is utilized in PROTAC synthesis[1].
价 格：￥电议型 号：T16058产 地：中国大陆
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T16057Methyltetrazine-PEG4-amine；化合物 T16057Methyltetrazine-PEG4-amine
Methyltetrazine-PEG4-amine is a polyethylene glycol (PEG) derivative serving as a PROTAC linker for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16057产 地：中国大陆
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T16056Methyltetrazine-DBCO；化合物 T16056Methyltetrazine-DBCO
Methyltetrazine-DBCO is a non-cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16056产 地：中国大陆
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T16055Methyltetrazine-acid；化合物 T16055Methyltetrazine-acid
Methyltetrazine-acid is an alkyl chain-derived linker employed for PROTAC synthesis[1].
价 格：￥电议型 号：T16055产 地：中国大陆
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T16046Methyl propionate-PEG12；化合物 T16046Methyl propionate-PEG12
Methyl propionate-PEG12, a PEG-based PROTAC linker, is utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16046产 地：中国大陆
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T15964Mal-amido-PEG9-acid；化合物 T15964Maleimide-NH-PEG9-CH2CH2COOH；Maleimide-NH-PEG9-CH2CH2COOH
Mal-amido-PEG9-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：T15964产 地：中国大陆
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T15960Mal-amido-PEG7-acid；化合物Mal-amido-PEG7-acidMaleimide-NH-PEG7-CH2CH2COOH|||Mal-NH-PEG7-COOH；Maleimide-
Mal-amido-PEG7-acid (Mal-NH-PEG7-COOH) is a PEG-based PROTAC linker that can be used to synthesize PROTACs.
价 格：￥电议型 号：T15960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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T15761Lipoamide-PEG3-Mal；化合物 T15761Lipoamide-PEG3-Mal
Lipoamide-PEG3-Mal 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：T15761产 地：中国大陆
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T15629JTE-013；化合物JTE-013JTE-013
JTE-013 is an effective and specific antagonist of S1P2. JTE-013 suppresses the specific binding of radiolabeled S1P to human and rat S1P2 (IC50s: 17 nM and 22 nM, respectively).
价 格：￥电议型 号：T15629产 地：中国大陆
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T15611JH-RE-06；化合物JH-RE-06JH-RE-06
JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POLζ. JH-RE-06 is an effective REV1-REV7 interface inhibitor (IC50=0.78 μM; Kd=0.42 μM), which targets REV1 that interacts with the REV7 subunit of POLζ. JH-RE-06 also improves chemotherapy.
价 格：￥电议型 号：T15611产 地：中国大陆
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T15561Imanixil；伊马昔尔HOE-402 free base；HOE-402 free base
Imanixil (HOE-402 free base) is an LDL receptor (LDLR) inducer, a hypolipidemic and hypocholesterolemic compound with antiatherogenic activity that inhibits the production of very low-density lipoproteins (VLDLs).Imanixil acts by stimulating the LDL receptor pathway.
价 格：￥电议型 号：T15561产 地：中国大陆
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T15543IA-Alkyne；化合物IA-AlkyneN-Hex-5-ynyl-2-iodo-acetamide|||Iodoacetamide-alkyne；N-Hex-5-ynyl-2-iodo-aceta
IA-Alkyne (Iodoacetamide-alkyne) is a TRP channel (TRPC) agonist. IA-Alkyne can be used to develop an isotopically tagged probe for quantitative cysteine-reactivity profiling. It also has the potential for the study of respiratory infection.
价 格：￥电议型 号：T15543产 地：中国大陆
