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T16397Ophiobolin A；化合物 T16397Ophiobolin A
Ophiobolin A is a fungal metabolite and a phytotoxin and is an effective and irreversibly inhibitor of calmodulin-activated cyclic nucleotide phosphodiesterase (IC50: 9 μM). Ophiobolin A also has antimicrobial and anticancer activity.
价 格：￥电议型 号：T16397产 地：中国大陆
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T16353Meseclazone；美西拉宗W2395|||NSC297623；美西拉宗|||W2395|||NSC297623
Meseclazone has anti-inflammatory, analgesic, and antipyretic activity. Meseclazone shows inhibitory potency of secondary phase ADP aggregation.
价 格：￥电议型 号：T16353产 地：中国大陆
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T16297NH-bis(m-PEG4)；化合物 T16297NH-bis(m-PEG4)
NH-bis(m-PEG4) 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：T16297产 地：中国大陆
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T16197N-(Azido-PEG4)-N-Boc-PEG4-Boc；化合物 T16197N-(Azido-PEG4)-N-Boc-PEG4-Boc
N-(Azido-PEG4)-N-Boc-PEG4-Boc is a polyethylene glycol (PEG) derived linker, specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16197产 地：中国大陆
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T16109ML402；化合物ML402ZINC3671497|||N-[2-(4-chloro-2-methylphenoxy)ethyl]thiophene-2-carboxamide；ZINC3671497
ML402 (ZINC3671497) is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.
价 格：￥电议型 号：T16109产 地：中国大陆
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T16097MK-8318；化合物 T16097MK-8318
MK-8318 is an effective and selective antagonist of the CRTh2 receptor (Ki: 5.0 nM).
价 格：￥电议型 号：T16097产 地：中国大陆
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T16093Telcagepant化合物 T16093MK-0974
Telcagepant is an orally active antagonist of calcitonin gene-related peptide (CGRP) receptor (Kis: 0.77 nM and 1.2 nM for human and rhesus CGRP receptors, respectively).
价 格：￥电议型 号：T16093产 地：中国大陆
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T16023L2(24S)-MC 976；化合物 T16023L2(24S)-MC 976
(24S)-MC 976 is a derivative of Vitamin D3.
价 格：￥电议型 号：T16023L2产 地：中国大陆
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T16023L(24R)-MC 976；化合物 T16023L(24R)-MC 976
(24R)-MC 976 is a derivative of Vitamin D3.
价 格：￥电议型 号：T16023L产 地：中国大陆
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T15997Mal-PEG5-NHS ester；化合物 T15997Mal-PEG5-NHS ester
Mal-PEG5-NHS ester, an alkyl/ether and PEG-based PROTAC linker, is utilized for the synthesis of PROTACs.
价 格：￥电议型 号：T15997产 地：中国大陆
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T1597LProadifen；化合物 T1597LAV-54315|||AV 54315|||AV54315；AV-54315|||AV 54315|||AV54315
Proadifen is a non-selective cytochrome P450 enzymes inhibitor, preventing some types of drug metabolism.
价 格：￥电议型 号：T1597L产 地：中国大陆
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T15979Mal-PEG2-alcohol；化合物 T15979Mal-PEG2-alcohol
Mal-PEG2-alcohol 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：T15979产 地：中国大陆
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T15978Mal-PEG2-acid；化合物 T15978Mal-PEG2-acid
Mal-PEG2-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Mal-PEG2-acid can be conjugated to Tubulysin and its derivative cytotoxic molecule[1].
价 格：￥电议型 号：T15978产 地：中国大陆
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T15977Mal-PEG1-PFP ester；化合物 T15977Mal-PEG1-PFP ester
Mal-PEG1-PFP ester, an alkyl/ether-based PROTAC linker, is utilized in PROTAC synthesis.
价 格：￥电议型 号：T15977产 地：中国大陆
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T15976Mal-PEG1-NHS ester；化合物Mal-PEG1-NHS esterMal-PEG1-NHS ester
Mal-PEG1-NHS ester is a cleavable and PEG-based ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It also is PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T15976产 地：中国大陆
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T15975Mal-PEG1-bromide；化合物 T15975Mal-PEG1-bromide
Mal-PEG1-bromide 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：T15975产 地：中国大陆
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T15974Mal-PEG1-Boc；化合物 T15974Mal-PEG1-Boc
Mal-PEG1-Boc is a alkyl/ether-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：T15974产 地：中国大陆
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T15973Mal-PEG1-acid；化合物 T15973Mal-PEG1-acid
Mal-PEG1-acid is a non-cleavable (1 unit PEG) ADC linker used in the synthesis of antibody-drug conjugates (ADCs)
价 格：￥电议型 号：T15973产 地：中国大陆
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T15972Mal-NH2 TFA；化合物 T15972Mal-NH2 TFA
Mal-NH2 TFA is a alkyl chain-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：T15972产 地：中国大陆
