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T24779SEN-1269；化合物 T24779SEN-1269
SEN-1269 is an amyloid-β (AB) aggregation inhibitor that acts by blocking Aβ(1-42) aggregation and protecting neuronal cell lines exposed to Aβ(1-42), reducing Aβ oligomer-induced LTP and memory deficits in vivo.
价 格：￥电议型 号：T24779产 地：中国大陆
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T23779BDM31827；化合物 T23779BDM 31827|||BDM-31827；BDM 31827|||BDM-31827
BDM31827 is an EthR inhibitor.
价 格：￥电议型 号：T23779产 地：中国大陆
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T22779Fenoldopam；非诺多泮Fenoldopam
Fenoldopam is a selective D1-like dopamine receptor partial agonist (EC50 = 57 nM).
价 格：￥电议型 号：T22779产 地：中国大陆
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T21857AR-R 17779 hydrochloride；化合物 T21857AR-R 17779 hydrochloride
AR-R17779 hydrochloride is a potent, selective full agonist of the nAChR, demonstrating K i values of 92 nM for the α7 subtype and 16,000 nM for the α4β2 subtype. It is noted for its ability to enhance learning and memory in rats, suggesting potential therapeutic applications. Additionally, this compound exhibits anxiolytic properties and can mitigate inflammation by activating anti-inflammatory cholinergic (vagal) pathways [1] [2] [4].
价 格：￥电议型 号：T21857产 地：中国大陆
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T2145Temsirolimus；西罗莫司脂化物NSC 683864|||CCI-779；NSC 683864|||CCI-779|||西罗莫司脂化物
Temsirolimus (CCI-779) is a specific mTOR inhibitor ( IC50: 1.76 μM), used in the treatment of advanced renal cell cancer.
价 格：￥电议型 号：T2145产 地：中国大陆
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T20779Kitasamycin tartrate；化合物 T20779Leucomycin tartrate；Leucomycin tartrate
Kitasamycin tartrate, a macrolide antibiotic produced by Streptomyces kitasatoensis, has a wide spectrum of antimicrobial activity.
价 格：￥电议型 号：T20779产 地：中国大陆
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T20031C.I. Direct Blue 2；化合物 T20031NSC 75779|||NSC-75779|||Pontamine Diazo Black BHSW|||Direct Blue 2|||CC
C.I. Direct Blue 2 is an agent of dye.
价 格：￥电议型 号：T20031产 地：中国大陆
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T19779SL-01；化合物 T19779Z L Phe chloromethyl ketone|||NSC-251810|||ZLPhe chloromethyl ketone|||Z-Phe-chlorom
SL-01 is an oral derivative of gemcitabine. SL-01 inhibited human breast cancer growth through the induction of apoptosis. SL-01 inhibited human cancer growth more potently than gemcitabine.
价 格：￥电议型 号：T19779产 地：中国大陆
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T19646Altizide；化合物 T19646CB-8093|||Aldactacine|||P 1779|||CB 8093|||P1779|||P-1779；CB-8093|||Aldactacine||
Altizide is a thiazide diuretic. It is used to treat oedema and hypertension.
价 格：￥电议型 号：T19646产 地：中国大陆
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T1953L-779450；化合物L-779450L 779450；L 779450
L-779450, an effective, ATP-competitive Raf kinase inhibitor (IC50: 10 nM) , displays > 7, > 30 and > 70-fold selectivity over p38α, GSK3β and Lck respectively.
价 格：￥电议型 号：T1953产 地：中国大陆
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T18954LCY7-SE Triethylamine (477908-53-5(free acid) )；化合物CY7-SE TriethylamineCY7-SE Triethylamine (477908-5
CY7-SE Triethylamine is a fluorescence labeling agent (Ex=700-770 nm，Em=790 nm) used for labeling proteins, peptides, antibodies, and oligonucleotides.
价 格：￥电议型 号：T18954L产 地：中国大陆
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T18779TCO-PEG8-acid；化合物 T18779TCO-PEG8-acid
TCO-PEG8-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：T18779产 地：中国大陆
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T17799DBCO-PEG4-SS-TCO；化合物 T17799DBCO-PEG4-SS-TCO
DBCO-PEG4-SS-TCO is a cleavable 4-unit polyethylene glycol (PEG) linker essential for the synthesis of antibody-drug conjugates (ADCs)[1]. It plays a crucial role in connecting the drug payload to the antibody, enabling targeted drug delivery.
价 格：￥电议型 号：T17799产 地：中国大陆
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T17798DBCO-PEG4-PFP ester；化合物 T17798DBCO-PEG4-PFP ester
DBCO-PEG4-PFP 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：T17798产 地：中国大陆
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T17797DBCO-PEG4-NH-Boc；化合物 T17797DBCO-PEG4-NH-Boc
DBCO-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：T17797产 地：中国大陆
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T17796DBCO-PEG4-Desthiobiotin；化合物 T17796DBCO-PEG4-Desthiobiotin
DBCO-PEG4-Desthiobiotin is a polyethylene glycol (PEG) derivative utilized as a linker for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T17796产 地：中国大陆
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T17795DBCO-PEG4-alkyne；化合物 T17795DBCO-PEG4-alkyne
DBCO-PEG4-alkyne is a four-unit PEG linker with non-cleavable properties, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17795产 地：中国大陆
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T17794DBCO-PEG4-alcohol；化合物 T17794DBCO-PEG4-alcohol
DBCO-PEG4-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：T17794产 地：中国大陆
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T17793DBCO-PEG4-Ahx-DM1；化合物 T17793DBCO-PEG4-Ahx-DM1
DBCO-PEG4-Ahx-DM1 is a drug-linker conjugate that combines the microtubulin inhibitor DM1 (mertansine), which is an antibody-conjugatable maytansinoid designed to reduce systemic toxicity and improve tumor-specific delivery, with the linker DBCO-PEG4-Ahx, for the development of antibody drug conjugates (ADCs).
价 格：￥电议型 号：T17793产 地：中国大陆
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T17792DBCO-PEG3-TCO；化合物 T17792DBCO-PEG3-TCO
DBCO-PEG3-TCO is a non-cleavable three-unit polyethylene glycol (PEG) linker employed for synthesizing antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17792产 地：中国大陆
