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T16216N-(Boc-PEG4)-NH-PEG4-NH-Boc；化合物 T16216N-(Boc-PEG4)-NH-PEG4-NH-Boc
N-(Boc-PEG4)-NH-PEG4-NH-Boc is a polyethylene glycol (PEG)-based PROteolysis TArgeting Chimera (PROTAC) linker, specifically designed for the synthesis of PROTACs [1].
价 格：￥电议型 号：T16216产 地：中国大陆
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T16215N-Boc-PEG4-bromide；化合物 T16215N-Boc-PEG4-bromide
N-Boc-PEG4-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16215产 地：中国大陆
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T16214N-(Boc-PEG3)-N-bis(PEG3-azide)；化合物 T16214N-(Boc-PEG3)-N-bis(PEG3-azide)
N-(Boc-PEG3)-N-bis(PEG3-azide) is a polyethylene glycol (PEG)-based linker, specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs) [1].
价 格：￥电议型 号：T16214产 地：中国大陆
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T16213N-(Boc-PEG3)-N-bis(PEG2-alcohol)；化合物 T16213N-(Boc-PEG3)-N-bis(PEG2-alcohol)
N-(Boc-PEG3)-N-bis(PEG2-alcohol) is a polyethylene glycol (PEG) based linker commonly employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16213产 地：中国大陆
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T16212N-Boc-PEG3-bromide；化合物 T16212N-Boc-PEG3-bromide
N-Boc-PEG3-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16212产 地：中国大陆
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T16211N-Boc-PEG2-bromide；化合物 T16211N-Boc-PEG2-bromide
N-Boc-PEG2-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16211产 地：中国大陆
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T16210N-(Boc-PEG1)-N-bis(PEG2-propargyl)；化合物 T16210N-(Boc-PEG1)-N-bis(PEG2-propargyl)
N-(Boc-PEG1)-N-bis(PEG2-propargyl) is a polyethylene glycol (PEG)-derived linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16210产 地：中国大陆
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T1621Imatinib Mesylate；甲磺酸伊马替尼ST-1571 Mesylate|||STI-571|||CGP-57148B；甲磺酸伊马替尼|||ST-1571 Mesylate|||STI-57
Imatinib Mesylate (STI571 Mesylate) is a multi-targeted receptor tyrosine kinase inhibitor that selectively inhibits the kinase activities of BCR/ABL, v-Abl, PDGFR, and c-kit with oral activity. Imatinib Mesylate has antitumor activity for the treatment of chronic granulocytic leukemia.
价 格：￥电议型 号：T1621产 地：中国大陆
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T15806LY2562175；化合物LY2562175LY2562175
LY2562175 is an effective and selective FXR agonist (EC50: 193 nM).
价 格：￥电议型 号：T15806产 地：中国大陆
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T15621Rilematovir；化合物RilematovirJNJ-53718678|||JNJ-678；JNJ-53718678|||JNJ-678
Rilematovir (JNJ-678) is an inhibitor of fusion protein with antiviral activity and low cytotoxicity. Rilematovir can be used in studies about respiratory syncytial virus treatment.
价 格：￥电议型 号：T15621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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T15134Dipraglurant；化合物 T15134ADX48621；ADX48621
Dipraglurant is a negative allosteric regulator (NAM) of blood-brain barrier transmissible mGluR5 with effective, selective and oral activity, with an IC50 value of 21 nM. Dipraglurant can treat levodopa-induced dyskinesia in Parkinson´s disease (PD-LID).
价 格：￥电议型 号：T15134产 地：中国大陆
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T14621Bis-aminooxy-PEG7；化合物 T14621Bis-aminooxy-PEG7
Bis-aminooxy-PEG7 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：T14621产 地：中国大陆
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T14068A-192621；化合物 T14068A-192621
A-192621 is a potent, nonpeptide, orally active and selective endothelin B (ETB) receptor antagonist with an IC50 of 4.5 nM and a Ki of 8.8 nM. A-192621 promotes apoptosis in PASMCs and it also causes elevation of arterial blood pressure and an elevation in the plasma ET-1 level[1][2][3]. The selectivity of A-192621 is 636-fold higher than ETA (IC50 of 4280 nM and Ki of 5600 nM).
价 格：￥电议型 号：T14068产 地：中国大陆
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T13621LCNDAC；化合物 T13621LCNDAC
CNDAC, a nucleoside analog, is a major metabolite of oral drug sapacitabine.
价 格：￥电议型 号：T13621L产 地：中国大陆
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T13621CNDAC hydrochloride；化合物CNDAC hydrochlorideCNDAC hydrochloride
CNDAC hydrochloride, a nucleoside analog, is a metabolite of the sapacitabine.
价 格：￥电议型 号：T13621产 地：中国大陆
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T13162117-hydroxy-17-methylandrost-4-ene-3,6-dione；化合物 17-hydroxy-17-methylandrost-4-ene-3,6-dione17-hydrox
17-hydroxy-17-methylandrost-4-ene-3,6-dione is a useful organic compound for research related to life sciences and the catalog number is T131621.
价 格：￥电议型 号：T131621产 地：中国大陆
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T12621LFT671化合物 T12621LFT671|||FT-671
FT671 is a non-covalent and selective inhibitor of USP7 (IC50: 52 nM) It also binds to the USP7 catalytic domain (Kd: 65 nM).
价 格：￥电议型 号：T12621L产 地：中国大陆
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T126218Gynosaponin V；化合物 Gynosaponin VGynosaponin V
Gynosaponin V is a useful organic compound for research related to life sciences. The catalog number is T126218 and the CAS number is 1207861-73-1.
价 格：￥电议型 号：T126218产 地：中国大陆
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