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T19689Raluridine；化合物 T19689FddClUrd|||935U-83|||FCU|||DRG-0215|||BW-935U-83；FddClUrd|||935U-83|||FCU|||DRG
Raluridine is a RNA-directed DNA polymerase inhibitor potentially for the treatment of HIV infection. 935U83 inhibited virus growth with an average 50% inhibitory concentration (IC50: 1.8 microM) corresponding IC50s were 0.10 microM for FLT (3´-deoxy-3´-fluorothymidine) and 0.23, 0.49, and 0.03 microM for the approved agents AZT, ddI (2´,3´-dideoxyinosine), and ddC (2´,3´-dideoxycytosine), respectively.
价 格：￥电议型 号：T19689产 地：中国大陆
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T19519Pimelic Diphenylamide 106 analog；化合物 T19519RGFA-8 analog|||TC-H 106 analog；RGFA-8 analog|||TC-H 106
Pimelic Diphenylamide 106 analog is an Pimelic Diphenylamide 106 analog .
价 格：￥电议型 号：T19519产 地：中国大陆
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T1951Asenapine Maleate；阿塞那平马来酸盐Org 5222 maleate|||Org 5222；Org 5222 maleate|||Org 5222|||马来酸阿塞那平|||阿塞那平马来
Asenapine Maleate (Org 5222 maleate) is a second generation (atypical) antipsychotic agent that is taken sublingually and used in the treatment of schizophrenia and manic or mixed episodes associated with bipolar 1 disorder. Asenapine is associated with a low rate of transient and mild serum aminotransferase elevations during therapy but has not been linked to instances of clinically apparent acute liver injury.
价 格：￥电议型 号：T1951产 地：中国大陆
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T19417Urinary Incontinence-Targeting Compound 1；化合物 T19417Urinary Incontinence-Targeting Compound 1
Urinary Incontinence-Targeting Compound 1, used in the research of urinary incontinence, is a sulfonanilide derivative.
价 格：￥电议型 号：T19417产 地：中国大陆
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T1936Alectinib；艾乐替尼RG-7853|||AF802|||CH5424802|||AF-802；阿来替尼|||RG-7853|||艾乐替尼|||AF802|||CH5424802|||AF-80
Alectinib (RG-7853) is an orally available inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) with antineoplastic activity.
价 格：￥电议型 号：T1936产 地：中国大陆
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T19349H-Arg-Lys-OH；化合物 T19349H-Arg-Lys-OH
H-Arg-Lys-OH is a dipeptide formed from L-lysine residues and L-arginyl.
价 格：￥电议型 号：T19349产 地：中国大陆
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T19348H-Arg-Lys-OH TFA (40968-46-5 free base)；化合物 T19348H-Arg-Lys-OH TFA；H-Arg-Lys-OH TFA
H-Arg-Lys-OH TFA is a dipeptide formed from L-lysine residues and L-arginyl.
价 格：￥电议型 号：T19348产 地：中国大陆
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T19347H-Arg-4MβNA；化合物H-Arg-4MβNAH-Arg-4MbNA；H-Arg-4MbNA
H-Arg-4MβNA (H-Arg-4MbNA) is a peptide that serves as a substrate for cathepsin H. The enzyme activity is often detected in gel electrophoresis.
价 格：￥电议型 号：T19347产 地：中国大陆
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T19315Ethyl nonanoate；壬酸乙酯Ethyl pelargonate；Ethyl pelargonate
Ethyl nonanoate (Ethyl pelargonate) is an abundant ester in spirits, and its presence is usually associated with the aroma of alcoholic beverages.
价 格：￥电议型 号：T19315产 地：中国大陆
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T19288DL-Arginine；DL-精氨酸DL-Arginine
DL-Arginine is deployed in the study of amino acid complexation dynamics and the formation of crystal structures.
价 格：￥电议型 号：T19288产 地：中国大陆
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T19197Argininic acid；化合物 T19197Argininic acid
Argininic acid is an α-amino acid used in the biosynthesis of proteins.
价 格：￥电议型 号：T19197产 地：中国大陆
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T1916Apitolisib；化合物ApitolisibRG 7422|||GNE 390|||GDC-0980；RG 7422|||GNE 390|||GDC-0980
Apitolisib (RG 7422), an effective, class I PI3K inhibitor for PI3Kα(IC50=5 nM), PI3Kβ(IC50=27 nM), PI3Kδ(IC50=7 nM), PI3Kγ (IC50=14 nM), is used in trials study of solid cancers, breast cancer, prostate cancer, renal cell carcinoma, and endometrial carcinoma, among others.
价 格：￥电议型 号：T1916产 地：中国大陆
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T18831Thalidomide-propargyl；化合物Thalidomide-propargylThalidomide-propargyl
Thalidomide-propargyl, a Thalidomide-derived Cereblon ligand, facilitates the recruitment of Cereblon. It can be attached to the protein ligand via a linker, producing IMiD-containing PROTACs.
价 格：￥电议型 号：T18831产 地：中国大陆
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T18826Thalidomide-O-PEG2-propargyl；化合物 T18826E3 ligase Ligand-Linker Conjugates 32；E3 ligase Ligand-Linker
Thalidomide-O-PEG2-propargyl (E3 Ligase Ligand-Linker Conjugates 32) is a chemical compound that has been synthesized as a conjugate of an E3 ligase ligand and a linker. It incorporates the cereblon ligand based on Thalidomide, along with a 2-unit PEG linker. This compound is specifically designed for use in PROTAC technology, which utilizes ligand-induced protein degradation [1].
价 格：￥电议型 号：T18826产 地：中国大陆
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T18823Thalidomide-O-amido-PEG4-propargyl；化合物 T18823Thalidomide-O-amido-PEG4-propargyl
Thalidomide-O-amido-PEG4-propargyl is a polyethylene glycol (PEG)-based linker employed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T18823产 地：中国大陆
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T18647Pyrene-PEG5-propargyl；化合物 T18647Pyrene-PEG5-propargyl
Pyrene-PEG5-propargyl 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：T18647产 地：中国大陆
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T18641SirReal1-O-propargyl；化合物 T18641PROTAC Sirt2-binding moiety 1；PROTAC Sirt2-binding moiety 1
SirReal1-O-propargyl, a moiety based on SirReal1, is a selective and highly potent inhibitor of Sirtuin 2 (Sirt2), demonstrating an IC50 of 2.4 μM. It operates by binding to the cereblon ligand through a linker, facilitating the formation of PROTAC for the degradation of Sirt2[1].
价 格：￥电议型 号：T18641产 地：中国大陆
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T18591Propargyl-PEG8-SH；化合物 T18591Propargyl-PEG8-SH
Propargyl-PEG8-SH 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：T18591产 地：中国大陆
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T18590Propargyl-PEG7-methane；化合物 T18590Propargyl-PEG7-methane
Propargyl-PEG7-methane 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：T18590产 地：中国大陆
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T18589Propargyl-PEG6-SH；化合物 T18589Propargyl-PEG6-SH
Propargyl-PEG6-SH 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：T18589产 地：中国大陆
