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T16193N-(Azido-PEG3)-NH-PEG3-acid；化合物 T16193N-(Azido-PEG3)-NH-PEG3-acid
N-(Azido-PEG3)-NH-PEG3-acid is a polyethylene glycol (PEG) derived linker utilized for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16193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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T16086MK-0493；化合物 T16086MK-0493
MK-0493 is an effective and selective agonist of the melanocortin receptor 4 (MC4R). It also demonstrated significant reductions in energy intake.
价 格：￥电议型 号：T16086产 地：中国大陆
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T15993Mal-PEG4-PFP ester；化合物 T15993Mal-PEG4-PFP ester
Mal-PEG4-PFP ester is a non-cleavable antibody-drug conjugate (ADC) linker that incorporates a Maleimide moiety, a 4-unit Polyethylene Glycol (PEG) backbone, and a Pentafluorophenyl (PFP) ester.
价 格：￥电议型 号：T15993产 地：中国大陆
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T15939m-PEG8-Tos；化合物 T15939m-PEG8-Tos
Tos-PEG8-m, a PEG-based PROTAC linker, is a derivative of silybin ethers. It is utilized in the synthesis of Silymarin[1].
价 格：￥电议型 号：T15939产 地：中国大陆
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T15938m-PEG8-thiol；化合物 T15938m-PEG8-thiol
m-PEG8-thiol 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：T15938产 地：中国大陆
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T15937m-PEG8-succinimidyl carbonate；化合物 T15937m-PEG8-succinimidyl carbonate
m-PEG8-succinimidyl carbonate is a polyethylene glycol (PEG)-derived linker, specifically designed for the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T15937产 地：中国大陆
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T15936m-PEG8-NHS ester；化合物 T15936m-PEG8-NHS ester
m-PEG8-NHS ester is a non-cleavable 8 unit polyethylene glycol (PEG) linker compound, employed in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15936产 地：中国大陆
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T15935m-PEG8-Ms；化合物 T15935m-PEG8-Ms
m-PEG8-Ms is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15935产 地：中国大陆
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T15934m-PEG8-Mal；化合物 T15934m-PEG8-Mal
m-PEG8-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：T15934产 地：中国大陆
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T15933m-PEG8-CH2COOH；化合物 T15933m-PEG8-CH2COOH
m-PEG8-CH2COOH is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T15933产 地：中国大陆
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T15932m-PEG9-NHS ester；化合物 T15932m-PEG8-CH2CH2-NHS ester；m-PEG8-CH2CH2-NHS ester
m-PEG8-CH2CH2-NHS ester is a PEG--based PROTAC linker can be used in the synthesis of PROTACs.
价 格：￥电议型 号：T15932产 地：中国大陆
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T1593Ezetimibe；依泽替米贝SCH 58235；依泽替米贝|||SCH 58235
Ezetimibe (SCH 58235) is a Dietary Cholesterol Absorption Inhibitor. The physiologic effect of ezetimibe is by means of Decreased Cholesterol Absorption.
价 格：￥电议型 号：T1593产 地：中国大陆
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T15893m-PEG5-CH2COOH；化合物 T15893m-PEG5-CH2COOH
m-PEG5-CH2COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15893产 地：中国大陆
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T15822Ly93；化合物 Ly93Ly93
Ly93 is a selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor (IC50: 91 nM) for the study of atherosclerosis.
价 格：￥电议型 号：T15822产 地：中国大陆
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T15807LY2794193；化合物 T15807LY2794193
LY2794193 is a highly effective and selective agonist of the mGlu3 receptor (hmGlu3 Ki=0.927 nM,EC50=0.47 nM; hmGlu2 Ki=412 nM,EC50=47.5 nM).
价 格：￥电议型 号：T15807产 地：中国大陆
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T15793Lurbinectedin；卢比克替定PM01183；卢比克替定|||PM01183
Lurbinectedin (PM01183) is a DNA minor groove covalent binder. Lurbinectedin also shows effective anti-tumor activity.
价 格：￥电议型 号：T15793产 地：中国大陆
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T15781LP-935509；化合物LP-935509LP-935509
LP-935509 is highly brain-penetrant and reverses fully established pain behavior following the SNL procedure. LP-935509 is an effective inhibitor of BIKE (IC50=14 nM) and a modest inhibitor of cyclin G-associated kinase(GAK, IC50=320 nM). LP-935509 is also a ATP-competitive inhibitor of adapter protein-2 associated kinase 1 (AAK1) (IC50 = 3.3 nM, Ki = 0.9 nM).
价 格：￥电议型 号：T15781产 地：中国大陆
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T15693L-Azidohomoalanine；化合物 T15693L-Azidohomoalanine
L-Azidohomoalanine, an alkyl chain-derived PROTAC linker, is utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15693产 地：中国大陆
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T1569Tigecycline；替加环素GAR-936；替加环素|||GAR-936
Tigecycline (GAR-936) is a broad-spectrum glycylcycline antibiotic derived from tetracycline. Tigecycline binds to the 30S ribosomal subunit, thereby interfering with the binding of aminoacyl-tRNA to the mRNA-ribosome complex.
价 格：￥电议型 号：T1569产 地：中国大陆
