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T23389SR1664SR 1664
SR1664 is a potent and selective PPARγ inhibitor with potential antidiabetic activity. SR1664 binds to PPARγ and potently inhibits Cdk5-mediated PPARγ phosphorylation (IC50 = 80 nM; Ki = 28.67 nM) without exhibiting PPARγ agonist activity.
价 格：￥电议型 号：T23389产 地：中国大陆
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T1664Meglutol美格鲁托；Dicrotalic acid；3-Hydroxy-3-methylglutaric acid
Meglutol is an antilipemic agent which lowers cholesterol, triglycerides, serum beta-lipoproteins and phospholipids. It acts by interfering with the enzymatic steps involved in the conversion of acetate to hydroxymethyl glutaryl coenzyme A as well as inhi
价 格：￥电议型 号：T1664产 地：中国大陆
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T1664MeglutolMeglutol,3-Hydroxy-3-methylglutaric acid,Dicrotalic acid
Meglutol is an antilipemic agent which lowers cholesterol, triglycerides, serum beta-lipoproteins and phospholipids. It acts by interfering with the enzymatic steps involved in the conversion of acetate to hydroxymethyl glutaryl coenzyme A as well as inhi
价 格：￥电议型 号：T1664产 地：美洲
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T81664NMB-1；化合物 NMB-1NMB-1
NMB-1, a conopeptide analogue, selectively inhibits sustained mechanically activated currents in sensory neurons with an IC50 of 1 μM, attenuating mechanical pain. It is utilized in research pertaining to hearing and pressure-evoked pain [1] [2].
价 格：￥电议型 号：T81664产 地：中国大陆
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T71664Mespirenone；美螺利酮Mespirenone
Mespirenone is a spironolactone derivative and aldosterone antagonist with diuretic effects.
价 格：￥电议型 号：T71664产 地：中国大陆
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T61664Benzoquinoquinoxaline；化合物 BenzoquinoquinoxalineBenzoquinoquinoxaline
Benzoquinoquinoxaline (BQQ) is a heterocyclic compound featuring an aminoalkyl side chain. BQQ exhibits preferential binding to DNA triplex structures, intercalating between the bases to stabilize the triplex conformation. Additionally, conjugation of BQQ to 1,10-phenanthroline enables specific binding and cleavage of double-strand DNA at the site where a triplex structure forms [1].
价 格：￥电议型 号：T61664产 地：中国大陆
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T31664Lysergamide, N-cyclopropyl-, maleate；化合物 T31664Ergoline-8-beta-carboxamide, N-cyclopropyl-9,10-dideh
Ergoline-8-beta-carboxamide, N-cyclopropyl-9,10-didehydro-6-methyl-, maleate is a bioactive chemical.
价 格：￥电议型 号：T31664产 地：中国大陆
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T28559Ro 16-6491；化合物 T28559Ro166491|||Ro-16-6491；Ro166491|||Ro-16-6491
Ro 16-6491 is a selective, reversible, orally-active inhibitor of MAO-B.
价 格：￥电议型 号：T28559产 地：中国大陆
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T23389SR1664；化合物SR 1664SR 1664；SR 1664
SR1664 is a potent and selective PPARγ inhibitor with potential antidiabetic activity. SR1664 binds to PPARγ and potently inhibits Cdk5-mediated PPARγ phosphorylation (IC50 = 80 nM; Ki = 28.67 nM) without exhibiting PPARγ agonist activity.
价 格：￥电议型 号：T23389产 地：中国大陆
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T23315SB 216641 hydrochloride；化合物 T23315SB 216641 hydrochloride
h5-HT1B antagonist
价 格：￥电议型 号：T23315产 地：中国大陆
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T16649Propargyl-PEG8-Boc；化合物 T16649Propargyl-PEG8-Boc
Propargyl-PEG8-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：T16649产 地：中国大陆
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T16648Propargyl-PEG8-acid；化合物 T16648Propargyl-PEG8-acid
Propargyl-PEG8-acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). The ADCs can be used in bacterial infections caused by Gram-negative bacteria[1].
价 格：￥电议型 号：T16648产 地：中国大陆
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T16647Propargyl-PEG8-NHS ester；化合物 T16647Propargyl-PEG8-NHS ester
Propargyl-PEG8-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16647产 地：中国大陆
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T16646Propargyl-PEG7-Boc；化合物 T16646Propargyl-PEG7-Boc
Propargyl-PEG7-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：T16646产 地：中国大陆
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T16644Propargyl-PEG7-acid；化合物 T16644Propargyl-PEG7-acid
Propargyl-PEG7-acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16644产 地：中国大陆
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T16643Propargyl-PEG6-NH2；化合物 T16643Propargyl-PEG6-NH2
Propargyl-PEG6-NH2 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：T16643产 地：中国大陆
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T16642Propargyl-PEG7-NHS ester；化合物 T16642Propargyl-PEG7-NHS ester
Propargyl-PEG7-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16642产 地：中国大陆
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T16641Propargyl-PEG6-Boc；化合物 T16641Propargyl-PEG6-Boc
Propargyl-PEG6-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：T16641产 地：中国大陆
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T16640Propargyl-PEG6-alcohol；化合物 T16640Propargyl-PEG6-alcohol
Propargyl-PEG6-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T16640产 地：中国大陆
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T1664Meglutol；美格鲁托Dicrotalic acid|||3-Hydroxy-3-methylglutaric acid；Dicrotalic acid|||3-Hydroxy-3-methylg
Meglutol (3-Hydroxy-3-methylglutaric acid) is an antilipemic agent which lowers cholesterol, triglycerides, serum beta-lipoproteins and phospholipids. It acts by interfering with the enzymatic steps involved in the conversion of acetate to hydroxymethyl glutaryl coenzyme A as well as inhibiting the activity of HYDROXYMETHYLGLUTARYL COA REDUCTASES which is the rate-limiting enzyme in the biosynthesis of cholesterol.
价 格：￥电议型 号：T1664产 地：中国大陆
