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T67817Besifovir PM；贝西福韦PMLB80331 PM；LB80331 PM
Besifovir PM (LB80331 PM) is n analogue of Besifovir, a novel orally available acyclic nucleotide phosphonate for the treatment of chronic hepatitis B infection.
价 格：￥电议型 号：T67817产 地：中国大陆
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T6726VU0361737；化合物VU 0361737ML-128|||VU 0361737；ML-128|||VU 0361737
VU0361737 (ML-128) is a specific positive allosteric modulator (PAM) of mGlu4 receptor.The EC50 of VU 0361737 is 240 nM for the human receptors. The EC50 of VU 0361737 is110 nM for rat receptors.It exhibits weak activity at mGlu5 and mGlu8 receptors, and is inactive at mGlu1, mGlu2, mGlu3, mGlu6 and mGlu7 receptors, can penetrate into CNS.
价 格：￥电议型 号：T6726产 地：中国大陆
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T66546Levothyroxine sodium；化合物 Levothyroxine sodiumLevothyroxine sodium
Levothyroxine sodium is a useful organic compound for research related to life sciences. The catalog number is T66546 and the CAS number is 25416-65-3.
价 格：￥电议型 号：T66546产 地：中国大陆
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T6593ML324；化合物ML324ML324
ML324(IC50=920 nM) is a specific inhibitor of jumonji histone demethylase (JMJD2).
价 格：￥电议型 号：T6593产 地：中国大陆
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T6592ML133 hydrochloride；(4-甲氧基苄基)(1-萘基甲基)胺盐酸盐ML133 HCl；ML133 HCl|||(4-甲氧基苄基)(1-萘基甲基)胺盐酸盐
ML133 hydrochloride (ML133 HCl) is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
价 格：￥电议型 号：T6592产 地：中国大陆
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T6591Nodinitib-1；化合物ML130ML130|||CID-1088438；ML130|||CID-1088438
Nodinitib-1 (CID-1088438) is a potent and selective NOD1 inhibitor with an IC50 of 0.56 μM.
价 格：￥电议型 号：T6591产 地：中国大陆
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T6568Licofelone；利克飞龙ML-3000；利克飞龙|||ML-3000
Licofelone (ML-3000) is a dual COX/LOX inhibitor potentially for the treatment of osteoarthritis. Licofelone is both an analgesic and an anti-inflammatory. Inhibition of 5-LOX may reduce the gastrointestinal toxicity associated with other non-steroidal anti-inflammatory drugs, which only inhibit COX (cyclooxygenase).
价 格：￥电议型 号：T6568产 地：中国大陆
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T65270L-Aspartic acid sodium；化合物 L-Aspartic acid sodiumL-Aspartic acid sodium
L-Aspartic acid sodium is a natural product for research related to life sciences. The catalog number is T65270 and the CAS number is 5598-53-8.
价 格：￥电议型 号：T65270产 地：中国大陆
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T6473816-(S)-ML188；化合物 16-(S)-ML18816-(S)-ML188
16-(S)-ML188 is a useful organic compound for research related to life sciences and the catalog number is T64738.
价 格：￥电议型 号：T64738产 地：中国大陆
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T64542Lactate potassium；化合物 Lactate potassiumLactate potassium
Lactate potassium is a useful organic compound for research related to life sciences. The catalog number is T64542 and the CAS number is 996-31-6.
价 格：￥电议型 号：T64542产 地：中国大陆
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T64523Locust bean gum；化合物 Locust bean gumLocust bean gum
Locust bean gum is a useful organic compound for research related to life sciences and the catalog number is T64523.
价 格：￥电议型 号：T64523产 地：中国大陆
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T64340ML267；化合物ML2674-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-car
ML267 (4-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-N-(4-methoxypyridin-2-yl)piperazine-1-carbothioamide trifluoroacetate) is a potent inhibitor of bacterial phosphopantetheinyl transferase that attenuates secondary metabolism and thwarts bacterial growth[1].
价 格：￥电议型 号：T64340产 地：中国大陆
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T64320ML251；化合物ML251u00A0ML251
ML251 is a potent novel nanomolar inhibitor of T. brucei and T. cruzi phosphofructokinase[1]. ML251 inhibits T. brucei PFK (IC50=0.37 μM) and T. cruzi PFK (IC50=0.13 μM). ML251 can be used for the research of parasite[1].
价 格：￥电议型 号：T64320产 地：中国大陆
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T64267Laropiprant sodium；化合物 Laropiprant sodiumLaropiprant sodium
Laropiprant sodium is a potent and selective DP receptor antagonist with Ki values of 0.57 nM for TP receptors and 2.95 nM for DP receptors.
价 格：￥电议型 号：T64267产 地：中国大陆
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T63779RmlA-IN-2；化合物 RmlA-IN-2RmlA-IN-2
RmlA-IN-2 is a potent inhibitor of 1-phosphoglucose thymidyltransferase (RmlA) (IC50: 0.303 μM).RmlA-IN-2 affects the monosaccharide l-rhamnose biosynthetic pathway and affects bacterial cell wall permeability.
价 格：￥电议型 号：T63779产 地：中国大陆
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T63674Imlunestrant；化合物 ImlunestrantImlunestrant
Imlunestrant is a selective, orally active estrogen receptor degrader (SERD) that can be used in ER+ and HER2 breast cancer studies.
价 格：￥电议型 号：T63674产 地：中国大陆
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T63445Amlodipine mesylate；化合物 Amlodipine mesylateAmlodipine mesylate
Amlodipine mesylate is an oral active dihydropyridine calcium channel blocker that blocks voltage-dependent L-type calcium channels and inhibits calcium inward flow, and is an anti-anginal agent. amlodipine mesylate can be used to study hypertension and cancer.
价 格：￥电议型 号：T63445产 地：中国大陆
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T6332Pevonedistat；化合物PevonedistatMLN4924；MLN4924
Pevonedistat (MLN4924) is a potent and selective NEDD8 activating enzyme (NAE) inhibitor (IC50=4.7 nM). Pevonedistat can be used for the treatment of myelodysplastic syndromes (MDS) and also has antitumor activity.
价 格：￥电议型 号：T6332产 地：中国大陆
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T6315MLN8054；化合物MLN8054MLN8054
MLN8054 is a potent and selective Aurora A kinase inhibitor with an IC50 of 4 nM.
价 格：￥电议型 号：T6315产 地：中国大陆
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T62692ML-SI1；化合物 ML-SI1ML-SI1
ML-SI1, a racemic mixture of diastereoisomers, is a TRPML inhibitor and acts on TRPML1 (IC50: 15 μM).
价 格：￥电议型 号：T62692产 地：中国大陆
