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T28603RO5353；化合物 T28603RO 5353|||RO-5353；RO 5353|||RO-5353
RO5353 is a potent and orally active inhibitor of p53-MDM2.
价 格：￥电议型 号：T28603产 地：中国大陆
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T28602RO5101576；化合物 T28602RO-5101576|||RO 5101576；RO-5101576|||RO 5101576
RO5101576 is a potent antagonist of LTB4 receptor.
价 格：￥电议型 号：T28602产 地：中国大陆
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T28601RO4988546；化合物 T28601RO-4988546|||RO 4988546；RO-4988546|||RO 4988546
RO4988546 is a potent negative allosteric modulator of mGlu?/?.
价 格：￥电议型 号：T28601产 地：中国大陆
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T28600Ro4491533；化合物 T28600Ro 4491533|||Ro-4491533；Ro 4491533|||Ro-4491533
Ro4491533 is a potent and selective negative allosteric modulator for group II of the metabotropic glutamate receptors (mGluR2/3).
价 格：￥电议型 号：T28600产 地：中国大陆
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T2860Vanillyl Alcohol；香兰醇4-Hydroxy-3-methoxybenzenemethanol|||3-Methoxy-4-hydroxybenzyl alcohol|||4-Hydro
Vanillyl Alcohol (3-Methoxy-4-hydroxybenzyl alcohol) possesses anti-angiogenic, anticonvulsive, anti-inflammatory, anti-oxidant, neuroprotective, and anti-nociceptive activities. Vanillyl alcohol can effectively inhibit the cytotoxicity and improved cell viability in 1-methyl-4-phenylpyridinium (MPP+)-induced MN9D dopaminergic cells, it also can attenuate the elevation of reactive oxygen species (ROS) levels, decrease in the Bax/Bcl-2 ratio and poly (ADP-ribose) polymerase proteolysis.
价 格：￥电议型 号：T2860产 地：中国大陆
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T28321PD 122860；化合物 T28321PD-122860|||PD122860；PD-122860|||PD122860
PD 122860 is a dihydropyridine with calcium channel blocking and sodium channel stimulating properties. In the rat heart, PD 122860 increased left ventricular contractility, decreased coronary resistance and altered the shape of the electrocardiogram T-wave. PD 122860 selectively relaxed potassium-contracted aortic rings and inhibited [3H]nitrendipine binding to rat brain membranes.
价 格：￥电议型 号：T28321产 地：中国大陆
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T28107MRT-68601 HCl；化合物 T28107MRT-68601 HCl
MRT-68601 HCl, a potent TBK1 (TANK-binding kinase-1), inhibits the formation of autophagosomes in lung cancer cells.
价 格：￥电议型 号：T28107产 地：中国大陆
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T27860Lu-AF11205；化合物 T27860Lu-AF11205
Lu-AF11205 is a potent positive allosteric modulator (PAM) of mGlu5 receptor.
价 格：￥电议型 号：T27860产 地：中国大陆
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T27832Lifibrol；利弗布罗U 83860|||K-12148|||K-12.148|||U-83860|||K12148；U 83860|||K-12148|||K-12.148|||U-83860|
Lifibrol (U-83860) is an inhibitor of cholesterol synthesis.Lifibrol has anticholesterol and hypolipidemic properties and promotes the conversion of LDL Apo B-100 in patients with hypercholesterolemia and mixed hyperlipidemia.
价 格：￥电议型 号：T27832产 地：中国大陆
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T27616BMS-986094；化合物 T27616INX 08189|||INX-189|||INX189|||INX08189|||INX-08189；INX 08189|||INX-189|||INX18
INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.
价 格：￥电议型 号：T27616产 地：中国大陆
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T27454GSK2008607；化合物GSK2008607GSK2008607
GSK2008607 is a potent B-RafV600E inhibitor with anticancer activity and can be used to study breast, colorectal, melanoma, thyroid, and ovarian cancers.
价 格：￥电议型 号：T27454产 地：中国大陆
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T27376FR-186054；化合物 T27376FR186054|||FR 186054；FR186054|||FR 186054
FR-186054 is a new, potent inhibitor of acyl-CoA:cholesterol O-acyltransferase (ACAT) and has oral activity. Compared to other ACAT inhibitors, this compound displayed excellent in vitro efficacy, irrespective of dosing method, indicating superior characteristics.
价 格：￥电议型 号：T27376产 地：中国大陆
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T26860BMS-814580；化合物 T26860BMS-814580
BMS-814580 is a potent and selective functional antagonist (Kb = 117 nM) of human MCHR1. BMS-814580 exhibits potent binding affinity (Ki = 17 nM) for human MCHR1. BMS-814580 also exhibits potent binding affinities for cynomolgus monkey and rat MCHR1 (Ki of 4.9 and 11.5 nM, respectively). MCHR1 antagonist demonstrates reduction in feeding and body weight in rats and mice.
价 格：￥电议型 号：T26860产 地：中国大陆
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T26826Bisindolylmaleimide I HCl化合物 T26826GF-109203X HCl|||BIS-I HCl|||GO-6860 HCl
Bisindolylmaleimide I HCl is a specific ATP-competitive PKC inhibitor.
价 格：￥电议型 号：T26826产 地：中国大陆
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T25860Neluxicapone；化合物 T25860Neluxicapona|||Neluxicaponum；Neluxicapona|||Neluxicaponum
Neluxicapone is an antiparkinsonian agent.
价 格：￥电议型 号：T25860产 地：中国大陆
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T25763LY 288601；化合物 T25763LY 288,601|||LY-288601|||LY-288,601|||LY288,601|||LY288601；LY 288,601|||LY-28860
LY 288601 is the 5,6-dihydro analog of LY231514 that has antitumor activity.
价 格：￥电议型 号：T25763产 地：中国大陆
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T24860TC-G1003；化合物 T24860TC G1003；TC G1003
TC-G1003 is an effective agonist of the somatostatin sst2 receptor.
价 格：￥电议型 号：T24860产 地：中国大陆
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T24808SMI-6860766；化合物 T24808TRAFSTOP 6860766|||TRAF-STOP 6860766|||SMI 6860766|||TRAFSTOP6860766|||SMI6860
SMI-6860766 is a CD40-Traf6 interactions blocker that acts by ameliorating the complications of diet-induced obesity in mice.
价 格：￥电议型 号：T24808产 地：中国大陆
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T24492Moflomycin；化合物 T24492F 860191|||F-860191|||F860191；F 860191|||F-860191|||F860191
Moflomycin is an anthracycline derivative. It exhibits a higher antileukemic activity compared to other anthracyclines.
价 格：￥电议型 号：T24492产 地：中国大陆
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T23860CAY10444；化合物 T23860BML-241|||CAY 10444|||CAY-10444|||BML241|||BML 241；BML-241|||CAY 10444|||CAY-1044
CAY10444 is an S1P3 specific antagonist.
价 格：￥电议型 号：T23860产 地：中国大陆
