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T30458Biphenyl-4-ylurea；化合物 T30458AI320179|||AI3-20179|||AI3 20179；AI320179|||AI3-20179|||AI3 20179
Biphenyl-4-ylurea is a biochemical.
价 格：￥电议型 号：T30458产 地：中国大陆
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T294585-Hydroxymebendazole化合物 T29458R 19167|||R19167|||R-19167
5-Hydroxymebendazole is a biochemical.
价 格：￥电议型 号：T29458产 地：中国大陆
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T2933025-Desacetylrifapentine；化合物 T29330L14583|||L-14583；L14583|||L-14583
25-Desacetylrifapentine is the main metabolite of DL 473-IT in plasma.
价 格：￥电议型 号：T29330产 地：中国大陆
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T28509RDR03871；化合物RDR03871RDR 03871|||ZINC20458540|||RDR-03871；RDR 03871|||ZINC20458540|||RDR-03871
RDR03871 is an MDM2 inhibitor.
价 格：￥电议型 号：T28509产 地：中国大陆
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T28493R-547 mesylate；化合物 T28493RO-4584820 mesylate|||RG-547 mesylate；RO-4584820 mesylate|||RG-547 mesylate
R547 Mesylate is a potent ATP-competitive inhibitor of CDK1, CDK2, CDK4 with Ki value of 2 nM, 3 nM, 1 nM respectively.
价 格：￥电议型 号：T28493产 地：中国大陆
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T28458PS432；化合物 T28458PS-432|||PS 432；PS-432|||PS 432
PS432 is an allosteric inhibitor of atypical PKCs. PS432 targets the PIF-pocket resulting in significantly reduce tumor growth without side effects in mouse xenograft model.
价 格：￥电议型 号：T28458产 地：中国大陆
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T28196NS-220；化合物 T28196LS-191458|||NS 220；LS-191458|||NS 220
NS-220, a selective agonist of peroxisome proliferator-activated receptor alpha, potently decreases plasma triglyceride and glucose levels and modifies lipoprotein profiles in KK-Ay mice.
价 格：￥电议型 号：T28196产 地：中国大陆
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T27708K-14585；化合物 T27708K-14585
K-14585 is a proteinase-activated receptor 2 antagonist. K-14585 inhibited PAR(2)-mediated p65 NFkappaB phosphorylation and NFkappaB-DNA binding. K-14585 inhibited SLIGKV-stimulated IL-8 production, but given alone increased IL-8.
价 格：￥电议型 号：T27708产 地：中国大陆
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T27480GSK494581A；化合物 T27480GSK 494581A|||GSK-494581A；GSK 494581A|||GSK-494581A
GSK494581A is a GPR55 agonist and glycine transporter subtype 1 inhibitor.
价 格：￥电议型 号：T27480产 地：中国大陆
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T27458GSK-2250665A；化合物 T27458GSK2250665|||GSK-2250665|||GSK 2250665A|||GSK 2250665；GSK2250665|||GSK-225066
GSK-2250665A is a Itk inhibitor with pKi value of 9.2.
价 格：￥电议型 号：T27458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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T26736Balapiravir hydrochloride；化合物 T26736R 1626|||Balapiravir HCl|||RO-4588161|||RO4588161|||R-1626|||R16
Balapiravir HCl, an NS5B inhibitor, is used potentially for the treatment of HCV infection.
价 格：￥电议型 号：T26736产 地：中国大陆
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T26458A 9145C；化合物 T26458A9145C|||A-9145C；A9145C|||A-9145C
A 9145C is an inhibitor of RNA methylase and cyclopropane fatty acid synthase.
价 格：￥电议型 号：T26458产 地：中国大陆
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T26360Benperidol；苯哌唑酮R4584|||R-4584|||Anquil|||McN-JR-4584|||R 4584；R4584|||R-4584|||Anquil|||McN-JR-4584|
Benperidol (Anquil) is a butanone analog with antipsychotic and stabilizing properties, and has been shown to be effective in blocking D2 receptors.Benperidol can be used in positron emission tomography (PET) scanning to measure D(2) dopamine receptor binding in vivo.Benperidol has been shown to be effective in blocking D2 receptors in vivo.Benperidol has been shown to be effective in blocking D2 receptors in vivo.
价 格：￥电议型 号：T26360产 地：中国大陆
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T25458Golexanolone；化合物 GolexanoloneGolexanolonum|||Golexanolona|||GR-3027；Golexanolonum|||Golexanolona|||G
Golexanolone (Golexanolona) is a novel GABA-A receptor-modulating steroid antagonist that reduces peripheral inflammation and neuroinflammation and improves cognitive and motor function in rats with chronic hyperammonemia, and may be used to study hepatic encephalopathy.
价 格：￥电议型 号：T25458产 地：中国大陆
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T24589Paldimycin A；化合物 T24589Antibiotic 273 A1-alpha；Antibiotic 273 A1-alpha
Paldimycin A is a semi-synthetic antibiotic from Streptomyces paulus.
价 格：￥电议型 号：T24589产 地：中国大陆
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T24588Palatrigine；化合物PalatrigineBW-A 256C|||BW A256C；BW-A 256C|||BW A256C
Palatrigine (BW-A 256C) is a compound with angiotensin-converting enzyme inhibitory and beta-adrenergic receptor blocking properties.
价 格：￥电议型 号：T24588产 地：中国大陆
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T24587Pafuramidine maleate；化合物 T24587DB-289|||DB289|||DB 289；DB-289|||DB289|||DB 289
Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis.
价 格：￥电议型 号：T24587产 地：中国大陆
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T24586PAFAH1b2；化合物 T24586PAFAH-1-b-2|||3-IN-P11|||3INP11|||3 IN P11|||PAFAH 1 b 2；PAFAH-1-b-2|||3-IN-P11||
PAFAH1b2 is a selective platelet-activating factor acetylhydrolases 1b2 and 1b3 inhibitor that acts by impairing cancer cell survival.
价 格：￥电议型 号：T24586产 地：中国大陆
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T24585PA-9；化合物 T24585PA 9；PA 9
PA-9 is the first small-molecule PAC1 receptor antagonist.
价 格：￥电议型 号：T24585产 地：中国大陆
