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TN7036N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamidebone formation,Beta catenin,inhibit,Inhibitor,N (
N-3-methoxylBenzyllinolenicamide induces osteogenic differentiation and subsequent bone formation of mesenchymal stem cells by activating the canonical Wnt/β-catenin signaling pathway that can be used for osteoporosis research.
价 格：￥电议型 号：TN7036产 地：中国大陆
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T9429ZZW-115ZZW115,ZZW 115
ZZW-115 is a potent NUPR1 inhibitor with a Kd of 2.1 μM. ZZW-115 is a derivative of Trifluoperazine (TFP). ZZW-115 shows a dose-dependent tumor regression with no neurological side effects and induces cell death mainly by necroptosis and apoptosis[1] [2].
价 格：￥电议型 号：T9429产 地：中国大陆
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TN1965N-?BenzyllinolenamideFatty acid amide hydrolase,Autophagy,N ?Benzyllinolenamide,inhibit,Inhibitor,N-
N-Benzyllinolenamide is a natural product. It is an inhibitor of fatty acid amide hydrolase (FAAH, IC50 of 41.8 μM).
价 格：￥电议型 号：TN1965产 地：中国大陆
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T14046Anandamide(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide；花生四烯酸乙醇胺
Anandamide, an immune modulator, acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55) in the central nervous system.
价 格：￥电议型 号：T14046产 地：中国大陆
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T14046AnandamideAnandamide,(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide,
Anandamide, an immune modulator, in the central nervous system acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55).
价 格：￥电议型 号：T14046产 地：美洲
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T140555Z-7-Oxozeaenol5Z-7-Oxozeaenol,FR148083,L783279
5Z-7-Oxozeaenol, a natural anti-protozoan compound from fungal origin, acting as a potent irreversible and selective inhibitor of TAK1 and VEGF-R2, with IC50s of 8 nM and 52 nM, respectively.
价 格：￥电议型 号：T14055产 地：美洲
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T1802ZLN005ZLN005
ZLN005 is an effective and tissue-specific transcriptional activator of PGC-1α.
价 格：￥电议型 号：T1802产 地：美洲
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T8396820-HETE Intermediate 15化合物 20-HETE Intermediate 15Methyl (5Z,8Z,11Z,14Z)-20-(acetyloxy)-5,8,11,14-ei
20-HETE Intermediate 15 is an intermediate of 20-hydroxyeicosatetraenoic acid.
价 格：￥电议型 号：T83968产 地：中国大陆
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T80724ZK-PI-5；化合物 ZK-PI-5ZK-PI-5
ZK-PI-5, a potent trehalase inhibitor, has the potential to regulate Spodoptera frugiperda reproduction and may serve as a novel insecticide with significant pest control capabilities [1].
价 格：￥电议型 号：T80724产 地：中国大陆
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T78733ZLD115；化合物 ZLD115ZLD115
ZLD115 (compound 44), a derivative of FB23, functions as an inhibitor of the Fat Mass and Obesity-associated Protein (FTO) and demonstrates antiproliferative properties as an antileukemic agent against leukemic cell lines [1].
价 格：￥电议型 号：T78733产 地：中国大陆
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T77752HMBR；化合物HMBR4-Thiazolidinone, 5-[(4-hydroxy-3-methylphenyl)methylene]-2-thioxo-, (5Z)-；4-Thiazolidin
HMBR are not fluorescent by themselves, but when combined with Y-FAST, they emit yellow light when excited by blue light.
价 格：￥电议型 号：T77752产 地：中国大陆
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T755604(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-1-yl-；化合物 4(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-
4(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-1-yl- (compound 2), a quinolone alkaloid extracted from Cnidium, demonstrates activity against methicillin-resistant Staphylococcus aureus (MRSA), exhibiting minimum inhibitory concentration (MIC) values of 32 μg/mL (ATCC 33591) and 16 μM/mL (ATCC 25923) respectively [1].
价 格：￥电议型 号：T75560产 地：中国大陆
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T73567ZT55；化合物 ZT55ZT55
ZT55, an orally active, highly-selective JAK2 inhibitor with an IC50 of 0.031 μM, inhibits proliferation of JAK2 V617F-expressing HEL cell lines, induces apoptosis and cycle arrest, and effectively inhibits HEL xenograft tumor growth in mice models. Suitable for studies on myeloproliferative neoplasms, polycythemia vera, and primary thrombocythemia, ZT55 offers promising applications.
价 格：￥电议型 号：T73567产 地：中国大陆
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T70380ZBH-1205；化合物 ZBH-1205ZBH-1205
ZBH-1205 is a novel camptothecin derivative, revealing potent antitumor activities mainly through cell apoptosis pathway, being more effective than cpt-11 and sn38 at inhibiting topoismerase-1
价 格：￥电议型 号：T70380产 地：中国大陆
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T7021ZM241385；化合物ZM241385ZM241385
ZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.
价 格：￥电议型 号：T7021产 地：中国大陆
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T64123ZIKV-IN-5；化合物 ZIKV-IN-5ZIKV-IN-5
ZIKV-IN-5 is an acid-stable, low cytotoxic anti-ZIKV agent with an EC50 value of 0.71 μM. ZIKV-IN-5 showed effective inhibition of ZIKV NS5 MTase activity.
价 格：￥电议型 号：T64123产 地：中国大陆
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T60748ZDWX-25；化合物 ZDWX-25ZDWX-25
ZDWX-25 is a highly potent dual inhibitor of GSK-3β and DYRK1A that possesses significant cytotoxic activities towards SH-SY5Y and HL-7702 cells. ZDWX-25 can be used for Alzheimer´s disease research with an IC 50 value of 71 nM for GSK-3β [1].
价 格：￥电议型 号：T60748产 地：中国大陆
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T36562(5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic Acid；(5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-yno
(5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic acid is a stable isomer of 15(S)-HETE , a major arachidonic acid metabolite from the 15-lipoxygenase pathway. (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic acid elicits concentration-dependent contraction of isolated pulmonary arteries from rabbits and inhibits the proliferation and migration of hormone-independent prostate carcinoma PC-3 cells.
价 格：￥电议型 号：T36562产 地：中国大陆
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T35315Zoloperone；化合物 T35315Zoloperonum|||LR511|||LR 511|||LR-511；Zoloperonum|||LR511|||LR 511|||LR-511
Zoloperone is a neuroleptic.
价 格：￥电议型 号：T35315产 地：中国大陆
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