9月
JC-229；化合物JC-229JC-229 (2024/9/14)
簡介：jc-229 is a potent and selective tbrpa1 inhibitor that can inhibit rpa1 in trypanosoma brucei. jc-229 can be used to study human african trypanosomiasis (hat).
XWLC-05細胞專用培養(yǎng)基 (2024/9/14)
簡介：xwlc-05細胞專用培養(yǎng)基已包含xwlc-05細胞生長所需的各種成分，無需添加任何成分，可直接用于xwlc-05細胞的培養(yǎng)
施耐德CPU模塊140DAO84000 (2024/9/14)
簡介：首先檢查各接線接口是否出現(xiàn)松動，然后檢查串口及中斷號是否有沖突，若有沖突，應(yīng)調(diào)整資源，避開沖突。再檢查觸摸屏表面是否出現(xiàn)裂縫，如有裂縫應(yīng)及時更換。還需要檢查觸摸屏表面是否有塵垢，若有，用軟布進行清除。觀察檢查控制盒上的指示燈是否工作正常，正常時，指示燈為綠色，并且閃爍。
2-(Chloromethyl)Imidazo[1,2-A]Pyridine；2-氯甲基咪唑并[1,2-A]吡啶鹽酸鹽2-(Chloromethyl)Imidazo[1,2-A]Pyridine (2024/9/14)
簡介：2-(chloromethyl)imidazo[1,2-a]pyridine has potential anthelmintic activity and can be used to synthesize active compounds.
1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride；1-(氨基甲基)環(huán)丙烷羧酸1-(aminomethyl)cyclopropanecar (2024/9/14)
簡介：1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride inhibits l amino acid transporter proteins and the α2δ subunit of voltage-gated calcium channels.1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride can be used as a biological module for the synthesis of active biochemical reagents.
5-Bromoimidazo[1,2-A]Pyrazine；5-溴咪唑并吡嗪5-Bromoimidazo[1,2-A]Pyrazine (2024/9/14)
簡介：5-bromoimidazo[1,2-a]pyrazine inhibits phosphodiesterase and beta-adrenergic receptors.5-bromoimidazo[1,2-a]pyrazine shows antibronchospastic activity in vitro.
Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate；4-氯-2-氧-1,2-二氫喹啉-3-羧酸乙酯Ethyl 4-chloro-2-oxo- (2024/9/14)
簡介：ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate inhibits nad(p)h: quinone oxidoreductase 1.
CCG-222740；化合物CCG-222740CCG-222740 (2024/9/14)
簡介：ccg-222740 is an inhibitor of rho/mrtf pathway
Pyridine-4-Acetamide；吡啶-4-乙酰胺4-Pyridineacetamide；4-Pyridineacetamide (2024/9/14)
簡介：pyridine-4-acetamide (4-pyridineacetamide) is a pyridine-based ligand involved in the synthesis of w6s8 clusters.
XWLC-05TEM8細胞專用培養(yǎng)基 (2024/9/14)
簡介：xwlc-05tem8細胞專用培養(yǎng)基已包含xwlc-05tem8細胞生長所需的各種成分，無需添加任何成分，可直接用于xwlc-05tem8細胞的培養(yǎng)
BIRM 271；化合物BIRM 271BIRM 271 (2024/9/14)
簡介：birm 271 is a novel arachidonic acid release inhibitor that blocks leukotriene b4 and platelet-activating factor biosynthesis in human neutrophils. birm 271 and birm 270 are enantiomers that inhibit the production of leukotriene b4 with ic50 of 40 nm.
LSD1-IN-27；LSD1抑制劑27LSD1-IN-27 (2024/9/14)
簡介：lsd1-in-27 is a potent lsd1 inhibitor with an ic50 value of 13 nm.lsd1-in-27 inhibited the stemness and migration of gastric cancer cells.lsd1-in-27 inhibited the expression of pd-l1 in bgc-823 and mfc cells.lsd1-in-27 potentiated the t-cell immune response against gastric cancer.
JHU 75528；化合物JHU 75528JHU75528|||JHU-75528；JHU75528|||JHU-75528 (2024/9/14)
簡介：jhu 75528 (jhu-75528) is a novel pet tracer with inhibitory effects on cb that can be used to study the cannabinoid system in schizophrenic patients.
徠佳圖20-60X80ED WF4K抓拍系統(tǒng) 數(shù)碼遠拍望遠鏡 (2024/9/14)
簡介：lcantu徠佳圖20-60x80ed wf4k望遠鏡抓拍系統(tǒng)采用新一代松下1600萬感光芯片，獨有的wifi技術(shù)，通過手機、平板電腦等方式觀看，從真正的意義上解放了雙眼，為用戶提供了一種便利、支持多人同時觀看，提高觀看的樂趣，并且提供了最輕松的拍攝保存方式。設(shè)備可無線連接ipad 或iphone/安卓系統(tǒng)手機
G43；化合物G43G 43|||G-43；G 43|||G-43 (2024/9/14)
簡介：g43 is a potent and selective glucosyltransferase inhibitor that inhibits gtfb and gtfc with kd values of 3.7 μm and 46.9 nm, respectively.g43 exhibits in vitro and in vivo anti-streptococcus mutans activity and can be used for caries studies.
Antiviral agent 34；抗病毒劑34Antiviral agent 34 (2024/9/14)
簡介：antiviral agent 34 is an orally available, potent antiviral compound that inhibits influenza a and b viruses.antiviral agent 34 inhibits the proliferation of influenza viruses by modulating rna polymerase.antiviral agent 34 is used in the study of viral infections.
Enpp/Carbonicu00A0anhydrase-IN-2；Enpp/Carbonicu00A0anhydras抑制劑2Enpp/Carbonicu00A0anhydrase-IN-2 (2024/9/14)
簡介：enpp/carbonic?anhydrase-in-2 is a potent dual inhibitor of enpp and carbonic anhydrase, inhibiting npp1, npp2, npp3, ca-ix, ca-xii, with ic50 values of 1.13, 1.07, 0.74, 0.33, 0.68, respectively.enpp/carbonic?anhydrase-in-2 induced apoptosis.enpp/carbonic anhydrase-in-2 has antiproliferative activity against cancer cells and low cytotoxicity against normal cells.
WM266-4細胞專用培養(yǎng)基 (2024/9/14)
簡介：wm266-4細胞專用培養(yǎng)基已包含wm266-4細胞生長所需的各種成分，無需添加任何成分，可直接用于wm266-4細胞的培養(yǎng)
EP3u00A0antagonistu00A04；EP3拮抗劑4EP3u00A0antagonistu00A04 (2024/9/14)
簡介：ep3?antagonist?4 is an ep3 antagonist that inhibits hep with a ki of 2 nm. ep3 antagonist 4 showed low in vivo clearance, high oral auc and good bioavailability in complete pk studies in rats. ep3 antagonist 4 can be used to study diabetes and cellular dysfunction.
深圳德邁盛電池燃燒（噴射）試驗機DMS-DC008 (2024/9/14)
簡介：深圳德邁盛電池燃燒（噴射）試驗機dms-dc008電池燃燒（噴射）試驗機 用于手持式電子產(chǎn)品用鋰離子電池組、可能置于口袋中攜帶或使用的便攜式電子產(chǎn)品用的鋰離子電池組、其他便攜式電子產(chǎn)品用可置于口袋中攜帶的電池組、安裝非用戶更換型電池/電池組的手持式電子產(chǎn)品的燃燒噴射試驗。電池燃燒（噴射）試驗機符合gb31241-2014等標準。
Thalidomide-4-OH化合物Thalidomide-4-OHCereblon ligand 2|||E3 ligase Ligand 2 (2024/9/14)
簡介：thalidomide-4-oh (e3 ligase ligand 2) (cereblon ligand 2) is the thalidomide-based cereblon ligand used to recruit of crbn protein. thalidomide-4-oh (cereblon ligand 2) is a linker to form protacs
FD274；化合物FD274FD 274|||FD-274；FD 274|||FD-274 (2024/9/14)
簡介：fd274 is a potent dual pi3k/mtor inhibitor with inhibitory effects on pi3kα/β/γ/δ and mtor, with ic50s of 0.65 nm, 1.57 nm, 0.65 nm, 0.42 nm, and 2.03 nm, respectively. fd274 showed significant antiproliferative activity in aml cell line antiproliferative assays. fd274 exhibited dose-dependent pit tumor growth activity in an hl-60 xenograft model. fd274 has potential for use in acute myeloid leukemia studies.
Bisindolylmaleimide III；雙辛基馬來酰亞胺IIIBisindolylmaleimide III (2024/9/14)
簡介：bisindolylmaleimide iii is a potent and selective inhibitor of protein kinase c (pkc).bisindolylmaleimide iii selectively interacts with pkcα or ribosomal s6 protein kinase 1 upon activation of these kinases.
GS9000步進頻連續(xù)波雷達全分辨率成像技術(shù) (2024/9/14)
簡介：步進頻連續(xù)波雷達全分辨率成像技術(shù)步進頻連續(xù)波雷達通過在一定頻率范圍內(nèi)按固定步長逐步改變發(fā)射信號的頻率。發(fā)射信號是由一系列離散頻率的正弦波組成，每個頻率的信號在時間上依次發(fā)射、
Opevesostat；化合物OpevesostatODM208|||ODM-208；ODM208|||ODM-208 (2024/9/14)
簡介：opevesostat (odm-208) is an inhibitor of lyase (cyp11a1) (the enzyme cleavage cholesterol side chain).
CCG-13514；化合物CCG-13514CCG-13514 (2024/9/14)
簡介：ccg-13514 is a biochemical reagent to be developed for biosynthesis.
WAY-270250；化合物WAY-270250WAY-270250 (2024/9/14)
簡介：way-270250 is an igf-1r/src inhibitor.
Z16078526化合物Z16078526Z 16078526|||Z16078526|||Z16078526 (2024/9/14)
簡介：z16078526 enhances thermogenesis in mice by inducing endogenous ucp1 expression, promoting p38 mapk phosphorylation, and stimulating lipolysis in primary mouse brown adipocytes. additionally, it activates thermogenic gene expression and mitochondrial activity, specifically uncoupled respiration, in these cells.
WM-115細胞專用培養(yǎng)基 (2024/9/14)
簡介：wm-115細胞專用培養(yǎng)基已包含wm-115細胞生長所需的各種成分，無需添加任何成分，可直接用于wm-115細胞的培養(yǎng)
LMTK3-IN-1；LMTK3抑制劑1LMTK3-IN-1 (2024/9/14)
簡介：lmtk3-in-1 is a potent atp-competitive lemur tyrosine kinase 3 (lmtk3) (kd=2.5 μm) inhibitor that degrades lmtk3 through the ubiquitin proteasome pathway. lmtk3-in-1 has shown anticancer activity in a variety of cancer cell lines and in vivo bc mouse models. lmtk3-in-1 (10-20 μm) can induce the apoptosis of bc cell line.
最新產(chǎn)品 最新資訊 技術(shù)文章 公司動態(tài) 最新求購 分類瀏覽搜索標簽
Copyright 2009-2012 app17.com,all rights reserved ICP備案號：浙ICP備08105869號
MSN交談
會員服務(wù)咨詢：0571-85363692 客服熱線：0571-85363691 采購技術(shù)交流群號：187637045
