Nigericin sodium salt 是從吸水鏈霉菌中得到的一種抗生素,作為 H
+,K
+ 和 Pb
2+ 離子載體起作用。
Nigericin sodium salt產(chǎn)品描述:Nigericin sodium salt is an antibiotic from Streptomyces hygroscopicus that works by acting as an H
+, K
+, and Pb
2+ ionophore.
In Vitro:Nigericin (0.1 μM) decreases inhibits proliferation and clo
nogenicity of
H460 lung cancer cells in a dose dependent manner. Nigericin inhibits
migration and invasion of H460 lung cancer cells
[1].
Nigericin (0.1-10 nM) has apparently a dual effect on cell volume, that
is a shrinking effect at lower Nigericin co
ncentrations and a swelling
effect at higher concentrations. Nigericin (0.1-1 nM) significantly
decreases cytosolic pH (pHi), and slightly increases the pHi at 5 and 10
nM
[2]. Nigericin exhibits higher toxicity on S18 cells than S26 cells, with IC
50 of 2.03±0.55 μM and 4.77±2.35 μM, respectively. Nigericin can
selectively kill cancer stem cells in NPC in vitro. Nigericin
dramatically reduces the migration ability of S18 and HONE-1 cells
[3]. Nigericin exhibits gteat toxicity for the HT29 and SW116 cell line with IC
50 of 12.92±0.25 μmol and 15.86±0.18 μmol. Nigericin also shows a
decreased ability to form colo
nies under anchorage-independent
co
nditions in a standard soft agar assay
[4].
In Vivo: Milrinone (1 μg/kg/min, i.v.) significantly
reduces PAP, PVR (?18.96 ± 1.7%), and LAP (?26.03 ± 2.3%) in co
ngestive
heart failure (CHF) rats. Milrinone (1 mg/mL, inhalation) results in a
near-maximal reduction of PAP without significant effects on AP,
decreases pulmo
nary artery pressure similarly in a larger collective of
CHF rats. Milrinone Ngericin (4 mg/kg, i.p.) significantly reduces tumor growth and acts
synergistically with the chemotherapeutic agent DDP, as shown by the
tumor volumes. Nigericin markedly decreases Bmi-1 in vivo.
Overex
pression of Bmi-1 partially restores CSC co
ntent and me
tastatic
ability of NPC cells under Nigericin treatment. The downregulation of
Bmi-1 may be involved in the inhibitory effect of Nigericin on CSCs in
NPC
[3].
公司介紹:MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、API及化合物庫,總部位于美國新澤西,分別在瑞典和上海設(shè)有歐洲區(qū)子公司和區(qū)總代理,營銷網(wǎng)點(diǎn)遍及20多個(gè)地區(qū)。MCE經(jīng)過多年努力已成為生物活性小分子領(lǐng)域的供應(yīng)商,
產(chǎn)品涵蓋癌癥、神經(jīng)科學(xué)、抗感染、表觀遺傳學(xué)等20個(gè)熱門研究領(lǐng)域,PI3K、MAPK等近千個(gè)細(xì)分靶點(diǎn),超過4000個(gè)活性小分子化合物現(xiàn)貨,以及GPCR、API、離子通道等超過20種不同類型的化合物庫,同時(shí)提供從毫克到千克的專業(yè)定制合成服務(wù)。
MCE 對(duì)每批產(chǎn)品都進(jìn)行嚴(yán)格的LCMS和NMR檢驗(yàn),其產(chǎn)品已被近萬名客戶廣泛使用并發(fā)表大量文章、;
MCE 定期增加各領(lǐng)域熱門抑制劑、激動(dòng)劑,不斷擴(kuò)增已有化合物庫,以滿足新的科研需求;
數(shù)千種產(chǎn)品在上海有充足備貨,24-48小時(shí)內(nèi)送達(dá)客戶;
大量產(chǎn)品提供試用裝; 已為多個(gè)知名企業(yè)、院校構(gòu)建各種定制型化合物庫。
Purity:98%
MWt:746.9432
Formula:C40H67NaO11
SMILES:C[C@H]1[C@](O[C@@H]2C[C@](CC[C@@H]3C)([H])O[C@@]3([H])[C@@H](C)C([O-])=O)([C@@H]([C@H](OC)C2)C)O[C@](C)([C@]4([H])O[C@](C)([C@]5([H])O[C@]([C@@]([C@H](C[C@H]6C)C)([H])O[C@@]6(O)CO)([H])C[C@@H]5C)CC4)C1.[Na+]
Pathway:Membrane Transporter/Ion Channel;
Mechanisms:Potassium Channel;
Research Area:Cancer
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