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PPI-2458

PPI-2458 Struktur
431077-35-9
CAS-Nr.
431077-35-9
Englisch Name:
PPI-2458
Synonyma:
PPI-2458;PPI 2458;QBDVVYNLLXGUGN-XGTBZJOHSA-N;Carbamic acid, N-[(1R)-1-(aminocarbonyl)-2-methylpropyl]-, (3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]oct-6-yl ester
CBNumber:
CB72668496
Summenformel:
C22H36N2O6
Molgewicht:
424.53
MOL-Datei:
431077-35-9.mol

PPI-2458 Eigenschaften

Siedepunkt:
578.9±50.0 °C(Predicted)
Dichte
1.17±0.1 g/cm3(Predicted)
pka
10.98±0.46(Predicted)

Sicherheit

PPI-2458 Chemische Eigenschaften,Einsatz,Produktion Methoden

Enzyminhibitor

This orally bioavailable, selectively cytotoxic agent (FWfree-acid = 424.54 g/mol; Photosensitive; Store in dark: IUPAC: [(3R,4S,5S,6R)-5-methoxy-4- [(2R,3R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro2.5]octan- 6-yl] N-[(2R)-1-amino-3-methyl-1-oxobutan-2-yl]carbamate), a synthetic analogue of an Aspergillus fumigatus secondary metabolite (See Fumagillin), suppresses the formation of new blood vessels and inhibits endothelial cell proliferation and angiogenesis. Its epoxide group reacts with an active-site histidyl residue in methionyl aminopeptidase type II. Because removal of the N-terminal methionine from many proteins is required for their biologic activity, subcellular localization, and stability, methionyl-aminopeptidase plays a pivotal co-regulatory role in translation. PPI-2458 potently inhibits the proliferation of human fibroblast-like synoviocytes, or HFLS-RA (GI50 = 0.04 nM) derived from RA patients, showing >95% inhibition at 1 nM. Proliferation of human umbilical vein endothelial cells (HUVEC) is similarly inhibited (GI50 = 0.2 nM) by PPI-2458. Moreover, PPI-2458 inhibition of MetAP-2 catalysis (IC50 = 0.2 nM) in HFLS-RA is directly correlated with cell growth inhibition and a decrease in the DNA polymerase processivity factor PCNA. PPP-2458 also protects the a-subunit of eukaryotic initiation factor 2 from inhibitory phosphorylation. Based on the structure of TNP-470, a fumagillin analogue that exhibits dose-limiting CNS toxicity, PPI-2458 was designed to retain antiproliferative activity while improving its CNS toxicity profile. PPI-2458 also inhibits proliferation of B16F10 melanoma cells in vitro, (GI50 = 0.2 nM). This property, coupled with the absence of detectable resistance to PPI-2458 and the induction of morphological features of differentiated melanocytes, commends this agent for melanoma chemotherapy. PPI-2458 also inhibits non-Hodgkin's lymphoma cell proliferation in vitro and in vivo. Metabolic data demonstrate the participation of active metabolites in the in vivo efficacy of PPI-2458.

PPI-2458 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


PPI-2458 Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 2)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Suzhou Meishi Biotechnology Co., Ltd. 1173954148q
meishipharma@126.com China 20033 58
TargetMol Chemicals Inc. 15002134094
marketing@targetmol.cn China 19704 58

  • PPI 2458
  • PPI-2458
  • Carbamic acid, N-[(1R)-1-(aminocarbonyl)-2-methylpropyl]-, (3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]oct-6-yl ester
  • QBDVVYNLLXGUGN-XGTBZJOHSA-N
  • 431077-35-9
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