China 130622-05-8 Tert-butoxycarbonyl-D-glutamicum acidum (methyl ester) - methyl ester Manufacturer and Factory |Jiayinglai

130622-05-8 Acidum glutamicum Tert-butoxycarbonyl-D-glutamicum (methyl ester) -methyl ester

Description:

Aspectus	Album ad Off-Crystallis alba vel crystallina pulveris.
MF	C12H21NO6
MW	275.3
Puritas	98+

Mitte ad nos inscriptio

Product Detail

Transportatio conditio & commendatur naviculas modum:
per aerem, per mare vel per express

Repono conditione:
Tene in obscuro loco, signatus in sicco, cella Temperature

Ordinis Qty minimum:
Negatio

Certification:
COA, HPLC, GC, HNMR, Assay, Aqua Content (KF), TLC available

Synonyma

dimethyl(tert-butoxycarbonyl)-D-glutamatum;
(R) -2-tert-butoxycarbonylamino-pentanedioicum acidum dimethyl niensis;
(Tert-Butoxy)Carbonyl D-Glu(OMe)-OMe (Syrup);
Boc-D-Glu(OMe)-OMe (Syrup);
dimethyl (2R)-2-[(2-methylpropan-2-yl) oxycarbonylamino] pentanedioate;
Alogliptin Impuritas 43;
1,5-dimethyl (2R)-2-{[(tert-butoxy) carbonyl]amino} pentanedioate

interiorem sarcina

Solent ad stipant pulveris.Et solem et aquam possunt prohibere mala questus.

exteriores sarcina

Lobortis duris res tuas ex fragore et umore questus protegere potest.

Applications

Fluoroquinolones latum habent spectrum antibacterial, actio antibacterial fortis, motus adversae humiles, bona texti permeabilitas, bioavailbilitas oris alta, longi temporis administratio et administratio opportuna.Communiter adhibentur in curatione morborum infectiosorum sicut infectio tractus respiratorii et infectionis tractus urinarii.Structura medicamentorum antibactalium fluoroquinolonorum praesente fluorino in sexto positione nuclei parentis quinolonis notatur.
Nuper autem X annis, ob pressionem selectivam, quae per late patentem huius generis medicamentorum genera generata est, modos medicamento-resistentes auget, praesertim his annis, quinolone resistens Streptococcus pneumoniae transversalem resistentiam habet, quae penicillini resistit; macrolide antibiotica et quinolone antibiotica.Eodem tempore, inventum est nonnullos fluoroquinolones QTc inter- cessionem facere posse electrocardiogram, hepatotoxicitatem et phototoxicitatem, quae applicationem eorum circumscripsit.
Ut supra defectus fluoroquinolonum superetur, urget ut novas compositiones structurales componat cum actione antibacterial bona, ampla spectrum antibacterial et quam minima quam maxime adversae reactiones contra multi-medicamentum bacteria resistentia.Series recentium novarum fluoroquinolone-liberorum (NFQ) medicamentorum quae 8-methoxylum continentium diversae sunt a fluoroquinolone antibioticorum in eo quod non habent fluorinum in positione 6 nuclei parentis quinoloni, sed adhuc valent in actione vitro antibacterial.nemonoxacin inhibitor bacterial topoisomerase nova NFQ selectiva est.
Comparatus cum fluoroquinolonibus nunc in foro, Nenofloxacin novum genus medicamentorum structurarum repraesentat.nemonocacin (TG-873870), novum medicamentum quinolone a Procter & Gamble (P&G evolutum), significantem actionem antibacterialem contra varios pathogenos cinematographicos pertinentes, inter Staphylococcus aureus et multidrug-repugnans Streptococcus pneumoniae.Eventus experimenti in muribus infectis demonstraverunt effectum antibacterial huius facti validiorem quam plures quinolones currentes.Praeterea productum optimum proprietates pharmacokineticae habet et bene toleratur.

Related Products

Fmoc-Gly-glu(otbu)-oh	Boc-D-Glu(OBzl)-Oet
HL-Glu-OH	Boc-D-Glu(Obzl)-OH
HD-Glu-OH	Boc-D-Glu(Ome)-OH
DL-Glu-OH	Boc-D-Glu(Ome)-OH.DCHA
DL-Glu-OH.H2O	Boc-Glu(OBzl)-Obzl
L-Glu(Obzl)-NCA	Boc-L-Glu-OBzl
D-Glu(Obzl)-NCA	Boc-D-Glu-Obzl
DL-Glu(Obzl)-NCA	Boc-D-Glu-Otbu-OH
L-Glu-Obzl	Boc-D-Glu(OMe)-OMe
Tos-Glu-Obzl	Boc-D-Glu(Obzl)-Obzl
L-Glu(Ome)-Obzl.TOS	Boc-L-Glu(Ome)-Ome
AC-Glu(OtBu)	Boc-L-Glu(OMe)-OH
DL-Glu(ome)	Boc-L-Glu(OBzl)-OH
HD-Glu(OMe)-OH	Boc-Glu-Otbu
HL-Glu(OME)-OH	Boc-L-Glu(Obzl)-Ome
L-Glu(Obzl)	Boc-L-Glu(Oet)
HL-Glu(OtBu)-OH	Fmoc-L-Glu-OH
HL-Glu(OEt)-OH	Fmoc-D-Glu-OH
L-Glu(Otbu)-Otbu-OH	Fmoc-D-Glu(Ome)-OH
HD-Glu(OBzl)-OH	Fmoc-L-Glu(OcHx)-OH
D-Glu-OBzl	Fmoc-L-Glu(OMe)-OH
HL-Glu(Ome) -Otbu.Hcl	Fmoc-L-Glu(OtBu)-OH
D-Glu(Obzl)-Otbu.HCL	Fmoc-D-Glu(OBzl)-OH
D-Glu(OtBu)-OtBu•HCl	Fmoc-D-Glu(Otbu)-OH
L-Glu(OcHx).hcl	Fmoc-L-Glu-OtBu
HL-Glu(OBzl)-OBzl.HCl	Fmoc-L-Glu(OBzl)-OH
HL-Glu-OBzl.HCl	Fmoc-L-Glu(Cbz-sic)
D-Glu(OBzl)-OBzl.HCl	Fmoc-N-Me-L-Glu(Otbu)-OH
DL-Glu(Ome)-Ome.Hcl	Fmoc-glu-obzl
HL-Glu(OtBu)-OtBu•HCl	Cbz-L-Glu-OH
HL-Glu(OMe)-OMe.HCl	Cbz-D-Glu-OH
L-Glu(Obzl)-OME.HCL	ZL-Glu-OBzl
HL-Glu(OEt)-OEt·HCl	ZD-Glu-OBzl
L-Glu(Obzl)-Otbu.HCl	Cbz-L-Glu-Otbu
HD-Glu(OMe)-OMe·HCl	Cbz-D-Glu(ome)
N-Pht-Glu	Cbz-L-Glu(OBzl)-OH
Boc-L-Glu-OH	Cbz-L-Glu(Otbu)
Boc-D-Glu-OH	Cbz-L-Glu(Ome)
Boc-Glu(obzl)-NH2	Cbz-D-Glu(OtBu)-OH
Boc-Glu（trt）-OH	Cbz-L-Glu(Ome)-OtBu
Boc-L-Glu(OcHx)-OH	Cbz-L-Glu-OBzl.DCHA
Boc-L-Glu(OtBu)-OH	Cbz-L-Glu(Oet)-OH
Boc-Glu(Osu)-Otbu	Boc-Glu-Otbu（Osu）

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