Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-)

Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) Struktur
3200-75-7
CAS-Nr.
3200-75-7
Englisch Name:
Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-)
Synonyma:
Sporidesmolide II;Sporidesmolide II (7CI,8CI,9CI);Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-)
CBNumber:
CB52344037
Summenformel:
C34H60N4O8
Molgewicht:
652.87
MOL-Datei:
3200-75-7.mol

Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) Eigenschaften

Schmelzpunkt:
228-230°
alpha 
D20 -195° (c = 0.6 in chloroform)
Siedepunkt:
892.7±65.0 °C(Predicted)
Dichte
1.009±0.06 g/cm3(Predicted)
Löslichkeit
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
Aggregatzustand
A solid
pka
12.26±0.70(Predicted)

Sicherheit

Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Sporidesmolide II is the most abundant of N-methyl analogues belonging to the hexadepsipeptide sporidesmolide complex. Biosynthesis of sporidesmolide II involves the use of D- and L- amino acids utilising D-alloisoleucine, leucine and four valine sub-units, where two of the valines are converted to the corresponding valic acid. The biological activity of sporidesmolide II has not been extensively investigated.

Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-)
  • Sporidesmolide II
  • Sporidesmolide II (7CI,8CI,9CI)
  • 3200-75-7
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