| Identification | Back Directory | [Name]
Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) | [CAS]
3200-75-7 | [Synonyms]
Sporidesmolide II
Sporidesmolide II (7CI,8CI,9CI)
Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-) | [Molecular Formula]
C34H60N4O8 | [MOL File]
3200-75-7.mol | [Molecular Weight]
652.87 |
| Chemical Properties | Back Directory | [Melting point ]
228-230° | [alpha ]
D20 -195° (c = 0.6 in chloroform) | [Boiling point ]
892.7±65.0 °C(Predicted) | [density ]
1.009±0.06 g/cm3(Predicted) | [solubility ]
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble | [form ]
A solid | [pka]
12.26±0.70(Predicted) |
| Hazard Information | Back Directory | [Uses]
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. |
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