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

Base Information

• Chemical Name: Cyclo(L-Hmb-D-aIle-D-Leu-L-Hmb-L-Val-N-methyl-L-Leu-)
• CAS No.: 3200-75-7
• Molecular Formula: C34H60 N4 O8
• Molecular Weight: 652.86
• Mol file: 3200-75-7.mol

Synonyms:SporidesmolideI, 2-D-alloisoleucine-; 1,10-Dioxa-4,7,13,16-tetraazacyclooctadecane, cyclicpeptide deriv.; Cyclo(D-alloisoleucyl-D-leucyl-3-methyl-L-2-hydroxybutanoyl-L-valyl-N-methyl-L-leucyl-3-methyl-L-2-hydroxybutanoyl);Cyclo(D-alloisoleucyl-D-leucyl-L-a-hydroxyisovaleryl-L-valyl-N-methyl-L-leucyl-L-a-hydroxyisovaleryl)

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

Chemical Property:

• Melting Point: 228-230°
• PSA: 170.68000
• LogP: 3.97690

Purity/Quality:

98% ^*data from raw suppliers

Sporidesmolide II ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• 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.