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Compounds

COMPOUND NPA003218

STRUCTURE
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PROPERTIES
NPAID NPA003218
CLUSTER ID 36
NODE ID 35
NAME [(2S)-2-hexadecanoyloxy-3-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S,6R)-4-hexadecanoyloxy-3,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxymethyl]-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxy-propyl] (9E,12E,15E)-octadeca-9,12,15-trienoate
FORMULA C65H116O16
MOLECULAR WEIGHT (Da) 1153.6270
ACCURATE MASS (Da) 1152.8263
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Cyanobacterium
ORIGIN SPECIES scytonema sp. (TAU strain SL-30-1-4)
InChIKey LUJVGUPZCJTKPB-FJYSWILXSA-N
InChI InChI=1S/C65H116O16/c1-4-7-10-13-16-19-22-25-26-29-30-33-36-39-42-45-55(67)75-49-52(78-56(68)46-43-40-37-34-31-27-23-20-17-14-11-8-5-2)50-76-64-61(73)60(72)58(70)54(80-64)51-77-65-62(74)63(59(71)53(48-66)79-65)81-57(69)47-44-41-38-35-32-28-24-21-18-15-12-9-6-3/h7,10,16,19,25-26,52-54,58-66,70-74H,4-6,8-9,11-15,17-18,20-24,27-51H2,1-3H3/b10-7-,19-16-,26-25-
SMILES CCCCCCCCCCCCCCCC(=O)OC1C(C(OC(C1O)OCC2C(C(C(C(O2)OCC(COC(=O)CCCCCCC/C=C\C/C=C\C/C=C\CC)OC(=O)CCCCCCCCCCCCCCC)O)O)O)CO)O
ORIGINAL ISOLATION REFERENCE
CITATION Reshef, V; Mizrachi, E; Maretzki, T; Silberstein, C; Loya, S; Hizi, A; Carmeli, S New acylated sulfoglycolipids and digalactolipids and related known glycolipids from cyanobacteria with a potential to inhibit the reverse transcriptase of HIV-1 Journal of Natural Products 1997 60 (12) 1251-1260.
DOI 10.1021/np970327m PMID 9428159
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Cyanobacteria LPSN 1117
Class Cyanophyceae LPSN -
Order Chroococcales LPSN 1118
Family Cyanobacteriaceae LPSN -
Genus Cyanobacterium LPSN 102234
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