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Compounds

COMPOUND NPA018950

STRUCTURE
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PROPERTIES
NPAID NPA018950
CLUSTER ID 26
NODE ID 25
NAME Scytonemide A
FORMULA C36H56N8O9
MOLECULAR WEIGHT (Da) 744.8910
ACCURATE MASS (Da) 744.4170
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Scytonema
ORIGIN SPECIES hofmannii UTEX 1834
InChIKey HJKXQQVDTIEFDD-ADDJGAGCSA-N
InChI InChI=1S/C36H56N8O9/c1-7-21(6)31-36(53)42-27(18-45)34(51)43-30(20(4)5)35(52)40-23(14-19(2)3)16-38-26(15-22-8-10-24(46)11-9-22)32(49)39-17-29(48)41-25(33(50)44-31)12-13-28(37)47/h8-11,16,19-21,23,25-27,30-31,45-46H,7,12-15,17-18H2,1-6H3,(H2,37,47)(H,39,49)(H,40,52)(H,41,48)(H,42,53)(H,43,51)(H,44,50)/t21-,23-,25+,26-,27-,30-,31-/m0/s1
SMILES CC[C@H](C)[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C=N[C@H](C(=O)NCC(=O)N[C@@H](C(=O)N1)CCC(=O)N)CC2=CC=C(C=C2)O)CC(C)C)C(C)C)CO
ORIGINAL ISOLATION REFERENCE
CITATION Krunic, Aleksej; Vallat, Armelle; Mo, Shunyan; Lantvit, Daniel D.; Swanson, Steven M.; Orjala, Jimmy Scytonemides A and B, cyclic peptides with 20S proteasome inhibitory activity from the cultured cyanobacterium scytonema hofmanii Journal of Natural Products 2010 73 (11) 1927-1932.
DOI 10.1021/np100600z PMID 21058727
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Cyanobacteria LPSN 1117
Class Cyanophyceae LPSN -
Order Nostocales LPSN 1161
Family Scytonemataceae LPSN 1182
Genus Scytonema LPSN 1203
SYNTHESES
CITATION 1 Wilson TA; Tokarski RJ; Sullivan P; Demoret RM; Orjala J; Rakotondraibe LH; Fuchs JR Total Synthesis of Scytonemide A Employing Weinreb AM Solid-Phase Resin. Journal of Natural Products 2018 81 (3) 534-542. DOI: 10.1021/acs.jnatprod.7b00912 PMID: 29400964
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