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Compounds

COMPOUND NPA033906

STRUCTURE
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PROJECT MOLECULE TO GLOBAL VIEW See Global
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PROPERTIES
NPAID NPA033906
CLUSTER ID 26
NODE ID 25
NAME Motobamide
FORMULA C63H95N11O10S
MOLECULAR WEIGHT (Da) 1198.5870
ACCURATE MASS (Da) 1197.6984
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Leptolyngbya
ORIGIN SPECIES sp.
InChIKey KGAZEHXLNKMYBU-PGTWJRKASA-N
InChI InChI=1S/C63H95N11O10S/c1-35(2)24-26-63-34-49-56(79)66-44(33-37(5)6)57(80)72-29-16-22-47(72)58(81)70-27-14-21-46(70)55(78)69-51(39(9)10)60(83)71-28-15-20-45(71)54(77)64-42(25-31-85-11)52(75)65-43(32-36(3)4)53(76)68-50(38(7)8)61(84)73-30-17-23-48(73)59(82)74(49)62(63)67-41-19-13-12-18-40(41)63/h12-13,18-19,24,36-39,42-51,62,67H,14-17,20-23,25-34H2,1-11H3,(H,64,77)(H,65,75)(H,66,79)(H,68,76)(H,69,78)/t42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,62-,63-/m0/s1
SMILES CSCC[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](C(C)C)NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@@H]2C[C@@]3(CC=C(C)C)C4=CC=CC=C4N[C@H]3N2C(=O)[C@@H]2CCCN2C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC1=O
ORIGINAL ISOLATION REFERENCE
CITATION Takahashi, Hiroki; Iwasaki, Arihiro; Kurisawa, Naoaki; Suzuki, Ryota; Jeelani, Ghulam; Matsubara, Teruhiko; Sato, Toshinori; Nozaki, Tomoyoshi; Suenaga, Kiyotake Motobamide, an Antitrypanosomal Cyclic Peptide from a Leptolyngbya sp. Marine Cyanobacterium. Journal of Natural Products 2021 84 (5) 1649-1655.
DOI 10.1021/acs.jnatprod.1c00234 PMID 33983736
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Cyanobacteria LPSN 1117
Class Cyanophyceae LPSN -
Order Synechococcales LPSN 1890424
Family Leptolyngbyaceae LPSN 1890438
Genus Leptolyngbya LPSN 47251
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