Loading...

Loading...

Compounds

COMPOUND NPA004716

STRUCTURE
Image structure
EXPORT OPTIONS PNG JSON SDF
PROJECT MOLECULE TO GLOBAL VIEW See Global
EXTERNAL LINKS
npmrd logo unichem logo
PROPERTIES
NPAID NPA004716
CLUSTER ID 263
NODE ID 141
NAME Trichorzin PA IX
FORMULA C85H142N20O22
MOLECULAR WEIGHT (Da) 1796.1890
ACCURATE MASS (Da) 1795.0608
ORIGIN ORGANISM TYPE Fungus
ORIGIN GENUS Trichoderma
ORIGIN SPECIES harzianum
InChIKey LSUGDYLGJSFGHM-UHFFFAOYSA-N
InChI InChI=1S/C85H142N20O22/c1-25-84(23,104-76(126)85(24,26-2)102-62(112)48(9)89-64(114)56(44-107)95-71(121)79(13,14)97-49(10)108)75(125)94-53(35-37-59(87)110)65(115)98-80(15,16)73(123)96-61(47(7)8)69(119)101-78(11,12)70(120)88-42-60(111)91-54(39-45(3)4)66(116)100-83(21,22)77(127)105-38-30-33-57(105)68(118)92-55(40-46(5)6)67(117)99-82(19,20)74(124)103-81(17,18)72(122)93-52(34-36-58(86)109)63(113)90-51(43-106)41-50-31-28-27-29-32-50/h27-29,31-32,45-48,51-57,61,106-107H,25-26,30,33-44H2,1-24H3,(H2,86,109)(H2,87,110)(H,88,120)(H,89,114)(H,90,113)(H,91,111)(H,92,118)(H,93,122)(H,94,125)(H,95,121)(H,96,123)(H,97,108)(H,98,115)(H,99,117)(H,100,116)(H,101,119)(H,102,112)(H,103,124)(H,104,126)
SMILES CCC(C)(NC(=O)C(C)NC(=O)C(CO)NC(=O)C(C)(C)NC(C)=O)C(=O)NC(C)(CC)C(=O)NC(CCC(N)=O)C(=O)NC(C)(C)C(=O)NC(C(C)C)C(=O)NC(C)(C)C(=O)NCC(=O)NC(CC(C)C)C(=O)NC(C)(C)C(=O)N1CCCC1C(=O)NC(CC(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NC(CCC(N)=O)C(=O)NC(CO)CC1=CC=CC=C1
ORIGINAL ISOLATION REFERENCE
CITATION Leclerc, G; Rebuffat, S; Goulard, C; Bodo, B Directed biosynthesis of peptaibol antibiotics in two Trichoderma strains. I. Fermentation and isolation Journal of Antibiotics 1998 51 (2) 170-177.
DOI 10.7164/antibiotics.51.170 PMID 9544938
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Eukarya - 2759
Kingdom Fungi MycoBank 4751
Phylum Ascomycota MycoBank 4890
Class Sordariomycetes MycoBank 147550
Order Hypocreales MycoBank 5125
Family Hypocreaceae MycoBank 5129
Genus Trichoderma MycoBank 5543
CLASSYFIRE
Show Hide
NP CLASSIFIER
Show Hide