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Compounds

COMPOUND NPA010550

STRUCTURE
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PROPERTIES
NPAID NPA010550
CLUSTER ID 1676
NODE ID 1370
NAME Amythiamicin D
FORMULA C43H42N12O7S6
MOLECULAR WEIGHT (Da) 1031.2880
ACCURATE MASS (Da) 1030.1624
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Amycolatopsis
ORIGIN SPECIES sp. MI481-42F4
InChIKey CEKXFMGPQFBJOI-UHFFFAOYSA-N
InChI InChI=1S/C43H42N12O7S6/c1-17(2)30-41-51-26(15-67-41)39-48-23(12-64-39)33-20(8-9-21(46-33)38-52-27(16-65-38)43(61)62-7)37-49-25(14-63-37)35(59)47-22(10-28(56)44-6)40-55-32(19(5)68-40)36(60)54-31(18(3)4)42-50-24(13-66-42)34(58)45-11-29(57)53-30/h8-9,12-18,22,30-31H,10-11H2,1-7H3,(H,44,56)(H,45,58)(H,47,59)(H,53,57)(H,54,60)
SMILES CC1=C2C(=O)NC(C3=NC(=CS3)C(=O)NCC(=O)NC(C4=NC(=CS4)C5=NC(=CS5)C6=C(C=CC(=N6)C7=NC(=CS7)C(=O)OC)C8=NC(=CS8)C(=O)NC(C(=N2)S1)CC(=O)NC)C(C)C)C(C)C
ORIGINAL ISOLATION REFERENCE
CITATION Shimanaka, K; Kinoshita, N; Iinuma, H; Hamada, M; Takeuchi, T Novel antibiotics, amythiamicins. I. Taxonomy, fermentation, isolation, physico-chemical properties, and antimicrobial activity. Journal of Antibiotics 1994 47 (6) 668-674.
DOI 10.7164/antibiotics.47.668 PMID 8040071
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Pseudonocardiales LPSN 85010
Family Pseudonocardiaceae LPSN 2070
Genus Amycolatopsis LPSN 1813
SYNTHESES
CITATION 1 Hughes RA; Thompson SP; Alcaraz L; Moody CJ Total synthesis of the thiopeptide amythiamicin D. Chemical Communications 2004 (8) 946-948. DOI: 10.1039/b401580k PMID: 15069488
CITATION 2 Hughes RA; Thompson SP; Alcaraz L; Moody CJ Total synthesis of the thiopeptide antibiotic amythiamicin D. Journal of the American Chemical Society 2005 127 (44) 15644-15651. DOI: 10.1021/ja0547937 PMID: 16262432
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