Loading...

Loading...

Compounds

COMPOUND NPA012713

STRUCTURE
Image structure
EXPORT OPTIONS PNG JSON SDF
PROJECT MOLECULE TO GLOBAL VIEW See Global
EXTERNAL LINKS
gnps logo npmrd logo unichem logo
PROPERTIES
NPAID NPA012713
CLUSTER ID 46
NODE ID 11
NAME Tetrangomycin
FORMULA C19H14O5
MOLECULAR WEIGHT (Da) 322.3160
ACCURATE MASS (Da) 322.0841
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES sp. CB01913
InChIKey UGEKKXLEYACFTD-LJQANCHMSA-N
InChI InChI=1S/C19H14O5/c1-19(24)7-9-5-6-11-16(14(9)13(21)8-19)18(23)10-3-2-4-12(20)15(10)17(11)22/h2-6,20,24H,7-8H2,1H3/t19-/m1/s1
SMILES C[C@]1(CC2=C(C(=O)C1)C3=C(C=C2)C(=O)C4=C(C3=O)C=CC=C4O)O
ORIGINAL ISOLATION REFERENCE
CITATION Ma, Ming; Rateb, Mostafa E.; Teng, Qihui; Yang, Dong; Rudolf, Jeffrey D.; Zhu, Xiangcheng; Huang, Yong; Zhao, Li-Xing; Jiang, Yi; Li, Xiuling; Rader, Christoph; Duan, Yanwen; Shen, Ben Angucyclines and Angucyclinones from Streptomyces sp. CB01913 Featuring C-Ring Cleavage and Expansion Journal of Natural Products 2015 78 (10) 2471-2480.
DOI 10.1021/acs.jnatprod.5b00601 PMID 26335269
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Streptomycetales LPSN 85011
Family Streptomycetaceae LPSN 2062
Genus Streptomyces LPSN 1883
SYNTHESES
CITATION 1 Kesenheimer C; Kalogerakis A; Meissner A; Groth U The cobalt way to angucyclinones: asymmetric total synthesis of the antibiotics (+)-rubiginone B2, (-)-tetrangomycin, and (-)-8-O-methyltetrangomycin. Chemistry - A European Journal 2010 16 (29) 8805-8821. DOI: 10.1002/chem.201000804 PMID: 20575121
CLASSYFIRE
Show Hide
NP CLASSIFIER
Show Hide