Loading...

Loading...

Compounds

COMPOUND NPA010752

STRUCTURE
Image structure
EXPORT OPTIONS PNG JSON SDF
PROJECT MOLECULE TO GLOBAL VIEW See Global
EXTERNAL LINKS
mibig logo npmrd logo unichem logo
PROPERTIES
NPAID NPA010752
CLUSTER ID 4252
NODE ID 3141
NAME Belactosin C
FORMULA C16H27N3O6
MOLECULAR WEIGHT (Da) 357.4070
ACCURATE MASS (Da) 357.1900
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES sp.
InChIKey ZFCGPWGFGUDLHO-UHFZAUJKSA-N
InChI InChI=1S/C16H27N3O6/c1-4-8(2)11-12(25-16(11)24)14(21)18-7-5-6-10(15(22)23)19-13(20)9(3)17/h8-12H,4-7,17H2,1-3H3,(H,18,21)(H,19,20)(H,22,23)/t8-,9-,10-,11-,12+/m0/s1
SMILES CC[C@H](C)[C@H]1[C@@H](OC1=O)C(=O)NCCC[C@@H](C(=O)O)NC(=O)[C@H](C)N
ORIGINAL ISOLATION REFERENCE
CITATION Asai, A; Hasegawa, A; Ochiai, K; Yamashita, Y; Mizukami, T Belactosin A, a novel antitumor antibiotic acting on cyclin/CDK mediated cell cycle regulation, produced by Streptomyces sp Journal of Antibiotics 2000 53 (1) 81-83.
DOI 10.7164/antibiotics.53.81 PMID 10724015
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 Cho SW; Romo D Total synthesis of (-)-belactosin C and derivatives via double diastereoselective tandem mukaiyama aldol lactonizations. Organic Letters 2007 9 (8) 1537-40. DOI: 10.1021/ol070275k PMID: 17378572
CLASSYFIRE
Show Hide
NP CLASSIFIER
Show Hide