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Compounds

COMPOUND NPA002961

STRUCTURE
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PROPERTIES
NPAID NPA002961
CLUSTER ID 1701
NODE ID 1389
NAME Decarestrictine L
FORMULA C9H16O3
MOLECULAR WEIGHT (Da) 172.2240
ACCURATE MASS (Da) 172.1099
ORIGIN ORGANISM TYPE Fungus
ORIGIN GENUS Penicillium
ORIGIN SPECIES sp.
InChIKey GDXDHEIQIIZPSF-YIZRAAEISA-N
InChI InChI=1S/C9H16O3/c1-6(10)5-9-8(11)4-3-7(2)12-9/h7-9,11H,3-5H2,1-2H3/t7-,8+,9-/m0/s1
SMILES C[C@H]1CC[C@H]([C@@H](O1)CC(=O)C)O
ORIGINAL ISOLATION REFERENCE
CITATION Grabley, S; Hammann, P; Hütter, K; Kirsch, R; Kluge, H; Thiericke, R; Mayer, M; Zeeck, A Secondary metabolites by chemical screening. 20. Decarestrictines, a new family of inhibitors of cholesterol biosynthesis from Penicillium: III. Decarestrictines E to M. Journal of Antibiotics 1992 45 (7) 1176-1181.
DOI 10.7164/antibiotics.45.1176 PMID 1517163
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Eukarya - 2759
Kingdom Fungi MycoBank 4751
Phylum Ascomycota MycoBank 4890
Class Eurotiomycetes MycoBank 147545
Order Eurotiales MycoBank 5042
Family Aspergillaceae MycoBank 1131492
Genus Penicillium MycoBank 5073
SYNTHESES
CITATION 1 Risi RM; Maza AM; Burke SD Asymmetric hydroformylation-initiated tandem sequences for syntheses of (+)-patulolide C, (-)-pyrenophorol, (+)-decarestrictine L, and (+)-prelog djerassi lactone. Journal of Organic Chemistry 2015 80 (1) 204-16. DOI: 10.1021/jo502301k PMID: 25398097
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