Lactimidomycin

Lactimidomycin
Identifiers
	IUPAC name 4-[(E,2R,5S)-2-hydroxy-5-methyl-7-[(2R,3S,4Z,6E,10E)-3-methyl-12-oxo-1-oxacyclododeca-4,6,10-trien-2-yl]-4-oxooct-6-enyl]piperidine-2,6-dione;
CAS Number	134869-15-1 ;
PubChem CID	11669726;
ChemSpider	9844457;
ChEMBL	ChEMBL1221911;
Chemical and physical data
Formula	C26H35NO6
Molar mass	457.567 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES N2C(=O)CC(CC2=O)CC(O)CC(=O)C(C)\C=C(/C)\C1OC(=O)C=CCCC=CC=CC1C;
	InChI InChI=1S/C26H35NO6/c1-17-10-8-6-4-5-7-9-11-25(32)33-26(17)19(3)12-18(2)22(29)16-21(28)13-20-14-23(30)27-24(31)15-20/h4,6,8-12,17-18,20-21,26,28H,5,7,13-16H2,1-3H3,(H,27,30,31)/b6-4+,10-8-,11-9+,19-12+/t17-,18-,21+,26+/m0/s1; Key:OYOKHBHOTQDIPM-BRHOHSSQSA-N;

Lactimidomycin is a glutarimide antibiotic derived from the bacteria Streptomyces amphibiosporus.^[1]^[2] It has antifungal, antiviral and anti-cancer properties, acting as a direct inhibitor of protein translation in ribosomes.^[3]^[4]^[5] Antiviral activity is seen against a variety of RNA viruses including flaviviruses such as dengue fever, Kunjin virus and Modoc virus, as well as vesicular stomatitis virus and poliovirus.^[6] As lactimidomycin is a natural product containing an unusual unsaturated 12-membered lactone ring, it has been the subject of numerous total synthesis approaches.^[7]^[8]^[9]^[10]

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Identifiers

IUPAC name 4-[(E,2R,5S)-2-hydroxy-5-methyl-7-[(2R,3S,4Z,6E,10E)-3-methyl-12-oxo-1-oxacyclododeca-4,6,10-trien-2-yl]-4-oxooct-6-enyl]piperidine-2,6-dione
CAS Number	134869-15-1^Y
PubChem CID	11669726
ChemSpider	9844457
ChEMBL	ChEMBL1221911
Chemical and physical data
Formula	C₂₆H₃₅NO₆
Molar mass	457.567 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES N2C(=O)CC(CC2=O)CC(O)CC(=O)C(C)\C=C(/C)\C1OC(=O)C=CCCC=CC=CC1C
InChI InChI=1S/C26H35NO6/c1-17-10-8-6-4-5-7-9-11-25(32)33-26(17)19(3)12-18(2)22(29)16-21(28)13-20-14-23(30)27-24(31)15-20/h4,6,8-12,17-18,20-21,26,28H,5,7,13-16H2,1-3H3,(H,27,30,31)/b6-4+,10-8-,11-9+,19-12+/t17-,18-,21+,26+/m0/s1 Key:OYOKHBHOTQDIPM-BRHOHSSQSA-N