
CAS 1000995-48-1
:Formel:C39H42O14
InChl:InChI=1S/C39H42O14/c1-15-7-8-49-25(40)5-6-26(41)50-13-17-18-11-23-34(3,19-9-22(19)37(23,47)14-51-30(15)42)24-12-36(46)21-10-20(21)35(4)29(36)28(38(18,24)52-32(17)44)27-16(2)31(43)53-39(27,48)33(35)45/h7,19-24,33,45-48H,5-6,8-14H2,1-4H3/b15-7+/t19-,20-,21+,22+,23-,24+,33-,34+,35+,36+,37+,38+,39+/m1/s1
InChI Key:VAOZXVGMCZGLOH-BQPKVCGRSA-N
SMILES:C/C/1=C\COC(=O)CCC(=O)OCC2=C3C[C@@H]4[C@]([C@@H]5C[C@@H]5[C@]4(COC1=O)O)([C@H]6[C@@]3(C7=C8[C@]([C@@H]9C[C@@H]9[C@]8(C6)O)([C@H]([C@@]1(C7=C(C(=O)O1)C)O)O)C)OC2=O)C
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Chloramultilide C
CAS:Chloramultilide C is a natural product of Chloranthus, Chloranthaceae.Formel:C39H42O14Reinheit:98%Farbe und Form:SolidMolekulargewicht:734.751Chloramultilide C
CAS:Chloramultilide C is a macrolide polyketide, which is a secondary metabolite produced by certain marine bacteria. Specifically, it is derived from the genus Streptomyces, isolated from oceanic environments known for their rich biodiversity and unique chemical ecosystems. The mode of action of chloramultilide C involves inhibiting bacterial protein synthesis, thus exerting its antimicrobial effects by targeting and binding to the bacterial ribosome, which disrupts the translation process. This compound has shown significant activity against a broad spectrum of bacterial pathogens, particularly Gram-positive bacteria.Formel:C39H42O14Reinheit:Min. 95%Molekulargewicht:734.7 g/mol




