Description
Niloticin, isolated from the barks of Phellodendron chinense, presented 83.2% ovicidal activity at 2ppm concentration after 120h post treatment and Niloticin exhibited significant growth disruption and morphological deformities at sub lethal concentrations against Ae.
Synonyms
(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one
IUPAC Name
(9R,10R,13S,14S,17R)-17-[(2S,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
Molecular Formula
C30H48O3
Canonical SMILES
CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C
InChI
InChI=1S/C30H48O3/c1-18(17-22(31)25-27(4,5)33-25)19-11-15-30(8)21-9-10-23-26(2,3)24(32)13-14-28(23,6)20(21)12-16-29(19,30)7/h9,18-20,22-23,25,31H,10-17H2,1-8H3/t18-,19+,20-,22+,23?,25-,28+,29-,30+/m0/s1
InChIKey
GKQMMZUXYRXFOH-IWPAKXEHSA-N
Boiling Point
538.5±45.0 °C(Predicted)
Density
1.07±0.1 g/cm3(Predicted)
pKa
14.37±0.20(Predicted)