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906366-79-8

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Articles about 906366-79-8Total 3 be found

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Inotilone derivatives as coherent biological response modifier (cBMR)
Optimal compositions of derivatives of 5-methyl-3(2H)-furanone compounds and phenylpropanoid polyketides related to inotilone, that exert biological response modification in health and disease, and their method of preparation, are disclosed. Methods of tr
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(2011/04/14)

Short synthesis of COX-2 inhibitor inotilone
An efficient three-step synthesis of COX-2 inhibitor inotilone from acetaldoxime is described. The structure of inotilone was elucidated via an aldol reaction between 5-methyl-3(2H)-furanone and 3,4-dihydroxybenzaldehyde. This approach describes a convenient pathway to 5-alkyl-3-furanones through isoxazole chemistry.
Al-Busafi, Saleh,Al-Belushi, Muna,Al-Muqbali, Khalid
experimental part
p. 1088 - 1092
(2010/05/18)

Convergent synthesis of potent COX-2 inhibitor inotilone
The first synthesis of potent COX-2 inhibitor inotilone is reported. The convergent route features a Mukaiyama aldol condensation that generates the target without the use of protecting groups or a separate dehydration step. The approach also highlights a
Shamshina, Julia L.,Snowden, Timothy S.
p. 3767 - 3769
(2008/02/06)

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Chemical Properties

Melting Point: 177.4 °C
Boiling Point: 491.9±45.0 °C(Predicted)
Density: 1.433±0.06 g/cm3(Predicted)
Solubility:≤1mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide
PKA: 8.58±0.35(Predicted)
PSA: 66.76000
LogP: 1.94180

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