Barbier P, Benezra C
J Med Chem. 1986 May;29(5):868-71. doi: 10.1021/jm00155a046.
(+/-)-Tulipalin B was prepared in six steps from phenyl sulfide and ethyl 2-bromopropionate. The sensitizing power in the skin of (+/-)-tulipalin A (1a) and B (1b) and of the beta-acetoxy derivatives (1c) was studied. All are able to induce allergic contact dermatitis (ACD) and give cross-reactions. gamma,gamma-Disubstituted analogues (with a -(CH2)5- chain in the gamma-position) were synthesized and used to induce ACD in guinea pigs: they all were sensitizers and cross-reacted. However no cross-reaction was demonstrated between gamma,gamma-unsubstituted and gamma,gamma-substituted compounds showing a great specificity of ACD.
(±)-土荆芥内酯B由苯硫醚和2-溴丙酸乙酯经六步反应制得。研究了(±)-土荆芥内酯A(1a)和B(1b)以及β-乙酰氧基衍生物(1c)在皮肤中的致敏能力。它们均能诱发过敏性接触性皮炎(ACD)并产生交叉反应。合成了γ,γ-二取代类似物(γ位带有-(CH2)5-链)并用于在豚鼠中诱发ACD:它们都是致敏剂且会发生交叉反应。然而,γ,γ-未取代和γ,γ-取代的化合物之间未显示交叉反应,这表明ACD具有高度特异性。