Juvenile hormone synthesis by ring glands of the blowfly Lucilia cuprina
✍ Scribed by P.D. East; T.D. Sutherland; S.C. Trowell; A.J. Herlt; R.W. Rickards
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 131 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0739-4462
No coin nor oath required. For personal study only.
✦ Synopsis
The major radiolabelled product released from ring gland and brain-ring gland complexes of third instar larval and pre-pupal stages of the sheep blowfly Lucilia cuprina upon incubation with L-[methyl-3 H]methionine corresponded to one diastereomer of juvenile hormone III bisepoxide (JHB 3 ). Endocrine glands incubated with the juvenile hormone precursor 2E,6E-farnesoic acid released increased quantities of JHB 3 , together with significant amounts of juvenile hormone III but not the isomeric methyl 2E-6,7-epoxyfarnesoate. Synthesis of JHB 3 was developmentally and neurally regulated. Ring glands and brain-ring gland complexes from third instar larvae released more JHB 3 than comparable preparations from pre-pupae, while isolated corpus allatum segments of the gland were more active than intact brain-gland complexes. These results reinforce the emerging status of JHB 3 as the characteristic juvenile hormone of dipteran insects.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
The paper reports the synthesis of some ethereal insect juvenile hormone analogs with a pinene or cyclohexene ring in the terminal position. ## Synthese von Juvenilhormon-Analogen von Insekten, IV I). -Synthese von Ether-Analogen mit einem Pinen-und Cyclohexenring in der terminalen Stellung Es wi
Treatment of the dimethyl acetals of citral (1) and farnesal be subjected to a Diels-Alder reaction, which allows further synthetic elaboration. In particular, in the case of farnesal (2) with the superbase "LICKOR" in THF at low temperatures induces regioselective metallation at the allylic methyl