Rutaceae

Hegnauer, Robert

doi:10.1007/978-3-0348-9379-4_10

Cited by 3 publications

(2 citation statements)

References 149 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The Rutaceae is well known as the source of a very wide range of secondary metabolites (Hegnauer, 1973) and the distribution and chemotaxonomic significance of alkaloids (Waterman, 1975;Waterman & Khalid, 1981), coumarins (Gray & Waterman, 1978), flavonoids (Grieve & Scora, 1980) and limonoids (Dreyer, Pickering & Cohan, 1972) have all been examined. Until recently comparatively little information was available on the occurrence of these classes of compounds in the Diosmeae.…”

Section: Introductionmentioning

confidence: 99%

Chemosystematics in the Rutaceae: A chemotaxonomic survey of flavonoids and monoterpenes in leaves of Acmadenia species

Waterman

Hussain

1983

Botanical Journal of the Linnean Society

View full text Add to dashboard Cite

By means of thin layer chromatography and gas liquid chromatography the distribution of monoterpenes and flavonoid aglycones in the leaves of 19 samples of 15 species of Acmadenia has been investigated. The distribution of flavonol and flavone aglycones shows a close agreement with recently proposed taxonomic divisions within the genus. It is proposed that these patterns may be of importance in interpreting the evolutionary development of the genus.

show abstract

Section: Introductionmentioning

confidence: 99%

Chemosystematics in the Rutaceae: A chemotaxonomic survey of flavonoids and monoterpenes in leaves of Acmadenia species

Waterman

Hussain

1983

Botanical Journal of the Linnean Society

View full text Add to dashboard Cite

show abstract

“…7000),293.4 (2630); IR vm.icm'l 3400, 1608, 1510; IH NMR (CDCI) S/ppm 7.31 (2H, d, J = 8.7 Hz, H-2 and H-6), 6.87 (2H, d, J =8.7 Hz, H-3 and H-5), 6.55 (lH, d, J =15.9Hz, H-7),6.22 (lH, dt, J =15.9,5.6 Hz,, 5.49 OH, t, J = 6 6. Hz, H-2'), 4.51 (2H, d, J= 6.6 Hz, 4.29 (2H, d, …”

mentioning

confidence: 99%

Structure and Synthesis of Evofolin‐C from Tetradium glabrifolium

Wu¹,

Yeh²,

Wu³

1995

J Chinese Chemical Soc

View full text Add to dashboard Cite

show abstract

Myristicin, safrole, and fagaramide as phytosynergists of xanthotoxin

Neal

1989

J Chem Ecol

View full text Add to dashboard Cite

The methylenedioxyphenyl-containing (MDP) inhibitors of mixed-function oxidase detoxification enzymes, myristicin, safrole, fagaramide, and isosafrole, occur with xanthotoxin or other toxic furanocoumarins in plants of the families Umbelliferae and Rutaceae. All four MDP compounds have a synergistic effect on the toxicity of xanthotoxin toHeliothis zea. Myristicin also increased the phototoxicity of xanthotoxin in the presence of UV light. The term phytosynergist is used to describe plant compounds that are present at concentrations producing no toxic effect by themselves but have a synergistic effect on cooccurring toxins.

show abstract

Rutaceae

Cited by 3 publications

References 149 publications

Chemosystematics in the Rutaceae: A chemotaxonomic survey of flavonoids and monoterpenes in leaves of Acmadenia species

Chemosystematics in the Rutaceae: A chemotaxonomic survey of flavonoids and monoterpenes in leaves of Acmadenia species

Structure and Synthesis of Evofolin‐C from Tetradium glabrifolium

Myristicin, safrole, and fagaramide as phytosynergists of xanthotoxin

Contact Info

Product

Resources

About