2002
DOI: 10.1021/np0101604
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A Benzochromene from the Roots of Pentas bussei

Abstract: A new homoprenylated benzochromene, methyl-5,10-dihydroxy-7-methoxy-3-methyl-3-[4-methyl-3-pentenyl]-3H-benzo[f]chromene-9-carboxylate (1), was isolated from the roots of Pentas bussei, collected from Kenya. The structure of this new compound was determined by spectroscopic data interpretation.

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Cited by 29 publications
(37 citation statements)
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“…Plants of the genus Hypericum (Gutiferae) present several kinds of phenolic compounds such as polycyclic quinones, xanthones, flavonoids, phloroglucinols and benzopyrans that can produce antiproliferative effects (Bukuru et al, 2002). In a previous study, our group detected this effect in four of six Hypericum native species studied (Ferraz et al, 2004).…”
Section: Introductionmentioning
confidence: 88%
“…Plants of the genus Hypericum (Gutiferae) present several kinds of phenolic compounds such as polycyclic quinones, xanthones, flavonoids, phloroglucinols and benzopyrans that can produce antiproliferative effects (Bukuru et al, 2002). In a previous study, our group detected this effect in four of six Hypericum native species studied (Ferraz et al, 2004).…”
Section: Introductionmentioning
confidence: 88%
“…K 2 CO 3 was added to neutralize the acid till no bubble occurs. The reaction mixture was filtered, and washed with a small amount of ethanol, dried to give (11,12,13). FT-IR -1 ): 3424 cm -1 (NH), 1735 cm -1 (C=O lacton), 1678 cm -1 (C=O amid), 1…”
Section: Synthesis Of Compound (11-13)mentioning
confidence: 99%
“…Scheme (2): preparation compounds (7)(8)(9)(10) Preparation and characterization of compound (11)(12)(13) For synthesis these compounds, compound (2) was also selected as a key intermediate for the synthesis of new fused and non-fused chromene derivatives. The synthetic reactions are summarized in Scheme (3).…”
Section: Scheme (1): Preparation Compounds (3-6)mentioning
confidence: 99%
“…Photochromic properties of 3H-naphtho [2,1-b]pyrans also make them valuable to be used for a variety of other applications such as electronic display systems, optical switches, and temporary or permanent memories [4][5][6]. Furthermore, 3H-naphtho [2,1-b]pyrans and their oxygenated and/or partially reduced congeners have also been isolated from natural sources [7][8][9]; several analogs are reported to posses interesting biological activities [8][9][10][11][12]. Molecular structures of several representative examples are shown in Figure 2.…”
Section: Known Properties Of Naphthopyran Derivativesmentioning
confidence: 99%
“…Molecular structures of several representative examples are shown in Figure 2. A homoprenylated 3H-naphtho[2,1-b]pyran 3 was isolated from the roots of Pentas bussei [7]. In another case, several naphthopyrans including Adenaflorins C (4) were isolated from young leaves of Adenaria floribunda and bioassays show these compounds have cytotoxic effect against human cancer cells [8].…”
Section: Known Properties Of Naphthopyran Derivativesmentioning
confidence: 99%