2007
DOI: 10.1002/mnfr.200600135
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Inhibition of human recombinant cytochromes P450 CYP1A1 and CYP1B1 by trans‐resveratrol methyl ethers

Abstract: CYP1A1 and CYP1B1 are the inducible forms of cytochrome P450 expressed in extrahepatic tissues, which are responsible for the biotransformation of polycyclic aromatic hydrocarbons, heterocyclic amines and estradiol to the carcinogenic intermediates. The aim of our research was to determine and compare the inhibitory effect of naturally occurring analogues of trans-resveratrol on the catalytic activities of human recombinant CYP1A1 and CYP1B1. Pinostilbene (3,4'-dihydroxy-5-methoxystilbene), desoxyrhapontigenin… Show more

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Cited by 98 publications
(61 citation statements)
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“…RME was purified using preparative TLC and HPLC, and characterized by GC-MS). RME characteristics corresponded to published data (l max 307 nm, 320 nm in 50% acetonitrile, ion at m/z 242; Katsuyama et al, 2007;Mikstacka et al, 2007). HPLC-grade solvents (acetonitrile, methanol) were from Merck and used in combination with sterilized water from Aguettant.…”
Section: Chemicals and Radiochemicalsmentioning
confidence: 87%
“…RME was purified using preparative TLC and HPLC, and characterized by GC-MS). RME characteristics corresponded to published data (l max 307 nm, 320 nm in 50% acetonitrile, ion at m/z 242; Katsuyama et al, 2007;Mikstacka et al, 2007). HPLC-grade solvents (acetonitrile, methanol) were from Merck and used in combination with sterilized water from Aguettant.…”
Section: Chemicals and Radiochemicalsmentioning
confidence: 87%
“…5). In addition to chemopreventive activity, methylated resveratrols, such as desoxyrhapontigenin (4Ј-O-methylresveratrol) and pinostilbene (1k: 3-O-methyl-resveratrol), exhibit higher CYP1A1 inhibitory activity than resveratrol (2f) [52]. Furthermore, a pinosylvin monomethyl ether (1k) as a nematicidal agent from Pinus massoniana shows a tentimes smaller LC 50 value than pinosylvin (1f) [53].…”
Section: -2 Production Of Stilbene Methyl Ethersmentioning
confidence: 99%
“…그러나 quercetin 자체는 생물 이용 성이 낮아 급여시 그 이용이 제한적이다. 이는 hydroxylated flavonoids인 quercetin이 혈액이나 장기에 도달하기 전에 in vivo 상태에서 신속하게 대사되어 배설되고 transcellular 수 송이 낮은 단점이 있기 때문이다 (Lee et al, 2011;Suresh Babu et al, 2004;Mikstacka et al, 2007). 이를 보완하기 위해 수 산화기를 메틸기로 치환함으로써 (methoxylation) 친수성인 quercetin의 지용성을 증가시키고, 음이온을 띠게 하여 대사 안정성과 세포내 수송율을 높일 수 있다 (Graf et al, 2005;Wilson et al, 2008).…”
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