αナフトフラボン
WordNet
- first in order of importance; "the alpha male in the group of chimpanzees"; "the alpha star in a constellation is the brightest or main star"
- the 1st letter of the Greek alphabet
- the beginning of a series or sequence; "the Alpha and Omega, the first and the last, the beginning and the end"--Revelations
- early testing stage of a software or hardware product; "alpha version"
- any high mountain
PrepTutorEJDIC
- アルファ(ギリシア語アルファベットの第1字A,α;英語のA,aに相当) / アルファ星(星座の主星)
- 高山,高峰
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/06/02 14:36:08」(JST)
[Wiki en表示]
alpha-Naphthoflavone
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Names |
IUPAC name
2-phenylbenzo[h]chromen-4-one
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Other names
7,8-Benzoflavone, ANF,2-phenylbenzo[h]chromen-4-one
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Identifiers |
CAS Number
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3D model (Jmol)
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ChEBI |
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ChemSpider |
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DrugBank |
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ECHA InfoCard |
100.009.156 |
InChI
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InChI=1S/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H Y
Key: VFMMPHCGEFXGIP-UHFFFAOYSA-N Y
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InChI=1/C19H12O2/c20-17-12-18(14-7-2-1-3-8-14)21-19-15-9-5-4-6-13(15)10-11-16(17)19/h1-12H
Key: VFMMPHCGEFXGIP-UHFFFAOYAW
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SMILES
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O=C\1c4c(O/C(=C/1)c2ccccc2)c3ccccc3cc4
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Properties |
Chemical formula
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C19H12O2 |
Molar mass |
272.30 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N verify (what is YN ?) |
Infobox references |
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alpha-Naphthoflavone, also known as 7,8-benzoflavone and 2-phenyl-benzo(h)chromen-4-one, is a synthetic[1][2] flavone derivative. It can be prepared from 2-naphthol and cinnamaldehyde.[3]
alpha-Naphthoflavone is a potent inhibitor of the enzyme aromatase, the enzyme that converts testosterone to estrogen.[1][2] alpha-Naphthoflavone has been shown to cause abnormal testicular development in young chickens.[4]
See also
References
- ^ a b Campbell, Deborah R.; Kurzer, Mindy S. (1993). "Flavonoid inhibition of aromatase enzyme activity in human preadipocytes". Journal of Steroid Biochemistry and Molecular Biology. 46 (3): 381–388. doi:10.1016/0960-0760(93)90228-O. PMID 9831487.
- ^ a b Kellis JT Jr; Vickery LE (1984). "Inhibition of human estrogen synthetase (aromatase) by flavones". Science. 225 (4666): 1032–1034. doi:10.1126/science.6474163. PMID 6474163.
- ^ Harvey, Ronald G.; Hahn, Jung Tai; Bukowska, Maria; Jackson, Henry (1990). "A new chromone and flavone synthesis and its utilization for the synthesis of potentially antitumorigenic polycyclic chromones and flavones". The Journal of Organic Chemistry. 55 (25): 6161. doi:10.1021/jo00312a023.
- ^ Trefil, P.; Micakova, A.; Stiborova, M.; Poplstein, M.; Brillard, J.P.; Hodek, P. (2004). "Effects of alpha-naphthoflavone on body growth and gonad development in chickens (Gallus domesticus)". Czech Journal of Animal Science - UZPI. 49 (6): 231–238.
UpToDate Contents
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English Journal
- Apoptosis induction and inhibition of HeLa cell proliferation by alpha-naphthoflavone and resveratrol are aryl hydrocarbon receptor-independent.
- Flores-Pérez A1, Elizondo G2.
- Chemico-biological interactions.Chem Biol Interact.2018 Feb 1;281:98-105. doi: 10.1016/j.cbi.2017.12.029. Epub 2017 Dec 20.
- PMID 29274324
- The synthesis of chalcones as anticancer prodrugs and their bioactivation in CYP1 expressing breast cancer cells.
- Ruparelia KC1, Zeka K1, Ijaz T1, Ankrett DN1, Wilsher NE1, Butler PC1, Tan HL1, Lodhi S1, Bhambra AS1, Potter GAPRRA1, Arroo RR1, Beresford KJM1.
- Medicinal chemistry (Shariqah (United Arab Emirates)).Med Chem.2018 Jan 12. doi: 10.2174/1573406414666180112120134. [Epub ahead of print]
- PMID 29332599
- Resveratrol supports and alpha-naphthoflavone disrupts growth of human ovarian follicles in an in vitro tissue culture model.
- Hao J1, Tuck AR2, Sjödin MOD2, Lindberg J2, Sand A3, Niklasson B4, Argyraki M4, Hovatta O4, Damdimopoulou P5.
- Toxicology and applied pharmacology.Toxicol Appl Pharmacol.2018 Jan 1;338:73-82. doi: 10.1016/j.taap.2017.11.009. Epub 2017 Nov 14.
- PMID 29146461
Japanese Journal
- Induction of cytochrome P-450 1A1 by omeprazole in human HepG2 cells is protein tyrosine kinase-dependent and is not inhibited by alpha-naphthoflavone
- Mechanism of action of alpha-naphthoflavone as an Ah receptor antagonist in MCF-7 human breast cancer cells
Related Links
- Sigma-Aldrich offers Aldrich-N5757, α-Naphthoflavone for your research needs. Find product specific information including CAS, MSDS, protocols and references. ... Dietary Antioxidants Antioxidants protect biological systems from ...
- [α-Naphthoflavone] [604-59-1] | 価格や在庫、物性値などの詳細情報ページです。 ... ・川口の在庫は即日,つくばの在庫は2〜3日以内の出荷となります。・詳細につきましては,お手数ですが営業部までお問い合わせください。
Related Pictures
★リンクテーブル★
[★]
- 英
- alpha-naphthoflavone
- 関
- α-ナフトフラボン
[★]
- 英
- alpha-naphthoflavone
- 関
- αナフトフラボン
[★]
α、アルファ
- 関
- alfa