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 ▣ 천연물에서 분리된 개별유효성분 레코드 등록정보

성 분 명 

Lutein

다른이름들 

Xanthophyll beta,epsilon-Carotene-3,3'-diol (3R,3'R,6'R-form)

함유 천연물 

Brassica juncea (L.) Czern. var. juncea[갓(Gat)](개채(芥菜))
Brassica juncea var. crispifolia L.H.Bailey[겨자(Gyeo-ja)](백개자(白芥子))
Brassica oleracea var. capitata L.[양배추(Yang-bae-chu)]()
Citrus aurantium var. daidai Makino[광귤(Gwang-gyul)](대대화(玳玳花),지실(枳實))
Citrus junos Siebold ex Tanaka[유자나무(Yu-ja-na-mu)](유자(柚子),유피(柚皮),등자피(橙子皮))
Citrus sinensis (L.) Osbeck[당귤나무(Dang-gyul-la-mu)](기실(枳實))
Equisetum hyemale L.[속새(Sok-sae)](목적(木賊))
Euonymus japonicus Thunb.[사철나무(Sa-cheol-na-mu)](조경초(調經草))
Ginkgo biloba L.[은행나무(Eun-haeng-na-mu)](은행엽(銀杏葉),백과(白果))
Glycine max (L.) Merr.[콩(Kong)](흑대두(黑大豆),담두시(淡豆시),대두황권(大豆黃卷))
Helianthus annuus L.[해바라기(Hae-ba-ra-gi)](향일규자(向日葵子),향일규화탁(向日葵花托),향일규엽(向日葵葉),향일규화(向日葵花))
Hibiscus syriacus L.[무궁화(Mu-gung-hwa)](목근피(木槿皮),목근화(木槿花),목근근(木槿根),목근자(木槿子))
Impatiens nolitangere L. var. nolitangere[노랑물봉선(No-rang-mul-bong-seon)](야봉선화(野鳳仙花))
Lactuca sativa L.[상추(Sang-chu)](와거(와거),와거자(와거子))
Lemna paucicostata (L.) Hegelm.[좀개구리밥(Jom-gae-gu-ri-bap)](부평(浮萍))
Matteuccia struthiopteris (L.) Tod.[청나래고사리(Cheong-na-rae-go-sa-ri)](협과궐(莢果蕨))
Medicago sativa L.[자주개자리(Ja-ju-gae-ja-ri)]()
Momordica charantia L.[여주(Yeo-ju)](고과(苦瓜))
Panax ginseng C.A.Mey.[인삼(In-sam)](인삼(人蔘),산삼(山蔘),장뇌(樟腦),인삼엽(人蔘葉),인삼로(人蔘蘆),미삼(尾蔘),인삼자(人蔘子),홍삼(紅蔘))
Physalis alkekengi var. francheti (Mast.) Hort[꽈리(Kkwa-ri)](산장(酸漿))
Pisum sativum L.[](완두화(豌豆花))
Rosa rugosa Thunb. var. rugosa[해당화(Hae-dang-hwa)](매괴화(매괴花),매괴화근(매괴花根))
Spinacia oleracea L.[시금치(Si-geum-chi)](파채(파菜))
Vitis vinifera L.[포도(Po-do)](포도(葡萄),포도근(葡萄根),포도경엽(葡萄莖葉),포도엽(葡萄葉))

분 자 식 

C₄₀H₅₆O₂

화학족 분류 

테트라테르페노이드(tetraterpenoid);

분 자 량 

568.891

녹 는 점 

196°C

생리학적효과 

Antioxidant.

UV_CHART 

(λmax, nm) (benzene):417, 439, 470, (EtOH): 417, 439, 469, (CHCl3): 424, 448, 478, (CS2): 438, 468, 498

HNMR_CHART 

(CDCl3,400 MHz) δ:0.85(3H, s, 1'beta-Me), 1.00(3H, s, 1'alpha-Me), 1.31(1H, d, 7, 3'-OH), 1.34(1H, d, 5, 3-OH), 1.37(1H, dd, 13.2, 7, H2'), 1.48(1H, t, 12, H2beta), 1.63(3H, br s, 5'-Me), 1.74(3H, s, 5-Me), 1.77(1H, ddd, 12.5, 4, 2, H2alpha), 1.90(3H, s, 9'-Me), 1.97(9H, br s, 9,13,13'-Me), 2.04(1H, br dd, 17, 10, H4beta), 2.38(1H, m, H4alpha), 2.41(1H, H6'alpha), 4.00(1H, m, H3), 4.35(1H, m, H3'), 5.43(1H, dd, 15.3, 9.5, H7'), 5.55(1H, br s, H4'), 6.11(1H, d, 16, H7), 6.13(2H, ea. d, 16, H8,8'), 6.14, 6.16(2H, ea. d, H10',10), 6.26(2H, m, H14,14'), 6.36(2H, ea. d, 15, H12',12), 6.61-6.64(4H, m, H11',15,15',11)

CNMR_CHART 

(CDCl3 + DMSO-d6) δ: 36.76, 48.41, 64.34, 42.61, 126.69, 137.26, 125.81, 137.92, 135.48, 131.03, 124.88, 137.27, 136.09, 132.44, 129.99, 28.63, 30.27, 21.55, 12.61, 12.68, 34.00, 44.89, 63.46, 125.97, 135.55, 54.77, 129.13, 137.35, 134.88, 130.52, 124.80, 137.27, 136.1

참고문헌 

· M. Baranyai et al., Tetrahedron, 37, 203, 1981(cmr) · T. Ohta et al., Chem. Pharm. Bull., 7, 254, 1959(uv) · M. Vecchi et al., Helv. Chim. Acta, 65, 1050, 1982(pmr) · GP. Moss, Pure Appl. Chem., 47, 97, 1976 · GM. Fishman et al., Chem. Nat. Comp., 24, 3, 395, 1988 · SL. Jensen et al., Acta Chem. Scand., 20, 1703, 1966 · R. Buchecker et al., Helv. Chim. Acta, 57, 631, 1974 · BCL. Weedon, Pure Appl. Chem., 47, 161, 1976 · BH. Davies, Int. Rev. Biochem., 14, 51, 1977 · H. Mayer et al., Helv. Chim. Acta, 63, 1451, 1980 · BV. Milborrow et al., Phytochemistry, 21, 2853, 1982 · W. Miki et al., Comp. Biochem. Physiol., B: Comp. Biochem., 80, 195, 1985 · T. Matsuno et al., Comp. Biochem. Physiol., B: Comp. Biochem., 80, 779, 1985 · M. Chopra et al., Ann. N.Y. Acad. Sci., 691, 246, 1993 · Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, London, 1428, 1993 · MH. Bui, J. Chromatogr., B: Biomed. Appl., 654, 129, 1994 · ES. Egeland et al., Phytochemistry, 40, 515, 1995 · HR. Sliwka et al., Acta Chem. Scand., 50, 637, 1996