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13C NMR (101 MHz, DMSO) ¦Ä12.98,13.06,13.35,21.95,23.02,24.23,29.01,29.47,29.49,29.94,30.74,34.22,36.97,43.12,45.18,48.98,54.86,63.09,64.01,125.54,125.62,126.04,126.99,127.35,129.71,130.81,131.07,131.78,133.06,133.13,135.00,135.31,135.88,136.66,136.70,137.46,137.61,137.78,137.86,138.12.
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1 .     compound 1
C40H56O2     ÏàËÆ¶È:87.5%
Korean Journal of Pharmacognosy          1999          30(4)          404-408
Isolation of Grb2-Shc Domain Binding Inhibition Component from Agastache rugosa
Lee, Eun-Sook; Ahn, Byung-Tae; Lee, Sae-Bom; Kim, Hyae-Kyeong; Bok, Song-Hae; Jeong, Tae-Sook
2 .     lutein
C40H56O2     ÏàËÆ¶È:87.5%
Acta Botanica Yunnanica          2010          32          455-462
A New Lignan from Elaeagnus lanceolata (Elaeagnaceae)
SONG We i-Wu, LIBo, LIU Ji-Kai

3 .     lutein
    ÏàËÆ¶È:87.5%
Chinese Journal of Natural Medicines          2012          10          0284-0286
A new triterpene from Glinus oppositifolius
Consolacion Y. Ragasa, Dinah L. Espineli, Emelina H. Mandia, Ming-Jaw Don, Chien-Chang Shen

4 .     all-E-lutein
C40H56O2     ÏàËÆ¶È:82.5%
Planta Medica          2012          78          957-961
Inhibition of Lysenin-induced Hemolysis by All-E-Lutein Derived from the Plant Dalbergia latifolia
Niwa, Yuki; Matsui, Chino; Sukumwang, Neelanun; Iinuma, Hironobu; Ikeda, Yoko; Koyano, Takashi; Kovitayakorn, Taworn; Simizu, Siro; Umezawa, Kazuo:

5 .     (13Z,13'Z-,3R,3'R,6'R)-Lutein
    ÏàËÆ¶È:82.5%
Journal of Agricultural and Food Chemistry          1999          47          455-461
Isolation and Structural Elucidation of (13Z,13¡®Z,3R,3¡®R,6¡®R)-Lutein from Marigold Flowers, Kale, and Human Plasma
Frederick Khachik, Andrea Steck, and Hanspeter Pfander

6 .     3,3'-Dimethoxylutein
    ÏàËÆ¶È:75%
Helvetica Chimica Acta          2004          Vol. 87          1254
Confirmation of the Structures of Lutein and Zeaxanthin
Anthony Linden, Bruno B¨¹rgi, and Conrad Hans Eugster

7 .     (30Z,50Z)-celaxanthin
C40H54O2     ÏàËÆ¶È:75%
Phytochemistry          2009          70          920-923
Sterically hindered carotenoids with 3Z, 5Z configuration from the seeds of oriental bitter sweet, Celastrus orbiculatus
Takashi Maoka

8 .     (8R)-mutatoxanthin
    ÏàËÆ¶È:75%
Phytochemistry          1991          30          2983-2986
Carotenoids from three red algae of the Corallinaceae
Jorge A. Palermo, Eduardo G. Gros, Alicia M. Seldes

9 .     (8S)-mutatoxanthin
    ÏàËÆ¶È:75%
Phytochemistry          1991          30          2983-2986
Carotenoids from three red algae of the Corallinaceae
Jorge A. Palermo, Eduardo G. Gros, Alicia M. Seldes

10 .     Compound 2
    ÏàËÆ¶È:73.1%
Magnetic Resonance in Chemistry          2002          40          797-799
NMR assignments of selected bacterial carotenoids
Bjart Frode Lutnaes, Jostein Krane and Synnøve Liaaen-Jensen

11 .     cucurbitaxanthin A
    ÏàËÆ¶È:72.5%
Helvetica Chimica Acta          1996          Vol. 79          1435
Reisolation of Carotenoid 3,6-Epoxides from Red Paprika (Capsicum annuum)
J¨®zsef Deli, P¨¦ter Moln¨¢r, Zolt¨¢n Matus, and Gyula T¨®th

12 .     ipomoeaxanthin A
C40H58O3     ÏàËÆ¶È:72.5%
Phytochemistry          2007          68          1740-1745
Carotenoids with a 5,6-dihydro-5,6-dihydroxy-b-end group,from yellow sweet potato "Benimasari", Ipomoea batatas LAM
Takashi Maoka , Naoshige Akimoto, Koji Ishiguro, Masaru Yoshinaga, Makoto Yoshimoto

13 .     (all E)-celaxanthin
    ÏàËÆ¶È:72.5%
Phytochemistry          2009          70          920-923
Sterically hindered carotenoids with 3Z, 5Z configuration from the seeds of oriental bitter sweet, Celastrus orbiculatus
Takashi Maoka
14 .     7',8',9',10'-Tetrahydro-¦Â-cryptoxanthin
C40H60O     ÏàËÆ¶È:72.5%
Chemical & Pharmaceutical Bulletin          2011          59(1)          140-145
Structures of Minor Carotenoids from the Japanese Common Catfish,Silurus asotus
Takashi MAOKA and Naoshige AKIMOTO

15 .     (3R,6'R)-¦Á-Cryptoxanthin
C40H56O     ÏàËÆ¶È:72.5%
Journal of Natural Products          2007          70          220-226
Partial Synthesis of (3R,6'R)-¦Á-Cryptoxanthin and (3R)-¦Â-Cryptoxanthin from (3R,3'R,6'R)-Lutein
Frederick Khachik, An-Ni Chang, Audry Gana, and Eugene Mazzola

16 .     (3R)-¦Â-Cryptoxanthin
C40H56O     ÏàËÆ¶È:72.5%
Journal of Natural Products          2007          70          220-226
Partial Synthesis of (3R,6'R)-¦Á-Cryptoxanthin and (3R)-¦Â-Cryptoxanthin from (3R,3'R,6'R)-Lutein
Frederick Khachik, An-Ni Chang, Audry Gana, and Eugene Mazzola

17 .     (3R,5'RS,6'R)-3',4'-Didehydro-5',6'-dihydro-¦Â,¦Â-caroten-3-ol
C40H56O     ÏàËÆ¶È:72.5%
Journal of Natural Products          2007          70          220-226
Partial Synthesis of (3R,6'R)-¦Á-Cryptoxanthin and (3R)-¦Â-Cryptoxanthin from (3R,3'R,6'R)-Lutein
Frederick Khachik, An-Ni Chang, Audry Gana, and Eugene Mazzola

18 .     (3S,5S,6R,3'R,6'R)-5,6-dihydro-b,e-carotene-3,5, 6,3'-tetrol [(3S,5S,6R,3'R,6'R)-5,6-dihydro-5,6-dihydroxylutein]
C40H56O4     ÏàËÆ¶È:70%
Phytochemistry          2004          65          2781-2787
Carotenoid composition in petals of chrysanthemum (Dendranthema grandiflorum (Ramat.) Kitamura)
Sanae Kishimoto, Takashi Maoka, Masayoshi Nakayama, Akemi Ohmiya

19 .     diadinoxanthin
    ÏàËÆ¶È:70%
Journal of Natural Products          2004          67          1067-1069
The Methylerythritol Phosphate Pathway Contributes to Carotenoid But Not Phytol Biosynthesis in Euglena gracilis
Dojung Kim, Michael R. Filtz, and Philip J. Proteau

20 .     compound 16 and 18
    ÏàËÆ¶È:70%
Helvetica Chimica Acta          1981          64          2469-2484
Synthese von optisch aktiven, nat¨¹rlichen Carotinoiden und strukturell verwandten Naturprodukten. IX. Synthese von (3R)-Hydroxyechinenon, (3R, 3¡äR)- und (3R, 3¡äS)-Adonixanthin, (3R)-Adonirubin, deren optischen Antipoden und verwandten Verbindungen
Kurt Bernhard, Gerhard Englert, Hans Mayer, Robert K. M¨¹ller, August R¨¹ttimann, Max Vecchi, Erich Widmer, Reinhard Zell
3Â¥2012-11-12 12:21:50
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