5,2′-Dihydroxyflavone-7-O-glucuronide (2′-Hydroxychrysin-7-O-glucuronide)

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Taxonomy: Physicochemical and Pharmacological Properties of Flavonoids – Flavons and Flavon-3-ols

Biological sources: Scutellaria comosa [1], S. Ikonnikovii [2], S. pycnoclada [3], S. Tournefortii [4]

C21H18O11: 446.0841

Mp: 230–235°C

[α]D−140.0° (EtOH)

UV: 270, 330; +ZrOCl2: 290, 390; +NaOH: 405 [1, 2]

1H NMR (DMSO-d6): 5.23 (1H, d, J = 6.9, H-1″), 6.44 (1H, d, J = 2.2, H-6), 6.82 (1H, d, J = 2.2, H-8), 6.98 (1H, t, H-5′), 7.07 (1H, d, J = 8.0, H-3′), 7.13 (1H, s, H-3), 7.39 (1H, t, H-4′), 7.83 (1H, d, J = 8.0, H-6′), 12.86 (1H, s, 5-OH) [1, 2]

13 C NMR (DMSO-d 6) [ 2]:

Table 1

C-2

163.07

C-1′

117.35

C-1″

99.45

3

105.34

2′

157.08

2″

72.96

4

182.20

3′

116.82

3″

74.11

5

161.0

4′

132.84

4″

71.89

6

99.37

5′

119.13

5″

76.32

7

161.73

6′

128.25

6″

172.02

8

94.69

       

9

157.34

       

10

109.12

       

References

  1. 1.
    B. Yusupova, R. Atadzhanov, Sh Toshmatov, Sh Abdullaev, V.I. Litvinenko, Chem. Nat. Comp. 31, 144 (1995)CrossRefGoogle Scholar
  2. 2.
    Y. Oi, K. Matsuzaki, K. Takanashi, T. Okuyama, S. Shibato, Chem. Pharm. Bull. 36, 3206 (1988)CrossRefGoogle Scholar
  3. 3.
    F.D. Nasrullaev, in Author's Abstract of a Candidate Dissertation in Chemical Sciences, Tashkent, 1993Google Scholar
  4. 4.
    T.P. Popova, D.A. Pakaln, V.I. Litvinenko, in Useful Plants of the Natural Flora and Their Use in the Economy [in Russian], (Kiev, 1980), p. 80Google Scholar

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© Springer Science+Business Media New York 2013

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