Taxonomy: Physicochemical and Pharmacological Properties of Triterpene Glycosides – Glycosides of Aglycones of Oleanene Type – Glycosides of Oleanolic Acid
C41H66O12: 750.455
Mp: 269–271°C [3]
[α] 20D + 41.6° (c 0.33, C5H5N) [1]
13 C NMR (75 MHz, C5D5N):[2]
Table 1
C-1 |
38.8 |
C-16 |
23.9 |
Ara-1 |
104.9 |
 2 |
26.5 |
 17 |
46.7 |
2 |
80.8 |
 3 |
89 |
 18 |
42.0 |
3 |
73.5 |
 4 |
39.6 |
 19 |
46.5 |
4 |
68.4 |
 5 |
55.9 |
 20 |
31.0 |
5 |
65.1 |
 6 |
18.6 |
 21 |
34.3 |
Glc-1 |
105.9 |
 7 |
33.2 |
 22 |
33.2 |
2 |
76.4 |
 8 |
39.8 |
 23 |
28.3 |
3 |
78.2 |
 9 |
48.1 |
 24 |
16.8 |
4 |
71.6 |
10 |
37.0 |
 25 |
15.5 |
5 |
78.2 |
11 |
23.9 |
 26 |
17.5 |
6 |
62.6 |
12 |
122.6 |
 27 |
26.2 |
||
13 |
144.9 |
 28 |
180.3 |
||
14 |
42.2 |
 29 |
33.2 |
||
15 |
28.3 |
 30 |
23.9 |
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References
V.I. Grishkovets, E.A. Sobolev, A.S. Shashkov, V.Ya. Chirva, Chem. Nat. Comp. 36(5), 501 (2000)
Z.S. Kemoklidze, G.E. Dekanosidze, O.D. Dzhikiya, M.M. Vugal’ter, E.P. Kemertelidze, Chem. Nat. Comp. 18(6), 757 (1982)
B. Demon, K. Hostettmann, Helv. Chim. Acta. 66, 422 (1983)
H. Kawai, M. Kuroyanagi, K. Umehara, A. Ueno, M. Satake, Chem. Pharm. Bull. 36(12), 4769 (1988)
R. Higuchi, T. Kawasaki, Chem. Pharm. Bull. 24(5), 1021 (1976)
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(2013). Fatsiaside C1 (Saponin PE). In: Azimova, S.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0541-2_129
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