Taxonomy: Physicochemical and Pharmacological Properties of Triterpene Glycosides – Glycosides of Aglycones of Oleanene Type – 2α,3β,6β,23-Tetrahydroxy-olean-12-en-28-oic Acid
C36H58O11: 666.397
Mp: 215°C (MeOH) [2]
[α]D + 25° (c 0.75, MeOH) [2]
IR (KBr) νmax cm−1: 3500–3200, 1730, 1635, 1450, 1060 [2]
LSI-MS m/z: 705 [M + K]+, 689 [M + Na]+ [2]
13 C NMR (100 MHz, C5D5N): [2]
Table 1
C-1 |
50.0 |
C-16 |
24.0 |
Glc-1 |
95.6 |
2 |
69.0 |
17 |
47.0 |
2 |
74.0 |
3 |
78.3 |
18 |
41.8 |
3 |
79.1 |
4 |
42.3 |
19 |
47.0 |
4 |
71.1 |
5 |
48.8 |
20 |
30.7 |
5 |
78.6 |
6 |
67.6 |
21 |
34.0 |
6 |
62.1 |
7 |
41.0 |
22 |
32.5 |
||
8 |
41.0 |
23 |
66.1 |
||
9 |
48.8 |
24 |
15.9 |
||
10 |
38.1 |
25 |
18.8 |
||
11 |
22.6 |
26 |
19.0 |
||
12 |
123.5 |
27 |
26.1 |
||
13 |
143.5 |
28 |
176.4 |
||
14 |
42.8 |
29 |
33.1 |
||
15 |
28.2 |
30 |
23.6 |
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References
I.K. Adnyana, Y. Tezuka, S. Awale, A.H. Banskota, K.Q. Tran, S. Kadota, Chem. Pharm. Bull. 48, 1114 (2000)
A.P. Kundu, S.B. Mahato, Phytochemistry 32(4), 999 (1993)
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(2013). Chebuloside II. In: Azimova, S.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0541-2_799
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