Common Name: Xuxuarine Cβ
Synonyms:
CAS Registry Number:
InChI: InChI=1S/C56H70O8/c1-29-23-39-47(4,28-36(29)58)15-19-53(10)41-27-35(57)43-31(3)45-37(25-34(43)49(41,6)17-20-52(39,53)9)63-56(62)42(59)26-33-32(55(56,12)64-45)13-14-38-48(33,5)16-21-54(11)40-24-30(2)44(60)46(61)50(40,7)18-22-51(38,54)8/h13-14,25-27,29-30,39-40,46,61-62H,15-24,28H2,1-12H3/t29-,30-,39-,40-,46-,47+,48+,49+,50-,51-,52+,53-,54+,55-,56+/m1/s1
InChIKey: InChIKey=OVGKPRSKOPTIPZ-UQRDLBQTSA-N
Formula: C56H70O8
Molecular Weight: 871.152302
Exact Mass: 870.507069
NMR Solvent: CDCl3
MHz:
Calibration:
NMR references: 13C - Shirota, O., Morita, H., Takeya, K., Itokawa, H. Tetrahedron (1995) 51, 1107-20
Species:
Notes: Family : Terpenoids, Type : Triterpenoids, Group : Celastranes; 13 C Spectrum from Naproc 13: José Luis López-Pérez, Roberto Therón, Esther del Olmo, David Díaz: NAPROC-13: a database for the dereplication of natural product mixtures in bioassay-guided protocols. Bioinformatics 23(23):3256-3257 (2007)
Position | PPM |
---|---|
1 (CH) | 115.05 |
2 (C) | 189.45 |
3 (C) | 91.17 |
4 (C) | 76.9 |
5 (C) | 132.15 |
6 (CH) | 128.61 |
7 (CH) | 117.28 |
8 (C) | 162.95 |
9 (C) | 43.52 |
10 (C) | 172.78 |
11 (CH2) | 33.32 |
12 (CH2) | 29.85 |
13 (C) | 39.75 |
14 (C) | 43.67 |
15 (CH2) | 28.22 |
16 (CH2) | 29.47 |
17 (C) | 44.78 |
18 (CH) | 45 |
19 (CH2) | 31.91 |
20 (CH) | 40.83 |
21 (C) | 213.44 |
22 (CH) | 76.35 |
23 (CH3) | 24.55 |
25 (CH3) | 39.78 |
26 (CH3) | 22.36 |
27 (CH3) | 20.39 |
28 (CH3) | 24.94 |
30 (CH3) | 14.7 |
1' (CH) | 110.49 |
2' (C) | 145.18 |
3' (C) | 137.65 |
4' (C) | 128.56 |
5' (C) | 123.88 |
6' (C) | 187.09 |
7' (CH) | 126.15 |
8' (C) | 170.09 |
9' (C) | 39.75 |
10' (C) | 151.14 |
11' (CH2) | 34.13 |
12' (CH2) | 30.09 |
13' (C) | 40.16 |
14' (C) | 144.29 |
15' (CH2) | 28.39 |
16' (CH2) | 35.52 |
17' (C) | 38.12 |
18' (CH) | 43.48 |
19' (CH2) | 31.91 |
20' (CH) | 41.85 |
21' (C) | 213.37 |
22' (CH2) | 52.61 |
23' (CH3) | 13.14 |
25' (CH3) | 38.68 |
26' (CH3) | 20.81 |
27' (CH3) | 19.77 |
28' (CH3) | 32.58 |
30' (CH3) | 15.06 |