Common Name: Xuxuarine Bα
Synonyms:
CAS Registry Number:
InChI: InChI=1S/C56H70O9/c1-28-23-37-49(6,45(61)42(28)59)17-21-51(8)36-14-13-31-32(47(36,4)15-19-52(37,51)9)26-40(58)56(63)55(31,12)65-44-30(3)41-33(25-35(44)64-56)48(5)16-20-53(10)38-24-29(2)43(60)46(62)50(38,7)18-22-54(53,11)39(48)27-34(41)57/h13-14,25-29,37-38,45-46,61-63H,15-24H2,1-12H3/t28-,29-,37-,38-,45-,46+,47+,48+,49-,50-,51-,52+,53+,54-,55+,56-/m1/s1
InChIKey: InChIKey=ZHALWCABSYEFBP-WIFRSEASSA-N
Formula: C56H70O9
Molecular Weight: 887.151707
Exact Mass: 886.501984
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) | 115.57 |
2 (C) | 190.18 |
3 (C) | 92.05 |
4 (C) | 79.36 |
5 (C) | 130.29 |
6 (CH) | 126.52 |
7 (CH) | 116.24 |
8 (C) | 160.12 |
9 (C) | 41.54 |
10 (C) | 173.56 |
11 (CH2) | 34.48 |
12 (CH2) | 29.74 |
13 (C) | 39.36 |
14 (C) | 43.96 |
15 (CH2) | 28.03 |
16 (CH2) | 29.43 |
17 (C) | 44.78 |
18 (CH) | 44.89 |
19 (CH2) | 32.03 |
20 (CH) | 40.76 |
21 (C) | 213.48 |
22 (CH) | 76.44 |
23 (CH3) | 22.17 |
25 (CH3) | 35.59 |
26 (CH3) | 22.32 |
27 (CH3) | 20.76 |
28 (CH3) | 24.92 |
30 (CH3) | 14.66 |
1' (CH) | 111.25 |
2' (C) | 144.69 |
3' (C) | 137.68 |
4' (C) | 127.82 |
5' (C) | 124.36 |
6' (C) | 187.44 |
7' (CH) | 126.11 |
8' (C) | 170.21 |
9' (C) | 39.62 |
10' (C) | 150.4 |
11' (CH2) | 33.43 |
12' (CH2) | 30.13 |
13' (C) | 40.11 |
14' (C) | 43.93 |
15' (CH2) | 28.15 |
16' (CH2) | 29.55 |
17' (C) | 44.78 |
18' (CH) | 45.03 |
19' (CH2) | 31.89 |
20' (CH) | 40.76 |
21' (C) | 213.42 |
22' (CH) | 76.4 |
23' (CH3) | 12.89 |
25' (CH3) | 38.61 |
26' (CH3) | 20.84 |
27' (CH3) | 20.45 |
28' (CH3) | 24.98 |
30' (CH3) | 14.66 |