Common Name: 7',8'-dihydroxuxuarine Aβ
Synonyms:
CAS Registry Number:
InChI: InChI=1S/C56H72O7/c1-30-23-41-47(4,28-37(30)58)15-19-51(8)40-14-13-33-34(49(40,6)17-21-52(41,51)9)26-44(60)56(61)55(33,12)63-46-32(3)45-35(25-39(46)62-56)50(7)18-22-53(10)42-24-31(2)38(59)29-48(42,5)16-20-54(53,11)43(50)27-36(45)57/h13-14,25-26,30-31,41-43,61H,15-24,27-29H2,1-12H3/t30-,31-,41-,42-,43+,47+,48+,49+,50+,51-,52+,53+,54-,55-,56+/m1/s1
InChIKey: InChIKey=FRSVTVPTKAPUES-QZQPZFNNSA-N
Formula: C56H72O7
Molecular Weight: 857.168779
Exact Mass: 856.527805
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) | 115.14 |
2 (C) | 189.45 |
3 (C) | 91.19 |
4 (C) | 76.85 |
5 (C) | 132.31 |
6 (CH) | 128.39 |
7 (CH) | 117.19 |
8 (C) | 163.23 |
9 (C) | 43.65 |
10 (C) | 172.71 |
11 (CH2) | 33.16 |
12 (CH2) | 29.88 |
13 (C) | 39.84 |
14 (C) | 44 |
15 (CH2) | 27.92 |
16 (CH2) | 35.52 |
17 (C) | 38.22 |
18 (CH) | 43.54 |
19 (CH2) | 31.96 |
20 (CH) | 42.31 |
21 (C) | 213.91 |
22 (CH2) | 52.41 |
23 (CH3) | 24.61 |
25 (CH3) | 26.39 |
26 (CH3) | 22.39 |
27 (CH3) | 19.64 |
28 (CH3) | 32.77 |
30 (CH3) | 15.17 |
1' (CH) | 108.82 |
2' (C) | 145.38 |
3' (C) | 137.53 |
4' (C) | 129.69 |
5' (C) | 125.27 |
6' (C) | 200.06 |
7' (CH2) | 37.49 |
8' (CH) | 41.9 |
9' (C) | 37.15 |
10' (C) | 152.32 |
11' (CH2) | 33.05 |
12' (CH2) | 29.71 |
13' (C) | 39.53 |
14' (C) | 40.04 |
15' (CH2) | 28.56 |
16' (CH2) | 35.38 |
17' (C) | 38.16 |
18' (CH) | 44 |
19' (CH2) | 31.77 |
20' (CH) | 41.95 |
21' (C) | 213.32 |
22' (CH2) | 53.61 |
23' (CH3) | 13.21 |
25' (CH3) | 39.71 |
26' (CH3) | 14.97 |
27' (CH3) | 18.14 |
28' (CH3) | 32.52 |
30' (CH3) | 15.11 |