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PANUOSTERONE

Year of first isolation: 1995
Formula:C28H46O7
Molecular weight:494
Occurence in plants:
Tapinella panuoides [Fungi] » Images of Tapinella panuoides Wikipedia: Tapinella panuoides [Fungi]
Occurence in animals:
 
PANUOSTERONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C)C(C)(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O
Isomeric SMILES
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C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1C2CC[C@]2([C@]1(CC[C@@H]2[C@]([C@@H](C[C@@](C(C)C)(C)O)O)(O)C)O)C)C » JSMol: View in 3D
IUPAC Name(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID100953175
InChiKey
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YXPVYQIMXPYFSF-DQVFBYKJSA-N
InChIInChI=1S/C28H46O7/c1-15(2)26(5,33)14-23(32)27(6,34)22-8-10-28(35)17-11-19(29)18-12-20(30)21(31)13-24(18,3)16(17)7-9-25(22,28)4/h11,15-16,18,20-23,30-35H,7-10,12-14H2,1-6H3/t16-,18-,20+,21-,22-,23+,24+,25+,26+,27+,28+/m0/s1

MASS SPECTRUM

EI-MS m/z (relative intensity %)494 (M)+ (0), 415 (4), 397 (3), 382 (3), 363 (33), 345 (79), 327 (15), 301 (6), 285 (8), 269 (14), 250 (10), 227 (7), 213 (10), 199 (7), 185 (12), 173 (14), 157 (15), 129 (29), 111 (26), 97 (42), 83 (52), 71 (79), 57 (100), 43 (88)
FAB-MS m/z517 (M+Na)+ (15), 495 (M+H)+ (14), 477 (13), 459 (7), 442 (6), 418 (5), 402 (6), 301 (11), 251 (10), 239 (18), 208 (15), 173 (30), 147 (89), 129 (31), 112 (48), 95 (57), 81 (57), 69 (84), 52 (100)

CARBON NMR

PROTON NMR

CD3OD
0137.38
0268.72
0368.52
0432.86
0551.80
06205.42
07122.30
08167.60
0934.90
1039.30
1121.54
1232.44
13a
1485.40
1531.83
1621.44
1750.19
1817.98
1924.40
2077.81
2120.69
2274.06
2341.18
2476.26
2537.28
2618.82
2717.30
2822.16
CD3OD
01-Ha1.43 (dd, 13.2, 12.4)
01-He1.79 (dd, 13.2, 4.0)
02-Ha3.83 (ddd, 12.4, 4.0, 3.4)
03-He3.95 (q )
04-Ha1.75
04-He1.69 (dt )
05-H2.38 (dd, 13.0, 4.5)
07-H5.81 (d, 2.6)
09-H3.15 (ddd, 10.5, 7.0, 2.6)
11-Ha1.79
11-He1.71
12-Ha2.11
12-He1.87
15-Ha1.95
15-Hb1.59
16-Ha2.02
16-Hb1.79
17-H2.26 (dd, 10.0, 8.5)
18-Me0.896 (s )
19-Me0.968 (s )
21-Me1.204 (s )
22-H3.78 (dd, 11.0, 1.7)
23-Ha1.73
23-Hb1.44 (dd, 14.7, 11.0)
25-H1.90 (h, 6.5)
26-Me0.980 (d, 6.5)
27-Me0.911 (d, 6.5)
28-Me1.079 (s )

PHYSICAL PROPERTIES

M.P.207-214 °C
[α]D20 
IR (KBr) ν max (cm-1)3416 (OH), 1653 (cyclohexanone)
UV (EtOH) λ max (log ε) 

CHROMATOGRAPHY

NP-HPLCcolumn Silasorb 600 (4 x 250 mm), flow-rate 0.8 ml.min-1, solvent Et2O-hexane-MeOH-H2O (440:430:120:10), Ret 23.5 min (20E 47.5 min)
HPTLC 
TLC 
GLC 
RP-HPLCcolumn Separon SIX C18 (4 x 250 mm), solvent MeOH-H2O, linear gradient 10 to 70 % MeOH in 50 min, flow-rate 0.6 ml.min-1, Ret 48.9min (20E 42.7 min).

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationVOKÁČ, K. et al. (1995) 16th Conference on Isoprenoids, Prague, Abstracts, pp. 77-78 Search more
IdentificationVOKÁČ, K. et al. (1998) Phytochemistry 49, 2109-2114 Search more

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© Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Prague, Czech Republic
© Institut National de la Recherche Agronomique, Versailles, France
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