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PARISTERONE

Year of first isolation: 1982
Formula:C27H44O7
Molecular weight:480
Occurence in plants:
Paris polyphylla [Melanthiaceae] » Images of Paris polyphylla Wikipedia: Paris polyphylla [Melanthiaceae]
Occurence in animals:
 
PARISTERONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(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](CCC(C)(C)O)O)(O)C)O)C)C » JSMol: View in 3D
IUPAC Name(2R,3R,5R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID16395231
InChiKey
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NKDFYOWSKOHCCO-VWEFCCBJSA-N
InChIInChI=1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15?,17-,19+,20+,21-,22+,24+,25+,26+,27+/m0/s1

MASS SPECTRUM

HR-MS426.2788 (C27H38O4) (calc. 426.2770); 363.2166 (C21H31O5) (calc. 363.2171); 345.2052 (C21H29O4) (calc.345.2066); 327.1962 (C21H27O3) (calc. 327.1960)
FD-MS m/z480.4 [M]+ (34%)
EI-MS m/z (relative intensity %)462, 444, 426, 411 (5), 363 (33), 345 (62), 327 (23), 320 (4), 309 (6), 301 (8), 300 (5), 285 (5), 269 (12), 250 (9), 225 (3), 213 (4), 191 (8), 173 (12), 161 (6), 143 (10), 117 (6), 99 (40), 81 (37), 69 (38), 58 (100)

CARBON NMR

PROTON NMR

DMSO-d6
0137.6
0266.8 *
0368.8 *
0433.2
0550.1
06202.7
07120.5
08165.2
0936.7
1038.5
1120.3
1230.9
1346.9
1483.1
1531.5
1623.8
1748.8
1817.1
1926.1
2075.8
2120.9
2276.2
2329.0
2441.3
2575.8
2629.8
2729.8
DMSO-d6
01-Ha 
02-He3.75 (m, w1/2 = 8)
03-He3.75 (m, w1/2 = 8)
04-Ha 
04-He 
05-H 
07-H5.65
09-Ha 
11-Ha 
11-He 
12-Ha 
12-He 
14-OH4.60
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H 
18-Me0.77
19-Me0.84
21-Me1.10
22-Hb3.20 (m, w1/2 = 10)
23-Ha 
24-Ha 
24-Hb 
26-Me1.10
27-Me1.10

PHYSICAL PROPERTIES

M.P.216-220 °C (decomp)
[α]D25+ 41.9° (c 0.5; pyridine)
IR (KBr) ν max (cm-1)3300 (OH, broad), 1650 (cyclohexenone), 1435, 1380 (CH3), 11
UV (EtOH) λ max (log ε)240 (4.013)

CHROMATOGRAPHY

HPTLC 
TLC 
GLC 
HPLC 

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationSINGH, S.B. et al. (1982) Tetrahedron 38, 2189-2194 Search more

see Important notice
© Université Pierre & Marie Curie, Paris 6, France
© Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Prague, Czech Republic
© Institut National de la Recherche Agronomique, Versailles, France
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