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5-HYDROXYECDYSONE

Year of first isolation: 2011
Formula:C27H44O7
Molecular weight:480
Occurence in plants:
Polypodium vulgare [Polypodiaceae] » Images of Polypodium vulgare Wikipedia: Polypodium vulgare [Polypodiaceae]
Occurence in animals:
 
5-HYDROXYECDYSONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C)O)C(CCC(C)(C)O)O
Isomeric SMILES
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C1[C@]2([C@@](C[C@H]([C@H]1O)O)(C(=O)C=C1[C@@H]2CC[C@]2([C@]1(CC[C@@H]2[C@H](C)[C@@H](CCC(C)(C)O)O)O)C)O)C » JSMol: View in 3D
IUPAC Name(2S,3R,5S,9R,10R,13R,14S,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-2,3,5,14-tetrahydroxy-10,13-dimethyl-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID101534441
InChiKey
[ ChemIDPlus: search ]
UMGDTBHEMFZFBZ-NJQDZGJSSA-N
InChIInChI=1S/C27H44O7/c1-15(19(28)8-9-23(2,3)32)16-7-11-26(33)18-12-22(31)27(34)14-21(30)20(29)13-25(27,5)17(18)6-10-24(16,26)4/h12,15-17,19-21,28-30,32-34H,6-11,13-14H2,1-5H3/t15-,16+,17-,19+,20-,21+,24+,25+,26+,27+/m0/s1

MASS SPECTRUM

HRESI-MS [M+H]+ = 481.3152, calculated for C27H45O7 481.3160, delta - 1.6 ppm
CI-MS (NH3) m/z
ESI-MS m/z (relative intensity %) 504 (30) [M+Na]+, 481 (0.1) (M+H]+, 463 (1) [M+H-H2O]+, 445 (27) [M+H-2H2O]+, 429 (4) [M-2H2O-CH3]+, 427 (15) [M+H-3H2O]+, 409 (5) [M+H-4H2O]+, 393 (1), 363 (7), 345 (35), 99 (100)

CARBON NMR

PROTON NMR

CD3OD
0134.3
0268.5
0370.4
0436.3
0580.4
06202.6
07120.6
08167.3
0939.3
1045.6
1122.7
1232.3
1348.3
1485.0
1532.2
1627.1
1748.9
1816.3
1917.1
2043.6
2113.4
2275.4
2325.5
2442.4
2571.6
2629.2
2729.1
CD3OD
01-Ha1.74
01-He1.74
02-Ha3.95 (ddd, 9.5, 6.9, 3.5)
03-He3.99 (q, 3.0)
04-Ha2.08 (dd, 14.8, 3.0°
04-He1.77
07-H5.86 (d, 2.7)
09-H3.19
11-Ha1.74
11-He1.82
12-Ha2.13
12-He1.79
15-Ha1.60
15-Hb1.97
16-Ha1.52
16-Hb1.97
17-H2.02
18-Me0.74 (s)
19-Me0.92 (s)
20-H1.76
21-Me0.95 (d, 6.7)
22-H3.59
23-Ha1.32
23-Hb1.55
24-Ha1.41
24-Hb1.80
26-Me1.19 (s)
27-Me1.21 (s)

PHYSICAL PROPERTIES

M.P.°C ;
[α]D28+31 ° (c 0.1 ; MeOH)
IR (KBr) ν max (cm-1)
UV (MeOH) λ max (log ε)241 (3.84) ;

CHROMATOGRAPHY

HPLC
GLC
HPTLC
TLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationSIMON, A. et al. (2011) Steroids 76, 1419-1424 Search more

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© 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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