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11β-HYDROXY-20-DEOXYSHIDASTERONE

Year of first isolation: 2013
Formula:C27H42O6
Molecular weight:462
Occurence in plants:
Vitex doniana [Lamiaceae (alt. Labiatae)] » Images of Vitex doniana Wikipedia: Vitex doniana [Lamiaceae (alt. Labiatae)]
Occurence in animals:
 
11β-HYDROXY-20-DEOXYSHIDASTERONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)C5CCC(O5)(C)C
Isomeric SMILES
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C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2[C@H](C[C@]2([C@]1(CC[C@@H]2[C@H](C)[C@H]1CCC(O1)(C)C)O)C)O)C » JSMol: View in 3D
IUPAC Name(2S,3R,5R,10R,11S,13R,14S,17R)-17-[(1S)-1-[(2S)-5,5-dimethyloxolan-2-yl]ethyl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID71533239
InChiKey
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JNZGVPFIDQLKCF-AADHXZMHSA-N
InChIInChI=1S/C27H42O6/c1-14(22-7-8-24(2,3)33-22)15-6-9-27(32)17-11-18(28)16-10-19(29)20(30)12-25(16,4)23(17)21(31)13-26(15,27)5/h11,14-16,19-23,29-32H,6-10,12-13H2,1-5H3/t14-,15+,16-,19+,20-,21-,22-,23?,25-,26+,27+/m0/s1

MASS SPECTRUM

HRESI-MS (ToF)m/z 463.3591 (calc. 453.3454 [M+H]+, 485.2652 (calc. 485.2636 [M+Na]+)
ESI-MS m/z (relative intensity %) 463 [M+H]+ (60), 445 [M+H-H2O]+ (100), 427 [M+H-2H2O]+ (30), 409 [M+H-3H2O]+ (60)

CARBON NMR

PROTON NMR

CD3OD
0139.4
0271.4
0368.8
0433.1
0551.9
06206.9
07121.7
08168.6
0942.5
10
1176.3
1243.5
13
1485.3
1532.4
1621.7
1750.6
1818.2
1924.5
2035.2
2121.2
2285.0
2329.7
2437.3
2579.5
2627.5
2727.3
CD3OD
01-Ha1.25-1.34 (m)
01-He2.49 (m)
02-Ha4.44 (m, w1/2=5.5)
03-He4.35 (m, w1/2=2.5)
04-Ha1.70-1.72 (m)
04-He1.70-1.72 (m)
05-H2.26 (dd, 13.1, 3.5)
07-H5.62 (d, 1.5)
09-H3.14 (m, w1/2=10)
11-Ha4.32 (m, w1/2=2.5)
12-H2.25 (dd, 12.5, 10.4), 2.23 (dd, 12.4, 6.0)
15-Ha1.47-1.49 (m)
15-Hb1.90-2.00 (m)
16-Ha1.58-1.60 (m)
16-Hb1.49-1.50 (m)
17-H2.52 (dd, 9.6, 8.5)
18-Me0.80 (s)
19-Me0.83 (s)
20-H2.44 (m)
21-Me0.92 (d, 6.5)
22-H3.75 (m)
23-Ha1.70-1.72 (m)
23-Hb1.97-2.00 (m)
24-Ha1.72-1.74 (m)
24-Hb1.72-1.74 (m)
26-Me1.05 (s)
27-Me1.01 (s)

PHYSICAL PROPERTIES

M.P.258-262 °C ;
[α]D20° (c ; MeOH)
IR (KBr) ν max (cm-1)3427, 2832, 1654, 1059
UV (MeOH) λ max (log ε)241 (3.54) ;

CHROMATOGRAPHY

HPLC
GLC
HPTLC
TLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationOCHIENG, C.O. et al. (2013) Planta Med. 79, 52-59 Search more

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© Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Prague, Czech Republic
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