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11-HYDROXY-CYASTERONE

Year of first isolation: 2015
Formula:C29H44O9
Molecular weight:536
Occurence in plants:
Ajuga turkestanica [Lamiaceae (alt. Labiatae)] » Images of Ajuga turkestanica Wikipedia: Ajuga turkestanica [Lamiaceae (alt. Labiatae)]
Occurence in animals:
 
11-HYDROXY-CYASTERONE

STRUCTURE DESCRIPTORS

Canonical SMILES 
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@](C)([C@@H](C[C@@H]1[C@H](OC(=O)[C@H]1C)C)O)O)O)C)O)C » JSMol: View in 3D
IUPAC Name(3S,4S,5R)-4-((2R,3R)-2,3-dihydroxy-3-((2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-6-oxo-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl)-3,5-dimethyldihydrofuran-2(3H)-one
CAS-RN 
PubChem CID 
InChiKey
[ ChemIDPlus: search ]
GYHHEOJCLAGQCK-HNWGTDKPSA-N
InChIInChI=1S/C29H44O9/c1-13-15(14(2)38-25(13)35)8-23(34)28(5,36)22-6-7-29(37)17-10-18(30)16-9-19(31)20(32)11-26(16,3)24(17)21(33)12-27(22,29)4/h10,13-16,19-24,31-34,36-37H,6-9,11-12H2,1-5H3/t13-,14+,15-,16-,19+,20-,21+,22-,23+,24+,26-,27+,28+,29+/m0/s1

MASS SPECTRUM

ESI-MS m/z 537 [M+H]+, 519 [MH - H2O]+, 501 [MH - 2H2O]+, 483 [MH - 3H2O]+, 465 [MH - 3H2O]+
HRESI-MS 559.28775 [M+Na]+, expected 559.28775 for C29H44O9Na
EI-MS m/z (relative intensity %)

CARBON NMR

PROTON NMR

D2O
0139.2
0269.3
0369.3
0433.6
0553.4
06210.6
07123.9
08167.9
0943.4
1040.3
1170.3
1243.8
1349.3
1486.6
1532.5
1622.1
1750.7
1819.7
1925.3
2079.9
2121.3
2275.9
2335.2
2449.7
2544.4
26185.9
2717.0
2884.1
2920.4
D2O
01-Ha1.39 (t, 13)
01-He2.48 (dd, 13.2, 4)
02-Ha4.09 (m, w1/2 = 11)
03-He4.09 (m, w1/2 = 11)
04-Ha1.77
04-He1.77
05-H2.31
07-H5.99 (d, 2.6)
09-H3.13 (dd, 8.8, 2.6)
11-Ha4.23 (m, w1/2 = 27, ddd 10.8, 9, 6.1)
12-Ha2.07
12-He2.28 (dd, 12.7, 6.1)
15-Ha2.06
15-Hb1.66 (m)
16-Ha1.93
16-Hb1.83
17-H2.32 (m)
18-Me0.87 (s)
19-Me1.10 (s)
21-Me1.26 (s)
22-H3.63 (d, 10.8)
23-Ha1.59 (m)
23-Hb1.76
24-Ha2.08
25-H2.67 (dq, 10.8, 7.1)
27-Me1.32 (d, 7.2)
28-H4.34 (dq, 9.4, 6.1)
29-Me1.45 (d, 6.1)

PHYSICAL PROPERTIES

M.P.°C ;
[α]D20° (c ; MeOH)
IR (KBr) ν max (cm-1)
UV (EtOH) λ max (log ε)() ;

CHROMATOGRAPHY

GLC
HPLC
HPTLC
TLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationGUIBOUT, L. et al. (2015) Phytochemical Analysis 26, 293-300 Search more

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