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AJUGASTERONE C 2,3;20,22-DIACETONIDE

Year of first isolation: 2001
Formula:C33H52O7
Molecular weight:560
Occurence in plants:
Rhaponticum uniflorum [Asteraceae] » Images of Rhaponticum uniflorum Wikipedia: Rhaponticum uniflorum [Asteraceae]
Occurence in animals:
 
AJUGASTERONE C 2,3;20,22-DIACETONIDE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C)CCC1C(OC(O1)(C)C)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC6C(C5)OC(O6)(C)C)C)O)C)O
Isomeric SMILES
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C1[C@]2([C@@H](C[C@@H]3[C@H]1OC(O3)(C)C)C(=O)C=C1[C@@H]2[C@@H](C[C@]2([C@]1(CCC2[C@]1(C)[C@@H](CCC(C)C)OC(O1)(C)C)O)C)O)C » JSMol: View in 3D
IUPAC Name(1R,2R,4S,8R,10R,14S,17S,18R,20R)-14,20-dihydroxy-2,6,6,18-tetramethyl-17-[(4R,5R)-2,2,4-trimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-5,7-dioxapentacyclo[11.7.0.02,10.04,8.014,18]icos-12-en-11-one
CAS-RN 
PubChem CID12044242
InChiKey
[ ChemIDPlus: search ]
PAYRGVCZJJHSFE-MPQXGJTKSA-N
InChIInChI=1S/C33H52O7/c1-18(2)10-11-26-32(9,40-29(5,6)39-26)25-12-13-33(36)20-14-21(34)19-15-23-24(38-28(3,4)37-23)17-30(19,7)27(20)22(35)16-31(25,33)8/h14,18-19,22-27,35-36H,10-13,15-17H2,1-9H3/t19-,22+,23+,24-,25-,26+,27+,30-,31+,32+,33+/m0/s1

MASS SPECTRUM

HR-MS
EI-MS m/z (relative intensity %)560 [M]+, 545 [M-CH3]+, 542 [M-H2O]+, 502, 484, 460, 410, 379, 361, 357, 325, 317, 306, 299, 185, 142, 127
CI-MS (NH3) m/z

CARBON NMR

PROTON NMR

CD3OD
0139.98
0272.64
0371.59
0436.35
0552.09
06203.29
07122.13
08161.14
0941.88
1038.58
1168.09
1242.39
1347.14
1484.42
1531.65
1621.16
1748.79
1817.70
1923.59
2083.90
2121.84
2281.57
2327.12
2436.38
2528.22
2622.45
2722.58
Me26.76, 26.83, 29.04, 30.87
O-C-O108.09, 106.81
CDCl3
01-Ha 
01-He 
02-Ha4.52 (m)
03-He4.29 (m)
04-Ha 
04-He 
05-H 
07-H5.84 (d, 2.4)
09-H2.83 (m)
11-He4.12 (m)
12-Ha 
12-He 
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H 
18-Me0.78 (s)
19-Me1.04 (s)
21-Me1.16 (s)
22-H3.60 (m)
23-Ha 
23-Hb 
24-Ha 
24-Hb 
25-H 
26-Me0.90 (d, 6.5)
27-Me0.90 (d, 6.5)
Me-ketals1.32 (s), 1.38 (s), 1.41 (s), 1.49 (s)

PHYSICAL PROPERTIES

M.P.134-136 °C ;
[α]D20+ 58.2 ? ° (c ; MeOH)
IR (KBr) ν max (cm-1)3431, 1662, 1459, 1056
UV (MeOH) λ max (log ε)243 (-) ;

CHROMATOGRAPHY

HPLC
GLC
HPTLC
TLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationZHANG, Y.-H. et al. (2001) Pharmazie 56(10), 828-829 Search more
GeneralCHENG, J.K. et al. (2002) Gaodeng Xuexiao Huaxue Xuebao 23(11), 2084-2088 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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