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ACHYRANTHESTERONE A

Year of first isolation: 2005
Formula:C27H44O8
Molecular weight:496
Occurence in plants:
Achyranthes bidentata [Amaranthaceae] » Images of Achyranthes bidentata Wikipedia: Achyranthes bidentata [Amaranthaceae]
Occurence in animals:
 
ACHYRANTHESTERONE A

STRUCTURE DESCRIPTORS

Canonical SMILESCC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(CO)(C(CCC(C)(C)O)O)O)O
Isomeric SMILES
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[ ChemSpider: search ]
C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2CC[C@]2([C@]1(CC[C@@H]2[C@](CO)([C@@H](CCC(C)(C)O)O)O)O)C)C » JSMol: View in 3D
IUPAC Name(2S,3R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,3R)-1,2,3,6-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID90910301
InChiKey
[ ChemIDPlus: search ]
UYDQOOHBGRAEBT-QZELUQRGSA-N
InChIInChI=1S/C27H44O8/c1-23(2,33)8-7-22(32)26(34,14-28)21-6-10-27(35)16-11-18(29)17-12-19(30)20(31)13-24(17,3)15(16)5-9-25(21,27)4/h11,15,17,19-22,28,30-35H,5-10,12-14H2,1-4H3/t15-,17?,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1

MASS SPECTRUM

ESI-MS m/z (positive ions)497.1 [M+H]+, 479.0 [M+H-H2O], 461.0 [M+H-2H2O], 443.1 [M+H-3H2O], 425.1 [M+H-4H2O]
HR-MS
EI-MS m/z (relative intensity %)

CARBON NMR

PROTON NMR

C5D5N
0138.0
0268.2
0368.1
0432.4
0551.4
06203.5
07121.8
08165.9
0934.5
1038.7
1121.1
1231.6
1347.8
1484.3
1531.4
1621.6
1747.9
1817.9
1924.5
2078.6
2166.8
2278.8
2327.9
2442.8
2569.8
2630.0
2730.1
C5D5N
01-Ha1.90 (m)
01-He2.10 (m)
02-Ha4.18 (m)
03-He4.22 (m)
04-Ha1.88 (m)
04-He1.98 (m)
05-H3.00 (dd, 3, 12)
07-H6.25 (d, 3)
09-H3.60 (m)
11-Ha1.68 (m)
11-He1.80 (m)
12-Ha2.16 (m)
12-He1.96 (m)
15-Ha2.56 (m)*
15-Hb1.96 (m)*
16-Ha2.51 (m)$
16-Hb2.08 (m)$
17-H3.11 (m)
18-Me1.20 (s)
19-Me1.02 (s)
21-CH20H4.42 (d, 19.2), 4.39 (d, 19.2)
22-H4.08 (m)
23-Ha2.34 (m)
23-Hb2.18 (m)
24-Ha2.32 (m)
24-Hb1.84 (m)
26-Me1.35 (s)
27-Me1.35 (s)

PHYSICAL PROPERTIES

M.P.> 300 °C ;
[α]D30+ 13.0 ° (c 0.001; MeOH)
IR (KBr) ν max (cm-1)
UV (MeOH) λ max (log ε)240.8 nm

CHROMATOGRAPHY

HPLC
GLC
HPTLC
TLC

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationMENG, D.-L. et al. (2005) J. Asian Nat. Prod. Res. 7(2), 181-184 Search more

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