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ECDYSONE 3-ACETATE 2-PHOSPHATE

Year of first isolation: 1984
Formula:C29H47O10P
Molecular weight:586
Occurence in plants:
 
Occurence in animals:
Schistocerca gregaria [Orthoptera] » Images of Schistocerca gregaria Wikipedia: Schistocerca gregaria [Orthoptera]
ECDYSONE 3-ACETATE 2-PHOSPHATE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC(=O)C)OP(=O)(O)O)C)C)O)C(CCC(C)(C)O)O
Isomeric SMILES
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C[C@@H]([C@H]1CC[C@@]2([C@@]1(CC[C@H]3C2=CC(=O)[C@H]4[C@@]3(C[C@@H]([C@@H](C4)OC(=O)C)OP(=O)(O)O)C)C)O)[C@@H](CCC(C)(C)O)O » JSMol: View in 3D
IUPAC Name[(2S,3R,5R,9R,10R,13R,14S,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-10,13-dimethyl-6-oxo-2-phosphonooxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
CAS-RN 
PubChem CID23657836
InChiKey
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MYOZIWALDKJCBG-KXCOSXAXSA-N
InChIInChI=1S/C29H47O10P/c1-16(22(31)9-10-26(3,4)33)18-8-12-29(34)20-13-23(32)21-14-24(38-17(2)30)25(39-40(35,36)37)15-27(21,5)19(20)7-11-28(18,29)6/h13,16,18-19,21-22,24-25,31,33-34H,7-12,14-15H2,1-6H3,(H2,35,36,37)/t16-,18+,19-,21-,22+,24+,25-,27+,28+,29+/m0/s1

MASS SPECTRUM

CI-MS (NH3) m/z 
EI-MS m/z (relative intensity %) 
FAB-MS m/z585 (M-H)-, 97 (H2PO4)-, 79 (PO3)-
HR-MS 

CARBON NMR

PROTON NMR

C5D5N
01 
02 
03 
04 
05 
06 
07 
08 
09 
10 
11 
12 
13 
14 
15 
16 
17 
18 
19 
20 
21 
22 
23 
24 
25 
26 
27 
CD3OD
01-Ha 
01-He 
02-Ha 
03-He 
04-Ha 
04-He 
05-H5.82
07-H 
09-Ha 
11-Ha 
11-He 
12-Ha 
12-He 
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H 
18-Me0.73 (s )
19-Me1.00 (s )
20-H 
21-Me0.94 (d, 6)
22-H3.58 (m, w1/2=16)
23-Ha 
23-Hb 
24-Ha 
24-Hb 
26-Me1.19 (s )
27-Me1.20 (s )
O-Ac2.09 (s )

PHYSICAL PROPERTIES

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

CHROMATOGRAPHY

HPTLC 
TLC 
GLC 
HPLC1-Retention volume 50 ml [column Partisil-ODS3, 25 cm long, 4.6 mm i.d., eluted with a linear gradient (30 min) of MeOH in 20 mM sodium citrate, pH 6.5, from 1:9 to 7:3, flow-rate 2 ml.min-1]; 2-Retention volume 35 ml [column Partisil-ODS3, 25 cm long, 4.6 mm i.d., eluted with a linear gradient (30 min) of MeOH in H2O from 1:19 to 1:1, flow rate 2 ml.min-1]; 3-Ret-ention volume 30 ml [column Partisil-SAX, 25 cm long, 4.6 mm i.d., eluted with 0.1M ammonium acetate, flow rate 2 ml.min-1]

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationISAAC, R.E. et al. (1984) Biochem. J. 217, 239-243 Search more
GeneralDIEHL, P.A. et al. (1985) Methods Enzymol. 111, 377-410 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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