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ECDYSONE 22-ADENOSINE-MONOPHOSPHATE

Year of first isolation: 1982
Formula:C37H56O12N5P
Molecular weight:792
Occurence in plants:
 
Occurence in animals:
Locusta migratoria [Orthoptera] » Images of Locusta migratoria Wikipedia: Locusta migratoria [Orthoptera]
ECDYSONE 22-ADENOSINE-MONOPHOSPHATE

STRUCTURE DESCRIPTORS

Canonical SMILES 
Isomeric SMILES
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C[C@]12[C@@]([H])(C[C@H]([C@H](C2)[O][H])[O][H])C(C=C3C1CC[C@]4([C@]3(CC[C@@]4([C@H](C)[C@@H](CCC([O][H])(C)C)[O][P]([O]C[C@H]5[O][C@H]([C@@H]([C@@H]5[O][H])[O][H])[N]6C=[N]C7=C6[N]=C[N]=C7[N]([H])[H])([O][H])=[O])[H])[O][H])C)=[O] » JSMol: View in 3D
IUPAC Name((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2S,3R)-6-hydroxy-6-methyl-2-((2S,3R,5R,10R,13R,14S,17R)-2,3,14-trihydroxy-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)heptan-3-yl) hydrogen phosphate
CAS-RN94036-01-8
PubChem CID 
InChiKey
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JPGNGCBJGFLVNO-HNJBQQIFSA-N
InChIInChI=1S/C37H56N5O12P/c1-18(19-7-11-37(49)21-12-23(43)22-13-24(44)25(45)14-35(22,4)20(21)6-10-36(19,37)5)26(8-9-34(2,3)48)54-55(50,51)52-15-27-29(46)30(47)33(53-27)42-17-41-28-31(38)39-16-40-32(28)42/h12,16-20,22,24-27,29-30,33,44-49H,6-11,13-15H2,1-5H3,(H,50,51)(H2,38,39,40)/t18-,19+,20?,22-,24+,25-,26+,27+,29+,30+,33+,35+,36+,37+/m0/s1

MASS SPECTRUM

CI-MS (NH3) m/z 
EI-MS m/z (relative intensity %) 
HR-MSMS-Laser ionization m/z: 79 (PO3)-, 63 (PO2)-

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 
D2O
01-Ha 
01-He 
02-Ha 
03-He 
04-Ha 
04-He 
05-H 
07-H 
09-Ha 
11-Ha 
11-He 
12-Ha 
12-He 
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H 
18-Me0.72 (s )
19-Me0.96 (s )
21-Me0.92 (d, 6.4)
22-H 
23-Ha 
23-Hb 
24-Ha 
24-Hb 
26-Me1.20 (s )
27-Me1.20 (s )
aromatic7.4 (2H)

PHYSICAL PROPERTIES

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

CHROMATOGRAPHY

HPTLC 
TLC 
GLC 
HPLCRetention time 17 min [column Lichroprep C18 10 ?m, 250 mm long, 4 mm i.d., eluted with a gradient 12% to 44% (in 32 min, gradient former Waters M660, curve 7) of acetonitrile in 20 mM tris-HCl, pH 7.5, flow-rate 1 ml.min-1]

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationTSOUPRAS, G. et al. (1982) Thesis, Strasbourg, France Search more
GeneralLAGUEUX, M. et al. (1984) In: Biosynthesis, Metabolism and Mode of Action of Invertebrate Hormones (eds., Hoffmann J.A., Porchet M.), Springer-Verlag, Berlin, pp. 168-180 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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