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| Year of first isolation: | 1982 |  | Formula: | C37H56O12N5P |  | Molecular weight: | 792 |  | Occurence in plants: |  |  |  | Occurence in animals: |  | Locusta migratoria [Orthoptera] »   ![Wikipedia: Locusta migratoria [Orthoptera]](/images/wikipedia.png) 
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 | | Canonical SMILES |  |  | Isomeric SMILES [ PubChem: search | XML ]
 [ ChemSpider: search ]
 | 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] »  
 |  | 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-RN | 94036-01-8 |  | PubChem CID |  |  | InChiKey [ ChemIDPlus: search ]
 | JPGNGCBJGFLVNO-HNJBQQIFSA-N |  | InChI | InChI=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 | 
 
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 | | CI-MS (NH3) m/z |  |  | EI-MS m/z (relative intensity %) |  |  | HR-MS | MS-Laser ionization m/z: 79 (PO3)-, 63 (PO2)- | 
 
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 | | 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-Me | 0.72 (s ) |  | 19-Me | 0.96 (s ) |  | 21-Me | 0.92 (d, 6.4) |  | 22-H |  |  | 23-Ha |  |  | 23-Hb |  |  | 24-Ha |  |  | 24-Hb |  |  | 26-Me | 1.20 (s ) |  | 27-Me | 1.20 (s ) |  | aromatic | 7.4 (2H) | 
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 | | M.P. |  |  | [α]D20 |  |  | IR (KBr) ν max (cm-1) |  |  | UV (EtOH) λ max (log ε) |  | 
 
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 | | HPTLC |  |  | TLC |  |  | GLC |  |  | HPLC | Retention 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] | 
 
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 | | First isolation | TSOUPRAS, G. et al. (1982) Thesis, Strasbourg, France |  |  | General | LAGUEUX, 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 |  | 
 
 |  | Permanent link to this datasheet: ECDYSONE 22-ADENOSINE-MONOPHOSPHATE |  |