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14-DEOXYECDYSONE

Year of first isolation: 1988
Formula:C27H44O5
Molecular weight:448
Occurence in plants:
 
Occurence in animals:
Mus musculus [Muridae] » Images of Mus musculus Wikipedia: Mus musculus [Muridae]
Gryllus bimaculatus [Orthoptera] » Images of Gryllus bimaculatus Wikipedia: Gryllus bimaculatus [Orthoptera]
metabolite of exogenous ecdysone » Images of metabolite of exogenous ecdysone
Locusta migratoria [Orthoptera] » Images of Locusta migratoria Wikipedia: Locusta migratoria [Orthoptera]
14-DEOXYECDYSONE

STRUCTURE DESCRIPTORS

Canonical SMILES 
Isomeric SMILES
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C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2CC[C@]2(C1CC[C@@H]2[C@H](C)[C@@H](CCC(C)(C)O)O)C)C  » JSMol: View in 3D
C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2CC[C@]2([C@H]1CC[C@@H]2[C@H](C)[C@@H](CCC(C)(C)O)O)C)C  » JSMol: View in 3D
C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2CC[C@]2([C@@H]1CC[C@@H]2[C@H](C)[C@@H](CCC(C)(C)O)O)C)C » JSMol: View in 3D
IUPAC Name(2S,3R,5R,9R,10R,13R,17R)-17-((2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl)-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-6H-cyclopenta[a]phenanthren-6-one
CAS-RN 
PubChem CID 
InChiKey
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GWHYLAWOMCRKRC-GVGVEOICSA-N
InChIInChI=1S/C27H44O5/c1-15(21(28)9-10-25(2,3)32)17-6-7-18-16-12-22(29)20-13-23(30)24(31)14-27(20,5)19(16)8-11-26(17,18)4/h12,15,17-21,23-24,28,30-32H,6-11,13-14H2,1-5H3/t15-,17+,18-,19-,20-,21+,23+,24-,26+,27+/m0/s1

MASS SPECTRUM

CI-MS (NH3) m/z466 (M+H+NH3)+, 449, 431, 413, 333, 315, 279
EI-MS m/z (relative intensity %) 
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-Ha1.43
01-He1.78
02-Ha3.84 (m, w1/2=22)
03-He3.94 (m, w1/2=8)
04-Ha1.65
04-He1.75
05-H2.38 (dd, 13,4)
07-H5.63 (t, ~2)
09-Ha2.69 (m, w1/2=22)
11-Ha 
11-He 
12-Ha1.55
12-He2.22
14-H2.2 (m )
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H1.48
18-Me0.68 (s )
19-Me0.97 (s )
21-Me0.99 (d, 6.5)
22-H3.58
23-Ha 
23-Hb 
24-Ha 
24-Hb 
26-Me1.19 (s )
27-Me1.20 (s )

PHYSICAL PROPERTIES

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

CHROMATOGRAPHY

HPTLC 
TLC 
GLC 
HPLCNP-HPLC [ Zorbax-Sil 250 mm x 4.6 mm i.d., flow-rate 1 ml.min-1] 1-Ret 9.6 min [solvent CH2Cl2-iPrOH-H2O 125:25:2 v/v/v] (E : 26 min); 2-Ret 11.6 min [solvent CH2Cl2-iPrOH-H2O 125:20:1.5 v/v/v] (E : 33.8 min); 3-Ret24.4 min [solvent isoC8-iPrOH-H2O 100:30:2 v/v/v] (E 31.2 min)RP-HPLC [Zorbax-ODS 250 mm x 4.6 mm i.d., solvent linear gradient 18% to 40% (in 30 min) of ACN in 0.1% TFA in H2O, flow-rate 1 ml. min-1] Ret 21.2 min (E : 14.8 min)

BIOLOGICAL ACTIVITIES

Calliphora assay: 7% (20-hydroxyecdysone = 100%)

REFERENCES

GeneralKERB, U. et al. (1966) Helv. Chim. Acta 49, 1601-1606 Search more
BioactivitiesBERGAMASCO, R. et al. (1980) In: Progress in Ecdysone Research (Ed. J.A. Hoffmann), Elsevier/North Holland Biomed. Press, Amsterdam 299-324 Search more
GeneralHAAG, T. et al. (1987) Insect Biochem. 17, 291-301 Search more
First isolationGIRAULT, J.-P. et al. (1988) Drug Metab. Dispos. 16, 716-720 Search more
GeneralTHIRY, E. et al. (1988) Dissertation thesis, University of Ulm, Search more
GeneralLAFONT, R. et al. (1988) Biochem. Pharmacol. 37, 1174-1177 Search more

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© 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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