Welcome to online ecdysteroids database ! . .
Access data · History · Contact

2-DEOXYECDYSONE

Year of first isolation: 1970
Formula:C27H44O5
Molecular weight:448
Occurence in plants:
Blechnum minus [Blechnaceae] » Images of Blechnum minus Wikipedia: Blechnum minus [Blechnaceae]
Occurence in animals:
Bombyx mori [Bombycidae] » Images of Bombyx mori Wikipedia: Bombyx mori [Bombycidae]
Locusta migratoria [Orthoptera] » Images of Locusta migratoria Wikipedia: Locusta migratoria [Orthoptera]
Schistocerca gregaria [Orthoptera] » Images of Schistocerca gregaria Wikipedia: Schistocerca gregaria [Orthoptera]
2-DEOXYECDYSONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CCC(C4)O)C)C)O)C(CCC(C)(C)O)O
Isomeric SMILES
[ PubChem: search | XML ]
[ ChemSpider: search ]
C1[C@]2([C@@H](C[C@H](C1)O)C(=O)C=C1[C@@H]2CC[C@]2([C@]1(CC[C@@H]2[C@H](C)[C@@H](CCC(C)(C)O)O)O)C)C » JSMol: View in 3D
IUPAC Name(3S,5R,9R,10R,13R,14S,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-3,14-dihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
CAS-RN31575-91-4
PubChem CID13939876
InChiKey
[ ChemIDPlus: search ]
CRAPXAGGASWTPU-VQOIUDCISA-N
InChIInChI=1S/C27H44O5/c1-16(22(29)9-10-24(2,3)31)18-8-13-27(32)20-15-23(30)21-14-17(28)6-11-25(21,4)19(20)7-12-26(18,27)5/h15-19,21-22,28-29,31-32H,6-14H2,1-5H3/t16-,17-,18+,19-,21-,22+,25+,26+,27+/m0/s1

MASS SPECTRUM

CI-MS (NH3) m/z466 (M+H+NH3)+, 449 (MH)+, 431, 415, 413, 333, 315
EI-MS m/z448, 430, 412, 361, 332, 314, 284, 99, 81
HR-MS 

CARBON NMR

PROTON NMR

C5D5N
0129.48 (t )
0229.07 (t )
0364.06 (d )
0433.07 (t )
0551.61 (d )
06203.20 (s )
07121.30 (d )
08166.01 (s )
0934.40 (d )
1036.96 (s )
1121.00 (t )
1231.70 (t )
1348.00 (s )
1484.01 (s )
1531.70 (t )
1625.50 (t )
1748.32 (d )
1815.80 (q )
1924.30 (q )
2042.99 (d )
2113.60 (q )
2273.90 (d )
2326.70 (t )
2442.46 (t )
2569.60 (s )
2629.98 (q )
2730.20 (q )
CD3OD
01-Ha 
01-He 
02-Ha 
03-He4.09 (m, w1/2=22)
04-Ha 
04-He 
05-H2.41 (dd, 12, 4)
07-H5.96 (d, 2)
09-Ha3.14 (m, w1/2=22)
11-Ha 
11-He 
12-Ha 
12-He 
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H2.02 (m )
18-Me0.74 (s )
19-Me0.98 (s )
21-Me0.94 (d, 6.5)
22-H3.69 (m, w1/2=16)
23-Ha 
23-Hb 
24-Ha 
24-Hb 
26-Me1.24 (s )
27-Me1.24 (s )
C5D5N
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-Me0.74 (s )
19-Me1.05 (s )
21-Me1.28 (d, 7)
22-H 
23-Ha 
23-Hb 
24-Ha 
24-Hb 
26-Me1.38 (s )
27-Me1.38 (s )

PHYSICAL PROPERTIES

M.P.231-232 °C ;
[α]D20 
IR (KBr) ν max (cm-1)3450 (OH), 1650 (cyclohexenone)
UV (EtOH) λ max (log ε)244 (4,111) ;

CHROMATOGRAPHY

TLC(silica plates) Rf 0.43 (solvent : EtOAc-MeOH-NH4OH 85:10:5 v/v/v) (20E : 0.18); Rf 0.40 (solvent : CH2Cl2-EtOH 85:15 v/v) (20E : 0.15); Rf 0.38 (solvent CHCl3-EtOH 4:1 v/v) (20E :0.15) RP-TLC (C18 bonded silica gel) Rf 0.19 (solvent MeOH-H2O 65:35 v/v) (20E : 0.47)
GLCas TMS ether on 1.5% OV101, 285°C, derivatized for 5h at 120°C, retention time 5.9 min (E : 6.9 min).
HPLCNP-HPLC, Retention time 11.6 min [Zorbax-Sil 250 mm x 4.6 mm i.d., solvent CH2Cl2- iPrOH-H2O, 125:25:2 v/v/v, flow-rate 1 ml.min-1] (20E 37.4 min); RP-HPLC, Retention time 34.1 min [Spherisorb-5ODS2 250 mm x 4.6 mm i.d., solvent ACN-0.1% TFA 23:77 v/v, flow-rate 1 ml.min-1] (20E : 5.5 min)

BIOLOGICAL ACTIVITIES

Drosophila melanogaster BII cell assay: EC50 = 5.0 x 10-5M
Drosophila melanogaster BII cell assay: EC50 = 2.0 x 10-5M
Galleria mellonella in vivo assay: ED50 = 15.6 ug/g
Sarcophaga bullata in vivo assay: ED50 = 31.3 ug/g
Calliphora assay: 100% (20-hydroxyecdysone = 100%)

REFERENCES

First isolationCHONG, Y.K. et al. (1970) J. Chem. Soc., Chem. Commun., 1217-1218 Search more
First isolationOHNISHI, E. et al. (1971) Science 197, 66-67 Search more
GeneralGALBRAITH, M.N. et al. (1975) Experientia 31, 873 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
GeneralWILSON, I.D. et al. (1985) J. Chromatogr. 318, 373-377 Search more
GeneralDIEHL, P.A. et al. (1985) Methods Enzymol. 111, 377-410 Search more
GeneralHETRU, C. et al. (1985) Methods Enzymol. 111, 411-419 Search more
GeneralBIELBY, C.R. et al. (1986) J. Chromatogr. 351, 57-64 Search more
GeneralGIRAULT, J.-P. et al. (1990) J. Nat. Prod. 53, 279-293 Search more
BioactivitiesSLÁMA, K. et al. (1993) Insect Biochem. Molec. Biol. 23, 181-185 Search more
BioactivitiesDINAN, L. et al. (1999) J. Computer-aided Mol. Design 13, 185-207 Search more
BioactivitiesDINAN, L. et al. (2003) In: Studies in Natural Products Chemisty (ed. Atta-ur-Rahman), Elsevier, Amsterdam, 29, 3-71 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
designed by Cybersales a.s.
Powered by Cybersales
PRINTER READY | MEDIUM | WIDE