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

CYATHISTERONE

Year of first isolation: 1994
Formula:C28H42O2
Molecular weight:410
Occurence in plants:
Calvatia cyathiformis [Fungi] » Images of Calvatia cyathiformis Wikipedia: Calvatia cyathiformis [Fungi]
Occurence in animals:
 
CYATHISTERONE

STRUCTURE DESCRIPTORS

Canonical SMILESCC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC(=O)C4C3(CCC(=O)C4)C)C
Isomeric SMILES
[ PubChem: search | XML ]
[ ChemSpider: search ]
C1[C@]2(C(CC(=O)C1)C(=O)C=C1[C@@H]2CC[C@]2(C1CC[C@@H]2[C@H](C)/C=C/[C@@H](C(C)C)C)C)C  » JSMol: View in 3D
C1[C@]2([C@@H](CC(=O)C1)C(=O)C=C1[C@@H]2CC[C@]2([C@@H]1CC[C@@H]2[C@H](C)/C=C/[C@@H](C(C)C)C)C)C  » JSMol: View in 3D
C1[C@]2([C@@H](CC(=O)C1)C(=O)C=C1[C@@H]2CC[C@]2([C@H]1CC[C@@H]2[C@H](C)/C=C/[C@@H](C(C)C)C)C)C  » JSMol: View in 3D
C1[C@]2([C@H](CC(=O)C1)C(=O)C=C1[C@@H]2CC[C@]2([C@H]1CC[C@@H]2[C@H](C)/C=C/[C@@H](C(C)C)C)C)C  » JSMol: View in 3D
C1[C@]2([C@H](CC(=O)C1)C(=O)C=C1[C@@H]2CC[C@]2([C@@H]1CC[C@@H]2[C@H](C)/C=C/[C@@H](C(C)C)C)C)C » JSMol: View in 3D
IUPAC Name(5S,9R,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,4,5,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,6-dione
CAS-RN 
PubChem CID70698238
InChiKey
[ ChemIDPlus: search ]
AGFWEYQAOQMEEO-KRGQBHGKSA-N
InChIInChI=1S/C28H42O2/c1-17(2)18(3)7-8-19(4)22-9-10-23-21-16-26(30)25-15-20(29)11-13-28(25,6)24(21)12-14-27(22,23)5/h7-8,16-19,22-25H,9-15H2,1-6H3/b8-7+/t18-,19+,22+,23-,24-,25+,27+,28+/m0/s1

MASS SPECTRUM

CI-MS (NH3) m/z 
EI-MS m/z (relative intensity %)410.3193 [M]+ (C28H42O2 requires 410.3185) (14), 285 [M - C9H17]+ (12), 259 (23), 109 (43).
HR-MS 

CARBON NMR

PROTON NMR

CDCl3
0138.3 (t)
0237.4 (t)
03211.7 (s)
0437.2 (t)
0554.8 (d)
06199.0 (s)
07123.3 (d)
08164.4 (s)
0949.9 (d)
1038.5 (s)
1122.1 (t)
1238.8 (t)
1344.7 (s)
1456.0 (d)
1522.7 (t)
1628.0 (t)
1756.3 (d)
1812.7 (q)
1912.9 (q)
2040.4 (d)
2121.2 (q)
22135.4 (d)
23133.1 (d)
2443.0 (d)
2533.2 (d)
2620.0 (q)
2719.7 (q)
2817.7 (q)
CDCl3
01-Ha 
01-He 
02-Ha 
02-He 
04-Ha2.56 (dd, 4.0, 15.5)
04-He2.60 (dd, 12.5, 15.5)
05-H2.66 (dd, 4.0, 12.5)
07-H5.78 (br t, 2.2)
09-H 
11-Ha 
11-He 
12-Ha 
12-He 
14-H 
15-Ha 
15-Hb 
16-Ha 
16-Hb 
17-H 
18-Me0.65 (s)
19-Me1.07 (s)
20-H 
21-Me1.05 (d, 6.6)
22-H5.17 (dd, 7.7, 15.3)
23-H5.27 (dd, 7.8, 15.3)
24-H 
25-H 
26-Me0.83 (d, 6.8)
27-Me0.84 (d, 6.8)
28-Me0.92 (d, 6.8)

PHYSICAL PROPERTIES

M.P.200-203 °C ;
[α]D25+ 12 ? ° (c 0.17; CHCl3)
IR (KBr) ν max (cm-1)1720 (CO), 1660 (CO)
UV (MeOH) λ max (log ε)242 (4.45) ;

CHROMATOGRAPHY

HPTLC 
TLC 
GLC 
HPLC 

BIOLOGICAL ACTIVITIES

 

REFERENCES

First isolationKAWAHARA, N. et al. (1994) Phytochemistry 37, 213-215 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