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| Year of first isolation: | 1975 |  | Formula: | C27H44O8 |  | Molecular weight: | 496 |  | Occurence in plants: |  | Ajuga turkestanica [Lamiaceae (alt. Labiatae)] »   ![Wikipedia: Ajuga turkestanica [Lamiaceae (alt. Labiatae)]](/images/wikipedia.png) Vitex glabrata [Lamiaceae (alt. Labiatae)] »
   ![Wikipedia: Vitex glabrata [Lamiaceae (alt. Labiatae)]](/images/wikipedia.png) Vitex canescens [Lamiaceae (alt. Labiatae)] »
   ![Wikipedia: Vitex canescens [Lamiaceae (alt. Labiatae)]](/images/wikipedia.png) Tapinella panuoides [Fungi] »
   ![Wikipedia: Tapinella panuoides [Fungi]](/images/wikipedia.png) Leuzea carthamoides [Asteraceae] »
   ![Wikipedia: Leuzea carthamoides [Asteraceae]](/images/wikipedia.png) 
 |  | Occurence in animals: |  |  |  |   |  |
 | | Canonical SMILES | CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O |  | Isomeric SMILES [ PubChem: search | XML ]
 [ ChemSpider: search ]
 | C1[C@]2([C@@H](C[C@H]([C@H]1O)O)C(=O)C=C1[C@@H]2[C@@H](C[C@]2([C@]1(CC[C@@H]2[C@](C)([C@@H](CCC(C)(C)O)O)O)O)C)O)C »  
 |  | IUPAC Name | (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one |  | CAS-RN | 41451-87-0 |  | PubChem CID | 14376672 |  | InChiKey [ ChemIDPlus: search ]
 | WSBAGDDNVWTLOM-XHZKDPLLSA-N |  | InChI | InChI=1S/C27H44O8/c1-23(2,33)8-7-21(32)26(5,34)20-6-9-27(35)15-11-16(28)14-10-17(29)18(30)12-24(14,3)22(15)19(31)13-25(20,27)4/h11,14,17-22,29-35H,6-10,12-13H2,1-5H3/t14-,17+,18-,19+,20-,21+,22+,24-,25+,26+,27+/m0/s1 | 
 
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 | | CI-MS (NH3) m/z |  |  | EI-MS m/z (relative intensity %) | 460 [M-2H2O], 442, 424, 409, 379, 361, 343, 325, 300, 143, 125, 99, 81, 69. |  | HR-MS |  | 
 
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 | | C5D5N |  | 01 | 39.6 |  | 02 | 68.0 * |  | 03 | 68.2 * |  | 04 | 32.6 |  | 05 | 52.5 |  | 06 | 204.0 |  | 07 | 122.1 |  | 08 | 164.2 |  | 09 | 42.4 |  | 10 | 39.3 |  | 11 | 68.7 * |  | 12 | 43.9 |  | 13 | 48.0 |  | 14 | 84.1 |  | 15 | 31.7 |  | 16 | 21.4 |  | 17 | 49.8 |  | 18 | 18.7 |  | 19 | 24.6 |  | 20 | 76.7 |  | 21 | 21.4 |  | 22 | 77.4 |  | 23 | 27.2 |  | 24 | 42.5 |  | 25 | 69.5 |  | 26 | 29.8 |  | 27 | 29.8 | 
 | CD3OD |  | 01 | 39.09 |  | 02 | 68.94 |  | 03 | 68.57 |  | 04 | 33.28 |  | 05 | 52.78 |  | 06 | 206.66 |  | 07 | 122.74 |  | 08 | 165.74 |  | 09 | 42.94 |  | 10 | 39.91 |  | 11 | 69.51 |  | 12 | 43.79 |  | 13 | a |  | 14 | 84.87 |  | 15 | 31.86 |  | 16 | 21.52 |  | 17 | 50.35 |  | 18 | 18.89 |  | 19 | 24.62 |  | 20 | 77.83 |  | 21 | 21.02 |  | 22 | 78.42 |  | 23 | 27.35 |  | 24 | 42.40 |  | 25 | 71.29 |  | 26 | 29.73 |  | 27 | 28.95 | 
 | | C5D5N |  | 01-Ha |  |  | 01-He |  |  | 02-Ha | 4.45 |  | 03-He | 4.06 |  | 04-Ha |  |  | 04-He |  |  | 05-H |  |  | 07-H | 6.12 |  | 09-Ha | 3.75 |  | 11-Ha | 4.45 |  | 12-Ha |  |  | 12-He |  |  | 15-Ha |  |  | 15-Hb |  |  | 16-Ha |  |  | 16-Hb |  |  | 17-H |  |  | 18-Me | 1.12 (s ) |  | 19-Me | 1.18 (s ) |  | 21-Me | 1.45 (s ) |  | 22-Hb | 3.75 |  | 23-Ha |  |  | 23-Hb |  |  | 24-Ha |  |  | 24-Hb |  |  | 26-Me | 1.24 (s ) |  | 27-Me | 1.24 (s ) | 
 | CD3OD |  | 01-Ha | 1.38 (dd, 13.0, 12.0) |  | 01-He | 2.59 dd, 13.0, 4.3) |  | 02-Ha | 4.01 (ddd, 12.0, 4.3, 3.4) |  | 03-He | 3.95 (q ) |  | 04-Ha | 1.78 |  | 04-He | 1.68 (dt, 14.2, 3.9, 3.5) |  | 05-H | 2.33 (dd, 13.2, 3.9) |  | 07-H | 5.80 (dd, 2.6, 1.0) |  | 09-Ha | 3.15 (dd, 9.0, 2.6) |  | 11-Ha | 4.10 (ddd, 10.6, 9.0, 6.2) |  | 12-Ha | 2.22 (dd, 12.4, 10.6) |  | 12-He | 2.16 (dd, 12.4, 6.2) |  | 15-Ha | 1.95 |  | 15-Hb | 1.58 |  | 16-Ha | 2.00 |  | 16-Hb | 1.75 |  | 17-H | 2.43 |  | 18-Me | 0.877 (s ) |  | 19-Me | 1.057 (s ) |  | 21-Me | 1.193 (s ) |  | 22-Hb | 3.32 (dd, 11.0, 1.8) |  | 23-Ha | 1.66 |  | 23-Hb | 1.29 |  | 24-Ha | 1.80 |  | 24-Hb | 1.43 (ddd, 13.6, 11.6, 4.3) |  | 26-Me | 1.206 (s ) |  | 27-Me | 1.220 (s ) | 
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 | | M.P. |  |  | [α]D20 |  |  | IR (KBr) ν max (cm-1) | 3300-3500 (OH), 1660 (CO) |  | UV (EtOH) λ max (log ε) | 244 (3.95) | 
 
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 | | NP-HPLC | column Silasorb 600 (4 x 250 mm), flow-rate 0.8 ml.min-1, solvent Et2O-hexane-MeOH-H2O (440:430:120:10), Ret 97.9 min (20E 47.5 min) |  | HPTLC |  |  | TLC |  |  | GLC |  |  | RP-HPLC | column Separon SIX C18 (4 x 250 mm), solvent MeOH-H2O, linear gradient 10 to 70 % MeOH in 50 min, flow-rate 0.6 ml.min-1, Ret 33.9 min (20E 42.7 min). | 
 
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 | | Drosophila melanogaster BII cell assay: EC50 = 1.3 x 10-6M |  | Drosophila melanogaster BII cell assay: EC50 = 3.0 x 10-7M |  | Drosophila melanogaster BII cell assay: EC50 = 8.0 x 10-7M |  | Galleria mellonella in vivo assay: ED50 = 62.5 ug/g |  | Sarcophaga bullata in vivo assay: ED50 = 0.3 ug/g |  | Dermestes vulpinus in vivo assay: ED50 = 4.2 ug/g | 
 
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 | | First isolation | USMANOV, B.Z. et al. (1975) Khim. Prir. Soedin. 466-470 |  |  | General | WERAWATTANAMETIN, K. et al. (1986) J. Nat. Prod. 49, 365-366 |  |  | Bioactivities | CLEMENT, C.Y. et al. (1993) Insect Biochem. Molec. Biol. 23, 187-193 |  |  | Bioactivities | SLÁMA, K. et al. (1993) Insect Biochem. Molec. Biol. 23, 181-185 |  |  | General | SUKSAMRARN, A. et al. (1997) Phytochemistry 45, 1149-1152 |  |  | Identification | VOKÁČ, K. et al. (1998) Phytochemistry 49, 2109-2114 |  |  | Bioactivities | DINAN, L. et al. (1999) J. Computer-aided Mol. Design 13, 185-207 |  |  | Bioactivities | DINAN, L. et al. (2005) In: Comprehensive Molecular Insect Science (eds. L. I. Gilbert, C. Iatrou, S. Gill), Elsevier, Oxford, III, 197-242 |  |  | General | BUDĚŠÍNSKÝ, M. et al. (2008) Steroids 73, 502-514 |  | 
 
 |  | Permanent link to this datasheet: TURKESTERONE |  |