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II.4.1 Mol fayllar

Nomi

Tuzilishi

























































































Mol fayl

HIN fayl

























Mos mol fayl

Mos HIN fayl

II.5.InChI va biologik aktivligi jadvali



compounds

InChi

HBL100




Jaborosalactol 28

InChI=1S/C30H40O7/c1-15(22-14-27(3)30(6,37-27)26(34)36-22)25-21(35-16(2)31)12-19-18-11-10-17-8-7-9-23(32)28(17,4)20(18)13-24(33)29(19,25)5/h7,9-10,15,18-22,25-26,34H,8,11-14H2,1-6H3/t15-,18+,19+,20+,21-,22-,25+,26-,27+,28+,29-,30-/m1/s1

34





Jaborosalactone R



InChI=1S/C28H36O7/c1-14-10-22(35-24(31)15(14)2)20-13-34-28(33)12-19-16(17-8-9-27(20,32)26(17,28)4)11-21(29)18-6-5-7-23(30)25(18,19)3/h5-7,16-17,19-22,29,32-33H,8-13H2,1-4H3/t16-,17-,19-,20+,21+,22+,25-,26-,27+,28-/m0/s1


35






Jaborosalactone 38


InChI=1S/C28H36O7/c1-14-10-20(34-23(30)15(14)2)19-13-33-28(32)12-18-16(17-7-9-26(19,31)25(17,28)4)11-22-27(35-22)8-5-6-21(29)24(18,27)3/h5-6,16-20,22,31-32H,7-13H2,1-4H3/t16-,17-,18-,19+,20+,22+,24-,25-,26+,27+,28-/m0/s1



4.0




Jaborosalactone 45

InChI=1S/C28H36O6/c1-15-12-22(34-24(30)16(15)2)21-14-33-28(32)13-20-18(19-10-11-27(21,31)26(19,28)4)9-8-17-6-5-7-23(29)25(17,20)3/h5,7-8,18-22,31-32H,6,9-14H2,1-4H3/t18-,19-,20-,21+,22+,25-,26-,27+,28-/m0/s1

24




11

0

90




12

0

33




13

0

4.7




14

0

6.0




Jaborosalactone 2

InChI=1S/C28H34O7/c1-13-15(3)28(35-23(13)32)22(31)14(2)17-8-9-18-16-11-21(30)26(33)10-6-7-20(29)25(26,5)19(16)12-27(28,34)24(17,18)4/h6-7,16,18-19,21,30,33-34H,8-12H2,1-5H3/t16-,18-,19-,21+,24+,25-,26-,27+,28-/m0/s1

0000




Jaborosalactone 3

InChI=1S/C28H33ClO6/c1-13-15(3)28(3523(13)33)22(32)14(2)17-8-9-18-16-11-21(31)26(29)10-6-7-20(30)25(26,5)19(16)12-27(28,34)24(17,18)4/h6-7,16,18-19,21,31,34H,8-12H2,1-5H3/t16-,18-,19-,21+,24+,25-,26-,27+,28-/m0/s1

2.9




Jaborosalactone 4

InChI=1S/C28H32O7/c1-13-14(2)28(35-23(13)32)22(31)16(12-29)18-8-7-17-15-10-21-26(34-21)9-5-6-20(30)25(26,4)19(15)1127(28,33)24(17,18)3/h5-6,15,17,19,21,29,33H,7-12H2,1-4H3/t15-,17-,19-,21+,24-,25-,26+,27+,28-/m0/s1

33




Jaborosalactone 5

InChI=1S/C28H32O6/c1-14-15(2)28(34-24(14)32)23(31)18(13-29)20-11-10-19-17-9-8-16-6-5-7-22(30)25(16,3)21(17)12-27(28,33)26(19,20)4/h5,7-8,17,19,21,29,33H,6,9-13H2,1-4H3/t17-,19-,21-,25-,26-,27+,28-/m0/s1

38

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2.”Antiproliferative activity of withanolide derivatives from Jaborosa cabrerae

and Jaborosa reflexa. Chemotaxonomic considerations”

Manuela E. García a, Gloria E. Barboza a, Juan C. Oberti a, Carla Ríos-Luci b, José M. Padrón b,Viviana E. Nicotra a,b,, Ana Estévez-Braun b,c, Angel G. Ravelo b,c,

3.”Antiproliferative and quinone reductase-inducing activities of withanolides derivatives” Manuela E. García a, b, *, Viviana E. Nicotra a, b, Juan C. Oberti a, b, Carla Ríos-Luci c, Leticia G. Leon c, Laura Marler d, Guannan Li e, John M. Pezzuto d,Richard B. van Breemen e, Jose M. Padronc, Idaira Hueso-Falconc, Ana Estevez-Braunc

4.”Withasteroids, a Growing Group of Naturally

5.”Occurring Steroidal Lactones” ANIL B. RAY and MOHINI GUPTA, Varanasi, India”

A.B. Ray, M. Gupta, Withasteroids, a growing group of naturally occurring

steroidal lactones, Prog. Chem. Org. Nat. Prod. 63 (1994) 1e106.

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7. L. Chen, H. He, F. Qiu, Natural withanolides: an overview, Nat. Prod. Rep. 28

(2011) 705e740.

8. R.I. Misico, V.E. Nicotra, J.C. Oberti, G.E. Barboza, R.R. Gil, G. Burton, in:

A.D. Kinghorn, H. Falk, J.Kobayashi (Eds.), Progress in the Chemistry of Organic

Natural Products, vol. 94, Springer, Wien New York, 2011, pp. 127e229

(Chapter 3).

9. G.E. Barboza, A. Hunziker, Estudios sobre Solanaceae XXV. Revision de

Jaborosa, Kurtziana 19 (1987) 77e153.

10. (a) E.S. Monteagudo, J.C. Oberti, E.G. Gros, G. Burton, A spiranic withanolide

from Jaborosa odonelliana, Phytochemistry 29 (1990) 933e935; (b) A.M. Cirigliano, A.S. Veleiro, G.M. Bonetto, J.C. Oberti, G. Burton, Spiranoid Withanolides from Jaborosa runcinata and Jaborosa araucana, J. Nat. Prod. 59(1996) 717e721;

(c) A.M. Cirigliano, A.S. Veleiro, J.C. Oberti, G. Burton, Spiranoid withanolides

from Jaborosa odonelliana, J. Nat. Prod. 65 (2002) 1049e1051;

(d) A.M. Cirigliano, R.I. Misico, Spiranoid withanolides from Jaborosa odonelliana and Jaborosa runcinata, Z. Naturforsch 60b (2005) 867e869.

10. R.P. Machin, A.S. Veleiro, V.E. Nicotra, J.C. Oberti, J.M. Padron, Antiproliferative activity of withanolides against human breast cancer cell lines, J. Nat. Prod. 73 (2010) 966e968.

11. R.I. Misico, L.L. Song, A.S. Veleiro, A.M. Cirigliano, M.C. Tettamanzi, G. Burton, G.M. Bonetto, V.E. Nicotra, G.L. Silva, R.R. Gil, J.C. Oberti, A.D. Kinghorn, J.M. Pezzuto, Induction of quinone reductase by withanolides, J. Nat. Prod. 65(2002) 677e680.

12. M.E. García, G.E. Barboza, J.C. Oberti, C. Ríos-Luci, J.M. Padron, V.E. Nicotra,A. Estevez-Braun, A.G. Ravelo, Antiproliferative activity of withanolide de-rivatives from Jaborosa cabrerae and J. reflexa. Chemotaxonomical considerations, Phytochemistry 76 (2012) 150e157.

13. S.K. Yousufa, R. Majeed, M. Ahmad, P. lal Sangwan, B. Purnima, A.K. Saxsena,K.A. Suri, D. Mukherjee, S.C. Taneja, Ring A structural modified derivatives of withaferin A and the evaluation of their cytotoxic potential, Steroids 76 (2011) 1213e1222.

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regulation of enzymes that detoxify carcinogens, Proc. Natl. Acad. Sci. USA 90

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against carcinogens and oxidants, Proc. Natl. Acad. Sci. USA 99 (2002) 11908e11913.

16. A.L. Eggler, K.A. Gay, A.D. Mesecar, Molecular mechanisms of natural products in chemoprevention: induction of cytoprotective enzymes by Nrf2, Mol. Nutr. Food Res. 52 (2008) S84eS94.

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