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Quim. Nova, Vol. 33, No. 4, S1-S10, 2010 Material Suplementar *e-mail: [email protected] STEROIDAL AND PHENOLIC COMPOUNDS FROM Sidastrum paniculatum (L.) FRYXELL AND EVALUATION OF CYTOTOXIC AND ANTI-INFLAMMATORY ACTIVITIES José Marcílio Sobral Cavalcante, Tiago Bezerra de Sá de Souza Nogueira, Anna Cláudia de Andrade Tomaz, Davi Antas e Silva, Maria de Fátima Agra e Maria de Fátima Vanderlei de Souza* Laboratório de Tecnologia Farmacêutica “Prof. Delby Fernandes de Medeiros”, Centro de Ciências da Saúde, Universidade Federal da Paraíba, CP 5009, 58051-970 João Pessoa - PB, Brasil Paulo Roberto Cavalcanti Carvalho, Sílvia Rafaelli Ramos, Silene Carneiro do Nascimento e Teresinha Gonçalves-Silva Departamento de Antibióticos, Universidade Federal de Pernambuco, 50670-901 Recife - PE, Brasil Figure 1S. IR spectrum of 4 (KBr, cm -1 )

et al. Quim. Nova - SBQsubmission.quimicanova.sbq.org.br/qn/qnol/2010/vol33n4/99-AR09380... · Quim. Nova, Vol. 33, No. 4, S1-S10, 2010 Material Suplementar *e-mail: [email protected]

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Quim. Nova, Vol. 33, No. 4, S1-S10, 2010

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*e-mail: [email protected]

STEROIDAL AND PHENOLIC COMPOUNDS FROM Sidastrum paniculatum (L.) FRYXELL AND EVALUATION OF CYTOTOXIC AND ANTI-INFLAMMATORY ACTIVITIES

José Marcílio Sobral Cavalcante, Tiago Bezerra de Sá de Souza Nogueira, Anna Cláudia de Andrade Tomaz, Davi Antas e Silva, Maria de Fátima Agra e Maria de Fátima Vanderlei de Souza*Laboratório de Tecnologia Farmacêutica “Prof. Delby Fernandes de Medeiros”, Centro de Ciências da Saúde, Universidade Federal da Paraíba, CP 5009, 58051-970 João Pessoa - PB, BrasilPaulo Roberto Cavalcanti Carvalho, Sílvia Rafaelli Ramos, Silene Carneiro do Nascimento e Teresinha Gonçalves-SilvaDepartamento de Antibióticos, Universidade Federal de Pernambuco, 50670-901 Recife - PE, Brasil

Figure 1S. IR spectrum of 4 (KBr, cm-1)

Cavalcante et al.2 Quim. Nova

Figure 2S. 1H NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 3S. Expansion of the 1H NRM spectrum of 4 (δ, CDCl3, 200 MHz)

Steroidal and phenolic compounds from Sidastrum paniculatum 3Vol. 33, No. 4

Figure 4S. Expansion of the 1H NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 5S. 13C-APT NMR spectrum of 4 (δ, CDCl3, 50 MHz)

Cavalcante et al.4 Quim. Nova

Figure 6S. Expansion of the 13C-APT NMR spectrum of 4 (δ, CDCl3, 50 MHz)

Figure 7S. Expansion of the 13C-APT NMR spectrum of 4 (δ, CDCl3, 50 MHz)

Steroidal and phenolic compounds from Sidastrum paniculatum 5Vol. 33, No. 4

Figure 8S. 1H x 1H-COSY NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 9S. Expansion of the 1H x 1H-COSY NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Cavalcante et al.6 Quim. Nova

Figure 10S. Expansion of the 1H x 1H-COSY NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 11S. 1H x 13C-HETCOR NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Steroidal and phenolic compounds from Sidastrum paniculatum 7Vol. 33, No. 4

Figure 12S. Expansion of the 1H x 13C-HETCOR NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 13S. Expansion of the 1H x 13C-HETCOR NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Cavalcante et al.8 Quim. Nova

Figure 14S. 1H x 13C-HMBC NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 15S. Expansion of the 1H x 13C-HMBC NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Steroidal and phenolic compounds from Sidastrum paniculatum 9Vol. 33, No. 4

Figure 16S. Expansion of the 1H x 13C-HMBC NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Figure 17S. 1H x 1H-NOESY NMR spectrum of 4 (δ, CDCl3, 200 MHz)

Cavalcante et al.10 Quim. Nova

Figure 18S. Expansion of the 1H x 1H-NOESY NMR spectrum of 4 (δ, CDCl3, 200 MHz)