Jomori, T., Setiawan, A., Sasaoka, M., and Arai, M. 2019a. Cytotoxicity of new diterpene alkaloids, ceylonamides G-I, isolated from Indonesian marine sponge of Spongia sp. NPC. 14: |
|
Chen, Q., Mao, Q., Bao, M., Mou, Y., Fang, C., Zhao, M., Jiang, W., Yu, X., Wang, C., Dai, L., He, W., Dong, J., Wu, J., and Yan, P. 2019. Spongian diterpenes including one with a rearranged skeleton from the marine sponge Spongia officinalis. J. Nat. Prod. 82:1714-1718. |
|
Liang, Y.-Q., Liao, X.-J., Lin, J.-L., Xu, W., Chen, G.-D., Zhao, B.-X., and Xu, S.-H. 2019. Spongiains A-C: three new spongian diterpenes with ring A rearrangement from the marine sponge Spongia sp. Tetrahedron. 75:3802-3808. |
|
Pech-Puch, D., Rodríguez, J., Cautain, B., Sandoval-Castro, C.A., and Jiménez, C. 2019. Cytotoxic furanoditerpenes from the sponge Spongia tubulifera collected in the Mexican Caribbean. Mar. Drugs. 17:416-425. |
|
Phan, C.-S., Kamada, T., Hamada, T., and Vairappan, C.S. 2018d. Cytotoxic sesterterpenoids from Bornean sponge Spongia sp. Rec. Nat. Prod. 12:643-647. |
|
Han, G.-Y., Sun, D.-Y., Liang, L.-F., Yao, L.-G., Chen, K.-X., and Guo, Y.-W. 2018. Spongian diterpenes from Chinese marine sponge Spongia officinalis. Fitoterapia. 127:159-165. |
|
Ito, T., Nguyen, H.M., Win, N.N., Vo, H.Q., Nguyen, H.T., and Morita, H. 2018. Three new sesquiterpene aminoquinones from a Vietnamese Spongia sp. and their biological activities. J. Nat. Med. 72:298-303. |
|
El-Desoky, A.H., Kato, H., and Tsukamoto, S. 2017b. Ceylonins G-I: spongian diterpenes from the marine sponge Spongia ceylonensis. J. Nat. Med. 71:765-769. |
|
Li, J., Gu, B.-B., Sun, F., Xu, J.-R., Jiao, W,.H., Yu, H.-B., Han, B.-N., Yang, F., Zhang, X.-C., and Lin, H.-W. 2017b. Sesquiterpene quinones/hydroquinones from the marine sponge Spongia pertusa Esper. J. Nat. Prod. 80:1436-1445. |
|
El-Desoky, A.H., Kato, H., Kagiyama, I., Hitora, Y., Losung, F., Mangindaan, R.E.P., de Voogd, N.J., and Tsukamoto, S. 2017a. Ceylonins A-F, spongian diterpene derivatives that inhibit RANKL-induced formation of multinuclear osteoclasts, from the marine sponge Spongia ceylonensis. J. Nat. Prod. 80:90-95. |
|
Nguyen, H.M., Ito, T., Kurimoto, S.-I., Ogawa, M., Win, N.N., Hung, V.Q., Nguyen, H.T., Kubota, T., Kobayashi, J., and Morita, H. 2017. New merosesquiterpenes from a Vietnamese marine sponge of Spongia sp. and their biological activity. Bioorg. Med. Chem. Lett. 27:3043-3047. |
|
El-Desoky, A.H., Kato, H., Angkouw, E.D., Mangindaan, R.E.P., de Voogd, N.J., and Tsukamoto, S. 2016. Ceylonamides A–F, nitrogenous spongian diterpenes that inhibit RANKL-induced osteoclastogenesis, from the marine sponge Spongia ceylonensis. J. Nat. Prod. 79:1922-1928. |
|
Nguyen, H.M., Ito, T., Win, N.N., Kodama, T., Hung, V.Q., Nguyen, H.T., and Morita, H. 2016. New antibacterial sesquiterpene aminoquinones from a Vietnamese marine sponge of Spongia sp. Phytochem. Lett. 17:288-292. |
|
Salim, A.A., Rae, J., Fontaine, F., Conte, M.M., Khalil, Z., Martin, S., Parton, R.G., and Capon, R.J. 2010. Heterofibrins: inhibitors of lipid droplet formation from a deep-water southern Australian marine sponge, Spongia (Heterofibria) sp. Org. Biomol. Chem. 8:3188-3194. |
|
Gross, H., Wright, A.D., Reinscheid, U., and König, G.M. 2009. Three new spongian diterpenes from the Fijian marine sponge Spongia sp. NPC. 4:315-322. |
|
Nam, S.J., Ko, H., Shin, M., Ham, J., Chin, J., Kim, Y., Kim, H., Shin, K., Choi, H., and Kang, H. 2006. Farnesoid X-activated receptor antagonists from a marine sponge Spongia sp. Bioorg. Med. Chem. Lett. 16:5398-5402. |
|
Takahashi, Y., Tsuda, M., Fromont, J., and Kobayashi, J. 2006. Metachromins J and K, new sesquiterpenoids from marine sponge Spongia species. Heterocycles. 67:791-795. |
|
Lin, C.-W., Su, J., Zeng, L., Wei, W., and Wei, T. 2005. Compounds containing nitrogen from Spongia zimocca ssp. irregularia (Lendenfeld). Youji Huaxue. 25:225-228. |
|
Cao, S., Gao, Z., Thomas, S.J., Hecht, S.M., Lazo, J.S., and Kingston, D.G.I. 2004. Marine sesquiterpenoids that inhibit the lyase activity of DNA polymerase b. J. Nat. Prod. 67:1716-1718. |
|
Tsukamoto, S., Miura, S., van Soest, R.W.M., and Ohta, T. 2003b. Three new cytotoxic sesterterpenes from a marine sponge Spongia sp. J. Nat. Prod. 66:438-440. |
|
Utkina, N.K., Denisenko, V.A., Scholokova, O.V., Virovaya, M.V., and Prokof’eva, N.G. 2003. Cyclosmenospongine, a new sesquiterpenoid aminoquinone from an Australian marine sponge Spongia sp. Tetrahedron Lett. 44:101-102. |
|
Capon, R.J., Jenkins, A., Rooney, F., and Ghisalberti, E.L. 2001b. Structure revision and assignment of absolute stereochemistry of a marine C21 bisfuranoterpene. J. Nat. Prod. 64:638-639. |
|
Zeng, L.-M., Guan, Z., Su, J.-Y., Feng, X.-L., and Cai, J.-W. 2001a. Two new spongian diterpene lactones. Acta Chim. Sin. 59:1675-1679. |
|
Aoki, S., Setiawan, A., Yoshioka, Y., Higuchia, K., Fudetani, R., Chen, Z.-S., Sumizawa, T., Akiyama, S.-I., and Kobayashi, M. 1999b. Reversal of multidrug resistance in human carcinoma cell line by agosterols, marine spongean sterols. Tetrahedron. 55:13965-13972. |
|
Rueda, A., Zubía, E., Ortega, M.J., Carballo, J.L., and Salvá, J. 1998a. New metabolites from the sponge Spongia agaricina. J. Nat. Prod. 61:258-261. |
|
Aoki, S., Yoshioka, Y., Miyamoto, Y., Higuchia, K., Setiawan, A., Murakami, N., Chen, Z.-S., Sumizawa, T., Akiyama, S.-I., and Kobayashi, M. 1998. Agosterol A, a novel polyhydroxylated sterol acetate reversing multidrug resistance from a marine sponge of Spongia sp. Tetrahedron Lett. 39:6303-5306. |
|
Garrido, L., Zubía, E., Ortega, M.J., and Salvá, J. 1997. New furanoterpenoids from the sponge Spongia officinalis. J. Nat. Prod. 60:794-797. |
|
Lu, Q., and Faulkner, D.J. 1997. Two new sesterterpenoids and a new 9,11-secosterol from Spongia matamata. J. Nat. Prod. 60:195-198. |
|
Fontana, A., Albarella, L., Scognamiglio, G., Uriz, M., and Cimino, G. 1996. Structural and stereochemical studies of C-21 terpenoids from Mediterranean Spongiidae sponges. J. Nat. Prod. 59:869-872. |
|
Pettit, G.R., Cichacz, Z.A., Gao, F., Boyd, M.R., Schmidt, J.M. 1994h. Isolation and structure of the cancer cell growth inhibitor dictyostatin 1. J. Chem. Soc. Chem. Comm. 1994:1111-1112. |
|
Searle, P.A., and Molinzki, T.F. 1994a. Scalemic 12-hydroxyambliofuran and 12-acetoxyambliofuran, five tetracyclic furanoditerpenes and a furanosesterterpene from Spongia sp. Tetrahedron. 50:9893-9908. |
|
He, H., Kulanthalvel, P., and Baker, B.J. 1994. New cytotoxic sesterterpenes from the marine sponge Spongia sp. Tetrahedron Lett. 35:7189-7192. |
|
Zubía, E., Gavagnin, M., Scognamiglio, G., Cimino, G., and Giusto, G.B. 1994. Spongiane and ent-isocopalane diterpenoids from the Mediterranean sponge Spongia zimocca. J. Nat. Prod. 57:725-731. |
|
Pettit, G.R., Cichacz, Z.A., Gao, F., Herald, C.L., and Boyd, M.R. 1993b. Isolation and structure of the remarkable human cancer cell growth inhibitors spongistatins 2 and 3 from an eastern Indian ocean spongia sp. J. Chem. Soc. Chem. Comm. 1993:1166-1168. |
|
Pettit, G.R., Cichacz, Z.A., Gao, F., Herald, C.L., Boyd, M.R., Schmidt, J.M., and Hooper, J.N.A. 1993a. Isolation and structure of spongistatin 1. J. Org. Chem. 58:1302-1304. |
|
Migliuolo, A., Piccialli, V., Sica, D., and Giordano, F. 1993. New ?8- and ?8(14)-5a,8a-epoxysterols from the marine sponge Spongia officinalis. Steroids. 58:134-140. |
|
Guella, G., Mancini, I., and Pietra, F. 1992c. C15 Acetogenins and terpenes of the dictyoceratid sponge Spongia zimocca of Il Rogiolo: a case of seaweed-metabolite transfer to, and elaboration within, a sponge? Comp. Biochem. Physiol. B. 103:1019-1023. |
|
Urban, S., and Capon, R.J. 1992. Cometins (A-C), new furanosesterterpenes from an Australian marine sponge, Spongia sp. Aust. J. Chem. 45:1255-1263. |
|
Carballeira, N.M., Shalabi, F., Cruz, C., Rodríguez, J., and Rodríguez, E. 1991b. Comparative study of the fatty acid composition of sponges of the genus Ircinia. Identification of the new 23-methyl-5,9-tetracosadienoic acid. Comp. Biochem. Physiol. B. 100:489-492. |
|
Guella, G., and Pietra, F. 1991. 5. Rogiolenyne A, B, and C: the first branched marine C15 acetogenins. Isolation from the red seaweed Laurencia microcladia or the sponge Spongia zimocca of Il Rogiolo. Helvet. Chim. Acta. 74:47-54. |
|
Migliuolo, A., Piccialli, V., and Sica, D. 1991. Structure elucidation and synthesis of 3ß,6a-dihydroxy-9-oxo-9,11-seco-5a-cholest-7-en-11-al, a novel 9,11-seco from the sponge Spongia officinalis. Tetrahedron. 47:7937-7950. |
|
Guella, G., Mancini, I., Chiasera, G., and Pietra, F. 1990. 144. Rogiolol acetate: a novel b-chamigrene-type sesquiterpene isolated from a marine sponge. Helvet. Chim. Acta. 73:1612-1620. |
|
Migliuolo, A., Notaro, G., Piccialli, V., and Sica, D. 1990a. New tetrahydroxylated sterols from the marine sponge Spongia officinalis. J. Nat. Prod. 53:1414-1424. |
|
Madaio, A., Piccialli, V., Sica, D., and Corriero, G. 1989. New polyhydrozysterols from the dictyoceratid sponges Hippospongia communis, Spongia officinalis, Ircinia variabilis, and Spongionella gracilis. J. Nat. Prod. 52:952-961. |
|
Aiello, A., Ciminiello, P., Fattorusso, E., and Magno, S. 1988. 3ß,5?-Dihydroxy-6ß-methoxycholest-7-enes from the marine sponge Spongia agaricina. J. Nat. Prod. 51:999-1002. |
|
Kakou, Y., Crews, P., and Bakus, G.J. 1987. Dendrolasin and latrunculin A from the Fijian sponge Spongia mycofijiensis and an associated nudibranch Chromodoris lochi. J. Nat. Prod. 50:482-484. |
|
Kohmoto, S., McConnell, O.J., Wright, A., and Cross, S. 1987. Isospongiadiol, a cytotoxic and antiviral diterpene from a Caribbean deep water marine sponge, Spongia sp. Chem. Lett. 16:1687-1690. |
|
González, A.G., Estrada, D.M., Martin, J.D., Martin, V.S., Pérez, C., and Pérez, R. 1984b. New antimicrobial diterpenes from the sponge Spongia officinalis. Tetrahedron. 40:4109-4113. |
|
Capelle, N., Braekman, J.-C., Dalňze, D., and Tursch, B. 1980. Chemical studies of marine invertebrates. XLIV. Three new spongian diterpenes from Spongia officinalis. Bull. Soc. Chim. Belg. 89:399-404. |
|
Walker, R.P., Thompson, J.E., and Faulkner, D.J. 1980. Sesterterpenes from Spongia idia. J. Org. Chem. 45:4976-4979. |
|
Kazlauskas, R., Murphy, P.T., Wells, R.J., Noack, K., Oberhänsli, W.E., and SchönhoIzer, P. 1979. A new series of diterpenes from Australian Spongia species. Aust. J. Chem. 32:867-880. |
|
Cimino, G., de Stefano, S., Minale, L., and Trivellone, E. 1977b. 12-Epi-scalarin and 12-epi-deoxoscalarin, sesterterpenes from the sponge Spongia nitens. J. Chem. Soc. Perkin Trans. 1:1587-1593. |
|
Kazlauskas, R., Murphy, P.T., Quinn, R.J., and Wells, R.J. 1976b. Tetradehydrofurospongin-1, a new C-21 furanoterpene from a sponge. Tetrahedron Lett. 17:1331-1332. |
|
Cimino, G., de Rosa, D., de Stefano, S., and Minale, L. 1974b. Isoagatholactone, a diterpene of a new structural type from the sponge Spongia officinalis. Tetrahedron. 30:645-649. |
|
Cimino, G., de Stefano, S., and Minale, L. 1972b. Further linear furanoterpenes from marine sponges. Tetrahedron. 28:5983-5991. |
|
Cimino, G., de Stefano, S., Minale, L., and Fattorusso, E. 1972a. Minor C-21 furanoterpenes from the sponges Spongia officinalis and Hippospongia communis. Tetrahedron. 28:267-273. |
|