References
- Bhattacharya D, Lai TK, Saha A, Selvin J, Mukherjee J. 2019. Structural elucidation and antimicrobial activity of a diketopiperazine isolated from a Bacillus sp. associated with the marine sponge Spongia officinalis. Nat Prod Res. 8(6):1–9.
- Carroll AR, Copp BR, Davis RA, Keyzers RA, Prinsep MR. 2020. Marine natural products. Nat Prod Rep. 37(2):175–223.
- Erdogan-Orhan I, Sener B, De Rosa S, Perez-Baz J, Lozach O, Leost M, Rakhilin S, Meijer L. 2004. Polyprenyl-hydroquinones and -furans from three marine sponges inhibit the cell cycle regulating phosphatase CDC25A. Nat Prod Res. 18(1):1–9.
- Fontana A, Mollo E, Ricciardi D, Fakhr I, Cimino G. 1997. Chemical studies of Egyptian Opisthobranchs: spongian diterpenoids from Glossodoris atromarginata. J Nat Prod. 60(5):444–448.
- Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Scalmani G, Barone V, Petersson GA, Nakatsuji H, et al. 2016. Gaussian 16 Version Revision A.03. Gaussian, Inc. Wallingford, CT.
- Gang Z, Jun C, Li X, Guoqiang L, Zhangzhe W, Lianzhong L. 2018. Study on secondary metabolites of cultured Mycale phyllophila. Ch J Mar Drugs. 37(4):17–22.
- Grimblat N, Zanardi MM, Sarotti AM. 2015. Beyond DP4: An improved probability for the stereochemical assignment of isomeric compounds using quantum chemical calculations of NMR shifts. J Org Chem. 80(24):12526–12534.
- Grimme S, Bannwarth C, Dohm S, Hansen A, Pisarek J, Pracht P, Seibert J, Neese F. 2017. Fully automated quantum-chemistry-based computation of spin-spin-coupled nuclear magnetic resonance spectra. Angew Chem Int Ed Engl. 56(46):14763–14769.
- Gross H, Wright AD, Reinscheid U, König GM. 2009. Three new spongian diterpenes from the Fijian marine sponge Spongia sp. Nat Prod Commun. 4(3):315–322.
- Han G-Y, Sun D-Y, Liang L-F, Yao L-G, Chen K-X, Guo Y-W. 2018. Spongian diterpenes from Chinese marine sponge Spongia officinalis. Fitoterapia. 127(3):159– 165.
- Humphrey W, Dalke A, Schulten K. 1996. VMD: Visual molecular dynamics. J Mol Graph. 14(1):33–38.
- Kazlauskas R, Murphy P, Wells R, Noack K, Oberhansli W, Schonholzer P. 1979. A new series of diterpenes from Australian spongia species. Aust J Chem. 32(4):867–868.
- Lenis LA, Nuñez L, Jiménez C, Riguera R. 1996. Isonitenin and acetylhomoagmatine new metabolites from the sponges Spongia officinalis and Cliona celata collected at the Galician coast (NW Spain). Nat Prod Lett. 8(1):15–23.
- Liang Y-Q, Liao X-J, Zhao B-X, Xu S-H. 2019. (+)- and (-)-Spongiterpene, a pair of new valerenane sesquiterpene enantiomers from the marine sponge Spongia sp. Nat Prod Res. 13(5):1–6.
- Liang Y-Q, Liao X-J, Zhao B-X, Xu S-H. 2020. Novel 3,4-seco-3,19-dinorspongian and 5,17-epoxy-19-norspongian diterpenes from the marine sponge Spongia sp. Org Chem Front. 7(20):3253–3261.
- Lu T, Chen F. 2012. Multiwfn: a multifunctional wavefunction analyzer. J Comput Chem. 33(5):580–592.
- Lu T, Chen Q. 2020. Shermo: A general code for calculating molecular thermochemistry properties. Version 2.0, http://bbs.keinsci.com/thread-17494-1-1.html.
- Lu T. 2020. molclus program, Version 1.9.6. http://www.keinsci.com/research/molclus.html.
- Marenich AV, Cramer CJ, Truhlar DG. 2009. Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the Bulk dielectric constant and atomic surface tensions. J Phys Chem B. 113(18):6378–6396.
- Maximo P, Ferreira LM, Branco P, Lima P, Lourenco A. 2016. The role of Spongia sp. in the discovery of marine Lead compounds. Mar Drugs. 14(8):139–210.
- Neese F. 2012. The ORCA program system. WIREs Comput Mol Sci. 2(1):73–78.
- Ou H, Zhai J, Wang D, Zhao J, Chen M, Ding S, Chen J. 2020. Cultivation of sponge Haliclona simulans juveniles in a floating sea raft. Aquaculture. 529(1):735660–735697.
- Sun D-Y, Han G-Y, Yang N-N, Lan L-F, Li X-W, Guo Y-W. 2018. Racemic trinorsesquiterpenoids from the Beihai sponge Spongia officinalis: structure and biomimetic total synthesis. Org Chem Front. 5(6):1022–1027.
- Sun J, Du Y, Zhang X, Wang Z, Lin Y, Song Q, Wang X, Guo J, Li S, Nan J, et al. 2020. Discovery and evaluation of Atopaxar hydrobromide, a novel JAK1 and JAK2 inhibitor, selectively induces apoptosis of cancer cells with constitutively activated STAT3. Invest New Drugs. 38(4):1003–1011.
- Wang Q, Sun Y, Yang L, Luo X, de Voogd NJ, Tang X, Li P, Li G. 2020. Bishomoscalarane sesterterpenoids from the sponge Dysidea granulosa collected in the South China Sea. J Nat Prod. 83(2):516–523.