Guangxi Zhuang Autonomous Region Food and Drug Administration (2011) Guangxi Zhuang Autonomous Region Zhuang Medicine Quality Standard. Guangxi Science and Technology Press, Guangxi

Google Scholar 

Liang X, Wang J, Guan RJ, Zhao L, Li DF, Long Z, Yang Q, Xu JY, Wang ZY, Xie JK, Lu WJ (2018) Limax extract ameliorates cigarette smoke-induced chronic obstructive pulmonary disease in mice. Int Immunopharmacol 54:210–220. https://doi.org/10.1016/j.intimp.2017.11.004

Article  CAS  PubMed  Google Scholar 

Lin GQ, Yan PK, Luo QF, Xie JK (2011) Therapeutic effect of freeze-dried slug powder in acute bronchitis. Guide of Chin Med 9:248–250. https://doi.org/10.15912/j.cnki.gocm.2011.21.040

Li LY (2019) Study on the antiasthmatic effect and mechanism of Limax extract and its quality control. Guangxi University of Chinese Medicine. https://doi.org/10.27879/d.cnki.ggxzy.2019.000218

Li LY, Wei QY, Tang XN, Long L, Tang RB (2019) Effects of limax lyophilized powder on asthma latency and levels of serum and bronchoalveolar lavage fluid interferon γ and interleukin 4 in rats with bronchial asthma. Guangxi Med J 41:1921–1924. https://doi.org/10.11675/j.issn.0253-4304.2019.15.13

Wei XY, Gao JP (2022) Research progress on chemical composition and pharmacological action of Limax maximus. Shanghai J Tradit Chin Med 56:89–95. https://doi.org/10.16305/j.1007-1334.2022.2103054

Yan PK, Lin GQ, Luo QF, Xie JK (2011) Effect of limax lyophilized powder on bronchial asthma. Chin Med Mat 34:1086–1089. https://doi.org/10.13863/j.issn1001-4454.2011.07.031

Liang X, Wu HB, Sun N, Liu T (2021) Effects of limax extract on LPS-induced acute inflammation of airway and pulmonary in mice. Chin J Mod Appl Pharm 38:2913–2920. https://doi.org/10.13748/j.cnki.issn1007-7693.2021.23.001

Huang YL, Wei YQ, He RJ, Li Y, Tang PD, Ruan J, Wang YF, Li DP (2018) Chemical constituents from Agriolimax agrestis. Chin Tradit Pat Med 40:2471–2474. https://doi.org/10.3969/j.issn.1001-1528.2018.11.022

Article  Google Scholar 

Zhang ZX, WangYF, He RJ, Huang YL (2021) GC-MS analysis of the volatile oil from Agriolimax Agrestis Linnaeus. Guangdong Chem Indus 48:217–219+201. https://doi.org/10.3969/j.issn.1007-1865.2021.05.085

Zhang ZX, Wang YF, Zhang Y, He RJ, Wei YQ, Yang BY, Ruan J, Huang YL (2022) Study on the chemical constituents of Agriolimax agrestis (II). Nat Prod Res Dev 34:63–69. https://doi.org/10.16333/j.1001-6880.2022.1.009

Rudi A, Yosief T, Schleyer M, Kashman Y (1999) Several new isoprenoids from two marine sponges of the family Axinellidae. Tetrahedron 55:5555–5566. https://doi.org/10.1016/S0040-4020(99)00221-5

Article  CAS  Google Scholar 

Cimino G, Madaio A, Trivellone E, Uriz M (1994) Minor triterpenoids from the mediterranean sponge, Raspaciona aculeata. J Nat Prod 57:784–790. https://doi.org/10.1021/np50108a015

Article  CAS  Google Scholar 

Rudi A, Goldberg I, Stein Z, Benayahu Y, Schleyer M, Kashman Y, Sodwanones A-C (1993) Three new triterpenoids from a marine sponge. Tetrahedron Lett 34:3943–3944. https://doi.org/10.1016/S0040-4039(00)79270-7

Article  CAS  Google Scholar 

Rudi A, Kashman Y, Benayahu Y, Schleyer M (1994) Sodwanones A-F, new triterpenoids from the marine sponge axinella weltneri. J Nat Prod 57:1416–1423. https://doi.org/10.1021/np50112a011

Article  CAS  Google Scholar 

Carmely S, Kashman Y (1983) The Sipholanes: a novel group of triterpenes from the marine sponge Siphonochalina siphonella. J Org Chem 48:3517–3525. https://doi.org/10.1021/jo00168a029

Article  CAS  Google Scholar 

José JF, María LS, Manuel N (2000) Marine polyether triterpenes. Nat Prod Rep 17:235–246. https://doi.org/10.1039/a909496b

Article  Google Scholar 

Xu D, Chen YJ, Cao XX, Zheng JJ, Wang Y, Ma YY, Zhang K, Zhao DG (2024) Anti-inflammatory activity of phenolics from Dianella ensifolia. Phytochem Lett 61:187–190. https://doi.org/10.1016/J.PHYTOL.2024.05.001

Article  CAS  Google Scholar 

Rizo MBA, Rodríguez FR, Romero TCJ, Riegos LCJ, Camacho RAM, Herrera ALA, Torre VEF, Góngora CE, Argáez AEV (2024) Models in vivo and in vitro for the study of acute and chronic inflammatory activity: a comprehensive review. Int Immunopharmacol 135:112292. https://doi.org/10.1016/J.INTIMP.2024.112292

Article  Google Scholar 

Liu Y, Wang AF, Anam N, Ye HL, Jiang P, Li XM, Wang SY, Pan J, Guan W, Lan W, Yang BY (2022) Phenylpropanoids and triterpenoids from Tripterygium regelii and their anti-inflammatory activities. Phytochem Lett 49:73–78. https://doi.org/10.1016/J.PHYTOL.2022.03.00

Article  CAS  Google Scholar 

Carmely S, Kashman Y (1986) Neviotine-A, a new triterpene from the red sea sponge Siphonochalina siphonella. J Org Chem 51:784–788. https://doi.org/10.1021/jo00356a003

Article  CAS  Google Scholar 

Carmely S, Loya Y, Kashman Y (1983) Siphenellinol, a new triterpene from the marine sponge siphonochalinasiphonella. Tetrahedron Lett 24:3673–3676. https://doi.org/10.1016/S0040-4039(00)88198-8

Article  CAS  Google Scholar 

Cimino G, Crispino A, Mattia CA, Mazzarella L, Puliti R, Trivellone E, Uriz MJ (1990) A new triterpenoid skeleton from the mediterranean sponge raspaciona aculeata: structure of raspacionin. Tetrahedron Lett 31:6565–6568. https://doi.org/10.1016/S0040-4039(00)97118-1

Article  CAS  Google Scholar 

Kusumi T, Ohtani I, Inouye Y, Kakisawa H (1988) Absolute configurations of cytotoxic marine cembranolides; consideration of mosher’s method. Tetrahedron Lett 29:4731–4734. https://doi.org/10.1016/S0040-4039(00)80593-6

Article  CAS  Google Scholar 

Ohtani I, Kusumi T, Ishitsuka OM, Kakisawa H (1989) Absolute configurations of marine diterpenes possessing a xenicane skeleton. An application of an advanced mosher’s method. Tetrahedron Lett 30:3147–3150. https://doi.org/10.1016/S0040-4039(00)99187-1

Article  CAS  Google Scholar 

Ohtani I, Kusumi T, Kashman Y, Kakisawa H (1991) A new aspect of the high-field NMR application of Mosher’s method. The absolute configuration of marine triterpene sipholenol A. J Org Chem 56:1296–1298. https://doi.org/10.1021/jo00003a067

Article  CAS  Google Scholar 

Ohtani I, Kusumi T, Kashman Y, Kakisawa H (1991) High-field FT NMR application of Mosher’s method. The absolute configurations of marine terpenoids. J Am Chem Soc 113:4092–4096. https://doi.org/10.1021/ja00011a006

Article  CAS  Google Scholar