메뉴 건너뛰기




Volumn 22, Issue 2, 2012, Pages 169-180

Modifications of andrographolide to increase some biological activities: A patent review (2006-2011)

Author keywords

Analgesic; Andrographolide; Anti inflammatory; Antibacterials; Anticancer; Antidiabetic; Antipyretic; Antivirals

Indexed keywords

11,12 DIDEHYDRO 14 DEOXYANDROGRAPHOLIDE; 14 ACETYL 3,19 ISOPROPYLIDENYLANDROGRAPHOLIDE; 14 ACETYLANDROGRAPHOLIDE; 14 DEOXYANDROGRAPHOLIDE; 3,19 DIPALMITOYL 14 DEOXY 11,12 DIDEHYDROANDROGRAPHOLIDE; 3,19 ISOPROPYLIDINYLANDROGARPHOLIDE; ALPHA GLUCOSIDASE; ANDROGRAPHOLIDE; ISOANDROGRAPHOLIDE; NEOANDROGRAPHOLIDE; UNCLASSIFIED DRUG;

EID: 84857577927     PISSN: 13543776     EISSN: 17447674     Source Type: Journal    
DOI: 10.1517/13543776.2012.661718     Document Type: Review
Times cited : (55)

References (93)
  • 3
    • 0029061240 scopus 로고
    • Analgesic antipyretic and antiulcerogenic effects of andrographolide
    • Madav S, Tripathi C, Tandan SK, Mishra S. Analgesic, antipyretic, and antiulcerogenic effects of andrographolide. Ind J Pharm Sci 1995;57:121-5
    • (1995) Ind. J. Pharm. Sci. , vol.57 , pp. 121-125
    • Madav, S.1    Tripathi, C.2    Tandan, S.K.3    Mishra, S.4
  • 4
    • 70349558444 scopus 로고    scopus 로고
    • Analgesic antipyretic anti-inflammatory and toxic effects of andrographolide derivatives in experimental animals
    • Suebsasana S, Pongnaratorn P, Sattayasai J, et al. Analgesic, antipyretic, anti-inflammatory and toxic effects of andrographolide derivatives in experimental animals. Arch Pharm Res 2009;32:1191-200
    • (2009) Arch. Pharm. Res. , vol.32 , pp. 1191-1200
    • Suebsasana, S.1    Pongnaratorn, P.2    Sattayasai, J.3
  • 5
    • 60249088269 scopus 로고    scopus 로고
    • In vitro and in vivo anti-inflammatory effects of andrographolide
    • Abu-Ghefreh AA, Canatan H, Ezeamuzie CI. In vitro and in vivo anti-inflammatory effects of andrographolide. Int Immunol 2009;9:313-18
    • (2009) Int. Immunol. , vol.9 , pp. 313-318
    • Abu-Ghefreh, A.A.1    Canatan, H.2    Ezeamuzie, C.I.3
  • 6
    • 33845936572 scopus 로고    scopus 로고
    • Antiangiogenic activity of Andrographis paniculata extract and andrographolide
    • Sheeja K, Guruvayoorappan C, Kuttan G. Antiangiogenic activity of Andrographis paniculata extract and andrographolide. Int Immunol 2007;7:211-21
    • (2007) Int. Immunol. , vol.7 , pp. 211-221
    • Sheeja, K.1    Guruvayoorappan, C.2    Kuttan, G.3
  • 7
    • 0036181416 scopus 로고    scopus 로고
    • Andrographolide prevents oxygen radical production by human neutrophils: Possible mechanism s involved in its anti-inflammatory effect
    • Shen Y-C, Chen C-F, Chiou W-F. Andrographolide prevents oxygen radical production by human neutrophils: possible mechanism(s) involved in its anti-inflammatory effect. Br J Pharmacol 2002;135:399-406
    • (2002) Br. J. Pharmacol. , vol.135 , pp. 399-406
    • Shen, Y.-C.1    Chen, C.-F.2    Chiou, W.-F.3
  • 8
    • 79955065706 scopus 로고    scopus 로고
    • Effect of the derivatives of Andrographolide on the morphology of B subtilis
    • Aromdee C, Seubsasana S, Sriubolmas N, et al. Effect of the derivatives of Andrographolide on the morphology of B. subtilis. Arch Pharm Res 2011;34:71-7
    • (2011) Arch. Pharm. Res. , vol.34 , pp. 71-77
    • Aromdee, C.1    Seubsasana, S.2    Sriubolmas, N.3
  • 9
    • 77953137432 scopus 로고    scopus 로고
    • Design synthesis and antibacterial activity of novel andrographolide derivatives
    • qourum sensing
    • Wang Z, Yu P, Xu L, et al. Design, synthesis and antibacterial activity of novel andrographolide derivatives. Bioorg Med Chem 2010;18:2469-74.qourum sensing
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 2469-2474
    • Wang, Z.1    Yu, P.2    Xu, L.3
  • 10
    • 70349924729 scopus 로고    scopus 로고
    • Preparation of acetylandrographolide and comparison of its antimicrobial activity and allopathic effect
    • Fan AL, Li XM, Gao JM, et al. Preparation of acetylandrographolide and comparison of its antimicrobial activity and allopathic effect. Acta Bot Boreal-Occid Sin 2006;26:1905
    • (2006) Acta. Bot. Boreal.-Occid. Sin. , vol.26 , pp. 1905
    • Fan, A.L.1    Li, X.M.2    Gao, J.M.3
  • 11
    • 33645969866 scopus 로고    scopus 로고
    • Ent-Labdane diterpenoids from andrographis paniculata
    • Shen YH, Li RT, Xiao WL, et al. ent-Labdane diterpenoids from Andrographis paniculata. J Nat Prod 2006;69:319-22
    • (2006) J. Nat. Prod. , vol.69 , pp. 319-322
    • Shen, Y.H.1    Li, R.T.2    Xiao, W.L.3
  • 12
    • 33747376146 scopus 로고    scopus 로고
    • The effect of medicinal plants used in Chinese folk medicine on RANTES secretion by virus-infected human epithelial cells
    • Ko H-C, Wei B-L, Chiou W-F. The effect of medicinal plants used in Chinese folk medicine on RANTES secretion by virus-infected human epithelial cells. J Ethnopharmacol 2006;107:205-10
    • (2006) J. Ethnopharmacol. , vol.107 , pp. 205-210
    • Ko, H.-C.1    Wei, B.-L.2    Chiou, W.-F.3
  • 13
    • 0034519360 scopus 로고    scopus 로고
    • Antiviral drugs against herpes infections
    • Vajpayee M, Malhotra N. Antiviral drugs against herpes infections. Ind J Pharmacol 2000;32:330-8
    • (2000) Ind. J. Pharmacol. , vol.32 , pp. 330-338
    • Vajpayee, M.1    Malhotra, N.2
  • 14
    • 31144431583 scopus 로고    scopus 로고
    • Antiviral properties of ent-labdene diterpenes of andrographis paniculata nees inhibitors of herpes simplex virus type 1
    • Wiart C, Kumar K, Yusof MY, et al. Antiviral properties of ent-labdene diterpenes of Andrographis paniculata Nees, inhibitors of herpes simplex virus type 1. Phytother Res 2005;19:1069-70
    • (2005) Phytother. Res. , vol.19 , pp. 1069-1070
    • Wiart, C.1    Kumar, K.2    Yusof, M.Y.3
  • 15
    • 79958815949 scopus 로고    scopus 로고
    • Stage of action of naturally occurring andrographolides and their semi-synthetic analogues against herpes simplex virus type 1 in vitro
    • Aromdee C, Seubsasana S, Ekalaksananan T, et al. Stage of action of naturally. occurring andrographolides and their semi-synthetic analogues against herpes simplex virus type 1 in vitro. Planta Med 2011;77:915-21
    • (2011) Planta. Med. , vol.77 , pp. 915-921
    • Aromdee, C.1    Seubsasana, S.2    Ekalaksananan, T.3
  • 16
    • 79955782902 scopus 로고    scopus 로고
    • A Potential Andrographolide analogue against the replication of herpes simplex virus type-1 in vero cells
    • Seubsasana S, Pientong C, Ekalaksananan T, et al. A Potential Andrographolide analogue against the replication of herpes simplex virus type-1 in vero cells. Med Chem 2011;7:237-44
    • (2011) Med. Chem. , vol.7 , pp. 237-244
    • Seubsasana, S.1    Pientong, C.2    Ekalaksananan, T.3
  • 17
    • 8544245691 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of andrographolide analogues as novel cytotoxic agents
    • Nanduri S, Nyavanandi VK, Thunuguntla SS, et al. Synthesis and structure-activity relationships of andrographolide analogues as novel cytotoxic agents. Bioorg Med Chem Lett 2004;14:4711-17
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 4711-4717
    • Nanduri, S.1    Nyavanandi, V.K.2    Thunuguntla, S.S.3
  • 18
    • 2342550564 scopus 로고    scopus 로고
    • Anticancer and immunostimulatory compounds from andrographis paniculata
    • Kumar RA, Sridevi K, Kumar NV, et al. Anticancer and immunostimulatory compounds from Andrographis paniculata. J Ethnopharmacol 2004;92:291-5
    • (2004) J. Ethnopharmacol. , vol.92 , pp. 291-295
    • Kumar, R.A.1    Sridevi, K.2    Kumar, N.V.3
  • 19
    • 33847248975 scopus 로고    scopus 로고
    • Semisynthesis and in vitro anticancer activities of andrographolide analogues
    • Jada SR, Subur GS, Matthews C, et al. Semisynthesis and in vitro anticancer activities of andrographolide analogues. Phytochemistry 2007;68:904-12
    • (2007) Phytochemistry , vol.68 , pp. 904-912
    • Jada, S.R.1    Subur, G.S.2    Matthews, C.3
  • 21
    • 1242329231 scopus 로고    scopus 로고
    • Antihyperglycemic effect of andrographolide in streptozotocin-induced diabetic rats
    • Yu BC, Hung CR, Chen WC, Cheng JT. Antihyperglycemic effect of andrographolide in streptozotocin-induced diabetic rats. Planta Med 2003;69:1075-9
    • (2003) Planta. Med. , vol.69 , pp. 1075-1079
    • Yu, B.C.1    Hung, C.R.2    Chen, W.C.3    Cheng, J.T.4
  • 22
    • 34247636613 scopus 로고    scopus 로고
    • Synthesis of andrographolide derivatives: A new family of a-glucosidae inhibitors
    • Xu HW, Dai GF, Lui GZ, et al. Synthesis of andrographolide derivatives: a new family of a-glucosidae inhibitors. Biorg Med Chem 2007;15:4247-55
    • (2007) Biorg. Med. Chem. , vol.15 , pp. 4247-4255
    • Xu, H.W.1    Dai, G.F.2    Lui, G.Z.3
  • 23
    • 68349146183 scopus 로고    scopus 로고
    • Hypoglycemic and beta cell protective effects of andrographolide analogue for diabetes treatment
    • Zhang Z, Jiang J, Yu P, et al. Hypoglycemic and beta cell protective effects of andrographolide analogue for diabetes treatment. J Transitional Med 2009;7:62
    • (2009) J. Transitional. Med. , vol.7 , pp. 62
    • Zhang, Z.1    Jiang, J.2    Yu, P.3
  • 24
    • 33645861668 scopus 로고    scopus 로고
    • Studies of the novel a-glucosidase inhibitory activity and structure-activity relationships for andrographolide analogues
    • Dai GF, Xu HW, Wang JF, et al. Studies of the novel a-glucosidase inhibitory activity and structure-activity relationships for andrographolide analogues. Bioorg Med Chem Lett 2006;16:2710-13
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 2710-2713
    • Dai, G.F.1    Xu, H.W.2    Wang, J.F.3
  • 25
    • 75849139352 scopus 로고    scopus 로고
    • Modification of 15-alkylidene andrographolide derivatives as alpha-glucosidase inhibitor
    • Xu HW, Lui GZ, Dai GF, et al. Modification of 15-alkylidene andrographolide derivatives as alpha-glucosidase inhibitor Drug Discov Ther. 2007;1:73-7
    • (2007) Drug Discov Ther. , vol.1 , pp. 73-77
    • Xu, H.W.1    Lui, G.Z.2    Dai, G.F.3
  • 27
    • 41949109020 scopus 로고    scopus 로고
    • Suppressionof v-src transformation via degradation of the v-src protein and attenuation of the erk signaling pathway
    • Liang FP, Lin CH, Kuo CD, et al. Suppressionof v-Src Transformation via degradation of the v-Src Protein and attenuation of the Erk signaling pathway. J Biol Chem 2008;283:5023-33
    • (2008) J. Biol. Chem. , vol.283 , pp. 5023-5033
    • Liang, F.P.1    Lin, C.H.2    Kuo, C.D.3
  • 28
    • 85011210216 scopus 로고
    • 1984 On the diterpenoids of andrographis paniculata: X-ray crystallographic analysis of andrographolide and structure determination of new minor diterpenoids
    • Fujita T, Fujitani R, Takeda Y, et al. 1984. On the diterpenoids of andrographis paniculata: X-ray crystallographic analysis of andrographolide and structure determination of new minor diterpenoids. Chem Pharm Bull 1984;32:2117-25
    • (1984) Chem. Pharm. Bull. , vol.32 , pp. 2117-2125
    • Fujita, T.1    Fujitani, R.2    Takeda, Y.3
  • 29
    • 4544257740 scopus 로고    scopus 로고
    • Flavonoids and andrographolides from andrographis paniculata
    • Rao YK, Vimalamma G, Rao CV, Tzeng Y-M. Flavonoids and andrographolides from Andrographis paniculata. Phytochemistry 2004;65:2317-21
    • (2004) Phytochemistry , vol.65 , pp. 2317-2321
    • Rao, Y.K.1    Vimalamma, G.2    Rao, C.V.3    Tzeng, Y.-M.4
  • 31
    • 33645892859 scopus 로고
    • Refined crystal and molecular structure of andrographolide-diterpene
    • Sambyal VS, Goswami KN. Refined crystal and molecular structure of andrographolide-diterpene. Cryst Res Tech 1995;30:629-36
    • (1995) Cryst. Res. Tech. , vol.30 , pp. 629-636
    • Sambyal, V.S.1    Goswami, K.N.2
  • 32
    • 34247636613 scopus 로고    scopus 로고
    • Synthesis of andrographolide derivatives: A new family of alpha-glucosidase inhibitors
    • Xu HW, Fu DG, Lui GZ, et al. Synthesis of andrographolide derivatives: a new family of alpha-glucosidase inhibitors. Bioorg Med Chem 2007;15:4247-55
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 4247-4255
    • Xu, H.W.1    Fu, D.G.2    Lui, G.Z.3
  • 33
    • 33644746091 scopus 로고    scopus 로고
    • 14-deoxy-11 12-didehydro-3 19- isopropylidenylandrographolide
    • published online 13 January 2006;:10.1107/S1600536806000699
    • Teh JBJ, Sagineedu RS, Fun HK, et al. 14-deoxy-11,12-didehydro-3,19- isopropylidenylandrographolide. Acta Cryst Sect E Struct Reports Online 2006;published online 13 January 2006; doi:10.1107/S1600536806000699
    • (2006) Acta. Cryst. Sect. E Struct. Reports Online
    • Teh, J.B.J.1    Sagineedu, R.S.2    Fun, H.K.3
  • 34
    • 77953543263 scopus 로고    scopus 로고
    • Effect of andrographolide on sexual function vascular reactivity and serum testosterone level in rodents
    • Sattayasai J, Srisuwan S, Arkaravichien T, Aromdee C. Effect of andrographolide on sexual function, vascular reactivity and serum testosterone level in rodents. Food Chem Toxicol 2010;48:1934-8
    • (2010) Food Chem. Toxicol. , vol.48 , pp. 1934-1938
    • Sattayasai, J.1    Srisuwan, S.2    Arkaravichien, T.3    Aromdee, C.4
  • 36
    • 79959733637 scopus 로고    scopus 로고
    • Protective role of 14-deoxy-11 12-didehydroandrographolide a noncytotoxic analogue of andrographolide
    • Guan HP, Kong LR, Cheng C, et al. Protective Role of 14-Deoxy-11, 12-didehydroandrographolide, a Noncytotoxic Analogue of Andrographolide, in Allergic Airway Inflammation J Nat Prod. 2011;74:1484-90
    • (2011) Allergic Airway Inflammation. J. Nat. Prod. , vol.74 , pp. 1484-1490
    • Guan, H.P.1    Kong, L.R.2    Cheng, C.3
  • 37
    • 77952055014 scopus 로고    scopus 로고
    • Isolation and identification of bioactive compounds in andrographis paniculata chuanxinliaz
    • Available from:
    • Chao WW, Lin BF. Isolation and Identification of Bioactive compounds in Andrographis paniculata (Chuanxinlian). Chin Med 2010;5:17-Available from: http://www. cmjournal.org/content/5/1/17
    • (2010) Chin. Med. , vol.5 , pp. 17
    • Chao, W.W.1    Lin, B.F.2
  • 38
    • 84857381831 scopus 로고    scopus 로고
    • Andrographolide and its analogues: Versatile bioactive molecules for combating inflammation and cancer
    • Accepted Article doi:10.1111/ j.1440-1681. 2011.05633.x
    • Lim CW, Chan TK, Ng DSW, et al. Andrographolide and its analogues: versatile bioactive molecules for combating inflammation and cancer. Clin Exp Pharmacol Physiol 2011;"Accepted Article"; doi:10.1111/ j.1440-1681.2011.05633.x
    • (2011) Clin. Exp. Pharmacol. Physiol.
    • Lim, C.W.1    Chan, T.K.2    Ng, D.S.W.3
  • 40
    • 0033772108 scopus 로고    scopus 로고
    • Pharmacokinetic and oral bioavalability of andrographolide from andrographis paniculata fixed combination kan jang in rats and humans
    • Panossian A, Hovhannisyan A, Mamikonyan G, et al. Pharmacokinetic and oral bioavalability of andrographolide from andrographis paniculata fixed combination Kan Jang in rats and humans. Phytomedicine 2000;7:351-64
    • (2000) Phytomedicine , vol.7 , pp. 351-364
    • Panossian, A.1    Hovhannisyan, A.2    Mamikonyan, G.3
  • 41
    • 0042703357 scopus 로고    scopus 로고
    • Four new andrographolide metabolites in rats
    • He X, Li J, Gao H, et al. Four new andrographolide metabolites in rats. Tetrahedron 2003;59:6603-7
    • (2003) Tetrahedron , vol.59 , pp. 6603-6607
    • He, X.1    Li, J.2    Gao, H.3
  • 42
    • 0642340617 scopus 로고    scopus 로고
    • Six new andrographolide metabolite in rats
    • He X, Li J, Gao H, Qui F. Six new andrographolide metabolite in rats. Chem Pharm Bull 2003;51:586-9
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 586-589
    • He, X.1    Li, J.2    Gao, H.3    Qui, F.4
  • 43
    • 84857563340 scopus 로고    scopus 로고
    • Isolation and identification of seven glucuronide conjugates of andrographolide human urine
    • Cui L, Qui F, Yao X. Isolation and identification of seven glucuronide conjugates of andrographolide human urine. Drug Metab Dispos 2005;25:285-93
    • (2005) Drug. Metab. Dispos. , vol.25 , pp. 285-293
    • Cui, L.1    Qui, F.2    Yao, X.3
  • 44
    • 33745012639 scopus 로고    scopus 로고
    • A new glucuronide metabolite of andrographolide in human
    • Available from:
    • Cui L, Qui F, Wang NL, et al. A new glucuronide metabolite of andrographolide in human. Chin Chem Lett 2005;16:369-71.Available from: http:// www.imm.ac.cn/journal/cc1.html
    • (2005) Chin. Chem. Lett. , vol.16 , pp. 369-371
    • Cui, L.1    Qui, F.2    Wang, N.L.3
  • 49
    • 79959998725 scopus 로고    scopus 로고
    • Enzymatic synthesis and antibacterial activity of andrographolide derivatives process
    • Chen ZG, Zhu Q, Zong MH, et al. Enzymatic synthesis and antibacterial activity of andrographolide derivatives Process. Biochemistry 2011;46:1649-53
    • (2011) Biochemistry , vol.46 , pp. 1649-1653
    • Chen, Z.G.1    Zhu, Q.2    Zong, M.H.3
  • 50
    • 67349136453 scopus 로고    scopus 로고
    • Synthesis and evaluation of antibacterial activities of andrographolide analogues
    • Jiang X, Yu P, Jiang J, et al. Synthesis and evaluation of antibacterial activities of andrographolide analogues. Eur J Med Chem 2009;44:2936-43
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 2936-2943
    • Jiang, X.1    Yu, P.2    Jiang, J.3
  • 52
    • 0033846074 scopus 로고    scopus 로고
    • A phase 1 trial of andrographolide in HIV positive patients and normal volunteers
    • Calbrese C, Berman SH, Babish JG, et al. A phase 1 trial of andrographolide in HIV positive patients and normal volunteers Phytother Res. 2000;14:333-8
    • (2000) Phytother Res. , vol.14 , pp. 333-338
    • Calbrese, C.1    Berman, S.H.2    Babish, J.G.3
  • 53
    • 0025911006 scopus 로고
    • Dehydroandrographolide succinic acid monoester as an inhibitor against the human immunodeficiency virus
    • Chang RH, Ding L, Chen G-Q et al. Dehydroandrographolide succinic acid monoester as an inhibitor against the human immunodeficiency virus. Proc Soc Exp Biol Med 1991;197:59-66
    • (1991) Proc. Soc Exp. Biol. Med. , vol.197 , pp. 59-66
    • Chang, R.H.1    Ding, L.2    Chen, G.-Q.3
  • 54
    • 78650216257 scopus 로고    scopus 로고
    • Synthesis and preliminary anti-HIV activities of andrographolide derivatives
    • Wang B, Ge L, Huang WL, et al. Synthesis and preliminary anti-HIV activities of andrographolide derivatives. Med Chem 2010;6:252-8
    • (2010) Med. Chem. , vol.6 , pp. 252-258
    • Wang, B.1    Ge, L.2    Huang, W.L.3
  • 55
    • 79957498305 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of andrographolide derivatives as potent anti-HIV agents
    • Wang B, Li J, Huang WL, et al. Synthesis and biological evaluation of andrographolide derivatives as potent anti-HIV agents. Chin Chem Lett 2011;22:781-4
    • (2011) Chin. Chem. Lett. , vol.22 , pp. 781-784
    • Wang, B.1    Li, J.2    Huang, W.L.3
  • 57
    • 84857536437 scopus 로고    scopus 로고
    • The replication of herpes simplex viruses
    • Knipe DM HowleyFields' PM editors. 5th edition. Lippincott -Williams and Wilkins; New York
    • Roizman B, Knipe DM, Whitley RJ. The replication of Herpes simplex viruses. In: Knipe DM, HowleyFields' PM, editors. Virology. 5th edition. Lippincott-Williams and Wilkins; New York: 2007
    • (2007) Virology
    • Roizman, B.1    Knipe, D.M.2    Whitley, R.J.3
  • 58
    • 58949101282 scopus 로고    scopus 로고
    • 5¢-O-Aliphatic and amino acid ester prodrugs of -b-D-2R4R- dioxolanethymine DOT: Syn thesis anti-HIV activity cytotoxicity and stability studies
    • Liang Y, Sharon A, Grier J, et al. 5¢-O-Aliphatic and amino acid ester prodrugs of (-)-b-D-(2R,4R)-dioxolanethymine (DOT): Synthesis, anti-HIV activity, cytotoxicity and stability studies. Bioorg Med Chem 2009;17:1404-9
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 1404-1409
    • Liang, Y.1    Sharon, A.2    Grier, J.3
  • 59
    • 84857533139 scopus 로고
    • Study of the phosphorylation of nucleosides with phosphorus trihalide
    • Yoshikawa M, Sakuraba M, Kusashio K. Study of the phosphorylation of nucleosides with phosphorus trihalide. Bull Chem Soc Jpn 1970;43:456-61
    • (1970) Bull. Chem. Soc. Jpn. , vol.43 , pp. 456-461
    • Yoshikawa, M.1    Sakuraba, M.2    Kusashio, K.3
  • 60
    • 69149103489 scopus 로고    scopus 로고
    • Activity of andrographolide and its derivatives against influenza virus in vivo and in vitro
    • Chen JX, Xue HJ, Ye WC, et al. Activity of andrographolide and its derivatives against influenza virus in vivo and in vitro. Biol Pharm Bull 2009;32:1385-91
    • (2009) Biol. Pharm. Bull. , vol.32 , pp. 1385-1391
    • Chen, J.X.1    Xue, H.J.2    Ye, W.C.3
  • 62
    • 0004282011 scopus 로고
    • Comparison of pharmacological effect of four andrographolides
    • Deng WL, Nie RJ, Lui JY. Comparison of pharmacological effect of four andrographolides. Yaoxue Tongbao 1982;17:195-8
    • (1982) Yaoxue. Tongbao. , vol.17 , pp. 195-198
    • Deng, W.L.1    Nie, R.J.2    Lui, J.Y.3
  • 63
    • 15944409586 scopus 로고    scopus 로고
    • Andrographolide interferes with binding of nuclear factor-kB to DNA in HL-60-derived neutrophilic cells
    • Hildalgo MA, Romero A, Figueroa J, et al. Andrographolide interferes with binding of nuclear factor-kB to DNA in HL-60-derived neutrophilic cells. Br J Pharmacol 2005;144:680-6
    • (2005) Br. J. Pharmacol. , vol.144 , pp. 680-686
    • Hildalgo, M.A.1    Romero, A.2    Figueroa, J.3
  • 64
    • 35848943019 scopus 로고    scopus 로고
    • Synthesis of andrographolide derivatives and their TNF-alpha and IL-6 expression inhibitory activities
    • Li J, Huang W, Zhang H, et al. Synthesis of andrographolide derivatives and their TNF-alpha and IL-6 expression inhibitory activities. Bioorg Med Chem 2007;17:6891-4
    • (2007) Bioorg. Med. Chem. , vol.17 , pp. 6891-6894
    • Li, J.1    Huang, W.2    Zhang, H.3
  • 66
    • 33645979959 scopus 로고    scopus 로고
    • Antidiabetic agents from medicinal plants
    • Jung M, Park M, Lee HC, et al. Antidiabetic agents from medicinal plants Curr Med Chem. 2006;13:1203-18
    • (2006) Curr. Med. Chem. , vol.13 , pp. 1203-1218
    • Jung, M.1    Park, M.2    Lee, H.C.3
  • 67
    • 0027977120 scopus 로고
    • Effect of lipoic acid on cyclophosphamide-induced diabetes and insulitis in non-obese diabetic mice
    • Faust A, Burkart V, Ulrich H, et al. Effect of lipoic acid on cyclophosphamide-induced diabetes and insulitis in non-obese diabetic mice. Int J Immunopharmacol 1994;16:61-6
    • (1994) Int. J. Immunopharmacol. , vol.16 , pp. 61-66
    • Faust, A.1    Burkart, V.2    Ulrich, H.3
  • 68
    • 0029909010 scopus 로고    scopus 로고
    • Neuroprotection by the metabolic antioxidant alpha-lipoic acis
    • Packer L, Tritschler HJ, Wessel K. Neuroprotection by the metabolic antioxidant alpha-lipoic acis. Free Radic Biol Med 1997;22:359-78
    • (1997) Free Radic. Biol. Med. , vol.22 , pp. 359-378
    • Packer, L.1    Tritschler, H.J.2    Wessel, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.