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Volumn 74, Issue 8, 2009, Pages 701-706

Corrigendum to "Synthesis and antimicrobial evaluation of bile acid tridentate conjugates" [Steroids 74 (2009) 701-706] (DOI:10.1016/j.steroids.2009.03.005);Synthesis and antimicrobial evaluation of bile acid tridentate conjugates

Author keywords

Antimicrobial activity; Bile acids; Tridentate conjugates

Indexed keywords

AMIDE; BILE ACID CONJUGATE; CHENODEOXYCHOLIC ACID DERIVATIVE; CHOLIC ACID DERIVATIVE; HYODEOXYCHOLIC ACID; N ETHYLAMINO 3ALPHA,6ALPHA DIHYDROXY 5BETA CHOLAN 24 HYODEOXYCHOLANOAMIDE; N ETHYLAMINO 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 CHENODEOXYCHOLANOAMIDE; N ETHYLAMINO 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 URSODEOXYCHOLANOAMIDE; N ETHYLAMINO 3ALPHA,7ALPHA,12ALPHA TRIHYDROXY 5BETA CHOLAN 24 CHOLANOAMIDE; N ETHYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,6ALPHA DIHYDROXY 5BETA CHOLAN 24 HYODEOXYCHOLANOAMIDE; N ETHYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 CHENODEOXYCHOLANOAMIDE; N ETHYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,7ALPHA,12ALPHA TRIHYDROXY 5BETA CHOLAN 24 CHOLANOAMIDE; N ETHYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 URSODEOXYCHOLANOAMIDE; N HEXYLAMINO 3ALPHA,6ALPHA DIHYDROXY 5BETA CHOLAN 24 HYODEOXYCHOLANOAMIDE; N HEXYLAMINO 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 CHENODEOXYCHOLANOAMIDE; N HEXYLAMINO 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 URSODEOXYCHOLANOAMIDE; N HEXYLAMINO 3ALPHA,7ALPHA,12ALPHA TRIHYDROXY 5BETA CHOLAN 24 CHOLANOAMIDE; N HEXYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,6ALPHA DIHYDROXY 5BETA CHOLAN 24 HYODEOXYCHOLANOAMIDE; N HEXYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,7ALPHA DIHYDROXY 5BETA CHOLAN 24 CHENODEOXYCHOLANOAMIDE; N HEXYLAMINO[BIS(PYRIDIN 2 YLMETHYL)] 3ALPHA,7ALPHA,12ALPHA TRIHYDROXY 5BETA CHOLAN 24 CHOLANOAMIDE; UNCLASSIFIED DRUG; URSODEOXYCHOLIC ACID DERIVATIVE;

EID: 67349266957     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2009.10.001     Document Type: Erratum
Times cited : (19)

References (30)
  • 1
    • 0031679779 scopus 로고    scopus 로고
    • Characterisation and optimization of in vitro assay conditions for (1,3)β-glucan synthase activity from Aspargillus fumigatus and Candida albicans for enzyme inhibition screening
    • Wood R.L., Miller T.K., Wright A., Mccarthy P., Taft C.S., Pomponi S., et al. Characterisation and optimization of in vitro assay conditions for (1,3)β-glucan synthase activity from Aspargillus fumigatus and Candida albicans for enzyme inhibition screening. J Antibiot 51 (1998) 665-675
    • (1998) J Antibiot , vol.51 , pp. 665-675
    • Wood, R.L.1    Miller, T.K.2    Wright, A.3    Mccarthy, P.4    Taft, C.S.5    Pomponi, S.6
  • 2
    • 0029868451 scopus 로고    scopus 로고
    • Resistance of clinically important yeasts to antifungal agents
    • Odds F.C. Resistance of clinically important yeasts to antifungal agents. Int J Antimicrob Agents 6 (1996) 145-147
    • (1996) Int J Antimicrob Agents , vol.6 , pp. 145-147
    • Odds, F.C.1
  • 3
    • 0031758332 scopus 로고    scopus 로고
    • Acanthosterol sulfates A-J: ten new antifungal steroidal sulfates from a marine sponge Acanthodendrilla sp.
    • Sachiko T., Shigeki M., Nobuhiro F., and Rob W.M. Acanthosterol sulfates A-J: ten new antifungal steroidal sulfates from a marine sponge Acanthodendrilla sp. J Nat Prod 61 (1998) 1374-1378
    • (1998) J Nat Prod , vol.61 , pp. 1374-1378
    • Sachiko, T.1    Shigeki, M.2    Nobuhiro, F.3    Rob, W.M.4
  • 5
    • 14844314862 scopus 로고    scopus 로고
    • Synthesis of biologically active steroid derivatives by the utility of Lawesson's reagent
    • Mohamed N.R., Elmegeed G.A., Abd-ElMalek H.A., and Younis M. Synthesis of biologically active steroid derivatives by the utility of Lawesson's reagent. Steroids 70 (2005) 131-136
    • (2005) Steroids , vol.70 , pp. 131-136
    • Mohamed, N.R.1    Elmegeed, G.A.2    Abd-ElMalek, H.A.3    Younis, M.4
  • 6
    • 27644436021 scopus 로고    scopus 로고
    • Synthesis and antifungal activity of oxygenated cholesterol derivatives
    • Jean M.B., Céline L., Nicolas V., Michel D., and Yves L. Synthesis and antifungal activity of oxygenated cholesterol derivatives. Steroids 70 (2005) 907-912
    • (2005) Steroids , vol.70 , pp. 907-912
    • Jean, M.B.1    Céline, L.2    Nicolas, V.3    Michel, D.4    Yves, L.5
  • 7
    • 33745587761 scopus 로고    scopus 로고
    • Atropurosides A-G, new steroidal saponins from Smilacina atropurpurea
    • Zh Y., Li H., Zh Y.J., Jacob M.R., Khan S.I., Li X.C., et al. Atropurosides A-G, new steroidal saponins from Smilacina atropurpurea. Steroids 71 (2006) 712-719
    • (2006) Steroids , vol.71 , pp. 712-719
    • Zh, Y.1    Li, H.2    Zh, Y.J.3    Jacob, M.R.4    Khan, S.I.5    Li, X.C.6
  • 8
    • 34250861451 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of water-soluble, dendritic derivatives of epimeric 5α-cholestan-3-aminesand 5α-cholestan-3-yl aminoethanoates
    • Eko W.S., Carla S., Joseph O.F., and Richard D.G. Synthesis and antimicrobial evaluation of water-soluble, dendritic derivatives of epimeric 5α-cholestan-3-aminesand 5α-cholestan-3-yl aminoethanoates. Steroids 72 (2007) 615-626
    • (2007) Steroids , vol.72 , pp. 615-626
    • Eko, W.S.1    Carla, S.2    Joseph, O.F.3    Richard, D.G.4
  • 9
    • 33845226177 scopus 로고    scopus 로고
    • A bioconjugate approach toward squalamine mimics: insight into the mechanism of biological action
    • Chen W.H., Shao X.B., Robert M., Christine W., and Regen S.L. A bioconjugate approach toward squalamine mimics: insight into the mechanism of biological action. Bioconjugate Chem 17 (2006) 1582-1591
    • (2006) Bioconjugate Chem , vol.17 , pp. 1582-1591
    • Chen, W.H.1    Shao, X.B.2    Robert, M.3    Christine, W.4    Regen, S.L.5
  • 10
    • 0033977927 scopus 로고    scopus 로고
    • Cholic acid derivatives: novel antimicrobials
    • Savage P.B., and Li C. Cholic acid derivatives: novel antimicrobials. Expert Opin Investig Drugs 9 (2000) 263-272
    • (2000) Expert Opin Investig Drugs , vol.9 , pp. 263-272
    • Savage, P.B.1    Li, C.2
  • 12
    • 0034944358 scopus 로고    scopus 로고
    • Synthesis and properties of bile acid phosphoramidites 5′-tethered to antisense oligodeoxynucleotides against HCV
    • Lehmann T.J., and Engels J.W. Synthesis and properties of bile acid phosphoramidites 5′-tethered to antisense oligodeoxynucleotides against HCV. Bioorg Med Chem 9 (2001) 1827-1835
    • (2001) Bioorg Med Chem , vol.9 , pp. 1827-1835
    • Lehmann, T.J.1    Engels, J.W.2
  • 14
    • 1642452632 scopus 로고    scopus 로고
    • Bile acid amides derived from chiral amino alcohols: novel antimicrobials and antifungals
    • Hazra B.G., Pore V.S., Dey S.K., Datta S., Darokar M.P., Saikia D., et al. Bile acid amides derived from chiral amino alcohols: novel antimicrobials and antifungals. Bioorg Med Chem Lett 14 (2004) 773-777
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 773-777
    • Hazra, B.G.1    Pore, V.S.2    Dey, S.K.3    Datta, S.4    Darokar, M.P.5    Saikia, D.6
  • 15
    • 0036200889 scopus 로고    scopus 로고
    • Design, synthesis and characterization of cationic peptide and steroid antibiotics
    • Savage P.B. Design, synthesis and characterization of cationic peptide and steroid antibiotics. Eur J Org Chem (2002) 759-768
    • (2002) Eur J Org Chem , pp. 759-768
    • Savage, P.B.1
  • 16
    • 0000854965 scopus 로고
    • Synthesis and aggregation properties of a new family of amphiphiles with an unusual headgroup topology
    • Stein T.M., and Gellman S.H. Synthesis and aggregation properties of a new family of amphiphiles with an unusual headgroup topology. J Am Chem Soc 114 (1992) 3943-3950
    • (1992) J Am Chem Soc , vol.114 , pp. 3943-3950
    • Stein, T.M.1    Gellman, S.H.2
  • 20
    • 34247392455 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles
    • Sugandhi E.W., Slebodnick C., Falkinham III J.O., and Gandour R.D. Synthesis and antimicrobial activity of symmetrical two-tailed dendritic tricarboxylato amphiphiles. Bioorg Med Chem 15 (2007) 3842-3853
    • (2007) Bioorg Med Chem , vol.15 , pp. 3842-3853
    • Sugandhi, E.W.1    Slebodnick, C.2    Falkinham III, J.O.3    Gandour, R.D.4
  • 22
    • 0034618315 scopus 로고    scopus 로고
    • Preparation and characterization of cholic acid-derived antimicrobial agents with controlled stabilities
    • Guan Q.Y., Li ChH, Schmidt E.J., Boswell S., Walsh J.P., Allman G.W., et al. Preparation and characterization of cholic acid-derived antimicrobial agents with controlled stabilities. Org Lett 2 (2000) 2837-2840
    • (2000) Org Lett , vol.2 , pp. 2837-2840
    • Guan, Q.Y.1    Li ChH2    Schmidt, E.J.3    Boswell, S.4    Walsh, J.P.5    Allman, G.W.6
  • 23
    • 0036000122 scopus 로고    scopus 로고
    • Efficient calf thymus DNA condensation upon binding with novel bile acid polyamine amides
    • Geall A.J., Al-Hadithi D., and Blagbrough I.S. Efficient calf thymus DNA condensation upon binding with novel bile acid polyamine amides. Bioconjugate Chem 13 (2002) 481-490
    • (2002) Bioconjugate Chem , vol.13 , pp. 481-490
    • Geall, A.J.1    Al-Hadithi, D.2    Blagbrough, I.S.3
  • 26
    • 53549097892 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam
    • Vatmurge N.S., Hazra B.G., Pore V.S., Shirazi F., Deshpande M.V., Kadreppa S., et al. Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam. Org Biomol Chem 6 (2008) 3823-3830
    • (2008) Org Biomol Chem , vol.6 , pp. 3823-3830
    • Vatmurge, N.S.1    Hazra, B.G.2    Pore, V.S.3    Shirazi, F.4    Deshpande, M.V.5    Kadreppa, S.6
  • 27
    • 33947507423 scopus 로고    scopus 로고
    • Novel bile acid derivatives (BANBs) with cytostatic activity obtained by conjugation of their side chain with nitrogenated bases
    • Vallejo M., Castro M.A., Medarde M., Rocio I.R., Macias R.I.R., Romero M.R., El-Mir M.Y., et al. Novel bile acid derivatives (BANBs) with cytostatic activity obtained by conjugation of their side chain with nitrogenated bases. Biochem Pharm 73 (2007) 1394-1404
    • (2007) Biochem Pharm , vol.73 , pp. 1394-1404
    • Vallejo, M.1    Castro, M.A.2    Medarde, M.3    Rocio, I.R.4    Macias, R.I.R.5    Romero, M.R.6    El-Mir, M.Y.7
  • 28
    • 0037377519 scopus 로고    scopus 로고
    • Cholic acid-carboplatin compounds (CarboChAPt) as models for specific drug delivery: synthesis of novel carboplatin analogous derivatives and comparison of the cytotoxic properties with corresponding cisplatin compounds
    • Paschke R., Kalbitz J., Paetz C., Luckner M., Mueller T., Schmoll H.J., et al. Cholic acid-carboplatin compounds (CarboChAPt) as models for specific drug delivery: synthesis of novel carboplatin analogous derivatives and comparison of the cytotoxic properties with corresponding cisplatin compounds. J Inorg Biochem 94 (2003) 335-342
    • (2003) J Inorg Biochem , vol.94 , pp. 335-342
    • Paschke, R.1    Kalbitz, J.2    Paetz, C.3    Luckner, M.4    Mueller, T.5    Schmoll, H.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.