Chromone derivatives from the filamentous fungus Lachnum sp. BCC 2424.
Rukachaisirikul V, Chantaruk S, Pongcharoen W, Isaka M, Lapanun S.
J Nat Prod · research support, non-u.s. gov't; journal article · DOI 10.1021/np060164e PUBLIKATIONSREGISTRET
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Publikationer i urvalet
50 träffarA cyclopeptide from the Insect pathogenic fungus Cordyceps sp. BCC 1788.
Rukachaisirikul V, Chantaruk S, Tansakul C, Saithong S, Chaicharernwimonkoon L, Pakawatchai C, Isaka M, Intereya K.
J Nat Prod · research support, non-u.s. gov't; journal article · DOI 10.1021/np050433lAntiangiogenic activity of deoxoartemisinin derivatives on chorioallantoic membrane.
Jung M, Tak J, Chung WY, Park KK.
Bioorg Med Chem Lett · research support, non-u.s. gov't; journal article · DOI 10.1016/j.bmcl.2005.11.074Hirsutane sesquiterpenes from the fungus Lentinus connatus BCC 8996.
Rukachaisirikul V, Tansakul C, Saithong S, Pakawatchai C, Isaka M, Suvannakad R.
J Nat Prod · research support, non-u.s. gov't; journal article · DOI 10.1021/np0502286Antifungal activity of artemisinin derivatives.
Galal AM, Ross SA, Jacob M, ElSohly MA.
J Nat Prod · research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/np050074uSpiro and dispiro-1,2,4-trioxolanes as antimalarial peroxides: charting a workable structure-activity relationship using simple prototypes.
Dong Y, Chollet J, Matile H, Charman SA, Chiu FC, Charman WN, Scorneaux B, Urwyler H, Santo Tomas J, Scheurer C, Snyder C, Dorn A, Wang X, Karle JM, Tang Y, Wittlin S, Brun R, Vennerstrom JL.
J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm049040u10-membered macrolides from the insect pathogenic fungus Cordyceps militaris BCC 2816.
Rukachaisirikul V, Pramjit S, Pakawatchai C, Isaka M, Supothina S.
J Nat Prod · research support, non-u.s. gov't; journal article · DOI 10.1021/np0401415Growth inhibition activity of thioacetal artemisinin derivatives against human umbilical vein endothelial cells.
Oh S, Jeong IH, Shin WS, Lee S.
Bioorg Med Chem Lett · research support, non-u.s. gov't; journal article · DOI 10.1016/j.bmcl.2003.08.023Structure-activity relationships of the antimalarial agent artemisinin. 8. design, synthesis, and CoMFA studies toward the development of artemisinin-based drugs against leishmaniasis and malaria.
Avery MA, Muraleedharan KM, Desai PV, Bandyopadhyaya AK, Furtado MM, Tekwani BL.
J Med Chem · comparative study; research support, u.s. gov't, p.h.s.; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/jm030181qStructure-activity relationships of the antimalarial agent artemisinin. 6. The development of predictive in vitro potency models using CoMFA and HQSAR methodologies.
Avery MA, Alvim-Gaston M, Rodrigues CR, Barreiro EJ, Cohen FE, Sabnis YA, Woolfrey JR.
J Med Chem · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; journal article · DOI 10.1021/jm0100234Synthesis, antimalarial activity, biomimetic iron(II) chemistry, and in vivo metabolism of novel, potent C-10-phenoxy derivatives of dihydroartemisinin.
O'Neill PM, Miller A, Bishop LP, Hindley S, Maggs JL, Ward SA, Roberts SM, Scheinmann F, Stachulski AV, Posner GH, Park BK.
J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm000987fSynthesis and antimalarial activity of sixteen dispiro-1,2,4, 5-tetraoxanes: alkyl-substituted 7,8,15,16-tetraoxadispiro[5.2.5. 2]hexadecanes.
Vennerstrom JL, Dong Y, Andersen SL, Ager AL, Fu H, Miller RE, Wesche DL, Kyle DE, Gerena L, Walters SM, Wood JK, Edwards G, Holme AD, McLean WG, Milhous WK.
J Med Chem · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/jm0000766Novel, potent, semisynthetic antimalarial carba analogues of the first-generation 1,2,4-trioxane artemether.
O'Neill PM, Searle NL, Kan KW, Storr RC, Maggs JL, Ward SA, Raynes K, Park BK.
J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm9903545Stability of acetal and non acetal-type analogs of artemisinin in simulated stomach acid.
Jung M, Lee S.
Bioorg Med Chem Lett · research support, non-u.s. gov't; journal article · DOI 10.1016/s0960-894x(98)00160-7Mechanism-based development of new antimalarials: synthesis of derivatives of artemisinin attached to iron chelators.
Kamchonwongpaisan S, Paitayatat S, Thebtaranonth Y, Wilairat P, Yuthavong Y.
J Med Chem · research support, u.s. gov't, p.h.s.; research support, non-u.s. gov't; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/jm00013a007Synthesis, characterization, and antimalarial activity of the glucuronides of the hydroxylated metabolites of arteether.
Ramu K, Baker JK.
J Med Chem · comparative study; research support, non-u.s. gov't; journal article · DOI 10.1021/jm00011a011Cytotoxicity of artemisinin-related endoperoxides to Ehrlich ascites tumor cells.
Woerdenbag HJ, Moskal TA, Pras N, Malingré TM, el-Feraly FS, Kampinga HH, Konings AW.
J Nat Prod · research support, non-u.s. gov't; journal article · DOI 10.1021/np50096a007Antimalarial activity of new water-soluble dihydroartemisinin derivatives. 2. Stereospecificity of the ether side chain.
Lin AJ, Lee M, Klayman DL.
J Med Chem · comparative study; journal article · DOI 10.1021/jm00126a017Arteether, a new antimalarial drug: synthesis and antimalarial properties.
Brossi A, Venugopalan B, Dominguez Gerpe L, Yeh HJ, Flippen-Anderson JL, Buchs P, Luo XD, Milhous W, Peters W.
J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm00398a026Antimalarial activity of new water-soluble dihydroartemisinin derivatives.
Lin AJ, Klayman DL, Milhous WK.
J Med Chem · journal article · DOI 10.1021/jm00394a037