Year |
Citation |
Score |
2023 |
Mi HTN, Chaiyasarn S, Eser BE, Tan SRS, Burapan S, Han J. Correction for Mi et al., "Allyl Aryl Ether Cleavage by sp. MRG-PMF1 Cocorrinoid -Demethylase". Microbiology Spectrum. e0007223. PMID 36715536 DOI: 10.1128/spectrum.00072-23 |
0.735 |
|
2022 |
Mi HTN, Chaiyasarn S, Eser BE, Tan SRS, Burapan S, Han J. Allyl Aryl Ether Cleavage by sp. MRG-PMF1 Cocorrinoid -Demethylase. Microbiology Spectrum. e0330522. PMID 36197289 DOI: 10.1128/spectrum.03305-22 |
0.766 |
|
2020 |
Burapan S, Kim M, Paisooksantivatana Y, Eser BE, Han J. Thai Species: Antioxidant and Bioactive Compounds. Foods (Basel, Switzerland). 9. PMID 32887356 DOI: 10.3390/Foods9091219 |
0.747 |
|
2018 |
Kim H, Moon JY, Burapan S, Han J, Cho SK. Induction of ER Stress-Mediated Apoptosis by the Major Component 5,7,4'-Trimethoxyflavone Isolated from Kaempferia parviflora Tea Infusion. Nutrition and Cancer. 1-13. PMID 30273054 DOI: 10.1080/01635581.2018.1491607 |
0.753 |
|
2017 |
Burapan S, Kim M, Han J. Curcuminoid Demethylation as an Alternative Metabolism by Human Intestinal Microbiota. Journal of Agricultural and Food Chemistry. PMID 28401758 DOI: 10.1021/Acs.Jafc.7B00943 |
0.758 |
|
2017 |
Burapan S, Kim M, Han J. Demethylation of Polymethoxyflavones by Human Gut Bacterium, Blautia sp. MRG-PMF1. Journal of Agricultural and Food Chemistry. PMID 28211698 DOI: 10.1021/Acs.Jafc.7B00408 |
0.769 |
|
2017 |
Shin BK, Kim M, Han J. Exceptionally high percentage of IPP synthesis by Ginkgo biloba IspH is mainly due to Phe residue in the active site. Phytochemistry. PMID 28139297 DOI: 10.1016/J.Phytochem.2017.01.012 |
0.618 |
|
2015 |
Shin BK, Ahn JH, Han J. N-Terminal Region of GbIspH1, Ginkgo biloba IspH Type 1, May Be Involved in the pH-Dependent Regulation of Enzyme Activity. Bioinorganic Chemistry and Applications. 2015: 241479. PMID 25892986 DOI: 10.1155/2015/241479 |
0.599 |
|
2015 |
Kim M, Lee J, Han J. Deglycosylation of isoflavone C-glycosides by newly isolated human intestinal bacteria. Journal of the Science of Food and Agriculture. 95: 1925-31. PMID 25199800 DOI: 10.1002/Jsfa.6900 |
0.307 |
|
2015 |
Kim M, Park Y, Cho S, Burapan S, Han J. Synthesis of alkyl quercetin derivatives Journal of the Korean Society For Applied Biological Chemistry. 58: 343-348. DOI: 10.1007/S13765-015-0050-X |
0.757 |
|
2014 |
Kim M, Kim N, Han J. Metabolism of Kaempferia parviflora polymethoxyflavones by human intestinal bacterium Bautia sp. MRG-PMF1. Journal of Agricultural and Food Chemistry. 62: 12377-83. PMID 25437273 DOI: 10.1021/Jf504074N |
0.343 |
|
2014 |
Kim HS, Shin B, Han J. High-throughput HDR inhibitor screening Journal of the Korean Society For Applied Biological Chemistry. 57: 67-72. DOI: 10.1007/S13765-013-4308-X |
0.608 |
|
2013 |
Seo J, Ryu JY, Han J, Ahn JH, Sadowsky MJ, Hur HG, Chong Y. Amino acid substitutions in naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4 result in regio- and stereo-specific hydroxylation of flavanone and isoflavanone. Applied Microbiology and Biotechnology. 97: 693-704. PMID 22391970 DOI: 10.1007/S00253-012-3962-Y |
0.315 |
|
2013 |
Kwon M, Shin B, Lee J, Han J, Kim S. Characterization of Burkholderia glumae BGR1 4-hydroxy-3-methylbut-2-enyl diphosphate reductase (HDR), the terminal enzyme in 2-C-methyl-d-erythritol 4-phosphate (MEP) pathway Journal of the Korean Society For Applied Biological Chemistry. 56: 35-40. DOI: 10.1007/S13765-012-2231-1 |
0.736 |
|
2012 |
Wongsrikaew N, Kim H, Vichitphan K, Cho SK, Han J. Antiproliferative activity and polymethoxyflavone composition analysis of Kaempferia parviflora extracts Journal of the Korean Society For Applied Biological Chemistry. 55: 813-817. DOI: 10.1007/S13765-012-2175-5 |
0.724 |
|
2012 |
Hossain MA, Wongsrikaew N, Yoo G, Han J, Shin C. Cytotoxic effects of polymethoxyflavones isolated from Kaempferia parviflora Journal of the Korean Society For Applied Biological Chemistry. 55: 471-476. DOI: 10.1007/S13765-012-2026-4 |
0.743 |
|
2011 |
Eser BE, Das D, Han J, Jones PR, Marsh EN. Oxygen-independent alkane formation by non-heme iron-dependent cyanobacterial aldehyde decarbonylase: investigation of kinetics and requirement for an external electron donor. Biochemistry. 50: 10743-50. PMID 22074177 DOI: 10.1021/Bi2012417 |
0.312 |
|
2011 |
Seo J, Kang SI, Kim M, Han J, Hur HG. Flavonoids biotransformation by bacterial non-heme dioxygenases, biphenyl and naphthalene dioxygenase. Applied Microbiology and Biotechnology. 91: 219-28. PMID 21626021 DOI: 10.1007/S00253-011-3334-Z |
0.334 |
|
2011 |
Park HY, Kim M, Han J. Stereospecific microbial production of isoflavanones from isoflavones and isoflavone glucosides. Applied Microbiology and Biotechnology. 91: 1173-81. PMID 21562980 DOI: 10.1007/S00253-011-3310-7 |
0.664 |
|
2011 |
Seo J, Kang SI, Won D, Kim M, Ryu JY, Kang SW, Um BH, Pan CH, Ahn JH, Chong Y, Kanaly RA, Han J, Hur HG. Absolute configuration-dependent epoxide formation from isoflavan-4-ol stereoisomers by biphenyl dioxygenase of Pseudomonas pseudoalcaligenes strain KF707. Applied Microbiology and Biotechnology. 89: 1773-82. PMID 21063701 DOI: 10.1007/S00253-010-2989-1 |
0.61 |
|
2011 |
Woo H, Shin B, Cho I, Koo H, Kim M, Han J. Anti-obesity Effect of Carbon Dioxide Supercritical Fluid Extracts of Panax Ginseng C. A. Meyer Journal of the Korean Society For Applied Biological Chemistry. 54: 738-743. DOI: 10.1007/Bf03253153 |
0.583 |
|
2010 |
Kim M, Won D, Han J. Absolute configuration determination of isoflavan-4-ol stereoisomers. Bioorganic & Medicinal Chemistry Letters. 20: 4337-41. PMID 20615704 DOI: 10.1016/J.Bmcl.2010.06.074 |
0.595 |
|
2010 |
Kim M, Marsh EN, Kim SU, Han J. Conversion of (3S,4R)-tetrahydrodaidzein to (3S)-equol by THD reductase: proposed mechanism involving a radical intermediate. Biochemistry. 49: 5582-7. PMID 20515029 DOI: 10.1021/Bi100465Y |
0.644 |
|
2010 |
Seo J, Kang SI, Ryu JY, Lee YJ, Park KD, Kim M, Won D, Park HY, Ahn JH, Chong Y, Kanaly RA, Han J, Hur HG. Location of flavone B-ring controls regioselectivity and stereoselectivity of naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4. Applied Microbiology and Biotechnology. 86: 1451-62. PMID 20091026 DOI: 10.1007/S00253-009-2389-6 |
0.738 |
|
2010 |
Seo J, Kang SI, Kim M, Won D, Takahashi H, Ahn JH, Chong Y, Lee E, Lim Y, Kanaly RA, Han J, Hur HG. Time-dependent density functional theory-assisted absolute configuration determination of cis-dihydrodiol metabolite produced from isoflavone by biphenyl dioxygenase. Analytical Biochemistry. 397: 29-36. PMID 19854147 DOI: 10.1016/J.Ab.2009.10.020 |
0.616 |
|
2010 |
Shin BK, Park HY, Han J. Enzymatic biotransformation of red ginseng and the compositional change of ginsenosides Journal of Applied Biological Chemistry. 53: 553-558. DOI: 10.3839/Jksabc.2010.085 |
0.725 |
|
2009 |
Kim M, Kim SI, Han J, Wang XL, Song DG, Kim SU. Stereospecific biotransformation of dihydrodaidzein into (3S)-equol by the human intestinal bacterium Eggerthella strain Julong 732. Applied and Environmental Microbiology. 75: 3062-8. PMID 19304836 DOI: 10.1128/Aem.02058-08 |
0.662 |
|
2008 |
Won D, Shin BK, Kang S, Hur HG, Kim M, Han J. Absolute configurations of isoflavan-4-ol stereoisomers. Bioorganic & Medicinal Chemistry Letters. 18: 1952-7. PMID 18281214 DOI: 10.1016/J.Bmcl.2008.01.116 |
0.713 |
|
2008 |
Shin B, Kim HM, Lee S, Han J. Axial Conformation of 3-Methyl-2-butenoyl Group in Pyranocoumarin Ring Endows Biological Activity of (+)-Decursin Bulletin of the Korean Chemical Society. 29: 1572-1574. DOI: 10.5012/Bkcs.2008.29.8.1572 |
0.604 |
|
2008 |
Shin B, Han J. Structure and Physical Properties of Copper Thiomolybdate Complex, ( n Bu 4 N) 3 [MoS 4 Cu 3 Cl 4 ] Bulletin of the Korean Chemical Society. 29: 2299-2302. DOI: 10.5012/Bkcs.2008.29.11.2299 |
0.602 |
|
2008 |
Kim M, Han J, Kim S. Isoflavone Daidzein: Chemistry and Bacterial Metabolism Journal of Applied Biological Chemistry. 51: 253-261. DOI: 10.3839/Jabc.2008.040 |
0.66 |
|
2007 |
Seo J, Jeon J, Kim SD, Kang S, Han J, Hur HG. Fungal biodegradation of carbofuran and carbofuran phenol by the fungus Mucor ramannianus: identification of metabolites. Water Science and Technology : a Journal of the International Association On Water Pollution Research. 55: 163-7. PMID 17305136 DOI: 10.2166/Wst.2007.051 |
0.31 |
|
2007 |
Shin B, Kim M, Han J. Structure of Mixed-Anions Tris(2-pyridylmethyl)amine Mn Complex, TPAMnη 2 -NO 3 )(η-CIO 4 ) Bulletin of the Korean Chemical Society. 28: 417-420. DOI: 10.5012/Bkcs.2007.28.3.417 |
0.6 |
|
2007 |
Shin B, Kim Y, Kim M, Han J. Synthesis, structure and catalase activity of the [TPA2Mn2(μ-Cl)2]2+ complex Polyhedron. 26: 4557-4566. DOI: 10.1016/J.Poly.2007.06.011 |
0.607 |
|
2007 |
Kim M, Kim Y, Han J. X-ray crystallographic structure and physical properties of the pentacoordinated [TPAFeCl]+ complex Polyhedron. 26: 4003-4008. DOI: 10.1016/J.Poly.2007.04.041 |
0.336 |
|
2006 |
Shin B, Han J. Rearrangement of the Mo/Fe/S Cluster under the Reducing Conditions; Alternative Synthesis of MoFe 4 S 6 (PEt 3 ) 4 Cl Cluster from [(Cl 4 -cat)Mo(MeCN)Fe 3 S 4 Cl 3 ](Et 4 N) 2 Bulletin of the Korean Chemical Society. 27: 35-36. DOI: 10.5012/Bkcs.2006.27.1.035 |
0.622 |
|
2005 |
Han J, Kim SY, Jung J, Lim Y, Ahn JH, Kim SI, Hur HG. Epoxide formation on the aromatic B ring of flavanone by biphenyl dioxygenase of Pseudomonas pseudoalcaligenes KF707. Applied and Environmental Microbiology. 71: 5354-61. PMID 16151125 DOI: 10.1128/Aem.71.9.5354-5361.2005 |
0.371 |
|
2005 |
Han J, Coucouvanis D. Synthesis and structure of the organometallic MFe2(mu3-S)2 clusters (M = Mo or Fe). Dalton Transactions (Cambridge, England : 2003). 1234-40. PMID 15782259 DOI: 10.1039/B419051C |
0.62 |
|
2004 |
Nava P, Han J, Ahlrichs R, Coucouvanis D. An evaluation by density functional theory of M-M interactions in organometallic clusters with the [Fe(3)MoS(3)](2+) cores. Inorganic Chemistry. 43: 3225-9. PMID 15132630 DOI: 10.1021/Ic0499392 |
0.6 |
|
2004 |
Han J, Newton WE. Differentiation of acetylene-reduction sites by stereoselective proton addition during Azotobacter vinelandii nitrogenase-catalyzed C2D2 reduction. Biochemistry. 43: 2947-56. PMID 15005631 DOI: 10.1021/Bi035247Y |
0.501 |
|
2003 |
Coucouvanis D, Han J, Ahlrichs R, Nava P, Huniar U. Density functional theory calculations on the nitrogenase cofactor and synthetic analogs Journal of Inorganic Biochemistry. 96: 19. DOI: 10.1016/S0162-0134(03)80435-X |
0.559 |
|
2002 |
Han J, Coucouvanis D. Synthesis and structure of singly bridged and doubly bridged [MoFe(3)S(4)] double cubanes with bidentate phosphine ligands. Inorganic Chemistry. 41: 2738-46. PMID 12005498 DOI: 10.1021/Ic010913+ |
0.628 |
|
2002 |
Coucouvanis D, Han J, Moon N. Synthesis and characterization of sulfur-voided cubanes. Structural analogues for the MoFe(3)S(3) subunit in the nitrogenase cofactor. Journal of the American Chemical Society. 124: 216-24. PMID 11782173 DOI: 10.1021/Ja0110832 |
0.613 |
|
2002 |
Han J, Huang M, Coucouvanis D. New heteronuclear Mo/Fe/S clusters. The syntheses and structures of (Cl4-cat)Mo(PEt3)Fe3S4(SPEt3)2Cl and (Cl4-cat)2MoFe2S2(PEt3)2(CO)4 clusters Polyhedron. 21: 2523-2530. DOI: 10.1016/S0277-5387(02)01208-1 |
0.61 |
|
2001 |
Han J, Koutmos M, Ahmad SA, Coucouvanis D. Rational synthesis of high nuclearity Mo/Fe/S clusters: the reductive coupling approach in the convenient synthesis of (Cl(4)-cat)(2)Mo(2)Fe(6)S(8)(PR(3))(6) [R = Et, (n)Pr, (n)Bu] and the new [(Cl(4)-cat)(2)Mo(2)Fe(2)S(3)O(PEt(3))(3)Cl]-1/2(Fe(PEt(3))(2)(MeCN)(4)) and (Cl(4)-cat)(2)Mo(2)Fe(3)S(5)(PEt(3))(5) clusters. Inorganic Chemistry. 40: 5985-99. PMID 11681915 DOI: 10.1021/Ic0104914 |
0.745 |
|
2001 |
Han J, Lee JG, Min SS, Park SH, Angerhofer CK, Cordell GA, Kim SU. Synthesis of new artemisinin analogues from artemisinic acid modified at C-3 and C-13 and their antimalarial activity. Journal of Natural Products. 64: 1201-5. PMID 11575956 DOI: 10.1021/Np0101752 |
0.659 |
|
2001 |
Stavrev KK, Urahata S, Herz T, Han J, Coucouvanis D. Theoretical study on the electronic structure and properties of synthetic MoFe3S3 compounds International Journal of Quantum Chemistry. 85: 469-474. DOI: 10.1002/Qua.1538 |
0.62 |
|
1996 |
Kim SU, Han J, Lim YH. Revised assignment of 1H-NMR signals of artemisinic acid Planta Medica. 62: 480-481. DOI: 10.1055/S-2006-957948 |
0.615 |
|
Show low-probability matches. |