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Journal Article
Bioorganic & medicinal chemistry, ISSN 0968-0896, 2019, Volume 27, Issue 7, pp. 1292 - 1307
[Display omitted] Bedaquiline is a new drug of the diarylquinoline class that has proven to be clinically effective against drug-resistant tuberculosis, but... 
HPLC, high-performance liquid chromatography | MABA, microplate alamar blue assay | M. tb, mycobacterium tuberculosis | LORA, low oxygen recovery assay | LiTMP, lithium tetramethylpiperidide | CFU, colony-forming units | TB, tuberculosis | LDA, lithium diisopropylamide | MIC90, minimum concentration for 90% inhibition of growth | hERG (human Ether-a-go-go Related Gene) | MDR, multidrug-resistant | QFVACMXSSGTRNB-UHFFFAOYSA-N | VRRHQOVTENICRT-UHFFFAOYSA-N | HPEZANWJRVQQPY-UHFFFAOYSA-N | UGUNGVBWXUEQAQ-UHFFFAOYSA-N | YJQCLWPGMHGBLU-UHFFFAOYSA-N | IKSKNYJMDKYTOW-UHFFFAOYSA-N | NBUAEURVOPSXCJ-UHFFFAOYSA-N | OYDTTXUPMJGJQF-UHFFFAOYSA-N | KLIQFVIIBDEFSR-UHFFFAOYSA-N | PTUDVOVIFTXCHK-UHFFFAOYSA-N | SNVWFSQDKYVAAG-UHFFFAOYSA-N | UXLVGNMLOBCENA-UHFFFAOYSA-N | GUWFEHMMBHOINR-UHFFFAOYSA-N | JJEGOJPMKLRSPJ-UHFFFAOYSA-N | PEJQWNBUKMHGGO-UHFFFAOYSA-N | CEKMWLSBGRPKES-UHFFFAOYSA-N | QZVLJNAOIGLPKW-UHFFFAOYSA-N | MAHMFPJJKAUVMB-UHFFFAOYSA-N | FROBLYAPPGEAGY-UHFFFAOYSA-N | XDKSYOXEWIYWFX-UHFFFAOYSA-N | LCXPUYSULUUQTQ-UHFFFAOYSA-N | VCZLKKRCINFNGE-UHFFFAOYSA-N | GQTLJYIGFBZGEF-UHFFFAOYSA-N | YCGHXWPDGDGPKQ-UHFFFAOYSA-N | GKYYBCNOEUQDTQ-UHFFFAOYSA-N | SVYKJBBFRWVRKZ-UHFFFAOYSA-N | HARUWTIOWZSVJY-UHFFFAOYSA-N | HHDDKDPLFXIPBX-UHFFFAOYSA-N | GRADMLRLWZORGX-UHFFFAOYSA-N | VDAOJOKLIXNFRY-UHFFFAOYSA-N | PDVNUOJSRPPQNZ-UHFFFAOYSA-N | ZIMZHZVDHBTFKS-UHFFFAOYSA-N | YEGWEZNQGSXHHQ-UHFFFAOYSA-N | HEUAVAYKJDRKNK-UHFFFAOYSA-N | IEDHWPCLYLYTME-UHFFFAOYSA-N | SNWMCNSZCLYXCK-UHFFFAOYSA-N | CHEMISTRY, MEDICINAL | ASSAY | MIC90, minimum concentration for 90 | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | inhibition of growth | HPLC, high-performance liquid | TUBERCULOSIS DRUG BEDAQUILINE | DIARYLQUINOLINES | chromatography LDA, lithium diisopropylamide | Antitubercular Agents - chemical synthesis | Antitubercular Agents - chemistry | Pyridines - chemistry | Humans | Antitubercular Agents - pharmacology | Pyridines - chemical synthesis | Ether-A-Go-Go Potassium Channels - metabolism | Structure-Activity Relationship | Potassium Channel Blockers - chemical synthesis | Diarylquinolines - pharmacology | Mycobacterium tuberculosis - drug effects | Dose-Response Relationship, Drug | Ether-A-Go-Go Potassium Channels - antagonists & inhibitors | Microbial Sensitivity Tests | Diarylquinolines - chemical synthesis | Molecular Structure | Pyridines - pharmacology | Diarylquinolines - chemistry | Potassium Channel Blockers - chemistry | Potassium Channel Blockers - pharmacology | Drug resistance in microorganisms | Tuberculosis | International cooperation | Chemical tests and reagents | Liability (Law) | Analysis | Research institutes | High performance liquid chromatography | Lithium compounds
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 08/2018, Volume 156, pp. 800 - 814
A number of 5-arylisatin derivatives were synthesized in 5–6 steps from readily available starting materials. Their structures were confirmed by 1H NMR and 13C... 
Angiogenesis | Synthesis | Proliferation | 5-phenylisatin | Migration | NQWUPWUECPPGIW-UHFFFAOYSA-N | ANLTXNNMSRCHCN-UHFFFAOYSA-N | PUNXJSZLFZQUAB-UHFFFAOYSA-N | VZNYACKYPSHSOU-UHFFFAOYSA-N | BHXSWBKMTUVULL-UHFFFAOYSA-N | DVVYNKPDVYRUCX-UHFFFAOYSA-N | HNLCFABWVBXZCD-UHFFFAOYSA-N | NLVWVQNXXBRNSF-UHFFFAOYSA-N | KFRCELJAQDCUFU-UHFFFAOYSA-N | LJIWGGIBHLOGIV-UHFFFAOYSA-N | KLRYXALRASRZSZ-UHFFFAOYSA-N | UZZKXZMLRJPWHY-UHFFFAOYSA-N | WJBPAFLRNLASSA-QRQIAZFYSA-N | WMKGTZOSXSVDFZ-UHFFFAOYSA-N | SRKOXUDYFFCIAD-UHFFFAOYSA-N | QRKGJDJKKVZLJZ-UHFFFAOYSA-N | ZDGMYXUBGVOAKW-UHFFFAOYSA-N | JNYHNYANZWQCGQ-UHFFFAOYSA-N | BMANTURQBSXOFX-UHFFFAOYSA-N | DRYRGMFBQMGXPB-UHFFFAOYSA-N | NUAMVJIXZFIQKX-UHFFFAOYSA-N | CALZDBFRPMTDQT-GYHWCHFESA-N | NDFUGRNSKABAHC-UHFFFAOYSA-N | DGSRGVDBCLLEQZ-JLPGSUDCSA-N | SCYQIRIBDBKXGG-UHFFFAOYSA-N | GLXDXOJIIXNBFX-UHFFFAOYSA-N | ORJDUBSLXFDEKU-UHFFFAOYSA-N | HMTMIKQLZXMAMT-UHFFFAOYSA-N | WOZYGCUDNFSAMU-UHFFFAOYSA-N | CGVRMPCDBYRPGV-UHFFFAOYSA-N | SZCKMTCYVDYGEB-UHFFFAOYSA-N | RKRAVBKCNMIBIK-UHFFFAOYSA-N | NFEWGBYJTMAOAE-UHFFFAOYSA-N | YIEYFAOUUYBIEG-UHFFFAOYSA-N | XQIGYJUCWBVHDV-UHFFFAOYSA-N | BOWDQFHYUWMVSK-UHFFFAOYSA-N | QJYUXPHANUMTLA-UHFFFAOYSA-N | JNWCIWDOWAVNEX-UHFFFAOYSA-N | MURNNTGIMOTEEI-UHFFFAOYSA-N | PQDURQOFPGFUFH-UHFFFAOYSA-N | LLGKXCGBYQERAR-UHFFFAOYSA-N | OEQVJYYMYNMBQR-UHFFFAOYSA-N | ZIFMYEUABOAUPY-UHFFFAOYSA-N | KKNIRCSVMWWEOY-UHFFFAOYSA-N | WPZWOMJBXSCVQY-UHFFFAOYSA-N | SZSAXLRFQKXWLL-UHFFFAOYSA-N | CGOUNXKCEGEARF-HAHDFKILSA-N | ZHYYSTBSIDKXEP-UHFFFAOYSA-N | JEAPPFRTYMXSOT-UHFFFAOYSA-N | RKCYEFAWSDGUSD-UHFFFAOYSA-N | VDJZRQWVBSDWGQ-UHFFFAOYSA-N | DPJQRIMBZXQXMJ-DXJNIWACSA-N | JGIUEALCJPSECX-UHFFFAOYSA-N | WXCWDAWGTWQPIB-VEILYXNESA-N | YNUKUKBQZLCNHO-UHFFFAOYSA-N | YRBIKCXVGGTAKX-UHFFFAOYSA-N | JPCMFBGBNFEZBC-UHFFFAOYSA-N | HDMORQPPXMLTHL-UHFFFAOYSA-N | APOPTOSIS | DESIGN | CHEMISTRY, MEDICINAL | DOCKING | ISATIN DERIVATIVES | INHIBITORS | Human Umbilical Vein Endothelial Cells | Leukemia - pathology | Apoptosis - drug effects | Antineoplastic Agents - chemical synthesis | Humans | Isatin - pharmacology | Leukemia - metabolism | Isatin - chemistry | Neovascularization, Pathologic - pathology | Liver Neoplasms - pathology | Antineoplastic Agents - pharmacology | Angiogenesis Inhibitors - chemical synthesis | Liver Neoplasms - drug therapy | Angiogenesis Inhibitors - pharmacology | Leukemia - drug therapy | Antineoplastic Agents - chemistry | Hep G2 Cells | Cell Movement - drug effects | Isatin - chemical synthesis | Neovascularization, Pathologic - drug therapy | K562 Cells | Liver Neoplasms - metabolism | Cell Proliferation - drug effects | Angiogenesis Inhibitors - chemistry | Drug Screening Assays, Antitumor | Prevention | Antimitotic agents | Liver cancer | Liver | Leukemia | Antineoplastic agents | Cancer
Journal Article
Tetrahedron, ISSN 0040-4020, 2018, Volume 74, Issue 32, pp. 4289 - 4294
The Diels-Alder reactivity of 1,2-heteroborines (H4C4B(H)X, X = NH, PH, AsH; O, S, Se) has been computationally explored by means of Density Functional Theory... 
1,2-Heteroborines | Diels-Alder | Reactivity | Aromaticity | Activation strain model | PONOWYVXWZVCCC-UHFFFAOYSA-N | SRHVNFUDFFIVRN-NUBCRITNSA-N | YCEGGNNGACCHFZ-UHFFFAOYSA-N | ZSTCCYWGIXBRPV-UHFFFAOYSA-N | NTNGMURAICZZPC-UHFFFAOYSA-N | QCUMWZDVNMRVET-DPYQTVNSSA-N | IOQJCJHBDWXZSD-LURJTMIESA-N | DTGYORVSPXZQBM-MOJAZDJTSA-N | VNAOUIBJUVIGLA-UHFFFAOYSA-N | CHKCLPJIWDOSQM-UHFFFAOYSA-N | UHOVQNZJYSORNB-UHFFFAOYSA-N | CLXFSILJZKQTSQ-DPYQTVNSSA-N | PGDUPBGRQSLJLK-UHFFFAOYSA-N | TVASWQMJDYUUIV-KVFPUHGPSA-N | PWZYIISNJZBZQV-UHFFFAOYSA-N | ZEXMUHQFTFFKEH-CJJZRWNGSA-N | CVNJOQLFFFUABC-UHFFFAOYSA-N | RQNTTXFSYWVJTC-UHFFFAOYSA-N | VCGYXDRALTWCFJ-FYZOBXCZSA-N | OGZZEGWWYQKMSO-UHFFFAOYSA-N | CLXFSILJZKQTSQ-MOJAZDJTSA-N | UMHSJEDRIIKSDA-ZETCQYMHSA-N | RWRJVRXWGGLQLS-UHFFFAOYSA-N | MEUCBUADBJJJIM-UHFFFAOYSA-N | VJFYALMMNXTWRN-UHFFFAOYSA-N | UJIZQFICYZHGNK-UHFFFAOYSA-N | RSGUYISAUVGSNH-UHFFFAOYSA-N | VXFHRPANTVCIPR-NRISCCJGSA-N | ZDPCTADKEKBXLZ-UHFFFAOYSA-N | WVGXAASCDWGORG-UHFFFAOYSA-N | DTGYORVSPXZQBM-DPYQTVNSSA-N | VCGYXDRALTWCFJ-UHFFFAOYSA-N | VMRUNHMEWAQXLH-RXMQYKEDSA-N | QCUMWZDVNMRVET-MOJAZDJTSA-N | BOVKNQHKMJRFDH-UHFFFAOYSA-N | ZEFWGXUSXKYOKS-ZETCQYMHSA-N | CDFJCQZIHBKYRZ-UHFFFAOYSA-N | VHAIUPZTODXARC-UHFFFAOYSA-N | AVJVLDDGYUJTPU-UHFFFAOYSA-N | NIPJKMZODYZYJG-LURJTMIESA-N | PYYOTYPDWAFLMT-ZCFIWIBFSA-N | GUSVGQFIPAJYNZ-UHFFFAOYSA-N | FPYJFEHAWHCUMM-UHFFFAOYSA-N | PROAEQOBVSNCIT-UHFFFAOYSA-N | JURIEQICPHEWPD-MOJAZDJTSA-N | VXFHRPANTVCIPR-CDRLLEPJSA-N | JURIEQICPHEWPD-DPYQTVNSSA-N | BUDIPYFWNYIQGI-UHFFFAOYSA-N | KMMASONFEWIHBO-UHFFFAOYSA-N | NOODIUXEUXWPLQ-LURJTMIESA-N | ISUNFWIKLIQVHH-UHFFFAOYSA-N | VBUPWSLICFIRTD-UHFFFAOYSA-N | ZEXMUHQFTFFKEH-WWGBPYKYSA-N | BORON | HYDROGENATION | S(N)2 REACTIONS | CHEMISTRY, ORGANIC | ENERGY DECOMPOSITION ANALYSIS | MULTIBOND REACTIONS | MOLECULAR-ORBITAL THEORY | CYCLOADDITION REACTION | SYNCHRONICITY | Density functionals | Specific gravity
Journal Article
Tetrahedron, ISSN 0040-4020, 2018, Volume 74, Issue 39, pp. 5683 - 5690
N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously... 
N-heterocyclic carbene-palladacyclic complex | Aryl chlorides | α-arylation | Synthetic methods | C-N coupling | LHEXQSNVSDFVSB-UHFFFAOYSA-N | CWUFBLXRZFLYCL-UHFFFAOYSA-N | CCHRTZDBCKYQGY-UHFFFAOYSA-N | DLIYPSUDXTYSKZ-UHFFFAOYSA-N | KEZRLEQDBNGXKA-UHFFFAOYSA-N | VZARMICIYMJKKP-UHFFFAOYSA-N | FHQRDEDZJIFJAL-UHFFFAOYSA-N | RQESRCNPCYZPJN-UHFFFAOYSA-N | VVYHEMDWUOTECJ-UHFFFAOYSA-N | BIMOAEQCESCJNJ-UHFFFAOYSA-N | VTYVRSMSJXKETA-UHFFFAOYSA-N | HYQQQBPBJZKKCK-UHFFFAOYSA-N | ZKKQSDFPMPSRNS-UHFFFAOYSA-N | FONVDCDJUVECGD-UHFFFAOYSA-N | LXZGVFCKZRHKMU-UHFFFAOYSA-N | XBJADZKTEUBHBI-UHFFFAOYSA-N | GANRUTSEZQVUIO-UHFFFAOYSA-N | NKWNLWFVNOMGNF-UHFFFAOYSA-N | RABKQBRVTCYEKB-UHFFFAOYSA-N | CEFXATQBOJMVRW-UHFFFAOYSA-N | FQKQCCVYAJVHAF-UHFFFAOYSA-N | LGROUUAKEVLNHD-UHFFFAOYSA-N | WZDHIQNTSAHSBB-UHFFFAOYSA-N | YAOBFBZFGOQMHL-UHFFFAOYSA-N | YKOLHVHMRGNMEZ-UHFFFAOYSA-N | ZQVAGPGHTQBLMM-UHFFFAOYSA-N | NFHIPZYAYZPXJE-UHFFFAOYSA-N | XSOVNHZUZFPETI-UHFFFAOYSA-N | YJCYHOQBCOTCDR-UHFFFAOYSA-N | SDWQEPLBCOZBFL-UHFFFAOYSA-N | AFOQGTQATMATIX-UHFFFAOYSA-M | GHTILTIFYAIUHV-UHFFFAOYSA-N | NLXYMNARXOOBEW-UHFFFAOYSA-N | BKPSCHXBECTTLS-UHFFFAOYSA-N | BXBCQWYERUFTQQ-UHFFFAOYSA-N | FQILZCAXBBSGEC-UHFFFAOYSA-N | PAAPAGLAGXSLNI-UHFFFAOYSA-N | HRCMEBQQAGTUCC-UHFFFAOYSA-N | OGLZSMPGMUDNKR-UHFFFAOYSA-N | CNKWMZSMRRWDGN-UHFFFAOYSA-N | KMMLCPOBCVFTPQ-UHFFFAOYSA-N | ZZFARUSNHHPINW-UHFFFAOYSA-N | PWJLYIDEFMLCPF-UHFFFAOYSA-N | GZGYOLIWTUXMAR-UHFFFAOYSA-N | PGPGRRQZSNCYDX-UHFFFAOYSA-N | OXMURBQZWNJHAO-UHFFFAOYSA-N | FCBHQTYZMFLZAH-UHFFFAOYSA-N | CQLXSFDDEBUZQZ-UHFFFAOYSA-N | OKNJNSJETRTQJI-UHFFFAOYSA-M | QQKNYXROGNWARI-UHFFFAOYSA-N | alpha-arylation | BOND-FORMING REACTIONS | CHEMISTRY, ORGANIC | NHC-PD(II)-IM NHC | BUCHWALD-HARTWIG AMINATION | PALLADIUM-CATALYZED AMINATION | EFFICIENT CATALYSTS | HETEROARYL CHLORIDES | VERSATILE CATALYST | LIGANDS | TEMPERATURE SUZUKI-MIYAURA | SELECTIVE MONOARYLATION
Journal Article
Bioorganic & medicinal chemistry letters, ISSN 0960-894X, 2018, Volume 28, Issue 17, pp. 2914 - 2919
[Display omitted] •Benign synthesis of new pyrazole derivatives.•29 novel molecules.•MIC as low as 0.78 μM (S. aureus, MRSA, B. subtilis, and A.... 
Antimicrobial | Acinetobacter baumannii | Hydrazone | Pyrazole | MRSA | LOERTZFIRUROPJ-DHRITJCHSA-N | UWGGQMGEFMBVLR-KKMKTNMSSA-N | HDYVUMZUWCJPKC-KKMKTNMSSA-N | JIXROJKYLGSGTF-LGJNPRDNSA-N | LFXQJGXFFMMSCD-KKMKTNMSSA-N | UUHAWRQSWYCALO-KKMKTNMSSA-N | RXERGSIGGJWJQK-KKMKTNMSSA-N | JORSTRRMGOZNNU-RPPGKUMJSA-N | SUWFPEZITOEUQR-IPBVOBEMSA-N | JYMHEGQCQAJSTQ-GLCIPLLTSA-N | FPMNUHFIZZDCKX-DHRITJCHSA-N | AVLRRMXQQJNKGP-DHRITJCHSA-N | AQVBDLJEOUZANE-KKMKTNMSSA-N | VAXHWIHXKIPNRD-IPBVOBEMSA-N | PFEMWRAYTCTHIG-OOEWDAAOSA-N | QEWMZDUKJDLAQH-PNQUVVCRSA-N | NIPISOWJKCIIHK-LGJNPRDNSA-N | RXESTGQXLDYIKG-IPBVOBEMSA-N | SBLBFRUAAPEBKY-KKMKTNMSSA-N | WIKWAYNIPJPLTA-OWNKRRAQSA-N | MVLUBVHJPZOZLV-KKMKTNMSSA-N | FETAFRLLXZXYCT-KKMKTNMSSA-N | UWBWHTJUAPCNHF-KKMKTNMSSA-N | IQLGHNZLARMWNN-KKMKTNMSSA-N | TWFYOLDKHQKSCA-IPBVOBEMSA-N | ADNDOVPYDVEIIC-KKMKTNMSSA-N | ZUGRLNIFEHJKOS-OOEWDAAOSA-N | HTHJFNCAJAARGB-RPPGKUMJSA-N | BACTERIA | CHEMISTRY, MEDICINAL | CHEMISTRY, ORGANIC | FLUORINE | AGENTS | IRAQ | Benzoates - chemistry | Benzoates - chemical synthesis | Hydrazones - chemical synthesis | Structure-Activity Relationship | Hydrazones - chemistry | Hydrazones - pharmacology | Anti-Bacterial Agents - chemical synthesis | Dose-Response Relationship, Drug | Microbial Sensitivity Tests | Anti-Bacterial Agents - chemistry | Benzoates - pharmacology | Anti-Bacterial Agents - pharmacology | Molecular Structure | Acinetobacter baumannii - drug effects | Staphylococcus aureus - drug effects | Bacillus subtilis - drug effects | Index Medicus
Journal Article
Tetrahedron, ISSN 0040-4020, 05/2019, Volume 75, Issue 19, pp. 2763 - 2770
KMnO -mediated oxidative C[sbnd]N bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride... 
KVZKXVUKFXXYMK-UHFFFAOYSA-N | WEWQWPBVOOSUPN-UHFFFAOYSA-N | LGSFCNQOKBXWSV-UHFFFAOYSA-N | UNHLIOCGYKIPMQ-UHFFFAOYSA-N | AHCKWEJCWNMPOC-UHFFFAOYSA-N | XWVZOCHPUVJKSD-UHFFFAOYSA-N | WHUZMDXNODMIIP-UHFFFAOYSA-N | OWUKKBKCYSHARY-UHFFFAOYSA-N | IXGKXDNXVMUNJE-UHFFFAOYSA-N | JTRXYDXSZLRHBM-UHFFFAOYSA-N | LCOPCEDFGGUYRD-UHFFFAOYSA-N | IHKIASZHUKYNEA-UHFFFAOYSA-N | SCIQYIYYMAPENJ-UHFFFAOYSA-N | XLMQTLGCVJWKGO-UHFFFAOYSA-N | MAZZBVWLOONVSQ-UHFFFAOYSA-N | Acyl chloride | LITQQXVRZFNDMV-UHFFFAOYSA-N | Amide | YJACBPFSRIMHFW-UHFFFAOYSA-N | MIPPUZLVNVNAPW-UHFFFAOYSA-N | VLJDAYGYFZKFGN-UHFFFAOYSA-N | CICSJMNWCSOMDH-UHFFFAOYSA-N | LUWGONODJOZTMQ-UHFFFAOYSA-N | MVDGHRIRJFXONZ-UHFFFAOYSA-N | WKDYQGMWPAPVBT-UHFFFAOYSA-N | NELWCGWIYQJYJY-UHFFFAOYSA-N | KMnO | IXAOBVXPTKIAED-UHFFFAOYSA-N | KRXAPUFKQQWAGK-UHFFFAOYSA-N | OEYWSNRVIODBJL-UHFFFAOYSA-N | UGHRBUNRVJUSFC-UHFFFAOYSA-N | VGFFGZGFETXMNS-UHFFFAOYSA-N | KFGDZDHOKBKEJZ-UHFFFAOYSA-N | RCOMQXDBEXYAML-UHFFFAOYSA-N | XGZZJMMAOGFTGG-UHFFFAOYSA-N | RAECVXWPFBWHOJ-UHFFFAOYSA-N | WJWGQMWVGSNLSI-UHFFFAOYSA-N | HEFFCQILGLLHQC-UHFFFAOYSA-N | GDTOEWWFOATDIW-UHFFFAOYSA-N | XGCAULAWUGUDFT-UHFFFAOYSA-N | HCQQGTYHBGXRTR-UHFFFAOYSA-N | VSURRQZMKWVYIC-UHFFFAOYSA-N | C[sbnd]N cleavage | Tertiary amine | FZIFUJULXRFHBB-UHFFFAOYSA-N | LQJYGXFRWWUKNT-UHFFFAOYSA-N | KJSQPVRSXVERSV-UHFFFAOYSA-N | OAZSHPNFKFANSG-UHFFFAOYSA-N | ACTIVATION | ALKYLATION | ARYLATION | AMIDATION | CHEMISTRY, ORGANIC | AMINATION | COOPERATIVE CATALYSIS | KMnO4 | C-N cleavage | CARBON-NITROGEN BOND | H BONDS | DERIVATIVES | METAL-FREE
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 12/2018, Volume 876, pp. 66 - 77
Bifunctional silanes ClCH2SiF3 and ClCH2SiF2Me react with N-trimethylsilyl-N-methylacetamide and its tautomer О-trimethylsilyl-N-methylacetimidate as ambident... 
Trans-silylation | Bifunctional (chloromethyl)fluorosilanes | N-trimethylsilyl-N-methylacetamide | O-trimethylsilyl-N-methylacetimidate | Alkylation | LZBXJLBYHFVKID-UHFFFAOYSA-N | GHULCXGKGMKDRP-YVFTVSHDSA-N | VNCINCFHIHBABX-UHFFFAOYSA-N | ZHMMUJBOBFHFGQ-FJXQXJEOSA-N | LEQPQYLSKOOZBC-OGFXRTJISA-N | NHVCXSOQGUQWPJ-UHDJGPCESA-N | DNZMWSMASHVUSH-UHFFFAOYSA-N | QZXIUIVNLBSEAV-SNVBAGLBSA-N | PXBXSQIAOCLLJL-XBXARRHUSA-N | IRKIANSIKSKTKR-VOTSOKGWSA-N | QHUOBLDKFGCVCG-UHFFFAOYSA-N | KJPHRQFOVIMVRY-SOFGYWHQSA-N | QHTVELKRMQXYEL-RMZRELHQSA-N | ZMQMFPJITFFNNN-UHFFFAOYSA-N | LYZQNNUMEMOAMJ-UHDJGPCESA-N | XVDDRRAIRVXXKL-UHFFFAOYSA-N | IJOOHPMOJXWVHK-UHFFFAOYSA-N | KMDJTGORMWBENH-XBXARRHUSA-N | LHMKUTKRLVWHGR-VMPITWQZSA-N | BUWVFXQXJZZXMB-JTQLQIEISA-N | CTIKAHQFRQTTAY-UHFFFAOYSA-N | GSSJYDPDBXWCQB-UHFFFAOYSA-N | KNBHNRSDNNQEDD-SOFGYWHQSA-N | HFYKLNXKBNFHFQ-UHFFFAOYSA-N | LBDKEDMWUNEPJA-KPKJPENVSA-N | YVAKMDBUZRKCCY-UHFFFAOYSA-N | JCCVPMDZJPSMKQ-QRPNPIFTSA-N | XZOLBVIGBYYFGV-UHFFFAOYSA-N | DQCRGAGEZPEQKW-VHODGJRUSA-N | OAAYVUOGEYBJKX-ZDTICIBISA-N | CWLUGSDHELAQNH-UHFFFAOYSA-N | GMVMMSWZWUKXFF-KMXZHCNGSA-N | QTEOOICTJFZYHL-XBXARRHUSA-N | PEELWXHICOPINM-UHFFFAOYSA-N | PPQLDFJGDNYQAV-SOFGYWHQSA-N | OVVYHHUTRRZFBO-UHFFFAOYSA-N | CHAMWPSLFQXIPT-UHFFFAOYSA-N | KATVUIAWELMJKD-UHFFFAOYSA-N | MZNJKFZRKLEMSZ-UHFFFAOYSA-N | PSYFYONVUBTXLR-UHDJGPCESA-N | YORSPWXYCHFRGC-UHFFFAOYSA-N | ICBLAYYRCPHQLM-UHFFFAOYSA-N | OIXFBORHATWXCM-UHFFFAOYSA-N | FPGLPOIMBLXJEY-UHFFFAOYSA-N | FESSCXXKADLNIV-YHNNWUSJSA-N | IGWTVVLXPBAHMC-UHFFFAOYSA-N | CRYSTAL-STRUCTURE | S(N)2 REACTIONS | REACTIVITY | CHEMISTRY, ORGANIC | INTRAMOLECULAR COORDINATION | CHEMISTRY, INORGANIC & NUCLEAR | REARRANGEMENT | SUBSTITUTED 2-PHENYLACETAMIDES | SILICON COMPLEXES | PENTACOORDINATE | DERIVATIVES | AMIDES | Amides | Nuclear magnetic resonance spectroscopy | Analysis | Silane
Journal Article
Journal of Catalysis, ISSN 0021-9517, 11/2016, Volume 343, pp. 240 - 247
[Display omitted] •Electrocarboxylation of 2,3-dimethyl-butadiene at an onset potential of −1.3V.•Elucidation of electrocarboxylation mechanism by first... 
Electrochemistry | Density functional theory | Nickel | Mechanism | Carbon dioxide | JCOADMTVEFEMRB-UHFFFAOYSA-N | DCWNMBVZNOMUIO-UHFFFAOYSA-L | KAXRPGOVDVRQRV-UHFFFAOYSA-N | RLERLEQTWMVLOE-UHFFFAOYSA-N | YCYXAVOSNLLCKA-UHFFFAOYSA-N | SUQIPZMRMITSOM-UHFFFAOYSA-N | VOHHNFLDCHAUIY-UHFFFAOYSA-N | Mmc1.pdf | LYNHTPHTJWVPKK-UHFFFAOYSA-N | MYPVOBFYUVCLMO-UHFFFAOYSA-N | QPVGPARGNKXDJE-UHFFFAOYSA-N | JFHMZJRGAJXOEP-UHFFFAOYSA-N | LABRWMOJSAYDPL-UHFFFAOYSA-N | BXCJKFHLMPZGKJ-UHFFFAOYSA-N | WFTITXXWBRVCLK-UHFFFAOYSA-M | JBLZCMLQVGGGBV-QDXJQGPWSA-N | KAKZBPTYRLMSJV-UHFFFAOYSA-N | CIVKECGAWHNMMH-SYOLFDCTSA-N | DIKBKLULQCNWFE-UHFFFAOYSA-N | VDDAQBBXEZSNHH-UHFFFAOYSA-N | FHNSZOZVRKRZGQ-UHFFFAOYSA-N | IQKPCYQRKHJALH-UHFFFAOYSA-N | UMVYXLXQXUEFRV-UHFFFAOYSA-N | VSVKXOLIOSGVCJ-UHFFFAOYSA-L | VTHXEJIWTGATJW-UHFFFAOYSA-N | SEUCQUZIPWXOBH-UHFFFAOYSA-N | LRQIISNFNXZOAK-UHFFFAOYSA-J | WDSKYSABKOOQRK-UHFFFAOYSA-L | APAHXRGQWURMJR-UHFFFAOYSA-N | HREOABIJUTZHCI-UHFFFAOYSA-N | KVWZPQIVNKDUHM-UHFFFAOYSA-N | VOBMDCAGKGENRH-UHFFFAOYSA-N | UXMFHNKDQFFOOL-UHFFFAOYSA-N | OLNHBSNIVFVGGW-UHFFFAOYSA-N | NVRSOWPNPLTMAQ-UHFFFAOYSA-N | LAFORKIOPBPCNS-UHFFFAOYSA-N | OXJZEDNDPPJTJD-UHFFFAOYSA-N | VGGSQFUCUMXWEO-UHFFFAOYSA-N | LPGZPZDKTWWAEO-UHFFFAOYSA-N | AKBIZVWCXJQZLG-UHFFFAOYSA-J | LYJAGSWTKGGDOJ-UHFFFAOYSA-N | VNPMSJOKLISNOE-UHFFFAOYSA-N | LTGQENGTSNJDEH-UHFFFAOYSA-N | XLNXLMGKHNRSHN-UHFFFAOYSA-N | GSDRCAHUZXIGOX-UHFFFAOYSA-L | GUFOFKDUFACARE-UHFFFAOYSA-M | DKEHOOAKLFRDNY-UTZZRDIYSA-N | FPTIZLYXVNJBHP-UHFFFAOYSA-N | FZRZIQSGOOKBPC-UHFFFAOYSA-N | XLEGCVYSYKDRSA-UHFFFAOYSA-N | PLPJELUSDATAJG-UHFFFAOYSA-L | JISVROCKRBFEIQ-UHFFFAOYSA-N | GENAZHJYHPJKOC-UHFFFAOYSA-N | YYLXMOBNWLHUAR-BWRCCWPFSA-N | XYAPAZVKBADAFD-UHFFFAOYSA-N | GPUUZTOWDDTBBG-UHFFFAOYSA-N | XIOSRWXZKNQBOL-UHFFFAOYSA-N | ACIDS | CO2 | CHEMISTRY, PHYSICAL | ELECTROCHEMICAL REDUCTION | CATHODE | ENGINEERING, CHEMICAL | ALKENES | CARBON-DIOXIDE | SURFACES | Olefins | Butadiene | Catalysts | Formic acid | Density functionals | Atoms | Organic acids | or physical chemistry | Catalysis | Chemical Sciences | Theoretical and
Journal Article
Bioorganic & medicinal chemistry, ISSN 0968-0896, 2018, Volume 26, Issue 15, pp. 4452 - 4460
[Display omitted] Syzygium is a large genus of flowering plants, with several species, including the clove tree, used as important resources in the food and... 
Cytotoxicity | NF-κB inhibition | Mitochondrial transmembrane potential inhibition | Pentacyclic triterpenoids | Syzygium corticosum | JPZKPTYPWSCQTN-LTFTTYLTSA-N | XUARCIYIVXVTAE-ZAPOICBTSA-N | VYKLRWGPNUVKNC-HNSJSBKASA-N | AOXTVVMIAYODJX-HCOAJINSSA-N | MDCGEAGEQVMWPE-SXGMEYSMSA-N | LXEQIOGTMDLLEC-UHFFFAOYSA-N | AQHKWALTXQHZKK-GLDUGTPFSA-N | ZOEYQETWCHEROV-DOMZBBRYSA-N | MKSFEZKHACTMCV-UHFFFAOYSA-N | WCGUUGGRBIKTOS-GPOJBZKASA-N | JJRYPZMXNLLZFH-URWSZGRFSA-N | QJSQOGJCHBXLAH-UHFFFAOYSA-N | KPQMCAKZRXOZLB-KOIHBYQTSA-N | QGJZLNKBHJESQX-FZFNOLFKSA-N | FVWJYYTZTCVBKE-ROUWMTJPSA-N | PFCVZKFJHRCLCC-PGOIBATFSA-N | KCDXJAYRVLXPFO-UHFFFAOYSA-N | QQLURXJDJDJYQV-UHFFFAOYSA-N | JWDDEDFQFOCWRN-LTQNRFLVSA-N | PSZDOEIIIJFCFE-OSQDELBUSA-N | RCOMNCICXWMEBP-BDCFQSRGSA-N | XEVQXKKKAVVSMW-WRWORJQWSA-N | VWWMSFMNICMFQB-AWEZNQCLSA-N | UXUVZTGGSMRNDQ-YMUSRRSASA-N | KWUXNWWMRBXQRC-BBBXVDCKSA-N | MIJYXULNPSFWEK-GTOFXWBISA-N | FRUITS | CHEMISTRY, MEDICINAL | NF-kappa B inhibition | CHEMICAL-SHIFTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PREVENTION | CHEMISTRY, ORGANIC | SUPPRESSION | STRUCTURE ELUCIDATION | DISCOVERY | URSOLIC ACID | NMR | ANTIOXIDANT | CONSTITUENTS | Plant Leaves - chemistry | Plant Extracts - chemistry | NF-kappa B - antagonists & inhibitors | Antineoplastic Agents, Phytogenic - chemical synthesis | Triterpenes - pharmacology | Humans | Molecular Conformation | Antineoplastic Agents, Phytogenic - chemistry | NF-kappa B - metabolism | Structure-Activity Relationship | Membrane Potential, Mitochondrial - drug effects | HT29 Cells | Syzygium - chemistry | Triterpenes - chemistry | Plant Leaves - metabolism | Triterpenes - chemical synthesis | Cell Line, Tumor | Cell Proliferation - drug effects | Antineoplastic Agents, Phytogenic - pharmacology | Syzygium - metabolism
Journal Article
European journal of medicinal chemistry, ISSN 0223-5234, 2019, Volume 165, pp. 93 - 106
Candida albicans biofilm represents a major clinical problem due to its intrinsic tolerance to anti-fungal compounds and it has been highly related to... 
Indole derivatives | Candida albicans biofilm | Galleria mellonella | STFYECVTJVAXEL-UHFFFAOYSA-N | ZDAZUJBASMCUAK-UHFFFAOYSA-N | QEOATOUNLDHSQK-UHFFFAOYSA-N | RNQKFVUQTYKTMI-UHFFFAOYSA-N | JGMIQSWMEOLVBB-UHFFFAOYSA-N | AUCXPEQZOQAAFS-UHFFFAOYSA-N | PDAACQKFXIJYAL-UHFFFAOYSA-N | SDJNCZDWCAXMSH-UHFFFAOYSA-N | ZQTZHAMHKFWIBB-UHFFFAOYSA-N | IDNLCTISTSJTCZ-UHFFFAOYSA-N | FYEXJEHODQMAQH-UHFFFAOYSA-N | KTEDBFKQSUUOQJ-UHFFFAOYSA-N | BQHATOAEKBHBSG-ONEGZZNKSA-N | QWXWNQKFHDHYQE-UHFFFAOYSA-N | HXFLQBANGDSGQG-RMKNXTFCSA-N | ZHHGIWYVPGOVQF-UHFFFAOYSA-N | CXRBEIYAJRAXGL-UHFFFAOYSA-N | RHFWDNPLXMRBPV-UHFFFAOYSA-N | QRDRJCVOWLBKAI-UHFFFAOYSA-N | SAYITMHVAPIHOJ-UHFFFAOYSA-N | XHZHVKZMLSMJMV-UHFFFAOYSA-N | BVYXKWDLASTCIQ-UHFFFAOYSA-N | TZEPSZHSUYEGHK-UHFFFAOYSA-N | GECISELQTBSFMH-UHFFFAOYSA-N | GACNYZFBTRNWNF-UHFFFAOYSA-N | RQALFBAYWUEKQO-UHFFFAOYSA-N | QTJRJEPSSNWTEU-UHFFFAOYSA-N | DPKPMCBKYQFKCM-UHFFFAOYSA-N | FTKBYDWYXDQBIR-UHFFFAOYSA-N | NJBOOOMGSPXXEY-UHFFFAOYSA-N | TYTXPTDMAYMPCH-UHFFFAOYSA-N | ZVXBCYQLTVSTIA-UHFFFAOYSA-N | NGDRNYOVDLWVSF-UHFFFAOYSA-N | PRRZWJAGZHENJJ-UHFFFAOYSA-N | NTJSXZMZJOFXBE-UHFFFAOYSA-N | VRHMOCLINRGJOD-UHFFFAOYSA-N | GOYOQVBBVIZNBX-UHFFFAOYSA-N | QFHXYQKTLIINHH-UHFFFAOYSA-N | UAGBXHLSSFEDDU-UHFFFAOYSA-N | RNFBXOBIDNOBJJ-UHFFFAOYSA-N | ZIEAAKFMVJDXHQ-UHFFFAOYSA-N | ACID-DERIVATIVES | CHEMISTRY, MEDICINAL | IN-VIVO | Derivatives (Financial instruments) | Index Medicus
Journal Article