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钱旭红 - 华东师范大学校长、党委副书记 免费编辑 修改义项名

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钱旭红,男,1962年生于江苏宝应。博士、教授、中国工程院院士

1978年9月进入华东化工学院(现华东理工大学)石油化工系,1982年7月获学士学位,1982年9月华东化工学院(现华东理工大学)精细化工系研究生,1985年4月获硕士学位,1988年7月华东理工大学获工学博士学位。

2011年当选中国工程院院士。

现任华东师范大学校长、党委副书记。

基本信息

  • 中文名

    钱旭红

  • 国籍

    中国

  • 出生地

    江苏宝应

  • 出生日期

    1962年

  • 职业

    科学家

  • 毕业院校

    华东化工学院(现华东理工大学)

  • 主要成就

    1996国务院政府特殊津贴1998中国青年科技奖;1999第六届上海十大科技精英

折叠 编辑本段 个人经历

1986-1987华东理工大学精细化工系党总支副书记;

1992.8-1995.4先后任华东理工大学精细化工学科主任、药物化工研究所所长;

1995.5-7国家高级教育行政学院学员;

1995.9-1996.2任华东理工大学校长助理、1996.3-2000.10 任副校长;

2000.9-2004.6 大连理工大学教育部奖励计划特聘教授。

2002.1-2010.1上海市化学生物学重点实验室主任(兼);

2003.3-2006国家南方农药创制中心(上海)主任(兼);

2004.7-华东理工大学校长。2007.4- 中国化工学会副理事长;

2007-2008,亚洲及太平洋化工联盟主席;

2011.12 当选中国工程院院士(化工、冶金与材料工程学部);

2015年3月,卸任华东理工大学校长一职;

2018年1月,任华东师范大学校长、党委副书记。

曾经先后入选或获得奖励计划、国家杰出青年基金者、国家“973”项目首席科学家、上海市科技精英,现为中国工程院院士、国家自然科学基金化学部咨询委员会委员、英国皇家化学会会士、德国洪堡基金会学术大使。

1992年获霍英东基金会高校优秀青年教师奖(科研类);1995年获全国优秀教师;1996年获国务院政府特殊津贴;1997年获入选国家百千万人才工程(第一、二层次);1998年获中国青年科技奖;1999年获第六届上海十大科技精英称号。作为第一完成人,获得1998年,2002年,2003年国家教育部科技进步一等奖、2008年获上海市自然科学一等奖和2008国家科技进步二等奖,作为第三完成人,获得2010上海市自然科学二等奖。[1]

折叠 编辑本段 职务信息

2018年1月17日上午,华东师范大学全校干部教师大会召开。教育部党组成员、部长助理刘大为宣布了教育部党组的任免决定。钱旭红任华东师范大学校长;钱旭红任华东师范大学党委委员、常委、党委副书记。[2]

折叠 编辑本段 学术论文

研究方向1.染料的化学生物学

ORG. LETT.-2006-3721: A series of polyamide receptor based PET fluorescent sensor molecules: Positively cooperative Hg2+ ion binding with high sensitivity

ORG. LETT. 2005-3029: Colorimetric and ratiometric fluorescent chemosensor with a large red-shift in emission: Cu(Ⅱ)-only sensing by deprotonation of secondary amines as receptor conjugated to naphthalimide fluorophore

ORG. LETT.-2005-889: Ratiometric and selective fluorescent sensor for Cu-Ⅱ based on internal charge transfer (ICT)

ORG. LETT. 2004-2757: Novel fluorescent pH sensors based on intramolecular hydrogen bonding ability of naphthalimide (SS)

J. ORG. CHEM.-2006-4308: Detecting Hg2+ ions with an ICT fluorescent sensor molecule: Remarkable emission spectra shift and unique selectivity

J. ORG. CHEM.-2007-3554: Ratiometric and highly selective fluorescent sensor for cadmium under physiological pH range: A new strategy to discriminate cadmium from zinc

CHEM. COMMUN.-2006-109: Two regioisomeric and exclusively selective Hg(Ⅱ) sensor molecules composed of a naphthalimide fluorophore and an o-phenylenediamine derived triamide receptor

CHEM. COMMUN.-2005-239: A new class of long-wavelength fluorophores: strong red fluorescence,convenient synthesis and easy derivation

CHEM. COMMUN.-2001-2656: Intramolecular aromatic 1,5-hydrogen transfer in preparation of oxacyclic naphthalic anhydride via unusual Pschorr cyclisation

NEW J. CHEM.-2003-337: A polyamidoamine dendrimer with peripheral 1,8-naphthalimide groups capable of acting as a PET fluorescent sensor for metal cations

NEW J. CHEM.-2002-920: Novel heterogeneous PET fluorescent sensors selective for transition metal ions or protons: polymers regularly labelled with naphthalimide

J. AM. CHEM. SOC.-2004-2272: A highly selective and sensitive fluorescent chemosensor for Hg2+ in neutral buffer aqueous solution

KIDNEY INTERNATIONAL-2004-2279: Fluorescent imaging of acute mercuric chloride exposure on cultured human kidney tubular epithelial cells

CHEM. RES. TOⅪC.-2005-1814: Visible study of mercuric ion and its conjugate in living cells of mammals and plants

CHEMBIOCHEM-2007-113: Novel Bcl-2 inhibitors: Discovery and mechanism study of small organic apoptosis-inducing agents (SS)

J. MATER. CHEM. -2005-2836: A pH-resistant Zn(Ⅱ) sensor derived from 4-aminonaphthalimide: design,synthesis and intracellular applications

MOL. CANCER THER.-2007-484: R16,a novel amonafide analogue,induces apoptosis and G2-M arrest via poisoning topoisomerase Ⅱ (SS)

BIOORG. MED. CHEM. LETT.-2006-1562: Synthesis and evaluation of novel 8-oxo-8H-cyclopenta[a]acenaphthylene-7-carbonitriles as long-wavelength fluorescent markers for hypoxic cells in solid tumor

BIOORG. MED. CHEM. LETT.-2005-5909: Novel synthetic isoquinolino[5,4-ab]phenazines: Inhibition toward topoisomerase I,antitumor and DNA photo-cleaving activities

BIOORG. MED. CHEM. LETT.-2005-4864: Novel thiazonaphthalimides as efficient antitumor and DNA photocleaving agents: Effects of intercalation,side chains,and substituent groups (SS)

BIOORG. MED. CHEM. LETT.-2005-4864: Synthesis,antitumor evaluation and DNA photocleaving activity of novel methylthiazonaphthalimides with aminoalkyl side chains (SS)

BIOORG. MED. CHEM. LETT.-2005-1139: Five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains: intercalation and photocleavage to DNA (SS)

BIOORG. MED. CHEM. LETT.-2003-5427: Novel naphthalimide hydroperoxide photonucleases: The role of thiocyclic-fused area and the difference in spectra,photochemistry and photobiological activity (SS)

BIOORG. MED. CHEM.-2007-1356: Novel antitumor agent family of 1H-benzo[c,d]indol-2-one with flexible basic side chains: Synthesis and biological evaluation (SS)

BIOORG. MED. CHEM.-2006-6962:Acenaphtho[1,2-b]pyrrole derivatives as new family of intercalators: Various DNA binding geometry and interesting antitumor capacity (SS)

BIOORG. MED. CHEM.-2006-4639: Design,synthesis,and antitumor evaluation of novel acenaphtho[1,2-b]pyrrole-carboxylic acid esters with amino chain substitution (SS)

BIOORG. MED. CHEM. -2005-3149: Novel heterocyclic family of phenyl naphthothiazole carboxamides derived from naphthalimides: synthesis,antitumor evaluation,and DNA photocleavage (SS)

BIOORG. MED. CHEM.-2005-1615: Thio-heterocylic naphthalimides with aminoalkyl side chains: novel alternative tools for photodegradation of genomic DNA without impairment on bioactivities of proteins (SS)

TETRAHEDRON LETT.-2005-6289: A proton sponge-based fluorescent switch

TETRAHEDRON LETT.-2004-3969: A novel chromatism switcher with double receptors selectively for Ag+ in neutral aqueous solution: 4,5-diaminoalkeneamino-N-alkyl-1,8-naphthalimides

TETRAHEDRON LETT.-2003-2087: Novel highly efficient fluoroionophores with a peri-effect and strong electron-donating receptors: TICT-promoted PET and signaling response to transition metal cations with low background emission

TETRAHEDRON LETT.-2003-795: Promoting effects of the hydroxymethyl group on the fluorescent signaling recognition of anions by thioureas

TETRAHEDRON LETT.-2002-2991: 4-Amino-1,8-dicyanonaphthalene derivatives as novel fluorophore and fluorescence switches: efficient synthesis and fluorescence enhancement induced by transition metal ions and protons

TETRAHEDRON LETT.-2002-2995: Synthesis and properties of benzothioxanthene dicarboximide hydroperoxide: an efficient 'time-resolved' DNA photocleaver with long-wavelength (SS)

TETRAHEDRON LETT.-2001-6175: N-aroyloxynaphthalimides as novel highly efficient DNA photocleavers: substituent effects

TETRAHEDRON LETT.-2000-7711: Novel and highly efficient DNA photocleavers: hydroperoxides of heterocyclic-fused naphthalimides

TETRAHEDRON-2005-11895: Novel DNA bis-intercalators of isoquinolino[4,5-bc]acridines: design,synthesis and evaluation of cytotoxic activity

TETRAHEDRON-2005-8717: Synthesis,antitumor and DNA photocleaving activities of novel naphthalene carboxamides: effects of different thio-heterocyclic rings and aminoalkyl side chains (SS)

TETRAHEDRON-2005-6634: Synthesis of thiazo- or thiadiazo- naphthalene carboxamides via mercuric intermediates and their antitumor and DNA photocleavage activities (SS)

TETRAHEDRON-2006-10117: Exploiting the deprotonation mechanism for the design of ratiometric and colorimetric Zn2+ fluorescent chemosensor with a large red-shift in emission

DYES PIGMENTS-2002-247: Synthesis and properties of oligonucleotides containing fluorescent ethenodeoxyadeno sine and ethenodeoxycytidine

DYES PIGMENTS-2001-51: Absorption and fluorescence spectral properties of tetra (fluoroalkoxy) metallophthalocyanines (FF)

DYES PIGMENTS-2001-43: Oxazolonaphthalimides and their hydroperoxides: photophysical and photobiological properties

DYES PIGMENTS-2004-9: Benzothioxanthene dyes as fluorescent label for DNA hybridization: synthesis and application (SS)

DYES PIGMENTS-2004-17: Synthesis and peroxidase-staining properties of novel water soluble polyhydroxylalkyl benzidine dyes

J. FLUORINE CHEM.-2002-161: Synthesis and photosensitizing properties of fluoroalkoxyl phthalocyanine metal complexes (FF)

J. FLUORINE CHEM.-2000-69: Synthesis of fluorine-containing oxazolonaphthalimide hydroperoxides as DNA photocleavers (FF)

CHINESE J. ORG. CHEM.1997-329: Synthesis and characterizations of the dye sensitized photooxygenation products and the heterocycles of naphthofuran derivatives

CHINESE J. ORG. CHEM.-1997-428: Synthesis,characterization and DNA intercalation of a furonaphthopyronone as a novel analogue of furocoumarin

CHINESE J. ORG. CHEM.-2000-338: Synthesis and structure characterization of two thienonaphthopyrones (SS)

CHINESE J. ORG. CHEM. 2006-504: Synthesis and properties of N-butyl-4-(aza-15-crown-5)-1,8-naphthalimide as a fluorescent probe

CHEM. RESEARCH IN CHINESE UNⅣ.-2005-480: A novel photocleaver with long wavelength absorption - Highly efficient antitumor agent: 4-(2-diethylamino -ethylamino)-8-oxo-8H-acenaphtho-[ 1,2-b] pyrrole-9-carbonitrile

CHEM. J. CHINESE UNⅣ.-1996-1399: Syntheses,DNA Intercalation Activities and Molecular Modelling on Structures of Tatramethyldifuronaphthalenes

J. PHOTOCHEM. PHOTOBIO. B-2001-35: Tetra-trifluoroethoxyl zinc phthalocyanine: potential photosensitizer for use in the photodynamic therapy of cancer (SS)

J. PHOTOCHEM. PHOTOBIO. B-2006-221: Isoquino[4,5-bc]acridines: Design,synthesis and evaluation of DNA binding,anti-tumor and DNA photo-damaging ability

J. CHEM. SOC.-PERKIN TRANSACTIONS 2-2000-715: Interaction of naphthyl heterocycles with DNA: effects of thiono and thio groups (SS)

MONATSH CHEM.-1999-1109: Synthesis of novel DNA-intercalating naphthopyrone derivatives with improved water solubility and photophysical properties

BULL. CHEM. SOC. JAPAN-1999-1571: Highly efficient photoinduced DNA cleavage by naphthopyrone hydroperoxides

CHEM. LETT.-2005-696: Novel naphthalimide fluorescent sensors selective for certain proteins on basis of non-covalent interactions between enzyme and inhibitor (SS)

SYNTHESIS-STUTTGART-1999-1109: General synthesis of thioxo-1,8-naphthalimides via thioxo-1,8-naphthalic anhydrides (SS)

HETEROATOM CHEM.-1999-141: The improved synthesis,Diels-Alder reactions,and desulfuration of trithio-1,8-naphthalic anhydride (SS)

POLYMER-2002-5731: Synthesis and photophysical properties of 1,8-naphthalimide-labelled PAMAM as PET sensors of protons and of transition metal ions

CHINESE J. ANAL. CHEM. -2004-837: Studies on the room temperature phosphorescence of halogen naphthalic anhydrides

CHINESE CHEM. LETT.-2004-118: Anthracylmethyl benzoazacrown ether as selective fluorescence sensors for Zn2+

HETEROCYCL. COMMUN.-2003-229: A new class of DNA intercalator and photocleaver: Bis-naphthailimides with bromo and nitro substituents

MONATSH. CHEM.-2003-393: New fluorescent conjugates of uridine nucleoside and substituted 1,8-naphthalimide: Synthesis,weak interactions and solvent effects on spectra

INT. J. BIO. MACROMOL.-2006-59: Study on the interaction between 4-(2-diethylanuno- ethylamino)-8-oxo-8H- acenaphtho[1,2-b]pyrrole-9-carbonitrile and DNA by molecular spectra

研究方向2.农药的化学与生物学

J. AGRI. FOOD CHEM.-2007-2288: Synthesis,insecticidal activity,and QSAR of novel nitromethylene neonicotinoids with tetrahydropyridine fixed cis configuration and exo-ring ether modification

J. AGRI. FOOD CHEM.-2006-125: Synthesis and herbicidal activity of novel 3-aminocarbonyl-2-oxazolidinethione derivatives containing a substituted pyridine ring

J. AGRI. FOOD CHEM.-2006-8793: Novel,unnatural benzo-1,2,3-thiadiazole-7-carboxylate elicitors of taxoid biosynthesis (SS,FF)

J. AGRI. FOOD CHEM.-2005-3120: Syntheses,antifeedant activity,and QSAR analysis of new oxa(thia)diazolyl 3(2H)-pyridazinones (SS)

J. AGRI. FOOD CHEM.-2005-3120: Syntheses,Antifeedant Activity,and QSAR Analysis of New Oxa(thia)diazolyl 3(2 H)-Pyridazinones (SS)

J. AGRI. FOOD CHEM.-2003-152: Synthesis and Antifeedant Activity of New Oxadiazolyl 3(2H)-Pyridazinones

J. AGRI. FOOD CHEM.-2001-124: Synthesis and Quantitative Structure-Activity Relationships of New 2,5-Disubstituted-1,3,4-oxadiazoles (FF)

J. AGRI. FOOD CHEM.-2001-5279: Synthesis and Quantitative Structure-Activity Relationships of Fluorine-Containing 4,4-Dihydroxylmethyl-2-aryl imino- oxazo (thiazo)lidines as Trehalase Inhibitors (SS,FF)

J. AGRI. FOOD CHEM.-1999-4415: Quantitative studies on structure-activity relationship of sulfonylurea and benzoylphenylurea type pesticides and their substituents' bioisosterism using synthons' activity contribution (SS,FF)

J. AGRI. FOOD CHEM.-1996-1538: Molecular modeling study on the structure-activity relationship of substituted dibenzoyl-1-tert-butylhydrazines and their structural similarity to 20-hydroxyecdysone

ACS SYMPOSIUM SERIES-2005(892)-273: Oxadiazole derivatives as novel insect-growth regulators: Synthesis and structure-bioactivity relationship (FF)

J. FLUORINE CHEM.-2006-182: Synthesis and herbicidal activities of fluorine-containing 3-pyridylmethyl-2- phenyliminothiazolidine derivatives (SS,FF)

J. FLUORINE CHEM.-2005-297: Synthesis and fungicidal activity of fluorine-containing phenylimino-thiazolidines derivatives (SS,FF)

J. FLUORINE CHEM.-2005-53: Synthesis and biological activities of hydroxyl-protected fluorine-containing 4,4-dihydroxylmethyl-2-aryl-iminothiazolidines (SS,FF)

J. FLUORINE CHEM.-2004-1159: Synthesis and fungicidal activity of Fluorine-containing Phenylimino-thiazolidines Derivatives (SS,FF)

J. FLUORINE CHEM.-2004-1609: Syntheses,structures and bioactivities of fluorine-containing phenylimino-thia(oxa)zolidine derivatives as agricultural bioregulators (SS,FF)

J. FLUORINE CHEM.-2003-163: Synthesis and insecticidal activities of novel 2,5-disubstituted 1,3,4-oxadiazoles (FF)

J. FLUORINE CHEM.-2003-51: Synthesis and insecticidal activity of new substituted N-aryl-N’-benzoylthiourea compounds (SS,FF)

J. FLUORINE CHEM.-2002-63: Syntheses and insecticidal activity of new 2-(5-(trifluoromethyl)pyridyloxymethyl) -1,3,4-oxadiazoles] (FF)

J. FLUORINE CHEM.-2000-111: Fluorine containing heterocyclic compounds: synthesis of 6-substituted-2-substituted-aryl-1,2,4-triazolo[5,1-b] 1,3,5- thia- diazin-7-one derivatives (SS,FF)

J. FLUORINE CHEM.-2000-173: Syntheses and insecticidal activities of novel 2-fluorophenyl-5-aryl/cyclopropyl-1,3,4-oxadiazoles (FF)

J. FLUORINE CHEM.-2001-143: Synthesis and biological activities of fluorine-containing N,N’-diphenylcarbamimidothioates (SS,FF)

J. FLUORINE CHEM.-1999-39: Syntheses and characterization of 2-amino-5-aryl-1,3,4-oxadiazoles containing trifluoroethoxy groups (FF)

J. FLUORINE CHEM.-1998-9: Polyfluoroalkoxylation and methoxylation of polychloropyridines (FF)

J. FLUORINE CHEM.-1996-9: Alcoholysis of trifluoromethyl groups attached to the pyridine ring (FF)

J. FLUORINE CHEM.-1991-143: A synthetic and MO-SCF study of the trifluoroethoxylation of chloro(trifluoromethyl)pyridine derivatives (FF)

CHEM. PHYS. LETT.-2003-489: Intramolecular noncovalent force in cyclic amidines: nonbonded interaction between carbon atoms and heteroatoms (SS,FF)

PEST. MANAG. SCI. -2003-933: The toxic and anti-feedant activity of 2H-pyridazin-3-one-substituted 1,3,4-oxadiazoles against the armyworm Pseudaletia separata (Walker) and other insects and mite

CARBOHYDRATE RESEARCH-2001-79: Syntheses and activities as trehalase inhibitors of N-arylglycosylamines derived from fluorinated anilines (FF)

J. CHEM. TECH. BIOTECH.-1996-124: Syntheses and insecticidal activities of novel 2,5-disubstituted-1,3,4-oxadiazoles (FF)

CAN. J. CHEM. -2003-272: N'-tert-Butyl-N'-aroyl-N-(alkoxycarbonylmethyl)-N-aroylhydrazines,a novel nonsteroidal ecdysone agonist: syntheses,insecticidal activity,conformational and crystal structure analysis

MONATSH CHEM.-2006-779: An efficient and practical method for the synthesis of 1-(2,6-difluorobenzoyl)-3-(2-alkyl-3-oxopyridazin-4-yl)ureas as potential chitin synthesis inhibitors (FF)

MONATSH CHEM.-2000-953: Novel fused heterocycles: Synthesis and activity of 5,6-dihydro-7-thia-1,3,3a,5-tetraazainden-4-one and 1-thia-3,4a,9-triazafluoren-4-one derivatives (SS)

J. CHEM. RES.-2006- 626: Synthesis and bioactivities of novel neonicotinoids dioxolane compounds

J. CHEM. RES.-2000-88: The crystal structure of 1-phenyl-3-methyl-5-[2 '-(4 ''-phenylmethoxylphenyl)ethoxyl]pyrazole,a potential insect juvenile hormone mimic

J. CHEM. RES.-1999-66: The crystal structure of N-(5-phenyl-1,3,4-oxadiazol-2-yl)-N '-benzoyl urea,a novel insect-growth regulator

J. CHEM. RES. -1998-478: Crystal structure of 1-(3,5-dichloro-2,4-difluorophenyl)-3-(2,6-difluorobenzoyl)urea,an inhibitor of chitin synthesis (SS,FF)

CHEM. J. CHINESE UNⅣ.-1994-224: Synthesis and bioactivities of novel trifluoromethylpyridine derivatives

CHINESE CHEM. LETT. -2004-7: Novel Analogues of -Terthienyl,Thienyl 1,3,4-Thia(oxa)diazoles as Potential Photoactivated Insecticides:Synthesis and Bioactivity (SS)

PESTICIDE BIOCHEM. PHYSIOLOGY-2004-42: Photolarvicidal effect of thienyl 1,3,4-thia(oxa)diazoles and their potential DNA photocleavage (SS)

ARKⅣOC-2003-141: Synthesis and insecticidal activity of 1,2,4-triazole derivatives

CHEM. LETT.-2001-54: A Novel and Practical Amination of 4,5-Dichloropyridazin-3-ones via Reduction with Hydrazine Hydrate

ORG. PREP. PROCEDURE INTL.-2000-571: A facile synthesis of aryl isothiocyanates from arylamines (SS)

ORG. PREP. PROCEDURE INTL.-1999-110: A facile synthesis of 3-chloro-4-(2 ',2 ',2 '-trifluoroethoxy)benzonitrile (FF)

研究方向3.化学生物技术与工程

CHEM. COMMUN.-2006-865: Baker's yeast-mediated enantioselective reduction of substituted fluorenones (FF)

CHEM. COMMUN.-2005-2338: A novel strategy for the preparation of arylhydroxylamines: chemoselective reduction of aromatic nitro compounds using bakers' yeast

CHEM. COMMUN.-2004-2339: A novel strategy for the preparation of arylhydroxylamines: chemoselective reduction of aromatic nitro compounds using bakers’ yeast

APPL. MICROBIO. BIOT.-2005-98: A novel synthetic fluoro-containing jasmonate derivative acts as a chemical inducing signal for plant secondary metabolism (FF)

APPL. MICROBIOL. BIOT.-2006-164: Novel synthetic 2,6-dichloroisonicotinate derivatives as effective elicitors for inducing the biosynthesis of plant secondary metabolites

APPLIED MICROBIO.BIOTECH.-2006-298: Efficient induction of ginsenoside biosynthesis and alteration of ginsenoside heterogeneity in cell cultures of Panax notoginseng by using chemically synthesized 2-hydroxyethyl jasmonate

BIOORG. MED. CHEM. LETT.-2005-1769: Novel 2-aminothiazonaphthalimides as visible light activatable photonucleases: effects of intercalation,heterocyclic-fused area and side chains (SS)

BIOORG. MED. CHEM. LETT.-2003-3513: Thiadiazole: A new family of intercalative photonuclease with electron transfer and radical mechanisms (SS,FF)

BIOORG. MED. CHEM. LETT.-2004-2665: Highly-efficient DNA photocleavers with long wavelength absorptions: thio-heterocyclic fused naphthalimides containing aminoalkyl side chains (SS)

BIOORG. MED. CHEM. LETT.-2004-2335: N-aroyloxylthioxo-naphthalimides as DNA photocleavers of aroyloxyl oxygen radicals: synthesis,evaluation,and substituents' effect (SS)

BIOORG. MED. CHEM. LETT.-2004-4755: Novel fluoro- and hydroxyl-containing jasmonate derivatives as highly efficient elicitors in suspension cultures of Taxus chinensis (FF)

BIOORG. MED. CHEM. LETT.-2006-803: Hydrolysis of plasmid DNA and RNA by amino alkyl naphthalimide as metal-free artificial nuclease (SS)

BIOORG. MED. CHEM.-2006-2935: Novel fluorescent markers for hypoxic cells of naphthalimides with two heterocyclic side chains for bioreductive binding

BIOORG. MED. CHEM.-2006-23: Eliminating nucleic acids contaminants by hydrogen peroxide-induced free radicals during the preparation of proteins (SS)

BIOTECH. BIOENG-2005-516: Highly efficient strategy for enhancing taxoid production by repeated elicitation with a newly synthesized jasmonate in fed- batch cultivation of Taxus chinensis cells

BIOTECH. BIOENG.-2004-809: Novel chemically synthesized hydroxyl-containing jasmonates as powerful inducing signals for plant secondary metabolism

BIOTECH. BIOENG.-2004-595: Novel synthetic jasmonates as highly efficient elicitors for taxoid production by suspension cultures of Taxus chinensis

BIOTECH. PROGR.-2006-331: Novel chemically synthesized salicylate derivative as an effective elicitor for inducing the biosynthesis of plant secondary metabolites

BIOTECH. AND BIOPROCESS ENGI.-2005-162: Efficient elicitation of ginsenoside biosynthesis in cell cultures of Panax notoginseng by using self-chemically-synthesized jasmonates

BIOCHEM. ENGINEERING. J.-2006-23: Eliminating nucleic acids contaminants by hydrogen peroxide-induced free radicals during the preparation of proteins

TETRAHEDRON LETT.-2004-1247: Naphthalimide-thiazoles as novel photonucleases: molecular design,synthesis,and evaluation (SS)

TETRAHEDRON-2005-11264: Versatile acenaphtho[1,2-b]pyrrol-carbonitriles as a new family of heterocycles: diverse Snar(H)H reactions,cytotoxicity and spectral behavior (SS)

DYES AND PIGMENTS-1999-139: Naphthalimide hydroperoxides as photonucleases: substituent effects and structural basis

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