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1. Full Text A blend of small molecules regulates both mating and development in Caenorhabditis elegans
by Zachariah, Cherian and Alborn, Hans T and Srinivasan, Jagan and Kaplan, Fatma and Teal, Peter E. A and Ajredini, Ramadan and Edison, Arthur S and Sternberg, Paul W and Schroeder, Frank C and Malik, Rabia U
Nature, ISSN 0028-0836, 08/2008, Volume 454, Issue 7208, pp. 1115 - 1118
In many organisms, population-density sensing and sexual attraction rely on small-molecule-based signalling systems. In the nematode Caenorhabditis elegans,... 
LONGEVITY | GENE | DAUER-INDUCING PHEROMONE | MULTIDISCIPLINARY SCIENCES | SEX | Sex Attractants - metabolism | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - growth & development | Sex Attractants - chemistry | Glycolipids - pharmacology | Glycolipids - isolation & purification | Male | Hexoses - metabolism | Glycolipids - metabolism | Sex Attractants - pharmacology | Sex Attractants - isolation & purification | Sexual Behavior, Animal - physiology | Caenorhabditis elegans - physiology | Animals | Caenorhabditis elegans - drug effects | Hexoses - isolation & purification | Population Density | Glycolipids - chemistry | Neurons - metabolism | Escherichia coli - physiology | Sexual Behavior, Animal - drug effects | Hexoses - chemistry | Hexoses - pharmacology | Disorders of Sex Development | Physiological aspects | Caenorhabditis elegans | Research | Courtship of animals | Sexual behavior | Thin films | E coli | Nematodes | Genetics | Molecular biology | Males | Mass spectrometry | Chemicals | Index Medicus
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2. Full Text Two-Step Synthesis of Carbohydrates by Selective Aldol Reactions
by Alan B. Northrup and David W. C. MacMillan
Science, ISSN 0036-8075, 9/2004, Volume 305, Issue 5691, pp. 1752 - 1755
Studies of carbohydrates have been hampered by the lack of chemical strategies for the expeditious construction and coupling of differentially protected... 
Carbohydrates | Solvents | Hydroxyls | Polysaccharides | Hexoses | Lewis acids | Reports | Aldehydes | Dimerization | Isomers | Chemicals | HEXOSES | ROUTE | ASYMMETRIC-SYNTHESIS | MULTIDISCIPLINARY SCIENCES | DIELS-ALDER REACTION | ALDEHYDES | SUGARS | Stereoisomerism | Molecular Conformation | Carbon Isotopes | Hexoses - chemical synthesis | Proline - chemistry | Acids | Cyclization | Hexoses - isolation & purification | Molecular Structure | Catalysis | Hexoses - chemistry | Aldehydes - chemistry | Stereoisomers | Design and construction | Observations | Properties | Alcohol | Chemical synthesis | Index Medicus
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3. Full Text Complete Hexose Isomer Identification with Mass Spectrometry
by Nagy, Gabe and Pohl, Nicola L. B
Journal of The American Society for Mass Spectrometry, ISSN 1044-0305, 4/2015, Volume 26, Issue 4, pp. 677 - 685
The first analytical method is presented for the identification and absolute configuration determination of all 24 aldohexose and 2-ketohexose isomers,... 
Biotechnology | Carbohydrates | Configuration determination | Chemistry | Analytical Chemistry | Monosaccharide | Chirality | Proteomics | Hexose isomers | Kinetic resolution | Bioinformatics | Mass spectrometry | Organic Chemistry | Sugar sequencing | Carbohydrate analysis | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, PHYSICAL | ANION-EXCHANGE CHROMATOGRAPHY | KINETIC METHOD | MONOSACCHARIDE ENANTIOMERS | FIXED LIGANDS | SPECTROSCOPY | AMINO-ACIDS | CHIRAL ANALYSIS | ION MOBILITY | PULSED AMPEROMETRIC DETECTION | ELECTROSPRAY-IONIZATION | Kinetics | Isomerism | Mass Spectrometry - methods | Hexoses - analysis | Hexoses - chemistry | Analysis | Glucose | Galactose | Enantiomers | Fructose | Dextrose | Hexoses | Sorbose | Identification | Mannose | Isomers | Index Medicus
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4. Full Text Physicochemical properties and skin permeation of Span 60/Tween 60 niosomes of ellagic acid
by Junyaprasert, Varaporn Buraphacheep and Singhsa, Pratyawadee and Suksiriworapong, Jiraphong and Chantasart, Doungdaw
International Journal of Pharmaceutics, ISSN 0378-5173, 02/2012, Volume 423, Issue 2, pp. 303 - 311
Ellagic acid (EA) is a potent antioxidant phytochemical substance which has limitation to use due to its poor biopharmaceutical properties, low solubility and... 
Skin distribution | Non-ionic surfactants | Ellagic acid | Niosomes | Skin permeation | SYSTEM | ASSAY | DRUG-DELIVERY | VACCINE DELIVERY | CARRIERS | IN-VITRO | NONIONIC SURFACTANT VESICLES | ETHER | PHARMACOLOGY & PHARMACY | LIPOSOMES | Antioxidants - chemistry | Polysorbates - chemistry | Ellagic Acid - metabolism | Skin - metabolism | Antioxidants - metabolism | Humans | Middle Aged | Administration, Cutaneous | Polysorbates - pharmacology | Hexoses - administration & dosage | Drug Compounding | Polysorbates - administration & dosage | Skin Absorption - drug effects | Adult | Female | Solubility | Ellagic Acid - chemistry | Technology, Pharmaceutical - methods | Permeability | Chemistry, Pharmaceutical | Surface-Active Agents - pharmacology | Ellagic Acid - administration & dosage | Particle Size | Microscopy, Confocal | Surface-Active Agents - administration & dosage | Antioxidants - administration & dosage | Surface-Active Agents - chemistry | Liposomes | Hexoses - chemistry | Hexoses - pharmacology | Skin - drug effects | Surface active agents | Skin | Index Medicus
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5. Full Text Triacetonide of Glucoheptonic Acid in the Scalable Syntheses of d -Gulose, 6-Deoxy- d -gulose, l -Glucose, 6-Deoxy- l -glucose, and Related Sugars
by Liu, Zilei and Yoshihara, Akihide and Jenkinson, Sarah F and Wormald, Mark R and Estévez, Ramón J and Fleet, George W.J and Izumori, Ken
Organic Letters, ISSN 1523-7060, 08/2016, Volume 18, Issue 16, pp. 4112 - 4115
Ease of separation of petrol-soluble acetonides derived from the triacetonide of methyl glucoheptonate allows scalable syntheses of rare sugars containing the... 
D-PSICOSE | 8 STEREOISOMERS | L-RHAMNOSE | LACTONES | D-SORBOSE | CHEMISTRY, ORGANIC | STEREOSELECTIVE-SYNTHESIS | CARBOHYDRATE BUILDING-BLOCKS | L-FUCOSE | DERIVATIVES | L-HEXOSES | Sugar Acids - chemistry | Sugars - chemical synthesis | Sugars - chemistry | Stereoisomerism | Molecular Conformation | Hexoses - chemical synthesis | Hexoses - chemistry | Index Medicus
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6. Full Text Direct amino acid catalyzed asymmetric synthesis of polyketide sugars
by Casas, Jesús and Engqvist, Magnus and Ibrahem, Ismail and Kaynak, Betul and Córdova, Armando and Stockholms universitet and Naturvetenskapliga fakulteten and Institutionen för organisk kemi
Angewandte Chemie - International Edition, ISSN 1433-7851, 02/2005, Volume 44, Issue 9, pp. 1343 - 1345
Carbohydrates | Aldol reaction | Hexoses | Aldehydes | Asymmetric catalysis | carbohydrates | aldol reaction | ORGANOCATALYSIS | ALDOL REACTIONS | asymmetric catalysis | CHEMISTRY, MULTIDISCIPLINARY | CHEMICAL SYNTHESIS | ALCOHOLS | 2-STEP SYNTHESIS | MANNICH REACTION | KETONES | aldehydes | BIOSYNTHESIS | hexoses | DERIVATIVES | Stereoisomerism | Molecular Conformation | Amino Acids - chemistry | Crystallography, X-Ray | Hexoses - chemical synthesis | Proline - chemistry | Lactones - chemical synthesis | Polyketide Synthases | Molecular Structure | Catalysis | Hexoses - chemistry | Aldehydes - chemistry | Lactones - chemistry | Index Medicus
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7. Full Text Correction: On the Evolution of Hexose Transporters in Kinetoplastid Potozoans
by Pereira, Claudio Alejandro and Silber, Ariel Mariano
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7
Pereira CA, Silber AM (2012) On the Evolution of Hexose Transporters in Kinetoplastid Protozoans. PLoS ONE 7(5): e36303. doi:10.1371/journal.pone.0036303... 
Hexose
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8. Full Text Optimizing polychlorinated biphenyl degradation by flavonoid-induced cells of the rhizobacterium Rhodococcus erythropolis U23A
by Pham, Thi Thanh My and Rodriguez, Nancy Johanna Pino and Hijri, Mohamed and Sylvestre, Michel
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, pp. e0126033 - e0126033
There is evidence that many plant secondary metabolites may act as signal molecules to trigger the bacterial ability to metabolize polychlorinated biphenyls... 
PCBS | REGULATOR | BACTERIA | BIOTRANSFORMATION | BIODEGRADATION | METABOLITES | TERPENES | REMOVAL | MULTIDISCIPLINARY SCIENCES | DIOXYGENASE | RHIZOSPHERE | Dioxygenases - metabolism | Disaccharides - metabolism | Plants - microbiology | Environmental Pollutants - metabolism | Disaccharides - pharmacology | Culture Media | Polymerase Chain Reaction | Biological Assay | Flavonoids - pharmacology | Rhodococcus - enzymology | Chlorobenzoates - chemistry | Rhizobiaceae - drug effects | Biodegradation, Environmental | Rhodococcus - drug effects | Bacterial Proteins - genetics | Hexoses - metabolism | Polychlorinated Biphenyls - metabolism | Plant Roots - microbiology | DNA Gyrase - metabolism | Dioxygenases - genetics | DNA Gyrase - genetics | Flavonoids - metabolism | Rhodococcus - genetics | Bacterial Proteins - metabolism | Rhizobiaceae - enzymology | Gene Expression Regulation, Bacterial | Hexoses - pharmacology | Hydrogen-Ion Concentration | Rhizobiaceae - genetics | Polychlorinated biphenyls | Plant metabolites | Isoflavones | Sucrose | Rhodococcus | Mannose | Optimization | Degradation | PCB compounds | Secondary metabolites | Metabolites | Mannitol | Biphenyl | Bacteria | Sugars | Inducers | Soil contamination | Biodegradation | Enzymes | Substrates | PCB | Sodium acetate | Polymerase chain reaction | Exudates | Flavonoids | Sodium | Polychlorinated biphenyls--PCB | Exudation | Acetic acid | Index Medicus | Hexoses | Disaccharides | Environmental Pollutants | Polychlorinated Biphenyls | DNA Gyrase | Plants | Dioxygenases | Bacteriology | Bacterial Proteins | Chlorobenzoates | Life Sciences | Microbiology and Parasitology | Plant Roots | Rhizobiaceae | Food engineering
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9. Full Text Tunable GLUT–Hexose Binding and Transport via Modulation of Hexose C‐3 Hydrogen‐Bonding Capabilities
by Kumar Kondapi, Venkata Pavan and Soueidan, Olivier‐Mohamad and Cheeseman, Christopher I and West, Frederick G
Chemistry – A European Journal, ISSN 0947-6539, 06/2017, Volume 23, Issue 33, pp. 8073 - 8081
The importance of the hydrogen bonding interactions in the GLUT–hexose binding process (GLUT=hexose transporter) has been demonstrated by studying the binding... 
hydrogen bonding | hexose | transport mechanisms | GLUT | structure–activity relationships | MEMBRANE TRANSPORTERS | EPOXIDE | RECOGNITION | GLUCOSE TRANSPORTERS | CANCER | CHEMISTRY, MULTIDISCIPLINARY | FRUCTOSE ANALOGS | THERAPY | structure-activity relationships | METABOLISM | TISSUES | EXPRESSION | Glucose Transporter Type 5 - metabolism | Oocytes - metabolism | Humans | RNA, Messenger - genetics | Glucose Transporter Type 1 - metabolism | Glucose Transporter Type 5 - chemistry | Hexoses - metabolism | RNA, Messenger - metabolism | Mannitol - analogs & derivatives | Microscopy, Confocal | Glucose Transporter Type 1 - chemistry | Animals | Biological Transport | Hydrogen Bonding | Xenopus laevis - metabolism | Cell Line, Tumor | Mannitol - chemistry | Mice | Monosaccharide Transport Proteins - chemistry | Xenopus laevis - growth & development | Glucose Transporter Type 5 - genetics | Monosaccharide Transport Proteins - metabolism | Hexoses - chemistry | Hydrogen | Hydrogen bonding | Fructose | Binding | Efflux | Installation | Hexose | Hexose transporter | Analogue | Tumor cells | Derivatives | Machinery | Glucose transporter type 5 | Hydrogen bonds | Modulation | Mannitol | Chemical bonds | Transport | Bonding | Transporter | Scaffolds | Recognition | Payloads | Index Medicus
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10. Full Text Distinct geographical distribution of the Miscanthus accessions with varied biomass enzymatic saccharification
by Li, Xukai and Liao, Haofeng and Fan, Chunfen and Hu, Huizhen and Li, Ying and Li, Jing and Yi, Zili and Cai, Xiwen and Peng, Liangcai and Tu, Yuanyuan
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, pp. e0160026 - e0160026
Miscanthus is a leading bioenergy candidate for biofuels, and it thus becomes essential to characterize the desire natural Miscanthus germplasm accessions with... 
EUROPE | PRETREATMENTS | BIOFUEL PRODUCTION | GRASSES | MULTIDISCIPLINARY SCIENCES | ENERGY CROPS | CELLULOSE | DIGESTIBILITY | LIGNIN | Lignin - analysis | Pentoses - analysis | Climate | Species Specificity | Colorimetry | Biomass | Biofuels | Hexoses - analysis | Poaceae - classification | Polysaccharides - metabolism | Hydrolysis | Lignin - metabolism | Poaceae - metabolism | Cell Wall - metabolism | China | Polysaccharides - chemistry | Poaceae - growth & development | Environmental aspects | Research | Grasses | Biomass energy | Distribution | Geographical distribution | Lignin | Biotechnology | Ethanol | Laboratories | Cell walls | Insolation | Cellulose | Alcohol | Saccharification | Raw materials | Sulfuric acid | Germplasm | Alternative energy sources | Lignocellulose | Mathematical analysis | Biodiesel fuels | Plant sciences | Polymers | Digestibility | Rice | Index Medicus
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11. Full Text Synthesis of All Eight L‐Glycopyranosyl Donors Using CH Activation
by Frihed, Tobias Gylling and Pedersen, Christian Marcus and Bols, Mikael
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2014, Volume 53, Issue 50, pp. 13889 - 13893
The synthesis of all eight rare, but biologically important L ‐hexoses as the according thioglycosyl donors was achieved through a procedure involving the CH... 
CH activation | iridium catalysis | glycosyl donors | L | hexoses | Fleming–Tamao oxidation | Glycosyl donors | Fleming-Tamao oxidation | L-hexoses | C-H activation | Iridium catalysis | ACID BUILDING-BLOCKS | CONVENIENT SYNTHESIS | ASYMMETRIC-SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | DE-NOVO SYNTHESIS | EFFICIENT SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | CATALYZED REGIOSELECTIVE SILYLATION | CH activation | L-GLUCOSE | DISACCHARIDE SUBUNIT | Hydrogen - chemistry | Carbon - chemistry | Hexoses - chemistry | Index Medicus | Activation | Oxidation | Synthesis | Acetylation | Iridium
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12. Full Text Novel hamamelitannin analogues for the treatment of biofilm related MRSA infections–A scaffold hopping approach
by Vermote, Arno and Brackman, Gilles and Risseeuw, Martijn D.P and Coenye, Tom and Van Calenbergh, Serge
European Journal of Medicinal Chemistry, ISSN 0223-5234, 02/2017, Volume 127, pp. 757 - 770
Antimicrobial research is increasingly being focused on the problem of resistance and biofilm formation. Hamamelitannin (HAM) was recently identified as an... 
Scaffold hopping | Antibiotic potentiators | Quorum sensing | Hamamelitannin analogues | MRSA | STAPHYLOCOCCUS-AUREUS PATHOGENESIS | TARGET | ANTIBIOTICS | CHEMISTRY, MEDICINAL | PROTEIN | SUSCEPTIBILITY | QUORUM-SENSING INHIBITOR | DISCOVERY | RIP | POTENTIATORS | Biofilms - drug effects | Methicillin-Resistant Staphylococcus aureus - physiology | User-Computer Interface | Gallic Acid - pharmacology | Methicillin-Resistant Staphylococcus aureus - drug effects | Hexoses - chemical synthesis | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Anti-Bacterial Agents - chemistry | Drug Design | Gallic Acid - chemical synthesis | Ligands | Anti-Bacterial Agents - pharmacology | Gallic Acid - analogs & derivatives | Drug Evaluation, Preclinical | Gallic Acid - chemistry | Hexoses - chemistry | Hexoses - pharmacology | Care and treatment | Health aspects | Staphylococcus aureus | Staphylococcus aureus infections | Antibacterial agents | Index Medicus
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13. Full Text Soluble Acid Invertases Act as Key Factors Influencing the Sucrose/Hexose Ratio and Sugar Receding in Longan (Dimocarpus longan Lour.) Pulp
by Luo, Tao and Shuai, Liang and Liao, Lingyan and Li, Jing and Duan, Zhenhua and Guo, Xiaomeng and Xue, Xiaoqing and Han, Dongmei and Wu, Zhenxian
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 01/2019, Volume 67, Issue 1, pp. 352 - 363
Soluble acid invertases (SAIs) cleave sucrose into hexose in vacuoles and play important roles in influencing fruit quality. However, their potential roles in... 
Dimocarpus longan Lour | sucrose/hexose ratio | sugar receding | sucrose metabolism | soluble acid invertases | VACUOLAR INVERTASE | FOOD SCIENCE & TECHNOLOGY | TRANSPORT | EVOLUTION | METABOLISM | ROLES | SYNTHASE ACTIVITY | GENES | STARCH | AGRICULTURE, MULTIDISCIPLINARY | ACCUMULATION | CHEMISTRY, APPLIED | EXPRESSION | Sucrose - chemistry | Fruit - chemistry | Glycoside Hydrolases - genetics | Sapindaceae - enzymology | Fruit - enzymology | Hexoses - metabolism | Sapindaceae - chemistry | Plant Proteins - genetics | Plant Proteins - chemistry | Sucrose - metabolism | Glycoside Hydrolases - chemistry | Sapindaceae - genetics | Plant Proteins - metabolism | Glycoside Hydrolases - metabolism | Kinetics | Fruit - metabolism | Sapindaceae - metabolism | Fruit - genetics | Hexoses - chemistry | Index Medicus
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14. Full Text Avoiding misannotation of in-source fragmentation products as cellular metabolites in liquid chromatography-mass spectrometry-based metabolomics
by Xu, Yi-Fan and Lu, Wenyun and Rabinowitz, Joshua D and Princeton Univ., NJ (United States)
Analytical Chemistry, ISSN 0003-2700, 02/2015, Volume 87, Issue 4, pp. 2273 - 2281
Liquid chromatographymass spectrometry (LC-MS) technology allows for rapid quantitation of cellular metabolites, with metabolites identified by mass... 
CHEMISTRY, ANALYTICAL | RAPIDFIRE(R) | PERFORMANCE | QUANTITATIVE METABOLOMICS | SEPARATION | INHIBITORS | IDENTIFICATION | CHALLENGES | REVERSED-PHASE | ELECTROSPRAY-IONIZATION | STRATEGIES | Metabolomics | Phosphates - metabolism | Nucleotides - analysis | Mass Spectrometry | Chromatography, Liquid | Hexoses - metabolism | Nucleotides - metabolism | Phosphates - analysis | Hexoses - analysis | Phosphates | Analytical chemistry | Yeast | Metabolites | Mass spectrometry | Chromatography | Index Medicus | Spectroscopy | Cellular | Liquids | Separation | Ionization | Fragmentation | INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
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