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Research > Chapter 10041

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2,3,7,8-Tetrachlorodibenzo-p-dioxin inhibits luminal cell differentiation and androgen responsiveness of the ventral prostate without inhibiting prostatic 5alpha-dihydrotestosterone formation or testicular androgen production in rat offspring

2,3,7,8-Tetrachlorodibenzo-p-dioxin interacts with endogenous estradiol to disrupt prostate gland morphogenesis in male rat fetuses

2,3,7,8-Tetrachlorodibenzo-p-dioxin suppresses apoptosis leads hyperphosphorylation p53 rat hepatocytes

2,3,7,8-Tetrachlorodibenzo-p-dioxin toxicity in the zebrafish embryo: Altered regional blood flow and impaired lower jaw development

2,3,7,8-Tetrachlorodibenzo-p-dioxin toxicity in the zebrafish embryo: Local circulation failure in the dorsal midbrain is associated with increased apoptosis

2,3,7,8-Tetrachlorodibenzo-p-dioxin cure induces c-Fos expression forebrain Long-Evans rat

2,3,7,8-Tetrachlorodibenzo-p-dioxin-dependent release contact inhibition WB-F344 cells - Involvement cyclin A

2,3,7,8-Tetrachlorodibenzo-p-dioxin-induced degradation of aryl hydrocarbon receptor (AhR) by the ubiquitin-proteasome pathway: Role of the transcription activaton and DNA binding of AhR

2,3,7,8-Tetrachlorodibenzo-p-dioxin-mediated oxidative stress CYP1A2 knockout (CYP1A2-/-) mice

2,3,7,8-dibenzo-p-dioxins mined clay products United States - Proof potential natural origin

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) alters the regulation and posttranslational modification of p27kip1 in lipopolysaccharide-activated B cells

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces Fas-dependent activation-induced cell death in superantigen-primed T cells

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces binding 50 kDa protein 3 untranslated area urokinase-type plasminogen activator mRNA

2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced activities nuclear protein kinases phosphatases affecting DNA binding activity c-Myc AP-1 livers guinea pigs

2,3,7,8-tetrachlorodibenzo-p-dioxin alters cardiovascular and craniofacial development and function in sac fry of rainbow trout (Oncorhynchus mykiss)

2,3,7,8-tetrachlorodibenzo-p-dioxin alters follicular steroidogenesis time- cell-specific manner

2,3,7,8-tetrachlorodibenzo-p-dioxin alters hippocampal astroglia-neuronal gap junctional communication

2,3,7,8-tetrachlorodibenzo-p-dioxin natural immunity - Lack influence complement scheme guinea swine model

2,3,7,8-tetrachlorodibenzo-p-dioxin decreases estradiol production without altering the enzyme activity of cytochrome P450 aromatase of human luteinized granulosa cells in vitro

2,3,7,8-tetrachlorodibenzo-p-dioxin increases serum kidney retinoic acid levels kidney retinol esterification rat

2,3,7,8-tetrachlorodibenzo-p-dioxin increases steady-state estrogen receptor-beta mRNA levels CYP1A1 CYP1B1 induction rat granulosa cells vitro

2,3,7,8-tetrachlorodibenzo-p-dioxin induces apoptosis in nervous scheme - Correlation local circulation failure apoptosis dorsal midbrain zebrafish embryos

2,3,7,8-tetrachlorodibenzo-p-dioxin induces lecithin - Retinol acyltransferase transcription rat kidney

2,3,7,8-tetrachlorodibenzo-p-dioxin potential activator human cytomegalovirus replication human fibroblast cell line

2,3,7,8-tetrachlorodibenzo-p-dioxin suppresses tumor necrosis factor-alpha and anti-CD40-induced activation of NF-kappaB/Rel in dendritic cells: p50 homodimer activation is not affected

2,3,7,8-tetrachlorodibenzo-p-dioxin - Its influence genes mandible traits mice

2,3-Anhydro sugars glycoside bond synthesis. Highly stereoselective syntheses oligosaccharides alpha- beta-arabinofuranosyl linkages

2,3-Butanediol production Enterobacter aerogenes - Selection optimal conditions function food industry residues

2,3-Butanedione monoxime (BDM) as a myosin inhibitor

2,3-Butanedione monoxime (BDM), a potent inhibitor of actin-myosin interaction, induces ion and fluid transport in MDCK monolayers

2,3-Butanedione monoxime cardioplegia - Advantages hyperkalemia blood-perfused extracted hearts

2,3-Butanedione monoxime increases speed relaxation single muscle fibres frog

2,3-Butanedione monoxime unmasks Ca2+-induced NADH structure inhibits electron transport rat hearts

2,3-DPG-Hb complex. theory asymmetric binding

2,3-Dibenzylbutyrolactones 1,2,3,4-tetrahydro-2-naphthoic acid gamma-lactones - Structure activity relation cytotoxic activity

2,3-Dihydrofarnesyl citronellyl esters paracloacal gland secretions brown caiman (Caiman crocodilus fuscus) Costa Rica

2,3-Dihydroisoindolones cyclisation rearomatisation lithiated benzamides

2,3-Dimercaptopropane-1-sulfonic acid meso-2,3-dimercaptosuccinic acid increase mercury- cadmium-induced inhibition delta-aminolevulinate dehydratase

2,3-Dimethoxybenzo(i)phenanthridines - Topoisomerase I-targeting anticancer agents

2,3-Dinor-5,6-dihydro-15-F2t-isoprostane. bioactive prostanoid metabolite

2,3-alpha-Epoxyjaeschkeanadiol 5-benzoate Ferula hermonis Boiss

2,3-butanedione monoxime suppresses primarily total calcium handling canine heart

2,3-diaryl-5-anilino(1,2,4)thiadiazoles melanocortin MC4 receptor agonists effects feeding behavior rats

2,3-diarylbenzopyran derivatives class selective cyclooxygenase-2 inhibitors

2,3-diarylcyclopentenones orally active, highly selective cyclooxygenase-2 inhibitors

2,3-dihydro-1H,7H-pyrimido(5,6,1-de)acridine-1,3,7-trione derivatives class cytotoxic agents active multidrug-resistant cell lines - Synthesis, biological evaluation, structure-activity relationships

2,3-dihydro-2-oxo-1H-benzimidazole-1-carboxamides selective affinity 5-HT4 receptor - Synthesis structure-affinity structure-activity relationships series partial agonist antagonist derivatives

2,3-dihydrobenzofuran neolignans Aristolochia pubescens

2,3-dihydrobiflavone Ginkgo biloba

2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(f)quinoxaline reduces glial loss and acute white matter pathology after experimental spinal cord contusion

2,3-dimercaptopropanol inhibits Ca2+ transport in microsomes from brain but not from fast-skeletal muscle

2,3-dimethyl-5-(2-methylpropyl)pyrazine, a trail pheromone component of Eutetramorium mocquerysi Emery (1899) (Hymenoptera: Formicidae)

2,3-disubstituted quinuclidines class dopamine transporter inhibitors

2,4'-Dihydroxyacetophenone dioxygenase (EC 1.13.11.41) from Alcaligenes sp. 4HAP: A novel enzyme with an atypical dioxygenase sequence

2,4,4-trichlorobiphenyl increases STAT5 transcriptional activity

2,4,5-Trichlorophenoxyacetic acid inhibits apoptosis PC12 cells

2,4,5-Trisubstituted imidazoles - New nontoxic modulators P-glycoprotein mediated multidrug resistance. Part 1

2,4,5-Trisubstituted imidazoles - New nontoxic modulators P-glycoprotein mediated multidrug resistance. Part 2

2,4,6,8-Tetraiodoglycoluril sulfuric acid powerful reagent iodination deactivated arenes

2,4,6-Triarylchalcogenopyrylium dyes similar formation antitumor substance AA1 vitro sensitizers photodynamic therapy cancer

2,4,6-Trichlorophenol degradation by river sediment exposed to bleached kraft mill discharge

2,4,6-Trinitrotoluene detection using recombinant antibodies

2,4,6-Trinitrotoluene reduction by an Fe-only hydrogenase in Clostridium acetobutylicum

2,4,6-Trinitrotoluene reduction by carbon monoxide dehydrogenase from Clostridium thermoaceticum

2,4,6-Triphenylpyrylium ion encapsulated within Y zeolite as photocatalyst for the degradation of methyl parathion

2,4,6-tri(3,5-dimethylpyrazoyl)-1,3,5-triazine modified carbon paste electrode trace Cobaltdetermination differential pulse anodic stripping voltammetry

2,4,6-trinitrotoluene (TNT) tolerance biotransformation potential microfungi extracted TNT-contaminated soil

2,4-(hydroxyphenl)-ethanol, antioxidative substance produced Candida spp., impairs neutrophilic yeast killing vitro

2,4-D Sclerotinia minor control usual dandelion

2,4-D degradation by electron beam irradiation: Influence of oxygen concentration

2,4-D treatment in tench (Tinca tinca L.): Pathological processes on the excretory kidney

2,4-Decadienal downregulates TNF-alpha gene expression THP-1 human macrophages

2,4-Decadienals produced (R)-11-HPITE arachidonic acid marine green alga Ulva conglobata

2,4-Dicarboxy-pyrroles selective non-competitive mGluR1 antagonists - Further characterization 3,5-dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-trimethyl-propyl) ester structure-activity relationships

2,4-Dichlorophenoxyacetate/alpha-ketoglutarate dioxygenases Burkholderia cepacia 2a Ralstonia eutropha JMP134

2,4-Dichlorophenoxyacetic acid and kinetin in anther culture of cultivated and wild oats and their interspecific crosses: Plant regeneration from A. sativa L

2,4-Dichlorophenoxyacetic acid disrupts the cytoskeleton and disorganizes the Golgi apparatus of cultured neurons

2,4-Dichlorophenoxyacetic acid developing rats alters behaviour, myelination regions brain gangliosides pattern

2,4-Dichlorophenoxyacetic acid residues semen Ontario farmers

2,4-Dichlorophenoxyacetic acid/partially methylated-beta-Cyclodextrin inclusion complexes

2,4-Dienoyl-CoA reductase Escherichia coli iron-sulfur flavoprotein functions fatty acid beta-oxidation

2,4-Dimethoxybenzyl: An amide protecting group for 2-acetamido glycosyl donors

2,4-Dinitrophenol. activating reagent nucleotide synthesis phosphoramidite route. Design effective phosphitylating reagents

2,4-Dinitrophenylhydrazine carbonyl assay metal-catalysed protein glycoxidation

2,4-Disubstituted pyrimidines. class KDR kinase inhibitors

2,4-Disubstituted pyrroles - Synthesis, traceless linking pharmacological studies leading dopamine D4 receptor partial agonist FAUC 356

2,4-Nonadienal benzaldehyde bioantimutagens Fushimi sweet pepper (Fushimi-togarashi)

2,4-Pentanedione: Evaluation of the genotoxic potential in vitro and in vivo

2,4-Thiazolidinediones potent selective human beta3 agonists

2,4-Toluenediisocyanate hexamethylene-diisocyanate adducts blood proteins - Assessment reactivity amino acid residues vitro

2,4-Trans-7,4-dihydroxy-4-methoxyflavan Cassia abbreviata

2,4-dinitrophenol acutely inhibits rabbit atrial Ca2+-sensitive Cl- current (ITO2)

2,4-diphenyl furan diamidines anti-Pneumocystis carinii pneumonia agents

2,5-Disubstituted adenosine derivatives - Evaluation selectivity efficacy adenosine A1, A2A, A3 receptor

2,5-Anhydro sugar diacid 2,5-anhydro sugar diamine based C2 symmetric peptidomimetics potential HIV-1 protease inhibitors

2,5-Anhydro-D-mannitol increases hepatocyte calcium - Implications hepatic hunger stimulus

2,5-Anhydro-D-mannitol increases hepatocyte sodium - Transduction hepatic hunger stimulus?

2,5-Bis-(2-hydroxybenzoylamino)pentanoic acid salicylic acid-metabolite extracted chicken - Characterization independent synthesis

2,5-Di-t-butyl-1,4-benzohydroquinone (BHQ) inhibits vascular L-type Ca2+ channel superoxide anion generation

2,5-Di-t-butyl-1,4-benzohydroquinone induces endothelium-dependent relaxation rat thoracic aorta

2,5-Di-tert-butyl-1,4-hydroquinone enhances cell transformation accompanied increase intracellular free calcium ion concentration

2,5-Dialkylresorcinol biosynthesis in Pseudomonas aurantiaca: Novel head-to-head condensation of two fatty acid-derived precursors

2,5-Diketo-D-gluconate production by a mixed culture of two newly-isolated strains: Flavimonas oryzihabitans and Pseudomonas cepacia

2,5-Dimethyl-4-hydroxy-2H-furan-3-one derivatives - Analysis, synthesis biosynthesis-A review

2,5-Dimethyl-4-hydroxy-3(2H)-furanone as a secondary metabolite from D-fructose-1,6-diphosphate metabolism by Zygosaccharomyces rouxii

2,5-Pyridinedicarboxylic acid derivatives non-nucleosidic reverse transcriptase inhibitors hepatitis B virus

2,576 ultrasounds blunt abdominal trauma

2,6,8,9-Tetrasubstituted purines CDK1 inhibitors

2,6,9-trisubstituted purines - Optimization highly potent selective CDK1 inhibitors

2,6-Di(omega-aminoalkyl)-2,5,6,7-tetrahydropyrazolo(3,4,5-mn)pyrimido(5,6,1-de)-acridine-5,7-diones - Novel, potent, cytotoxic, DNA-binding agents

2,6-Diamino-5,8-diaza-7,9-dicarba-purine

2,6-Dibromobiphenyl primes extensive dechlorination Aroclor 1260 contaminated sediment 8-30 C stimulating growth PCB-dehalogenating microorganisms

2,6-Dichlorobenzonitrile cellulose biosynthesis inhibitor, affects morphology structural integrity petunia lily pollen tubes

2,6-Dichloroquinone chlorimide 7,7,8,8-tetracyanoquinodimethane reagents spectrophotometric measurement salbutamol pure dosage forms

2,6-Dimethyltyrosine analogues stereodiversified ligand library - Highly potent, selective, non-peptidic mu opioid receptor agonists

2,6-diaminopurine TNA - Influence duplex stabilities efficiency template-controlled ligations

2,6-dichloro-phenol indophenol prevents switch-over electrons cyanide-sensitive -insensitive pathway mitochondrial electron transport chain presence inhibitors

2,6-difluorophenol bioisostere carboxylic acid - Bioisosteric analogues gamma-aminobutyric acid

2,6-disubstituted pyran-4-one thiopyran-4-one inhibitors DNA-dependent protein kinase (DNA-PK)

2,7,12,18-Tetramethyl-13,17-di(3-hydroxypropyl)porphyrin - Synthesis photosensitivity

2,7-Di-tert-butyl-Fmoc-P-OSu. polymer-supported reagent protection amino group

2,7-Diaminofluorene is a sensitive substrate for detection and characterization of plant root peroxidase activities

2,7-Diazabicyclo(3.3.0)octanes h5-HT1D receptor agonists

2,7-Dichlorofluorescin oxidation reactive oxygen species - What measure?

2,7-Dioxo-2,3,4,5,6,7-hexahydro-1H-benzo(h)(1,4)diazonine template design CCK2 receptor antagonists

2,7-Disubstituted amidofluorenone derivatives inhibitors human telomerase

2,8-Disubstituted adenosine derivatives partial agonists adenosine A2A receptor

2,8-dihydroxyadenine urolithiasis due partial insufficiency adenine phosphoribosyltransferase. case report

2,8-dihydroxyadenine urolithiasis patient considerable residual adenine phosphoribosyltransferase activity cell extracts mutations copies APRT

2- And 8-alkynyladenosines - Conformational investigations docking human adenosine A3 receptor explain diverse biological behavior

2- 3-substituted 1,4-naphthoquinone derivatives subversive substrates trypanothione reductase lipoamide dehydrogenase Trypanosoma cruzi - Synthesis correlation redox cycling activities vitro cytotoxicity

2- 6-(1-azidoalkyl)-5,8-dimethoxy-1,4-naphthoquinone - Synthesis, assessment cytotoxic activity, antitumor activity inhibitory influence DNA topoisomerase-I

2-((2-((Dimethylamino)methyl)phenyl)thio)-5-iodophenylamine (ADAM) - An good serotonin transporter ligand

2-(1-Aminoacetyloxyalkyl)-1,4-dihydroxy-9,10-anthraquinone derivatives - Synthesis cytotoxic activity

2-(1-hydroxyiminoalkyl)-1,4-dimethoxy-9,10-anthraquinones - Synthesis assessment cytotoxicity

2-(11C)thymidine positron emission tomography as an indicator of thymidylate synthase inhibition in patients treated with AG337

2-(18F)F-A-85380: A PET radioligand for alpha4beta2 nicotinic acetylcholine receptors

2-(18F)F-A-85380: PET imaging of brain nicotinic acetylcholine receptors and whole body distribution in humans

2-(18F)fluoropyridines no-carrier-added nucleophilic aromatic substitution (18F)FK-K222. comparative study

2-(2-Hydroxy-2-substituted) ethyl-1,2,3,4-tetrahydropyrrolo(1,2-a)-pyrazines. group compounds possessing antiarrhythmic activity

2-(2-Hydroxy-3-alkoxyphenyl)-1H-benzimidazole-5-carboxamidine derivatives potent selective urokinase-type plasminogen activator inhibitors

2-(2-Oxo-1,4-dihydro-2H-quinazolin-3-yl)- 2-(2,2-dioxo-1,4-dihydro-2H-2lambda6-benzo(1,2,6)thiadiazin-3-yl)-N-hydroxy-acetamides potent selective peptide deformylase inhibitors

2-(2-Piperidyl)- 2-(2-pyrrolidyl)chromans nicotine agonists - Synthesis pharmacological characterization

2-(3,4-Dihydro-1H-isoquinolin-2yl)-pyridines class NR1/2B subtype selective NMDA receptor antagonists

2-(3,5-Dimethylphenyl)tryptamine derivatives bind GnRH receptor

2-(3-(2-thioxopyrrolidin-3-ylidene)methyl)-tryptophan yellow pigment salted radish roots

2-(3-Halogen-4-hydroxyphenyl)-1,4-naphthoquinones 2-(3,5-di-tert-butyl-4-hydroxyphenyl) congeners, potent 5-lipoxygenase inhibitors - 1,4-Naphthoquinones, XXVII

2-(3-aminopropyl)-4-pentenoic acid bio-compatible/cleavable linker solid-phase organic synthesis

2-(3-methyl-3H-diaziren-3-yl)ethyl 1-(1-phenylethyl)-1H-imidazole-5-carboxylate. derivative stereoselective general anesthetic etomidate photolabeling ligand-gated ion channels

2-(3-pyridyl)thiazolidine-4-carboxamide derivatives. Structure-activity relationships active configuration 2-(3-pyridyl)thiazolidine-4-carboxamides platelet-activating factor receptor antagonists

2-(3-pyridyl)thiazolidine-4-carboxamide derivatives. Synthesis metabolites metabolism 2-(3-pyridyl)thiazolidine-4-carboxamides YM461 YM264 platelet-activating factor (PAF) receptor antagonists

2-(4-(3-(4-Aryl/heteroaryl-1-piperazinyl)propoxy)phenyl)-2H-benzotriazoles N-oxides ligands serotonin dopamine receptors

2-(4-(7-Chloro-2-quinoxalinyloxyphenoxy)-propionic acid (XK469), an inhibitor of topoisomerase (Topo) IIbeta, up-regulates Topo IIalpha and enhances Topo IIalpha-mediated cytotoxicity

2-(4-(7-chloro-2-quinoxalinyloxy)phenoxy)-propionic acid (XK469) inhibition of topoisomerase IIbeta is not sufficient for therapeutic response in human Waldenstrom's macroglobulinemia xenograft model

2-(4-(omega-(4-(2-methoxyphenyl)-1-piperazinyl)alkoxy)phenyl) phthalimides ligands 5-HT, dopamine adrenergic receptor subtypes

2-(4-(omega-(4-(2-methoxyphenyl)-1-piperazinyl)alkoxy)phenyl)-2H-benzotriazoles N-oxides ligands 5-hydroxytryptamine, dopamine adrenergic receptor subtypes

2-(4-Carboxyphenyl)-6-N,N-diethylaminobenzofuran. reagent sensitive measurement alcohols high-performance liquid chromatography fluorimetric detection

2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002) inhibits nitric oxide production cultured murine astrocytes

2-(4-R-Phenoxy/phenylthio)alkanoic esters 1-lupinine

2-(Alk-1-ynyl)-4,6-dimethoxy-1,3,5-triazines Pd-mediated alkynylation 2-chloro-4,6-dimethoxy-1,3,5-triazine

2-(Alkylthio)pyrimidin-4-ones novel, reversible inhibitors lipoprotein-associated phospholipase A2

2-(Allylthio)pyrazine inhibition aflatoxin B1-induced hepatocarcinogenesis rats

2-(Allylthio)pyrazine inhibition aflatoxin B1-induced hepatotoxicity rats - Inhibition cytochrome P450 2B- 3A2-mediated bioactivation

2-(Allylthio)pyrazine suppresses growth proliferation human promyelocytic leukemia (HL-60) cells induction apoptosis

2-(Allylthio)pyrazine cancer chemopreventive agent, inhibits liver fibrosis stimulated dimethylnitrosamine rats - Role inhibition transforming growth factor-beta1 expression

2-(Anilinomethyl)imidazolines alpha1 adrenergic receptor agonists - The discovery alpha1a subtype selective 2-alkylsulfonyl-substituted analogues

2-(Anilinomethyl)imidazolines alpha1 adrenergic receptor agonists - alpha1a subtype selective 2-heteroaryl compounds

2-(Anilinomethyl)imidazolines alpha1-adrenoceptor agonists - The diagnosis alpha1A subtype selective 2-carboxylic acid esters amides

2-(Azidomethyl)benzoyl protecting group nucleosides

2-(C-11)Thymidine imaging of malignant brain tumors

2-(Dimethylaminomethyl)-tetrahydroisoxazolopyridobenzazepine derivatives. Synthesis 5-HT2C antagonist potential anxiolytic properties

2-(N-methylanilino)-3-formylchromone. versatile synthon incorporation chromone moiety cultivar heterocyclic systems macrocycles reactions bifunctional nucleophiles

2-(N1-2-pyrimidyl-aminobenzenesulfonamido) ethyl 4-bis(2-chloroethyl) aminophenyl butyrate. potent antitumor substance

2-(Oxalylamino)-benzoic acid is a general, competitive inhibitor of protein-tyrosine phosphatases

2-(anilinomethyl)imidazolines alpha1A adrenergic receptor agonists - 2-heteroaryl 2-oxime ether series

2-(aryloxy)ethylamine derivatives - Ring opened congeners long chain 1-arylpiperazines high 5-HT1A receptor affinity selectivity D2 alpha1 receptors

2-(diethylamino)thieno(1,3)oxazin-4-ones stable inhibitors human leukocyte elastase

2-(ethoxycarbonylmethyl)-1H-naphtho(1,8-de)-1,2,3-triazine anion. glycine enolate equivalent

2-(fluorine-18) fluoro-2-deoxy-D-glucose PET scan brain maple syrup urine disease

2-(fluorine-18)-fluoro-2-deoxy-D-glucose positron emission tomography identification recurrent ovarian cancer

2-(fluorine-18)fluoro-2-deoxy-D-glucose positron emission tomography detection staging malignant lymphoma. bicenter experiment

2-36(K4,RYYSA19-23)PP Y5-receptor preferring ligand strong stimulatory influence food intake

2-4 Years results posterior doublerod instrumentation cure idiopathic scoliosis

2-5A antisense directed telomerase RNA produces apoptosis ovarian cancer cells

2-5A antisense telomerase RNA therapy for intracranial malignant gliomas

2-5A antisense therapy directed human telomerase RNA inhibits telomerase activity induces apoptosis telomere impairment cervical cancer cells

2-5A-DNA conjugate inhibition respiratory syncytial virus replication - Influences oligonucleotide formation modifications RNA target site selection

2-5A-PNA complexes. class antisense compounds

2-Acetaminofluorene blocks cell cycle progression hepatectomy p21 induction lack Cyclin E expression

2-Acetoxyacrylonitrile - Use electrophile equivalent acetaldehyde asymmetric Michael response chiral imines

2-Acetylaminofluorene up-regulates rat mdr1b expression through generating reactive oxygen species that activate NF-kappaB pathway

2-Acylimino-3H-thiazoline derivatives. template platelet GPIIb/IIIa receptor antagonists

2-Alkoxycarbonylaminopyridines: Inhibitors of Mycobacterium tuberculosis FtsZ

2-Alkyl-1-(2-aryl-1,1-difluoro-2-hydroxyethyl)benzimidazoles - Potential angiotensin II receptor antagonists

2-Alkyl-3-alkylamino-2H-benzo- pyridothiadiazine 1,1-dioxides - From KATP+ channel openers Ca++ channel blockers?

2-Alkylcyclobutanones as irradiation dose indicators in irradiated ground beef patties

2-Alkylcyclobutanones markers irradiated foodstuffs - Improvement field function EN 1785 technique silver ion chromatography

2-Alkyloxyalkylthiohypoxanthines potent inhibitors xanthine oxidase

2-Alkylthio-substituted platelet P2Y12 receptor antagonists reveal pharmacological identity rat brain Gi-linked ADP receptors P2Y12

2-Amidinylindole-3-carbaldehydes - Synthesis tetracyclic compounds pyrrolo(1,2-c)1,4-diazepine ring

2-Amidinylindole-3-carbaldehydes - Versatile synthons preparation alpha-carboline derivatives

2-Amino-1-methyl-6-(5-hydroxy-)phenylimidazo(4,5-b)pyridine (5-OH-PhIP) biomarker genotoxic dose heterocyclic amine, 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP)

2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) modulates lactogenic hormone-mediated differentiation and gene expression in HC11 mouse mammary epithelial cells

2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) retards mammary gland involution in lactating Sprague-Dawley rats

2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhlP)-induced mutagenesis cultured Large BlueTM rat mammary epithelial fibroblast cells

2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine induces a higher number of aberrant crypt foci in Fischer 344 (rapid) than in Wistar Kyoto (slow) acetylator inbred rats

2-Amino-2-oxazolines subtype selective alpha2 adrenoceptor agonists

2-Amino-3-aroyl-4,5-alkylthiophenes - Agonist allosteric enhancers human A1 adenosine receptors

2-Amino-3-benzoylthiophene allosteric enhancers A1 adenosine agonist binding - Novel 3, 4-, 5-modifications

2-Amino-3-carboxy-1,4-naphthoquinone affects the end-product profile of bifidobacteria through the mediated oxidation of NAD(P)H

2-Amino-3-methylimidazo(4,5-f)quinoline inhibits nitric oxide production lipopolysaccharide-stimulated RAW 264.7 cells blocking p38 kinase activation

2-Amino-3-phenylpyrazine sensitive, fluorescence prelabeling reagent chromatographic electrophoretic measurement saccharides

2-Amino-3-substituted-6-((E)-1-phenyl-2-(N-methylcarbamoyl)vinyl)imidazo-(1,2-a)pyridines class inhibitors human rhinovirus - Stereospecific synthesis antiviral activity

2-Amino-4,6-diarylpyridines ligands estrogen receptor

2-Amino-4-(3-hydroxyphenyl)-4-hydroxybutanoic acid; potent inhibitor rat recombinant human kynureninase

2-Amino-5-oxo-2-tetrahydrofuran carboxylic acids, gamma-lactone antibacterial agents

2-Amino-6-(1,2,4-triazol-4-yl)-purine. intermediate synthesis 9-alkylguanines

2-Amino-6-arylsulfonylbenzonitriles non-nucleoside reverse transcriptase inhibitors HIV-1

2-Amino-7-deazaadenine forms stable base pairs cytosine thymine

2-Amino-N-(2-furylmethyl)propanamide alanylglycine equivalent synthesized bacilysin synthetase

2-Aminoanthracene analytical tool acetylation response catalyzed arylamine N-acetyltransferase

2-Aminoethoxydiphenyl borane activates a novel calcium-permeable cation channel

2-Aminoethoxydiphenyl borate (2-APB) antagonises inositol 1,4,5-trisphosphate-induced calcium release, inhibits calcium pumps use-dependent slowly reversible effect store-operated calcium entry channels

2-Aminoethoxydiphenyl borate (2-APB) is a reliable blocker of store-operated Ca2+ entry but an inconsistent inhibitor of InsP3-induced Ca2+ release

2-Aminoethoxydiphenyl borate affects inositol 1,4,5-trisphosphate receptor, intracellular Ca2+ pump non-specific Ca2+ leak non-mitochondrial Ca2+ stores permeabilized A7r5 cells

2-Aminoethoxydiphenyl borate causes dissociation between membrane electrical and mechanical activity in guinea-pig urinary bladder smooth muscle

2-Aminoethoxydiphenyl borate directly inhibits store-operated calcium entry channels in human platelets

2-Aminoethoxydiphenyl borate inhibits inositol 1,4,5-trisphosphate receptor function, ubiquitination downregulation, acts variable characteristics diverse cell types

2-Aminoethoxydiphenyl borate inhibits phototransduction blocks voltage-gated potassium channels Limulus ventral photoreceptors

2-Aminoethoxydiphenyl borate modulates kinetics of intracellular Ca2+ signals mediated by inositol 1,4,5-trisphosphate-sensitive Ca2+ stores in single pancreatic acinar cells of mouse

2-Aminoethoxydiphenyl borate reveals heterogeneity receptor-activated Ca2+ discharge store-operated Ca2+ influx

2-Aminopurine allows interspecies recombination by a reversible inactivation of the Escherichia coli mismatch repair system

2-Aminopurine electronic formation fluorescence properties DNA

2-Aminopyrimidine directed self-assembly zinc porphyrins bulky 3,5-di-tert-butylphenyl groups

2-Aminothiazoles. class agonist allosteric enhancers A1 adenosine receptors

2-Arachidonoylglycerol cannabinoid receptors

2-Arachidonoylglycerol induces the migration of HL-60 cells differentiated into macrophage-like cells and human peripheral blood monocytes through the cannabinoid CB2 receptor-dependent mechanism

2-Arachidonoylglycerol candidate endothelium-derived hyperpolarizing factor

2-Arachidonyl glyceryl ether, an endogenous agonist of the cannabinoid CB1 receptor

2-Arachidonyl-glycerol stimulates nitric oxide release human immune vascular tissues invertebrate immunocytes cannabinoid receptor 1

2-Arachidonylglycerol, endogenous cannabinoid, inhibits tumor necrosis factor-alpha production murine macrophages, mice

2-Aroylindoles, a novel class of potent, orally active small molecule tubulin inhibitors

2-Aryl indole NK1 antagonists - Optimisation amide substituent

2-Aryl indole NK1 receptor antagonists - Optimisation indole substitution

2-Aryl indole NK1 receptor antagonists - Optimisation 2-aryl ring indole nitrogen substituent

2-Aryl-3,6-dialkyl-5-dialkylaminopyrimidin-4-ones CRF-1 receptor antagonists

2-Aryl-3-arylaminoisoxazol-5(2H)-ones sources indoles imidazo(1,2-a)pyridines

2-Arylalkyl-substituted anthracenones inhibitors 12-lipoxygenase enzymes. Structure-activity relationships terminal aryl ring

2-Azabenzonorbornanes 7-azabenzonorbornanols nitrogen-directed neophyl-type radical rearrangement

2-Azabicyclo(2.2.1)hept-5-en-3-one epoxide. versatile intermediate synthesis cyclopentyl carbocyclic 2-deoxy-, 3-deoxy- ara- ribonucleoside analogues

2-Benzoxazolyl 2-benzimidazolyl hydrazones derived 2-acetylpyridine. class antitumor agents

2-Benzyl-3,4-iminobutanoic acid inhibitor carboxypeptidase A

2-Benzyloxybenzaldehyde inhibits formyl-methionyl-leucyl-phenylalanine stimulation phospholipase D activation rat neutrophils

2-Bromoadenosine-substituted 2,5-oligoadenylates modulate binding activation abilities human recombinant RNase L

2-Bromoethanesulfonate affects bacteria in a trichloroethene-dechlorinating culture

2-Bromoethanesulfonate, sulfate, molybdate, and ethanesulfonate inhibit anaerobic dechlorination of polychlorobiphenyls by pasteurized microorganisms

2-Bromoethylamine suicide inhibitor tissue-bound semicarbazide-sensitive amine oxidase

2-Bromopropane ovarian dysfunction damaging primordial follicles oocytes female rats

2-Bromopropane induced germ cell apoptosis during spermatogenesis in male rat

2-Bromopropane induces DNA damage, impairs functional antioxidant cellular defenses, enhances lipid peroxidation process primary cultures rat Leydig cells

2-Buten-4-olide, endogenous feeding suppressant, improves spatial performance brain acidic fibroblast growth factor mice

2-Butoxyethanol enhances the adherence of red blood cells

2-C-trifluoromethyl substituted pentoses

2-COM - An instrument facilitate patient-professional communication routine medical practice

2-Carbomethoxy-3-aryl-8-bicyclo(3.2.1)octanes - Potent non-nitrogen inhibitors monoamine transporters

2-Chloro N6-methyl-(N)-methanocarba-2-deoxyadenosine-3,5-bisphosphate selective high affinity P2Y1 receptor antagonist

2-Chloro-1,4-dimethoxybenzene mediator lignin peroxidase catalyzed oxidations

2-Chloro-1,4-dimethoxybenzene cation radical - Formation function lignin peroxidase oxidation anisyl alcohol

2-Chloro-2-deoxyadenosine induces apoptosis Fas/Fas ligand pathway human leukemia cell line MOLT-4

2-Chloro-2-deoxyadenosine inhibits DNA repair synthesis potentiates UVC cytotoxicity chronic lymphocytic leukemia B lymphocytes

2-Chloro-3-substituted-1,4-naphthoquinone inactivators human cytomegalovirus protease

2-Chloro-N6-cyclopentyladenosine, adenosine A1 receptor agonist, antagonizes adenosine A3 receptor

2-Chloro-N6-cyclopentyladenosine-elicited attenuation evoked glutamate release sufficient giving complete protection pilocarpine-induced seizures rats

2-Chloro-adenosine induces glutamate-dependent calcium answer C2C12 myotubes

2-Chloro-s-triazine herbicides induce aromatase (CYP19) activity in H295R human adrenocortical carcinoma cells: A novel mechanism for estrogenicity?

2-Chloroacetaldehyde induces epsilondA DNA adducts in DNA of Raji cells as demonstrated by an improved HPLC-fluorimetry method

2-Chloroadenosine adenosine induces apoptosis rheumatoid fibroblasts independently cell surface adenosine receptor signalling

2-Chlorodeoxyadenosine (Cladribine) cure patients chronic lymphocytic leukemia 55 years younger

2-Chlorodeoxyadenosine (cladribine) cure hairy cell leukemia hairy cell leukemia variant - 7-year experience Poland

2-Cyclopentadienylglycine alpha-amino acid eta5-complex structure

2-Cyclopenten-1-one prostaglandin J2 reduce restenosis balloon angioplasty rats - Role NF-kappaB

2-Cys peroxiredoxin PfTrx-Px1 is involved in the antioxidant defence of Plasmodium falciparum

2-D 3-D endoluminal ultrasound - Vascular nonvascular functions

2-D 3-D reconstructions spiral computed tomography localization inferior alveolar canal dental implants

2-D Doppler ultrasonic appearance normal human eyes

2-D echocardiography characteristics acute ventricle myocardial infarction

2-D gel densitometer high-contrast selective imaging chlorophyll-containing protein complexes separated non-denaturing polyacrylamide gel electrophoresis

2-D index means estimating complexity level 3-D sinusoidal structures normal cirrhotic liver hepatocellular carcinoma

2-D optical quantification particle reworking activities marine surface sediments

2-DE study relation heart role ventricular configuration pulmonary hypertension

2-Dehydro-3-epi-20-hydroxyecdysone Froelichia florida

2-Deoxy 5-azacytidine and fetal hemoglobin induction in sickle cell anemia

2-Deoxy-2-iodo-beta-glucopyranosyl fluorides - Mild highly stereoselective glycosyl donors synthesis 2-deoxy-beta-glycosides beta-hydroxy ketones

2-Deo