听力与言语-语言病理学

行为科学

医学伦理学

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  • Nelumbinis Semen reverses a decrease in 5-HT1A receptor binding induced by chronic mild stress, a depression-like symptom.

    abstract::Depression is associated with a dysfunctional serotonin (5-hydroxytryptamine; 5-HT) system. More recently, several lines of evidence suggest that an important factor in the development of depression may be a deficit in the function and expression of 5-HT1A receptors. The present study assessed ifNelumbinis Semen (N. s...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02975433

    authors: Jang CG,Kang M,Cho JH,Lee SB,Kim H,Park S,Lee J,Park SK,Hong M,Shin MK,Shim IS,Bae H

    更新日期:2004-10-01 00:00:00

  • Constituents of the halophyte Salicornia herbacea.

    abstract::Four compounds were isolated from Salicornia herbacea by repeated column chromatography. Their structures were identified as beta-sitosterol (1), stigmasterol (2), uracil (3), and isorhamnetin-3-O-beta-D-glucopyranoside (4) by spectral analysis and comparison with the published data. ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02975427

    authors: Lee YS,Lee HS,Shin KH,Kim BK,Lee S

    更新日期:2004-10-01 00:00:00

  • Pulsatilla saponin D: the antitumor principle from Pulsatilla koreana.

    abstract::By bioassay-guided separation, an already known saponin, Pulsatilla saponin D was isolated from the root of Pulsatilla koreana Nakai as a antitumor component when evaluated by in vivo antitumor activity as well as in vitro cytotoxic activity test. It showed potent inhibition rate of tumor growth (IR, 82%) at the dose ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02975843

    authors: Kim Y,Bang SC,Lee JH,Ahn BZ

    更新日期:2004-09-01 00:00:00

  • Enantioselective pharmacokinetics of carvedilol in human volunteers.

    abstract::Carvedilol is administered as a racemic mixture of the R(+)- and S(-)-enantiomers, although they exhibit different pharmacological effects. To investigate the stereoselective pharmacokinetics, the enantiomeric separation of carvedilol in human plasma was undertaken using capillary electrophoresis (CE). Resolution of t...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02975853

    authors: Phuong NT,Lee BJ,Choi JK,Kang JS,Kwon KI

    更新日期:2004-09-01 00:00:00

  • Synthesis of new diselenide compounds as anti-inflammatory agents.

    abstract::Many diselenide compounds are used as antioxidants, enzyme inhibitors and cytokine inducers. Three new diselenide compounds, bis-(2-hydroxyphenyl) diselenide, bis-(3-hydroxyphenyl) diselenide and bis-(4-hydroxyphenyl) diselenide were designed and synthesized as anti-inflammatory agent. All of them were found to have s...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980171

    authors: Shen L,Shin KM,Lee KT,Jeong JH

    更新日期:2004-08-01 00:00:00

  • Oxidative stress in ovariectomy menopause and role of chondroitin sulfate.

    abstract::Oxidative stress due to reactive oxygen species (ROS) can cause oxidative damage to cells. Cells have a number of defense mechanisms to protect themselves from the toxicity of ROS. Mitochondria are especially important in the oxidative stress as ROS have been found to be constantly generated as an endogen threat. Mito...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980181

    authors: Ha BJ

    更新日期:2004-08-01 00:00:00

  • Cytotoxic constituents of Diadema setosum.

    abstract::5,8-Epidioxycholest-6-en-3-ol (1), cholesterol (2), glycerol 1-palmitate (3) and glycerol 1,3-dioleate-2-stearate (4) were isolated from the methanol extract of the sea urchin Diadema setosum, which was collected from the Halong sea, Vietnam. Chemical structures were established based on extensive 1D, 2D-NMR, FAB-MS, ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980141

    authors: Minh CV,Kiem PV,Huong le M,Kim YH

    更新日期:2004-07-01 00:00:00

  • Optimizing the novel formulation of liposome-polycation-DNA complexes (LPD) by central composite design.

    abstract::LPD vectors are non-viral vehicles for gene delivery comprised of polycation-condensed plasmid DNA and liposomes. Here, we described a novel anionic LPD formulation containing protamine-DNA complexes and pH sensitive liposomes composed of DOPE and cholesteryl hemisuccinate (Chems). Central composite design (CCD) was e...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980151

    authors: Sun X,Zhang Z

    更新日期:2004-07-01 00:00:00

  • A new indolinepeptide from Paecilomyces sp. J300.

    abstract::A new indolinepeptide (3) was isolated, together with two known compounds, a cerebroside (1) and an alloxazine (2), from silkworm larvae infected with Paecilomyces sp. J300. On the basis of spectroscopic data, their structures were elucidated as (4E, 8E, 2S, 2'R, 3R)-N-2'-hydroxyhexadecanoyl-1-O-beta-D-glucopyranosyl-...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980157

    authors: Kwon HC,Kim KR,Zee SD,Cho SY,Lee KR

    更新日期:2004-06-01 00:00:00

  • Water soluble cyclosporine monomethoxy poly(ethyleneglycol) conjugates as potential prodrugs.

    abstract::The highly water-soluble monomethoxypoly(ethyleneglycol) (mPEG) prodrugs of cyclosporin A (CsA) were synthesized. These prodrugs were prepared by initially preparing intermediate in the form of carbonate at the 3'-positions of CsA with chloromethyl chloroformate, in the presence of a base to provide a 3'-carbonated Cs...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980167

    authors: Cho H,Chung Y

    更新日期:2004-06-01 00:00:00

  • Synthesis and biological evaluation of new thiazolopyrimidines.

    abstract::In this study, a series of 4-amino-5-cyano-3-substituted-2,3-dihydrothiazol-2-thiones (1a-c), as well as their triazolo and triazinopyrimidine derivatives such as 8-substituted-3-benzyl-5-methylthiazolo[5,4-e][1,2,4] triazolo[1,5-c]pyrimidin-2-thiones (4-6, 10) and 3-benzyl-5-methyl thiazolo[5,4-e]pyrimidino[3,4-b][1,...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980118

    authors: Said M,Abouzid K,Mouneer A,Ahmedy A,Osman AM

    更新日期:2004-05-01 00:00:00

  • Solid-phase extraction of L-muscone from aqueous samples with Amberlite XAD-4 for gas chromatographic assay.

    abstract::An efficient analytical method was devised for the accurate L-muscone assay in aqueous samples. It involves solid-phase extraction of L-muscone in adsorption mode using XAD-4 as the sorbent and dichloromethane modified with 10% (v/v) methanol as the eluting solvent. The gas chromatographic analysis of the eluate resid...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980128

    authors: Paik MJ,Kim KR

    更新日期:2004-05-01 00:00:00

  • Anti-platelet pentacyclic triterpenoids from leaves of Campsis grandiflora.

    abstract::Five pentacyclic triterpenoids, oleanolic acid (1), hederagenin (2), ursolic acid (3), tormentic acid (4) and myrianthic acid (5), were isolated from the methanol extract of the leaves of Campsis grandiflora, and structures of the compounds were established by the spectroscopic methods. Compounds 2, 3, 4, and 5 were i...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980076

    authors: Jin JL,Lee YY,Heo JE,Lee S,Kim JM,Yun-Choi HS

    更新日期:2004-04-01 00:00:00

  • Microtubule inhibitory effects of various SJ compounds on tissue culture cells.

    abstract::SJ compounds (SJ8002 and related compounds) are a group of novel anticancer agents (Cho, Chung, Lee, Kwon, Kang, Joo, and Oh. PCT/KR02/00392). To explore the anticancer mechanism of these compounds, we examined the effect of SJ8002 on microtubules of six human cell lines. At a high concentration (2 microg/mL), SJ8002 ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980086

    authors: Lee JH,Kang DW,Kwon HS,Lee SH,Park SK,Chung SG,Cho EH,Paik SY,Lee JH

    更新日期:2004-04-01 00:00:00

  • Synthesis and biological activities of 8-arylflavones.

    abstract::A number of 8-arylflavones have been synthesized as congeners of wogonin and evaluated for their inhibitory activities of PGE2 production. 8-Arylflavones were obtained from commercially available chrysin via two different synthetic pathways. Most 8-arylflavones exhibited much reduced inhibitory activities against COX-...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980059

    authors: Dao TT,Kim SB,Sin KS,Kim S,Kim HP,Park H

    更新日期:2004-03-01 00:00:00

  • (-)-Epigallocatechin-3-gallate and hinokitiol reduce melanin synthesis via decreased MITF production.

    abstract::In this study, the effects of (-)-epigallocatechin-3-gallate (EGCG) and/or hinokitiol (beta-thujaplicin) on melanogenesis were investigated. Our results showed that both EGCG and hinokitiol significantly inhibited melanin synthesis in a concentration-dependent manner, and that their hypopigmenting effects were stronge...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980069

    authors: Kim DS,Park SH,Kwon SB,Li K,Youn SW,Park KC

    更新日期:2004-03-01 00:00:00

  • Absorption, distribution, metabolism, and excretion of CKD-732, a novel antiangiogenic fumagillin derivative, in rats, mice, and dogs.

    abstract::The pharmacokinetics of CKD-732 (6-O-4-[dimethyl-aminoethoxy)cinnamoyl]-fumagillol x hemioxalate) was investigated in male SD rats and beagle dogs after bolus intravenous administration. The parent compound and metabolites obtained from in vitro and in vivo samples were determined by LC/MS. The main metabolite was iso...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980116

    authors: Lee HS,Choi WK,Son HJ,Lee SS,Kim JK,Ahn SK,Hong CI,Min HK,Kim M,Myung SW

    更新日期:2004-02-01 00:00:00

  • Antioxidant activities of isoflavones from the rhizomes of Belamcanda chinensis on carbon tetrachloride-induced hepatic injury in rats.

    abstract::The present study was carried out to clarify whether tectorigenin and tectoridin isolated from the rhizomes of Belamcanda chinensis (Iridaceae) inhibit hepatic damage induced by carbon tetrachloride (CCl4)-intoxication in rats by the experimental methods in vitro and in vivo. Tectorigenin and tectoridin exhibited a si...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980104

    authors: Jung SH,Lee YS,Lim SS,Lee S,Shin KH,Kim YS

    更新日期:2004-02-01 00:00:00

  • The influence of cimetidine on the pharmacokinetics of diltiazem and its main metabolite in rabbits.

    abstract::The purpose of this study was to investigate the pharmacokinetic alteration of diltiazem and its main metabolite, deacetyldiltiazem, after oral administration of diltiazem in rabbits with or without cimetidine co-administration. The area under the plasma concentration-time curve (AUC) of diltiazem was significantly el...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980114

    authors: Choi JS,Burm JP

    更新日期:2004-02-01 00:00:00

  • Control of encapsulation efficiency and initial burst in polymeric microparticle systems.

    abstract::Initial burst is one of the major challenges in protein-encapsulated microparticle systems. Since protein release during the initial stage depends mostly on the diffusional escape of the protein, major approaches to prevent the initial burst have focused on efficient encapsulation of the protein within the micropartic...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章,评审

    doi:10.1007/BF02980037

    authors: Yeo Y,Park K

    更新日期:2004-01-01 00:00:00

  • Anti-allergic activity of 18beta-glycyrrhetinic acid-3-O-beta-D-glucuronide.

    abstract::Glycyrrhizin (18beta-glycyrrhetinic acid-3-O-beta-D-glucuronopyranosyl-(1 --> 2)-beta-D-glucuronide, GL) was transformed to 18beta-glycyrrhetinic acid-3-O-beta-D-glucuronide (GAMG) by Streptococcus LJ-22. The antiallergic activities of GL and GAMG was measured using a RBL cell assay system and contact hypersensitivity...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980047

    authors: Park HY,Park SH,Yoon HK,Han MJ,Kim DH

    更新日期:2004-01-01 00:00:00

  • Preparation of alginate/chitosan microcapsules and enteric coated granules of mistletoe lectin.

    abstract::The aqueous extract of European mistletoe (Viscum album, L.) has been used in cancer therapy. The purified mistletoe lectins, main components of mistletoe, have demonstrated cytotoxic and immune-system-stimulating activities. Korean mistletoe (Viscum album L. coloratum), a subspecies of European mistletoe, has also be...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980057

    authors: Lyu SY,Kwon YJ,Joo HJ,Park WB

    更新日期:2004-01-01 00:00:00

  • Lipase mediated chiral resolution of 4-arylthio-2-butanol as an intermediate for beta-lactam antibiotics.

    abstract::This paper deals with chiral enzymatic resolution of 4-arylthio-2-butanols by lipase to prepare potential intermediates of beta-lactam antibiotics. Among several lipases employed, lipase P type enzyme gave the highest ee value to prepare (R)-4-arylthio-2-butyl acetate. The enzymatic resolution of phenyl substituted al...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02994748

    authors: Hwang KJ,Lee J,Chin S,Moon CJ,Lee W,Baek CS,Kim HJ

    更新日期:2003-12-01 00:00:00

  • Lysophosphatidic acid inhibits melanocyte proliferation via cell cycle arrest.

    abstract::Lysophosphatidic acid (LPA) is a well-known mitogen in various cell types. However, we found that LPA inhibits melanocyte proliferation. Thus, we further investigated the possible signaling pathways involved in melanocyte growth inhibition. We first examined the regulation of the three major subfamilies of mitogen-act...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02994758

    authors: Kim DS,Park SH,Kim SE,Kwon SB,Park ES,Youn SW,Park KC

    更新日期:2003-12-01 00:00:00

  • JNK/SAPK is required in nitric oxide-induced apoptosis in osteoblasts.

    abstract::Nitric oxide(NO) induces apoptosis in human osteoblasts. Treatment with exogenous NO donors, SNAP (S-Nitroso-N-acetylpenicillamine) and SNP (sodium nitroprusside), to MG-63 osteoblasts resulted in apoptotic morphological changes, as shown by a bright blue-fluorescent condensed nuclei and chromatin fragmentation by flu...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980203

    authors: Kang YJ,Chae SW

    更新日期:2003-11-01 00:00:00

  • Antioxidant and memory enhancing effects of purple sweet potato anthocyanin and cordyceps mushroom extract.

    abstract::The effects of purple sweet potato anthocyanin (SPA) and Cordyceps mushroom extract (CME) on lipid peroxidation, 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals and cognitive deficits were examined. Both SPA and CME exhibited DPPH radical scavenging activities with similar potency. In contrast, only SPA was shown to eff...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02980027

    authors: Cho J,Kang JS,Long PH,Jing J,Back Y,Chung KS

    更新日期:2003-10-01 00:00:00

  • Platelet anti-aggregatory effects of coumarins from the roots of Angelica genuflexa and A. gigas.

    abstract::Five coumarins, isoimperatorin (1), pabulenol (2), isooxypeucedanin (3), oxypeucedanin hydrate (4) and osthol (5) were isolated from the MeOH extract of Angelica genuflexa in the course of searching for anti-platelet and anti-coagulant components from plants. Pabulenol (2) was isolated from A. genuflexa for the first ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976681

    authors: Lee YY,Lee S,Jin JL,Yun-Choi HS

    更新日期:2003-09-01 00:00:00

  • Compounds obtained from sida acuta with the potential to induce quinone reductase and to inhibit 7,12-dimethylbenz[a]anthracene-induced preneoplastic lesions in a mouse mammary organ culture model.

    abstract::Activity-guided fractionation of the EtOAc-soluble extract of the whole plants of Sida acuta using a bioassay based on the induction of quinone reductase (QR) in cultured Hepa 1c1c7 mouse hepatoma cells, led to the isolation of ten active compounds of previously known structure, quindolinone (1), cryptolepinone (2), 1...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976704

    authors: Jang DS,Park EJ,Kang YH,Su BN,Hawthorne ME,Vigo JS,Graham JG,Cabieses F,Fong HH,Mehta RG,Pezzuto JM,Kinghorn AD

    更新日期:2003-08-01 00:00:00

  • In vitro percutaneous absorption of ondansetron hydrochloride from pressure-sensitive adhesive matrices through hairless mouse skin.

    abstract::To investigate the feasibility of developing a new ondansetron transdermal system, the effects of vehicles and penetration enhancers on the in vitro permeation of ondansetron hydrochloride (OS) from a pressure-sensitive adhesive (PSA) matrices across dorsal hairless mouse skin were studied. Vehicles employed in this s...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976714

    authors: Gwak HS,Oh IS,Chun IK

    更新日期:2003-08-01 00:00:00

  • Effect of active synthetic 2-substituted quinazolinones on anti-platelet aggregation and the inhibition of superoxide anion generation by neutrophils.

    abstract::Quinazolinones, 2-substituted and 3-substituted, mainly synthesized by microwave irradiation, were subjected to anti-platelet aggregation and inhibition of superoxide anion generation assays. Interestingly, 2-phenyl-4-quinazolinone (4) exhibited significant inhibitory activities toward platelet aggregation and neutrop...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976872

    authors: Chang FR,Wu CC,Hwang TL,Patnam R,Kuo RY,Wang WY,Lan YH,Wu YC

    更新日期:2003-07-01 00:00:00

  • Pharmacokinetic and pharmacodynamic characterization of gliclazide in healthy volunteers.

    abstract::Pharmacokinetic and pharmacodynamic properties of gliclazide were studied after an oral administration of gliclazide tablets in healthy volunteers. After an overnight fasting, gliclazide tablet was orally administered to 11 volunteers. Additional 10 volunteers were used as a control group (i.e., no gliclazide administ...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976882

    authors: Kim H,Yun M,Kwon KI

    更新日期:2003-07-01 00:00:00

  • Synthesis and anti-HIV activity of sulfonated amino ribofuranans.

    abstract::New sulfonated amino ribofuranans were synthesized to elucidate the relationship between structure and specific biological activities such as anti-HIV and blood anticoagulant activities. The synthesis was performed by sulfonation of copolymers having various proportion of (1 --> 5)-alpha-D-ribofuranosidic unit. The su...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976858

    authors: Kang BW

    更新日期:2003-06-01 00:00:00

  • The influences of extremely low frequency magnetic fields on drug-induced convulsion in mouse.

    abstract::This study investigated the effects of extremely low frequency magnetic fields (ELF-MFs) on the sensitivity of seizure response to bicuculline, picrotoxin and NMDA in mice. The mice were exposed to either a sham or 20 G ELF-MFs for 24 hours. Convulsants were then administered i.p. at various doses. The seizure inducti...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976868

    authors: Sung JH,Jeong JH,Kim JS,Choi TS,Park JH,Kang HY,Kim YS,Kim DS,Sohn UD

    更新日期:2003-06-01 00:00:00

  • Synthesis of allylthiopyridazine derivatives and inhibition of aflatoxin B1-induced hepatotoxicity in rats.

    abstract::Five kinds of allylthiopyridazine derivatives were synthesized and their chemoprotective activities examined in rats exposed to aflatoxin B1-toxicant. Rats were pretreated with five allylthiopyridazine derivatives at daily oral doses of 50 mg/kg for 10 consecutive days, and during this period with one or three repeate...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976691

    authors: Shin HS,Kwon SK

    更新日期:2003-05-01 00:00:00

  • Enhanced ex vivo buccal transport of propranolol: evaluation of phospholipids as permeation enhancers.

    abstract::The aim of the present study was to evaluate the effects of two phospholipid permeation enhancers, lysophosphatidylcholine (LPC) and didecanoylphosphatidylcholine (DDPC), along with a fusidic acid derivative, sodium taurodihydrofusidate (STDHF) and ethanol (EtOH) on the buccal transport of propranolol hydrochloride (P...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976701

    authors: Lee J,Choi YW

    更新日期:2003-05-01 00:00:00

  • Synthesis and evaluation of cytotoxicity of stilbene analogues.

    abstract::Resveratrol analogs were newly synthesized and evaluated for cytotoxicity in cultured human lung and colon cancer cells. 3,5,4-Trimethoxy-trans-stilbene and 3,5,2',4'-tetramethoxy-trans-stilbene were found to be more potent rather than resveratrol. 3,4,5-Trimethoxy-4'-bromo-cis-stilbene was the most active among the t...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976951

    authors: Lee SK,Nam KA,Hoe YH,Min HY,Kim EY,Ko H,Song S,Lee T,Kim S

    更新日期:2003-04-01 00:00:00

  • Prevention of macrophage-related inflammatory diseases by allergina.

    abstract::The oriental herbal combination allergina has been shown to inhibit allergic inflammation. In the present study, we demonstrate that the oral administration of allergina markedly inhibits the progression of inflammatory diseases, such as graft-versus-host diseases (in the allogeneic bone marrow transplantation and the...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976961

    authors: Han SB,Lee CW,Park SK,Yoon WK,Moon JS,Lee KH,Kim HC,Kim HM

    更新日期:2003-04-01 00:00:00

  • Synthesis and immunosuppressive activity of novel succinylacetone analogues.

    abstract::This study describes the synthesis of novel enol esters (3) and triketones (4) as analogues of succinylacetone (SA) (Ed- this abbreviation is introduced here based on your use of it in the body of the paper) and the evaluation on the mouse allogeneic mixed lymphocyte reaction (MLR) and the murine model of antigen-indu...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976828

    authors: Kim TH,Oh DR,Na HS,Lee HC

    更新日期:2003-03-01 00:00:00

  • Cerebrosides from Longan Arillus.

    abstract::From the pulp of Euphoria longana (Longan Arillus), three cerebroside molecular species have been isolated. Six known cerebrosides, soyacerebrosides I and II, 1-O-beta-D-glucopyranosyl-(2S,3R,4E,8E)-2-(2'-lignoceroylamino)-4,8-octadecadiene-1,3-diol (longan cerebroside I) and its 8Z isomer (longan cerebroside II), mom...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF02976659

    authors: Ryu J,Kim JS,Kang SS

    更新日期:2003-02-01 00:00:00

  • Importance of sulfonylimidazolidinone motif of 4-phenyl-1-arylsulfonylimidazolidinones for their cytotoxicity: synthesis of 2-benzoyl-4-phenyl[1,2,5]thiazolidine-1,1-dioxides and their cytotoxcity.

    abstract::For probing the importance of planarity of imidazolidinone motif of 4-phenyl-1-(benzenesulfonyl)imidazolidinones 1 for their cytotoxicity, 4-phenyl-2-(benzoyl)[1,2,5]thiadiazolidine-1,1-dioxide (2a), 4-phenyl-2-(p-toluoyl)[1,2,5]thiadiazolidine-1,1-dioxide (2b), 4-phenyl-2-(phenylcarbamoyl)[1,2,5]thiadiazolidine-1,1-d...

    journal_title:Archives of pharmacal research

    pub_type: 杂志文章

    doi:10.1007/BF03179923

    authors: Kim IW,Lee CK,Kim HS,Jung SH

    更新日期:2003-01-01 00:00:00

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