筛选出 2 条数据

    品牌 产品 货期 价格 货号 规格 /
    合成52809-07-1

    CAS号:52809-07-1

    品名:使君子氨酸(+)-QuisqualicAcid

    中文别名:L-使君子氨酸;

    英文别名:L-Quisqualicacid,(L)-(+)-α-Amino-3,5-dioxo-1,2,4-oxadiazolidine-2-propanoicacid;

    分子式:C5H7N3O5

    分子量:189.126

    精确质量:189.039

    Psa:131.32

    MDL号:MFCD00069337

    外观与性状:白色粉末

    密度:1.679g/cm3

    熔点:185-187ºC dec.

    折射率:1.571

    稳定性:Stable. Incompatible with strong oxidizing agents.

    储存条件:2-8ºC

    安全说明:S26; S36

    危险类别码:R20/21/22

    海关编码:2934999090

    危险品标志:Xn

    信号词:Warning

    危险性防范说明:P280

    危险标志:GHS07

    危险性描述:H302; H312; H332

    简介:QuisqualicacidisanagonistoftheAMPA,kainate,andgroupImetabotropicglutamatereceptors,andoneofthemostpotentAMPAreceptoragonistsknown.Itcausesexcitotoxicityandisusedinneurosciencetoselectivelydestroyneuronsinthebrainorspinalcord.QuisqualicacidoccursnaturallyintheseedsofQuisqualisspecies.[α]20D=+17(6MHCl);ResearchconductedbytheUSDAAgriculturalResearchService,hasdemonstratedquisqualicacidisalsopresentwithintheflowerpetalsofzonalgeranium(Pelargoniumxhortorum)andisresponsibleforcausingrigidparalysisoftheJapanesebeetle.QuisqualicacidisthoughttomimicL-glutamicacid,whichisaneurotransmitterintheinsectneuromuscularjunctionandmammaliancentralnervoussystem.

    用途:生化研究,使君子酸受体的兴奋剂,拮抗谷氨酸能竞争中枢神经元的谷氨酸受体。

     52809-07-1 详细信息

    合成

    CAS号:52809-07-1

    品名:使君子氨酸(+)-QuisqualicAcid

    中文别名:L-使君子氨酸;

    英文别名:L-Quisqualicacid,(L)-(+)-α-Amino-3,5-dioxo-1,2,4-oxadiazolidine-2-propanoicacid;

    分子式:C5H7N3O5

    分子量:189.126

    精确质量:189.039

    Psa:131.32

    MDL号:MFCD00069337

    外观与性状:白色粉末

    密度:1.679g/cm3

    熔点:185-187ºC dec.

    折射率:1.571

    稳定性:Stable. Incompatible with strong oxidizing agents.

    储存条件:2-8ºC

    安全说明:S26; S36

    危险类别码:R20/21/22

    海关编码:2934999090

    危险品标志:Xn

    信号词:Warning

    危险性防范说明:P280

    危险标志:GHS07

    危险性描述:H302; H312; H332

    简介:QuisqualicacidisanagonistoftheAMPA,kainate,andgroupImetabotropicglutamatereceptors,andoneofthemostpotentAMPAreceptoragonistsknown.Itcausesexcitotoxicityandisusedinneurosciencetoselectivelydestroyneuronsinthebrainorspinalcord.QuisqualicacidoccursnaturallyintheseedsofQuisqualisspecies.[α]20D=+17(6MHCl);ResearchconductedbytheUSDAAgriculturalResearchService,hasdemonstratedquisqualicacidisalsopresentwithintheflowerpetalsofzonalgeranium(Pelargoniumxhortorum)andisresponsibleforcausingrigidparalysisoftheJapanesebeetle.QuisqualicacidisthoughttomimicL-glutamicacid,whichisaneurotransmitterintheinsectneuromuscularjunctionandmammaliancentralnervoussystem.

    用途:生化研究,使君子酸受体的兴奋剂,拮抗谷氨酸能竞争中枢神经元的谷氨酸受体。

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    合成52809-07-1
    阿拉丁 异喹啉酸 Quisqualicacid 期货,请咨询

     570.90
    Q276562 Moligand™,≥99%
    膜转运/离子通道122647-32-9

    CAS号:122647-32-9

    品名:富马酸伊布利特IbutilideHemifumarate

    中文别名:伊布利特;N-[4-[4-(乙基庚基胺)-1-羟基丁基]苯基]甲磺酰胺富马酸盐;伊布利特半富马酸盐;

    英文别名:Ibutilidehemifumaratesalt;Ibutilidefumarate;IbutilideFumarate;

    分子式:C44H76N4O10S2

    分子量:885.225

    精确质量:884.5

    Psa:230.64

    UNII号:9L5X4M5L6I

    密度:

    沸点:522.4ºC at 760 mmHg

    闪点:269.7ºC

    蒸汽压:9.71E-12mmHg at 25°C

    信号词:Warning

    危险标志:GHS07

    危险性描述:H302

    简介:IbutilideisaClassIIIantiarrhythmicagentthatisindicatedforacutecardioconversionofatrialfibrillationandatrialflutterofarecentonsettosinusrhythm.Itexertsitsantiarrhythmiceffectbyinductionofslowinwardsodiumcurrent,whichprolongsactionpotentialandrefractoryperiod(physiology)ofmyocardialcells.BecauseofitsClassIIIantiarrhythmicactivity,thereshouldnotbeconcomitantadministrationofClassIaandClassIIIagents.

     122647-32-9 详细信息

    膜转运/离子通道

    CAS号:122647-32-9

    品名:富马酸伊布利特IbutilideHemifumarate

    中文别名:伊布利特;N-[4-[4-(乙基庚基胺)-1-羟基丁基]苯基]甲磺酰胺富马酸盐;伊布利特半富马酸盐;

    英文别名:Ibutilidehemifumaratesalt;Ibutilidefumarate;IbutilideFumarate;

    分子式:C44H76N4O10S2

    分子量:885.225

    精确质量:884.5

    Psa:230.64

    UNII号:9L5X4M5L6I

    密度:

    沸点:522.4ºC at 760 mmHg

    闪点:269.7ºC

    蒸汽压:9.71E-12mmHg at 25°C

    信号词:Warning

    危险标志:GHS07

    危险性描述:H302

    简介:IbutilideisaClassIIIantiarrhythmicagentthatisindicatedforacutecardioconversionofatrialfibrillationandatrialflutterofarecentonsettosinusrhythm.Itexertsitsantiarrhythmiceffectbyinductionofslowinwardsodiumcurrent,whichprolongsactionpotentialandrefractoryperiod(physiology)ofmyocardialcells.BecauseofitsClassIIIantiarrhythmicactivity,thereshouldnotbeconcomitantadministrationofClassIaandClassIIIagents.

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    膜转运/离子通道122647-32-9
    阿拉丁 富马酸依布利特 Ibutilidefumarate 期货,请咨询

     600.90
    I276579 ≥99%
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