筛选出 5 条数据

    品牌 产品 货期 价格 货号 规格 /
    生物缓冲液26305-03-3

    CAS号:26305-03-3

    品名:胃酶抑素APepstatinA

    中文别名:抑肽素;胃蛋白酶抑制剂;

    英文别名:pepsininhibitors735a;peptistatinA;PEPSTATINASYNTHETIC;Isovalerylpepstatin;procidins735a;PepstainA;PEPSTATIN;pepstatineA;ahpatininc;IVA-VAL-VAL-STA-ALA-STA;

    分子式:C34H63N5O9

    分子量:685.892

    精确质量:685.463

    Psa:223.26

    RTECS号:SC6155000

    BRN号:2201362

    EINECS号:247-600-0

    MDL号:MFCD00060740

    PubChem号:24898620

    外观与性状:固体

    密度:1.117 g/cm3

    沸点:997.6ºC at 760 mmHg

    熔点:233°C (dec.)(lit.)

    闪点:557.1ºC

    折射率:1.504

    稳定性:Stable. Incompatible with strong bases, strong acids.

    储存条件:2-8ºC

    蒸汽压:0mmHg at 25°C

    安全说明:S22-S24/25

    WGK Germany:2

    简介:Pepstatinisapotentinhibitorofaspartylproteases.Itisahexa-peptidecontainingtheunusualaminoacidstatine(Sta,(3S,4S)-4-amino-3-hydroxy-6-methylheptanoicacid),havingthesequenceIsovaleryl-Val-Val-Sta-Ala-Sta(Iva-Val-Val-Sta-Ala-Sta).ItwasoriginallyisolatedfromculturesofvariousspeciesofActinomycesduetoitsabilitytoinhibitpepsinatpicomolarconcentrations.PepstatinAiswellknowntobeaninhibitorofasparticproteinasessuchaspepsin,cathepsinsDandE.Exceptforitsroleasaproteinaseinhibitor,however,thepharmacologicalactionofpepstatinAuponcellsremainunclear.PepstatinAsuppressesreceptoractivatorofNF-κBligand(RANKL)–inducedosteoclastdifferentiation.PepstatinAsuppressestheformationofmultinuclearosteoclastsdose-dependently.Thisinhibitionoftheformationonlyaffectedosteoclastcells,i.e.,notosteoblast-likecells.Furthermore,pepstatinAalsosuppressesdifferentiationfrompre-osteoclastcellstomononuclearosteoclastcellsdose-dependently.ThisinhibitionseemstobeindependentoftheactivitiesofproteinasessuchascathepsinD,becausetheformationofosteoclastswasnotsuppressedwiththeconcentrationthatinhibitedtheactivityofcathepsinD.CellsignalinganalysisindicatedthatthephosphorylationofERKwasinhibitedinpepstatinA-treatedcells,whilethephosphorylationofIκBandAktshowedalmostnochange.Furthermore,pepstatinAdecreasedtheexpressionofnuclearfactorofactivatedTcellsc1(NFATc1).TheseresultssuggestthatpepstatinAsuppressesthedifferentiationofosteoclaststhroughtheblockadeofERKsignalingandtheinhibitionofNFATc1expression.

     26305-03-3 详细信息

    生物缓冲液

    CAS号:26305-03-3

    品名:胃酶抑素APepstatinA

    中文别名:抑肽素;胃蛋白酶抑制剂;

    英文别名:pepsininhibitors735a;peptistatinA;PEPSTATINASYNTHETIC;Isovalerylpepstatin;procidins735a;PepstainA;PEPSTATIN;pepstatineA;ahpatininc;IVA-VAL-VAL-STA-ALA-STA;

    分子式:C34H63N5O9

    分子量:685.892

    精确质量:685.463

    Psa:223.26

    RTECS号:SC6155000

    BRN号:2201362

    EINECS号:247-600-0

    MDL号:MFCD00060740

    PubChem号:24898620

    外观与性状:固体

    密度:1.117 g/cm3

    沸点:997.6ºC at 760 mmHg

    熔点:233°C (dec.)(lit.)

    闪点:557.1ºC

    折射率:1.504

    稳定性:Stable. Incompatible with strong bases, strong acids.

    储存条件:2-8ºC

    蒸汽压:0mmHg at 25°C

    安全说明:S22-S24/25

    WGK Germany:2

    简介:Pepstatinisapotentinhibitorofaspartylproteases.Itisahexa-peptidecontainingtheunusualaminoacidstatine(Sta,(3S,4S)-4-amino-3-hydroxy-6-methylheptanoicacid),havingthesequenceIsovaleryl-Val-Val-Sta-Ala-Sta(Iva-Val-Val-Sta-Ala-Sta).ItwasoriginallyisolatedfromculturesofvariousspeciesofActinomycesduetoitsabilitytoinhibitpepsinatpicomolarconcentrations.PepstatinAiswellknowntobeaninhibitorofasparticproteinasessuchaspepsin,cathepsinsDandE.Exceptforitsroleasaproteinaseinhibitor,however,thepharmacologicalactionofpepstatinAuponcellsremainunclear.PepstatinAsuppressesreceptoractivatorofNF-κBligand(RANKL)–inducedosteoclastdifferentiation.PepstatinAsuppressestheformationofmultinuclearosteoclastsdose-dependently.Thisinhibitionoftheformationonlyaffectedosteoclastcells,i.e.,notosteoblast-likecells.Furthermore,pepstatinAalsosuppressesdifferentiationfrompre-osteoclastcellstomononuclearosteoclastcellsdose-dependently.ThisinhibitionseemstobeindependentoftheactivitiesofproteinasessuchascathepsinD,becausetheformationofosteoclastswasnotsuppressedwiththeconcentrationthatinhibitedtheactivityofcathepsinD.CellsignalinganalysisindicatedthatthephosphorylationofERKwasinhibitedinpepstatinA-treatedcells,whilethephosphorylationofIκBandAktshowedalmostnochange.Furthermore,pepstatinAdecreasedtheexpressionofnuclearfactorofactivatedTcellsc1(NFATc1).TheseresultssuggestthatpepstatinAsuppressesthedifferentiationofosteoclaststhroughtheblockadeofERKsignalingandtheinhibitionofNFATc1expression.

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    生物缓冲液26305-03-3
    MCE Pepstatin Pepstatin 现货

     343.00
    HY-P0018 98.59%
    梯希爱 胃酶抑素A PepstatinA 现货

     360.00
    P3041 90.0%
    TargetMol 抑肽素 Pepstatin 现货

     428.00
    T3695 99.94%
    Am PepstatinA PepstatinA 现货

     495.00
    A135194 98%
    生物缓冲液103476-89-7

    CAS号:103476-89-7

    品名:亮抑酶肽Leupeptinhemisulfate

    中文别名:亮抑蛋白酶肽;亮抑肽酶;

    英文别名:Leupeptin,synthetic;LEUPEPTIN1/2H2SO4;Leupeptin,Microbial;AC-LEU-LEU-ARGININAL;AC-LEU-LEU-ARG-CHO;SynonymAcetyl-Leu-L;LEUPEPTINSULFATE;AC-LLR-CHO;

    分子式:C20H38N6O4

    分子量:426.554

    精确质量:426.295

    Psa:166.27

    MDL号:MFCD00037012

    PubChem号:24896328

    外观与性状:白色固体

    密度:

    储存条件:-20ºC

    安全说明:S22; S24/25; S36/37; S36

    危险类别码:R20/21/22

    WGK Germany:3

    海关编码:29241900

    危险品标志:Xn

    信号词:Warning

    危险性防范说明:P261; P264; P280; P302 + P352 + P312; P304 + P340 + P312; P501

    危险标志:GHS07

    危险性描述:H302 + H312 + H332

     103476-89-7 详细信息

    生物缓冲液

    CAS号:103476-89-7

    品名:亮抑酶肽Leupeptinhemisulfate

    中文别名:亮抑蛋白酶肽;亮抑肽酶;

    英文别名:Leupeptin,synthetic;LEUPEPTIN1/2H2SO4;Leupeptin,Microbial;AC-LEU-LEU-ARGININAL;AC-LEU-LEU-ARG-CHO;SynonymAcetyl-Leu-L;LEUPEPTINSULFATE;AC-LLR-CHO;

    分子式:C20H38N6O4

    分子量:426.554

    精确质量:426.295

    Psa:166.27

    MDL号:MFCD00037012

    PubChem号:24896328

    外观与性状:白色固体

    密度:

    储存条件:-20ºC

    安全说明:S22; S24/25; S36/37; S36

    危险类别码:R20/21/22

    WGK Germany:3

    海关编码:29241900

    危险品标志:Xn

    信号词:Warning

    危险性防范说明:P261; P264; P280; P302 + P352 + P312; P304 + P340 + P312; P501

    危险标志:GHS07

    危险性描述:H302 + H312 + H332

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    生物缓冲液103476-89-7
    MCE Leupeptinhemisulfate Leupeptinhemisulfate 现货

     495.00
    HY-18234A ≥98.0%
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