筛选出 12 条数据

    品牌 产品 货期 价格 货号 规格 /
    干细胞与Wnt信号879085-55-9

    CAS号:879085-55-9

    品名:2-氯-N-[4-氯-3-(2-吡啶基)苯基]-4-(甲磺酰基)苯甲酰胺vismodegib

    中文别名:维莫德吉;2-氯-n-[4-氯-3-(2-吡啶)苯基]-4-(甲基磺酰基)苯甲酰胺;

    英文别名:Vismodegib;2-Chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide;

    分子式:C19H14Cl2N2O3S

    分子量:421.297

    精确质量:420.01

    Psa:84.51

    MDL号:MFCD12407408

    密度:1.44

    沸点:561.6ºC at 760 mmHg

    闪点:293.4ºC

    折射率:1.64

    海关编码:2933399090

    简介:TargetstheHedgehog(Hh)pathway.InhibitionoftheHhsignalingmaybeeffectiveinthetreatmentandpreventionofmanytypesofhumancancers.

     879085-55-9 详细信息

    干细胞与Wnt信号

    CAS号:879085-55-9

    品名:2-氯-N-[4-氯-3-(2-吡啶基)苯基]-4-(甲磺酰基)苯甲酰胺vismodegib

    中文别名:维莫德吉;2-氯-n-[4-氯-3-(2-吡啶)苯基]-4-(甲基磺酰基)苯甲酰胺;

    英文别名:Vismodegib;2-Chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide;

    分子式:C19H14Cl2N2O3S

    分子量:421.297

    精确质量:420.01

    Psa:84.51

    MDL号:MFCD12407408

    密度:1.44

    沸点:561.6ºC at 760 mmHg

    闪点:293.4ºC

    折射率:1.64

    海关编码:2933399090

    简介:TargetstheHedgehog(Hh)pathway.InhibitionoftheHhsignalingmaybeeffectiveinthetreatmentandpreventionofmanytypesofhumancancers.

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    干细胞与Wnt信号879085-55-9
    MCE Vismodegib Vismodegi 现货

     700.00
    HY-10440 99.97%
    干细胞与Wnt信号1243243-89-1

    CAS号:1243243-89-1

    品名:2-(4-(2-甲基吡啶-4-基)苯基)-n-(4-(吡啶-3-基)苯基)乙酰胺2-[4-(2-methylpyridin-4-yl)phenyl]-N-(4-pyridin-3-ylphenyl)acetamide

    中文别名:硫酸特布他林.硫酸叔丁宁按;

    英文别名:QC-8389;2-[4-(2-methylpyridin-4-yl)phenyl]-N-[4-(pyridin-3-yl)phenyl]acetamide;S7037,C59;CS-1420;Wnt-C59(C59);Wnt-C59;

    分子式:C25H21N3O

    分子量:379.454

    精确质量:379.168

    Psa:54.88

    MDL号:MFCD22201167

    密度:1.2±0.1g/cm3

    沸点:628.3±55.0°Cat760mmHg

    闪点:333.8±31.5°C

    折射率:1.648

    储存条件:-20°C

    蒸汽压:0.0±1.8mmHgat25°C

    海关编码:2933399090

    简介:Wnt-C59isaporcupinehomolog–Drosophila(PORCN)inhibitorforWnt3A-mediatedactivationofamultimerizedTCF-bindingsitedrivingluciferase.

     1243243-89-1 详细信息

    干细胞与Wnt信号

    CAS号:1243243-89-1

    品名:2-(4-(2-甲基吡啶-4-基)苯基)-n-(4-(吡啶-3-基)苯基)乙酰胺2-[4-(2-methylpyridin-4-yl)phenyl]-N-(4-pyridin-3-ylphenyl)acetamide

    中文别名:硫酸特布他林.硫酸叔丁宁按;

    英文别名:QC-8389;2-[4-(2-methylpyridin-4-yl)phenyl]-N-[4-(pyridin-3-yl)phenyl]acetamide;S7037,C59;CS-1420;Wnt-C59(C59);Wnt-C59;

    分子式:C25H21N3O

    分子量:379.454

    精确质量:379.168

    Psa:54.88

    MDL号:MFCD22201167

    密度:1.2±0.1g/cm3

    沸点:628.3±55.0°Cat760mmHg

    闪点:333.8±31.5°C

    折射率:1.648

    储存条件:-20°C

    蒸汽压:0.0±1.8mmHgat25°C

    海关编码:2933399090

    简介:Wnt-C59isaporcupinehomolog–Drosophila(PORCN)inhibitorforWnt3A-mediatedactivationofamultimerizedTCF-bindingsitedrivingluciferase.

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    干细胞与Wnt信号1243243-89-1
    MCE Wnt-C59 Wnt-C59 现货

     800.00
    HY-15659 99.86%
    干细胞与Wnt信号956697-53-3

    CAS号:956697-53-3

    品名:雷特格韦Erismodegib

    中文别名:REL-N-[6-[(2R,6S)-2,6-二甲基-4-吗啉基]-3-吡啶基]-2-甲基-4'-(三氟甲氧基)-[1,1'-联苯]-3-甲酰胺;

    英文别名:NVP-LDE225LDE225;LDE225(NVP-LDE225)Erismodegib;LDE225(NVP-LDE225,Erismodegib);NVP-LDE225;

    分子式:C26H26F3N3O3

    分子量:485.498

    精确质量:485.193

    Psa:63.69

    MDL号:MFCD16038928

    密度:

    简介:Apotent,selectiveandorallybioavailableSmoothened(SMO)antagonist;itinhibitshedgehog(Hh)signalingpathwayviaantagonismoftheSmoothenedreceptor(SMO).Antineoplastic.

     956697-53-3 详细信息

    干细胞与Wnt信号

    CAS号:956697-53-3

    品名:雷特格韦Erismodegib

    中文别名:REL-N-[6-[(2R,6S)-2,6-二甲基-4-吗啉基]-3-吡啶基]-2-甲基-4'-(三氟甲氧基)-[1,1'-联苯]-3-甲酰胺;

    英文别名:NVP-LDE225LDE225;LDE225(NVP-LDE225)Erismodegib;LDE225(NVP-LDE225,Erismodegib);NVP-LDE225;

    分子式:C26H26F3N3O3

    分子量:485.498

    精确质量:485.193

    Psa:63.69

    MDL号:MFCD16038928

    密度:

    简介:Apotent,selectiveandorallybioavailableSmoothened(SMO)antagonist;itinhibitshedgehog(Hh)signalingpathwayviaantagonismoftheSmoothenedreceptor(SMO).Antineoplastic.

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    干细胞与Wnt信号956697-53-3
    MCE Sonidegib Sonidegi 现货

     660.00
    HY-16582A 99.91%
    干细胞与Wnt信号4449-51-8

    CAS号:4449-51-8

    品名:环巴胺Cyclopamine

    中文别名:环杷明;11-去氧芥芬胺;

    英文别名:11-DEOXYJERVINE;alkaloidv;(3β,23R)-17,23-Epoxyveratraman-3-ol;deoxojervine;11-Desoxo-jervin;(2′R,3S,3′R,3′aS,6′S,6aS,6bS,7′aR,11aS,11bR)-1,2,3,3′a,4,4′,5′,6,6′,6a,6b,7,7′,7'a,8,11,11a,11b-octadecahydro-3′,6′,10,11b-tetramethyl-spiro[9H-benzo[a]fluorene-9,2′(3′H)-furo[3,2-b]pyridin]-3-ol;Cyclopamine;11-DEOXOJERVINE;11-deoxojervine;(3β,​23R)-​17,​23-​epoxyveratraman-​3-​ol;11-deoxo-jervin;

    分子式:C27H41NO2

    分子量:411.62

    精确质量:411.314

    Psa:41.49

    UNII号:ZH658AJ192

    外观与性状:白色结晶固体

    密度:1.14g/cm3

    沸点:550.8ºC at 760mmHg

    熔点:236-238ºC

    闪点:286.9ºC

    折射率:1.583

    稳定性:Store in Freezer at - 20ºC

    储存条件:2-8ºC

    安全说明:S22; S24/25

    危险品标志:Xi

    简介:环杷明(环巴胺,11-去氧芥芬胺,英语:Cyclopamine)是自然产生的化学物质,属于甾族的介藜芦生物碱。它是从玉米百合花加州藜芦中分离出的致畸胎剂,可导致独眼畸形(前脑无裂畸形)。环杷明是以放牧于爱达荷州野生玉米百合花农场的绵羊生下的独眼畸形羊羔命名的。1957年美国农业部的科学家开始了长达11年的研究,最终发现环杷明是导致出生缺陷的罪魁祸首。

    用途:能与Hedgehog信号通路中的Smoothened(Smo)蛋白结合,从而抑制该蛋白活性。因其致畸作用而于20世纪60年代被发现,但九十年代以后的研究表明,环巴胺是一种hedgehog信号通路抑制剂,已经在在果蝇体中得到证实,由于hedgehog信号通路的突变与多种肿瘤的发病有关联,最近研究发现,环巴胺在成体中具有抗肿瘤作用,且在胰腺癌、胆管癌、卵巢癌、肝癌等的体内或体外实验中均得到证实,但关于其在胃癌细胞中的研究,国内尚未见相关报道。目前环巴胺作为一种潜在的抗肿瘤新药在世界范围内掀起了研究热潮。

     4449-51-8 详细信息

    干细胞与Wnt信号

    CAS号:4449-51-8

    品名:环巴胺Cyclopamine

    中文别名:环杷明;11-去氧芥芬胺;

    英文别名:11-DEOXYJERVINE;alkaloidv;(3β,23R)-17,23-Epoxyveratraman-3-ol;deoxojervine;11-Desoxo-jervin;(2′R,3S,3′R,3′aS,6′S,6aS,6bS,7′aR,11aS,11bR)-1,2,3,3′a,4,4′,5′,6,6′,6a,6b,7,7′,7'a,8,11,11a,11b-octadecahydro-3′,6′,10,11b-tetramethyl-spiro[9H-benzo[a]fluorene-9,2′(3′H)-furo[3,2-b]pyridin]-3-ol;Cyclopamine;11-DEOXOJERVINE;11-deoxojervine;(3β,​23R)-​17,​23-​epoxyveratraman-​3-​ol;11-deoxo-jervin;

    分子式:C27H41NO2

    分子量:411.62

    精确质量:411.314

    Psa:41.49

    UNII号:ZH658AJ192

    外观与性状:白色结晶固体

    密度:1.14g/cm3

    沸点:550.8ºC at 760mmHg

    熔点:236-238ºC

    闪点:286.9ºC

    折射率:1.583

    稳定性:Store in Freezer at - 20ºC

    储存条件:2-8ºC

    安全说明:S22; S24/25

    危险品标志:Xi

    简介:环杷明(环巴胺,11-去氧芥芬胺,英语:Cyclopamine)是自然产生的化学物质,属于甾族的介藜芦生物碱。它是从玉米百合花加州藜芦中分离出的致畸胎剂,可导致独眼畸形(前脑无裂畸形)。环杷明是以放牧于爱达荷州野生玉米百合花农场的绵羊生下的独眼畸形羊羔命名的。1957年美国农业部的科学家开始了长达11年的研究,最终发现环杷明是导致出生缺陷的罪魁祸首。

    用途:能与Hedgehog信号通路中的Smoothened(Smo)蛋白结合,从而抑制该蛋白活性。因其致畸作用而于20世纪60年代被发现,但九十年代以后的研究表明,环巴胺是一种hedgehog信号通路抑制剂,已经在在果蝇体中得到证实,由于hedgehog信号通路的突变与多种肿瘤的发病有关联,最近研究发现,环巴胺在成体中具有抗肿瘤作用,且在胰腺癌、胆管癌、卵巢癌、肝癌等的体内或体外实验中均得到证实,但关于其在胃癌细胞中的研究,国内尚未见相关报道。目前环巴胺作为一种潜在的抗肿瘤新药在世界范围内掀起了研究热潮。

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    干细胞与Wnt信号4449-51-8
    MCE Cyclopamine Cyclopamine 现货

     272.00
    HY-17024 99.97%
    干细胞与Wnt信号284028-89-3

    CAS号:284028-89-3

    品名:3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-d]嘧啶-4-酮2-[4-(trifluoromethyl)phenyl]-1,5,7,8-tetrahydrothiopyrano[4,3-d]pyrimidin-4-one

    中文别名:3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-d]嘧啶-4-酮

    英文别名:XAV939,XAV-939;XAV939;3,5,7,8-Tetrahydro-2-[4-(trifluoromethyl)phenyl]-4H-thiopyrano[4,3-d]pyrimidin-4-one;NVP-XAV939;

    分子式:C14H11F3N2OS

    分子量:312.31

    精确质量:312.054

    Psa:71.31

    MDL号:MFCD16879017

    密度:1.5 g/cm3

    沸点:429.3ºC at 760 mmHg

    闪点:213.4ºC

    安全说明:S26-S45

    危险类别码:R25; R36

    危险品运输编码:UN 2811

    简介:Atankyrase(TNKS)inhibitorthatantagonizesWntsignalingviastimulationofβ-catenindegradationandstabilizationofaxin.XAV939inhibitsproliferationoftheμ-catenin-dependentcoloncarcinomacelllineDLD-1.

     284028-89-3 详细信息

    干细胞与Wnt信号

    CAS号:284028-89-3

    品名:3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-d]嘧啶-4-酮2-[4-(trifluoromethyl)phenyl]-1,5,7,8-tetrahydrothiopyrano[4,3-d]pyrimidin-4-one

    中文别名:3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-d]嘧啶-4-酮

    英文别名:XAV939,XAV-939;XAV939;3,5,7,8-Tetrahydro-2-[4-(trifluoromethyl)phenyl]-4H-thiopyrano[4,3-d]pyrimidin-4-one;NVP-XAV939;

    分子式:C14H11F3N2OS

    分子量:312.31

    精确质量:312.054

    Psa:71.31

    MDL号:MFCD16879017

    密度:1.5 g/cm3

    沸点:429.3ºC at 760 mmHg

    闪点:213.4ºC

    安全说明:S26-S45

    危险类别码:R25; R36

    危险品运输编码:UN 2811

    简介:Atankyrase(TNKS)inhibitorthatantagonizesWntsignalingviastimulationofβ-catenindegradationandstabilizationofaxin.XAV939inhibitsproliferationoftheμ-catenin-dependentcoloncarcinomacelllineDLD-1.

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    干细胞与Wnt信号284028-89-3
    MCE XAV-939 XAV-939 现货

     418.00
    HY-15147 99.91%
    干细胞与Wnt信号1127442-82-3

    CAS号:1127442-82-3

    品名:rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-六氢-1,3-二氧代-4,7-甲桥-2H-异吲哚-2-基]-N-8-喹啉基苯甲酰胺IWR-1-endo

    中文别名:rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-六氢-1,3-二氧代-4,7-甲桥-2H-异吲哚-2-基]-N-8-喹啉基苯甲酰胺

    英文别名:IWR-1-endo

    分子式:C25H19N3O3

    分子量:409.437

    精确质量:409.143

    Psa:79.37

    密度:1.4±0.1g/cm3

    沸点:643.9±55.0°Cat760mmHg

    闪点:343.2±31.5°C

    折射率:1.741

    储存条件:StoreatRT

    蒸汽压:0.0±1.9mmHgat25°C

    简介:IWR-3actasinhibitorsofWntresponse.ItappearthatIWRcompoundsinducestabilizationofAxinproteinsviaadirectinteraction,whichisapartoftheb-catenindestructioncomplex(consistsofApc,Axin,Ck1andGsk3b).\nSuchcompoundsmaybeusedinthetreatmentofWntproteinsignaling-relateddiseasesandconditionssuchascancer,degenerativediseases,typeIIdiabetesandosteopetrosis.

     1127442-82-3 详细信息

    干细胞与Wnt信号

    CAS号:1127442-82-3

    品名:rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-六氢-1,3-二氧代-4,7-甲桥-2H-异吲哚-2-基]-N-8-喹啉基苯甲酰胺IWR-1-endo

    中文别名:rel-4-[(3aR,4S,7R,7aS)-1,3,3a,4,7,7a-六氢-1,3-二氧代-4,7-甲桥-2H-异吲哚-2-基]-N-8-喹啉基苯甲酰胺

    英文别名:IWR-1-endo

    分子式:C25H19N3O3

    分子量:409.437

    精确质量:409.143

    Psa:79.37

    密度:1.4±0.1g/cm3

    沸点:643.9±55.0°Cat760mmHg

    闪点:343.2±31.5°C

    折射率:1.741

    储存条件:StoreatRT

    蒸汽压:0.0±1.9mmHgat25°C

    简介:IWR-3actasinhibitorsofWntresponse.ItappearthatIWRcompoundsinducestabilizationofAxinproteinsviaadirectinteraction,whichisapartoftheb-catenindestructioncomplex(consistsofApc,Axin,Ck1andGsk3b).\nSuchcompoundsmaybeusedinthetreatmentofWntproteinsignaling-relateddiseasesandconditionssuchascancer,degenerativediseases,typeIIdiabetesandosteopetrosis.

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    干细胞与Wnt信号1127442-82-3
    MCE IWR-1 IWR-1 现货

     400.00
    HY-12238 99.49%
    干细胞与Wnt信号780757-88-2

    CAS号:780757-88-2

    品名:2,3-二氢-1,4-苯并恶嗪2H-PYRAZINO[1,2-A]PYRIMIDINE-1(6H)-CARBOXAMIDE,HEXAHYDRO-6-[(4-HYDROXYPHENYL)METHYL]-8-(1-NAPHTHALENYLMETHYL)-4,7-DIOXO-N-(PHENYLMETHYL)-,(6R,9AR)-REL-

    中文别名:(6S,9AS)-6-(4-HYDROXYBENZYL)-N-BENZYL-8-(NAPHTHALEN-1-YLMETHYL)-4,7-DIOXO-HEXAHYDRO-2H-PYRAZINO[1,2-A]PYRIMIDINE-1(6H)-CARBOXAMIDE;(6S,9as)-n-苄基-6-(4-羟基苄基)-8-(萘-1-甲基)-4,7-二氧代八氢-1H-吡嗪o[1,2-a]嘧啶-1-羧酰胺;香紫苏醇.硬尾醇;ICG001;(6R,9AR)-REL-六氢-6-[(4-羟基苯基)甲基]-8-(1-萘基甲基)-4,7-二氧代-N-(苯基甲基)-2H-吡嗪并[1,2-A]嘧啶-1(6H)-甲酰胺;

    英文别名:(6S,9aS)-N-benzyl-6-(4-hydroxybenzyl)-8-(naphthalen-1-ylMethyl);(6S,9aS)-N-benzyl-6-(4-hydroxybenzyl)-8-(naphthalen-1-ylmethyl)-4,7-dioxooctahydro-1H-pyrazino[1,2-a]pyrimidine-1-carboxamide;(6S,9aS)-6-(4-hydroxybenzyl)-N-benzyl-8-(naphthalen-1-ylmethyl)-4,7-dioxo-hexahydro-2H-pyrazino[1,2-a]pyrimidine-1(6H)-carboxamide;(S,S)-ICG001;(6R,9aR)-rel-Hexahydro-6-[(4-hydroxyphenyl)methyl]-8-(1-naphthalenylmethyl)-4,7-dioxo-N-(phenylmethyl)-2H-pyrazino[1,2-a]pyrimidine-1(6H)-carboxamide;(6S,9AS)-6-(4-HYDROXYBENZYL)-8-NAPHTHALEN-1-YLMETHYL-4,7-DIOXO-HEXAHYDRO-PYRAZINO[1,2-A]PYRIMIDINE-1-CARBOXYLICACIDBENZYLAMIDE;(6S,9aS)-rel-Hexahydro-6-[(4-hydroxyphenyl)Methyl]-8-(1-naphthalenylMethyl)-4,7-dioxo-N-(phenylMethyl)-2H-pyrazino[1,2-a]pyriMidine-1(6H)-carboxaMide;

    分子式:C33H32N4O4

    分子量:548.632

    精确质量:548.242

    Psa:93.19

    密度:1.37g/cm3

    沸点:895.6ºC at 760 mmHg

    熔点:133-134ºC

    闪点:495.4ºC

    折射率:1.722

     780757-88-2 详细信息

    干细胞与Wnt信号

    CAS号:780757-88-2

    品名:2,3-二氢-1,4-苯并恶嗪2H-PYRAZINO[1,2-A]PYRIMIDINE-1(6H)-CARBOXAMIDE,HEXAHYDRO-6-[(4-HYDROXYPHENYL)METHYL]-8-(1-NAPHTHALENYLMETHYL)-4,7-DIOXO-N-(PHENYLMETHYL)-,(6R,9AR)-REL-

    中文别名:(6S,9AS)-6-(4-HYDROXYBENZYL)-N-BENZYL-8-(NAPHTHALEN-1-YLMETHYL)-4,7-DIOXO-HEXAHYDRO-2H-PYRAZINO[1,2-A]PYRIMIDINE-1(6H)-CARBOXAMIDE;(6S,9as)-n-苄基-6-(4-羟基苄基)-8-(萘-1-甲基)-4,7-二氧代八氢-1H-吡嗪o[1,2-a]嘧啶-1-羧酰胺;香紫苏醇.硬尾醇;ICG001;(6R,9AR)-REL-六氢-6-[(4-羟基苯基)甲基]-8-(1-萘基甲基)-4,7-二氧代-N-(苯基甲基)-2H-吡嗪并[1,2-A]嘧啶-1(6H)-甲酰胺;

    英文别名:(6S,9aS)-N-benzyl-6-(4-hydroxybenzyl)-8-(naphthalen-1-ylMethyl);(6S,9aS)-N-benzyl-6-(4-hydroxybenzyl)-8-(naphthalen-1-ylmethyl)-4,7-dioxooctahydro-1H-pyrazino[1,2-a]pyrimidine-1-carboxamide;(6S,9aS)-6-(4-hydroxybenzyl)-N-benzyl-8-(naphthalen-1-ylmethyl)-4,7-dioxo-hexahydro-2H-pyrazino[1,2-a]pyrimidine-1(6H)-carboxamide;(S,S)-ICG001;(6R,9aR)-rel-Hexahydro-6-[(4-hydroxyphenyl)methyl]-8-(1-naphthalenylmethyl)-4,7-dioxo-N-(phenylmethyl)-2H-pyrazino[1,2-a]pyrimidine-1(6H)-carboxamide;(6S,9AS)-6-(4-HYDROXYBENZYL)-8-NAPHTHALEN-1-YLMETHYL-4,7-DIOXO-HEXAHYDRO-PYRAZINO[1,2-A]PYRIMIDINE-1-CARBOXYLICACIDBENZYLAMIDE;(6S,9aS)-rel-Hexahydro-6-[(4-hydroxyphenyl)Methyl]-8-(1-naphthalenylMethyl)-4,7-dioxo-N-(phenylMethyl)-2H-pyrazino[1,2-a]pyriMidine-1(6H)-carboxaMide;

    分子式:C33H32N4O4

    分子量:548.632

    精确质量:548.242

    Psa:93.19

    密度:1.37g/cm3

    沸点:895.6ºC at 760 mmHg

    熔点:133-134ºC

    闪点:495.4ºC

    折射率:1.722

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    干细胞与Wnt信号780757-88-2
    MCE ICG-001 ICG-001 现货

     921.00
    HY-14428 99.86%
    干细胞与Wnt信号1118807-13-8

    CAS号:1118807-13-8

    品名:N-(6-氯-2-苯并噻唑)-3,4-二甲氧基苯丙酰胺N-(6-chloro-1,3-benzothiazol-2-yl)-3-(3,4-dimethoxyphenyl)propanamide

    中文别名:N-(6-氯-2-苯并噻唑)-3,4-二甲氧基苯丙酰胺

    英文别名:QC-8207;2-(3-(3,4-dimethoxyphenyl)propanamido)-6-chlorobenzothiazole;

    分子式:C18H17ClN2O3S

    分子量:376.857

    精确质量:376.065

    Psa:92.18

    MDL号:MFCD08483062

    密度:1.4±0.1g/cm3

    折射率:1.661

    储存条件:2-8°C

    简介:KY0211,allowsforinducingdifferentiationofpluripotentstemcellintocardiacmuscle.

     1118807-13-8 详细信息

    干细胞与Wnt信号

    CAS号:1118807-13-8

    品名:N-(6-氯-2-苯并噻唑)-3,4-二甲氧基苯丙酰胺N-(6-chloro-1,3-benzothiazol-2-yl)-3-(3,4-dimethoxyphenyl)propanamide

    中文别名:N-(6-氯-2-苯并噻唑)-3,4-二甲氧基苯丙酰胺

    英文别名:QC-8207;2-(3-(3,4-dimethoxyphenyl)propanamido)-6-chlorobenzothiazole;

    分子式:C18H17ClN2O3S

    分子量:376.857

    精确质量:376.065

    Psa:92.18

    MDL号:MFCD08483062

    密度:1.4±0.1g/cm3

    折射率:1.661

    储存条件:2-8°C

    简介:KY0211,allowsforinducingdifferentiationofpluripotentstemcellintocardiacmuscle.

    展开

    干细胞与Wnt信号1118807-13-8
    MCE KY02111 KY02111 现货

     506.00
    HY-13815 99.74%
    干细胞与Wnt信号1258861-20-9

    CAS号:1258861-20-9

    品名:LY2940680;4-氟-N-甲基-N-[1-[4-(1-甲基-1H-吡唑-5-基)-1-酞嗪基]-4-哌啶基]-2-(三氟甲基)苯甲酰胺4-fluoro-N-methyl-N-[1-[4-(2-methylpyrazol-3-yl)phthalazin-1-yl]piperidin-4-yl]-2-(trifluoromethyl)benzamide

    中文别名:LY2940680;4-氟-N-甲基-N-[1-[4-(1-甲基-1H-吡唑-5-基)-1-酞嗪基]-4-哌啶基]-2-(三氟甲基)苯甲酰胺

    英文别名:4-fluoro-N-methyl-N-(1-(4-(1-methyl-1H-pyrazol-5-yl)phthalazin-1-yl)piperidin-4-yl)-2-(trifluoromethyl)benzamide;Taladegib;

    分子式:C26H24F4N6O

    分子量:512.502

    精确质量:512.195

    Psa:67.15

    UNII号:QY8BWX1LJ5

    密度:1.4±0.1g/cm3

    沸点:703.5±60.0°Cat760mmHg

    闪点:379.3±32.9°C

    折射率:1.634

    储存条件:-20°C

    蒸汽压:0.0±2.2mmHgat25°C

    简介:LY2940680bindstotheSmoothened(Smo)receptorandpotentlyinhibitsHedgehog(Hh)signaling.

     1258861-20-9 详细信息

    干细胞与Wnt信号

    CAS号:1258861-20-9

    品名:LY2940680;4-氟-N-甲基-N-[1-[4-(1-甲基-1H-吡唑-5-基)-1-酞嗪基]-4-哌啶基]-2-(三氟甲基)苯甲酰胺4-fluoro-N-methyl-N-[1-[4-(2-methylpyrazol-3-yl)phthalazin-1-yl]piperidin-4-yl]-2-(trifluoromethyl)benzamide

    中文别名:LY2940680;4-氟-N-甲基-N-[1-[4-(1-甲基-1H-吡唑-5-基)-1-酞嗪基]-4-哌啶基]-2-(三氟甲基)苯甲酰胺

    英文别名:4-fluoro-N-methyl-N-(1-(4-(1-methyl-1H-pyrazol-5-yl)phthalazin-1-yl)piperidin-4-yl)-2-(trifluoromethyl)benzamide;Taladegib;

    分子式:C26H24F4N6O

    分子量:512.502

    精确质量:512.195

    Psa:67.15

    UNII号:QY8BWX1LJ5

    密度:1.4±0.1g/cm3

    沸点:703.5±60.0°Cat760mmHg

    闪点:379.3±32.9°C

    折射率:1.634

    储存条件:-20°C

    蒸汽压:0.0±2.2mmHgat25°C

    简介:LY2940680bindstotheSmoothened(Smo)receptorandpotentlyinhibitsHedgehog(Hh)signaling.

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    干细胞与Wnt信号1258861-20-9
    MCE Taladegib Taladegi 现货

     500.00
    HY-13242 99.57%
    干细胞与Wnt信号483367-10-8

    CAS号:483367-10-8

    品名:Purmorphamine

    中文别名:Purmorphamine

    英文别名:2-(1-Naphthoxy)-6-(4-morpholinoanilino)-9-cyclohexylpurine;9-Cyclohexyl-N-[4-(4-morpholinyl)phenyl]-2-(1-naphthalenyloxy);9H-Purin-6-amine(9-cyclohexyl-N-[4-(4-morpholinyl)phenyl]-2-(1-naphthalenyloxy);9-cyclohexyl-N-(4-morpholin-4-ylphenyl)-2-naphthalen-1-yloxypurin-6-amine;

    分子式:C31H32N6O2

    分子量:520.625

    精确质量:520.259

    Psa:77.33

    MDL号:MFCD09037557

    密度:1.353 g/cm3

    沸点:790.313ºC at 760 mmHg

    熔点:210-212ºC

    闪点:431.766ºC

    简介:ActivatestheHedgehogpathway\n.

     483367-10-8 详细信息

    干细胞与Wnt信号

    CAS号:483367-10-8

    品名:Purmorphamine

    中文别名:Purmorphamine

    英文别名:2-(1-Naphthoxy)-6-(4-morpholinoanilino)-9-cyclohexylpurine;9-Cyclohexyl-N-[4-(4-morpholinyl)phenyl]-2-(1-naphthalenyloxy);9H-Purin-6-amine(9-cyclohexyl-N-[4-(4-morpholinyl)phenyl]-2-(1-naphthalenyloxy);9-cyclohexyl-N-(4-morpholin-4-ylphenyl)-2-naphthalen-1-yloxypurin-6-amine;

    分子式:C31H32N6O2

    分子量:520.625

    精确质量:520.259

    Psa:77.33

    MDL号:MFCD09037557

    密度:1.353 g/cm3

    沸点:790.313ºC at 760 mmHg

    熔点:210-212ºC

    闪点:431.766ºC

    简介:ActivatestheHedgehogpathway\n.

    展开

    干细胞与Wnt信号483367-10-8
    MCE Purmorphamine Purmorphamine 现货

     492.00
    HY-15108 99.89%
    干细胞与Wnt信号1373615-35-0

    CAS号:1373615-35-0

    品名:1-[4-(5'-氯-3,5-二甲基[2,4'-联吡啶]-2'-基)-1-哌嗪基]-3-(甲基磺酰基)-1-丙酮1-[4-[5-chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl]piperazin-1-yl]-3-methylsulfonylpropan-1-one

    中文别名:1-[4-(5'-氯-3,5-二甲基[2,4'-联吡啶]-2'-基)-1-哌嗪基]-3-(甲基磺酰基)-1-丙酮

    英文别名:1-(4-(5'-chloro-3,5-dimethyl-2,4'-bipyridin-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one;1-(4-(5-chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one;CS-1206;QC-1145;

    分子式:C20H25ClN4O3S

    分子量:436.956

    精确质量:436.134

    Psa:91.85

    密度:1.3±0.1g/cm3

    沸点:686.0±55.0°Cat760mmHg

    闪点:368.7±31.5°C

    折射率:1.590

    储存条件:roomtemp

    蒸汽压:0.0±2.1mmHgat25°C

    简介:PF-5274857isapotentandselectiveSmoothened(Smo)antagonist,inhibitsHedgehog(Hh)signaling,respectively,andcanpenetratetheblood–brainbarrier.

     1373615-35-0 详细信息

    干细胞与Wnt信号

    CAS号:1373615-35-0

    品名:1-[4-(5'-氯-3,5-二甲基[2,4'-联吡啶]-2'-基)-1-哌嗪基]-3-(甲基磺酰基)-1-丙酮1-[4-[5-chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl]piperazin-1-yl]-3-methylsulfonylpropan-1-one

    中文别名:1-[4-(5'-氯-3,5-二甲基[2,4'-联吡啶]-2'-基)-1-哌嗪基]-3-(甲基磺酰基)-1-丙酮

    英文别名:1-(4-(5'-chloro-3,5-dimethyl-2,4'-bipyridin-2'-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one;1-(4-(5-chloro-4-(3,5-dimethylpyridin-2-yl)pyridin-2-yl)piperazin-1-yl)-3-(methylsulfonyl)propan-1-one;CS-1206;QC-1145;

    分子式:C20H25ClN4O3S

    分子量:436.956

    精确质量:436.134

    Psa:91.85

    密度:1.3±0.1g/cm3

    沸点:686.0±55.0°Cat760mmHg

    闪点:368.7±31.5°C

    折射率:1.590

    储存条件:roomtemp

    蒸汽压:0.0±2.1mmHgat25°C

    简介:PF-5274857isapotentandselectiveSmoothened(Smo)antagonist,inhibitsHedgehog(Hh)signaling,respectively,andcanpenetratetheblood–brainbarrier.

    展开

    干细胞与Wnt信号1373615-35-0
    MCE PF-5274857 PF-5274857 现货

     1600.00
    HY-13459 98.89%
    干细胞与Wnt信号304909-07-7

    CAS号:304909-07-7

    品名:(E)-N-(4-苄基-1-哌嗪基)-1-(3,5-二甲基-1-苯基-1H-吡唑-4-基)甲亚胺(E)-N-(4-benzylpiperazin-1-yl)-1-(3,5-dimethyl-1-phenylpyrazol-4-yl)methanimine

    中文别名:(E)-N-(4-苄基-1-哌嗪基)-1-(3,5-二甲基-1-苯基-1H-吡唑-4-基)甲亚胺

    英文别名:SANT-1;1-Piperazinamine(N-[(3,5-dimethyl-1-phenyl-1H-pyrazol-4-yl)methylene]-4-(phenylmethyl);ShhSignalingAntagonistV;(4-Benzyl-piperazin-1-yl)-(3,5-dimethyl-1-phenyl-1H-pyrazol-4-ylmethylene)-amine;

    分子式:C23H27N5

    分子量:373.494

    精确质量:373.227

    Psa:36.66

    密度:1.13g/cm3

    沸点:547.4ºC at 760mmHg

    熔点:104-106ºC

    闪点:284.8ºC

    折射率:1.623

    储存条件:-20ºC

    简介:Apotentantagonistofthesonichedgehog(Shh)signalingpathway(IC50=20nminShh-LIGHT2assayandinPtch1-/-cells)thatactsbybindingtosmoothened(Smo:KD=1.2nM),adistantrelativeofGprotein-coupledreceptors.Incontrasttocyclopamine,SNAT-1inhibitstheactivitiesofbothwildtypeandoncogenicSmowithequalpotency(IC50=30nminSmoA1-LIGHT2assay).

     304909-07-7 详细信息

    干细胞与Wnt信号

    CAS号:304909-07-7

    品名:(E)-N-(4-苄基-1-哌嗪基)-1-(3,5-二甲基-1-苯基-1H-吡唑-4-基)甲亚胺(E)-N-(4-benzylpiperazin-1-yl)-1-(3,5-dimethyl-1-phenylpyrazol-4-yl)methanimine

    中文别名:(E)-N-(4-苄基-1-哌嗪基)-1-(3,5-二甲基-1-苯基-1H-吡唑-4-基)甲亚胺

    英文别名:SANT-1;1-Piperazinamine(N-[(3,5-dimethyl-1-phenyl-1H-pyrazol-4-yl)methylene]-4-(phenylmethyl);ShhSignalingAntagonistV;(4-Benzyl-piperazin-1-yl)-(3,5-dimethyl-1-phenyl-1H-pyrazol-4-ylmethylene)-amine;

    分子式:C23H27N5

    分子量:373.494

    精确质量:373.227

    Psa:36.66

    密度:1.13g/cm3

    沸点:547.4ºC at 760mmHg

    熔点:104-106ºC

    闪点:284.8ºC

    折射率:1.623

    储存条件:-20ºC

    简介:Apotentantagonistofthesonichedgehog(Shh)signalingpathway(IC50=20nminShh-LIGHT2assayandinPtch1-/-cells)thatactsbybindingtosmoothened(Smo:KD=1.2nM),adistantrelativeofGprotein-coupledreceptors.Incontrasttocyclopamine,SNAT-1inhibitstheactivitiesofbothwildtypeandoncogenicSmowithequalpotency(IC50=30nminSmoA1-LIGHT2assay).

    展开

    干细胞与Wnt信号304909-07-7
    MCE SANT-1 SANT-1 现货

     600.00
    HY-100224 99.88%
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