筛选出 6 条数据

    品牌 产品 货期 价格 货号 规格 /
    PI3K/Akt/mTOR1032568-63-0

    CAS号:1032568-63-0

    品名:Copanlisib2-amino-N-[7-methoxy-8-(3-morpholinopropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide

    中文别名:Copanlisib

    英文别名:BAY80-6946;2-Amino-N.N-diaethyl-toluolsulfonamid-(4);2-amino-N-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide;2-amino-toluene-4-sulfonicaciddiethylamide;2-Amino-toluol-4-sulfonsaeure-diaethylamid;

    分子式:C23H28N8O4

    分子量:480.52

    精确质量:480.223

    Psa:146.23

    密度:1.5±0.1g/cm3

    折射率:1.722

    储存条件:-20℃

    简介:Copanlisib(BAY80-6946),developedbyBayer,isaselectiveClassIphosphoinositide3-kinaseinhibitorwhichhasshownpromiseinPhaseI/IIclinicaltrialsforthetreatmentofnon-Hodgkinlymphomaandchroniclymphocyticleukemia.

     1032568-63-0 详细信息

    PI3K/Akt/mTOR

    CAS号:1032568-63-0

    品名:Copanlisib2-amino-N-[7-methoxy-8-(3-morpholinopropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide

    中文别名:Copanlisib

    英文别名:BAY80-6946;2-Amino-N.N-diaethyl-toluolsulfonamid-(4);2-amino-N-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide;2-amino-toluene-4-sulfonicaciddiethylamide;2-Amino-toluol-4-sulfonsaeure-diaethylamid;

    分子式:C23H28N8O4

    分子量:480.52

    精确质量:480.223

    Psa:146.23

    密度:1.5±0.1g/cm3

    折射率:1.722

    储存条件:-20℃

    简介:Copanlisib(BAY80-6946),developedbyBayer,isaselectiveClassIphosphoinositide3-kinaseinhibitorwhichhasshownpromiseinPhaseI/IIclinicaltrialsforthetreatmentofnon-Hodgkinlymphomaandchroniclymphocyticleukemia.

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    PI3K/Akt/mTOR1032568-63-0
    源叶 BAY80-6946(Copanlisib) BAY80-6946(Copanlisib) 现货

     1550.00
    T29380 10mMinDMSO
    PI3K/Akt/mTOR1251156-08-7

    CAS号:1251156-08-7

    品名:[7-(6-氨基-3-吡啶基)-2,3-二氢-1,4-苯并氧氮杂卓-4(5H)-基][3-氟-2-甲基-4-(甲基磺酰基)苯基]-甲酮[7-(6-aminopyridin-3-yl)-3,5-dihydro-2H-1,4-benzoxazepin-4-yl]-(3-fluoro-2-methyl-4-methylsulfonylphenyl)methanone

    中文别名:[7-(6-氨基-3-吡啶基)-2,3-二氢-1,4-苯并氧氮杂卓-4(5H)-基][3-氟-2-甲基-4-(甲基磺酰基)苯基]-甲酮

    英文别名:S7035;[7-(6-aminopyridin-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl][3-fluoro-2-methyl-4-(methylsulfonyl)phenyl]methanone;XL388;

    分子式:C23H22FN3O4S

    分子量:455.502

    精确质量:455.132

    Psa:111.7

    密度:1.4±0.1g/cm3

    沸点:738.6±60.0°Cat760mmHg

    闪点:400.5±32.9°C

    折射率:1.619

    储存条件:-20℃

    蒸汽压:0.0±2.4mmHgat25°C

    简介:XL388isahighlypotent,orallybioavailable,selective,ATP-competitivemammaliantargetofrapamycin(mTOR)inhibitor.XL388hasshownsignificantanddose-dependentantitumoractivityinathymicnudemiceimplantedwithhumantumorxenografts.

     1251156-08-7 详细信息

    PI3K/Akt/mTOR

    CAS号:1251156-08-7

    品名:[7-(6-氨基-3-吡啶基)-2,3-二氢-1,4-苯并氧氮杂卓-4(5H)-基][3-氟-2-甲基-4-(甲基磺酰基)苯基]-甲酮[7-(6-aminopyridin-3-yl)-3,5-dihydro-2H-1,4-benzoxazepin-4-yl]-(3-fluoro-2-methyl-4-methylsulfonylphenyl)methanone

    中文别名:[7-(6-氨基-3-吡啶基)-2,3-二氢-1,4-苯并氧氮杂卓-4(5H)-基][3-氟-2-甲基-4-(甲基磺酰基)苯基]-甲酮

    英文别名:S7035;[7-(6-aminopyridin-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl][3-fluoro-2-methyl-4-(methylsulfonyl)phenyl]methanone;XL388;

    分子式:C23H22FN3O4S

    分子量:455.502

    精确质量:455.132

    Psa:111.7

    密度:1.4±0.1g/cm3

    沸点:738.6±60.0°Cat760mmHg

    闪点:400.5±32.9°C

    折射率:1.619

    储存条件:-20℃

    蒸汽压:0.0±2.4mmHgat25°C

    简介:XL388isahighlypotent,orallybioavailable,selective,ATP-competitivemammaliantargetofrapamycin(mTOR)inhibitor.XL388hasshownsignificantanddose-dependentantitumoractivityinathymicnudemiceimplantedwithhumantumorxenografts.

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    PI3K/Akt/mTOR1251156-08-7
    源叶 XL388 XL388 现货

     1599.00
    S58999 2mMinDMSO
    PI3K/Akt/mTOR1349796-36-6

    CAS号:1349796-36-6

    品名:Benzamide,N-​[4-​[[[3-​[(3,​5-​dimethoxyphenyl)​amino]​-​2-​quinoxalinyl]​amino]​sulfonyl]​phenyl]​-​3-​methoxy-​4-​methyl-

    中文别名:Benzamide,N-​[4-​[[[3-​[(3,​5-​dimethoxyphenyl)​amino]​-​2-​quinoxalinyl]​amino]​sulfonyl]​phenyl]​-​3-​methoxy-​4-​methyl-

    英文别名:SAR245409(XL765);

    分子式:C31H29N5O6S

    分子量:599.657

    精确质量:599.184

    Psa:149.15

    密度:

    简介:XL765isisalow-molecularmassPI3KinhibitorthatalsoinhibitsDNA-PKandmTOR.

     1349796-36-6 详细信息

    PI3K/Akt/mTOR

    CAS号:1349796-36-6

    品名:Benzamide,N-​[4-​[[[3-​[(3,​5-​dimethoxyphenyl)​amino]​-​2-​quinoxalinyl]​amino]​sulfonyl]​phenyl]​-​3-​methoxy-​4-​methyl-

    中文别名:Benzamide,N-​[4-​[[[3-​[(3,​5-​dimethoxyphenyl)​amino]​-​2-​quinoxalinyl]​amino]​sulfonyl]​phenyl]​-​3-​methoxy-​4-​methyl-

    英文别名:SAR245409(XL765);

    分子式:C31H29N5O6S

    分子量:599.657

    精确质量:599.184

    Psa:149.15

    密度:

    简介:XL765isisalow-molecularmassPI3KinhibitorthatalsoinhibitsDNA-PKandmTOR.

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    PI3K/Akt/mTOR1349796-36-6
    源叶 Voxtalisib(XL765)Analogue Voxtalisib(XL765)Analogue 现货

     1551.00
    T93281 10mMinDMSO
    PI3K/Akt/mTOR1372540-25-4

    CAS号:1372540-25-4

    品名:2-甲基-1-[[2-甲基-3-(三氟甲基)苯基]甲基]-6-(4-吗啉基)-1H-苯并咪唑-4-羧酸2-methyl-1-[[2-methyl-3-(trifluoromethyl)phenyl]methyl]-6-morpholin-4-ylbenzimidazole-4-carboxylicacid

    中文别名:2-甲基-1-[[2-甲基-3-(三氟甲基)苯基]甲基]-6-(4-吗啉基)-1H-苯并咪唑-4-羧酸

    英文别名:QCR-187;UNII-DW94IAT0LS;CS-0747;2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylicacid;

    分子式:C22H22F3N3O3

    分子量:433.424

    精确质量:433.161

    Psa:67.59

    密度:1.4±0.1g/cm3

    沸点:641.3±55.0°Cat760mmHg

    闪点:341.7±31.5°C

    折射率:1.606

    储存条件:室温,干燥,密封

    蒸汽压:0.0±2.0mmHgat25°C

    简介:GSK2636771isapotent,orallybioavailable,PI3Kβ-selectiveinhibitor,sensitivetoPTENnullcelllines.

     1372540-25-4 详细信息

    PI3K/Akt/mTOR

    CAS号:1372540-25-4

    品名:2-甲基-1-[[2-甲基-3-(三氟甲基)苯基]甲基]-6-(4-吗啉基)-1H-苯并咪唑-4-羧酸2-methyl-1-[[2-methyl-3-(trifluoromethyl)phenyl]methyl]-6-morpholin-4-ylbenzimidazole-4-carboxylicacid

    中文别名:2-甲基-1-[[2-甲基-3-(三氟甲基)苯基]甲基]-6-(4-吗啉基)-1H-苯并咪唑-4-羧酸

    英文别名:QCR-187;UNII-DW94IAT0LS;CS-0747;2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylicacid;

    分子式:C22H22F3N3O3

    分子量:433.424

    精确质量:433.161

    Psa:67.59

    密度:1.4±0.1g/cm3

    沸点:641.3±55.0°Cat760mmHg

    闪点:341.7±31.5°C

    折射率:1.606

    储存条件:室温,干燥,密封

    蒸汽压:0.0±2.0mmHgat25°C

    简介:GSK2636771isapotent,orallybioavailable,PI3Kβ-selectiveinhibitor,sensitivetoPTENnullcelllines.

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    PI3K/Akt/mTOR1372540-25-4
    源叶 GSK2636771 GSK2636771 现货

     1816.00
    T93311 10mMinDMSO
    PI3K/Akt/mTOR572924-54-0

    CAS号:572924-54-0

    品名:42-(二甲基亚膦酰)雷帕霉素Ridaforolimus

    中文别名:雷帕霉素衍生物;

    英文别名:Deforolimus;AP23573;42-(Dimethylphosphinate)rapamycin;MK8669;Ridaforolimus;

    分子式:C53H84NO14P

    分子量:990.206

    精确质量:989.563

    Psa:211.31

    UNII号:48Z35KB15K

    外观与性状:灰白色固体

    密度:1.18 g/cm3

    沸点:996.16ºC at 760 mmHg

    熔点:95-98ºC

    折射率:1.539

    储存条件:Hygroscopic, -20ºC Freezer, Under Inert Atmosphere

    简介:Animmunosupressantandiscurrentlybeinginvestigatedforuseincancertreatments.Ridaforolimusmayactasaregulatorofproteinsynthesis,cellproliferation,cellcycleprogressionandcellsurvival.Ridaforolimus,wasformerlyknownasDeforolimus.

     572924-54-0 详细信息

    PI3K/Akt/mTOR

    CAS号:572924-54-0

    品名:42-(二甲基亚膦酰)雷帕霉素Ridaforolimus

    中文别名:雷帕霉素衍生物;

    英文别名:Deforolimus;AP23573;42-(Dimethylphosphinate)rapamycin;MK8669;Ridaforolimus;

    分子式:C53H84NO14P

    分子量:990.206

    精确质量:989.563

    Psa:211.31

    UNII号:48Z35KB15K

    外观与性状:灰白色固体

    密度:1.18 g/cm3

    沸点:996.16ºC at 760 mmHg

    熔点:95-98ºC

    折射率:1.539

    储存条件:Hygroscopic, -20ºC Freezer, Under Inert Atmosphere

    简介:Animmunosupressantandiscurrentlybeinginvestigatedforuseincancertreatments.Ridaforolimusmayactasaregulatorofproteinsynthesis,cellproliferation,cellcycleprogressionandcellsurvival.Ridaforolimus,wasformerlyknownasDeforolimus.

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    PI3K/Akt/mTOR572924-54-0
    源叶 Ridaforolimus(Deforolimus,... Ridaforolimus(Deforolimus,... 现货

     1702.00
    T94144 10mMinDMSO
    PI3K/Akt/mTOR1007207-67-1

    CAS号:1007207-67-1

    品名:[5-[7-甲磺酰基-2-(吗啉-4-基)-6,7-二氢-5H-吡咯并[2,3-d]嘧啶-4-基]嘧啶-2-基]胺5-(7-methylsulfonyl-2-morpholin-4-yl-5,6-dihydropyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine

    中文别名:[5-[7-甲磺酰基-2-(吗啉-4-基)-6,7-二氢-5H-吡咯并[2,3-d]嘧啶-4-基]嘧啶-2-基]胺

    英文别名:QCR-47;5-(7-(methylsulfonyl)-2-morpholino-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine;5-(7-methanesulfonyl-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-ylamine;

    分子式:C15H19N7O3S

    分子量:377.421

    精确质量:377.127

    Psa:136.54

    UNII号:JCL936W835

    密度:1.6±0.1g/cm3

    沸点:751.1±70.0°Cat760mmHg

    闪点:408.1±35.7°C

    折射率:1.706

    储存条件:-20℃

    蒸汽压:0.0±2.5mmHgat25°C

    简介:CH5132799isaselectiveclassIphosphoinositide3-kinase(PI3K)inhibitorthattargetshumancancersharboringoncogenicPIK3CAmutations.CH5132799alsoshowedpotentantiproliferativeandantitumoractivity.

     1007207-67-1 详细信息

    PI3K/Akt/mTOR

    CAS号:1007207-67-1

    品名:[5-[7-甲磺酰基-2-(吗啉-4-基)-6,7-二氢-5H-吡咯并[2,3-d]嘧啶-4-基]嘧啶-2-基]胺5-(7-methylsulfonyl-2-morpholin-4-yl-5,6-dihydropyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine

    中文别名:[5-[7-甲磺酰基-2-(吗啉-4-基)-6,7-二氢-5H-吡咯并[2,3-d]嘧啶-4-基]嘧啶-2-基]胺

    英文别名:QCR-47;5-(7-(methylsulfonyl)-2-morpholino-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine;5-(7-methanesulfonyl-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-ylamine;

    分子式:C15H19N7O3S

    分子量:377.421

    精确质量:377.127

    Psa:136.54

    UNII号:JCL936W835

    密度:1.6±0.1g/cm3

    沸点:751.1±70.0°Cat760mmHg

    闪点:408.1±35.7°C

    折射率:1.706

    储存条件:-20℃

    蒸汽压:0.0±2.5mmHgat25°C

    简介:CH5132799isaselectiveclassIphosphoinositide3-kinase(PI3K)inhibitorthattargetshumancancersharboringoncogenicPIK3CAmutations.CH5132799alsoshowedpotentantiproliferativeandantitumoractivity.

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    PI3K/Akt/mTOR1007207-67-1
    源叶 CH5132799 CH5132799 现货

     1550.00
    S59340 10mMinDMSO
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