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CAS:918505-84-7|PLX-4720

CAS:918505-84-7|PLX-4720

作者:德尔塔 日期:2022-03-21

产品名称 PLX-4720 英文名称 PLX-4720 规格或纯度 ≥99% 别名 N-(3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonamide 英文别名 N-(3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluorophenyl)propane-1-sulfonamide 运输条件 超低温冰袋运输 生化机理 PLX-4720 is a B-raf inhibitor with IC50 of 160 nM.Potent B-Raf inhibitor (IC 50 values are 6.7, 13 and 160 nM for C-Raf-1 Y340D/Y341D , B-Raf V600E and B-Raf wild-type respectively). Shows antiproliferative effects. Shows antitumor effects in vivo. Orally ac

CAS:586379-66-0|PH-797804

CAS:586379-66-0|PH-797804

作者:德尔塔 日期:2022-03-21

产品名称 PH-797804 英文名称 PH-797804 规格或纯度 ≥99% 别名 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-[(methylamino)carbonyl]-2-methylphenyl]-6-methylpyridin-2(1H)-one,3-[3-Bromo-4-[(2,4-difluorophenyl)methoxy]-6-methyl-2-oxo-1(2H)-pyridinyl]-N,4-dimethyl-benzamide,PH 797804 英文别名 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-[(methylamino)carbonyl]-2-methylphenyl]-6-methylpyridin-2(1H)-one,3-[3-Bromo-4-[(2,4-difluorophenyl)methoxy]-6-methyl-2-oxo-1(2H)-pyridinyl]-N,4-dimethyl-benzamide,PH 797804 运输条件 超低温冰袋运输 生化机理 PH-797804 is an ATP-competitive, rea

CAS:271576-80-8|SD-06

CAS:271576-80-8|SD-06

作者:德尔塔 日期:2022-03-21

产品名称 SD-06 英文名称 SD-06 生化机理 SD-06 is a p38 MAP kinase inhibitor. SD-06 inhibits p38α with an IC50 value of 170nM and inhibits LPS-stimulated TNF-release in rats (83% inhibition at 1mg/kg, po).CAS编号 271576-80-8 溶解性 DMSO 储存温度 储存温度-20°C

CAS:934660-93-2|考比替尼

CAS:934660-93-2|考比替尼

作者:德尔塔 日期:2022-03-21

产品名称 考比替尼 英文名称 Cobimetinib 规格或纯度 98% 运输条件 超低温冰袋运输 生化机理 GDC-0973(XL-518; GDC 0973) is a selective inhibitor of MEK. GDC-0973 is also known as mitogen activated protein kinase kinase (MAPKK), is a key component of the RAS/RAF/MEK/ERK pathway, which is frequently activated in human tumors. Inappropriate activation of the MEK/ERK pathway promotes cell growth in the absence of exogenous growth factors.CAS编号 934660-93-2 熔点 165 - 166°C

CAS:899805-25-5|CC-930

CAS:899805-25-5|CC-930

作者:德尔塔 日期:2022-03-21

产品名称 CC-930 英文名称 CC-930 规格或纯度 98% 英文别名 Tanzisertib;CC930;CC 930;4-[[9-[(3S)-oxolan-3-yl]-8-(2,4,6-trifluoroanilino)purin-2-yl]amino]cyclohexan-1-ol 运输条件 超低温冰袋运输CAS编号 899805-25-5 溶解性 25°C: DMSO 储存温度 -20°C储存

CAS:208260-29-1|ZM 336372

CAS:208260-29-1|ZM 336372

作者:德尔塔 日期:2022-03-21

产品名称 ZM 336372 英文名称 ZM 336372 应用 A potent and selective Raf-1 inhibitor. 规格或纯度 ≥98% 别名 ZM-336372 英文别名 3-(Dimethylamino)-N-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]-benzamide;ZM336372; ZM-336372 运输条件 冰袋运输 生化机理 ZM 336372 is a reversible, selective inhibitor of the protein kinase Raf-1 (IC50 = 70nM). Althoμgh ZM 336372 weakly inhibits Raf-B, it is 10 fold more potent against Raf

CAS:209410-46-8|VX-745

CAS:209410-46-8|VX-745

作者:德尔塔 日期:2022-03-21

产品名称 VX-745 英文名称 VX-745 规格或纯度 ≥98% 别名 5-(2,6-Dichlorophenyl)-2-(2,4-difluorophenylthio)-6H-pyrimido[1,6-b]pyridazin-6-one 英文别名 5-(2,6-dichlorophenyl)-2-(2,4-difluorophenyl)sulfanylpyrimido[1,6-b]pyridazin-6-one;Neflamapimod 运输条件 超低温冰袋运输 生化机理 VX-745 is highly potent and selective p38α inhibitor (IC50 = 10 nM). VX-745 also blocks TNFα production in LPS-stimulated HWB in vitro (IC50 = 177 nM). VX-745 displays 1000-fold selectivity over closely related kinases, including ERK1,

CAS:1094614-84-2|BIX 02188

CAS:1094614-84-2|BIX 02188

作者:德尔塔 日期:2022-03-21

产品名称 BIX 02188 英文名称 BIX 02188 规格或纯度 ≥98%CAS编号 1094614-84-2 溶解性 DMSO 43 mg/mL Water

CAS:334949-59-6|BIX02188

CAS:334949-59-6|BIX02188

作者:德尔塔 日期:2022-03-21

产品名称 BIX02188 英文名称 BIX02188 规格或纯度 ≥98% 英文别名 BIX-02188;BIX 02188 运输条件 超低温冰袋运输 生化机理 BIX02188 is a MEK5-selective inhibitor with an IC50 of 0.8 ± 1.0 μM.Potent, selective MEK5 inhibitor (IC 50 = 4.3 nM). Blocks phosphorlyation of ERK5, without affecting phosphorylation of ERK1/2. Induces apoptosis in FLT3-ITD cells. Centrally active in vivo.CAS编号 334949-59-6

CAS:1265916-41-3|BIX02189

CAS:1265916-41-3|BIX02189

作者:德尔塔 日期:2022-03-21

产品名称 BIX02189 英文名称 BIX02189 规格或纯度 98% 别名 BIX 02189;(3Z)-3-[[[3-[(Dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-N,N-dimethyl-2-oxo-1H-indole-6-carboxamide;(Z)-3-((3-((Dimethylamino)methyl)phenylamino)(phenyl)methylene)-N,N-dimethyl-2-oxoindoline-6-carboxamide;(3Z)-3-[[[3-[(Dimeth 英文别名 BIX 02189;(3Z)-3-[[[3-[(Dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-N,N-dimethyl-2-oxo-1H-indole-6-carboxamide;(Z)-3-((3-((Dimethylamino)methyl)phenylamino)(phenyl)methylene)-N,N-dimethyl-2-oxoindoline-6-carboxamide;(3Z)-3-[[[3-[(Dimeth 运输条件 超低温冰袋运输 生化机理

CAS:479543-46-9|VX-702

CAS:479543-46-9|VX-702

作者:德尔塔 日期:2022-03-21

产品名称 VX-702 英文名称 VX-702 规格或纯度 ≥98% 运输条件 超低温冰袋运输 生化机理 VX-702 is a P38 MAPK inhibitor , IL-6, IL-1β and TNFα (IC50 = 59, 122 and 99 ng/ml, respectively).Potent, selective p38 MAP kinase inhibitor (K d values are 3.7 and 17 nM for p38α and p38β, respectively). Active in vitro and in vivo . Orally active.CAS编号 479543-46-9 溶解性 DMSO ≥78mg/mL Water

CAS:918504-65-1|Vemurafenib(PLX4032,RG7204)

CAS:918504-65-1|Vemurafenib(PLX4032,RG7204)

作者:德尔塔 日期:2022-03-21

产品名称 Vemurafenib(PLX4032,RG7204) 英文名称 Vemurafenib (PLX4032, RG7204) 应用 A novel and potent inhibitor of B-RAFV600E with IC50 of 31 nM. 规格或纯度 ≥98% 别名 维罗非尼 生化机理 Vemurafenib is a novel and potent inhibitor of B-RAFV600E with IC50 of 31 nM. Has been shown to kill melanoma cells in vitro.CAS编号 918504-65-1 熔点 260-262 °C

CAS:1173097-76-1|U0126-EtOH

CAS:1173097-76-1|U0126-EtOH

作者:德尔塔 日期:2022-03-21

产品名称 U0126-EtOH 英文名称 U0126-EtOH 规格或纯度 ≥97% 别名 U 0126;U-0126 生化机理 U0126-EtOH functionally antagonizes AP- 1 transcriptional activity and blocks the production of a variety of cytokines and metalloproteinases involved in the inflammatory response. U0126-EtOH inhibits T cell proliferation in response to antigenic stimulation or cross-linked anti-CD3 plus anti-CD28 Abs without effect on IL-2-induced proliferation by down-regulating IL-2 mRNA levels . A recent study shows that U0126-EtOH antagonizes resveratrol-induced apoptosis in castration-resistant human prostate cancer C4-2 cells, inhibits mitochondrial function and shifts cells to aerobic glycolysis independently of MEK .CAS编号 1173097-76-1

CAS:869357-68-6|AZD8330

CAS:869357-68-6|AZD8330

作者:德尔塔 日期:2022-03-21

产品名称 AZD8330 英文名称 AZD8330 应用 An antineoplastic selective MEK inhibitor 规格或纯度 ≥98% 别名 ARRY-424704; ARRY424704;ARRY704; AZD8330 英文别名 AZD-8330; ARRY-704;2-(2-氟-4-碘苯氨基)-N-(2-羟基乙氧基)-1,5-二甲基-6-氧代-1,6-二氢吡啶-3-甲酰胺; 运输条件 超低温冰袋运输 生化机理 AZD8330 potently and strongly inhibits MEK 1/2. AZD8330 has no inhibitory activity against over 200 other kinases including at conce

CAS:1628838-42-5|RAF709

CAS:1628838-42-5|RAF709

作者:德尔塔 日期:2022-03-21

产品名称 RAF709 英文名称 RAF709 规格或纯度 98% 英文别名 N-[2-methyl-5'-(4-morpholinyl)-6'-[(tetrahydro-2H-pyran-4-yl)oxy][3,3'-bipyridin]-5-yl]-3-(trifluoromethyl)-benzamide 运输条件 超低温冰袋运输CAS编号 1628838-42-5 溶解性 溶于DMSO, 最高浓度 (mg/mL):100, 最高浓度(mM):184.31;溶于Ethanol, 最高浓度 (mg/mL):100, 最高浓度(mM):184.31