EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE

EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE

中文名称EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE
中文同义词N4-(9-乙基-9H-咔唑-3-基)-N2-[3-(4-吗啉基)丙基]-2,4-嘧啶二胺;RAC GTPASE抑制剂(EHOP-016);EHOP-016游离态;N4-(9-乙基-9H-咔唑-3-基)-N2-(3-吗啉丙基)嘧啶-2,4-二胺;EHOP-016,RAC抑制剂;EHOP-016,RAC GTPASE抑制剂;化合物EHOP-016,10 MM DMSO 溶液;EHop-016 试剂
英文名称N4-(9-Ethyl-9H-carbazol-3-yl)-N2-(3-Morpholin-4-yl-propyl)-pyriMidine-2,4-diaMine
英文同义词EHop-016;EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE;N4-(9-Ethyl-9H-carbazol-3-yl)-N2-(3-Morpholin-4-yl-propyl)-pyriMidine-2,4-diaMine;N4-(9-Ethyl-9H-carbazol-3-yl)-N2-[3-(4-morpholinyl)propyl]-2,4-pyrimidinediamine;N4-(9-Ethyl-9H-carbazol-3-yl)-N2-[3-(4-morpholinyl)propyl]-2,4-pyrimidinediamine Ehop-016;EHop-016, >=98%;EHOP016; EHOP-016; EHOP 016; EHOP016; EHOP-016; EHOP 016.;EHOP 016;EHOP016
CAS号1380432-32-5
分子式C25H30N6O
分子量430.55
EINECS号
相关类别细胞生物学试剂;细胞周期;小分子抑制剂;小分子抑制剂,天然产物;Inhibitors
Mol文件1380432-32-5.mol
结构式EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE 结构式

EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE 性质

沸点633.9±65.0 °C(Predicted)
密度1.27
储存条件2-8°C
溶解度DMSO:可溶10mg/mL,澄清
酸度系数(pKa)7.30±0.10(Predicted)
形态粉末
颜色白色至米色
InChIKeyAFTZZRFCMOAFCR-UHFFFAOYSA-N
SMILESCCn1c2ccccc2c3cc(Nc4ccnc(NCCCN5CCOCC5)n4)ccc13

EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE 用途与合成方法

EHop-016 是一种有效的选择性的 Rac GTPase Rac1 和 Rac3 抑制剂。EHop-016 在 MDA-MB-435 细胞中抑制 Rac1 活性,IC50 为 1.1 μM。EHop-016 抑制 Vav2 与 Rac,Rac 激活的 PAK1 相互作用,片状脂蛋白形成和细胞迁移。

EHop-016 (1-10 μM; 24 hours; MDA-MB-435 cells) treatment inhibits Rac1 and Rac3 activity. At higher concentrations, EHop-016 inhibits the close homolog Cdc42. In MDA-MB-435 cells that demonstrate high active levels of the Rac GEF Vav2, EHop-016 inhibits the association of Vav2 with a nucleotide-free Rac1(G15A) .
EHop-016 also inhibits the Rac activity of MDA-MB-231 metastatic breast cancer cells and reduces Rac-directed lamellipodia formation in both cell lines. EHop-016 decreases Rac downstream effects of PAK1 (p21-activated kinase 1) activity and directed migration of metastatic cancer cells.
EHop-016 affectes cell viability by down-regulating Akt and Jun kinase activities and c-Myc and Cyclin D expression, as well as increasing caspase 3/7 activities in metastatic cancer cells.

Western Blot Analysis

Cell Line: MDA-MB-435 cells
Concentration: 1 μM, 2 μM, 4 μM, 5 μM, 10 μM
Incubation Time: 24 hours
Result: The activity Rac3 was inhibited by 58%.

EHop-016 (10-25 mg/kg; intraperitoneal injection; 3 times a week; for 55 days; nu/nu mice) treatment significantly reduces mammary fat pad tumor growth, metastasis, and angiogenesis.

Animal Model: Female athymic nu/nu mice (4-5 weeks old) injected with GFP-MDA-MB-435 cells
Dosage: 10 mg/kg, 25 mg/kg
Administration: Intraperitoneal injection; 3 times a week; for 55 days
Result: Significantly reduced mammary fat pad tumor growth, metastasis, and angiogenesis.
生产方法 
N-(3-氨丙基)吗啉

123-00-2

9H-Carbazol-3-amine, N-(2-chloro-4-pyrimidinyl)-9-ethyl-

1380432-31-4

EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE

1380432-32-5

EHop-016的合成在Bruker 400MHz光谱仪上记录1H和13C NMR光谱。在Hewlett Packard 6890N GC/MS光谱仪上获得质谱。所有化学品均购自Sigma Aldrich Chemical Company。根据图1中提供的反应方案,EHop-016(5)的合成分两步进行。如图1(A)所示,进行与文献中描述的过程类似的过程。得到(2-氯-嘧啶-4-基)-(9-乙基-9H-咔唑-3-基)-胺3,为纯化合物,收率为53%。通过TLC、NMR和GC/MS鉴定产物。Rf = 0.23(3:1,己烷-乙酸乙酯);1H NMR(DMSO-d6, 400MHz)δ 1.32(t, J = 6.9Hz, 3H), 4.45(q, J = 6.6Hz, 2H), 6.72(s, 1H), 7.20(t, J = 7.36Hz, 1H), 7.47(t, J = 7.30Hz, 1H), 7.56(s, 1H), 7.62(t, J = 8.68Hz, 1H), 8.11(t, J = 7.36Hz, 1H), 8.27(s, 1H), 10.1(s, 1H);13C NMR(DMSO-d6, 100MHz)δ 13.7, 37.0, 109.2, 109.4, 115.0, 118.7, 120.3, 121.3, 121.9, 122.3, 125.9, 129.9, 136.9, 140.0, 156.9, 159.6, 162.4;LRGC-MS m/z(相对百分比):[M]+ 276(100), [M-Cl]+ 241(40), [M-C5H5N3Cl]+ 134(26)。得到N4-(9-乙基-9H-咔唑-3-基)-N2-(3-吗啉-4-基-丙基)-嘧啶-2,4-二胺5(EHop-016),为纯化合物,收率为93%。通过TLC和NMR鉴定产物基本上是纯的:Rf = 0.34(9:1,CH2Cl2-MeOH);1H NMR(DMSO-d6, 400MHz)δ 1.31(t, J = 7.0Hz, 3H), 1.73(m, 2H), 2.32(m, 2H), 2.34(t, J = 6.89Hz, 8H), 3.52(m, 2H), 4.42(q, J = 7.0Hz, 2H), 5.98(d, J = 5.7Hz, 1H), 6.69(t, J = 5.3Hz, 1H), 7.16(t, J = 7.4Hz, 1H), 7.43(t, J = 7.2Hz, 1H), 7.53(t, J = 9.0Hz, 4H), 7.81(d, J = 5.4Hz, 1H), 8.10(s, 1H), 8.66(s, 1H), 9.1(s, 1H);13C NMR(DMSO-d6, 100MHz)δ 13.7, 26.2, 36.9, 53.4, 56.3, 66.2, 108.9, 109.0, 118.2, 119.7, 120.2, 122.0, 122.2, 125.6, 132.5, 135.5, 139.9, 159.8, 160.9, 162.1。

参考文献:

[1] Patent: US2013/172552, 2013, A1. Location in patent: Paragraph 0031

安全信息

WGK Germany3
存储类别11 - 可燃固体

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2025/12/22HY-12810EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE
EHop-016
1380432-32-51 mg199元
2025/12/22HY-12810EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE
EHop-016
1380432-32-510mM * 1mLin DMSO398元

EHOP-016;N4-(9-ETHYL-9H-CARBAZOL-3-YL)-N2-(3-MORPHOLIN-4-YL-PROPYL)-PYRIMIDINE-2,4-DIAMINE 上下游产品信息

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