2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇

2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇

中文名称2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇
中文同义词2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇;2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇, >98%;CDC28P和PHO85P激酶抑制剂(NG 52);化合物NG-52
英文名称COMPOUND 52
英文同义词NG-52;2-(2-HYDROXYETHYLAMINO)-6-(3-CHLORANILINO)-9-ISOPROPYLPURINE;2-(2-HYDROXYETHYLAMINO)-6-(3-CHLOROANILINO)-9-ISOPROPYLPURINE;COMPOUND 52;2-(2-Hydroxyethylamino)-6-(3-chloroanilino)-9-isopropylpurine, NG-52;2-((6-((3-chlorophenyl)aMino)-9-isopropyl-9H-purin-2-yl)aMino)ethanol;2-[[6-[(3-Chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]ethanol;NG 52 (Compound 52 )
CAS号212779-48-1
分子式C16H19ClN6O
分子量346.81
EINECS号
相关类别小分子抑制剂;小分子抑制剂,天然产物;细胞生物学试剂;Inhibitors
Mol文件Mol File
结构式2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇 结构式

2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇 性质

沸点587.7±60.0 °C(Predicted)
密度1.42±0.1 g/cm3(Predicted)
储存条件Keep in dark place,Sealed in dry,2-8°C
溶解度二氯甲烷:50 mg/mL,澄清,无色
形态粉末
酸度系数(pKa)14.54±0.10(Predicted)
颜色白色至类白色

2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇 用途与合成方法

NG-52是三取代嘌呤,可结合酵母CDK的ATP结合区域,抑制Cdc28p和Pho85p,IC50分别为7 μM和2 μM。
TargetValue
Pho85p
(Cell-free assay)
2 μM
Cdc28p
(Cell-free assay)
7 μM

NG 52 (Compound 52) inhibits growth in a drug-sensitized yeast strain ( S. cerevisiae ) with a GI 50 of 30 μM. NG 52 is active against cdc2-cyclin B with an IC 50 value of 340 nM.
NG 52 dose-dependently inhibits the proliferation of glioma U87 and U251 cell lines with GI 50 values of 7.8 μM and 5.2 μM, respectively, meanwhile it potently inhibits the proliferation of primary glioma cells.
NG 52 (12.5-50 μM) effectively inhibits the phosphorylation of PDHK1 at Thr338 site and the phosphorylation of PDH at Ser293 site in U87 and U251 cells, resulting in more pyruvic acid entering the Krebs cycle with increased production of ATP and ROS.
NG 52 can reverse the Warburg effect by enhancing the activity of pyruvate dehydrogenase (PDH) through inhibiting the activity of PGK1, and switched cellular glucose metabolism from anaerobic mode to aerobic mode.

Cell Proliferation Assay

Cell Line: Glioma U87 and U251 cells
Concentration: 0 μM, 12.5 μM, 25 μM, 50 μM
Incubation Time: 6 days
Result: Potently inhibited the proliferation of primary glioma cells.

Western Blot Analysis

Cell Line: Glioma U87 and U251 cells
Concentration: 0 μM, 12.5 μM, 25 μM, 50 μM
Incubation Time: 12 hours or 24 hours
Result: Potently inhibited the proliferation of primary glioma cells.

NG 52 (50-150 mg/kg; oral administration; daily; for 13 days) treatment dose-dependently suppresses the growth of glioma xenograft.

Animal Model: Female nu/nu mice (5-week-old) injected with glioma cells
Dosage: 50 mg/kg, 100 mg/kg, 150 mg/kg
Administration: Oral administration; daily; for 13 days
Result: Dose-dependently suppressed the growth of glioma xenograft.

安全信息

危险品标志Xn
危险类别码40-68
安全说明36/37
WGK Germany3

MSDS信息

提供商 语言
英文
更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-15154NG 521 mg659元
2024/04/30S65402-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇
NG 52
212779-48-12mg1204.43元

2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇 上下游产品信息

"2-[[6-[(3-氯苯基)氨基]-9-异丙基-9H-嘌呤-2-基]氨基]乙醇"相关产品信息
氯苯基硅烷 2,2-双(对氯苯基)-1,1,1-三氯乙烷
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