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Merck
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文件

P0042

Sigma-Aldrich

PP2

≥98% (HPLC)

同義詞:

4-氨基-3-(4-氯苯基)-1-(叔丁基)-1H-吡唑并 [3,4-d] 嘧啶, 4-氨基-5-(4-氯苯基)-7-(叔丁基)吡唑并 [3,4-d] 嘧啶, AG 1879

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About This Item

經驗公式(希爾表示法):
C15H16ClN5
CAS號碼:
分子量::
301.77
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

white to off-white

溶解度

DMSO: >10 mg/mL

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)n1nc(-c2ccc(Cl)cc2)c3c(N)ncnc13

InChI

1S/C15H16ClN5/c1-15(2,3)21-14-11(13(17)18-8-19-14)12(20-21)9-4-6-10(16)7-5-9/h4-8H,1-3H3,(H2,17,18,19)

InChI 密鑰

PBBRWFOVCUAONR-UHFFFAOYSA-N

應用

PP2 已被用于:
  • 分析 Src/粘着斑激酶(FAK)信号传导对 IQ 结构域 GTP酶激活蛋白 1 (IQGAP1)介导的失巢凋亡抗性的影响
  • 用于 Src 抑制以研究其对非小细胞肺癌 (NSCLC) 细胞中表皮生长因子受体(EGFR) 和核因子E 2 相关因子 2(Nrf2) 磷酸化的影响
  • 用于MDA-MB-231 乳腺癌细胞中 SRC的药物抑制

生化/生理作用

PP2 是非受体酪氨酸激酶(nRTK) 的Src-家族酪氨酸激酶的选择性抑制剂。它对ζ链TCR相关蛋白激酶70(ZAP-70)和 Janus激酶 2(JAK2)的选择性>10000 倍。PP2 在体外体内有效地减少宫颈癌增殖。

特點和優勢

该化合物是激酶磷酸酶生物学研究的特色产品。 点击此处 ,发现更多特色激酶磷酸酶生物学产品。在 sigma.com/discover-bsm了解更多关于其他研究领域的生物活性小分子。

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

防範說明

危險分類

Acute Tox. 3 Oral

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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