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Merck

D8946

Sigma-Aldrich

DMH1

≥98% (HPLC), powder, BMP inhibitor

别名:

4- [6- [4-(1-甲基乙氧基)苯基] 吡唑并 [1,5-a] 嘧啶-3-基]-喹啉, 4-[6-(4-异丙氧基苯基)吡唑并 [1,5-a] 嘧啶-3-基] 喹啉

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About This Item

经验公式(希尔记法):
C24H20N4O
分子量:
380.44
MDL號碼:
分類程式碼代碼:
51111800
PubChem物質ID:
NACRES:
NA.77

product name

DMH1, ≥98% (HPLC)

品質等級

化驗

≥98% (HPLC)

形狀

powder

儲存條件

desiccated

顏色

light yellow to orange

溶解度

DMSO: 5 mg/mL, clear (warmed)

儲存溫度

2-8°C

SMILES 字串

CC(C)OC(C=C1)=CC=C1C(C=N2)=CN3C2=C(C4=CC=NC5=C4C=CC=C5)C=N3

InChI

1S/C24H20N4O/c1-16(2)29-19-9-7-17(8-10-19)18-13-26-24-22(14-27-28(24)15-18)20-11-12-25-23-6-4-3-5-21(20)23/h3-16H,1-2H3

InChI 密鑰

JMIFGARJSWXZSH-UHFFFAOYSA-N

一般說明

DMH1 刺激人类诱导多能干细胞 (hiPSCs) 的神经发生并抑制肺癌的生长和转移。它阻止细胞自噬反应。

應用

DMH1 已被用于骨形态发生蛋白 (BMP) 抑制。 也被用于阻断血管内皮生长因子 (VEGF) 信号。

生化/生理作用

DMH1 是一种高选择性骨形态发生蛋白 (BMP) 抑制剂。DMH1 是一种 Dorsomorphin 类似物,仅靶向 BMP ,但不是 VEGF 通路。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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An organizing role for the TGF-β signaling pathway in axes formation of the annelid Capitella teleta
Lanza AR, et al.
Developmental Biology, 435(1), 26-40 (2018)
Silvia Colucci et al.
Blood, 130(19), 2111-2120 (2017-09-03)
The expression of the key regulator of iron homeostasis hepcidin is activated by the BMP-SMAD pathway in response to iron and inflammation and among drugs, by rapamycin, which inhibits mTOR in complex with the immunophilin FKBP12. FKBP12 interacts with BMP
DMH1 (4-[6-(4-isopropoxyphenyl) pyrazolo [1, 5-a] pyrimidin-3-yl] quinoline) inhibits chemotherapeutic drug-induced autophagy
Sheng Y, et al.
Acta Pharmaceutica Sinica. B, 5(4), 330-336 (2015)
Richard H Row et al.
eLife, 7 (2018-06-08)
The mesodermal germ layer is patterned into mediolateral subtypes by signaling factors including BMP and FGF. How these pathways are integrated to induce specific mediolateral cell fates is not well understood. We used mesoderm derived from post-gastrulation neuromesodermal progenitors (NMPs)
Kwang Bo Jung et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 32(1), 111-122 (2017-09-01)
Human intestinal organoids (hIOs) derived from human pluripotent stem cells (hPSCs) have immense potential as a source of intestines. Therefore, an efficient system is needed for visualizing the stage of intestinal differentiation and further identifying hIOs derived from hPSCs. Here

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