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产品名称
环盐酸吗甲吡嗪酸 来源于圆弧青霉菌, ≥98% (HPLC), powder
品質等級
化驗
≥98% (HPLC)
形狀
powder
顏色
white to off-white
溶解度
DMSO: soluble
chloroform: soluble
儲存溫度
−20°C
SMILES 字串
CN1C(=O)C(=C(\C)O)\C(=O)C2C(Cc3cccc4[nH]cc2c34)C1(C)C
InChI
1S/C20H22N2O3/c1-10(23)15-18(24)17-12-9-21-14-7-5-6-11(16(12)14)8-13(17)20(2,3)22(4)19(15)25/h5-7,9,13,17,21,23H,8H2,1-4H3/b15-10-
InChI 密鑰
WJCPGKDPOYBOOJ-GDNBJRDFSA-N
基因資訊
human ... ADORA1(134) , ADORA2A(135) , ADORA3(140)
mouse ... Adora1(11539)
rat ... Adora1(29290) , Adora2a(25369) , Adora3(25370)
一般說明
圆弧偶氮酸(CPA)是由多种 曲霉 和 青霉菌 种合成的tetramic酸。
應用
圆弧青霉菌来源圆弧偶氮酸用于:
- 作为标准品,用于薄层色谱法(TLC)检测和定量黄曲霉毒素
- 作为培养基成分,用于不含Ca2+的DMEM(含10%胎牛血清(FBS))
- 作为肌质网/内质网Ca2+ -ATP酶的可逆抑制剂,检测腔内钙在内质网(ER)-至-高尔基体转运过程中的作用
- 作为内质网Ca2+-ATP酶的阻滞剂,处理神经元;研究内质网(ER)在Ca2+诱导的Ca2+ 释放(CICR)抑制 SERCA 过程中,对释放和维持Ca2+ 的影响
生化/生理作用
抑制肌质网 Ca 2 + -泵。
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 2 Oral
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
其他客户在看
Plant and fungal toxins as contaminants of feed and meat
Improving the Safety of Fresh Meat, 77-101 (2005)
N Demaurex et al.
The Journal of biological chemistry, 267(4), 2318-2324 (1992-02-05)
The filling state of intracellular Ca2+ stores has been proposed to regulate Ca2+ influx across the plasma membrane in a variety of tissues. To test this hypothesis, we have used three structurally unrelated inhibitors of the Ca(2+)-ATPase of intracellular Ca2+
Toxigenic Aspergillus flavus and other fungi of public health concern in food and organic matter in southwest Nigeria
Fapohunda SO, et al.
Mycology, 3, 210-219 (2012)
Ca2+-Induced Ca2+ Release in Aplysia Bag Cell Neurons Requires Interaction Between Mitochondrial and Endoplasmic Reticulum Stores
Geiger JE, et al.
Journal of Neurophysiology (2008)
Sakiko Ujita et al.
Cerebral cortex (New York, N.Y. : 1991), 27(2), 1602-1614 (2016-01-24)
Astrocytes in various brain regions exhibit spontaneous intracellular calcium elevations both in vitro and in vivo; however, neither the temporal pattern underlying this activity nor its function has been fully evaluated. Here, we utilized a long-term optical imaging technique to
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