推荐产品
产品线
BioUltra
方案
≥99%
杂质
<0.005% Phosphorus (P)
灼烧残渣
<0.1%
mp
200-201 °C (lit.)
溶解性
DMSO: soluble 1 M (with gentle warming)
痕量阴离子
sulfate (SO42-): <0.05%
痕量阳离子
Al: <0.0005%
Ca: <0.005%
Cu: <0.0005%
Fe: <0.005%
K: <0.05%
Mg: <0.005%
NH4+: <0.05%
Na: <0.005%
Pb: <0.001%
Zn: <0.0005%
储存温度
−20°C
SMILES字符串
CC(C)CN1C(=O)N(C)C(=O)c2[nH]cnc12
InChI
1S/C10H14N4O2/c1-6(2)4-14-8-7(11-5-12-8)9(15)13(3)10(14)16/h5-6H,4H2,1-3H3,(H,11,12)
InChI key
APIXJSLKIYYUKG-UHFFFAOYSA-N
基因信息
rat ... Adora1(29290) , Adora2a(25369)
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应用
3-异丁基-1-甲基黄嘌呤是一种腺苷3′,5′-环但但磷酸磷酸二酯酶 (cAMP PDE)抑制剂,已用于:
- 成脂分化
- 组织培养
- 3T3-L1脂肪前体细胞分化
生化/生理作用
由IBMX对磷酸二酯酶的抑制而引起的cAMP水平的增加可激活PKA,而引起增殖减少、分化增加并诱导细胞凋亡。IBMX可抑制苯肾上腺素诱导的气道粘膜神经内分泌上皮细胞5-羟色胺释放。(IC50:1.3 μM)。IBMX还可作为一种腺苷受体拮抗剂。其已表现出对神经肌肉接头、GH3细胞和血管平滑肌细胞中离子通道的抑制作用。IBMX可诱导感觉神经元释放储存在细胞内的钙。
由IBMX对磷酸二酯酶的抑制而引起的cAMP水平的增加可激活PKA,而引起增殖减少、分化增加并诱导细胞凋亡。IBMX可抑制苯肾上腺素诱导的气道粘膜神经内分泌上皮细胞5-羟色胺释放(IC50:1.3 μM)。IBMX还可作为一种腺苷受体拮抗剂。其已表现出对神经肌肉接头、GH3细胞和血管平滑肌细胞中离子通道的抑制作用。IBMX可诱导感觉神经元释放储存在细胞内的钙。
特点和优势
- ICP法痕量元素检测
- ICP检测痕量硫(硫酸盐形式)和磷(磷酸盐形式)含量
- 离子色谱法检测痕量铵含量
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
其他客户在看
Preferential apelin-13 production by the proprotein convertase PCSK3 is implicated in obesity
Shin K, et al.
FEBS Open Bio, 3(1), 328-333 (2013)
Distinct roles of the phosphatidate phosphatases lipin 1 and 2 during adipogenesis and lipid droplet biogenesis in 3T3-L1 cells
Sembongi H, et al.
The Journal of biological chemistry, jbc-M113 (2013)
Ryan D Rose et al.
Theriogenology, 79(1), 142-148 (2012-10-30)
Physical removal of mammalian cumulus-oocyte complexes (COCs) from ovarian follicles results in spontaneous resumption of meiosis, largely because of a decrease in cAMP concentrations, causing asynchrony between cytoplasmic and nuclear maturation and decreased oocyte developmental competence. The aim of this
Uniaxial mechanical strain modulates the differentiation of neural crest stem cells into smooth muscle lineage on micropatterned surfaces
Li X, et al.
PLoS ONE, 6(10), e26029-e26029 (2011)
The next generation of phosphodiesterase inhibitors: structural clues to ligand and substrate selectivity of phosphodiesterases.
David T Manallack et al.
Journal of medicinal chemistry, 48(10), 3449-3462 (2005-05-13)
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