IBMX
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IBMX

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品牌: Absin
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    分子式:
    C10H14N4O2
    C10H14N4O2
    分子量:
    222.24
    222.24
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    产品介绍
    产品信息
    抗原名称
    Phosphodiesterase (PDE)
    商品描述
    IBMX is a potent cyclic nucleotide phosphodiesterase inhibitor; due to this action, the compound increases cyclic AMP and cyclic GMP in tissue and thereby activates CYCLIC NUCLEOTIDE-REGULATED PROTEIN KINASES
    分子量
    222.24
    纯度

    99%

    可溶性
    DMSO : 50 mg/mL (224.98 mM; Need ultrasonic)
    Ethanol : ≥ 7.14 mg/mL (32.13 mM)
    外观
    off-white powder
    In vitro(体外研究)
    At 100 μM, KMUP-1 (a xanthine derivative) and IBMX are the most effective at inducing tracheal relaxation; the magnitude of the relaxation responses induced by KMUP-1 and IBMX are not significantly different. IBMX (100 μM) activates renal outer medullary K+ (ROMK) channels (n=6, P+ (HK)-fed rats with IBMX (100 μM) for 20 min leads to a significant increase in tubular cAMP content to 1.43±0.35 pg/mm tubule length (n=14) compare with that measured in vehicle-treated controls (0.61±0.13 pg/mm tubule length, n=12, P.
    In vivo(体内研究)
    IBMX, a non-selective PDE inhibitor significantly decreases the liver glycogen storage (mg/g, IBMX 22±1.5 P0.05) also mc2 does not change plasma glucose (control=141±3 and mc2=145±5). IBMX has the highest efficacy on increasing plasma glucose. Treatments with IBMX and Apocynin significantly decrease cold-induced elevation of right ventricular (RV) systolic pressure (23.5±1.8 and 24.2±0.6 mmHg, respectively) although they do not decrease RV pressure to the warm control levels. IBMX or Apocynin significantly reduces medial layer thickness (19.0±0.9, and 16.9±0.8 μm, respectively) and increases lumen diameter (62.7±4.2, and 59.5±4.3 μm, respectively) of small PAs in cold-exposed rats.
    背景
    别名
    3-异丁基-1-甲基黄嘌呤
    分子式
    C10H14N4O2
    CAS号
    28822-58-4
    制备和贮存
    保存方式
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.

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    货号:
    abs817348-25mg
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