
Diethyl aminoethyl hexanoate citrate
CAS No. 220439-24-7
Diethyl aminoethyl hexanoate citrate ( DA-6 citrate | 2-Diethylaminoethyl hexanoate citrate )
产品货号. M27070 CAS No. 220439-24-7
二乙基氨乙基己酸柠檬酸盐是一种广泛用作植物生长调节剂的化合物,可刺激不定芽的再生。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
100MG | ¥332 | 有现货 |
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200MG | ¥470 | 有现货 |
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500MG | ¥786 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Diethyl aminoethyl hexanoate citrate
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述二乙基氨乙基己酸柠檬酸盐是一种广泛用作植物生长调节剂的化合物,可刺激不定芽的再生。
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产品描述Diethyl aminoethyl hexanoate citrate is a compound that is widely used as a plant growth regulator stimulates the regeneration of adventitious buds.(In Vitro):Diethyl aminoethyl hexanoate citrate absorbs UV-A radiation and its peak is at 354 nm. At 25 °C, the molar absorption coefficient of Diethyl aminoethyl hexanoate citrate in EtOH is 39 000 mol/dm3/cm.
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体外实验Diethyl aminoethyl hexanoate citrate is used as a plant growth regulator, stimulates the regeneration of adventitious buds. Diethyl aminoethyl hexanoate (DA-6, 1 μM) with EDTA effectively causes theCd extraction. Diethyl aminoethyl hexanoate fixes more Cd in cell walls and reduces Cd migration in shoot to reduce metal toxicity. Furthermore, Diethyl aminoethyl hexanoate/gibberellic acid 3 in combination with EDTA alleviates the adverse effect of EDTA on plant growth.
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体内实验——
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同义词DA-6 citrate | 2-Diethylaminoethyl hexanoate citrate
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通路Others
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靶点Other Targets
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受体Microtubule/Tubulin
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研究领域——
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适应症——
化学信息
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CAS Number220439-24-7
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分子量407.46
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分子式C18H33NO9
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (245.42 mM)
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SMILESOC(=O)CC(O)(CC(O)=O)C(O)=O.CCCCCC(=O)OCCN(CC)CC
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献




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Calcitonin (8-32), s...
Calcitonin (8-32), salmon is a highly selective amylin receptor antagonist.Calcitonin is a hormone known to participate in calcium and phosphorus metabolism. In mammals, the major source of calcitonin is from the parafollicular or C cells in the thyroid gland. Calcitonin is a 32 amino acid peptide cleaved from a larger prohormone.
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CRSP-1
Endogenous central calcitonin (CT) receptor agonist that stimulates cAMP formation at a potency 350-fold greater than CT (ED50 values are 0.2 and 71 nM respectively). Displays no activity at calcitonin-gene related peptide (CGRP) and adrenomedullin receptors. Inhibits formation of multinuclear osteoclasts with similar efficacy to CT in vitro. Suppresses food intake and increases body temperature in free-feeding rats, and significantly decreases plasma calcium levels in vivo.
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cGMP Dependent Kinas...
Competitive inhibitor of cGMP-dependent protein kinase (PKG); analog of a substrate peptide corresponding to a phosphorylation site of histone H2B. Competes with synthetic substrates (Ki = 86 mM) but does not inhibit phosphorylation of intact histones by PKG. Inhibits phosphorylation of intact histones by PKA.