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The proteins that combine with DNA are generally of characteristic types called histones and protamines.

核糖核酸结合者通常属于被称为组蛋白或鱼精蛋白的特殊

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OBJECTIVE To establish a method for determination of hyodeoxycholic acid (HDCA) and chenodeoxycholic acid (CDCA) in Ligan tablets.

立利肝片中猪胆酸(HDCA)及鹅胆酸(CDCA)的含测定方法。

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HPLC method for determination of phenylephrine hydrochloride, paracetamol, caffeine anhydrous,salicylamide and brompheniramine maleate in Liufenkamin tablets was established.

立了HPLC法测定柳酚咖敏片中盐酸上腺素、对乙酰氨基酚、无水咖啡因、水杨酰胺、马来酸溴苯那敏的含

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Diester deoxyaconitine is very toxic.When deoxyaconitine was transformed into mono-ester aconitum alkaloids and lipo-alkaloids by human intestinal bacteria, the toxicity decreased.

双酯型的乌头碱的毒性较高,当它被肠内细菌转化为单酯型和脂生物碱时会使其毒性降低。

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

They didn't review phenylephrine nasal sprays.

刘易斯:他们没有审查鼻喷雾剂。

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

Fischman: Overall, though, if oral phenylephrine doesn't work, what should people use instead of it?

Fischman:不过,总的来说,如果口服不起作用,人们应该用什么来代替它?

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

So, more products started using phenylephrine.

因此,更多的产品

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

Fischman: But I've been taking these cold medications with phenylephrine for years and they do make me feel better.

Fischman:但是我多年来一直服用这些感冒药和,它们确实让我感觉好多了。

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

Phenylephrine was actually approved in the 1970s, so it had been around a while.

实际是在 20 世纪 70 年代获得批准的,所以它已经存在了一段时间了。

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

In addition to that, three trials of oral phenylephrine showed it was no better than a placebo at relieving congestion.

除此之外,三项口服试验表明,它在缓解充血方面并不比安慰剂更好。

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学快报-学美国人Science Quickly, from SCIENTIFIC AMERICAN

And the pharmacologic data side indicated that when you take oral phenylephrine, most of it is metabolized to inactive forms, so very little of the active drug—in fact, one percent, based on FDA data—actually gets into the blood.

Le:药理学数据方面表明,当您服用口服时,大部分会被代谢为非活性形式,因此活性药物的含量极少(根据 FDA 数据,实际只有 1%)真正进入血液。

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