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102029-73-2

中文名稱 乙酰輔酶 A 鈉鹽
英文名稱 Acetyl coenzyme A sodium salt
CAS 102029-73-2
分子式 C23H38N7O17P3S
分子量 809.57
MOL 文件 102029-73-2.mol
更新日期 2025/01/14 09:12:30
102029-73-2 結(jié)構(gòu)式 102029-73-2 結(jié)構(gòu)式

基本信息

中文別名
乙醯輔酶A
乙醯COA
乙酰COA
乙酰輔酶 A
乙酰輔酶A鈉
乙酰輔酶A三鈉鹽
乙酰輔酶 A 鈉鹽
乙酰輔酶A鈉鹽(進(jìn)分)
乙酰輔酶 A(乙酰輔酶 A 鈉鹽)
ACETYL COENZYME A 鈉鹽
英文別名
C2:0
acetyl coa
Acetyl-S- CoA
Acetyl-Coenzym A
ACETYL COENZYME A
Acetyl Coenzyme A trisodium
ACETYL COENZYME A SODIUM SALT
ACETHYL COENZYME A SODIUM SALT
Acethyl coenzyme alpha sodium salt
Acetyl coenzyme A sodium salt,Acetyl CoA

物理化學(xué)性質(zhì)

儲存條件−20°C
溶解度H2O: 100 mg/mL
形態(tài)powder
顏色White to off-white
InChIKeyZSLZBFCDCINBPY-KMYLAXNMSA-N

安全數(shù)據(jù)

安全說明24-36/37-45
WGK Germany1
海關(guān)編碼29349990

常見問題列表

應(yīng)用及發(fā)展前景
乙酸乙酯是清香型白酒的主體香,一直備受關(guān)注。通過基因工程手段提高釀酒酵母分泌乙酰輔酶A的能力,從而提高乙酸乙酯生成量。通過ACH1基因缺失的α5ΔACH1菌株表達(dá)發(fā)現(xiàn),乙酰輔酶A含量較親本菌株α5稍有提高,但對提高乙酸乙酯生成量的效果并不明顯,分析原因可能是ACH1基因定位于線粒體中,其增加的是線粒體中乙酰輔酶A的含量,線粒體中的乙酰輔酶A無法流向乙酸乙酯的合成。在ACH1基因缺失的基礎(chǔ)上,過表達(dá)ACS1和ACS2基因得到工程菌株α5-A1和α5-A2,乙酸乙酯生成量分別比親本菌株α5提高26.12%和23.70%;乙酰輔酶A含量分別比α5ΔACH1提高了80.33%和52.79%;結(jié)果表明,過表達(dá)ACS1和ACS2基因均能提高乙酰輔酶A含量和乙酸乙酯生成量,且乙酸乙酯生成量和胞內(nèi)乙酰輔酶A的增加量呈正相關(guān)。在過表達(dá)ACS1和ACS2基因的基礎(chǔ)上,過表達(dá)醇乙?;D(zhuǎn)移酶ATF1基因得到工程菌株A1-ATF1和
A2-ATF1,乙酸乙酯含量分別為72.52 mg/L和44.80 mg/L,分別是單獨(dú)過表達(dá)ATF1基因a5-ATF1的204.14%和125.67%,且ΔA-ATF1比α5-ATF1產(chǎn)乙酸乙酯顯著增加,結(jié)果表明,在底物乙酰輔酶A充足的條件下,提高醇乙?;D(zhuǎn)移酶活性,能夠提高乙酸乙酯的生成量。  
生物活性
Acetyl Coenzyme A trisodium (Acetyl-CoA trisodium) 是一種重要的代謝中間產(chǎn)物。Acetyl Coenzyme A trisodium 是糖酵解丙酮酸進(jìn)入三羧酸 (TCA) 循環(huán)的實(shí)際分子,是脂質(zhì)合成的關(guān)鍵前體,并且是乙?;阴;奈ㄒ还w,還是一種丙酮酸羧化酶 (PC) 的有效變構(gòu)活化劑。
體外研究

Acetyl-coenzyme A (Acetyl-CoA) is a membrane-impermeant molecule constituted by an acetyl moiety (CH3CO) linked to coenzyme A (CoA), a derivative of vitamin B5 and cysteine, through a thioester bond. As thioester bonds are energy rich, the chemical structure of acetyl-CoA facilitates the transfer of the acetyl moiety to a variety of acceptor molecules, including amino groups on proteins.
In most mammalian cells, Acetyl-coenzyme A (Acetyl-CoA) is predominantly generated in the mitochondrial matrix by various metabolic circuitries, namely glycolysis, β-oxidation, and the catabolism of branched amino acids. Cytosolic Acetyl-coenzyme A is the precursor of multiple anabolic reactions that underlie the synthesis of fatty acids and steroids, as well as specific amino acids including glutamate, proline, and arginine.

體內(nèi)研究

Mice deprived of food (but with access to water ad libitum) for 24 hr exhibit a significant reduction in total Acetyl-coenzyme A (Acetyl-CoA) levels in several organs, including the heart and muscles, corresponding to a decrease in protein acetylation levels. However, the same experimental conditions have no major effects on Acetyl-coenzyme A concentrations in the brain and actually increase hepatic Acetyl-coenzyme A and protein acetylation levels. Ethanol intake augments Acetyl-coenzyme A levels in hepatic mitochondria.

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