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96574-01-5

中文名稱 丹酚酸 A
英文名稱 Salvianolic acid
CAS 96574-01-5
分子式 C26H22O10
分子量 494.45
MOL 文件 96574-01-5.mol
更新日期 2024/12/24 09:24:12
96574-01-5 結(jié)構(gòu)式 96574-01-5 結(jié)構(gòu)式

基本信息

中文別名
丹參酚酸A
丹酚酸 A
丹酚酸A對照品,
丹酚酸A(標(biāo)準(zhǔn)品)
丹酚酸A(丹參酚酸A)
丹參酚酸A, 來源于丹參根莖
SALVIANOLIC ACID A 丹酚酸A
(R)-3-(3,4-二羥基苯基)-2-((E)-3-(2-((E)-3,4-二羥基苯乙烯基)-3,4-二羥基苯基)丙烯?;?氧基)丙酸
(2R)-3-(3,4-二羥基苯基)-2-[(E)-3-[2-[(E)-2-(3,4-二羥基苯基)乙烯基]-3,4-二羥基苯基]丙-2-烯酰]氧丙酸
英文別名
SALVIANOLIC ACID
Danphenolic acid A
SALVIANOLIC ACID A
Salvianolic acid A, >=98%
Salvianolic acid A hydrate
Dan phenolic acid A hydrate
Salvianolic acid A 96574-01-5
SALVIANOLIC ACID A 98.0% BY HPLC
Salvianolic acid A, froM Salvia Miltiorrhiza
Salvianolic acid A, 98%, from Salvia miltiorrhiza Bunge
所屬類別
生物化工:提取物

物理化學(xué)性質(zhì)

外觀性狀黃色針狀結(jié)晶,可溶于甲醇、乙醇、DMSO等有機(jī)溶劑,來源于丹參根莖。
熔點(diǎn)164-167°C
沸點(diǎn)858.7±65.0 °C(Predicted)
密度1.580±0.06 g/cm3(Predicted)
儲存條件2-8°C
溶解度在水中的溶解度為≥19mg/mL
酸度系數(shù)(pKa)2.78±0.10(Predicted)
形態(tài)粉末
顏色黃色
BRN2660108
InChIKeyYMGFTDKNIWPMGF-UCPJVGPRSA-N

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
安全說明24/25
WGK Germany3
海關(guān)編碼29189900

應(yīng)用領(lǐng)域

用途1
用于含量測定/鑒定/藥理實(shí)驗(yàn)等。
藥理藥效:抗凝血作用和顯著的抗血小板聚集作用,抗分泌和抗?jié)冏饔玫取?/span>
用途2
丹酚酸A適用于心絞痛及急性心肌梗塞,腦血栓形成的后遺癥。

常見問題列表

生物活性
Salvianolic acid A 可通過抑制基質(zhì)金屬鈦酶 9 (MMP-9) 和抗炎作用來保護(hù)血腦屏障。
靶點(diǎn)

MMP-9

體內(nèi)研究

A significant beneficial effect of Salvianolic acid A (SAA) is observed in the Salvianolic acid A treatment groups. Salvianolic acid A (20 mg/kg) could significantly prolonged the retention time of rats on the plate. While compared with sham operation group, the brain water content in model group significantly increases, which is attenuated significantly by Salvianolic acid A (10 and 20 mg/kg). Compared with the model group, Salvianolic acid A (5, 10, and 20 mg/kg) could maintain the normal structures of neurons and increase neurons number. It is also found that Salvianolic acid A (20 mg/kg) could significantly reduce I/R induced MMP-9 upregulation. While the MMP-2 expression is not significantly affected by Salvianolic acid A. Tissue inhibitors of metalloproteinases (TIMPs) could inhibit the activity of MMPs through high affinity binding to MMPs catalytic domain.

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