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152-95-4

中文名稱 槐角苷
英文名稱 Sophoricoside
CAS 152-95-4
分子式 C21H20O10
MDL 編號(hào) MFCD01075138
分子量 432.38
MOL 文件 152-95-4.mol
更新日期 2024/12/20 18:42:03
152-95-4 結(jié)構(gòu)式 152-95-4 結(jié)構(gòu)式

基本信息

中文別名
槐角苷
英文別名
5,7-dihydroxy-3-[4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
GENISTEIN-4'-GLUCOSIDE
GENISTEIN-4'-O-GLUCOSIDE
ISOGENISTIN
SOPHORICOSIDE
4'-beta-D-glucopyranosyloxy-5,7-dihydroxyisoflavone
5,7-Dihydroxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
4H-1-Benzopyran-4-one,3-[4-(β-
D-glucopyranosyloxy)phenyl]-5,7-dihydroxy-
Sophoricoside ,98%
3-[4-(β-D-Glucopyranosyloxy)phenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one
所屬類別
天然產(chǎn)物:黃酮類化合物

物理化學(xué)性質(zhì)

外觀性狀白色結(jié)晶粉末,溶于甲醇,來源于槐角。
熔點(diǎn)298°
比旋光度D20 -47° (pyridine); D20 -32° (10% aq pyridine)
沸點(diǎn)466.08°C (rough estimate)
密度1.3597 (rough estimate)
折射率1.5376 (estimate)
儲(chǔ)存條件under inert gas (nitrogen or Argon) at 2–8 °C
溶解度可溶于水基(輕微)、DMSO(輕微、加熱)、吡啶(輕微、超聲處理)
酸度系數(shù)(pKa)6.45±0.20(Predicted)
形態(tài)固體
顏色白色至淺棕色
最大波長(zhǎng)(λmax)271nm(MeOH)(lit.)
檢測(cè)方法HPLC,NMR
CAS 數(shù)據(jù)庫(kù)152-95-4(CAS DataBase Reference)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302
安全說明22-24/25
海關(guān)編碼29329990

應(yīng)用領(lǐng)域

用途一
升血糖作用;槐角浸羔注射于家兔,能使血糖一時(shí)性增高。據(jù)南京藥物研究所報(bào)道,從槐角中提出的染料木素和山柰酚,具有干擾孕卵運(yùn)輸、終止孕卵著床和抗早期妊娠等作用,可能與其雌性激素活性有關(guān);小量長(zhǎng)期服用染料木素和槐角甙,對(duì)雌性小鼠在不影響交配率和生長(zhǎng)的情況下,有顯著的抗生育作用。毒性作用,槐角浸羔能使家兔及豚鼠的紅細(xì)胞減少,尤以莢果作用為大?;睒浞N子提取液能使兔、豬、人的紅細(xì)胞凝集,種子、莢、果肉均含有抗A、抗B、抗H凝集素;中國(guó)槐為含有植物血凝素類藥物,并具有促進(jìn)淋巴細(xì)胞的轉(zhuǎn)化作用

常見問題列表

概述
現(xiàn)代藥理研究表明,槐角苷對(duì)慢性肝炎病人的降谷丙轉(zhuǎn)氨酶效果良好,還能同時(shí)抑制由巴豆油誘導(dǎo)的耳水腫和角叉菜膠引起的爪水腫。臨床研究也證實(shí),槐角苷可用于防治婦女絕經(jīng)后骨質(zhì)疏松的癥狀。
生物活性
Sophoricoside 是一種從槐花中分離得到的異黃酮糖苷,具有抗炎,抗癌和免疫抑制作用。
體外研究

Sophoricoside is an isoflavone glycoside isolated from Sophora japonica and has anti-inflammatory, anti-cancer and immunosuppressive effects. The results show that Sophoricoside (50 μM) significantly inhibits the PMACI-induced histamine release. The inhibition rate reaches up to 30.24%. The maximal rates of TNF-α, IL-8 and IL-6 inhibition by Sophoricoside (50 μM) are approximately 31.42%, 43.43% and 34.24%, respectively. The rates of the levels of Rel/p65 inhibition in nuclear by Sophoricoside (50 μM) is approximately 50.14%. Results show that the enhanced caspase-1 activity induced by PMACI is significantly reduced by Sophoricoside in a dose-dependent manner.

體內(nèi)研究

When the Sophoricoside is orally administered 1 h before compound 48/80 injections, the scratching behaviors is reduced. The inhibition rate of Sophoricoside (2 mg/kg) is approximately 41.21%. Orally administered Sophoricoside inhibits the scratching behaviors by 47.31%. When mice are treated for 2 weeks with Sophoricoside, the atopic dermatitis is recovered to a significant extent.

槐角苷價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/11/08HY-N0423槐角苷
Sophoricoside
152-95-4100mg900元
2024/11/08HY-N0423槐角苷
Sophoricoside
152-95-410mM * 1mLin DMSO990元
2024/11/08XW080076槐角苷
sophoricoside;5,7-dihydroxy-3-[4-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
152-95-420MG222元
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