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476-28-8

中文名稱 石蒜堿鹽酸鹽
英文名稱 LYCORINE
CAS 476-28-8
分子式 C16H17NO4
分子量 287.31
MOL 文件 476-28-8.mol
更新日期 2024/11/05 11:02:39
476-28-8 結(jié)構(gòu)式 476-28-8 結(jié)構(gòu)式

基本信息

中文別名
水仙鹼
石蒜鹼
石蒜堿
石蒜堿標(biāo)準(zhǔn)品
石蒜堿鹽酸鹽
石蒜堿 HPL
石蒜堿(水仙堿)
石蒜提取物.石蒜堿
LYCORINE 石蒜堿
英文別名
LYCORIN
LYCORINE
Amaryline
Belamarine
amarylline
narcissine
NSC 401360
NSC 683873
LYCORINE HCL
(-)-LYCORINE
所屬類別
原料藥:抗阿米巴病及抗滴蟲病藥

物理化學(xué)性質(zhì)

外觀性狀棱形大結(jié)晶。熔點275-280℃(分解)。溶于稀酸,難溶于醇、氯仿和石油醚,幾乎水溶于水和堿類,對石蕊呈堿性反應(yīng)。其鹽酸鹽為長針狀結(jié)晶,熔點217℃(分解),帶一分子結(jié)晶水的石蒜堿鹽酸鹽的熔點為206℃??扇苡?0份水。
熔點253-255℃ (dec.)
比旋光度D16 -129° (c = 0.16 in 98% alc)
沸點429.61°C (rough estimate)
密度1.53
折射率1.5500 (estimate)
儲存條件2-8°C
溶解度Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
酸度系數(shù)(pKa)13.55±0.40(Predicted)
形態(tài)powder
顏色White to off-white

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS06
警示詞危險
危險性描述H301
危險品標(biāo)志T
危險類別碼25
安全說明45
危險品運輸編號UN 2811 6.1/PG 3
WGK Germany3

應(yīng)用領(lǐng)域

用途1
石蒜堿經(jīng)口給藥或皮下注射有流涎、亞心及增加氣管分泌的作用,故在一些時候曾用其制劑作祛痰劑。石蒜堿有較顯著的催吐作用。效力比吐根堿強,但不如阿相嗎啡。石蒜堿經(jīng)氫化后生成二氫石蒜堿,后者具有較強的抗阿米巴痢的作用,且毒較小,已供臨床使用。石蒜堿制成的內(nèi)胺鹽在動物上表現(xiàn)出抗種瘤作用。中藥鐵色箭、烏蒜具有祛痰催葉作用,其原因是含有石蒜堿。

制備方法

方法1
該品是廣泛存在于石蒜科植物中的異喹啉生物堿,可從石蒜(Lycoris radiata)等的鱗莖中提取。

上下游產(chǎn)品信息

上游原料
異喹啉

常見問題列表

生物活性
Lycorine 是從金眼科植物科中提取的天然生物堿。Lycorine 是強效具有口服活性的 SCAP?抑制劑,Kd 值 15.24 nM。Lycorine 下調(diào) SCAP 蛋白水平而不改變其轉(zhuǎn)錄。Lycorine 也是黑色素瘤血管生成抑制劑。Lycorine 有潛力用于前列腺癌和代謝疾病的研究。
靶點

Kd: 15.24 nM (SCAP)

體外研究

Lycorine inhibits cell proliferation in a dose-dependent manner in the abovementioned 4 PCa cell lines, and the IC 50 ranged from 5 μM to 10 μM., it also shows Lycorine has little effects on PNT1A cell's proliferation.SCAP (SREBF chaperone) is an ER-toGolgi transport protein, undergoes a conformational change, and regulates/preserves SREBFs in the ER by forming a complex with INSIG1 (insulin induced gene 1).Lycorine (5-40 μM; 16 hours) significantly suppresses SREBFs activity (up to -70%) in a dosedependent manner and does not cause obvious cytotoxicity in cells.Lycorine (10-20 μM; 2-16 hours) dose- and time-dependently decreases the mature SREBF1 and SREBF2 proteins in HL-7702 cells.Lycorine (20 μM; 16 hours) neither activates NR1H3 transcription nor affect NR1H3 target genes, including ABCG5 and ABCG8, but Sterols activates NR1H3 transcription activity.Lycorine hydrochloride (0-25 μM; 48 hours) treatment markedly suppresses the expression of vascular endothelial (VE)-cadherin in a dose-dependent manner and also slightly diminishes the expression of Sema4D in C8161 cells. However, the expression of the other six genes is not affected.Lycorine hydrochloride (0-25 μM; 48 hours) treatment markedly reduces VE-cadherin protein levels in C8161 cells in a dose-dependent fashion.

Cell Viability Assay

Cell Line: HL-7702/SRE-Luc cells
Concentration: 16 hours
Incubation Time: 5 μM; 10 μM; 20 μM; 40 μM
Result: Had no cytotoxicity on HL-7702 cells.

Western Blot Analysis

Cell Line: HL-7702/SRE-Luc cells
Concentration: 2 hours, 4 hours, 8 hours, 12 hours, 16 hours
Incubation Time: 10 μM; 20 μM
Result: Decreased p-SREBF1, m-SREBF1, p-SREBF2 and p-SREBF1 protein expression.

RT-PCR

Cell Line: C8161 cells
Concentration: 0 μM, 1.56 μM, 3.13 μM, 6.25 μM, 12.5 μM, 25 μM
Incubation Time: 48 hours
Result: Markedly suppressed the expression of VE-cadherin in a dose-dependent manner and also slightly diminished the expression of Sema4D in C8161 cells.
體內(nèi)研究

Lycorine (oral chow; 15 mg/kg, 30 mg/kg; once daily) alleviates fat accumulation and metabolic syndrome, increases lipolysis and betaoxidation of fatty acid along with precursor and mature SREBFs in mice .

Animal Model: High-fat diet (HFD)-fed C57BL/6J mice
Dosage: 15 mg/kg, 30 mg/kg
Administration: Oral chow; once daily
Result: Ameliorated high-fat diet-induced hyperlipidemia, hepatic steatosis, and insulin resistance in mice.
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