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142741-24-0

中文名稱 CONOPHYLLINE
英文名稱 Cophylline
CAS 142741-24-0
分子式 C44H50N4O10
分子量 794.9
MOL 文件 142741-24-0.mol
更新日期 2025/10/17 11:59:05
142741-24-0 結(jié)構(gòu)式 142741-24-0 結(jié)構(gòu)式

基本信息

中文別名
長春堿衍生物
長春花堿 III-121C
長春花生物堿III-121C
英文別名
Cophylline
Vinca alkaloid III-121C
[8,15'-Biaspidospermidine]-3,3'-dicarboxylicacid,2,2',3,3'-tetradehydro-6',7':7,16'-diepoxy-6,15-dihydroxy-16,17-dimethoxy-,dimethyl ester, (5a,6b,7a,8a,12R,19a)-(5'a,6'b,7'b,12'R,19'a)-
[8,15'-Biaspidospermidine]-3,3'-dicarboxylic acid, 2,2',3,3'-tetradehydro-6',7':7,16'-diepoxy-6,15-dihydroxy-16,17-dimethoxy-, dimethyl ester, (5α,6β,7α,8α,12R,19α)-(5'α,6'β,7'β,12'R,19'α)-
所屬類別
天然產(chǎn)物:生物堿

物理化學性質(zhì)

密度1.53±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
酸度系數(shù)(pKa)10.73±0.70(Predicted)
形態(tài)Solid
顏色Off-white to light yellow
CONOPHYLLINE價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/06/05HY-N3619CONOPHYLLINE
Conophylline
142741-24-01 mg6500元

常見問題列表

生物活性
Conophylline 是一種從熱帶植物 Ervatamia microphylla 中提取的長春花生物堿。Conophylline 是胰腺細胞分化的誘導(dǎo)劑。Conophylline 能抑制 HSC,誘導(dǎo)其凋亡。
體外研究

Conophylline (100 ng/ml; 48 hours) reproduces differentiationinducing activity but not apoptosis-inducing activity of activin.
Conophylline (100 ng/ml; 72 hours) exhibits the differentiation-inducing activity in AR42J cells and converts these cells to endocrine cells.
Conophylline increases the expression of neurogenin-3 by activating p38 mitogen-activated protein kinase to induce differentiation of AR42J cells.
Conophylline reduces the expression of α-SMA and collagen-1 in rat HSC and Lx-2 cells.
Conophylline inhibits DNA synthesis induced by serum.
Conophylline also promots activation of caspase-3 and induces apoptosis in Lx-2 Cells.

Apoptosis Analysis

Cell Line: Lx-2 Cells
Concentration: 12 hours
Incubation Time: 0.1 μg/ml
Result: Induced apoptosis

Western Blot Analysis

Cell Line: Lx-2 cells
Concentration: 0.1 μg/ml
Incubation Time: 15 minutes, 30 minutes, 60 minutes, 120 minutes
Result: Increased phospho-JNK.
體內(nèi)研究

Conophylline (0.9 mg/kg; p.o.; daily; for 12 weeks) attenuates formation of the liver fibrosis induced by TAA in vivo.

Animal Model: Sprague-Dawley rats (70-80 g)
Dosage: 0.9 mg/kg
Administration: Oral administration; daily; for 12 weeks
Result: Attenuated formation of the liver fibrosis induced by TAA.
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