CasImg
荷叶碱 , 来源于荷叶
产品纠错
CAS号:475-83-2 | 英文名称:Nuciferine, from Lotus Leaf
分子式
分子量
EINECS号
MDL
Smiles
InChIKey
乙二醇化学百科
基本信息
中文名称 荷叶碱
英文名称 NUCIFERINE
CAS号 475-83-2
分子式 C19H21NO2
分子量 295.38
EINECS号 618-170-5
物化性质
熔点 165.5°C
沸点 437.06°C (rough estimate)
密度 1.1156 (rough estimate)
折射率 1.5000 (estimate)
LogP 2.357 (est)
溶解度 DMSO : 11.11 mg/mL (37.61 mM; 需要超声波)H2O : < 0.1 mg/mL (不溶)
形态 粉末
酸度系数(pKa) 7.87±0.20(Predicted)
颜色 白色至米色
旋光性 (optical activity) [α]/D -145 to -165°, c = 0.5 in ethanol
安全信息
安全说明 24/25
危险品运输编号 UN 1544PSN1 6.1 / PGIII
海关编码 29389090
毒性 LD50 orl-rat: 280 mg/kg AIPTAK 197,261,72
生产及用途
荷叶碱是从睡莲科植物莲的干燥叶中提取的一种阿朴啡型生物碱,为荷叶中的主要降脂活性成分,以晒干粉碎的荷叶为原料,采用纤维素酶预处理、稀盐酸浸提、超声波辅助提取、氯仿萃取一系列方法提取而成。
中医学认为,荷叶性味苦涩,平,归肝、脾、胃、心经。有清暑利湿、升发清阳、凉血止血等功效。荷叶的主要化学成分有荷叶碱、柠檬酸、草酸等,起主要减肥作用的是荷叶碱,药理研究表明,荷叶具有利尿通便、通肠毒、降脂除油、清暑解热等作用,能明显降低血清中甘油三醇和胆固醇含量,具有调节血脂的保健作用。采用荷叶减肥不需要刻意节食,对人体无任何副作用。Nuciferine 是一种 5-HT2A,5-HT2C 和 5-HT2B 拮抗剂,IC50 分别为 478 nM,131 nM 和 1 μM;也是 5-HT7 的反向激动剂,IC50 为 150 nM。

5-HT 2C Receptor

131 nM (IC 50 )

5-HT 7 Receptor

150 nM (IC 50 )

5-HT 2A Receptor

478 nM (IC 50 )

5-HT 2B Receptor

1 μM (IC 50 )

5-HT 6 Receptor

700 nM (EC 50 )

5-HT 1A Receptor

3.2 μM (EC 50 )

D 2 Receptor

64 nM (EC 50 )

D 4 Receptor

2 μM (EC 50 )

D 5 Receptor

2.6 μM (EC 50 )

Nuciferine is a partial agonist at DD 2 receptor with an activity (E max =67% of dopamine) similar to aripiprazole (E max =50% of dopamine). In line with its partial agonist activity, Nuciferine inhibited dopamine-induced activation of G i with a potency similar to clozapine (Nuciferine K B =62 nM; Clozapine K B =20 nM) as determined via Schild regression analysis. The natural product Nuciferine acts as an effective inhibitor of adult worm motility. Nuciferine is effective at inhibiting both basal and 5-HT evoked motility of adult schistosomes. Nuciferine inhibits Sm.5HTR L and schistosomule with 0.24±0.04 and 0.62±0.22 μM, respectively.

In rodent models relevant to antipsychotic drug action, Nuciferine blocks head-twitch responses and discriminative stimulus effects of a 5-HT 2A agonist, substituted for clozapine discriminative stimulus, enhanced amphetamine induced locomotor activity, inhibited phencyclidine (PCP)-induced locomotor activity, and rescued PCP-induced disruption of prepulse inhibition without induction of catalepsy. In the presence of 1 or 3 mg/kg Nuciferine, cumulative PCP doses produce similar substitution to PCP alone. In the clozapine-trained animals, a dose-dependent substitution for 1.25 mg/kg clozapine is seen at 10 mg/kg Nuciferine (80.63% drug lever responding), with an ED 50 value of 5.42 mg/kg (95% CI 3.09-9.48 mg/kg) while the lower doses tested (0.1 mg/kg-3 mg/kg) fails to produce substitution for clozapine’s discriminative cue. In addition to a high percentage of responding on the clozapine-appropriate lever, 10 mg/kg Nuciferine also produces significant rate suppression as compared to vehicle control points (p<0.001).

化学性质 
易溶于苯、乙醚、氯仿、卤代烷烃等极性较低的有机溶剂,在丙酮、乙醇等亲水性有机溶剂中也有较好的溶解度,而在水中溶解度较小或几乎不溶 来源于睡莲科植物莲的干燥叶
用途 
用于含量测定/鉴定/药理实验等
药理药效:具有减肥降脂的作用。
用途 
清热解暑,升发清阳,凉血止血。
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产品供应商
Nuciferine
询价
上海阿拉丁生化科技股份有限公司
2023-10-02

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