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延胡索甲素

(+)- Corydaline

CAS: 518-69-4

Molecular Formula: C22H27NO4

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延胡索甲素 - Names and Identifiers

Name (+)- Corydaline
Synonyms Corydalis A
d-Corydaline
(13s-e)-thyl
(+)- Corydaline
2,3,9,10-tetramethoxy-13-methyl-berbin
2,3,9,10-TetraMethoxy-13-Methylberbine, 8CI
2,3,9,10-tetramethoxy-13-alpha-methyl-13a-beta-berbin
6h-dibenzo(a,g)quinolizine,5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-13-me
[7S,13S,13aR,(+)]-5,8,13,13a-Tetrahydro-2,3,9,10-tetramethoxy-13-methyl-6H-dibenzo[a,g]quinolizine
CAS 518-69-4
InChIKey VRSRXLJTYQVOHC-YEJXKQKISA-N

延胡索甲素 - Physico-chemical Properties

Molecular FormulaC22H27NO4
Molar Mass369.45
Density1.1771 (rough estimate)
Melting Point135°
Boling Point499.57°C (rough estimate)
Specific Rotation(α)D20 +311° (c = 0.8 in alc)
Solubility Soluble in chloroform, soluble in ether, slightly soluble in methanol, actually insoluble in water.
Appearanceprism crystallization
ColorWhite to Off-White
pKa6.57±0.40(Predicted)
Storage Condition2-8°C(protect from light)
Refractive Index1.5614 (estimate)
MDLMFCD00065280
Physical and Chemical PropertiesWhite crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, from Corydalis tubers, Corydalis Koizumi whole grass, deep mountain Corydalis root, Marcha Corydalis tubers and aboveground parts.

延胡索甲素 - Risk and Safety

ToxicityLD50 in mice (mg/kg): 135.5 ± 12.8 i.v. (Anderson, Chen)

延胡索甲素 - Reference

Reference
Show more
1. Antrum Zenghua, du Lianping. Simultaneous determination of six components in compound yuanhu Zhitong tablets by HPLC [J]. Chinese patent medicine 2017 39(02):312-315.
2. Zhang Dan, Wang Chang-Li, ji diao, et al. Simultaneous determination of five alkaloids in Corydalis yanhusuo by HPLC [J]. Central South pharmacy, 2018, 16(12):1759-1762.
3. Li can, Tang Lijun, Ru Qin, etc. Study on the fingerprint of detoxification drug 1 by high performance liquid chromatography [J]. Journal of Jianghan University (Natural Science Edition), 2018, 46(05):471-476.
4. Zhang, Y., wang, Z., xu, J. et al. Optimization of the extraction and purification of Corydalis yanhusuo W.T. Wang based on the Q-marker uniform design method. BMC Chemistry 14, 9 (2020). https://doi.org/10.1186/s13065-020-00666-6
5. [IF=4.759] Lvhuan Wang et al."Online screening of acetylcholinesterase inhibitors in natural products using monolith-based immobilized capillary enzyme reactors combined with liquid chromatography-mass spectrometry."J Chromatogr A. 2018 Aug;1563:135
6. [IF=4.411] Simona S. Ghanem et al."Natural Alkaloid Compounds as Inhibitors for Alpha-Synuclein Seeded Fibril Formation and Toxicity."Molecules. 2021 Jan;26(12):3736
7. [IF=3.963] Zhong-min Zhao et al."Anti-phytopathogenic activity and the possible mechanisms of action of isoquinoline alkaloid sanguinarine."Pestic Biochem Phys. 2019 Sep;159:51
8. [IF=3.373] Xueyan Zhao et al."An integrated strategy for the establishment of a protoberberine alkaloid profile: Exploration of the differences in composition between Tinosporae radix and Fibraurea caulis."Phytochem Analysis. 2021 Nov;32(6):1131-1140

延胡索甲素 - Reference Information

1.23 µm (Omega-opiid receptor)
Overview Corydalis yanhusuo (Corydalis yanhusuo) is a quaternary amine alkaloid. T.Wang) one of the main active ingredients in tubers. Modern pharmacology shows that Corydalis a not only has analgesic, exciting uterus, anti-arrhythmic effect, Corydalis A has anti-morphine-like effect, can also be used for the preparation of drug detoxification.
Application of Corydalis a can effectively inhibit Virus of the replication of the respiratory tract in a non-toxic range, it can be further developed into a drug for treating or preventing Virus respiratory diseases, and has a wide application prospect.
biological activity Corydaline (( )-Corydaline) is an isoquinoline alkaloid extracted from Corydalis yanhusuo, it is an AChE inhibitor with an IC50 of 226 μm. Corydaline is a μ-opioid receptor (Ki 1.23 µm) agonist that inhibits intestinal Virus 71 (EV71) replication (IC50 25.23 µm). Corydaline has anti-angiogenic, anti-allergic, gastric emptying and antinociceptive effects.
Target IC50: 226 µm (AChE); 25.23 µm (Enterovirus 71) Ki:
Cell Line: Vero cells infected with EV71
Concentration: 12.5 µM, 25 µM, 50 µM
Incubation Time: 24 hours
Result: Reduced the phosphorylation of P38 MAPK and JNK MAPK and the expression of COX-2.
Showed antinociceptive effects in mice.
Animal Model: Male CD1 mice (30-35 g, 7-8 weeks old) injected with acetic acid
Dosage: 10 mg/kg
Administration: Subcutaneous administration; once
Use Corydalis a analgesic, sedative, hypnotic effect.
for content determination/identification/pharmacological experiments. Pharmacological Efficacy: analgesic effect.
Last Update:2024-04-09 20:52:54
延胡索甲素
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Mobile: +8618958170122
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SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
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Product Name: (+)- Corydaline Visit Supplier Webpage Request for quotation
CAS: 518-69-4
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
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Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: Corydaline Visit Supplier Webpage Request for quotation
CAS: 518-69-4
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Yuanye Bio-Technology Co., Ltd.
Multiple SpecificationsSpot supply
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CAS: 518-69-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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延胡索甲素
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