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L-Tetrahydropalmatine hydrochloride is a chemical compound belonging to the tetrahydroprotoberberine class, traditionally used in Chinese medicine for its potential therapeutic effects on neurological and psychiatric disorders. It exhibits analgesic, anxiolytic, and sedative properties and is being studied for its potential in treating anxiety, depression, and substance abuse disorders by modulating neurotransmitter systems in the brain.

2506-20-9

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2506-20-9 Usage

Uses

Used in Pharmaceutical Industry:
L-Tetrahydropalmatine hydrochloride is used as a therapeutic agent for neurological and psychiatric disorders due to its analgesic, anxiolytic, and sedative properties.
Used in Treatment of Drug Addiction and Withdrawal:
L-Tetrahydropalmatine hydrochloride is used as an alleviating agent for symptoms of drug addiction and withdrawal, potentially aiding in the management of substance abuse disorders.
Used in Research and Development:
L-Tetrahydropalmatine hydrochloride is used as a subject of ongoing research for its potential as a treatment for conditions such as anxiety, depression, and substance abuse disorders, with its effects on neurotransmitter systems in the brain being a key area of investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 2506-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2506-20:
(6*2)+(5*5)+(4*0)+(3*6)+(2*2)+(1*0)=59
59 % 10 = 9
So 2506-20-9 is a valid CAS Registry Number.

2506-20-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Tetrahydropalmatinehydrochloride

1.2 Other means of identification

Product number -
Other names L-TETRAHYDROPALMATINE HYDROCHLORIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2506-20-9 SDS

2506-20-9Upstream product

2506-20-9Downstream Products

2506-20-9Relevant academic research and scientific papers

Bioactive isoquinoline alkaloids from Corydalis saxicola

Huang, Qiao-Qin,Bi, Jun-Long,Sun, Qian-Yun,Yang, Fu-Mei,Wang, Yue-Hu,Tang, Gui-Hua,Zhao, Fu-Wei,Wang, Huan,Xu, Jin-Jin,Kennelly, Edward J.,Long, Chun-Lin,Yin, Ge-Fen

experimental part, p. 65 - 70 (2012/06/18)

Twelve isoquinoline alkaloids including two new nitro-containing tetrahydroprotoberberines, (-)-2,9-dihydroxyl-3,11-dimethoxy-1,10- dinitrotetrahydroprotoberberine (1) and (+)-4-nitroisoapocavidine (2), were isolated from the whole plant of Corydalis saxicola Bunting. The structures of the new compounds were established by spectroscopic analysis and chemical evidence. The inhibitory activity of these isolates against cholinesterase and canine parvovirus were evaluated. Compounds 1 and 1a, (+)-1-nitroapocavidine (5), berberine (8), palmatine (9), dehydrocavidine (10), and sanguinarine (11) showed potent inhibitory activity against acetylcholinesterase with IC 50 values of less than 10M, while only compound 1 possessed weak activity against canine parvovirus. Structure-activity studies demonstrated that the nitro substituents at ring A in the tetrahydroprotoberberines led to an increase in the anti-acetylcholinesterase activity.

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