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Corydaline, a natural alkaloid derived from the plant Corydalis, is known for its analgesic properties and potential anti-angiogenic effects. It is widely used in traditional Chinese medicine for its therapeutic benefits.

518-69-4

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518-69-4 Usage

Uses

Used in Traditional Chinese Medicine:
Corydaline is used as an analgesic for [relieving pain] due to its natural pain-relieving properties.
Used in Anticancer Applications:
Corydaline is used as an anti-angiogenic agent for [inhibiting the growth of new blood vessels in tumors], which can help in slowing down the progression of cancer.
Used in Pharmaceutical Industry:
Corydaline is used as a key ingredient in the development of new drugs for [treating pain and potentially cancer] due to its analgesic and anti-angiogenic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 518-69-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 518-69:
(5*5)+(4*1)+(3*8)+(2*6)+(1*9)=74
74 % 10 = 4
So 518-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO4/c1-13-15-6-7-18(24-2)22(27-5)17(15)12-23-9-8-14-10-19(25-3)20(26-4)11-16(14)21(13)23/h6-7,10-11,13,21H,8-9,12H2,1-5H3

518-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name corydaline

1.2 Other means of identification

Product number -
Other names (13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline

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:518-69-4 SDS

518-69-4Relevant academic research and scientific papers

Three-Step Catalytic Asymmetric Total Syntheses of 13-Methyltetrahydroprotoberberine Alkaloids

Zhou, Shiqiang,Tong, Rongbiao

, p. 1594 - 1597 (2017/04/13)

(S,R)-N-PINAP was identified to be the chiral ligand for highly enantioselective CuI-catalyzed reaction of tetrahydroisoquinolines (THIQs), alkynes, and 2-bromobenzaldehyde derivatives. This enables us to accomplish the first asymmetric total synthesis of 12 natural 13-methyltetrahydroprotoberberine (13-MeTHPB) alkaloids in only three catalytic steps with 47-64% overall yields. In addition, the Pd-catalyzed reductive Heck cyclization was successfully extended to three Pd-catalyzed domino reactions (Heck/Suzuki, Heck/Sonogashira, and Heck/Heck), which greatly expands the synthetic utility of this catalytic strategy and allows expeditious access to 13-substituted tetrahydroprotoberberines for further bioactivity evaluation.

CORYDALINE DERIVATIVES USEFUL FOR REDUCING LIPID LEVELS

-

Page/Page column 62, (2010/07/09)

The present technology relates to compounds of Formulas (V) and (VI) and methods of making and using such compounds. Methods of use include prevention and treatment of hyperlipidemia, hypercholesterolemia, hypertriglyceridemia, hepatic steatosis, and metabolic syndrome. Compounds disclosed herein also lower total cholesterol, LDL- cholesterol, and triglycerides and increase hepatic LDL receptor expression, inhibit PCSK9 expression, and activate AMP-activated potein kinase.

STEREOCHEMICAL CHARACTERISTICS OF SET-PROMOTED PHOTOCHEMICAL REACTIONS OF DIHYDROISOQUINOLINIUM SALTS

Cho, In-Seop,Chang, Shirley S. S.,Ho, Chihmei,Lee, Chao-Pin,Ammon, Herman L.,Mariano, Patrick S.

, p. 2161 - 2192 (2007/10/02)

Single electron transfer (SET) promoted photocyclisation reactions of a series of silylbenzyl- and silylalkenyl-dihydroisoquinolinium perchlorates have been explored in order to evaluate the extent and source of stereochemical control in these N-heterocycle forming, diradical cyclization processes.

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