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Home > Encyclopedia > Chelidonic acid

Chelidonic acid

pharmaceutical raw materials
Chelidonic acid structure

Chelidonic acid 

structure
  • CAS No:

    99-32-1

  • Formula:

    C7H4O6

  • Chemical Name:

    Chelidonic acid

  • Synonyms:

    4H-Pyran-2,6-dicarboxylic acid,4-oxo-;Chelidonic acid;4-Oxo-4H-pyran-2,6-dicarboxylic acid;Jerva acid;Jervaic acid;Jervasic acid;4-Oxo-1,4-pyran-2,6-dicarboxylic acid;γ-Pyrone-2,6-dicarboxylic acid;2,6-Dicarboxy-4-pyrone;4-Pyranone-2,6-dicarboxylic acid;NSC 3979

  • Categories:

    Biochemical Engineering  >  Plant Extracts

Description

Chelidonic acid is a component of Chelidonium majus L., used as a mild analgesic, an antimicrobial, an acentral nervous system sedative. Chelidonic acid also shows anti-inflammatory activity. Chelidonic acid has potential to inhibit IL-6 production by blocking NF-κB and caspase-1[1]. Chelidonic acid is a glutamate decarboxylase inhibitor, with a Ki of 1.2 μM[2].


Chelidonic acid is a carbonyl compound and a member of pyrans.

Chelidonic acid Basic Attributes

184.1

184.10

202-749-0

T33U4W5K6O

3979

DTXSID30243928

2932999099

Characteristics

101

-0.4

1.571 g/cm3

262 °C

204.1ºC

14.3g/L(25 ºC)

Safety Information

NONH for all modes of transport

3

36/37/38

26-36

UP7350000

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

chelidonic acid

Chelidonic acid Use and Manufacturing

Methods of Manufacturing

From the reaction of diethyl oxalate and acetone.

Uses

Used in organic synthesis.

Computed Properties

Molecular Weight:184.10
XLogP3:-0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:184.00078784
Monoisotopic Mass:184.00078784
Topological Polar Surface Area:101
Heavy Atom Count:13
Complexity:316
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

It has a significant inhibitory effect on pain and can inhibit inflammatory responses. It has a certain sedative effect on mice. When used in combination with cyclophosphamide, it can increase the tumor inhibition rate and prolong survival time. It has no tolerance and physical dependence.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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