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Dehydroevodiamine

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Dehydroevodiamine Basic information

Product Name:
Dehydroevodiamine
Synonyms:
  • Dehydroevodiamine
  • 14-Methyl-5(7H)-oxo-8,13-dihydroindolo[2',3':3,4]pyrido[2,1-b]quinazoline-14-ium
  • 5,7,8,13-Tetrahydro-14-methyl-5-oxoindolo[2',3':3,4]pyrido[2,1-b]quinazolin-14-ium
  • 8,13-Dihydro-14-methyl-5-oxoindolo[2',3':3,4]pyrido[2,1-b]quinazolinium inner salt
  • 14-Methyl-5-oxo-7,8-dihydro-5H-indolo[2',3':3,4]-pyrido[2,1-b]quinazolin-14-ium-13-ide
  • Indolo[2',3':3,4]pyrido[2,1-b]quinazolinium,8,13-dihydro-14-methyl-5-oxo-, inner salt
  • dehydrovodiamine
  • 14-Methyl-5-oxo-7,8-dihydro-5H-indolo[2',3':3,4]pyrido[2,1-b]quinazolin-14-ium-13-ide
CAS:
67909-49-3
MF:
C19H15N3O
MW:
301.35
EINECS:
200-258-5
Product Categories:
  • reagent
  • standard substance
Mol File:
67909-49-3.mol
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Dehydroevodiamine Chemical Properties

Melting point:
190-192℃
storage temp. 
2-8°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
powder
color 
Yellow
InChI
InChI=1S/C19H15N3O/c1-21-16-9-5-3-7-14(16)19(23)22-11-10-13-12-6-2-4-8-15(12)20-17(13)18(21)22/h2-9H,10-11H2,1H3
InChIKey
VXHNSVKJHXSKKM-UHFFFAOYSA-N
SMILES
O=C1C2C=CC=CC=2[N+](C)=C2C3=C(CCN12)C1C=CC=CC=1[N-]3
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Dehydroevodiamine Usage And Synthesis

Chemical Properties

White crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from dried near-ripe fruit of Evodia sclerosus.

Uses

Dehydroevodiamine is a novel alkaloid which displays butyrylcholinesterase inhibitory activity in vivo.

Biological Activity

Dehydroevodiamine, a quinazoline alkaloid isolated from Evodiae Fructus, has antiarrhythmic effects on guinea pig ventricular myocytes. It inhibits LPS-induced expression of iNOS, COX-2, PGE2 and NF-κB in mouse macrophages.

Physiological effects

Dehydroevodiamine has an antihypertensive and antitumor effects.

in vitro

Dehydroevodiamine (0-50 μM; 2 hours) inhibits iNOS and COX-2 expression and prevents degradation of IκB-α in LPS induced RAW 264.7 macrophages. Dehydroevodiamine (0-50 μM; 2 hours) inhibits a LPS -induced increase in the iNOS and COX-2 mRNA expression.

Western Blot Analysis

Cell Line:

td>
RAW 264.7 macrophage cells
Concentration: 10 μM, 30 μM, 50 μM
Incubation Time: pretreated 2 hours
Result: Reduced iNOS and COX-2 expression and increased IκB-α expression.

RT-PCR

< td class="col1"> Cell Line: td>
RAW 264.7 macrophage cells
Concentration: 10 μM, 30 μM, 50 μM
Incubation Time: pretreated 2 hours
Result: Reduced iNOS and COX-2 mRNA expression.

target

TargetValue
NF-κB
()
COX-2
()
iNOS
()
PGE2
()

DehydroevodiamineSupplier

Chengdu Peter-like Biotechnology Co., Ltd. Gold
Tel
18108052721
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2850505130@qq.com
Adamas Reagent, Ltd.
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400-6009262 16621234537
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chenyj@titansci.com
ShangHai YuanYe Biotechnology Co., Ltd.
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021-61312847 13636370518
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shyysw007@163.com
Chengdu Climax Biotech Co., Ltd.
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028-83311324 1278112614
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climaxbiotech@gmail.com
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66113011 17798518460
Email
cfzhang@aikonchem.com