Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H27NO5 |
Molecular Weight | 361.4321 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)COC1=CC2=C(C=C1)C(C)=C(CCN(CC)CC)C(=O)O2
InChI
InChIKey=KLOIYEQEVSIOOO-UHFFFAOYSA-N
InChI=1S/C20H27NO5/c1-5-21(6-2)11-10-17-14(4)16-9-8-15(12-18(16)26-20(17)23)25-13-19(22)24-7-3/h8-9,12H,5-7,10-11,13H2,1-4H3
DescriptionSources: http://lekarstwo.ru/en/preparati/carbocromenum.htmlCurator's Comment: Description was created based on several sources, including http://adisinsight.springer.com/drugs/800000219
Sources: http://lekarstwo.ru/en/preparati/carbocromenum.html
Curator's Comment: Description was created based on several sources, including http://adisinsight.springer.com/drugs/800000219
Chromonar is a coronary vasodilator agent, it dilates coronary vessels and increases coronary blood flow volume rate, contributes to the development of collateral circulation (with prolonged use), improves metabolic processes in myocardium. The mechanism of action of a role played by its inhibitory effect on phosphodiesterase, accompanied by accumulation in the cells of cyclic 3 ', 5'-adenosine monophosphate. Due to the relatively low therapeutic efficacy Chromonar use is limited, mainly in the early stages of coronary heart disease with angina pectoris in the absence of long-standing and long strokes, when there is no expressed stenotic process.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: WP1884 Sources: http://www.ncbi.nlm.nih.gov/pubmed/947200 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Intensain Approved UseIndications for use: Angina without expressed stenotic process protracted and prolonged attacks, postinfarction period. |
PubMed
Title | Date | PubMed |
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Cardioprotective effects of carbocromen in awake and anesthetized dogs with amitriptyline poisoning. | 1985 Jul-Aug |
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Protective actions of carbocromene against amitriptyline-induced cardiotoxicity in anesthetized rats. | 1986 Jan |
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Intradermal injection vs. oral treatment of tinnitus. | 2001 Jul-Aug |
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Simultaneous determination of cloricromene and its active metabolite in rabbit aqueous humor by high-performance liquid chromatography. | 2002 Feb 5 |
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Effects of cloricromene, a coumarin derivative, on endotoxin-induced uveitis in Lewis rats. | 2003 Mar |
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Preparation and characterization of solid lipid nanoparticles containing cloricromene. | 2003 Oct-Dec |
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In vitro evaluation of PLA nanoparticles containing a lipophilic drug in water-soluble or insoluble form. | 2004 Jun 18 |
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Preparation and characterization of eudragit retard nanosuspensions for the ocular delivery of cloricromene. | 2006 Mar 24 |
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Protective effects of a coumarin derivative in diabetic rats. | 2009 Aug |
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Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-halo-3-phenylcoumarins. | 2010 Jan 12 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://lekarstwo.ru/en/preparati/carbocromenum.html
Inside after food: 0,075 - 0,15 g (1 - 2 tablets) 3 times a day.
In more severe cases, to begin receiving 0.15 g 4 times a day, and after improving the dose is reduced to 0.075 g of 3 - 4 times daily. It is noted that the effect of the drug increases (to 10 - 30th day) and lasts a long time.
Take in a few weeks or months (up to 6 months).
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6279121
In bovine heart mitochondria ho/h-1 ratios in repeated scans increased in presence of carbocromen (20--40 umol/l)
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WHO-ATC |
C01DX05
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NCI_THESAURUS |
C29707
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WHO-VATC |
QC01DX05
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CARBOCROMEN
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804-10-4
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3098
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m3513
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100000084566
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DTXSID60230301
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C79586
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D002866
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212-356-6
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2508
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CHEMBL163672
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DB13279
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)