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72509-76-3 molecular structure
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3-ethyl 5-methyl (4S)-4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

ChemBase ID: 168875
Molecular Formular: C18H19Cl2NO4
Molecular Mass: 384.25376
Monoisotopic Mass: 383.06911345
SMILES and InChIs

SMILES:
N1C(=C([C@@H](C(=C1C)C(=O)OCC)c1cccc(c1Cl)Cl)C(=O)OC)C
Canonical SMILES:
CCOC(=O)C1=C(C)NC(=C([C@@H]1c1cccc(c1Cl)Cl)C(=O)OC)C
InChI:
InChI=1S/C18H19Cl2NO4/c1-5-25-18(23)14-10(3)21-9(2)13(17(22)24-4)15(14)11-7-6-8-12(19)16(11)20/h6-8,15,21H,5H2,1-4H3/t15-/m0/s1
InChIKey:
RZTAMFZIAATZDJ-HNNXBMFYSA-N

Cite this record

CBID:168875 http://www.chembase.cn/molecule-168875.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
3-ethyl 5-methyl (4S)-4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
IUPAC Traditional name
3-ethyl 5-methyl (4S)-4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
Synonyms
(4R)-4-(2,3-Dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic Acid 3-Ethyl 5-Methyl Ester
(+)-Felodipine
(R)-Felodipine
(R)-(+)-Felodipine
Agon
Feloc
Fensel
Hydac
Modip
Plandil
Plendil
Splendil
Felodipine
CAS Number
72509-76-3
119945-59-4
PubChem SID
162263007
PubChem CID
941699

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 941699 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 3.1918502  LogD (pH = 7.4) 3.436203 
Log P 3.4404075  Molar Refractivity 99.1982 cm3
Polarizability 37.720104 Å3 Polar Surface Area 64.63 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
MSDS Link
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Mechanism of Action
Blocks voltage-dependent calcium currents in vascular smooth muscle and cultured rabbit atrial cells, and blocks potassium-induced contracture of the rat portal vein expand Show data source
By blocking the calcium channels, inhibits the influx of extracellular calcium across the myocardial and vascular smooth muscle cell membranes and expand Show data source
Calcium channel blocker expand Show data source
results in a decrease of peripheral vascular resistance. expand Show data source
Reversibly competes with nitrendipine and other calcium channel blockers for dihydropyridine binding sites expand Show data source
Certificate of Analysis
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Application(s)
Antihypertensive agent expand Show data source
Used to treat hypertension, chronic stable angina pectoris, and Prinzmetal's variant angina expand Show data source
Vasodilator expand Show data source

DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - F232365 external link
A dihydropyridine calcium channel blocker. Enantiomer R of Felodipine.

REFERENCES

REFERENCES

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  • • Haria, M. et al., Drugs, 2000, 59, 141-157, (rev)
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PATENTS

PATENTS

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INTERNET

INTERNET

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