Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H20N2O7 |
Molecular Weight | 388.3713 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=C(C)NC(C)=C(C1C2=C(C=CC=C2)[N+]([O-])=O)C(=O)OCC(C)=O
InChI
InChIKey=NCUCGYYHUFIYNU-UHFFFAOYSA-N
InChI=1S/C19H20N2O7/c1-10(22)9-28-19(24)16-12(3)20-11(2)15(18(23)27-4)17(16)13-7-5-6-8-14(13)21(25)26/h5-8,17,20H,9H2,1-4H3
Molecular Formula | C19H20N2O7 |
Molecular Weight | 388.3713 |
Charge | 0 |
Count |
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Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionCurator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/15992104
Curator's Comment: description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/15992104
Aranidipine (INN, trade name Sapresta) is a calcium channel blocker. Calcium channel antagonists have become popular medications for the management of hypertension. These agents belong to the diphenylalkylamine, benzothiazepine, dihydropyridine, or tetralol chemical classes. Although the medications share a common pharmacological mechanism in reducing peripheral vascular resistance, clinical differences between the sub-classes can be linked to structural profiles. This heterogeneity is manifested by differences in vascular selectivity, effects on cardiac conduction and adverse events. The lack of differentiation between calcium channel antagonists in clinical trials has contributed to uncertainty associated with their impact on morbidity and mortality. Administartion of aranidipine once daily had a high potent antihypertensive effect and clinical utility in all the clinical trials conducted in Japan. Aranidipine is now under registration.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2363032 Sources: http://www.ncbi.nlm.nih.gov/pubmed/7582390 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/24314165
5 mg/d for 4 weeks
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/10940777
In myocytes, aranidipine (10 nmol/l to 1 uM) concentration-dependently decreased T-type and L-type Ca(2+) currents. In the sinoatrial node, 0.1 uM aranidipine increased cycle length, and decreased +V(max) and the slope of the phase 4 depolarization
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:34:12 GMT 2023
by
admin
on
Fri Dec 15 15:34:12 GMT 2023
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Record UNII |
4Y7UR6X2PO
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C333
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86780-90-7
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m2026
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C73022
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2225
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SUB05550MIG
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CHEMBL2104030
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C059427
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ARANIDIPINE
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4Y7UR6X2PO
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100000087185
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |