Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H14O3 |
Molecular Weight | 242.2699 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(C(=O)OCC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=JFKWZVQEMSKSBU-UHFFFAOYSA-N
InChI=1S/C15H14O3/c16-14(13-9-5-2-6-10-13)15(17)18-11-12-7-3-1-4-8-12/h1-10,14,16H,11H2
Benzyl mandelate is of comparatively low toxicity on the one hand and is pharmacologically effective on the other hand. The most important pharmacological action of the drug is on smooth muscle. Benzyl mandelate has been used for its antispasmodic actions. It has also been included in preparations with analgesics in an attempt to increase the analgesic effect. Drugs with benzyl maleate were indicated for the angina prevention and for pain condition treatment.
Originator
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: http://www.catalog.md/drugs/spasmocor.html |
Preventing | Spasmocor Approved UseSpasmocor is indicated for the prevention of angina |
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Primary | Fohnetten N Approved UseUnknown |
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100000077163
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DTXSID301035097
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SUB13032MIG
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13461
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C004535
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9522
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2QN49PWH71
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890-98-2
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212-965-7
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SUBSTANCE RECORD