Details
Stereochemistry | RACEMIC |
Molecular Formula | C18H23N.ClH |
Molecular Weight | 289.843 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(CC(C1=CC=CC=C1)C2=CC=CC=C2)N(C)C
InChI
InChIKey=JCFRXWVRVBVWNY-UHFFFAOYSA-N
InChI=1S/C18H23N.ClH/c1-15(19(2)3)14-18(16-10-6-4-7-11-16)17-12-8-5-9-13-17;/h4-13,15,18H,14H2,1-3H3;1H
Molecular Formula | C18H23N |
Molecular Weight | 253.3819 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Trimethyldiphenylpropylamine (Recipavrin) is a methadon analog with antispasmodic properties. It exerts both musculotropic (antibarium) and anticholinergic action, relieves smooth muscle spasms, e.g. dysmenorrhea and pains associated with gallstones. It was marketed in Sweden in the 1960s as a spasmolytic drug under tradename Recipavrin.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:48:32 GMT 2023
by
admin
on
Sat Dec 16 09:48:32 GMT 2023
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Record UNII |
54985Y1A6A
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Record Status |
Validated (UNII)
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SUB127738
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54985Y1A6A
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DTXSID70944821
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30965
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244-814-6
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22173-83-7
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100000153606
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SUB15619MIG
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