Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H16ClNO3.ClH |
| Molecular Weight | 342.217 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.OC1=CC2=C(C=C1O)C(COC3=CC=C(Cl)C=C3)NCC2
InChI
InChIKey=YZURDQOXVMKLGY-UHFFFAOYSA-N
InChI=1S/C16H16ClNO3.ClH/c17-11-1-3-12(4-2-11)21-9-14-13-8-16(20)15(19)7-10(13)5-6-18-14;/h1-4,7-8,14,18-20H,5-6,9H2;1H
| Molecular Formula | C16H16ClNO3 |
| Molecular Weight | 305.756 |
| 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 |
Clofeverine is a compound synthesized by the Japanese company Fujisawa Pharmaceutical. Clofeverine is a highly selective relaxant for gastrointestinal smooth muscles with a beta-receptor stimulative nature. On isolated ileum, the inhibitory effect of clofeverine for spontaneous motility was comparable to that of isoproterenol and 100 times higher than that of papaverine.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 13:28:14 GMT 2023
by
admin
on
Sat Dec 16 13:28:14 GMT 2023
|
| Record UNII |
32FN39XWR3
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
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37969-58-7
Created by
admin on Sat Dec 16 13:28:14 GMT 2023 , Edited by admin on Sat Dec 16 13:28:14 GMT 2023
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20511252
Created by
admin on Sat Dec 16 13:28:14 GMT 2023 , Edited by admin on Sat Dec 16 13:28:14 GMT 2023
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32FN39XWR3
Created by
admin on Sat Dec 16 13:28:14 GMT 2023 , Edited by admin on Sat Dec 16 13:28:14 GMT 2023
|
PRIMARY |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |