Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H23ClN4O2.C4H6O4 |
| Molecular Weight | 444.91 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CCC(O)=O.CCN1CC(CN1CC)NC(=O)C2=C(OC)C=C(N)C(Cl)=C2
InChI
InChIKey=HLDCRAZAHFKARV-UHFFFAOYSA-N
InChI=1S/C15H23ClN4O2.C4H6O4/c1-4-19-8-10(9-20(19)5-2)18-15(21)11-6-12(16)13(17)7-14(11)22-3;5-3(6)1-2-4(7)8/h6-7,10H,4-5,8-9,17H2,1-3H3,(H,18,21);1-2H2,(H,5,6)(H,7,8)
| Molecular Formula | C15H23ClN4O2 |
| Molecular Weight | 326.822 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C4H6O4 |
| Molecular Weight | 118.088 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Dazopride is an antagonist of the 5-HT3 receptor and agonist of the 5-HT4 receptor, structurally related to metoclopramide. Dazopride was developed by A. H. Robins Company as an antiemetic and gastroprokinetic drug. Dazoptide demonstrated an antiemetic effect in the clinic after i.v. infusion to patients, receiving anticancer therapy.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:12:46 UTC 2023
by
admin
on
Fri Dec 15 15:12:46 UTC 2023
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| Record UNII |
25S5HB67BK
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| Record Status |
Validated (UNII)
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| Record Version |
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6917727
Created by
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100981-14-4
Created by
admin on Fri Dec 15 15:12:46 UTC 2023 , Edited by admin on Fri Dec 15 15:12:46 UTC 2023
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NON-SPECIFIC STOICHIOMETRY | |||
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106613-26-7
Created by
admin on Fri Dec 15 15:12:46 UTC 2023 , Edited by admin on Fri Dec 15 15:12:46 UTC 2023
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25S5HB67BK
Created by
admin on Fri Dec 15 15:12:46 UTC 2023 , Edited by admin on Fri Dec 15 15:12:46 UTC 2023
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PARENT -> SALT/SOLVATE | |||
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |