Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | 2C10H15N3O.H2O4S |
| Molecular Weight | 484.57 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(O)(=O)=O.NC(=N)NCCCOC1=CC=CC=C1.NC(=N)NCCCOC2=CC=CC=C2
InChI
InChIKey=CXDPVKRPWPEWCT-UHFFFAOYSA-N
InChI=1S/2C10H15N3O.H2O4S/c2*11-10(12)13-7-4-8-14-9-5-2-1-3-6-9;1-5(2,3)4/h2*1-3,5-6H,4,7-8H2,(H4,11,12,13);(H2,1,2,3,4)
| Molecular Formula | H2O4S |
| Molecular Weight | 98.078 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C10H15N3O |
| Molecular Weight | 193.2456 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Guanoxyfen sulfate is an antidepressant, antihypertensive. Guanoxyfen sulfate is an inhibitor of vasoconstrictor responses to sympathetic nerve stimulation. It could potentiate the actions of adrenaline and noradrenaline. It also could increase the blood glucose concentration and decrease the appetite.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:57:05 GMT 2025
by
admin
on
Mon Mar 31 17:57:05 GMT 2025
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| Record UNII |
47XBA61Y31
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C270
Created by
admin on Mon Mar 31 17:57:05 GMT 2025 , Edited by admin on Mon Mar 31 17:57:05 GMT 2025
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172118
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1021-11-0
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13922
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DTXSID80144633
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C65836
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CHEMBL2110935
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300000055139
Created by
admin on Mon Mar 31 17:57:05 GMT 2025 , Edited by admin on Mon Mar 31 17:57:05 GMT 2025
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47XBA61Y31
Created by
admin on Mon Mar 31 17:57:05 GMT 2025 , Edited by admin on Mon Mar 31 17:57:05 GMT 2025
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PRIMARY |
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