Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H18N4.H2O4S |
| Molecular Weight | 280.345 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(O)(=O)=O.CC1=CCN(CCNC(N)=N)CC1
InChI
InChIKey=FLZPKJNDZPCKJG-UHFFFAOYSA-N
InChI=1S/C9H18N4.H2O4S/c1-8-2-5-13(6-3-8)7-4-12-9(10)11;1-5(2,3)4/h2H,3-7H2,1H3,(H4,10,11,12);(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 | C9H18N4 |
| Molecular Weight | 182.266 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/5420832
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5420832
Guanacline was studied in the treatment of hypertension. However, information about the current use of this compound is not available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Species and structural specificity of the lipopigment accumulation and neuronal destruction induced by N-(2-guanidinoethyl)-4-methyl-1,2,5,6-tetrahydropyridine (guanacline). | 1986-09-24 |
|
| Clinical experiences with Leron (guanacline) in the treatment of hypertension. | 1970-05-09 |
|
| Guanacline, a new hypotensive drug. | 1969-01-25 |
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 17:45:53 GMT 2025
by
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Mon Mar 31 17:45:53 GMT 2025
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| Record UNII |
UE69UT7F2Y
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Validated (UNII)
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