Details
| Stereochemistry | MIXED |
| Molecular Formula | C18H35NO2 |
| Molecular Weight | 297.476 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCN(CC)CC1COC2(CCC(CC2)C(C)(C)C)O1
InChI
InChIKey=PUYXTUJWRLOUCW-UHFFFAOYSA-N
InChI=1S/C18H35NO2/c1-6-12-19(7-2)13-16-14-20-18(21-16)10-8-15(9-11-18)17(3,4)5/h15-16H,6-14H2,1-5H3
| Molecular Formula | C18H35NO2 |
| Molecular Weight | 297.476 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Spiroxamine is a spirodecane derivative patented by German multinational pharmaceutical and life sciences company Bayer A.-G. as agrochemical fungicide. Spiroxamine acts as a sterol biosynthesis inhibitor with systemic activity. This active ingredient provides control of powdery mildew caused by the ascomycetous fungus, Uncinula necator (syn. Erysiphe necator) in grapes. In laboratory animals, the technical grade Spiroxamine was moderate to highly acutely toxic by the oral route and slightly acutely toxic by the dermal and inhalation routes of exposure. Spiroxamine was non-irritating to the eyes but moderately irritating to the skin. Spiroxamine caused an allergic skin reaction. Health effects in animals given repeated doses of Spiroxamine included effects on the liver, lining of the gastrointestinal and urogenital tracts, the eye and body weight. Spiroxamine did not cause cancer in animals and did not damage genetic material.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:51:46 GMT 2025
by
admin
on
Mon Mar 31 21:51:46 GMT 2025
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| Record UNII |
OUT5YHB7BO
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID1034212
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9242
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118134-30-8
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spiroxamine
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OUT5YHB7BO
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m10159
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86160
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