Details
| Stereochemistry | MIXED |
| Molecular Formula | C14H16Cl6O5 |
| Molecular Weight | 476.992 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CC=C1OCC(COC(O)C(Cl)(Cl)Cl)OC(O)C(Cl)(Cl)Cl
InChI
InChIKey=IPVVZYZTTKHXKK-UHFFFAOYSA-N
InChI=1S/C14H16Cl6O5/c1-8-4-2-3-5-10(8)23-6-9(25-12(22)14(18,19)20)7-24-11(21)13(15,16)17/h2-5,9,11-12,21-22H,6-7H2,1H3
| Molecular Formula | C14H16Cl6O5 |
| Molecular Weight | 476.992 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Toloxychlorinol is a sedative agent. It is more pleasant alternative to chloral. Toloxychlorinol had low toxicity in the mouse, rat and guinea pig. Large doses of toloxychlorinol induced hypnosis rapidly. The duration of action was intermediate between that induced by moderate-, and long-acting barbiturates. Small doses, insufficient to cause outward signs of depression, significantly prolonged the period of sleep induced by hexobarbital. Toloxychlorinol antagonized convulsions induced by pentylenetetrazole. It displayed no analgesic activity. Pentylenetetrazole completely antagonized the effects of overdosage with toloxychlorinol.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:04:49 GMT 2025
by
admin
on
Mon Mar 31 18:04:49 GMT 2025
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| Record UNII |
A41Z78SD75
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| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 18:04:49 GMT 2025 , Edited by admin on Mon Mar 31 18:04:49 GMT 2025
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| Code System | Code | Type | Description | ||
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SUB11170MIG
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71215
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906
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6055-48-7
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CHEMBL2107227
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A41Z78SD75
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100000077781
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C152687
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DTXSID50863682
Created by
admin on Mon Mar 31 18:04:49 GMT 2025 , Edited by admin on Mon Mar 31 18:04:49 GMT 2025
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PRIMARY |
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ACTIVE MOIETY |