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
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
| 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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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
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ACTIVE MOIETY