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=C(OCC(COC(O)C(Cl)(Cl)Cl)OC(O)C(Cl)(Cl)Cl)C=CC=C1
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
Fri Dec 15 15:40:06 GMT 2023
by
admin
on
Fri Dec 15 15:40:06 GMT 2023
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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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-
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NCI_THESAURUS |
C29756
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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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
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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A41Z78SD75
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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100000077781
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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C152687
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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DTXSID50863682
Created by
admin on Fri Dec 15 15:40:06 GMT 2023 , Edited by admin on Fri Dec 15 15:40:06 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |