Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H20Cl2N6O3.ClH |
| Molecular Weight | 511.789 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(C)C(=O)C1=NN(C(CNC(=O)CN)=N1)C2=CC=C(Cl)C=C2C(=O)C3=CC=CC=C3Cl
InChI
InChIKey=KHINGHZNENOVFD-UHFFFAOYSA-N
InChI=1S/C21H20Cl2N6O3.ClH/c1-28(2)21(32)20-26-17(11-25-18(30)10-24)29(27-20)16-8-7-12(22)9-14(16)19(31)13-5-3-4-6-15(13)23;/h3-9H,10-11,24H2,1-2H3,(H,25,30);1H
| Molecular Formula | C21H20Cl2N6O3 |
| Molecular Weight | 475.328 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/3428781Curator's Comment: description was created based on several sources, including
https://www.jstage.jst.go.jp/article/jjsca1981/8/4/8_4_384/_article
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3428781
Curator's Comment: description was created based on several sources, including
https://www.jstage.jst.go.jp/article/jjsca1981/8/4/8_4_384/_article
Rilmazafone (previously known as 450191-S) is a water-soluble benzodiazepine prodrug developed in Japan. It has sedative and hypnotic effects. Rilmazafone induces impairment of motor function and has hypnotic properties. Rilmazafone has no effects on benzodiazepine receptors itself, but once inside the body is metabolised by aminopeptidase enzymes in the small intestine to form the active benzodiazepine 8-chloro-6-(2-chlorophenyl)-N,N-dimethyl-4H-1,2,4-triazolo benzodiazepine-2-carboxamide. Preclinical studies have shown its excellent effects inducing and maintaining sleep with little effect on the skeletal muscle. Earlier the clinical dose for this drug as a premedicant was found to be 2-4mg.
CNS Activity
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6145419
Curator's Comment: Known to be CNS penetrant in rat. Human data not available.
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6149175 |
Curative | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Hypnotic and sleep quality-enhancing properties of kavain in sleep-disturbed rats. | 2009-11 |
|
| Evaluation of anxiolytic-like effects of some short-acting benzodiazepine hypnotics in mice. | 2008-07 |
|
| Effects of melatonin and rilmazafone on nocturia in the elderly. | 2007-09-29 |
|
| Potentiation of ethanol in spatial memory deficits induced by some benzodiazepines. | 2006-08 |
|
| [Pharmacological profiles of benzodiazepinergic hypnotics and correlations with receptor subtypes]. | 2005-06 |
|
| Safety evaluation and drug development based on biological fate of drugs -efforts made to overcome drug interaction in drug development-. | 2002 |
Patents
| Substance Class |
Chemical
Created
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admin
on
Edited
Mon Mar 31 19:07:42 GMT 2025
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Mon Mar 31 19:07:42 GMT 2025
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| Record UNII |
25T258X8BV
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| Record Status |
Validated (UNII)
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SUB22078
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ACTIVE MOIETY |