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Details

Stereochemistry ACHIRAL
Molecular Formula C21H20Cl2N6O3.ClH.2H2O
Molecular Weight 547.819
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RILMAZAFONE HYDROCHLORIDE DIHYDRATE

SMILES

O.O.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=UWTWLIQPJSLNEN-UHFFFAOYSA-N
InChI=1S/C21H20Cl2N6O3.ClH.2H2O/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;2*1H2

HIDE SMILES / InChI

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 H2O
Molecular Weight 18.0153
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

Description
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

Curator's Comment: Known to be CNS penetrant in rat. Human data not available.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Safety evaluation and drug development based on biological fate of drugs -efforts made to overcome drug interaction in drug development-.
2002
[Pharmacological profiles of benzodiazepinergic hypnotics and correlations with receptor subtypes].
2005 Jun
Potentiation of ethanol in spatial memory deficits induced by some benzodiazepines.
2006 Aug
Effects of melatonin and rilmazafone on nocturia in the elderly.
2007 Sep-Oct
Evaluation of anxiolytic-like effects of some short-acting benzodiazepine hypnotics in mice.
2008 Jul
Hypnotic and sleep quality-enhancing properties of kavain in sleep-disturbed rats.
2009 Nov
Patents

Patents

Sample Use Guides

clinical dose for this drug as a premedicant was found to be 2-4 mg
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:14:25 GMT 2023
Edited
by admin
on Sat Dec 16 05:14:25 GMT 2023
Record UNII
3Q7B0F12KD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RILMAZAFONE HYDROCHLORIDE DIHYDRATE
Common Name English
RILMAZAFONE HYDROCHLORIDE HYDRATE
JAN  
Common Name English
RILMAZAFONE MONOHYDROCHLORIDE DIHYDRATE
MI  
Common Name English
RHYTHMY
Brand Name English
RILMAZAFONE HYDROCHLORIDE HYDRATE [JAN]
Common Name English
450191-S
Code English
RILMAZAFONE MONOHYDROCHLORIDE DIHYDRATE [MI]
Common Name English
Code System Code Type Description
FDA UNII
3Q7B0F12KD
Created by admin on Sat Dec 16 05:14:25 GMT 2023 , Edited by admin on Sat Dec 16 05:14:25 GMT 2023
PRIMARY
MERCK INDEX
m9616
Created by admin on Sat Dec 16 05:14:25 GMT 2023 , Edited by admin on Sat Dec 16 05:14:25 GMT 2023
PRIMARY Merck Index
PUBCHEM
135366
Created by admin on Sat Dec 16 05:14:25 GMT 2023 , Edited by admin on Sat Dec 16 05:14:25 GMT 2023
PRIMARY
EVMPD
SUB194917
Created by admin on Sat Dec 16 05:14:25 GMT 2023 , Edited by admin on Sat Dec 16 05:14:25 GMT 2023
PRIMARY
SMS_ID
100000181320
Created by admin on Sat Dec 16 05:14:25 GMT 2023 , Edited by admin on Sat Dec 16 05:14:25 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY