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Mexazolam

HCID 4177
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
31868-18-5
Standard SMILES
CC1COC2(c3ccccc3Cl)c3cc(Cl)ccc3NC(=O)CN12
InChIKey
ANUCDXCTICZJRH-UHFFFAOYSA-N
Molecular formula
C18H16Cl2N2O2
Average molar mass
363.2 g/mol
Monoisotopic mass
362.0588831

Overview

Mexazolam is a hemiaminal ether and an oxazolobenzodiazepine.

Names & identifiers

Preferred name
Mexazolam
IUPAC
10-chloro-11b-(2-chlorophenyl)-3-methyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
English name
mexazolam
Molecular formula
C18H16Cl2N2O2
Molecular weight
363.24

Names & synonyms

mexazolamMelex31868-18-5CS-386MexazolamumDTXSID9057715DTXCID0031504S5969B6237CHEBI:3184210-Chloro-11b-(2-chlorophenyl)-2,3,7,11b-tetrahydro-3-methyloxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-one10-chloro-2,3,7,11b-tetrahydro-3-methyl-11b-(2-chlorophenyl)oxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneRefChem:818798
Show more names
Sedoxilmexazolam APImexazolam USP/EP/BPMexazolam (1 mg/mL in Acetonitrile)MexazolamQ: What is Mexazolam Q: What is the CAS Number of Mexazolam
13-chloro-2-(2-chlorophenyl)-5-methyl-3-oxa-6,9-diazatricyclo(8.4.0.0^(2,6))tetradeca-1(10),8,11,13-tetraen-8-ol13-chloro-2-(2-chlorophenyl)-5-methyl-3-oxa-6,9-diazatricyclo(8.4.0.02,6)tetradeca-1(10),8,11,13-tetraen-8-ol10-chloro-11b-(2-chlorophenyl)-3-methyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one10-Chloro-11b-(o-chlorophenyl)-2,3,7,11b-tetrahydro-3-methyloxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneMexazolam [INN:JAN]Mexazolamum [INN-Latin]Mexazolam (1.0mg/ml in Acetonitrile)CS 386

Database identifiers

Properties

Computed structural properties

XLogP
3.7
Topological polar surface area
41.6 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
1
Heavy atoms
24
Formal charge
0
Complexity
505

Physicochemical properties

Melting point
172 · 172-175°
Boiling point
522.2 · 522.2±50.0 °C(Predicted)
Density
1.3817 · 1.3817 (rough estimate)
refractive index
1.61 · 1.6100 (estimate)
solubility
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form
Solid
pka
6.69 · 6.69(at 25℃)
color
White to Off-White
FDA UNII
5969 B6237 · S5969B6237
Toxicity
50 in · LD50 in male, female mice; male, female rats (mg/kg): 4687, 4571, 810, 4500 orally; >6000, >6000, >4000, >4000 i.p. or s.c. (Masuda)

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Toxicology

Treatment · 1 item

General supportive measures should be employed, along with intravenous fluids, and an adequate airway maintained. Hypotension may be combated by the use of norepinephrine or metaraminol. Dialysis is of limited value. Flumazenil (Anexate) is a competitive benzodiazepine receptor antagonist that can be used as an antidote for benzodiazepine overdose. In particular, flumazenil is very effective at reversing the CNS depression associated with benzodiazepines but is less effective at reversing respiratory depression. Its use, however, is controversial as it has numerous contraindications. It is contraindicated in patients who are on long-term benzodiazepines, those who have ingested a substance that lowers the seizure threshold, or in patients who have tachycardia or a history of seizures. As a general rule, medical observation and supportive care are the mainstay of treatment of benzodiazepine overdose. Although benzodiazepines are absorbed by activated charcoal, gastric decontamination with activated charcoal is not beneficial in pure benzodiazepine overdose as the risk of adverse effects often outweigh any potential benefit from the procedure. It is recommended only if benzodiazepines have been taken in combination with other drugs that may benefit from decontamination. Gastric lavage (stomach pumping) or whole bowel irrigation are also not recommended.

Toxicity Summary · 1 item

Benzodiazepines bind nonspecifically to benzodiazepine receptors BNZ1, which mediates sleep, and BNZ2, which affects affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABAA) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

Safety data

Chemistry & industry

Pharmacology

ATC Code · 2 items

N - Nervous system

QN - Nervous system

Protein BindingMexazolam is >90% protein bound in plasma.
Mechanism of ActionMexazolam is a benzodiazepine that binds to benzodiazepine-type receptors, inhibiting gamma-aminobutyric acid.
Biological Half-LifeMexazolam follows a 2 compartment model with a first half life of 1.4h and a second half life of 76h.
Metabolism/MetabolitesMexazolam is rapidly metabolized to the active metabolites chloronordiazepam and chloroxazepam.
Absorption, Distribution and Excretion · 2 items

The active metabolite chloronordiazepam has a Tmax of 1-2h.

Mexazolam is mainly eliminated in the bile and feces, with <10% eliminated as metabolites in the urine. >50% of a dose of mexazolam is eliminated as the metabolite chloroxazepam.

Uses & manufacturing

Uses · 1 item

Mexazolam has been trialed for anxiety and was found to be effective in alleviating anxiety at one week follow-up, however, after three weeks of therapy mexazolam had lost its therapeutic anxiolytic properties becoming no more effective than placebo, presumably due to benzodiazepine tolerance.

Applications

DescriptionMexazolam is a benzodiazepine anxiolytic closely related to flutazolam. It is reported to be particularly effective against psychosomatic essential hypertension, peptic ulcer, irritable colon and autonomic dystonia.

UsesMexazolam is a benzodiazepine derivative and have been investigated for its therapeutic value in treating anxiety. Mexazolam is known to be metabolized via the CYP3A4 pathway.

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
CAS
31868-18-5
PubChem CID
4177
DTXSID
DTXSID9057715
ChEMBL
CHEMBL1743261
ChEBI
CHEBI:31842
UNII
S5969B6237
Nikkaji
J3.491F
Toxicity
LD50 in male, female mice; male, female rats (mg/kg): 4687, 4571, 810, 4500 orally; >6000, >6000, >4000, >4000 i.p. or s.c. (Masuda)

Suppliers11 total

安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
Zhejiang J&C Biological Technology Co.,Limited+1-2135480471 · [email protected]
湖北扬信医药科技有限公司0714-3999001 19171453112 · [email protected]
宝鸡缔都医药化工有限公司029-81145305 17791533577 · [email protected]
艾吉析科技(上海)有限公司17717235263 17717235263 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
河南天孚化工有限公司+86-0371-55170693 +86-19937530512 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
TLC梯尔希(南京)药物研发有限公司18012923235 · [email protected]
Dideu Industries Group Limited+86-29-81148696 +86-15129568250 · [email protected]

Additional notes

DefinitionChEBI: Mexazolam is an oxazolobenzodiazepine and a hemiaminal ether.