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Molecule
ID:130342
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₂Cl₂N₂O₂
Molecular Mass
335.18468
Exact Mass
334.02758299
Charge
0
InChI
InChI=1S/C16H12Cl2N2O2/c1-20-13-7-6-9(17)8-11(13)14(19-15(21)16(20)22)10-4-2-3-5-12(10)18/h2-8,15,21H,1H3
InChIKey
FJIKWRGCXUCUIG-UHFFFAOYSA-N
Canonic Smiles
Clc1ccc2c(c1)C(=NC(C(=O)N2C)O)c1ccccc1Cl
Isomeric Smiles
Clc1ccccc1C1=NC(C(=O)N(C)c2c1cc(cc2)Cl)O
Calculated Properties
JChem
Acid pKa
10.67647
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
3.3913887
LogD (pH = 7.4)
3.3911622
Log P
3.3913915
Molar Refractivity
85.8151
Polarizability
32.86259
Polar Surface Area
52.9
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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Lormetazepam
PubChem
13314
Commercial Catalog
TRC
L469930
Names and Identifiers
Synonyms
''N''-methyllorazepam
Lormetazepam
methyl-lorazepam
(+/-)-Lormetazepam
Noctamid
7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-1-methyl-2H-1,4-benzodiazepin-2-one
Ergocalm
WY 4082
Ro 5-5516
Methyllorazepam
Loramet
N-Methyllorazepam
Noctamide
(RS)-Lormetazepam
IUPAC Traditional name
lormetazepam
IUPAC name
7-chloro-5-(2-chlorophenyl)-3-hydroxy-1-methyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one
Registration numbers
ATC CODE
N05CD06
Wikipedia Title
Lormetazepam
Unique Ingredient Identifier
GU56C842ZA
CHEMBL
22097
CHEBI ID
52993
CAS Number
848-75-9
KEGG ID
D01657
PubChem CID
13314
Chemspider ID
12750
PubChem SID
162224621
Molecule Details
Wikipedia
Lormetazepam
TRC
L469930
An analog of Lorazepam (L469850). Sedative, hypnotic.Controlled substance (depressant).
References
PubChem Literature
From Data Sources
•
Nudelman, A., et al.: J. Pharma. Sci., 63, 1886 (1974)
•
Humpel, M., et al.: Eur. J. Drug Metab. Pharmacokinet., 4, 237 (1974)
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Girkin, R., et al.: Xenobiotica, 10, 401 (1974)
Bioactivity
PubChem BioAssay
Registration numbers
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ATC CODE
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Wikipedia Title
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Unique Ingredient Identifier
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CHEMBL
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CHEBI ID
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CAS Number
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KEGG ID
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PubChem CID
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Chemspider ID
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PubChem SID
Properties
Pharmacology Properties
Metabolism
Hepatic
Source
Bioavailability
80%
Source
Pregnancy Category
D
Source
Legal Status
Schedule IV (US)
Source
Admin Routes
Oral
Source
Half Life
10–12 hours
Source
Renal
Source
Safety Information
Controlled Substance, -20°C Freezer
Source
Download link
Source
Physical Property
Pale Green Solid
Source
Chloroform
Source
Ethyl Acetate
Source
163-168°C
Source
Product Information
Download link
Source
Excretion
Storage Condition
MSDS Link
Apperance
Solubility
Melting Point
Certificate of Analysis