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SL-164
Sign in to saveSL-164, also known as dicloqualone or DCQ, is an analogue of methaqualone developed in the late 1960s by a team at Sumitomo. SL-164 has similar sedative, hypnotic and properties to the parent compound, but was never marketed for clinical use, due to higher risk of convulsions. Like other 4-substituted analogues, such as methylmethaqualone, SL-164 may cause seizures.
In the Vinony graph
Vinony's link graph records 589 inbound references to SL-164, and connects out to benzodiazepine drug, allopregnanolone and isovaleric acid.
It sits within the topics Chemical pages without DrugBank identifier, Drugs not assigned an ATC code and Drugs with no legal status.
Vinony links it to 7 Wikipedia language editions.
Chemical data
- Formula
- C16H12Cl2N2O
- Molecular weight
- 319.2 g/mol
- IUPAC name
- 5-chloro-3-(4-chloro-2-methylphenyl)-2-methylquinazolin-4-one
- SMILES
- CC1=C(C=CC(=C1)Cl)N2C(=NC3=C(C2=O)C(=CC=C3)Cl)C
- InChIKey
- KUIHLOHNUGOCTO-UHFFFAOYSA-N
- XLogP
- 3.8
- Polar surface area
- 32.7 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 318.032668
Show 3 more facts
- chemical formula
- C₁₆H₁₂Cl₂N₂O
- canonical SMILES
- CC1=C(C=CC(=C1)Cl)N2C(=NC3=C(C2=O)C(=CC=C3)Cl)C
- Commons category
- SL-164
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
SL-164, also known as dicloqualone or DCQ, is an analogue of methaqualone developed in the late 1960s by a team at Sumitomo. SL-164 has similar sedative, hypnotic and properties to the parent compound, but was never marketed for clinical use, due to higher risk of convulsions. Like other 4-substituted analogues, such as methylmethaqualone, SL-164 may cause seizures.
==See also== List of methaqualone analogues
Excerpted from Wikipedia’s “SL-164” article, available under the CC BY-SA 4.0 licence.