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Chemistry

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Also known as: Zolazepam hcl, 33754-49-3, Ci-716, 45sj093q1n, 4-(2-fluorophenyl)-1,3,8-trimethyl-6h-pyrazolo[3,4-e][1,4]diazepin-7-one;hydrochloride, 4-(o-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo(3,4-e)(1,4)diazepin-7(1h)-one monohydrochloride
Molecular Formula
C15H16ClFN4O
Molecular Weight
322.76  g/mol
InChI Key
NJERAXSSDSHLGE-UHFFFAOYSA-N
FDA UNII
45SJ093Q1N

Zolazepam Hydrochloride
A pyrazolodiazepinone with pharmacological actions similar to ANTI-ANXIETY AGENTS. It is commonly used in combination with TILETAMINE to obtain immobilization and anesthesia in animals.
1 2D Structure

Zolazepam Hydrochloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-(2-fluorophenyl)-1,3,8-trimethyl-6H-pyrazolo[3,4-e][1,4]diazepin-7-one;hydrochloride
2.1.2 InChI
InChI=1S/C15H15FN4O.ClH/c1-9-13-14(10-6-4-5-7-11(10)16)17-8-12(21)19(2)15(13)20(3)18-9;/h4-7H,8H2,1-3H3;1H
2.1.3 InChI Key
NJERAXSSDSHLGE-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC1=NN(C2=C1C(=NCC(=O)N2C)C3=CC=CC=C3F)C.Cl
2.2 Other Identifiers
2.2.1 UNII
45SJ093Q1N
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Ci 716

2. Ci-716

3. Ci716

4. Flupyrazapon

5. Flupyrazopon

6. Hydrochloride, Zolazepam

7. Zolasepam

8. Zolazepam

2.3.2 Depositor-Supplied Synonyms

1. Zolazepam Hcl

2. 33754-49-3

3. Ci-716

4. 45sj093q1n

5. 4-(2-fluorophenyl)-1,3,8-trimethyl-6h-pyrazolo[3,4-e][1,4]diazepin-7-one;hydrochloride

6. 4-(o-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo(3,4-e)(1,4)diazepin-7(1h)-one Monohydrochloride

7. Pyrazolo(3,4-e)(1,4)diazepin-7(1h)-one, 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethyl-, Monohydrochloride

8. Unii-45sj093q1n

9. Zolazepam Hydrochloride [usan]

10. Einecs 251-668-7

11. Zolazepam Hydrochloride [usan:usp]

12. Schembl73002

13. Zolazepam Hydrochloride (usp)

14. Chembl2107559

15. Dtxsid00955349

16. Zolazepam Hydrochloride(500 Mg)

17. Zolazepam Hydrochloride [mi]

18. Zolazepam Hydrochloride [usp-rs]

19. Zolazepam Hydrochloride [green Book]

20. Ft-0775057

21. Zolazepam Hydrochloride [usp Impurity]

22. D06377

23. Zolazepam Hydrochloride [usp Monograph]

24. Q27258863

25. 4-(2-fluorophenyl)-1,3,8-trimethyl-6h-pyrazolo[3,4-e][1,4]diazepin-7-one,hydrochloride

26. 4-(2-fluorophenyl)-1,3,8-trimethyl-6,8-dihydropyrazolo[3,4-e][1,4]diazepin-7(1h)-one--hydrogen Chloride (1/1)

27. 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo(3,4-e)(1,4)diazepin-7(1h)-one Monohydrochloride

28. 42551-17-7

29. Pyrazolo(3,4-e)(1,4)diazepin-7(1h)-one, 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethyl-, Hydrochloride

2.4 Create Date
2005-08-08
3 Chemical and Physical Properties
Molecular Weight 322.76 g/mol
Molecular Formula C15H16ClFN4O
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass322.0996670 g/mol
Monoisotopic Mass322.0996670 g/mol
Topological Polar Surface Area50.5 Ų
Heavy Atom Count22
Formal Charge0
Complexity455
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Anti-Anxiety Agents

Agents that alleviate ANXIETY, tension, and ANXIETY DISORDERS, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions. ADRENERGIC BETA-ANTAGONISTS are commonly used in the symptomatic treatment of anxiety but are not included here. (See all compounds classified as Anti-Anxiety Agents.)


GABA Modulators

Substances that do not act as agonists or antagonists but do affect the GAMMA-AMINOBUTYRIC ACID receptor-ionophore complex. GABA-A receptors (RECEPTORS, GABA-A) appear to have at least three allosteric sites at which modulators act: a site at which BENZODIAZEPINES act by increasing the opening frequency of GAMMA-AMINOBUTYRIC ACID-activated chloride channels; a site at which BARBITURATES act to prolong the duration of channel opening; and a site at which some steroids may act. GENERAL ANESTHETICS probably act at least partly by potentiating GABAergic responses, but they are not included here. (See all compounds classified as GABA Modulators.)


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