Azaperone
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Azaperone
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CAS No:
1649-18-9
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Formula:
C19H22FN3O
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Chemical Name:
Azaperone
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Synonyms:
1-Butanone,1-(4-fluorophenyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-;Butyrophenone,4′-fluoro-4-[4-(2-pyridyl)-1-piperazinyl]-;1-(4-Fluorophenyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-1-butanone;4′-Fluoro-4-[4-(2-pyridyl)-1-piperazinyl]butyrophenone;Azaperone;Fluoperidol;Stresnil;R-1929;Suicalm;NSC 170976
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CAS No:
Description
Azaperone (R-1929) acts as a dopamine antagonist but also has some antihistaminic and anticholinergic properties. Azaperone is a pyridinylpiperazine and butyrophenone neuroleptic drug with sedative and antiemetic effects, which is used mainly as a tranquilizer in veterinary medicine.
Azaperone is an N-arylpiperazine that is 2-(piperazin-1-yl)pyridine in which the amino hydrogen is replaced by a 3-(4-fluobenzoyl)propyl group. Used mainly as a tranquiliser for pigs and elephants. It has a role as an antipsychotic agent and a dopaminergic antagonist. It is a N-arylpiperazine, a N-alkylpiperazine, an aminopyridine, a tertiary amino compound, a member of monofluorobenzenes and an aromatic ketone.|Azaperone is a pyridinylpiperazine and butyrophenone agent that is capable of eliciting neuroleptic sedative and antiemetic effects. It is subsequently employed predominantly as a veterinary tranquilizer and mainly for pigs and elephants. At the same time, the agent generally does not see equine use as particular adverse reactions may happen. More rarely it may be used in humans as an antipsychotic drug, but this is uncommon.|A butyrophenone used in the treatment of PSYCHOSES.
Characteristics
36.4
3.3
White or off-white crystalline
1.2±0.1 g/cm3
73-75 °C
499.5°C at 760 mmHg
255.9±28.7 °C
1.568
0-6°C
4.14E-10mmHg at 25°C
180 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]|180.3 Ų [M+H]+ [CCS Type: TW]|181.99 Ų [M+H]+
Safety Information
Ⅲ
UN28116.1/PG3
22
EU4550000
Xn
Missing Phrase - N15.00950417
H301
|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P301+P310, P321, P330, P405, and P501|Aggregated GHS information provided by 42 companies from 3 notifications to the ECHA C&L Inventory.
Drug Information
Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus. (See all compounds classified as Antipsychotic Agents.)|Drugs used to induce drowsiness or sleep or to reduce psychological excitement or anxiety. (See all compounds classified as Hypnotics and Sedatives.)|Drugs that bind to but do not activate DOPAMINE RECEPTORS, thereby blocking the actions of dopamine or exogenous agonists. Many drugs used in the treatment of psychotic disorders (ANTIPSYCHOTIC AGENTS) are dopamine antagonists, although their therapeutic effects may be due to long-term adjustments of the brain rather than to the acute effects of blocking dopamine receptors. Dopamine antagonists have been used for several other clinical purposes including as ANTIEMETICS, in the treatment of Tourette syndrome, and for hiccup. Dopamine receptor blockade is associated with NEUROLEPTIC MALIGNANT SYNDROME. (See all compounds classified as Dopamine Antagonists.)
Azaperone
Azaperone Use and Manufacturing
Sedative; tranquilizer.
Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients|Pharmaceuticals -> Animal Drugs -> Approved in Taiwan
Veterinary Drug -> TRANQUILLIZING_AGENT;
Computed Properties
Molecular Weight:327.4
XLogP3:3.3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:327.17469050
Monoisotopic Mass:327.17469050
Topological Polar Surface Area:36.4
Heavy Atom Count:24
Complexity:390
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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