Citalopram
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Citalopram
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CAS No:
59729-33-8
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Formula:
C20H21FN2O
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Chemical Name:
Citalopram
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Synonyms:
5-Isobenzofurancarbonitrile,1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-;1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile;Lu 10-171;Citalopram;Nitalapram;(±)-Citalopram;1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile;Bonitrile;1-(3-Dimethylaminopropyl)-1-(4-fluorophenyl)-5-cyanophthalan;Prepram;1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-5-carbonitrile;103146-27-6;128196-03-2
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CAS No:
Description
ChEBI: A nitrile that is 1,3-dihydro-2-benzofuran-5-carbonitrile in which one of the hydrogens at position 1 is replaced by a p-fluorophenyl group, while the other is replaced by a 3-(dimethylamino)propyl group.
Characteristics
36.3
3.5
Solid
1.2±0.1 g/cm3
156-157 °C
178 °C
212.8±28.7 °C
1.591
Sparingly soluble
Store at RT
1.13X10-7 mm Hg at 25 °C (est)
9.78None
Safety Information
III
6.1(b)
3249
Stable under recommended storage conditions. /Citalopram hydrobromide/
P201, P202, P261, P264, P270, P271, P272, P273, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P333+P313, P337+P313, P363, P391, P403+P233, P405, P501
H302
Computed Properties
Molecular Weight:324.4
XLogP3:3.2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:324.16379146
Monoisotopic Mass:324.16379146
Topological Polar Surface Area:36.3
Heavy Atom Count:24
Complexity:466
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Citalopram is an antidepressant and a dicyclic hydrogenated phthalide derivative. Its antidepressant mechanism may be related to inhibiting the reuptake of 5-HT by neurons in the central nervous system, thereby enhancing the function of central serotonergic nerves. In vitro and animal experiments indicate that citalopram is a highly selective 5-HT reuptake inhibitor with little effect on the reuptake of norepinephrine and dopamine. Rats were given citalopram for 14 days, and the effect of inhibiting 5-HT uptake was not tolerated. Citalopram is a racemic body, and its effect of inhibiting 5-HT reuptake is mainly exerted by its (S)-enantiomer. Citalopram has no obvious affinity for 5-HT1A, 5-HT2A, D1 receptor, D2 receptor, а1 receptor, а2 receptor, β receptor, H1 receptor, GABA receptor, etc.
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Citalopram Related Compound B Formula
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Citalopram Related Compound H (25 mg) (1-(4'-fluorophenyl)-1-(3-dimethylaminopropyl)-5-bromophthalane hydrobromide) Formula
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Desfluoro Citalopram Oxalate Structure
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Citalopram hydrochloride Structure
85118-27-0
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What is CitalopraM Carboxaldehyde
227954-87-2
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What is Citalopram hydrobromide
59729-32-7