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Suppliers for
Escitalopram
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Properties | CAS |
128196-01-0 | Formula |
C20H21FN2O |
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9 Registered suppliers
Molecular Formula: C20H21FN2O Molecular Weight: 324,39
More details are to be found here
Molecular Formula: C20H21FN2O Molecular Weight: 324,39
More details are to be found here
Description : Escitalopram, the S-enantiomer of citalopram, belongs to a class of antidepressant agents known as selective serotonin-reuptake inhibitors (SSRIs). Escitalopram may be used to treat major depressive disorder (MDD) and generalized anxiety disorder (GAD). Escitalopram has no significant affinity for adrenergic (alpha1, alpha2, beta), cholinergic, GABA, dopaminergic, histaminergic, serotonergic (5HT1A, 5HT1B, 5HT2), or benzodiazepine receptors; antagonism of such receptors has been hypothesized to be associated with various anticholinergic, sedative, and cardiovascular effects for other psychotropic drugs. The chronic administration of escitalopram is found to downregulate brain norepinephrine receptors, as has been observed with other drugs effective in the treatment of major depressive disorder. Escitalopram does not inhibit monoamine oxidase. - Molecular Weight :324.39
- Melting Point :147-152C
- Purity :> 98%
Molecular Formula : C20H21FN2O Canonical SMILES : CN(C)CCCC1(C2=C(CO1)C=C(C=C2)C#N)C3=CC=C(C=C3)F InChI : InChI=1S/C20H21FN2O/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20/h4-9,12H,3,10-11,14H2,1-2H3/t20-/m0/s1 InChIKey : WSEQXVZVJXJVFP-FQEVSTJZSA-N Solubility : Sparingly soluble Application : Serotonin uptake inhibitors; antidepressive agents, Second-generation Synonyms : (S)-Citalopram; S-(+)-Citalopram; Seroplex
More details are to be found here
Description : Escitalopram, the S-enantiomer of citalopram, belongs to a class of antidepressant agents known as selective serotonin-reuptake inhibitors (SSRIs). Escitalopram may be used to treat major depressive disorder (MDD) and generalized anxiety disorder (GAD). Escitalopram has no significant affinity for adrenergic (alpha1, alpha2, beta), cholinergic, GABA, dopaminergic, histaminergic, serotonergic (5HT1A, 5HT1B, 5HT2), or benzodiazepine receptors; antagonism of such receptors has been hypothesized to be associated with various anticholinergic, sedative, and cardiovascular effects for other psychotropic drugs. The chronic administration of escitalopram is found to downregulate brain norepinephrine receptors, as has been observed with other drugs effective in the treatment of major depressive disorder. Escitalopram does not inhibit monoamine oxidase. - Molecular Weight :324.39
- Melting Point :147-152C
- Purity :> 98%
Molecular Formula : C20H21FN2O Canonical SMILES : CN(C)CCCC1(C2=C(CO1)C=C(C=C2)C#N)C3=CC=C(C=C3)F InChI : InChI=1S/C20H21FN2O/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20/h4-9,12H,3,10-11,14H2,1-2H3/t20-/m0/s1 InChIKey : WSEQXVZVJXJVFP-FQEVSTJZSA-N Solubility : Sparingly soluble Application : Serotonin uptake inhibitors; antidepressive agents, Second-generation Synonyms : (S)-Citalopram; S-(+)-Citalopram; Seroplex
More details are to be found here
More details are to be found here
More details are to be found here
More details are to be found here
More details are to be found here
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Properties:
... more properties and specification on Escitalopram
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Last update 2024-06-10
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