Escitalopram
CAS No. 128196-01-0
Escitalopram ( (S)-Citalopram )
Catalog No. M11157 CAS No. 128196-01-0
Escitalopram is a selective serotonin reuptake inhibitor (SSRI) with Ki of 0.89 nM.
Purity : >98%(HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 37 | In Stock |
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10MG | 51 | In Stock |
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25MG | 104 | In Stock |
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50MG | 164 | In Stock |
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100MG | 247 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameEscitalopram
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NoteResearch use only, not for human use.
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Brief DescriptionEscitalopram is a selective serotonin reuptake inhibitor (SSRI) with Ki of 0.89 nM.
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DescriptionEscitalopram is a selective serotonin reuptake inhibitor (SSRI) with Ki of 0.89 nM.
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Synonyms(S)-Citalopram
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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RecptorSert (Sodium-dependent); mAChR; α-adrenergic receptor; DA transporter; H1 receptor; Noradrenaline transporter (Sodium-dependent)
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number128196-01-0
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Formula Weight414.43
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Molecular FormulaC20H21FN2O·C2H2O4
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Purity>98%(HPLC)
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SolubilityDMSO: ≥15 mg/mL
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SMILESN#CC1=CC2=C([C@@](C3=CC=C(F)C=C3)(CCCN(C)C)OC2)C=C1
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Chemical Name(S)-1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Ziprasidone
A full antagonist of D2 and 5-HT2A receptors with Ki of 6.8 and 0.6 nM, respectively; also is a partial agonist of 5-HT1A, and a partial antagonist of 5-HT2C and 5-HT1D receptors.
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Homoeriodictyol
Homoeriodictyol, a naturally occurring, bitter-masking flavanone, as a promising agent to increase appetite and food intake. The flavanone homoeriodictyol can increase SGLT-1-mediated glucose uptake but decrease serotonin release in differentiated Caco-2 cells.In contrast to other polyphenols, the flavanon Homoeriodictyol promotes glucose uptake by 29.0 ± 3.83% at a concentration of 100 μM.
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Haloperidol
Haloperidol has been found to be highlt potent neuroleptic by relieving nervous through the depression of nerve function.