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About This Item
Empirical Formula (Hill Notation):
C20H21FN2O · C2H2O4
CAS Number:
Molecular Weight:
414.43
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Product Name
Escitalopram oxalate, ≥98% (HPLC), powder
Quality Level
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to tan
solubility
DMSO: ≥15 mg/mL
originator
Forest Labs
storage temp.
2-8°C
SMILES string
OC(=O)C(O)=O.CN(C)CCC[C@]1(OCc2cc(ccc12)C#N)c3ccc(F)cc3
InChI
1S/C20H21FN2O.C2H2O4/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;3-1(4)2(5)6/h4-9,12H,3,10-11,14H2,1-2H3;(H,3,4)(H,5,6)/t20-;/m0./s1
InChI key
KTGRHKOEFSJQNS-BDQAORGHSA-N
Gene Information
human ... SLC6A4(6532)
General description
Escitalopram oxalate is an anti-depressant. It is used to treat panic disorder and major depressive disorder(MDD).
Application
Escitalopram oxalate has been used as an antidepressant in rats exposed to chronic mild stress (CMS). It has also been used for scintillation proximity-based thermostability assay.
Biochem/physiol Actions
Escitalopram is a selective serotonin reuptake inhibitor (SSRI), the S-enantiomer and eutomer of citalopram.
Escitalopram oxalate is a selective serotonin reuptake inhibitor (SSRI); the S-enantiomer and eutomer of citalopram.
Features and Benefits
This compound was developed by Forest Labs. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Escitalopram
Waugh J and Goa KL
CNS Drugs, 17(5), 343-362 (2003)
Modulation of the antioxidant nuclear factor (erythroid 2-derived)-like 2 pathway by antidepressants in rats
Martin-Hernandez D, et al.
Neuropharmacology, 103, 79-91 (2016)
Jasmin N Beaver et al.
Cells, 11(12) (2022-06-25)
Plasma membrane monoamine transporter (PMAT, Slc29a4) transports monoamine neurotransmitters, including dopamine and serotonin, faster than more studied monoamine transporters, e.g., dopamine transporter (DAT), or serotonin transporter (SERT), but with ~400-600-fold less affinity. A considerable challenge in understanding PMAT's monoamine clearance
