Amoxapine

For research use only. Not for therapeutic Use.

  • CAT Number: A000936
  • CAS Number: 14028-44-5
  • Molecular Formula: C17H16ClN3O
  • Molecular Weight: 313.8
  • Purity: ≥95%
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Amoxapine (Cat. No.:A000936) is a tricyclic antidepressant with rapid onset of action, low cardiotoxicity, and weak anticholinergic and sedative effects. It can produce strong antidepressant and psychostimulant effects by inhibiting the reuptake of norepinephrine by the presynaptic membrane in the brain.


Catalog Number A000936
CAS Number 14028-44-5
Synonyms

14028-44-5; Asendin; Demolox; Moxadil; Amoxan

Molecular Formula C17H16ClN3O
Purity ≥95%
Storage -20°C
InChI 1S/C17H16ClN3O/c18-12-5-6-15-13(11-12)17(21-9-7-19-8-10-21)20-14-3-1-2-4-16(14)22-15/h1-6,11,19H,7-10H2
InChIKey QWGDMFLQWFTERH-UHFFFAOYSA-N
SMILES C1CN(CCN1)C2=NC3=CC=CC=C3OC4=C2C=C(C=C4)Cl
Reference

1: Yang W, Wei B, Yan R. Amoxapine Demonstrates Incomplete Inhibition of
β-Glucuronidase Activity from Human Gut Microbiota. SLAS Discov. 2018
Jan;23(1):76-83. doi: 10.1177/2472555217725264. Epub 2017 Aug 15. PubMed PMID:
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2: Li X, Wang Q, Hu T, Wang Y, Zhao J, Lu J, Pei G. A tricyclic antidepressant,
amoxapine, reduces amyloid-β generation through multiple serotonin receptor
6-mediated targets. Sci Rep. 2017 Jul 10;7(1):4983. doi:
10.1038/s41598-017-04144-3. PubMed PMID: 28694424; PubMed Central PMCID:
PMC5504036.
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3: Hu J, Nagao K, Tai T, Kobayashi H, Nakajima K. Randomized Crossover Trial of
Amoxapine Versus Vitamin B12 for Retrograde Ejaculation. Int Braz J Urol. 2017
May-Jun;43(3):496-504. doi: 10.1590/S1677-5538.IBJU.2016.0468. PubMed PMID:
28266821; PubMed Central PMCID: PMC5462141.
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4: Meng M, Zhao N, Pederson CC, Harrison E, Green C, Gorman SH, Reuschel S.
Simultaneous quantification of loxapine, loxapine N-oxide, amoxapine,
8-hydroxyloxapine and 7-hydroxyloxapine in human plasma using LC-MS/MS. J
Chromatogr B Analyt Technol Biomed Life Sci. 2017 Mar 1;1046:87-97. doi:
10.1016/j.jchromb.2017.01.007. Epub 2017 Jan 9. PubMed PMID: 28152454.
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5: Bhardwaj RM, Raval V, Oswald ID, Florence AJ. Crystal structure of a mixed
solvated form of amoxapine acetate. Acta Crystallogr E Crystallogr Commun. 2015
Jan 10;71(Pt 2):139-41. doi: 10.1107/S2056989014028096. eCollection 2015 Feb 1.
PubMed PMID: 25878802; PubMed Central PMCID: PMC4384552.
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6: Kong R, Liu T, Zhu X, Ahmad S, Williams AL, Phan AT, Zhao H, Scott JE, Yeh LA,
Wong ST. Old drug new use–amoxapine and its metabolites as potent bacterial
β-glucuronidase inhibitors for alleviating cancer drug toxicity. Clin Cancer Res.
2014 Jul 1;20(13):3521-30. doi: 10.1158/1078-0432.CCR-14-0395. Epub 2014 Apr 29.
PubMed PMID: 24780296; PubMed Central PMCID: PMC4079752.
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7: Reeves KC, Virk S, Niedermier J, Duchemin AM. Addition of amoxapine improves
positive and negative symptoms in a patient with schizophrenia. Ther Adv
Psychopharmacol. 2013 Dec;3(6):340-2. doi: 10.1177/2045125313499363. PubMed PMID:
24294487; PubMed Central PMCID: PMC3840811.
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8: Karasakal A, Ulu ST. Development and validation of a sensitive
spectrofluorimetric method for the determination of amoxapine in human plasma and
urine. Luminescence. 2014 May;29(3):284-7. doi: 10.1002/bio.2541. Epub 2013 Jun
19. PubMed PMID: 23780763.
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9: Wong YC, Wo SK, Zuo Z. Investigation of the disposition of loxapine, amoxapine
and their hydroxylated metabolites in different brain regions, CSF and plasma of
rat by LC-MS/MS. J Pharm Biomed Anal. 2012 Jan 25;58:83-93. doi:
10.1016/j.jpba.2011.09.020. Epub 2011 Sep 22. PubMed PMID: 21993198.
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10: Yang G, Zhou MH, Ren Z, Xu JJ, Mei YA. Amoxapine inhibits delayed outward
rectifier K(+) currents in cerebellar granule cells via dopamine receptor and
protein kinase A activation. Cell Physiol Biochem. 2011;28(1):163-74. doi:
10.1159/000331725. Epub 2011 Aug 16. PubMed PMID: 21865859.

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