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Duloxetine Hydrochloride (CAS 136434-34-9)

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Alternate Names:
(γS)-N-Methyl-γ-(1-naphthalenyloxy)-2-thiophenepropanamine Hydrochloride; (+)-(S)-N-Methyl-γ-(1-naphthyloxy)-2-thiophenepropylamine Hydrochloride
Application:
Duloxetine Hydrochloride is a dual serotonin and norepinephrine reuptake inhibitor
CAS Number:
136434-34-9
Purity:
≥99%
Molecular Weight:
333.88
Molecular Formula:
C18H19NOS•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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SRP14 Inhibitors are a specialized class of chemical compounds that target the SRP14 protein, a crucial component of the Signal Recognition Particle (SRP) complex. The SRP complex is an essential part of the cellular machinery responsible for targeting and translocating nascent proteins to the endoplasmic reticulum (ER) in eukaryotic cells. Specifically, SRP14, along with SRP9, forms a heterodimer that binds to the Alu domain of SRP RNA, playing a pivotal role in the pausing of ribosomal translation. This pausing ensures that the nascent polypeptide chain is properly targeted to the ER, where it can enter the secretory pathway. Inhibitors of SRP14 disrupt this critical interaction, leading to a breakdown in the coordination between translation and protein targeting. The inhibition of SRP14 offers valuable insights into the fundamental processes of protein synthesis and targeting. By interfering with SRP14 function, researchers can study the effects on protein translation, folding, and trafficking, shedding light on how cells maintain protein homeostasis under various conditions. Furthermore, SRP14 Inhibitors serve as powerful tools for investigating the broader functions of the SRP complex in cellular physiology. These inhibitors can be used to dissect the molecular details of SRP-dependent targeting pathways, understand the consequences of mistargeted proteins, and explore the cellular stress responses triggered by such disruptions. Overall, SRP14 Inhibitors contribute significantly to our understanding of the complex network of protein synthesis and targeting, offering a window into the intricate balance cells must maintain to ensure proper function and survival.


Duloxetine Hydrochloride (CAS 136434-34-9) References

  1. Duloxetine hydrochloride.  |  Waitekus, AB. and Kirkpatrick, P. 2004. Nat Rev Drug Discov. 3: 907-8. PMID: 15558861
  2. Duloxetine hydrochloride: a new dual-acting medication for the treatment of major depressive disorder.  |  Hunziker, ME., et al. 2005. Clin Ther. 27: 1126-43. PMID: 16199241
  3. Polymorphism and a metastable solvate of duloxetine hydrochloride.  |  Marjo, CE., et al. 2011. Mol Pharm. 8: 2454-64. PMID: 22050389
  4. Retraction: Disposable screen-printed sensors for determination of Duloxetine Hydrochloride.  |  Alarfaj, NA., et al. 2012. Chem Cent J. 6: 72. PMID: 22828180
  5. Excessive sweating induced by interaction between agomelatine and duloxetine hydrochloride: case report and review of the literature.  |  Štuhec, M. 2015. Wien Klin Wochenschr. 127: 703-6. PMID: 25576334
  6. Duloxetine Hydrochloride-Induced Oral Lichenoid Reaction: A Case Report.  |  Kadam, NS., et al. 2015. Med Princ Pract. 24: 394-7. PMID: 26022117
  7. Comparative study of the effects of venlafaxine and duloxetine on chemotherapy-induced peripheral neuropathy.  |  Farshchian, N., et al. 2018. Cancer Chemother Pharmacol. 82: 787-793. PMID: 30105459
  8. Prurigo successfully treated with duloxetine hydrochloride.  |  Hashimoto, T., et al. 2019. Australas J Dermatol. 60: 237-239. PMID: 30675900
  9. Efficacy and safety of duloxetine in osteoarthritis: a systematic review and meta-analysis.  |  Osani, MC. and Bannuru, RR. 2019. Korean J Intern Med. 34: 966-973. PMID: 30871298
  10. Preparation and evaluation of duloxetine hydrochloride enteric-coated pellets with different enteric polymers.  |  Kuang, C., et al. 2017. Asian J Pharm Sci. 12: 216-226. PMID: 32104333
  11. Duloxetine hydrochloride loaded film forming dermal gel enriched with methylcobalamin and geranium oil attenuates paclitaxel-induced peripheral neuropathy in rats.  |  Chahal, SK., et al. 2020. IBRO Rep. 9: 85-95. PMID: 32760845
  12. Duloxetine-Associated Photodistributed Erythema Multiforme.  |  Gay, P., et al. 2022. Prim Care Companion CNS Disord. 24: PMID: 35522835
  13. LY248686, a new inhibitor of serotonin and norepinephrine uptake.  |  Wong, DT., et al. 1993. Neuropsychopharmacology. 8: 23-33. PMID: 8424846

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Duloxetine Hydrochloride, 10 mg

sc-207599
10 mg
$199.00

Duloxetine Hydrochloride, 100 mg

sc-207599A
100 mg
$317.00

Duloxetine Hydrochloride, 1 g

sc-207599B
1 g
$671.00

Hi, Could you please give me estimated shipping time for Duloxetine Hydrochloride (CAS 136434-34-9)? Thank you

Asked by: Larisa Kizima
Thank you for contacting Santa Cruz Biotechnology. To request a price quote and ship date please email scbt@scbt.com.
Answered by: BlakeJ
Date published: 2025-05-29

What is the appearance of the compound?

Asked by: two2igm05
Thank you for your question. Duloxetine Hydrochloride, sc-207599, is an off-white or white crystalline powder.
Answered by: TechService7
Date published: 2018-09-07
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Rated 5 out of 5 by from DuloxetineDuloxetine, a known dual serotonin and norepinephrine re-uptake inhibitor, has been reported to be commonly used for treatment of depression, diabetic neuropathic pain, fibromyalgia, anxiety, and urinary incontinence in women. -SCBT Publication Review
Date published: 2015-01-17
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Duloxetine Hydrochloride is rated 5.0 out of 5 by 1.
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