Amitriptyline HCl - 10mM in DMSO , Norepinephrine transporter inhibitor, CAS No.549-18-8, Norepinephrine transporter inhibitor

CAS: 549-18-8 Cat. No.: A408601 Molecular Weight: 313.86 EC Number: 208-964-6
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GRADE & PURITY 10mM in DMSO
Synonyms
1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N,N-dimethyl-, hydrochloride (1:1)
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
A408601-1ml
2
$37.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Amitriptyline HCl is an inhibitor of bothserotonin transporter (SERT)andnorepinephrine transporter (NET)with Ki of 3.45 nM and 13.3 nM, respectively. Amitriptyline HCl also inhibitshistamine receptor H1,histamine receptor H4,5-HT2andsigma 1 receptorwith K
In vitro

Amitriptyline inhibits Forskolin-stimulated cyclic AMP accumulation with EC50 values of 16.2 μM in intact CHO/DOR cells. Amitriptyline causes a concentration-dependent stimulation of ERK1/2 and GSK-3β phosphorylation with EC50 values of 9.0 μM in CHO/DOR cells. Amitriptyline (15 μM) causes a stimulation of ERK1/2 phosphorylation in C6 cells. Amitriptyline (30 μM) inhibits Forskolin-stimulated adenylyl cyclase activity and antagonizes (−)-U50,488 inhibitory effect in rat nucleus accumbens. Amitriptyline binds the extracellular domain of both TrkA and TrkB and promotes TrkA-TrkB receptor heterodimerization. Amitriptyline (< 500 nM) promotes TrkA autophosphorylation in primary neurons and induces neurite outgrowth in PC12 cells. Amitriptyline selectively protects T17 cells from apoptosis with EC50 of 50 nM. [6]

In vivo

Amitriptyline (15 mg/kg, i.p.) activates TrkA and TrkB receptors and significantly reduces kainic acid-triggered neuronal cell death in mice. Amitriptyline (15 mg/kg and 30 mg/kg, i.p.) dose-dependently decreases the immobility time in the forced swimming test (FST) of mice. Amitriptyline (15 mg/kg, i.p.) shows a significant 24-h rhythm in the immobility time in the forced swimming test (FST) of mice. Amitriptyline (1 mg/kg and 3 mg/kg) significantly increases the total distance travelled of mice in novel cages. Amitriptyline (10 mg/kg p.o., twice daily) considerably attenuates the hypothermic response to 8-OHDPAT and mCPP in mice. Amitriptyline (10 mg/kg p.o., twice daily) significantly reduces serotonin transporter density by approximately 20% in cortex of mice.
Cell Data

cell lines:Mutant cell lines (G401, A204, G402, KYM-1), Wild type cell line (RD, 293, SJCRH30)

Concentrations:

Incubation Time:

Powder Purity:≥99%

Specifications

Synonyms
1-Propanamine, 3-(10, 11-dihydro-5H-dibenzo[a, d]cyclohepten-5-ylidene)-N, N-dimethyl-, hydrochloride (1:1)
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Amitriptyline HCl is an inhibitor of both serotonin transporter (SERT) and norepinephrine transporter (NET) with Ki of 3.45 nM and 13.3 nM, respectively. Amitriptyline HCl also inhibits histamine receptor H1, histamine receptor H4, 5-HT2 and sigma 1 recep
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Norepinephrine transporter inhibitor
Names and Identifiers
Isomeric SMILES CN(C)CCC=C1C2=CC=CC=C2CCC3=CC=CC=C31.Cl
WGK Germany 3
RTECS HO9450000
Alternate CAS 50-48-6
Molecular Weight 313.86
Reaxy-Rn 4164595
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4164595&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro Water: 37 mg/mL (201.01 mM); DMSO: 3 mg/mL (16.29 mM); Ethanol: Insoluble;
Melt Point(°C)195 °C
Citations of This Product
References
1. Cong Lu, Zhen Wei, Yongquan Wang, Shuying Li, Litao Tong, Xinmin Liu, Bei Fan, Fengzhong Wang.  (2022)  Soy isoflavones alleviate lipopolysaccharide-induced depressive-like behavior by suppressing neuroinflammation, mediating tryptophan metabolism and promoting synaptic plasticity.  Food & Function,  13  (18): (9513-9522).  [PMID:35993820] [10.1039/D2FO01437H]
2. Cong Lu, Rongjing Gao, Yingyu Zhang, Ning Jiang, Ying Chen, Jing Sun, Qiong Wang, Bei Fan, Xinmin Liu, Fengzhong Wang.  (2021)  S-equol, a metabolite of dietary soy isoflavones, alleviates lipopolysaccharide-induced depressive-like behavior in mice by inhibiting neuroinflammation and enhancing synaptic plasticity.  Food & Function,  12  (13): (5770-5778).  [PMID:34038497] [10.1039/D1FO00547B]
3. Libin Wan, Bin Lin, Ruiqin Zhu, Chuixiu Huang, Stig Pedersen-Bjergaard, Xiantao Shen.  (2019)  Liquid-Phase Microextraction or Electromembrane Extraction?.  ANALYTICAL CHEMISTRY,      [PMID:31141346] [10.1021/acs.analchem.9b00946]
4. Dan Liu, Ting Qiao, Haiyan Liu, Xiaoling Wang, Zhi-guo Shi.  (2017)  A simple approach to prepare a sulfone-embedded stationary phase for HPLC.  JOURNAL OF SEPARATION SCIENCE,  41  (4): (877-885).  [PMID:29205869] [10.1002/jssc.201700751]
5. Qianqian Shang, Yangyang Liu, Menghan Hou, Zhuangzhuang Dong, Stig Pedersen-Bjergaard, Chuixiu Huang, Xiantao Shen.  (2025)  Automated Formation of Supported Liquid Membranes by Molecular Self-Assembly: A Step Forward for Liquid-Phase Microextraction.  ANALYTICAL CHEMISTRY,      [PMID:41166073] [10.1021/acs.analchem.5c05134]
Solution Calculators
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