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Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Information
Amitriptyline Amitriptyline (MK-230, N-750, Ro41575) is a tricyclic antidepressant (TCA) with analgesic properties, widely used to treat depression and neuropathic pain. Amitriptyline is an inhibitor of both serotonin transporter (SERT) and norepinephrine transporter (NET) with Ki of 3.45 nM and 13.3 nM, respectively. Amitriptyline also inhibits histamine receptor H1 , histamine receptor H4 , 5-HT2 and sigma 1 receptor with Ki of 0.5 nM, 7.31 nM, 235 nM and 287 nM, respectively. This product is a waxy solid.
| Canonical Smiles | CN(C)CCC=C1C2=CC=CC=C2CCC3=CC=CC=C31 |
|---|---|
| IUPAC Name | N,N-dimethyl-3-(2-tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaenylidene)propan-1-amine |
| InChIKey | KRMDCWKBEZIMAB-UHFFFAOYSA-N |
| INCHI | 1S/C20H23N/c1-21(2)15-7-12-20-18-10-5-3-8-16(18)13-14-17-9-4-6-11-19(17)20/h3-6,8-12H,7,13-15H2,1-2H3 |
| Isomeric SMILES | CN(C)CCC=C1C2=CC=CC=C2CCC3=CC=CC=C31 |
| Molecular Weight | 277.41 |
| Reaxy-Rn | 2217885 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2217885&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Dibenzocycloheptenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dibenzocycloheptenes |
| Alternative Parents | Trialkylamines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Dibenzocycloheptene - Tertiary aliphatic amine - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as dibenzocycloheptenes. These are compounds containing a dibenzocycloheptene moiety, which consists of two benzene rings connected by a cycloheptene ring. |
| External Descriptors | tertiary amine - organic tricyclic compound |
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| Molecular Weight | 277.400 g/mol |
|---|---|
| XLogP3 | 5.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 277.183 Da |
| Monoisotopic Mass | 277.183 Da |
| Topological Polar Surface Area | 3.200 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 331.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Yujie Cao, Tianran Sheng, Jinfei Mei, Peng Qian, Deqian Huang, Liangquan Sheng, Guoping Sheng. (2022) Abundant oxygen vacancies constructed by deep reduction strategy to achieve ultra-high peroxomonosulfate activation efficiency for degrading organic pollutions in water. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2022.121892] |
| 2. Zhihong Yao, Shishi Li, Zifei Qin, Xiaodan Hong, Yi Dai, Baojian Wu, Wencai Ye, Frank J. Gonzalez, Xinsheng Yao. (2017) Characterization of human UDP-glucuronosyltransferases responsible for glucuronidation and inhibition of norbakuchinic acid, a primary metabolite of hepatotoxicity and nephrotoxicity component bakuchiol in Psoralea corylifolia L.. RSC Advances, 7 (83): (52661-52671). [PMID:] [10.1039/C7RA10376J] |
| 3. Pengchao Xie, Yizhou Guo, Yiqun Chen, Zongping Wang, Ran Shang, Songlin Wang, Jiaqi Ding, Ying Wan, Wei Jiang, Jun Ma. (2016) Application of a novel advanced oxidation process using sulfite and zero-valent iron in treatment of organic pollutants. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2016.12.094] |
| 4. Ximei Li, Lihua Xin, Lan Yang, Yi Yang, Wei Li, Mingyu Zhang, Yufen Liao, Chen Sun, Weiwei Li, Ying Peng, Jiang Zheng. (2024) Identification of an Epoxide Metabolite of Amitriptyline In Vitro and In Vivo. CHEMICAL RESEARCH IN TOXICOLOGY, [PMID:38761382] [10.1021/acs.chemrestox.4c00008] |
| 5. Lu Yang, Zijin Lin, Ruijing Mu, Wenhan Wu, Hao Zhi, Xiaodong Liu, Hanyu Yang, Li Liu. (2024) Neurons enhance blood–brain barrier function via upregulating claudin-5 and VE-cadherin expression due to glial cell line-derived neurotrophic factor secretion. eLife, [PMID:39475379] [10.7554/eLife.96161] |
| 6. Moying Yang, Yan Yao, Haotian Shen, Fei Teng, Yunuo Liu, Yuyang Ma, Bin Di, Mengxiang Su. (2025) Detection of antidepressants in wastewater from four provinces of China by UPLC-MS/MS to assess the regional prevalence of depression. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2025.114446] |
| 7. Teer Wen, Fangying Hu, Yao Yue, Chuqiao Li, Yunfei He, Jiafeng Ding. (2025) Enhanced Amitriptyline Degradation by Electrochemical Activation of Peroxydisulfate: Mechanisms of Interfacial Catalysis and Mass Transfer. MOLECULES, 30 (18): (3835). [PMID:41011726] [10.3390/molecules30183835] |
| 8. Wenjie Yuan, Yicheng Wu, Yeling Zhou, Bingjun Shu, Jinqi Cai, Haiyan Fu. (2025) Amitriptyline toxicity mechanisms in Chlorella vulgaris and potential for bioremediation of contaminated wastewater. Algal Research-Biomass Biofuels and Bioproducts, [PMID:] [10.1016/j.algal.2025.104475] |
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