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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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A425890-1ml
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1ml |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$69.90
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| Synonyms | amantadine | 1-Adamantanamine | 768-94-5 | adamantan-1-amine | 1-Adamantylamine | 1-Aminoadamantane | Adamantanamine | Adamantylamine | Aminoadamantane | Amantidine | Pk-merz | Adamantamine | Symadine | 1-Adamantamine | Amantadina | Amantadinum | adamantan-1-ylamine | Gocovri | Amantadinum |
|---|---|
| Specifications & Purity | Moligand™, 2mM in DMSO |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | CHANNEL BLOCKER |
| Mechanism of action | Channel blocker of GluN2A;Channel blocker of GluN2B;Channel blocker of GluN2C;Channel blocker of GluN2D |
| Product Description |
Building block for an L-piperidinamide catalyst used in an enantioselective Strecker reaction of phosphinoyl imines. application: 1-Adamantanamine acts as a catalyst in enantioselective strecker reaction of phosphinoyl imines. It is also useful for making adamantane derivatives, i.e. amantadine hydrochloride. It is used in the pharmaceutical industry as antiviral and an antiparkinsonian drug. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Primary amines |
| Direct Parent | Monoalkylamines |
| Alternative Parents | Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group. |
| External Descriptors | adamantanes - primary aliphatic amine |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| IUPAC Name | adamantan-1-amine |
|---|---|
| INCHI | InChI=1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2 |
| InChIKey | DKNWSYNQZKUICI-UHFFFAOYSA-N |
| Smiles | C1C2CC3CC1CC(C2)(C3)N |
| Isomeric SMILES | C1C2CC3CC1CC(C2)(C3)N |
| WGK Germany | 3 |
| RTECS | YD1925000 |
| Molecular Weight | 151.25 |
| Beilstein | 2204333 |
| Reaxy-Rn | 2204333 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2204333&ln= |
| Sensitivity | air sensitive |
|---|---|
| Melt Point(°C) | 206-208 °C |
| Molecular Weight | 151.250 g/mol |
| XLogP3 | 2.400 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 151.136 Da |
| Monoisotopic Mass | 151.136 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 144.000 |
| 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 |
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| 4. Cheng Gao, Cheryl H. T. Kwong, Qingfu Wang, Hiotong Kam, Beibei Xie, Simon Ming-Yuen Lee, Guosong Chen, Ruibing Wang. (2023) Conjugation of Macrophage-Mimetic Microalgae and Liposome for Antitumor Sonodynamic Immunotherapy via Hypoxia Alleviation and Autophagy Inhibition. ACS Nano, 17 (4): (4034–4049). |
| 5. Yuan-Yuan Liu, Jie Liu, Hao Wu, Qiangqiang Zhang, Xue-Rui Tang, Dan Li, Chen-Si Li, Yuanfang Liu, Aoneng Cao, Haifang Wang. (2023) Endocytosis, Distribution, and Exocytosis of Polystyrene Nanoparticles in Human Lung Cells. Nanomaterials, 13 (1): (84). |
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| 12. Q. Wang, X. Yu, Y. Zhao, Y. Wang, K. Chen, Y. Liu, B. Wang, H. Zhang, Y. Sun. (2022) Friction-induced supramolecular nanovalves for the potential treatment of osteoarthritis. Materials Today Chemistry, 24 (100876). |
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| 21. Xiaoming Ma, Shan He, Ying Zhang, Jianguo Xu, Huifang Zhang, Zhen Wang, Jun Xue, Xun Li, Wenbo Yu, Xiaolin Fan. (2020) Signal-off tuned signal-on (SF-T-SN) colorimetric immunoassay for amantadine using activity-metalmodulated peroxidase-mimicking nanozyme. SENSORS AND ACTUATORS B-CHEMICAL, 311 (127933). |
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| 23. Ying Kuang, Hui Chen, Zhongyin Chen, Lihui Wan, Jia Liu, Ziqiang Xu, Xueqin Chen, Bingbing Jiang, Cao Li. (2019) Poly(amino acid)/ZnO/mesoporous silica nanoparticle based complex drug delivery system with a charge-reversal property for cancer therapy. COLLOIDS AND SURFACES B-BIOINTERFACES, 181 (461). |
| 24. Zhiwu Chen, Hui Cao, Tianwei Tan. (2019) Preparation of functionalized star polymer nanoparticles by RAFT polymerization and their application in positionally assembled enzymes for cascade reactions. NEW JOURNAL OF CHEMISTRY, 43 (22): (8517-8526). |
| 25. Sa Liu, Chunting Zhong, Weiwei Wang, Yongguang Jia, Lin Wang, Li Ren. (2018) α-Cyclodextrins Polyrotaxane Loading Silver Sulfadiazine. Polymers, 10 (2): (190). |
| 26. Zhao Zheng, Jingjing Hu, Hui Wang, Junlin Huang, Yihua Yu, Qiang Zhang, Yiyun Cheng. (2017) Dynamic Softening or Stiffening a Supramolecular Hydrogel by Ultraviolet or Near-Infrared Light. ACS Applied Materials & Interfaces, 9 (29): (24511–24517). |
| 27. Liuyang Wang, Guoying Zhao, Xiaoqian Yao, Baozeng Ren, Suojiang Zhang. (2017) Adamantane-Based Cation and [MFn]− Anion Synergistically Enhanced Catalytic Performance of Sulfuric Acid for Isobutane Alkylation. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 56 (28): (7920–7929). |
| 28. Pin Lv, Cheng Zhou, Yulin Zhao, Xiali Liao, Bo Yang. (2017) Modified-epsilon-polylysine-grafted-PEI-β-cyclodextrin supramolecular carrier for gene delivery. CARBOHYDRATE POLYMERS, 168 (103). |
| 29. Wan-Fen Pu, Yang Yang, Bing Wei, Cheng-Dong Yuan. (2016) Potential of a β-Cyclodextrin/Adamantane Modified Copolymer in Enhancing Oil Recovery through Host–Guest Interactions. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 55 (31): (8679–8689). |
| 30. Xia Hao, Na Li, Zhen Xu, Nian Bing Li, Hong Qun Luo. (2016) An Electrochemical Sensing Strategy for Amantadine Detection Based on Competitive Host-guest Interaction of Methylene Blue/β-cyclodextrin/Poly(N-acetylaniline) Modified Electrode. ELECTROANALYSIS, 28 (7): (1489-1494). |
| 31. Jiaqiang Zhao, Lizhi Peng, Wenhua Zheng, Rikang Wang, Lei Zhang, Jian Yang, Heru Chen. (2015) Chemically Bonding of Amantadine with Gardenamide A Enhances the Neuroprotective Effects against Corticosterone-Induced Insults in PC12 Cells. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 16 (9): (22795-22810). |
| 32. Rongqiang Liao,Shouhui Yi,Manshuo Liu,Wenling Jin,Bo Yang. (2015-06-03) Folic-Acid-Targeted Self-Assembling Supramolecular Carrier for Gene Delivery.. Chembiochem : a European journal of chemical biology, 16 ((11)): (1622-1628). |
| 33. Dongjing Zhang,Cheng Zhou,Pin Lv,Yulin Zhao,Jing Liang,Xiali Liao,Bo Yang. (2018-03-12) Preparation and characterization of a novel host-guest complex based on folate-modified β-cyclodextrin and artesunate.. Materials science & engineering. C, Materials for biological applications, 86 (48-55). |
| 34. Luo Yusong, Liu Ruolan, Zhang He, Wang Hongyu, Yin Hang, Tian Guopeng, Wang Bo, Yan Yunji, Ding Zilin, Dai Junqiang, Niu Liang, Yuan Guoqiang, Pan Yawen. (2024) Amantadine against glioma via ROS-mediated apoptosis and autophagy arrest. Cell Death & Disease, 15 (11): (1-10). |
| 35. Xinyi Wang, Jing Wang, Houcheng Ding, Yongping Dong. (2025) Detection of acetylcholinesterase based on ECL resonance energy transfer between luminol and gold nanoparticle decorated covalent organic framework. MICROCHEMICAL JOURNAL, (112774). |
| 36. Rui-Dong Wang, Yi-Fei Zhang, Xiao-Long Han, Yu-Kun Gao, Ting-Ting You, Peng-Gang Yin. (2025) Development of hydroxypropylated polyrotaxane networks with macromolecular PEG crosslinkers: Strategies for enhanced ionic conductivity. EUROPEAN POLYMER JOURNAL, 230 (113893). |
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| 38. 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, (2024 Oct). |
| 39. Pan Ran, Bo Qiu, Huan Zheng, Shuang Xie, Guiyuan Zhang, Wenxiong Cao, Xiaohong Li. (2024) On-demand bactericidal and self-adaptive antifouling hydrogels for self-healing and lubricant coatings of catheters. Acta Biomaterialia, |
| 40. Rui-Dong Wang, Yi-Fei Zhang, Xiao-Long Han, Xiao-Yang Fan, Jun Tian, Yu-Kun Gao, Ting-Ting You, Peng-Gang Yin. (2024) Polyrotaxane-Based Solid Polymer Electrolyte with a Macromolecular Crosslinker. ACS Applied Polymer Materials, 6 (24): (15124-15135). |
| 41. Lei Chen, Yang Song, Lian Deng, Jianpeng Liu, Jiabao Liu, Daobing Jiang, Xiaoshuang Dai, Ke Mei, Junda Liu, Neng Qiu. (2025) Self-assembled stimuli-responsive adamantanamine-podophyllotoxin conjugate/β-cyclodextrins inclusion complex for enhanced solubility and anticancer activity. JOURNAL OF MOLECULAR STRUCTURE, 1324 (140752). |