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Basic Description
| Synonyms | Ac-Gly-OH | acetamidoacetate | ACETURIC ACID [MI] | bmse000610 | DB02713 | F0921-6976 | N-Acetylglycine, Vetec(TM) reagent grade, 98% | 2-acetamidoacetate | MFCD00004275 | U2UT4677KR | EU-0096429 | BDBM82197 | EINECS 208-839-6 | NSC7605 | NSC-7605 | Ac Gl |
|---|---|
| Specifications & Purity | ≥99% |
| Storage Temp | Desiccated |
| Shipped In | Normal |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
- Superclass Organic acids and derivatives
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives |
| Direct Parent | N-acyl-alpha amino acids |
| Alternative Parents | Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | N-acyl-alpha-amino acid - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. |
| External Descriptors | N-acylglycine - N-acetyl-amino acid |
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Associated Targets(Human)
PAM
Tchem
Peptidyl-glycine alpha-amidating monooxygenase (90 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| Pubchem Sid | 488181236 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181236 |
| IUPAC Name | 2-acetamidoacetic acid |
| INCHI | InChI=1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8) |
| InChIKey | OKJIRPAQVSHGFK-UHFFFAOYSA-N |
| Smiles | CC(=O)NCC(=O)O |
| Isomeric SMILES | CC(=O)NCC(=O)O |
| WGK Germany | 3 |
| Molecular Weight | 117.1 |
| Beilstein | 774114 |
| Reaxy-Rn | 774114 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774114&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 H2012082 |
Certificate of Analysis | May 31, 2024 | A103973 |
| H2012080 |
Certificate of Analysis | May 31, 2024 | A103973 |
| H2012083 |
Certificate of Analysis | May 31, 2024 | A103973 |
| H2012081 |
Certificate of Analysis | May 31, 2024 | A103973 |
| G2402087 |
Certificate of Analysis | Apr 11, 2024 | A103973 |
| G2402088 |
Certificate of Analysis | Apr 11, 2024 | A103973 |
| G2402089 |
Certificate of Analysis | Apr 11, 2024 | A103973 |
| B2313021 |
Certificate of Analysis | Feb 16, 2023 | A103973 |
| L2216081 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| L2216083 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| L2216084 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| L2216082 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| L2216080 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| L2216079 |
Certificate of Analysis | Oct 25, 2022 | A103973 |
| I2226236 |
Certificate of Analysis | Oct 10, 2022 | A103973 |
| I2226237 |
Certificate of Analysis | Sep 29, 2022 | A103973 |
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Chemical and Physical Properties
| Solubility | Solubility in Water:almost transparency |
|---|---|
| Melt Point(°C) | 206～208℃ |
| Molecular Weight | 117.100 g/mol |
| XLogP3 | -1.200 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 117.043 Da |
| Monoisotopic Mass | 117.043 Da |
| Topological Polar Surface Area | 66.400 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 110.000 |
| 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 |
Citations of This Product
| 1. Fangyuan Xu, Mengyue Fan, Saisai Kang, Xinrui Duan. (2019) A genetically encoded fluorescent biosensor for detecting nitroreductase activity in living cancer cells. ANALYTICA CHIMICA ACTA, 1088 (131). |
| 2. Hui Guo, Mengyue Fan, Zengjin Li, Wei Tang, Xinrui Duan. (2018) Ratiometric RNA aptamer/fluorophore complex for RNA synthesis detection. Analytical Methods, 10 (47): (5629-5633). |
| 3. Guo Song, Yang Wenge, Hu Yonghong, Wang Kai, Luan Yuanyuan. (2013) Measurement and Correlation of the Solubility of N-Acetylglycine in Different Solvents at Temperatures from 278.15 to 319.15 K. JOURNAL OF SOLUTION CHEMISTRY, 42 (10): (1879-1887). |
| 4. Jinqiang Jiang, Chao Gou, Jing Luo, Chenglin Yi, Xiaoya Liu. (2012) A novel highly selective colorimetric sensor for Ni(II) ion using coumarin derivatives. INORGANIC CHEMISTRY COMMUNICATIONS, 15 (12). |
| 5. Wenqing Zhang, Hao Zhu, Wenjie Xie, Chuanyuan Du, Xiuqiang Fang, Ruiming Zhang, Xiaosong Hu, Yawei Lin. (2024) Highly sensitive analysis of fatty aldehydes in vegetable oils using a novel coumarin-based fluorescent probe by HPLC for quality control. MICROCHEMICAL JOURNAL, 205 (111180). |
| 6. Hui Huang, Wendi Xuan, Jiakang Hai, Xue Wang, Meng Chen, Guobing Hong, Xinyue Dai, Lili Xia, Wei Feng, Yu Chen. (2024) NIR-II light-activated and Cu nanocatalyst-enabled bioorthogonal reaction in living systems for efficient tumor therapy. Nano Today, 59 (102483). |
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