| Record Information |
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| Version | 2.0 |
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| Created at | 2005-11-16 15:48:42 UTC |
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| Updated at | 2025-02-11 15:41:27 UTC |
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| NP-MRD ID | NP0000693 |
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| Secondary Accession Numbers | None |
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| Natural Product Identification |
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| Common Name | Deoxyadenosine monophosphate |
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| Description | Deoxyadenosine monophosphate (dAMP), also known as deoxyadenylic acid or deoxyadenylate in its conjugate acid and conjugate base forms, respectively, is a derivative of the common nucleic acid AMP, or adenosine monophosphate, in which the -OH (hydroxyl) group on the 2' carbon on the nucleotide's pentose has been reduced to just a hydrogen atom (hence the "deoxy-" part of the name). Additionally, the monophosphate of the name indicates that two of the phosphoryl groups of GTP have been removed, most likely by hydrolysis. It is a monomer used in DNA. |
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| Structure | NC1=NC=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](COP(O)(O)=O)O1 InChI=1S/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 |
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| Synonyms | | Value | Source |
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| 2'-dAMP | ChEBI | | 2'-Deoxy-5'-adenosine monophosphate | ChEBI | | 2'-Deoxy-AMP | ChEBI | | 2'-Deoxyadenosine 5'-(dihydrogen phosphate) | ChEBI | | 2'-Deoxyadenosine 5'-phosphate | ChEBI | | 2'-Deoxyadenosine monophosphate | ChEBI | | 2'-DEOXYADENOSINE-5'-monophosphATE | ChEBI | | 2'-Deoxyadenylic acid | ChEBI | | dAMP | ChEBI | | Deoxy-5'-adenylic acid | ChEBI | | Deoxy-AMP | ChEBI | | Deoxyadenosine 5'-monophosphate | ChEBI | | Deoxyadenosine 5'-phosphate | ChEBI | | Deoxyadenylic acid | ChEBI | | 2'-Deoxyadenosine 5'-monophosphate | Kegg | | 2'-Deoxy-5'-adenosine monophosphoric acid | Generator | | 2'-Deoxyadenosine 5'-(dihydrogen phosphoric acid) | Generator | | 2'-Deoxyadenosine 5'-phosphoric acid | Generator | | 2'-Deoxyadenosine monophosphoric acid | Generator | | 2'-DEOXYADENOSINE-5'-monophosphoric acid | Generator | | 2'-Deoxyadenylate | Generator | | Deoxy-5'-adenylate | Generator | | Deoxyadenosine 5'-monophosphoric acid | Generator | | Deoxyadenosine 5'-phosphoric acid | Generator | | Deoxyadenylate | Generator | | 2'-Deoxyadenosine 5'-monophosphoric acid | Generator | | Deoxyadenosine monophosphoric acid | Generator | | 2'-Deoxy-5'-adenylate | HMDB | | 2'-Deoxy-5'-adenylic acid | HMDB | | 2'-Deoxy-adenosine 5'-phosphorate | HMDB | | 2'-Deoxy-adenosine 5'-phosphoric acid | HMDB | | 2'-Deoxyadenosine-5'-phosphate | HMDB | | Deoxyadenosine-phosphate | HMDB | | PdA | HMDB | | 2'-Deoxy-5'-adenosine monophosphate, ammonium salt | HMDB | | 2'-Deoxy-5'-adenosine monophosphate, disodium salt | HMDB | | 2'Deoxy-5'-AMP | HMDB | | dAMP CPD | HMDB |
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| Chemical Formula | C10H14N5O6P |
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| Average Mass | 331.2218 Da |
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| Monoisotopic Mass | 331.06817 Da |
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| IUPAC Name | {[(2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonic acid |
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| Traditional Name | DAMP |
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| CAS Registry Number | 653-63-4 |
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| SMILES | NC1=NC=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](COP(O)(O)=O)O1 |
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| InChI Identifier | InChI=1S/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 |
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| InChI Key | KHWCHTKSEGGWEX-RRKCRQDMSA-N |
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| Experimental Spectra |
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| | Spectrum Type | Description | Depositor Email | Depositor Organization | Depositor | Deposition Date | View |
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| 1D NMR | 1H NMR Spectrum (1D, 500 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | | 2D NMR | [1H, 13C]-HSQC NMR Spectrum (2D, 400 MHz, H2O, experimental) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| | Predicted Spectra |
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| Not Available | | Chemical Shift Submissions |
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| | Spectrum Type | Description | Depositor Email | Depositor Organization | Depositor | Deposition Date | View |
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| 1D NMR | 13C NMR Spectrum (1D, 400 MHz, H2O, simulated) | v.dorna83@yahoo.com | Not Available | Not Available | 2021-08-07 | View Spectrum |
| | Species |
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| Species of Origin | |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. |
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| Kingdom | Organic compounds |
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| Super Class | Nucleosides, nucleotides, and analogues |
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| Class | Purine nucleotides |
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| Sub Class | Purine deoxyribonucleotides |
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| Direct Parent | Purine 2'-deoxyribonucleoside monophosphates |
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| Alternative Parents | |
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| Substituents | - Purine 2'-deoxyribonucleoside monophosphate
- 6-aminopurine
- Imidazopyrimidine
- Purine
- Aminopyrimidine
- Monoalkyl phosphate
- N-substituted imidazole
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Pyrimidine
- Imidolactam
- Alkyl phosphate
- Azole
- Imidazole
- Heteroaromatic compound
- Tetrahydrofuran
- Secondary alcohol
- Azacycle
- Oxacycle
- Organoheterocyclic compound
- Organic oxygen compound
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Amine
- Organic nitrogen compound
- Organic oxide
- Organopnictogen compound
- Alcohol
- Hydrocarbon derivative
- Aromatic heteropolycyclic compound
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| Molecular Framework | Aromatic heteropolycyclic compounds |
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| External Descriptors | |
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| Physical Properties |
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| State | Solid |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | 148 °C | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties | |
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| General References | - Hohenester E, Hutchinson WL, Pepys MB, Wood SP: Crystal structure of a decameric complex of human serum amyloid P component with bound dAMP. J Mol Biol. 1997 Jun 20;269(4):570-8. [PubMed:9217261 ]
- Avkin S, Adar S, Blander G, Livneh Z: Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase. Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3764-9. Epub 2002 Mar 12. [PubMed:11891323 ]
- Duarte V, Muller JG, Burrows CJ: Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine. Nucleic Acids Res. 1999 Jan 15;27(2):496-502. [PubMed:9862971 ]
- Chen XR, Li GM, Wang JR, Chen JJ: [Portal hemodynamics in patients with different syndromes of cirrhosis]. Zhong Xi Yi Jie He Xue Bao. 2004 May;2(3):178-81. [PubMed:15339437 ]
- Zhong H, Zang KT: Therapeutic approaches for chronic gastralgia based on differentiation of symptoms and signs. Di Yi Jun Yi Da Xue Xue Bao. 2002 Jul;22(7):639-40. [PubMed:12376299 ]
- Hashimoto K, Tominaga Y, Nakabeppu Y, Moriya M: Futile short-patch DNA base excision repair of adenine:8-oxoguanine mispair. Nucleic Acids Res. 2004 Nov 5;32(19):5928-34. Print 2004. [PubMed:15531653 ]
- Zhang Q, Zhang WT, Wei JJ, Wang XB, Liu P: [Combined use of factor analysis and cluster analysis in classification of traditional Chinese medical syndromes in patients with posthepatitic cirrhosis]. Zhong Xi Yi Jie He Xue Bao. 2005 Jan;3(1):14-8. [PubMed:15644152 ]
- Levine RL, Yang IY, Hossain M, Pandya GA, Grollman AP, Moriya M: Mutagenesis induced by a single 1,N6-ethenodeoxyadenosine adduct in human cells. Cancer Res. 2000 Aug 1;60(15):4098-104. [PubMed:10945616 ]
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