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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB001614 |
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Identification |
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| Name: |
Dihydroneopterin monophosphate |
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| Description: | Dihydroneopterin monophosphate is a member of the chemical class known as Biopterins and Derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. Dihdroneopterin monophosphate is an intermediate involved in tetrahydrofolate biosynthesis and salvage in Pseudomonas aeruginosa. It is converted to 7,8-dihydroneopterin through an unknown phosphorylase enzyme. |
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Structure |
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| Synonyms: | - 2-Amino-4-hydroxy-6-(erythro-1,2,3-trihydroxypropyl)dihydropteridine phosphate
- 2-amino-4-Hydroxy-6-(erythro-1,2,3-trihydroxypropyl)dihydropteridine phosphoric acid
- 7,8-Dihydro-D-neopterin 3'-phosphate
- 7,8-dihydro-D-Neopterin 3'-phosphoric acid
- Dihydroneopterin 3'-monophosphate
- Dihydroneopterin 3'-monophosphoric acid
- Dihydroneopterin 3'-phosphate
- Dihydroneopterin 3'-phosphoric acid
- Dihydroneopterin monophosphoric acid
- Dihydroneopterin-P
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Chemical Formula: |
C9H12N5O7P |
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| Average Molecular Weight: |
333.1946 |
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| Monoisotopic Molecular
Weight: |
333.047434275 |
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| InChI Key: |
PLSQMGZYOGSOCE-XINAWCOVSA-L |
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| InChI: | InChI=1S/C9H14N5O7P/c10-9-13-7-5(8(17)14-9)12-3(1-11-7)6(16)4(15)2-21-22(18,19)20/h4,6,15-16H,1-2H2,(H2,18,19,20)(H4,10,11,13,14,17)/p-2/t4-,6+/m1/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | 6-[(1S,2R)-3-(hydrogen phosphonatooxy)-1,2-dihydroxypropyl]-2-imino-1,2,7,8-tetrahydropteridin-4-olate |
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Traditional IUPAC Name: |
6-[(1S,2R)-3-(hydrogen phosphonatooxy)-1,2-dihydroxypropyl]-2-imino-7,8-dihydro-1H-pteridin-4-olate |
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| SMILES: | [H][C@@](O)(COP(O)([O-])=O)[C@@]([H])(O)C1=NC2=C(NC1)NC(=N)N=C2[O-] |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as biopterins and derivatives. These are coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland. |
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Kingdom |
Organic compounds |
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| Super Class | Organoheterocyclic compounds |
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Class |
Pteridines and derivatives |
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| Sub Class | Pterins and derivatives |
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Direct Parent |
Biopterins and derivatives |
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| Alternative Parents |
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| Substituents |
- Biopterin
- Secondary aliphatic/aromatic amine
- Alkyl phosphate
- Pyrimidine
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Organic phosphate
- Saccharide
- Heteroaromatic compound
- Secondary alcohol
- Ketimine
- 1,2-diol
- Azacycle
- Secondary amine
- Hydrocarbon derivative
- Organooxygen compound
- Organonitrogen compound
- Imine
- Amine
- Alcohol
- Organic anion
- 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: |
Not Available |
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| Charge: | -1 |
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Melting point: |
Not Available |
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| Experimental Properties: |
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| Predicted Properties |
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Biological Properties |
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| Cellular Locations: |
Cytoplasm |
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| Reactions: | |
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Pathways: |
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Spectra |
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| Spectra: |
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References |
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| References: |
- Keseler, I. M., Collado-Vides, J., Santos-Zavaleta, A., Peralta-Gil, M., Gama-Castro, S., Muniz-Rascado, L., Bonavides-Martinez, C., Paley, S., Krummenacker, M., Altman, T., Kaipa, P., Spaulding, A., Pacheco, J., Latendresse, M., Fulcher, C., Sarker, M., Shearer, A. G., Mackie, A., Paulsen, I., Gunsalus, R. P., Karp, P. D. (2011). "EcoCyc: a comprehensive database of Escherichia coli biology." Nucleic Acids Res 39:D583-D590. Pubmed: 21097882
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| Synthesis Reference: |
Not Available |
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| Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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| External Links: |
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