Record Information |
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Version | 1.0 |
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Created at | 2022-04-28 17:01:40 UTC |
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Updated at | 2022-04-28 17:01:40 UTC |
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NP-MRD ID | NP0071683 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | Purpuramine H |
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Description | Aplysamine 3 belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. Purpuramine H is found in Psammaplysilla purpurea and Suberea sp.. It was first documented in 2012 (PMID: 22620987). Based on a literature review a significant number of articles have been published on Aplysamine 3 (PMID: 25532280) (PMID: 24758268) (PMID: 22515429) (PMID: 22476960). |
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Structure | COC1=C(Br)C=C(C\C(=N/O)C(=O)NCCC2=CC(Br)=C(OCCCN)C(Br)=C2)C=C1 InChI=1S/C21H24Br3N3O4/c1-30-19-4-3-13(9-15(19)22)12-18(27-29)21(28)26-7-5-14-10-16(23)20(17(24)11-14)31-8-2-6-25/h3-4,9-11,29H,2,5-8,12,25H2,1H3,(H,26,28)/b27-18+ |
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Synonyms | Not Available |
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Chemical Formula | C21H24Br3N3O4 |
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Average Mass | 622.1520 Da |
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Monoisotopic Mass | 618.93170 Da |
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IUPAC Name | (2E)-N-{2-[4-(3-aminopropoxy)-3,5-dibromophenyl]ethyl}-3-(3-bromo-4-methoxyphenyl)-2-(N-hydroxyimino)propanamide |
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Traditional Name | (2E)-N-{2-[4-(3-aminopropoxy)-3,5-dibromophenyl]ethyl}-3-(3-bromo-4-methoxyphenyl)-2-(N-hydroxyimino)propanamide |
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CAS Registry Number | Not Available |
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SMILES | COC1=C(Br)C=C(C\C(=N/O)C(=O)NCCC2=CC(Br)=C(OCCCN)C(Br)=C2)C=C1 |
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InChI Identifier | InChI=1S/C21H24Br3N3O4/c1-30-19-4-3-13(9-15(19)22)12-18(27-29)21(28)26-7-5-14-10-16(23)20(17(24)11-14)31-8-2-6-25/h3-4,9-11,29H,2,5-8,12,25H2,1H3,(H,26,28)/b27-18+ |
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InChI Key | QQOOTUXDNKJQSN-OVVQPSECSA-N |
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Experimental Spectra |
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| Not Available | Predicted Spectra |
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| Spectrum Type | Description | Depositor ID | Depositor Organization | Depositor | Deposition Date | View |
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1D NMR | 13C NMR Spectrum (1D, 25 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 252 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 50 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 75 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 101 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 126 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 151 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 176 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 201 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 13C NMR Spectrum (1D, 226 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, predicted) | Wishart Lab | Wishart Lab | David Wishart | 2021-06-20 | View Spectrum |
| Chemical Shift Submissions |
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| Not Available | 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 anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. |
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Kingdom | Organic compounds |
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Super Class | Benzenoids |
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Class | Phenol ethers |
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Sub Class | Anisoles |
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Direct Parent | Anisoles |
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Alternative Parents | |
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Substituents | - Phenoxy compound
- Anisole
- Methoxybenzene
- Alkyl aryl ether
- Halobenzene
- Bromobenzene
- Fatty amide
- Aryl bromide
- Monocyclic benzene moiety
- Aryl halide
- Fatty acyl
- Ketoxime
- Amino acid or derivatives
- Secondary carboxylic acid amide
- Carboxamide group
- Ether
- Oxime
- Carboxylic acid derivative
- Organic nitrogen compound
- Primary aliphatic amine
- Organohalogen compound
- Organobromide
- Carbonyl group
- Organonitrogen compound
- Organooxygen compound
- Primary amine
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Amine
- Aromatic homomonocyclic compound
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Molecular Framework | Aromatic homomonocyclic compounds |
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External Descriptors | Not Available |
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Physical Properties |
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State | Not Available |
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Experimental Properties | Property | Value | Reference |
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Melting Point | Not Available | 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 | - Olatunji OJ, Ogundajo AL, Oladosu IA, Changwichit K, Ingkaninan K, Yuenyongsawad S, Plubrukarn A: Non-competitive inhibition of acetylcholinesterase by bromotyrosine alkaloids. Nat Prod Commun. 2014 Nov;9(11):1559-61. [PubMed:25532280 ]
- Kottakota SK, Evangelopoulos D, Alnimr A, Bhakta S, McHugh TD, Gray M, Groundwater PW, Marrs EC, Perry JD, Spilling CD, Harburn JJ: Synthesis and biological evaluation of purpurealidin E-derived marine sponge metabolites: aplysamine-2, aplyzanzine A, and suberedamines A and B. J Nat Prod. 2012 Jun 22;75(6):1090-101. doi: 10.1021/np300102z. Epub 2012 May 23. [PubMed:22620987 ]
- Tian LW, Feng Y, Shimizu Y, Pfeifer T, Wellington C, Hooper JN, Quinn RJ: Aplysinellamides A-C, bromotyrosine-derived metabolites from an Australian Aplysinella sp. marine sponge. J Nat Prod. 2014 May 23;77(5):1210-4. doi: 10.1021/np500119e. Epub 2014 Apr 23. [PubMed:24758268 ]
- Xu M, Davis RA, Feng Y, Sykes ML, Shelper T, Avery VM, Camp D, Quinn RJ: Ianthelliformisamines A-C, antibacterial bromotyrosine-derived metabolites from the marine sponge Suberea ianthelliformis. J Nat Prod. 2012 May 25;75(5):1001-5. doi: 10.1021/np300147d. Epub 2012 Apr 19. [PubMed:22515429 ]
- Gochfeld DJ, Kamel HN, Olson JB, Thacker RW: Trade-offs in defensive metabolite production but not ecological function in healthy and diseased sponges. J Chem Ecol. 2012 May;38(5):451-62. doi: 10.1007/s10886-012-0099-5. Epub 2012 Apr 4. [PubMed:22476960 ]
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