Record Information |
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Version | 2.0 |
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Created at | 2024-03-14 02:35:27 UTC |
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Updated at | 2024-11-01 01:35:53 UTC |
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NP-MRD ID | NP0332617 |
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Natural Product DOI | https://doi.org/10.57994/1877 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | Leptochelin C |
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Description | Leptochelin C belongs to the class of organic compounds known as phenylalanine and derivatives. Phenylalanine and derivatives are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on Leptochelin C. |
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Structure | [H]OC(=O)[C@]1([H])CSC(=N1)[C@@]1(C)O[C@H]1[C@]1([H])CSC(=N1)[C@@](C)(N)[C@@H](O)[C@H](C)NC(=O)[C@H](CC1=CC=C(Br)C=C1)NC(=O)[C@@]1([H])COC(=N1)C1=CC=CC(Br)=C1O InChI=1S/C34H38Br2N6O8S2/c1-15(25(44)33(2,37)31-41-22(13-51-31)26-34(3,50-26)32-42-23(14-52-32)30(47)48)38-27(45)20(11-16-7-9-17(35)10-8-16)39-28(46)21-12-49-29(40-21)18-5-4-6-19(36)24(18)43/h4-10,15,20-23,25-26,43-44H,11-14,37H2,1-3H3,(H,38,45)(H,39,46)(H,47,48)/t15-,20-,21+,22-,23-,25-,26-,33-,34-/m0/s1 |
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Synonyms | Not Available |
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Chemical Formula | C34H38Br2N6O8S2 |
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Average Mass | 882.6400 Da |
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Monoisotopic Mass | 880.05593 Da |
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IUPAC Name | (4R)-2-[(2S,3S)-3-[(4R)-2-[(2S,3S,4S)-2-amino-4-[(2S)-2-{[(4R)-2-(3-bromo-2-hydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl]formamido}-3-(4-bromophenyl)propanamido]-3-hydroxypentan-2-yl]-4,5-dihydro-1,3-thiazol-4-yl]-2-methyloxiran-2-yl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid |
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Traditional Name | (4R)-2-[(2S,3S)-3-[(4R)-2-[(2S,3S,4S)-2-amino-4-[(2S)-2-{[(4R)-2-(3-bromo-2-hydroxyphenyl)-4,5-dihydro-1,3-oxazol-4-yl]formamido}-3-(4-bromophenyl)propanamido]-3-hydroxypentan-2-yl]-4,5-dihydro-1,3-thiazol-4-yl]-2-methyloxiran-2-yl]-4,5-dihydro-1,3-thiazole-4-carboxylic acid |
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CAS Registry Number | Not Available |
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SMILES | [H]OC(=O)[C@]1([H])CSC(=N1)[C@@]1(C)O[C@H]1[C@]1([H])CSC(=N1)[C@@](C)(N)[C@@H](O)[C@H](C)NC(=O)[C@H](CC1=CC=C(Br)C=C1)NC(=O)[C@@]1([H])COC(=N1)C1=CC=CC(Br)=C1O |
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InChI Identifier | InChI=1S/C34H38Br2N6O8S2/c1-15(25(44)33(2,37)31-41-22(13-51-31)26-34(3,50-26)32-42-23(14-52-32)30(47)48)38-27(45)20(11-16-7-9-17(35)10-8-16)39-28(46)21-12-49-29(40-21)18-5-4-6-19(36)24(18)43/h4-10,15,20-23,25-26,43-44H,11-14,37H2,1-3H3,(H,38,45)(H,39,46)(H,47,48)/t15-,20-,21+,22-,23-,25-,26-,33-,34-/m0/s1 |
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InChI Key | WQNBAVRYYSCIFR-ALXBNCHJSA-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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NOESY NMR | [1H, 1H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental) | navalon@ucsd.edu | CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal | Mariana A. Reis | 2024-06-20 | View Spectrum | COSY NMR | [1H, 1H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental) | navalon@ucsd.edu | CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal | Mariana A. Reis | 2024-06-20 | View Spectrum | HSQC NMR | [1H, 13C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental) | navalon@ucsd.edu | CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal | Mariana A. Reis | 2024-06-20 | View Spectrum | HMBC NMR | [1H, 13C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental) | navalon@ucsd.edu | CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal | Mariana A. Reis | 2024-06-20 | View Spectrum | 1D NMR | 1H NMR Spectrum (1D, 600 MHz, CDCl3, experimental) | navalon@ucsd.edu | CIIMAR/CIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal | Mariana A. Reis | 2024-06-20 | View Spectrum |
| Predicted Spectra |
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| Spectrum Type | Description | Depositor ID | Depositor Organization | Depositor | Deposition Date | View |
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| Chemical Shift Submissions |
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| Not Available | Species |
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Species of Origin | Species Name | Source | Reference |
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sp. | | |
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Chemical Taxonomy |
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Description | This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
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Kingdom | Organic compounds |
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Super Class | Organic acids and derivatives |
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Class | Carboxylic acids and derivatives |
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Sub Class | Amino acids, peptides, and analogues |
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Direct Parent | Phenylalanine and derivatives |
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Alternative Parents | |
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Substituents | - Phenylalanine or derivatives
- N-acyl-alpha amino acid or derivatives
- Cysteine or derivatives
- Alpha-amino acid amide
- Amphetamine or derivatives
- 2-bromophenol
- 2-halophenol
- 1-hydroxy-4-unsubstituted benzenoid
- Phenol
- Halobenzene
- Bromobenzene
- Fatty acyl
- Imidothiolactone
- Benzenoid
- N-acyl-amine
- Fatty amide
- Monocyclic benzene moiety
- Meta-thiazoline
- Oxazoline
- Secondary alcohol
- Imidothioester
- Carboxamide group
- Oxacycle
- Azacycle
- Bromoalkene
- Haloalkene
- Organoheterocyclic compound
- Organic 1,3-dipolar compound
- Propargyl-type 1,3-dipolar organic compound
- Sulfenyl compound
- Vinyl halide
- Vinyl bromide
- Monocarboxylic acid or derivatives
- Imidothioic acid or derivatives
- Ether
- Oxirane
- Dialkyl ether
- Carboxylic acid
- Organic nitrogen compound
- Organic oxygen compound
- Organopnictogen compound
- Organic oxide
- Hydrocarbon derivative
- Organosulfur compound
- Organooxygen compound
- Organonitrogen compound
- Organobromide
- Organohalogen compound
- Primary aliphatic amine
- Alcohol
- Aromatic heteromonocyclic compound
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Molecular Framework | Aromatic heteromonocyclic 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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