Record Information |
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Version | 1.0 |
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Created at | 2021-01-05 23:30:01 UTC |
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Updated at | 2021-07-15 17:16:53 UTC |
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NP-MRD ID | NP0014287 |
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Secondary Accession Numbers | None |
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Natural Product Identification |
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Common Name | Suncheonoside B |
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Provided By | NPAtlas |
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Description | Suncheonoside B is found in Streptomyces sp. It was first documented in 2015 (PMID: 26078114). Based on a literature review a significant number of articles have been published on Suncheonoside B (PMID: 34607305) (PMID: 34607338) (PMID: 34607315) (PMID: 34607308). |
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Structure | [H]O[C@@]1([H])[C@]([H])(OC2=C(C(=O)SC([H])([H])[H])C(=C(C(OC([H])([H])[H])=C2C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])O[C@@]([H])(C([H])([H])[H])[C@]([H])(O[H])[C@@]1([H])O[H] InChI=1S/C20H30O7S/c1-8(2)12-9(3)17(25-6)10(4)18(13(12)19(24)28-7)27-20-16(23)15(22)14(21)11(5)26-20/h8,11,14-16,20-23H,1-7H3/t11-,14-,15+,16+,20-/m0/s1 |
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Synonyms | Value | Source |
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[4-Methoxy-3,5-dimethyl-2-(propan-2-yl)-6-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl](methylsulphanyl)methanone | Generator |
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Chemical Formula | C20H30O7S |
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Average Mass | 414.5100 Da |
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Monoisotopic Mass | 414.17122 Da |
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IUPAC Name | [4-methoxy-3,5-dimethyl-2-(propan-2-yl)-6-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl](methylsulfanyl)methanone |
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Traditional Name | (2-isopropyl-4-methoxy-3,5-dimethyl-6-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)(methylsulfanyl)methanone |
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CAS Registry Number | Not Available |
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SMILES | COC1=C(C)C(C(C)C)=C(C(=O)SC)C(O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)=C1C |
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InChI Identifier | InChI=1S/C20H30O7S/c1-8(2)12-9(3)17(25-6)10(4)18(13(12)19(24)28-7)27-20-16(23)15(22)14(21)11(5)26-20/h8,11,14-16,20-23H,1-7H3/t11-,14-,15+,16+,20-/m0/s1 |
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InChI Key | CMVHZNYTKJFYLM-WAPRPUHNSA-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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Classification | Not classified |
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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 | - Shin B, Ahn S, Noh M, Shin J, Oh DC: Suncheonosides A-D, Benzothioate Glycosides from a Marine-Derived Streptomyces sp. J Nat Prod. 2015 Jun 26;78(6):1390-6. doi: 10.1021/acs.jnatprod.5b00284. Epub 2015 Jun 16. [PubMed:26078114 ]
- Amirhashchi F, Azaran A, Seyedian SS, Jalilian S, Keikhaei B: Occult Hepatitis B Virus Infection among beta-Thalassemia Major Patients in Ahvaz City, Iran. Am J Trop Med Hyg. 2021 Oct 4. pii: tpmd210785. doi: 10.4269/ajtmh.21-0785. [PubMed:34607305 ]
- Ansari SA, Manjunatha C, Parveen N, Shivaraj BW, Hari Krishna R: Mechanistic insights into defect chemistry and tailored photoluminescence and photocatalytic properties of aliovalent cation substituted Zn0.94M0.06-xLixO (M: Fe(3+), Al(3+), Cr(3+)) nanoparticles. Dalton Trans. 2021 Oct 4. doi: 10.1039/d1dt01706c. [PubMed:34607338 ]
- Li H, Gong Y, Guo Z, Dong Z, Liao J, Tao Q, Dong J, Chen D: Unusual suppression of tungsten 5d electron depletion in superhard tungsten tetraboride solid solution with chromium under compression. J Phys Condens Matter. 2021 Oct 4. doi: 10.1088/1361-648X/ac2caa. [PubMed:34607315 ]
- El-Gendy AA, Hassan SHMET, Gertz B, Bernard B, Ahmed MM, Elzohry HA, El Tawab GA, El-Sayed ME, Kamel SY, Zakaria H, Mahros AM, Ahmed MH, Tahoon MA, Sakr MA, Gadallah AA, Ahmed FE, Elgazzar MF: Serotyping and Antibiotic Susceptibility of Invasive Streptococcus agalactiae in Egyptian Patients with or without Diabetes Mellitus. Am J Trop Med Hyg. 2021 Oct 4. pii: tpmd210300. doi: 10.4269/ajtmh.21-0300. [PubMed:34607308 ]
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