Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA009989
PROPERTIES
| NPAID | NPA009989 |
|---|---|
| CLUSTER ID | 626 |
| NODE ID | 556 |
| NAME | Nocarbenzoxazole G |
| FORMULA | C15H13NO4 |
| MOLECULAR WEIGHT (Da) | 271.2720 |
| ACCURATE MASS (Da) | 271.0845 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Nocardiopsis |
| ORIGIN SPECIES | lucentensis DSM 44048 |
| InChIKey | RFRAUDLICAGVNB-UHFFFAOYSA-N |
| InChI | InChI=1S/C15H13NO4/c1-19-14-7-10(3-4-12(14)18)15-16-11-6-9(8-17)2-5-13(11)20-15/h2-7,17-18H,8H2,1H3 |
| SMILES | COC1=C(O)C=CC(C2=NC3=C(C=CC(CO)=C3)O2)=C1 |
ORIGINAL ISOLATION REFERENCE
| CITATION | Sun, Mingwei; Zhang, Xiaomei; Hao, Huilin; Li, Wenjun; Lu, Chunhua Nocarbenzoxazoles A-G, Benzoxazoles Produced by Halophilic Nocardiopsis lucentensis DSM 44048 Journal of Natural Products 2015 78 (8) 2123-2127. | ||
|---|---|---|---|
| DOI | 10.1021/acs.jnatprod.5b00031 | PMID | 26270803 |
SYNTHESES
| CITATION 1 | Kim T; Lee SA; Noh T; Choi P; Choi SJ; Song BG; Kim Y; Park YT; Huh G; Kim YJ; Ham J Synthesis, Structure Revision, and Cytotoxicity of Nocarbenzoxazole G. Journal of Natural Products 2019 82 (5) 1325-1330. DOI: 10.1021/acs.jnatprod.9b00072 PMID: 30958679 | ||
|---|---|---|---|
REVISIONS
| VERSION | SMILES | CITATION | ||
|---|---|---|---|---|
| Original Isolation | COC1=C(C=CC(=C1)O)C2=NC3=C(O2)C=CC(=C3)CO | Sun, Mingwei; Zhang, Xiaomei; Hao, Huilin; Li, Wenjun; Lu, Chunhua Nocarbenzoxazoles A-G, Benzoxazoles Produced by Halophilic Nocardiopsis lucentensis DSM 44048 Journal of Natural Products 2015 78 (8) 2123-2127. DOI: 10.1021/acs.jnatprod.5b00031 PMID: 26270803 | ||
| 2 | COC1=C(O)C=CC(C2=NC3=C(C=CC(CO)=C3)O2)=C1 | Kim T; Lee SA; Noh T; Choi P; Choi SJ; Song BG; Kim Y; Park YT; Huh G; Kim YJ; Ham J Synthesis, Structure Revision, and Cytotoxicity of Nocarbenzoxazole G. Journal of Natural Products 2019 82 (5) 1325-1330. DOI: 10.1021/acs.jnatprod.9b00072 PMID: 30958679 | ||
