Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA029975
PROPERTIES
| NPAID | NPA029975 |
|---|---|
| CLUSTER ID | 16 |
| NODE ID | 16 |
| NAME | Gliomasolide E |
| FORMULA | C18H32O5 |
| MOLECULAR WEIGHT (Da) | 328.4490 |
| ACCURATE MASS (Da) | 328.2250 |
| ORIGIN ORGANISM TYPE | Fungus |
| ORIGIN GENUS | Gliomastix |
| ORIGIN SPECIES | sp. ZSDS1-F7-2 |
| InChIKey | CIKXQDGRSUPQKJ-IGSZESLRSA-N |
| InChI | InChI=1S/C18H32O5/c1-2-3-4-9-17-10-5-7-14(19)12-16(21)13-15(20)8-6-11-18(22)23-17/h6,11,14-17,19-21H,2-5,7-10,12-13H2,1H3/b11-6+/t14-,15-,16-,17-/m1/s1 |
| SMILES | CCCCC[C@@H]1CCC[C@@H](O)C[C@@H](O)C[C@H](O)C/C=C/C(=O)O1 |
ORIGINAL ISOLATION REFERENCE
| CITATION | Zhang J; Lin X; Li L; Zhong B; Liao X; Liu Y; Xu S Gliomasolides A–E, unusual macrolides from a sponge-derived fungus Gliomastix sp. ZSDS1-F7-2 RSC Advances 2015 5 (67) 54645-54648. | ||
|---|---|---|---|
| DOI | 10.1039/c5ra08559d | PMID | - |
REVISIONS
| VERSION | SMILES | CITATION | ||
|---|---|---|---|---|
| Original Isolation | CCCCC[C@@H]1CCCC(O)C[C@@H](O)C[C@H](O)C/C=C/C(=O)O1 | Zhang J; Lin X; Li L; Zhong B; Liao X; Liu Y; Xu S Gliomasolides A–E, unusual macrolides from a sponge-derived fungus Gliomastix sp. ZSDS1-F7-2 RSC Advances 2015 5 (67) 54645-54648. DOI: 10.1039/c5ra08559d | ||
| 2 | CCCCC[C@@H]1CCC[C@@H](O)C[C@@H](O)C[C@H](O)C/C=C/C(=O)O1 | Reddy, Ramidi Gopal; Venkateshwarlu, Ravula; Ramakrishna, Kallaganti V S; Yadav, Jhillu S; Mohapatra, Debendra K Asymmetric Total Syntheses of Two Possible Diastereomers of Gliomasolide E and Its Structural Elucidation. Journal of Organic Chemistry 2017 82 (2) 1053-1063. DOI: 10.1021/acs.joc.6b02611 PMID: 27992722 | ||
