Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA031289
PROPERTIES
| NPAID | NPA031289 |
|---|---|
| CLUSTER ID | 2376 |
| NODE ID | 1872 |
| NAME | Hapalonamide V |
| FORMULA | C21H23ClN2O3 |
| MOLECULAR WEIGHT (Da) | 386.8790 |
| ACCURATE MASS (Da) | 386.1397 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Hapalosiphon |
| ORIGIN SPECIES | fontinalis |
| InChIKey | MCXMMTXVFGCBFA-JBJCYXPGSA-N |
| InChI | InChI=1S/C21H23ClN2O3/c1-6-20(4)15(22)10-14-19(2,3)12-8-7-9-13(24-11-25)16(12)17(26)21(14,27)18(20)23-5/h6-9,11,14-15,18,27H,1,10H2,2-4H3,(H,24,25)/t14-,15-,18+,20+,21-/m1/s1 |
| SMILES | [C-]#[N+][C@@H]1[C@]2(O)C(=O)C3=C(C=CC=C3NC=O)C(C)(C)[C@H]2C[C@@H](Cl)[C@]1(C)C=C |
ORIGINAL ISOLATION REFERENCE
| CITATION | Richard E. Moore, Xu-qiang G. Yang, Gregory M.L. Patterson, Rosanne Bonjouklian, Tim A. Smitk Hapalonamides and other oxidized hapalindoles from Hapalosiphon fontinalis Phytochemistry 1989 28 (5) 1565-1567. | ||
|---|---|---|---|
| DOI | 10.1016/S0031-9422(00)97798-7 | PMID | - |
