Compounds
| ID | Spectrum Quality | Annotated Name |
|---|---|---|
| CCMSLIB00000424917 | Bronze | Hapalindole&D |
| CCMSLIB00000424918 | Bronze | Hapalindole&D |
COMPOUND NPA004538
PROPERTIES
| NPAID | NPA004538 |
|---|---|
| CLUSTER ID | 719 |
| NODE ID | 628 |
| NAME | Hapalindole Q |
| FORMULA | C21H24N2S |
| MOLECULAR WEIGHT (Da) | 336.5040 |
| ACCURATE MASS (Da) | 336.1660 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Hapalosiphon |
| ORIGIN SPECIES | fontinalis |
| InChIKey | PPHWDUZMWNUINO-NOOVBMIQSA-N |
| InChI | InChI=1S/C21H24N2S/c1-5-21(4)11-10-15(14(2)3)19(20(21)23-13-24)17-12-22-18-9-7-6-8-16(17)18/h5-9,12,15,19-20,22H,1-2,10-11H2,3-4H3/t15-,19+,20+,21-/m0/s1 |
| SMILES | CC(=C)[C@@H]1CC[C@]([C@@H]([C@H]1C2=CNC3=CC=CC=C32)N=C=S)(C)C=C |
ORIGINAL ISOLATION REFERENCE
| CITATION | Moore, Richard E.; Cheuk, Chad; Yang, Xu-Qiang G.; Patterson, Gregory M. L.; Bonjouklian, Rosanne; et al. Hapalindoles, Antibacterial and Antimycotic Alkaloids from the Cyanophyte Hapalosiphon fontinalis Journal of Organic Chemistry 1987 52 (6) 1036-1043. | ||
|---|---|---|---|
| DOI | 10.1021/jo00382a012 | PMID | - |
SYNTHESES
| CITATION 1 | Kinsman AC; Kerr MA The total synthesis of (+)-hapalindole Q by an organomediated Diels-Alder reaction. Journal of the American Chemical Society 2003 125 (46) 14120-14125. DOI: 10.1021/ja036191y PMID: 14611249 | ||
|---|---|---|---|
| CITATION 2 | Kinsman AC; Kerr MA Total synthesis of (+/-)-hapalindole Q. Organic Letters 2001 3 (20) 3189-3191. DOI: 10.1021/ol0165138 PMID: 11574027 | ||
