Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA015665
PROPERTIES
| NPAID | NPA015665 |
|---|---|
| CLUSTER ID | 5440 |
| NODE ID | 3868 |
| NAME | Cispentacin |
| FORMULA | C6H11NO2 |
| MOLECULAR WEIGHT (Da) | 129.1590 |
| ACCURATE MASS (Da) | 129.0790 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Bacillus |
| ORIGIN SPECIES | cereus (L450-B2) |
| InChIKey | JWYOAMOZLZXDER-UHNVWZDZSA-N |
| InChI | InChI=1S/C6H11NO2/c7-5-3-1-2-4(5)6(8)9/h4-5H,1-3,7H2,(H,8,9)/t4-,5+/m1/s1 |
| SMILES | N[C@H]1CCC[C@H]1C(=O)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Konishi; Nishio; Saitoh; Miyaki; Oki; Kawaguchi Cispentacin, a new antifungal antibiotic. I. Production, isolation, physico-chemical properties and structure Journal of Antibiotics 1989 42 (12) 1749-1755. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.42.1749 | PMID | 2516082 |
SYNTHESES
| CITATION 1 | Aggarwal VK; Roseblade S; Alexander R The use of enantiomerically pure ketene dithioacetal bis(sulfoxides) in highly diastereoselective intramolecular nitrone cycloadditions. Application in the total synthesis of the beta-amino acid (-)-cispentacin and the first asymmetric synthesis of cis-(3R,4R)-4-amino-pyrrolidine-3-carboxylic acid. Organic & Biomolecular Chemistry 2003 1 (4) 684-91. DOI: 10.1039/B212719A PMID: 12929455 | ||
|---|---|---|---|
