Compounds
ID | Spectrum Quality | Annotated Name |
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COMPOUND NPA011341
PROPERTIES
NPAID | NPA011341 |
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CLUSTER ID | 4394 |
NODE ID | 1727 |
NAME | Cyclophellitol |
FORMULA | C7H12O5 |
MOLECULAR WEIGHT (Da) | 176.1680 |
ACCURATE MASS (Da) | 176.0685 |
ORIGIN ORGANISM TYPE | Fungus |
ORIGIN GENUS | Phellinus |
ORIGIN SPECIES | sp. |
InChIKey | YQLWKYQDOQEWRD-GEGSFZHJSA-N |
InChI | InChI=1S/C7H12O5/c8-1-2-3(9)4(10)5(11)7-6(2)12-7/h2-11H,1H2/t2-,3-,4+,5-,6-,7+/m1/s1 |
SMILES | C([C@@H]1[C@H]([C@@H]([C@H]([C@H]2[C@@H]1O2)O)O)O)O |
ORIGINAL ISOLATION REFERENCE
CITATION | Atsumi, Sonoko; Umezawa, Kazou; Iinuma, Hironobu; Naganawa, Hiroshi; Nakamura, Hikaru; Iitaka, Yoichi; Takeuchi, Tomoi; PRODUCTION, ISOLATION AND STRUCTURE DETERMINATION OF A NOVEL β-GLUCOSIDASE INHIBITOR, CYCLOPHELLITOL, FROM PHELLINUS SP Journal of Antibiotics 1990 43 (1) 49-53. | ||
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DOI | 10.7164/antibiotics.43.49 | PMID | 2106502 |
SYNTHESES
CITATION 1 | Ishikawa T; Shimizu Y; Kudoh T; Saito S Conversion of D-glucose to cyclitol with hydroxymethyl substituent via intramolecular silyl nitronate cycloaddition reaction: application to total synthesis of (+)-cyclophellitol. Organic Letters 2003 5 (21) 3879-82. DOI: 10.1021/ol035424n PMID: 14535733 |
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