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| Product | Description | |
|---|---|---|
| Stachybotrylactam | An unusual spirodihydrobenzofuranlactam mycotoxin isolated from Stachybotrys sp. It shows immunosuppressant and weak HIV protease activity and shows diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Synonyms: Stachybotrylactam; 163391-76-2; 3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-furo[2,3-e]isoindole]-6'-one; Spiro[2H-furo[2,3-e]isoindole-2,1'(2'H)-naphthalen]-6(3H)-one, 3',4',4'a,5',6',7,7',8,8',8'a-decahydro-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-, (1'R,2'R,4'aS,6'R,8'aS)-; CID 45934402; Compound NP-020819; DTXSID70672955; CHEBI:201797; AKOS040737949; J-010041; (3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-7,8-dihydro-3H-uro[2,3-e]isoindole]-6'-one; 4,6'-DIHYDROXY-2',5',5',8'A-TETRAMETHYL-3',4',4'A,6',7,7',8,8'-OCTAHYDRO-2'H,3H-SPIRO[FURO[2,3-E]ISOINDOLE-2,1'-NAPHTHALEN]-6-ONE. Grade: >95% by HPLC. CAS No. 163391-76-2. Molecular formula: C23H31NO4. Mole weight: 385.50. |  |
| Stachybotrylactam (2-deoxy Antibiotic F1839A) | Isolated from a Stachybotrys sp., this unusual spirodi hydrobenzofuranlactam mycotoxin shows immuno-suppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. Group: Biochemicals. Alternative Names: 2-deoxy Antibiotic F1839A. Grades: Highly Purified. CAS No. 163391-76-2. Pack Sizes: 500ug. US Biological Life Sciences. |  Worldwide |
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