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| STACHYBOTRYLACTAM Basic information |
Product Name: | STACHYBOTRYLACTAM | Synonyms: | STACHYBOTRYLACTAM;2-deoxy F1839A;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)- | CAS: | 163391-76-2 | MF: | C23H31NO4 | MW: | 385.5 | EINECS: | | Product Categories: | | Mol File: | 163391-76-2.mol | |
| STACHYBOTRYLACTAM Chemical Properties |
Melting point | 210℃ (Decomposition) (ethyl acetate ) | Boiling point | 630.0±55.0 °C(Predicted) | density | 1.28±0.1 g/cm3(Predicted) | storage temp. | -20°C | solubility | DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble | form | neat | pka | 9.39±0.70(Predicted) |
| STACHYBOTRYLACTAM Usage And Synthesis |
Uses | Stachybotrylactam is an unusual, spirodihydrobenzofuranlactam mycotoxin isolated from a Stachybotrys sp., showing immunosuppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. | Uses | Stachybotrylactam is an unusual spirodihydrobenzofuranlactam mycotoxin isolated from a Stachybotrys sp. that has immunosuppressant and weak HIV protease activity. Members of this structural class show diverse activity including antiviral, endothelin and pancreatic cholesterase inhibition. |
| STACHYBOTRYLACTAM Preparation Products And Raw materials |
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