Spinosyn J → HCID 101045613, compound

HRID 611796Notes

Reaction equation

HRID 611796 reaction equation
CC[C@@H]1OC(=O)C[C@@H]2C(=C[C@@H]3[C@H]2C=C[C@H]2[C@H]3C[C@H](O[C@@H]3O[C@@H](C)[C@H](OC)[C@@H](O)[C@H]3OC)C2)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](N(C)C)CC2)CCC1.[CH3:52][CH2:53][C@@H:54]1[O:77][C:75](=[O:76])[CH2:74][C@@H:73]2[C:62](=[CH:63][C@@H:64]3[C@@H:72]2[CH:71]=[C:70]([CH3:78])[C@@H:69]2[C@@H:65]3[CH2:66][C@@H:67]([O:79][C@@H:80]3[O:85][C@@H:84]([CH3:86])[C@H:83]([O:87][CH3:88])[C@@H:82]([OH:89])[C@H:81]3[O:90][CH3:91])[CH2:68]2)[C:60](=[O:61])[C@H:59]([CH3:92])[C@@H:58]([O:93][C@@H:94]2[O:99][C@H:98]([CH3:100])[C@@H:97]([N:101](C)[CH3:102])[CH2:96][CH2:95]2)[CH2:57][CH2:56][CH2:55]1.CC[C@@H]1OC(=O)C[C@@H]2C(=C[C@@H]3[C@H]2C=C[C@H]2[C@H]3C[C@H](O[C@@H]3O[C@@H](C)[C@H](OC)[C@@H](O)[C@H]3OC)C2)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](NC)CC2)CCC1>>[CH3:52][CH2:53][C@@H:54]1[O:77][C:75](=[O:76])[CH2:74][C@@H:73]2[C:62](=[CH:63][C@@H:64]3[C@H:72]2[CH:71]=[C:70]([CH3:78])[C@H:69]2[C@H:65]3[CH2:66][C@@H:67]([O:79][C@@H:80]3[O:85][C@@H:84]([CH3:86])[C@H:83]([O:87][CH3:88])[C@@H:82]([OH:89])[C@H:81]3[O:90][CH3:91])[CH2:68]2)[C:60](=[O:61])[C@H:59]([CH3:92])[C@@H:58]([O:93][C@@H:94]2[O:99][C@H:98]([CH3:100])[C@@H:97]([NH:101][CH3:102])[CH2:96][CH2:95]2)[CH2:57][CH2:56][CH2:55]1

Participants

4

Procedure

The following tables illustrate the amount of Spinosyn J, Spinosyn L, Spinosyn M, and Spinosyn N that were produced by culture NRRL 18719

Sources & evidence

ORD record
ord-41f48c8fb3994653bcf882896740ca02
Source dataset
uspto-grants-1999_12
Patent number
US06001981

Reaction notes

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