InChI=1S/C48H72O14/c1- 11- 25(2) 43- 28(5) 17- 18- 47(62- 43) 23- 34- 20- 33(61- 47) 16- 15- 27(4) 42(26(3) 13- 12- 14- 32- 24- 55- 45- 40(49) 29(6) 19- 35(46(51) 58- 34) 48(32,45) 52) 59- 39- 22- 37(54- 10) 44(31(8) 57- 39) 60- 38- 21- 36(53- 9) 41(50) 30(7) 56- 38/h12- 15,17- 19,25- 26,28,30- 31,33- 45,49- 50,52H,11,16,20- 24H2,1- 10H3/b13- 12+,27- 15+,32- 14+/t25- ,26- ,28- ,30- ,31- ,33+,34- ,35- ,36- ,37- ,38- ,39- ,40+,41- ,42- ,43+,44- ,45+,47+,48+/m0/s1 |
RRZXIRBKKLTSOM-XPNPUAGNSA-N |
CC[C@H] (C) [C@H] 1O[C@@] 2(C[C@@H] 3C[C@@H] (C\C=C(C) \[C@@H] (O[C@H] 4C[C@H] (OC) [C@@H] (O[C@H] 5C[C@H] (OC) [C@@H] (O) [C@H] (C) O5) [C@H] (C) O4) [C@@H] (C) \C=C\C=C4/CO[C@@H] 5[C@H] (O) C(C) =C[C@@H] (C(=O) O3) [C@] 45O) O2) C=C[C@@H] 1C |
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Streptomyces avermitilis
(NCBI:txid33903)
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See:
PubMed
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bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via avermectin )
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View more via ChEBI Ontology
(2aE,4E,5'S,6S,6'R,7S,8E,11R,13S,15S,17aR,20R,20aR,20bS)- 20,20b- dihydroxy- 5',6,8,19- tetramethyl- 6'- [(1S)- 1- methylpropyl]- 17- oxo- 5',6,6',10,11,14,15,17,17a,20,20a,20b- dodecahydro- 2H,7H- spiro[11,15- methanofuro[4,3,2- pq][2,6]benzodioxacyclooctadecine- 13,2'- pyran]- 7- yl 2,6- dideoxy- 4- O- (2,6- dideoxy- 3- O- methyl- α- L- arabino- hexopyranosyl)- 3- O- methyl- α- L- arabino- hexopyranoside
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abamectin component B1a
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ChemIDplus
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Avermectin B1a
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KEGG COMPOUND
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3645625
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Beilstein Registry Number
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Beilstein
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65195-55-3
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CAS Registry Number
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KEGG COMPOUND
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65195-55-3
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CAS Registry Number
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ChemIDplus
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