Name |
RES 701-2 |
Formula |
C103H115N23O24 |
Mw |
2057.84853177 |
CAS RN |
171927-41-6 |
C_ID |
C00016600
,
|
InChIKey |
CXJFFNSFXUKNNN-ZITSZQLINA-N |
InChICode |
InChI=1S/C103H115N23O24/c1-53-102(148)126-34-14-24-81(126)100(146)123-79(45-85(133)109-50-86(134)114-77(43-83(104)131)97(143)119-75(40-60-47-108-69-23-12-10-20-66(60)69)96(142)121-76(42-62-49-106-52-112-62)90(136)111-51-87(135)125-88(54(2)127)101(147)113-53)99(145)120-74(39-59-46-107-68-22-11-9-19-65(59)68)95(141)117-70(35-55-15-5-3-6-16-55)91(137)115-71(36-56-17-7-4-8-18-56)93(139)122-78(44-84(105)132)98(144)118-72(37-57-26-30-63(128)31-27-57)92(138)116-73(38-58-28-32-64(129)33-29-58)94(140)124-80(103(149)150)41-61-48-110-89-67(61)21-13-25-82(89)130/h3-13,15-23,25-33,46-49,52-54,70-81,88,107-108,110,127-130H,14,24,34-45,50-51H2,1-2H3,(H2,104,131)(H2,105,132)(H,106,112)(H,109,133)(H,111,136)(H,113,147)(H,114,134)(H,115,137)(H,116,138)(H,117,141)(H,118,144)(H,119,143)(H,120,145)(H,121,142)(H,122,139)(H,123,146)(H,124,140)(H,125,135)(H,149,150)/t53-,54+,70-,71-,72-,73-,74-,75-,76-,77-,78-,79-,80-,81-,88-/m0/s1 |
SMILES |
c1ccc2c(c1)c(c[nH]2)C[C@H]1C(=O)N[C@H](C(=O)NCC(=O)N[C@H](C(=O)N[C@H](C(=O)N2[C@H](C(=O)N[C@@H](CC(=O)NCC(=O)N[C@H](C(=O)N1)CC(=O)N)C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)O)Cc1c[nH]c3c1cccc3O)Cc1ccc(cc1)O)Cc1ccc(cc1)O)CC(=O)N)Cc1ccccc1)Cc1ccccc1)Cc1c[nH]c3c1cccc3)CCC2)C)[C@H](O)C)Cc1[nH]cnc1 |
Start Substs in Alk. Biosynthesis (Prediction) |
L-Trp Anthranilate |
Organism |
Kingdom |
Family |
Species |
Reference |
Bacteria | Streptomycetaceae | Streptomyces sp. RE-896 | Ref. |
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zoom in
Organism | Streptomyces sp. RE-896 | Reference | Ogawa,J.Antibiotics 48,(1995),1213 |
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