Ascr#8 leneuridine Synthesis and biological activity of

Synthesis and biological activity of retinoic acid receptor-alpha specific amides

25 mg/kg/day or 0

2R)-1-hydroxy-1-phenylpropan-2-yl]amino]-1-methoxy-2-methyl-3-oxopropyl]pyrrolidin-1-yl]-3-methoxy-5-methyl-1-oxoheptan-4-yl]-methylamino]-3-methyl-1-oxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]-methylcarbamoyl]oxymethyl]phenoxy]-3

InChi: InChI=1S/C27H25N3O4S2/c1-20-11-15-23(16-12-20)35(31

Smiles: C[C@H]1C[C@@H](NC2=CC=C(Cl)C=C2)C2C=C(C=CC=2N1C(C)=O)C1=CC=C(C=C1)C(=O)NCCOCCOCCOCC(=O)N[C@H](C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC1=CC=C(C=C1)C1SC=NC=1C)C(C)(C)C

Ascr#8 leneuridine Synthesis and biological activity ofAscr#8 is an dauer inducing ascaroside isolated from Caenorhabditis elegans, synergizes with ascr#2 and ascr#3, and strongly enhances male attraction. Product information CAS Number: 1172120 40 9 Molecular Weight: 393. 43 Formula: C20H27NO7 Chemical Name: 4 [(2E,6R) 6 {[(2R,3R,5R,6S) 3,5 dihydroxy 6 methyloxan 2 yl]oxy}hept 2 enamido]benzoic acid Smiles: C[C@H](CC C=C C(=O)NC1C=CC(=CC=1)C(O)=O)O[C@@H]1O[C@@H](C)[C@H](O)C[C@H]1O InChiKey: