Table 2 NMR data of Cabanillasin (D20, 298 K)

From: Cabanillasin, a new antifungal metabolite, produced by entomopathogenic Xenorhabdus cabanillasii JM26

  Chemical shifts
Groups or atoms 1 H in p.p.m. (number of protons) 13 C in p.p.m.
C29H2 3.36 (2 protons) 40.70
C5H2, C10H2, C13H2, C18H2, C21H2, C26H2 3.28–3.16 (12 protons) 41.04–40.44
C2H2 3.03 (2 protons) 39.06
C35H3 2.24 (3 protons) 23.70
C3H2, C4H2, C11H2, C12H2, C19H2, C20H2, C27H2, C28H2 1.80 (16 protons) 25.42–23.86
C34 174.79
C7, C15, C23 155.72
C31 152.93