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. 2022 Sep 20;11(10):1847. doi: 10.3390/antiox11101847

Table 1.

1H NMR and 13C NMR Spectroscopic Data for Compounds 1.

Peripolin (1)
Position δH (J in Hz) δC Mult
2 5.34 dd (2.90, 12.7) 80.6, CH
3a 3.12 dd (12.7, 17.2) 44.0, CH2
3b 2.74 dd (2.9, 17.2) 44.3, CH2
4 198.4, qC
5 164.9, qC
6 6.16 m, ar 97.0, CH
7 166.5, qC
8 6.14 m, ar 98.1, CH
9 164.6, qC
10 105.1. qC
1′ 131.7, qC
2′ 6.79 m, ar 116.5, CH
3′ 147.0, qC
4′ 146.6, qC
5′ 6.80 m, ar 119.4, CH
6′ 6.93 m, ar 114.9, CH
1″ 5.08 d (7.6) 99.5, CH
2″ 3.66 dd (7.7, 9.0) 78.9, CH
3″ 3.60 dd (8.3, 9.0) 79.1, CH
4″ 3.36 dd (8.3, 10.4) 71.8, CH
5″ 3.69 ddd (2.0, 7.5, 11.9) 75.5, CH
6″a 4.40 dd (2.0, 11.9) 64.6, CH2
6″b 4.19 dd (7.5, 11.9)
1‴ 5.25 d (1.4) 102.5, CH
2‴ 3.93 dd (1.4, 3.2) 72.2, CH
3‴ 3.0 m 72.3, CH
4‴ 3.40 dd (1.6, 9.5) 74.1, CH
5‴ 3.90 ddd (3.9, 6.2, 9.5) 70.0, CH
6‴ 1.30 d (6.2) 18.2, CH3
1⁗ 172.5, qC
2⁗ 2.72–2.52 m 45.0, CH2
3⁗ 70.7, qC
4⁗ 2.72–2.52 m 46.5, CH2
5⁗ 174.9, qC
6⁗ 1.27 s 27.7, CH3