Position

1

Piperine [13]

δH (mult., J in Hz)

δC

COSY

HMBC

δH (mult., J in Hz)

δC

1

---

165.5

---

---

---

165.6

2

6.42, d, J = 14.8 Hz

120.1

H3

C1, C4

6.38, d, J = 14.7 Hz

119.7

3

7.38, ddd, J = 14.3, 8.4, 1.8 Hz

142.5

H2, H4

-

7.36, ddd, J = 14.7, 8.3, 1.9 Hz

142.8

4

6.74, m

125.4

H3

C3, C1'

overlapping

125.2

5

6.74, m

138.2

H3

C3, C1', C2'

overlapping

138.4

1'

131.1

-

-

---

130.9

2'

6.96, s

105.7

H6'

C5, C3', C4', C6'

6.93, d, J = 1.5 Hz

105.6

3'

---

148.2

-

---

---

148.06

4'

---

148.1

-

---

---

148.09

5'

6.76, d, J = 8.0 Hz

108.5

H6'

C1', C3', C4'

overlapping

108.4

6'

6.88, d, J = 8.0 Hz

122.5

H2', H5'

C5, C2', C4'

6.84, dd, J = 6.0, 1.5 Hz

122.5

Methylenedioxy

5.96, s

101.3

-

C3', C4'

5.9, s

101.2

2''

3.62, m

43.3

H3''

---

3.48, brs

43.3

3''

1.58, m

26.8

H2'', H4''

C5''

1.54, m

26.6

4''

1.65, m

24.7

H3'', H5''

---

1.54, m

24.5

5''

1.58, m

25.7

H4'', H6''

C3''

1.54, m

25.5

6''

3.51, m

46.9

H5''

3.57, brs

46.9