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Plant Sources
Structural Classes
Microbial Sources
Flagship Varieties
Synthetic Compounds
All
CAS No.
NAME
Molecular Formula
Molecular Weight
Purity
Price
2D Structure
1401419-90-6
Pterisolic acid F
CC1(CCCC2(C1CCC34C2(CCC(C3)C(C4=O)(CO)O)O)C)C(=O)O
C
20
H
30
O
6
366.4
HPLC≥98%
Click to inquire
644967-44-2
Rubianthraquinone
CC1=C(C=C2C(=C1OC)C(=O)C3=C(C2=O)C=C(C=C3)O)O
C
16
H
12
O
5
284.26
HPLC≥98%
Click to inquire
1059671-65-6
Sulfocostunolide B
C=C1CCC2C(C(=O)OC2C3C1CCC3=C)CS(=O)(=O)O
C
15
H
20
O
5
S
312.4
HPLC≥98%
Click to inquire
1042143-83-8
CID 129316815
CC(C)C1CCC2(C3CCC45CCCC4C2(C1N5C3)CCC6C7(CCC(C6(C(=O)O7)C)O)C)C
C
30
H
47
NO
3
469.7
HPLC≥98%
Click to inquire
1227375-09-8
Bi-linderone
COC1=CC(C2(C(C1C(=C3C(=O)C(=C(C3=O)OC)OC)OC)C4=CC=CC=C4)C(=O)C(=C(C2=O)OC)OC)C5=CC=CC=C5
C
34
H
32
O
10
600.6
HPLC≥98%
Click to inquire
1195760-68-9
CID 137796327
CCC1=NC2CC3(C4CC1C2CO4)C5=C(C=C(C=C5)O)N(C3=O)OC
C
19
H
22
N
2
O
4
342.4
HPLC≥98%
Click to inquire
122590-03-8
11-Hydroxyrankinidine
CC=C1CNC2CC3(C4CC1C2CO4)C5=C(C=C(C=C5)O)N(C3=O)OC
C
20
H
24
N
2
O
4
356.4
HPLC≥98%
Click to inquire
1351338-14-1
7,2'-Dihydroxy-5,8-dimethoxyflavanone
COC1=C2C(=O)CC(OC2=C(C(=C1)O)OC)C3=CC=CC=C3O
C
17
H
16
O
6
316.30
HPLC≥98%
Click to inquire
1372558-33-2
Chlorantholide A
CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3=C2)C)C
C
15
H
16
O
3
244.28
HPLC≥98%
Click to inquire
1372558-34-3
Chlorantholide B
CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C
C
15
H
18
O
3
246.30
HPLC≥98%
Click to inquire
1401419-90-6
Pterisolic acid F
Pterisolic acid F
C
20
H
30
O
6
366.4
644967-44-2
Rubianthraquinone
Rubianthraquinone
C
16
H
12
O
5
284.26
1059671-65-6
Sulfocostunolide B
Sulfocostunolide B
C
15
H
20
O
5
S
312.4
1042143-83-8
CID 129316815
Yunnandaphninine G
C
30
H
47
NO
3
469.7
1227375-09-8
Bi-linderone
Bi-linderone
C
34
H
32
O
10
600.6
1195760-68-9
CID 137796327
11-Hydroxygelsenicine
C
19
H
22
N
2
O
4
342.4
122590-03-8
11-Hydroxyrankinidine
11-Hydroxyrankinidine
C
20
H
24
N
2
O
4
356.4
1351338-14-1
7,2'-Dihydroxy-5,8-dimethoxyflavanone
7,2'-Dihydroxy-5,8-dimethoxyflavanone
C
17
H
16
O
6
316.30
1372558-33-2
Chlorantholide A
Chlorantholide A
C
15
H
16
O
3
244.28
1372558-34-3
Chlorantholide B
Chlorantholide B
C
15
H
18
O
3
246.30
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