Name |
Ponicidin |
Formula |
C20H26O6 |
Mw |
362.17293856 |
CAS RN |
52617-37-5 |
C_ID |
C00031075
,
|
InChIKey |
WHRDRHNMTIXZNY-FRZNRLFCNA-N |
InChICode |
InChI=1S/C20H26O6/c1-8-9-4-5-10-18-11(21)6-7-17(2,3)12(18)14(23)20(24)19(10,13(8)22)15(9)25-16(18)26-20/h9-12,14-16,21,23-24H,1,4-7H2,2-3H3/t9-,10-,11-,12+,14-,15-,16-,18-,19-,20+/m0/s1 |
SMILES |
[C@@H]12O[C@@H]3[C@]45[C@@H](C(CC[C@@H]4O)(C)C)[C@@H]([C@@]([C@@]41[C@H]5CC[C@H]2C(=C)C4=O)(O)O3)O |
Start Substs in Alk. Biosynthesis (Prediction) |
|
Organism |
Kingdom |
Family |
Species |
Reference |
Plantae | Labiatae | Isodon japonica | Ref. |
Plantae | Labiatae | Isodon japonicus Hara. | Ref. |
Plantae | Labiatae | Isodon rubescens var. lushanensis | Ref. |
Plantae | Labiatae | Isodon xerophilus | Ref. |
Plantae | Lamiaceae | Rabdosia nervosa | Ref. |
Plantae | Lamiaceae | Rabdosia rubescens | Ref. |
|
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zoom in
Organism | Isodon japonica | Reference | Ji, et al., Pharmacological Action and Application of Available Antitumor Composition of Traditional Chinese Medicine, Heilongjiang Science and technology Press, Heilongjiang, (1998).
Gao, et al., CCMM, 19, (1994), 295.
Buckingham(Executive Editor), Dictionary of Natural Products, Chapman & Hall, 1994, Vol1-7
1995, Vol8
1996, Vol9
1997, Vol10
1998, Vol11.
Meade-Tollin, et al., JNP, 67, (2004), 2.
Sun, et al., Diterpenoids from Isodon Species, Science Press, Beijing, (2001).
HAN, et al., Chem Pharm Bull, 51, (2003), 790.
Chen, Liu, et al., Determination of Effective Components in Traditional Chinese medicines, People's Medical Publishing House, Beijing, (2009) |
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