Ganoderic acid

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Ganoderic acid A
Ganoderic acid.png
Names
IUPAC names
(2R,6R)-6-[(5R,7S,10S,13R,14R,15S,17R)
-7,15-dihydroxy-4,4,10,13,14-pentamethyl-3,
11-dioxo-2,5,6,7,12,15,16,17
-octahydro-1H-cyclopenta[a]phenanthren-17-yl]
-2-methyl-4-oxoheptanoic acid
Identifiers
81907-62-2 YesY
ChemSpider 413668 N
Jmol 3D model Interactive image
PubChem 471002
  • InChI=1S/C30H44O7/c1-15(10-17(31)11-16(2)26(36)37)18-12-23(35)30(7)25-19(32)13-21-27(3,4)22(34)8-9-28(21,5)24(25)20(33)14-29(18,30)6/h15-16,18-19,21,23,32,35H,8-14H2,1-7H3,(H,36,37)/t15-,16-,18-,19+,21+,23+,28+,29-,30+/m1/s1 N
    Key: DYOKDAQBNHPJFD-JNTBEZBXSA-N N
  • InChI=1/C30H44O7/c1-15(10-17(31)11-16(2)26(36)37)18-12-23(35)30(7)25-19(32)13-21-27(3,4)22(34)8-9-28(21,5)24(25)20(33)14-29(18,30)6/h15-16,18-19,21,23,32,35H,8-14H2,1-7H3,(H,36,37)/t15-,16-,18-,19+,21+,23+,28+,29-,30+/m1/s1
    Key: DYOKDAQBNHPJFD-JNTBEZBXBK
  • OC(=O)[C@H](C)CC(=O)C[C@@H](C)[C@H]2C[C@H](O)[C@@]1(C)C/3=C(\C(=O)C[C@@]12C)[C@@]4(C)CCC(=O)[C@](C)(C)[C@@H]4C[C@@H]\3O
Properties
C30H44O7
Molar mass 516.67
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Ganoderic acids are a class of closely related triterpenoids (derivatives from lanosterol) found in Ganoderma mushrooms. For thousands of years, the fruiting bodies of Ganoderma fungi have been used in traditional medicines in East Asia.[1][2] Consequently, there have been efforts to identify the chemical constituents that may be responsible for the putative pharmacological effects. There are dozens of ganoderic acids that have been isolated and characterized, of which ganoderic acid A and ganoderic acid B are the most well characterized. Some ganoderic acids have been found to possess biological activities including hepatoprotection,[citation needed] anti-tumor effects,[3] and 5-alpha reductase inhibition.[4]

References

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