From Wikipedia, the free encyclopedia
Trachyspic acid
|
Names
|
IUPAC name
2-(Carboxymethyl)-8-nonyl-9-oxo-1,6-dioxaspiro[4.4]non-7-ene-2,3-dicarboxylic acid
|
Identifiers
|
|
|
|
|
ChEBI
|
|
ChemSpider
|
|
|
|
UNII
|
|
InChI=1S/C19H26O9/c1-2-3-4-5-6-7-8-12-11-27-19(15(12)22)9-13(16(23)24)18(28-19,17(25)26)10-14(20)21/h11,13H,2-10H2,1H3,(H,20,21)(H,23,24)(H,25,26)/t13-,18+,19+/m0/s1 Key: NYTZRXWHGZGDDX-MJXNMMHHSA-N
|
CCCCCCCCC1=CO[C@]2(C1=O)C[C@H]([C@](O2)(CC(=O)O)C(=O)O)C(=O)O
|
Properties
|
|
C20H28O9
|
Molar mass
|
412.435 g·mol−1
|
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Chemical compound
Trachyspic acid is a fungal isolate that can inhibit
heparanase.
[1]
References
-
^ Shiozawa H, Takahashi M, Takatsu T, Kinoshita T, Tanzawa K, Hosoya T, Furuya K, Takahashi S, Furihata K, Seto H (1995).
"Trachyspic acid, a new metabolite produced by Talaromyces trachyspermus, that inhibits tumor cell heparanase: taxonomy of the producing strain, fermentation, isolation, structural elucidation, and biological activity". J Antibiot (Tokyo). 48 (5): 357–362.
doi:
10.7164/antibiotics.48.357.
PMID
7797435.