Desaspidin
Chemical compound
- P02DX01 (WHO)
- 2-Butanoyl-4-[(3-butanoyl-2,4-dihydroxy-6-methoxyphenyl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one
- 114-43-2
Y
- 8238
- 10295071
N
- KV3495SGKS
- D07365
Y
- ChEMBL2105606
N
- DTXSID00976317 DTXSID6074461, DTXSID00976317
![Edit this at Wikidata](http://upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png)
- Interactive image
- CCCC(=O)C1=C(C(=C(C=C1O)OC)CC2=C(C(C(=C(C2=O)C(=O)CCC)O)(C)C)O)O
InChI
- InChI=1S/C24H30O8/c1-6-8-14(25)18-16(27)11-17(32-5)12(20(18)28)10-13-21(29)19(15(26)9-7-2)23(31)24(3,4)22(13)30/h11,27-28,30-31H,6-10H2,1-5H3
N
- Key:GAHOBHHMYUYJDT-UHFFFAOYSA-N
N
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![check](http://upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png)
Desaspidin is an anthelmintic. Desapidin may occur in natural form within some plants such as Coastal woodfern, Dryopteris arguta.[1] Since the 1950s the inhibition effects of desapidins upon phosphorylation in chloroplasts has been noted and studied.[2]
References
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Antitrematodals (schistosomicides) |
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Anticestodals (taeniacides) |
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(including
macrofilaricides)
Binds tubulin | |
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Glutamate-gated chloride channel, GABA receptor | |
NMDA |
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Other/unknown |
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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