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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
08. Chemical Category
08. Chemical Category
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
aplysiallene [CHEBI:65416] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65416]
ChEBI Compound Description :
A furofuran that is hexahydrofuro[3,2-b]furan which is substituted at position 2 by a (1E,3E)-4-bromohexa-1,3-dien-1-yl group and at position 5 by a (1R)-3-bromopropadienyl group (the 2R,3aS,5R,6aS diastereoisomer). A natural product first isolated from the red alga Laurencia okamurai Yamada and subsequently found in the sea hare Aplysia kurodai, aplysiallene is an inhibitor of sodium-potassium adenosine triphosphatase.
ChEBI Compound Identification Number :
65416
ChEBI InChI Value :
InChI=1S/C15H18Br2O2/c1-2-11(17)5-3-6-12-9-14-15(18-12)10-13(19-14)7-4-8-16/h3,5-8,12-15H,2,9-10H2,1H3/b6-3+,11-5+/t4-,12-,13-,14-,15-/m0/s1
ChEBI InChIKey Value :
UEQYOOYTFGFGQB-BTWUOVCESA-N
ChEBI Compound Name :
aplysiallene
ChEBI SMILES Value :
[H]C(Br)=C=C([H])[C@@]1([H])C[C@]2([H])O[C@]([H])(C[C@]2([H])O1)\C=C\C=C(\Br)CC
ChEBI Substance ID :
160644877
ChEBI URL :
ChEBI:65416
ChemSpider ID :
NS
Ontomatica Chemical Accession Key (OnChAKey) :
UEQYOOYTFGFGQB_BTWUOVCESA_N_000_000000
PubChem Compound ID :
17756329