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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
aphidicolin [CHEBI:2766] (1)
aphidicolin [CHEBI:2766] (1)
aphidicolin [CHEBI:2766] (1)
aphidicolin [CHEBI:2766] (1)
05. Industrial Uses
05. Industrial Uses
aphidicolin [CHEBI:2766] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Tolypocladium inflatum (9)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
unspecified structure [PO:0000004] (703)
08. Chemical Category
08. Chemical Category
aphidicolin [CHEBI:2766] (1)
aphidicolin [CHEBI:2766] (1)
ChEBI Compound Accession Identifier :
[CHEBI:2766]
ChEBI Compound Description :
A tetracyclic diterpenoid that has an tetradecahydro-8,11a-methanocyclohepta[a]naphthalene skeleton with two hydroxymethyl substituents at positions 4 and 9, two methyl substituents at positions 4 and 11b and two hydroxy substituents at positions 3 and 9. An antibiotic with antiviral and antimitotical properties. Aphidicolin is a reversible inhibitor of eukaryotic nuclear DNA replication.
ChEBI Compound Identification Number :
2766
ChEBI InChI Value :
InChI=1S/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1
ChEBI InChIKey Value :
NOFOAYPPHIUXJR-APNQCZIXSA-N
ChEBI Compound Name :
aphidicolin
ChEBI SMILES Value :
[H][C@@]12CC[C@@]3([H])[C@](C)(CO)[C@H](O)CC[C@]3(C)[C@]11CC[C@](O)(CO)[C@H](C2)C1
ChEBI Substance ID :
135610169
ChEBI URL :
ChEBI:2766
ChemSpider ID :
10280269
Ontomatica Chemical Accession Key (OnChAKey) :
NOFOAYPPHIUXJR_APNQCZIXSA_N_000_000000
PubChem Compound ID :
457964