CHEBI:73171 - ancymidol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name ancymidol
ChEBI ID CHEBI:73171
Definition A tertiary alcohol that is methanol in which the hydrogens attached to the carbon are replaced by cyclopropyl, p-methoxyphenyl and pyrimidin-5-yl groups. By inhibiting gibberellin biosynthesis, ancymidol reduces plant growth, resulting in reduced internode elongation and thus more compact plants. It is used in the commercial production of a wide variety of container-grown bedding and foliage plants, including chrysanthemums, Easter lilies and poinsettias.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Johnny Lloyd
Supplier Information
Download Molfile XML SDF
Formula C15H16N2O2
Net Charge 0
Average Mass 256.29970
Monoisotopic Mass 256.12118
InChI InChI=1S/C15H16N2O2/c1-19-14-6-4-12(5-7-14)15(18,11-2-3-11)13-8-16-10-17-9-13/h4-11,18H,2-3H2,1H3
InChIKey HUTDUHSNJYTCAR-UHFFFAOYSA-N
SMILES COc1ccc(cc1)C(O)(C1CC1)c1cncnc1
Roles Classification
Biological Role(s): plant growth retardant

cellulose synthesis inhibitor
An pathway inhibitor that inhibits the synthesis of cellulose.
gibberellin biosynthesis inhibitor
Any compound that inhibits one or more steps in the pathway leading to the synthesis of gibberellins.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing ancymidol (CHEBI:73171) has role cellulose synthesis inhibitor (CHEBI:63958)
ancymidol (CHEBI:73171) has role gibberellin biosynthesis inhibitor (CHEBI:73193)
ancymidol (CHEBI:73171) has role plant growth retardant (CHEBI:35219)
ancymidol (CHEBI:73171) is a pyrimidines (CHEBI:39447)
ancymidol (CHEBI:73171) is a tertiary alcohol (CHEBI:26878)
IUPAC Name
cyclopropyl(4-methoxyphenyl)pyrimidin-5-ylmethanol
Synonyms Sources
α-cyclopropyl-4-methoxy-α-(pyrimidin-5-yl)benzyl alcohol ChemIDplus
α-Cyclopropyl-4-methoxy-α-(pyrimidin-5-yl)benzylalkohol ChemIDplus
α-cyclopropyl-α-(4-methoxyphenyl)-5-pyrimidinemethanol ChemIDplus
ancymidole ChemIDplus
EL-531 ChEBI
Brand Names Sources
A-rest ChemIDplus
Abide ChEBI
Reducymol ChEBI
Manual Xrefs Databases
38 PPDB
C18774 KEGG COMPOUND
CPD-4022 MetaCyc
FR1569940 Patent
US3818009 Patent
View more database links
Registry Numbers Types Sources
12771-68-5 CAS Registry Number ChemIDplus
12771-68-5 CAS Registry Number NIST Chemistry WebBook
6212277 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
18832186 PubMed citation Europe PMC
22749285 PubMed citation Europe PMC
Last Modified
28 July 2014