EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C15H16N2O2 |
| Net Charge | 0 |
| Average Mass | 256.305 |
| Monoisotopic Mass | 256.12118 |
| SMILES | COc1ccc(C(O)(c2cncnc2)C2CC2)cc1 |
| 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 |
| Roles Classification |
|---|
| Biological Roles: | 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. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 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 | Source |
|---|---|
| ancymidole | ChemIDplus |
| EL-531 | ChEBI |
| 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 |
| Brand Names | Source |
|---|---|
| Abide | ChEBI |
| A-rest | ChemIDplus |
| Reducymol | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:6212277 | Reaxys |
| CAS:12771-68-5 | ChemIDplus |
| CAS:12771-68-5 | NIST Chemistry WebBook |
| CAS:12771-68-5 | KEGG COMPOUND |
| Citations |
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