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Merck

A9431

Sigma-Aldrich

Ancymidol

suitable for plant cell culture, BioReagent

Synonym(e):

α-Cyclopropyl-α-(4-methoxyphenyl)-5-pyrimidinmethanol

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About This Item

Empirische Formel (Hill-System):
C15H16N2O2
CAS-Nummer:
Molekulargewicht:
256.30
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
10171502
PubChem Substanz-ID:
NACRES:
NA.72

Produktlinie

BioReagent

Qualitätsniveau

Form

powder

Methode(n)

cell culture | plant: suitable

Anwendung(en)

agriculture

Lagertemp.

2-8°C

SMILES String

COc1ccc(cc1)C(O)(C2CC2)c3cncnc3

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

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Allgemeine Beschreibung

Ancymidol, a-cyclopropyl-a-(4-methoxyphenyl)-5-pyrimidinemethanol (EL-53 1), a plant growth retardant is a synthetic pyrimidine analogue. It is also a weak fungitoxic.

Anwendung

Ancymidol has been used as the cytochrome P450 inhibitor to study its effects on Cyanidioschyzon merolae strain.

Biochem./physiol. Wirkung

Ancymidol is a pyrimidine-class plant cell endocrine disruptor plant growth regulator that interferes with gibberellin and cellulose biosynthesis.
Ancymidol acts as a monooxygenase inhibitor. It is capable of interrupting gibberellin biosynthesis and growth in plants.

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type N95 (US)


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

S Tongpim et al.
Canadian journal of microbiology, 45(5), 369-376 (1999-08-14)
Mycobacterium strain S1, originally described as Rhodococcus strain S1 by chemotaxonomic criteria, was isolated by growth on anthracene, and is unable to use any of nine other polycyclic aromatic compounds as carbon source. Metabolism of phenanthrene during growth on anthracene
Carotenoid Biosynthesis in the Primitive Red Alga Cyanidioschyzon merolae
Cunningham FX, et al.
Eukaryotic Cell, 6(3), 533-545 (2007)
Rajesh Thakur et al.
Plant cell reports, 25(5), 382-391 (2005-12-22)
Effect of growth retardants (paclobutrazol or ancymidol) was studied in Lilium plantlets growing in liquid culture. A significant increase in leaf chlorophyll, epicuticular wax, plant dry weight and bulb starch contents were found in plantlets treated with growth retardants. A
Effect of ancymidol on cell wall metabolism in growing maize cells
Hernaandez-AJM, et al.
Planta, 247(4), 987-999 (2018)
C N McDaniel et al.
Development (Cambridge, England), 122(11), 3661-3668 (1996-11-01)
We investigated floral initiation in the long-day monocot Lolium temulentum, strain Ceres, by culturing apices explanted from photoperiodically induced plants at various times after one inductive long day onto medium with, and without, gibberellin. Apices cultured on the first day

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