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A9431

Sigma-Aldrich

Ancymidol

suitable for plant cell culture, BioReagent

Synonym(e):

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

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25 MG
CHF 63.50
100 MG
CHF 218.00

CHF 63.50


Voraussichtliches Versanddatum30. Mai 2025


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25 MG
CHF 63.50
100 MG
CHF 218.00

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

CHF 63.50


Voraussichtliches Versanddatum30. Mai 2025


Bulk-Bestellung anfordern

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[1] is a synthetic pyrimidine analogue. It is also a weak fungitoxic.[2]

Anwendung

Ancymidol has been used as the cytochrome P450 inhibitor to study its effects on Cyanidioschyzon merolae strain.[3]

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[1] and growth in plants.[4]

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type N95 (US)


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Marina Varbanova et al.
The Plant cell, 19(1), 32-45 (2007-01-16)
Arabidopsis thaliana GAMT1 and GAMT2 encode enzymes that catalyze formation of the methyl esters of gibberellins (GAs). Ectopic expression of GAMT1 or GAMT2 in Arabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plants with GA deficiency and typical
A E Desjardins et al.
Applied and environmental microbiology, 53(8), 1860-1865 (1987-08-01)
Ancymidol, a plant growth regulator, inhibited biosynthesis of diacetoxyscirpenol by Gibberella pulicaris (Fusarium sambucinum) in a defined liquid medium. Ancymidol also inhibited biosynthesis of T-2 toxin by a wild-type strain of Fusarium sporotrichioides and biosynthesis of diacetoxyscirpenol, deacetylated calonectrin, and
Luisa M Trindade et al.
Gene, 303, 77-87 (2003-02-01)
In the search for time- and tissue-specific promoters an RNA fingerprinting technique called cDNA-AFLP was used. A transcript derived fragment (TDF511) was isolated which showed high similarity to alcohol dehydrogenases. The gene corresponding to this TDF, named Stgan, is likely
F Le Guen-Le Saos et al.
Annals of botany, 89(4), 419-425 (2002-07-05)
Bulbing was studied in shallot plants cultured in vitro. Bulbing occurred under a 16 h photoperiod with fluorescent + incandescent light and 30-50 g 1(-1) sucrose in the culture medium. Exogenous gibberellin (10 microM GA3) inhibited leaf and root growth
Hongyan Zheng et al.
Scientific reports, 6, 24778-24778 (2016-04-23)
The primary root plays essential roles in root development, nutrient absorption, and root architectural establishment. Primary root growth is generally suppressed by phosphate (P) deficiency in A. thaliana; however, the underlying molecular mechanisms are largely elusive to date. We found

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