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A9431

Sigma-Aldrich

Ancymidol

suitable for plant cell culture, BioReagent

Sinônimo(s):

reducymol, thritone, α-Cyclopropyl-α-(4-methoxyphenyl)-5-pyrimidinemethanol

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About This Item

Fórmula empírica (Notação de Hill):
C15H16N2O2
Número CAS:
12771-68-5
Peso molecular:
256.30
Número CE:
235-814-7
Número MDL:
MFCD00072501
Código UNSPSC:
10171502
ID de substância PubChem:
24891450
NACRES:
NA.72

linha de produto

BioReagent

Nível de qualidade

200

forma

powder

técnica(s)

cell culture | plant: suitable

aplicação(ões)

agriculture

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

HUTDUHSNJYTCAR-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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

Ações bioquímicas/fisiológicas

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.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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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
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
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
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
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
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