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Merck
CN

A9431

Ancymidol

BioReagent, suitable for plant cell culture

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C15H16N2O2
CAS Number:
12771-68-5
Molecular Weight:
256.30
NACRES:
NA.72
PubChem Substance ID:
24891450
UNSPSC Code:
10171502
EC Number:
235-814-7
MDL number:
MFCD00072501
Form:
powder

Key Documents

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InChI key

HUTDUHSNJYTCAR-UHFFFAOYSA-N

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

SMILES string

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

product line

BioReagent

form

powder

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

2-8°C

Quality Level

200

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General description

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.

Application

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

Biochem/physiol Actions

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type N95 (US)

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000532638
0000532638
0000490220
0000490220
0000490221

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Effect of ancymidol on cell wall metabolism in growing maize cells
Hernaandez-AJM, et al.
Planta, 247(4), 987-999 (2018)
A B Pereira-Netto et al.
Plant cell reports, 21(5), 491-496 (2003-06-06)
Gibberellins (GAs) A(1), A(3), A(4) and A(7), all 3beta-hydroxylated, growth-active GAs, significantly inhibited shoot elongation and the formation of nodes in in vitro-grown Hancornia speciosa, as did GA(20), a 3-deoxy precursor of GA(1). Ancymidol, an early-stage inhibitor of GA biosynthesis
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
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
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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