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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:
Molecular Weight:
256.30
NACRES:
NA.72
PubChem Substance ID:
UNSPSC Code:
10171502
EC Number:
235-814-7
MDL number:
Form:
powder
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product line

BioReagent

Quality Level

form

powder

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

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

InChI key

HUTDUHSNJYTCAR-UHFFFAOYSA-N

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.[1]

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This Item
3252343563A6166
Quality Level

200

Quality Level

100

Quality Level

300

Quality Level

200

storage temp.

2-8°C

storage temp.

-

storage temp.

−20°C

storage temp.

2-8°C

form

powder

form

-

form

-

form

powder

product line

BioReagent

product line

PESTANAL®

product line

TraceCERT®

product line

-

application(s)

agriculture

application(s)

agriculture
environmental

application(s)

-

application(s)

-

technique(s)

cell culture | plant: suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

-


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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)



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Related Content


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
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
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



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