A9431
嘧啶醇
suitable for plant cell culture, BioReagent
别名:
α-环丙基-α-(4-环丙基)-5-嘧啶
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关于此项目
经验公式（希尔记法）:
C15H16N2O2
化学文摘社编号:
分子量:
256.30
EC 号:
MDL编号:
UNSPSC代码:
10171502
PubChem化学物质编号:
NACRES:
NA.72
产品线
BioReagent
质量水平
表单
powder
技术
cell culture | plant: suitable
应用
agriculture
储存温度
2-8°C
SMILES字符串
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
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一般描述
环丙嘧啶醇，a-环丙基-a-(4--甲氧基苯)-5-嘧啶甲醇(EL-53 1)，一种植物生长延缓剂，是人工合成的嘧啶类似物。它也是一种较弱的真菌毒素。
应用
环丙嘧啶醇已用作细胞色素P450抑制剂，研究其对Cyanidioschyzon merolae红藻的影响。
生化/生理作用
Ancymidol是一种嘧啶类植物细胞内分泌干扰物以及植物生长调节剂，可干扰赤霉素和纤维素的生物合成。
环丙嘧啶醇是单加氧酶抑制剂。它可干扰赤霉素生物合成和植物生长。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type N95 (US)
法规信息
农药列管产品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
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
Carotenoid Biosynthesis in the Primitive Red Alga Cyanidioschyzon merolae
Cunningham FX, et al.
Eukaryotic Cell, 6(3), 533-545 (2007)
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
Chromatograms
application for HPLC
application for HPLC
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