Uniconazole
(Synonyms: 烯效唑,S 3307D,XE 1019D) 目录号 : GC17112
A plant growth regulator
Cas No.:83657-22-1
Sample solution is provided at 25 µL, 10mM.
;)
,-1-7$$$37316672.jpg');)
;)
;)
$$$36806353.jpg');)
;33(7)%EF%BC%9A546-561$$$37156877.jpg');)
;)
;)
;)
%201124-1138.$$$35908550.jpg');)
%20766-780.$$$37100057.jpg');)
%20418-432.$$$36893736.jpg');)
%EF%BC%9A-240-255.$$$35108512.jpg');)
533-545$$$36543525.jpg');)
%201-13.$$$36600053.jpg');)
;)
Ki = 68 nM
Uniconazole is a cytochrome P450 707As inhibitor.
Plant growth retardants (PGRs) can reduce the shoot growth of plants via inhibiting gibberellin biosynthesis. The inhibitory effects of PGRs on Arabidopsis abscisic acid (ABA) 8'-hydroxylase, a major ABA catabolic enzyme, recently identified as CYP707As, have been reported.
In vitro: In an in-vitro assay with CYP707A3 microsomes expressed in insect cells, uniconazole could inhibit CYP707A3 activity more effectively than paclobutrazol or tetcyclacis, while the other tested PGRs could not significantly inhibit it. In addition, uniconazole was also found to be a strong competitive inhibitor of ABA 8'-hydroxylase [1].
In vivo: Uniconazole-treated Arabidopsis plants displayed enhanced drought tolerance. In uniconazole-treated plants, endogenous ABA levels increased 2-fold as compared with the control, and co-application of GA(4) could not suppress such effects, suggesting that these effects were not because of gibberellin deficiency. Therefore uniconazole could effectively inhibit ABA catabolism in Arabidopsis plants [1].
Clinical trial: So far, no clinical study has been conducted.
Reference:
[1] Saito, S. ,Okamoto, M.,Shinoda, S., et al. A plant growth retardant, uniconazole, is a potent inhibitor of ABA catabolism in Arabidopsis. Bioscience, Biotechnology, and Biochemistry 70(7), 1731-1739 (2006).
| Cas No. | 83657-22-1 | SDF | |
| 别名 | 烯效唑,S 3307D,XE 1019D | ||
| 化学名 | βE-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol | ||
| Canonical SMILES | ClC1=CC=C(/C=C(C(O)C(C)(C)C)/N2N=CN=C2)C=C1 | ||
| 分子式 | C15H18ClN3O | 分子量 | 291.8 |
| 溶解度 | ≥ 11.65mg/mL in DMSO | 储存条件 | Store at RT |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
||
| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
 |
1 mg | 5 mg | 10 mg |
| 1 mM | 3.427 mL | 17.135 mL | 34.27 mL |
| 5 mM | 0.6854 mL | 3.427 mL | 6.854 mL |
| 10 mM | 0.3427 mL | 1.7135 mL | 3.427 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet