Myclobutanil
CAS No. 88671-89-0
Myclobutanil ( RH 3866 )
产品货号. M16414 CAS No. 88671-89-0
腈菌唑是一种用作杀菌剂的三唑化学品。它是一种类固醇去甲基化抑制剂,专门抑制麦角甾醇的生物合成。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥157 | 有现货 |
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| 50MG | ¥217 | 有现货 |
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| 100MG | ¥295 | 有现货 |
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| 500MG | ¥651 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥164 | 有现货 |
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生物学信息
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产品名称Myclobutanil
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述腈菌唑是一种用作杀菌剂的三唑化学品。它是一种类固醇去甲基化抑制剂,专门抑制麦角甾醇的生物合成。
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产品描述Myclobutanil is a triazole chemical used as a fungicide. It is a steroid demethylation inhibitor, specifically inhibiting ergosterol biosynthesis. Ergosterol is a critical component of fungal cell membranes.(In Vitro):Myclobutanil reduces cell viability to <50% at 100 ppm and to <10% at 500 ppm. Myclobutanil promotes a slight, but significant, increase in fatty acid (FA)-induced steatotosis at doses from 1 to 100 ppm. Anti-apoptotic biomarkers are significantly reduced by Myclobutanil.
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体外实验Myclobutanil reduces cell viability to <50% at 100 ppm and to <10% at 500 ppm. Myclobutanil promotes a slight, but significant, increase in fatty acid (FA)-induced steatotosis at doses from 1 to 100 ppm. Anti-apoptotic biomarkers are significantly reduced by Myclobutanil.
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体内实验——
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同义词RH 3866
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通路Others
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靶点Other Targets
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受体Others
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研究领域——
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适应症——
化学信息
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CAS Number88671-89-0
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分子量288.78
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分子式C15H17ClN4
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纯度>98% (HPLC)
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溶解度Soluble in Water
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SMILESN#CC(C1=CC=C(Cl)C=C1)(CCCC)CN2N=CN=C2
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化学全称2-((1H-1,2,4-triazol-1-yl)methyl)-2-(4-chlorophenyl)hexanenitrile
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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CGS 20625
CGS 20625 是一种有效的、选择性的、具有口服活性的中枢苯二氮卓受体 (benzodiazepine receptor) 的部分激动剂。CGS 20625 抑制 [3H]-氟硝西泮与中枢苯二氮卓受体的结合,其 IC50 为 1.3 nM。CGS 20625 可用于 pentylenetetrazol 导致的癫痫发作的研究。
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Mequitamium
Mequitamium is an effective pharmaceutical intermediate that can be used to synthesize Mequitazium iodid.
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α-CGRP (mouse, rat)
α-CGRP (mouse, rat), a neuropeptide (calcitonin gene-related peptide (CGRP)) mainly expressed in neuromuscular junction, is a potent vasodilator. α-CGRP (mouse, rat) can lead to a fall in blood pressure and an increase in heart rate by peripheral administration, also relax colonie smooth muscle. α-CGRP (mouse, rat) has the potential in cardiovascular, pro-inflammatory, migraine and metabolic studies.
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