Mer-NF5003F
(Synonyms: F 1839M, NF 5003F, Stachybotrydial) 目录号 : GC46169A sesquiterpene with diverse biological activities
Cas No.:149598-70-9
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Mer-NF5003F is a sesquiterpene originally isolated from Stachybotrys with diverse biological activities.1,2,3 It inhibits avian myeloblastosis virus (AMV) protease (IC50 = 7.8 μM).1 Mer-NF5003F inhibits sialyltransferase 6N (ST6N), ST3O, and ST3N (IC50s = 0.61, 6.7, and 10 μg/ml, respectively), as well as fucosyltransferase (IC50 = 11.3 μg/ml).2 It is active against herpes simplex virus 1 (HSV-1) in vitro (IC50 = 4.32 μg/ml).3 Mer-NF5003F is also active against the multidrug-resistant P. falciparum strain K1 (IC50 = 0.85 μg/ml).
|1. Kaneto, R., Dobashi, K., Kojima, I., et al. Mer-NF5003B, E and F, novel sesquiterpenoids as avian myeloblastosis virus protease inhibitors produced by Stachybotrys sp. J. Antibiot. (Tokyo) 47(6), 727-730 (1994).|2. Lin, T.-W., Chang, W.-W., Chen, C.-C., et al. Stachybotrydial, a potent inhibitor of fucosyltransferase and sialyltransferase. Biochem. Biophys. Res. Commun. 331(4), 953-957 (2005).|3. Sawadjoon, S., Kittakoop, P., Isaka, M., et al. Antiviral and antiplasmodial spirodihydrobenzofuran terpenes from the fungus Stachybotrys nephrospora. Planta Med. 70(11), 1085-1087 (2004).
| Cas No. | 149598-70-9 | SDF | |
| 别名 | F 1839M, NF 5003F, Stachybotrydial | ||
| Canonical SMILES | O[C@@H]1CC[C@@]2(C)[C@](CC[C@@H](C)[C@@]23OC(C(C=O)=C(C=O)C=C4O)=C4C3)([H])C1(C)C | ||
| 分子式 | C23H30O5 | 分子量 | 386.5 |
| 溶解度 | DMF: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble | 储存条件 | Store at -20°C |
| 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。 |
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| 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 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.5873 mL | 12.9366 mL | 25.8732 mL |
| 5 mM | 0.5175 mL | 2.5873 mL | 5.1746 mL |
| 10 mM | 0.2587 mL | 1.2937 mL | 2.5873 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。
Antiviral and antiplasmodial spirodihydrobenzofuran terpenes from the fungus Stachybotrys nephrospora
Planta Med 2004 Nov;70(11):1085-7.PMID:15549667DOI:10.1055/s-2004-832652.
Two known spirodihydrobenzofuran terpenes (1 and 2) were isolated from a mycelium extract of the fungus Stachybotrys nephrospora BCC 3900. Compound 1 (Mer-NF5003F or stachybotrydial) exhibited potent antiviral activity (the IC50 value of 4.32 microg/mL) comparable to the standard drug, acyclovir, while compound 2 was inactive against the HSV-1 virus. Both 1 and 2 possessed antiplasmodial activity (IC50 values of 0.85 and 0.15 microg/mL for 1 and 2, respectively), and were not toxic towards the Vero cell line. A regiospecific conversion of the dialdehyde 1 to the lactone 2 proceeded simply under acidic conditions.