Himandridine
(Synonyms: NSC 23972) 目录号 : GC46156
An alkaloid
Cas No.:15521-76-3
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
Himandridine is an alkaloid that has been found in Galbulimima.1
|1. Mander, L.N., Ritchie, E., and Taylor, W.C. The chemical constituents of Galbulimima species. VI. The structure of himandridine. Aust. J. Chem. 20(5), 981-1019 (1967).
| Cas No. | 15521-76-3 | SDF | |
| 别名 | NSC 23972 | ||
| Canonical SMILES | O[C@]1([C@]2([H])CC3)C([C@@]([C@@](CC[C@@H]4O)([H])[C@]([C@H]4OC)([H])[C@@H]5OC(C6=CC=CC=C6)=O)(N([C@H]3C)[C@]2([H])C7)C7C1)=C5C(OC)=O | ||
| 分子式 | C30H37NO7 | 分子量 | 523.6 |
| 溶解度 | Soluble in DMSO | 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 | 1.9099 mL | 9.5493 mL | 19.0985 mL |
| 5 mM | 0.382 mL | 1.9099 mL | 3.8197 mL |
| 10 mM | 0.191 mL | 0.9549 mL | 1.9099 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。
Progress toward the syntheses of (+)-GB 13, (+)-himgaline, and Himandridine. new insights into intramolecular imine/enamine aldol cyclizations
J Am Chem Soc 2012 May 16;134(19):8162-70.PMID:22533781DOI:10.1021/ja3001776
A full account of our total synthesis of the galbulimima alkaloids GB 13 and himgaline is provided. Using a strategy adapted from the proposed biosynthesis of the GB alkaloid family, a linear precursor underwent successive intramolecular Diels-Alder, Michael, and imine aldol cyclizations to form the polycyclic alkaloid core. We now show that modification of this strategy can also deliver an advanced intermediate en route to the related alkaloid Himandridine. The success of the key imine aldol cyclization is acutely sensitive to substrate structure and solvent, including a case in which cyclization was spontaneous in protic solvents. A detailed computational investigation of the course of the reaction closely correlates with, and suggests a rationale for, the observed patterns of imine aldol reactivity.