跳转至内容
Merck
CN

E100

(-)-氧化毒扁豆碱 富马酸盐

analytical standard, for drug analysis

登录 查看组织和合同定价。

选择尺寸

关于此项目

经验公式（希尔记法）:
C13H18N2O · C4H4O4
化学文摘社编号:
70310-73-5
分子量:
334.37
UNSPSC Code:
41116107
PubChem Substance ID:
329798872
MDL number:
MFCD00055202

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

color

white

InChI

1S/C13H18N2O.C4H4O4/c1-13-6-7-14(2)12(13)15(3)11-5-4-9(16)8-10(11)13;5-3(6)1-2-4(7)8/h4-5,8,12,16H,6-7H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b;2-1+/t12-,13+;/m1./s1

SMILES string

[H]\C(=C(\[H])C(O)=O)C(O)=O.[H][C@]12N(C)CC[C@@]1(C)c3cc(O)ccc3N2C

InChI key

PBZRRADJWNBPNY-XDRMOJKASA-N

form

solid

optical activity

[α]23/D −107.9°, c = 0.5 in methanol(lit.)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

solubility

0.1 M HCl: soluble (Solutions should be freshly prepared.), 0.1 M NaOH: soluble (Solutions should be freshly prepared.), H2O: soluble (Solutions should be freshly prepared.), methanol: slightly soluble (Solutions should be freshly prepared.)

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

storage temp.

2-8°C

Quality Level

100

Gene Information

human ... ACHE(43)

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem/physiol Actions

毒扁豆碱（依色林）代谢物，其在某些神经元细胞系中具有细胞毒性；它同时具有抗乙酰胆碱酯酶和阿片激动剂活性；强效镇痛药。

Disclaimer

吸湿、光敏

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
074M4617V

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

A Galli et al.
The Journal of pharmacy and pharmacology, 37(1), 42-48 (1985-01-01)
The protective action of eseroline--(3aS,8aR)-1,2,3,3a,8,8a-hexahydro-1,3 a, 8-trimethyl-pyrrolo[2,3-b]indol-5-ol--salicylate against (DFP) diisopropyl fluorophosphate and carbamate poisoning of cholinesterases (ChEs) has been examined in-vitro with human erythrocytes and purified preparations of electric eel acetylcholinesterase (AChE) and of horse serum butyrylcholinesterase (BuChE), and in-vivo
S Fürst et al.
European journal of pharmacology, 83(3-4), 233-241 (1982-09-24)
The opiate-like effects of eseroline, a physostigmine derivative, were studied in different tests. The antinociceptive effect of eseroline given s.c. and intracerebrally could be detected in the rat hot plate test and was reversed by naloxone. The apparent pA2 values
Ross T Fennessy et al.
Nucleic acids research, 44(15), 7189-7203 (2016-04-24)
Nucleosomes, the fundamental subunits of eukaryotic chromatin, are organized with respect to transcriptional start sites. A major challenge to the persistence of this organization is the disassembly of nucleosomes during DNA replication. Here, we use complimentary approaches to map the
Swapnalee Sarmah et al.
Scientific reports, 10(1), 3951-3951 (2020-03-05)
Ethanol exposure during prenatal development causes fetal alcohol spectrum disorder (FASD), the most frequent preventable birth defect and neurodevelopmental disability syndrome. The molecular targets of ethanol toxicity during development are poorly understood. Developmental stages surrounding gastrulation are very sensitive to
A Galli et al.
Biochemical pharmacology, 31(7), 1233-1238 (1982-04-01)
The action of eseroline--(3aS,8aR)-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indo l-5-ol--salicylate was tested on preparations of ChE from different sources and on the longitudinal muscle of guinea-pig ileum. While eseroline is eseroline is extremely weak-acting on horse serum BuChE (Ki = 208 +/- 42 microM), it
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持