Company Name: |
BioBioPha Co., Ltd.
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Tel: |
0871-65217109 13211707573; |
Email: |
y.liu@mail.biobiopha.com |
Products Intro: |
CAS:639-36-1 Purity:>97.0% Package:5mg Remarks:BBP03110
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| (+)-Polyneuridine Basic information |
Product Name: | (+)-Polyneuridine | Synonyms: | 17-Hydroxysarpagane-16-carboxylic acid methyl ester;Rhazin;SARPAGAN-16-CARBOXYLIC ACID17-HYDROXY-,METHYL ESTER;Akuammidine;Rhazine;(+)-Polyneuridine | CAS: | 639-36-1 | MF: | C21H24N2O3 | MW: | 352.43 | EINECS: | | Product Categories: | | Mol File: | 639-36-1.mol |  |
| (+)-Polyneuridine Chemical Properties |
Melting point | 243-246℃ | Boiling point | 513.0±50.0 °C(Predicted) | density | 1.34±0.1 g/cm3(Predicted) | pka | 14.79±0.10(Predicted) |
| (+)-Polyneuridine Usage And Synthesis |
Uses | Akuammidine, isolated from the seeds of Picralima nitida, shows a preference for μ-opioid binding sites with Ki values of 0.6, 2.4 and 8.6 μM at μ-, σ- and κ-opioid binding sites, respectively. Akuammidine possesses anti-inflammatory and anti-asthmatic properties[1][2]. | IC 50 | κ Opioid Receptor/KOR | References | [1] Yuanyuan Hou, et al. Microfractionation Bioactivity-Based Ultra Performance Liquid Chromatography/Quadrupole Time-Of-Flight Mass Spectrometry for the Identification of Nuclear factor-κB Inhibitors and β2 Adrenergic Receptor Agonists in an Alkaloidal Extract of the Folk Herb Alstonia Scholaris. J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Nov 1;908:98-104. DOI:10.1016/j.jchromb.2012.10.004 [2] J R Menzies, et al. Opioid Activity of Alkaloids Extracted From Picralima Nitida (Fam. Apocynaceae). Eur J Pharmacol. 1998 May 29;350(1):101-8. DOI:10.1016/s0014-2999(98)00232-5 |
| (+)-Polyneuridine Preparation Products And Raw materials |
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