rescinnamine
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kemia kombinaĵo
estas
speco de kemiaĵo
subaro de
yohimbinoid alkaloid
uzado
kemia strukturo
maso
634,289031±0 daltono[17]
stereoizomero de
Methyl (15beta,16beta,17alpha,18beta,20alpha)-11,17-dimethoxy-18-{[(2E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]oxy}yohimban-16-carboxylate[11][18]
(1R,15S,17R,18R,19S,20S)-6,18-dimethoxy-17-[1-oxo-3-(3,4,5-trimethoxyphenyl)prop-2-enoxy]-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylic acid methyl ester[18]
kemia formulo
C₃₅H₄₂N₂O₉[3]
ĉefforma SMILES
COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C=CC6=CC(=C(C(=C6)OC)OC)OC[3]
izomera SMILES
CO[C@H]1[C@@H](C[C@@H]2CN3CCC4=C([C@H]3C[C@@H]2[C@@H]1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)/C=C/C6=CC(=C(C(=C6)OC)OC)OC[3]
Referenco
- ↑ 1,0 1,1 1,2 1,3 1,4 1,5 Global Substance Registration System, 19 nov. 2016, angla lingvo, rescinnamine, Q6W1F7DJ2D
- ↑ CAS Common Chemistry, 10 apr. 2021, SZLZWPPUNLXJEA-QEGASFHISA-N, https://commonchemistry.cas.org/detail?cas_rn=24815-24-5
- ↑ 3,0 3,1 3,2 3,3 3,4 3,5 PubChem, 19 nov. 2016, angla lingvo, 5280954, rescinnamine
- ↑ 4,0 4,1 UniChem
- ↑ 5,0 5,1 5,2 Kemiaj Entoj de Biologia Intereso, 3 okt. 2016, angla lingvo, rescinnamine, 28572
- ↑ 6,0 6,1 ChEMBL, 19 nov. 2016, angla lingvo, RESCINNAMINE, CHEMBL1668
- ↑ ChEBI release 2020-09-01
- ↑ DrugBank, 19 nov. 2016, angla lingvo, 01180, Rescinnamine
- ↑ 9,0 9,1 9,2 9,3 SZLZWPPUNLXJEA-QEGASFHISA-N, InChIKey
- ↑ Internacia Kemia Identigilo, InChI=1S/C35H42N2O9/c1-40-21-8-9-22-23-11-12-37-18-20-15-29(46-30(38)10-7-19-13-27(41-2)33(43-4)28(14-19)42-3)34(44-5)31(35(39)45-6)24(20)17-26(37)32(23)36-25(22)16-21/h7-10,13-14,16,20,24,26,29,31,34,36H,11-12,15,17-18H2,1-6H3/b10-7+/t20-,24+,26-,29-,31+,34+/m1/s1
- ↑ 11,0 11,1 inferred from InChIKey
- ↑ Freebase Data Dumps, 28 okt. 2013
- ↑ DrugBank, angla lingvo, 17 nov. 2015, 01180, Rescinnamine
- ↑ IUPHAR/BPS Guide to PHARMACOLOGY, 19 nov. 2016, angla lingvo, 7098, rescinnamine
- ↑ ECHA Substance Infocard database, 27 dec. 2018, 100.042.232, Rescinnamine, CAS no.: 24815-24-5
- ↑ ChemSpider, 3 okt. 2016, angla lingvo, 4444446, rescinnamine
- ↑ PubChem, 3 okt. 2016, angla lingvo, 5280954, rescinnamine
- ↑ 18,0 18,1 inferred from InChI
- ↑ Alkaloid distribution in some african rauvolfia species.
- ↑ The alkaloids of Rauwolfia volkensii
- ↑ Centrifugal thin-layer chromatography of alkaloids from vegetable sources using an aluminium oxide layer
- ↑ The Alkaloids of Rauwolfia cumminsii.
- ↑ Further alkaloids from the roots of Rauwolfia obscura
- ↑ Root alkaloids of Rauwolfia cumminsii Stapf
- ↑ Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications.
- ↑ Inhibitory effects of plant secondary metabolites on cytotoxic activity of polymorphonuclear leucocytes
- ↑ Analysis of Rauwolfia Alkaloids Employing Capillary Electrophoresis-Mass Spectrometry
- ↑ Identification and Estimation of the Alkaloids of Rauwolfia serpentina by High Performance Liquid Chromatography and Thin Layer Chromatography
- ↑ Determination of Reserpine and Rescinnamine in Rauwolfia serpentina Preparations by Liquid Chromatography with Fluorescence Detection
- ↑ Determination of Reserpine and Rescinnamine in Rauwolfia serpentina Powders and Tablets: Collaborative Study
- ↑ 31,0 31,1 31,2 Vinca Alkaloids
- ↑ Investigation of the alkaloids ofVinca major,V. pubescens, andV. rosea. The structure of majdine [1]
- ↑ Alkaloids of Vinca major introduced into Georgia
- ↑ Alkaloids of the roots of Vinca major introduced into Georgia
- ↑ Alkaloids from Vinca major
- ↑ 36,0 36,1 Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum
- ↑ Alcaoëdes d'Ochrosia alyxioides
- ↑ The Alkaloids of Rauwolfia mombasiana Roots
- ↑ Estimation of the alkaloids of Rauwolfia caffra by quantitative thin-layer chromatography. African Rauwolfia species. XIV