Alkaloids of the Australian Rutaceae: Melicope fareana. II. Preliminary Examination of Melicopine, Melicopidine, and Melicopicine

1949 ◽  
Vol 2 (2) ◽  
pp. 255
Author(s):  
WD Crow ◽  
JR Price

Four of the five oxygen atoms in the alkaloids melicopine, melicopidine, and melicopicine are present as alkoxyl groups, either methoxyl or methylenedioxy. In each alkaloid one of the methoxyl groups is remarkably sensitive to hydrolysis by acids. The resulting hydroxy compound is an alcohol, or more likely, an unreactive phenol. The methylenedioxy group in melicopine and melicopidine is attacked by alcoholic alkali and replaced by an hydroxyl and an alkoxyl group. The resulting phenols still contain the easily hydrolysed methoxyl group, the loss of which gives rise to a series of dihydroxy compounds. A number of acidic oxidation products is described.

2015 ◽  
Vol 19 (09) ◽  
pp. 1007-1013 ◽  
Author(s):  
Patrick C. Loughlin ◽  
Robert D. Willows ◽  
Min Chen

Following extraction from photosynthetic organisms, chlorophylls are prone to reactions including demetalation, dephytylation and specific oxidations of the exocyclic ring E, termed allomerizations. Allomerization of chlorophylls has been well-characterized in methanol and to a lesser extent in aqueous solution. Here we detail novel allomerization-like reactions of chlorophyll a and chlorophyll b. In the presence of heme, detergent-solubilized chlorophyll a is hydroxylated at its C 132 position in ring E and, surprisingly, the C 18 position in ring D. Two major oxidation products are synthesized — a C 132- OH and a C 132- OH , C 18- OH derivative of chlorophyll a. We track the origin of the oxygen atoms added in these hydroxylated chlorophylls using 18 O 2 labeling and demonstrate that the additional oxygen atoms are derived from molecular oxygen. A similar heme-catalyzed reaction is also observed using chlorophyll b as a substrate. These results highlight the need for care when dealing with extracted chlorophylls and demonstrate an unusual hydroxylation of the C 18 position of chlorophylls in the presence of heme.


1952 ◽  
Vol 5 (3) ◽  
pp. 563
Author(s):  
ER Nelson ◽  
JR Price

The alkaloid C15H10O2N2, present in the bark of Pentaceras australis Hook. f., has been shown to be 5-methoxycanthin-6-one. It is oxidized by potassium permanganate to β-carboline-1-carboxylic acid and its lactam ring may be opened by alkali to give a β-carbolylmethoxyacrylic acid which readily recyclizes to the alkaloid. The position of the methoxyl group is demonstrated by demethylation and condensation of the resulting hydroxy-compound with o-phenylenediamine to give a hydroxyquinoxaline. Attempted hydrogenation of the alkaloid or the derived methoxyacrylic acid led to elimination of methoxyl.


1982 ◽  
Vol 201 (3) ◽  
pp. 569-580 ◽  
Author(s):  
Muhammad Akhtar ◽  
Michael R. Calder ◽  
David L. Corina ◽  
J. Neville Wright

Mechanistic aspects of the biosynthesis of oestrogen have been studied with a microsomal preparation from full-term human placenta. The overall transformation, termed the aromatization process, involves three steps using O2 and NADPH, in which the C-19 methyl group of an androgen is oxidised to formic acid with concomitant production of the aromatic ring of oestrogen: [Formula: see text] To study the mechanism of this process in terms of the involvement of the oxygen atoms, a number of labelled precursors were synthesized. Notable amongst these were 19-hydroxy-4-androstene-3,17-dione (II) and 19-oxo-4-androstene-3,17-dione (IV) in which the C-19 was labelled with2H in addition to18O. In order to follow the fate of the labelled atoms at C-19 of (II) and (IV) during the aromatization, the formic acid released from C-19 was benzylated and analysed by mass spectrometry. Experimental procedures were devised to minimize the exchange of oxygen atoms in substrates and product with oxygens of the medium. In the conversion of the 19-[18O] compounds of types (II) and (IV) into 3-hydroxy-1,3,5-(10)-oestratriene-17-one (V, oestrone), it was found that the formic acid from C-19 retained the original substrate oxygen. When the equivalent16O substrates were aromatized under18O2, the formic acid from both substrates contained one atom of18O. It is argued that in the conversion of the 19-hydroxy compound (II) into the 19-oxo compound (IV), the C-19 oxygen of the former remains intact and that one atom of oxygen from O2 is incorporated into formic acid during the conversion of the 19-oxo compound (IV) into oestrogen. This conclusion was further substantiated by demonstrating that in the aromatization of 4-androstene-3,17-dione (I), both the oxygen atoms in the formic acid originated from molecular oxygen. 10β-Hydroxy-4-oestrene-3,17-dione formate, a possible intermediate in the aromatization, was synthesized and shown not to be converted into oestrogen. In the light of the cumulative evidence available to date, stereochemical aspects of the conversion of the 19-hydroxy compound (II) into the 19-oxo compound (IV), and mechanistic features of the C-10–C-19 bond cleavage step during the conversion of the 19-oxo compound (IV) into oestrogen are discussed.


2020 ◽  
Author(s):  
Meri Räty ◽  
Otso Peräkylä ◽  
Matthieu Riva ◽  
Lauriane Quéléver ◽  
Olga Garmash ◽  
...  

Abstract. Cyclohexene (C6H10) is commonly used as a proxy for biogenic monoterpenes, when studying their oxidation mechanisms and secondary organic aerosol (SOA) formation. The ozonolysis of cyclohexene has been shown to be effective at producing highly oxygenated organic molecules (HOM), a group of molecules known to be important in the formation of SOA. Here, we provide an in depth look at how, on a molecular level, the HOM formation and fate changed with perturbations from NOx and seed particles. HOM were produced in a chamber from cyclohexene ozonolysis, and measured with a chemical ionisation mass spectrometer (CIMS) using nitrate (NO3−) as reagent ion. As high-resolution CIMS instruments provide mass spectra with numerous ion signals and a wealth of information that can be hard to manage, we employed a primarily statistical approach for the data analysis. To utilise as many individual HOM signals as possible, each compound was assigned a parameter describing the quality of the observed signal. These parameters were then used as weights or to determine the inclusion of a given signal in further analyses. Under unperturbed ozonolysis conditions, known HOM peaks were observed in the chamber, including C6H8O9 as the largest HOM signal, and C12H20O9 as the largest dimer product. With the addition of nitric oxide (NO) into the chamber, the spectrum changed considerably, as expected. Dimer product signals decreased overall, but an increase in dimers with nitrate functionalities was seen, as a result of NO3 radical oxidation. The response of monomer signals to NO addition varied, and while nitrate-containing monomers increased, non-nitrate signals either increased or decreased, depending on the individual molecules. The addition of seed aerosol increased the condensation sink, which markedly decreased the signals of all low-volatility compounds. Larger molecules were seen to have a higher affinity for condensation, but a more detailed analysis showed that the uptake was controlled mainly by the number of oxygen atoms in each molecule. All non-nitrate compounds with at least 7 oxygen atoms were observed to condense onto the seed aerosol at close to equal rates. Nitrates required higher mass and higher oxygen content to condense at similar rates as the non-nitrate HOM. A comparison to experiments with alpha-pinene reported earlier, showed quite a similar relationship between elemental composition and volatility, although products from alpha-pinene ozonolysis appeared to require slightly higher oxygen numbers for the same decrease in volatility. In addition, two models developed for predicting volatilities of volatile organic compound (VOC) oxidation products were tested on the ozonolysis products of cyclohexene.


2008 ◽  
Vol 416 (3) ◽  
pp. 441-452 ◽  
Author(s):  
Clare L. Hawkins ◽  
David I. Pattison ◽  
Naomi R. Stanley ◽  
Michael J. Davies

Myeloperoxidase, released by activated phagocytes, forms reactive oxidants by catalysing the reaction of halide and pseudo-halide ions with H2O2. These oxidants have been linked to tissue damage in a range of inflammatory diseases. With physiological levels of halide and pseudo-halide ions, similar amounts of HOCl (hypochlorous acid) and HOSCN (hypothiocyanous acid) are produced by myeloperoxidase. Although the importance of HOSCN in initiating cellular damage via thiol oxidation is becoming increasingly recognized, there are limited data on the reactions of HOSCN with other targets. In the present study, the products of the reaction of HOSCN with proteins has been studied. With albumin, thiols are oxidized preferentially forming unstable sulfenyl thiocyanate derivatives, as evidenced by the reversible incorporation of 14C from HOS14CN. On consumption of the HSA (human serum albumin) free thiol group, the formation of stable 14C-containing products and oxidation of tryptophan residues are observed. Oxidation of tryptophan residues is observed on reaction of HOSCN with other proteins (including myoglobin, lysozyme and trypsin inhibitor), but not free tryptophan, or tryptophan-containing peptides. Peptide mass mapping studies with HOSCN-treated myoglobin, showed the addition of two oxygen atoms on either Trp7 or Trp14 with equimolar or less oxidant, and the addition of a further two oxygen atoms to the other tryptophan with higher oxidant concentrations (≥2-fold). Tryptophan oxidation was observed on treating myoglobin with HOSCN in the presence of glutathione and ascorbate. Thus tryptophan residues are likely to be favourable targets for the reaction in biological systems, and the oxidation products formed may be useful biomarkers of HOSCN-mediated protein oxidation.


2020 ◽  
Vol 295 (19) ◽  
pp. 6665-6676 ◽  
Author(s):  
Natalia Rios ◽  
Rafael Radi ◽  
Balaraman Kalyanaraman ◽  
Jacek Zielonka

Reactive oxygen and nitrogen species have been implicated in many biological processes and diseases, including immune responses, cardiovascular dysfunction, neurodegeneration, and cancer. These chemical species are short-lived in biological settings, and detecting them in these conditions and diseases requires the use of molecular probes that form stable, easily detectable, products. The chemical mechanisms and limitations of many of the currently used probes are not well-understood, hampering their effective applications. Boronates have emerged as a class of probes for the detection of nucleophilic two-electron oxidants. Here, we report the results of an oxygen-18–labeling MS study to identify the origin of oxygen atoms in the oxidation products of phenylboronate targeted to mitochondria. We demonstrate that boronate oxidation by hydrogen peroxide, peroxymonocarbonate, hypochlorite, or peroxynitrite involves the incorporation of oxygen atoms from these oxidants. We therefore conclude that boronates can be used as probes to track isotopically labeled oxidants. This suggests that the detection of specific products formed from these redox probes could enable precise identification of oxidants formed in biological systems. We discuss the implications of these results for understanding the mechanism of conversion of the boronate-based redox probes to oxidant-specific products.


1996 ◽  
Vol 100 (3) ◽  
pp. 1048-1054 ◽  
Author(s):  
Tsuyoshi Sueyoshi ◽  
Takehiko Sasaki ◽  
Yasuhiro Iwasawa

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