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Download Lecture 11 We started to discuss alkaloids possessing pipyridine
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Lecture 11 We started to discuss alkaloids possessing pipyridine ring in their structures, and we verified that pipyridine ring ring is originated from the amino acid (lysine) , But we now that in nature there isn’t black and white , there is always alternative pathways, we can obtain pipyridine ring not only from lysine but by other alternative pathways Today we’ll see such alternative pathways before continue to aromatic amino acids as aromatic precursor . Coniine : possessing pipyridine nucleus ,isolated as liquid alkaloid from Conium Maculatum ,family : Apiaceae Biogenesis : carbon skeleton of pipyridine nucleus is originated from acetate metabolism . Last year we discussed acetate- malonate pathway by which we are adding acetyl and malonyl coA , elongation always by 2 carbons to get poly keto methylene chain (each carbonyl grp separated by methylene grp),carbon skeleton of ciniine is originated from acetate-malonate pathway forming poly keto methylene chain using four acetate units - For Carbonyl and keto grps , it,s easily to start transamination rxn (keto grp vs amino grp), by donation amino grp from L alanine, we convert our acetate originated chain into precursor of coniine which is coniceine , coniceine will be reduced to coniine . - The consistency of the alkaloids , if it is liquid or solid depends on the presence of oxygen , oxygenated alkaloids are solids , non oxygenated are liquids - Coniine is lacking oxygen, so it is liquid. - U have to read in your reference text book extrarotatory and levo rotator coniine occurring in the plant , - 3 carbon side chain is attached to the alpha carbon to nitrogen , it is not alkylation rxn required . 1 - - - - In plant coniine and coniceine are occurring together Conium maculatum seeds or fruits (because the seeds and fruits are together)are similar in their appearance to anise seed but it is very difficult to mix between them together because this substance has very unpleasant smell , so we will immediately recognize even small quantinty of conium seeds in a cup with anise , this bad smell is due to coniceine(it is not the major toxic compound) keep in mind coniine is very toxic Antiquities was used it for criminals to punish them , they were forced to drink acup of extracted conium maculatum seeds in order to affect the brain centers People used it in the past as anti spasmodic agent in very low conc but now it has not medical utilization Coniine primary affects peripheral muscles causing paralysis , it is very similar to curare , so in consciousness cause paralysis starting from peripheral and reaches diaphragm and causing death . All parts of the plant are poisonous but the highest percentage in unripe fruits The doctor said it is not originated from precursor amino acid and she said that the carbon skeleton and the nitrogen is not originated from an amino acid precursor. She wants u to say what is the grp of this alkaloid , if u refer to the book u will find coniine under the grp of alkaloids derived from deamination rxns sub class acetate derived alkaloids (page no. 401 from medicinal natural products a biosynthetic approach 3rd eddition ) There is another possibility to synthesize pipyridine ring using nicotinic acid - The doctor assumed that a 4th year student knows nicotinic acid , pipyridine neucleotide cycle ,involvement of nicotinic acid in co enzymes , NAD,NADH 2 - - - - - - - Nicotinic acid can provide us mono unsaturated pipyridine and this another alternative way To produce pipyridine starting this time with another precursor . these compounds are arecoline, Arecaidine , guvacoline, and guvacine will ba isolated from areca catecha ,family palmae, it is temed as bitternut Bitternut chewing is a social or religious attitude in south Asia especially India , chewing its seeds not leaves continuously mixed with other ingredient , they crush bitter nut , mix it with other aromatic ingredient and chewed in the early morning by Indian . It is classified as stimulator musticatory , it does not cause any hallucination , it causes relaxation . Chewing bitternut is visible when Indian people smile because they have yellowish teeth , it causes staining of the teeth , people always spitting very dark yellow spots . Long term use of chewing gum can cause loosing of the teeth, full teething is rarely recognized in south Asia, it also can cause other inflammation in oral cavity, inflammation in stomach .. etc , these are common observation but they are not reported . In medicine it used as anti emetic Nicotinic acid incorporated in pipyridine nucleus synthesis , the more important to us for formation of other subclasses of alkaloids which we say alkaloid derived from nicotinic acid . In fact this sub classification from references is different because nucleus of nicotinic acid when we use carboxyl grp is pyridine We have seen pipyridine as derivative or incorporated as into alkaloids, now we’ll see what are the pyridine incorporated , in some references are referred as pyridine- popyridine alkaloids In the past they were studying enolate alkaloids originated from ornithine, lysine, and aspartic acid (aliphatic a.a), with time this aspartic acid has been excluded from titles , and the text books included alkaloids originated from nicotinic acid or alkaloids containing pyridine –pipyridine, but what were studying before reflects the reality more than the current condition because alkaloids which are based on nicotinic acid or pyridine nucleus they can be obtained like we have in our mammalian organism using amino acid tryptophan , it can be via quinolinic acid under hereto pyridine nucleotide cycle and we yield the nicotinic acid or more common niacin (vit B3) But what we concern about is how do we obtain nicotinic acid from plant kingdom We start condensation with aspartic acid with glyceraldehyde-3phosphate Because of this condensation we can obtain poly substituted pipyridine intermediate ,which well be converted to quinolinic acid aspartic acid is a derivative of oxalacetic acid , oxalacetic acid is obtained from kreb’s cycle , and glyceraldehydes 3 phosphate is obtained from photosynthesis ,u see very basic primary metabolites yielding glyceraldehyde 3 phoshphate and aspartic acid(secondary metabolites) , without these essentially steps of photosynthesis and kreb’s cycle u can’t get any of tese secondary metabolite quinolinic acid is a di carboxylic acid , the two carboxyl grps are obtained from oxalacetic acid 3 - - conversion of piyridine to pyridine needs dehydrogenation sense we have poly substituted pipyridine ring , in addition to dehydrogenase ,we have to eliminate the hydroxyl grp by simle dehydration (first dehydration step, second dehydration step and dehydrogenation step), to convert it to nicotinic acid we need an oxidative moiety , the pyridine nucleotide will be decarboxylated , and nicotinic acid will be released , now we have a building block . note that nicotinic acid itself is not the alkaloid , it is the parent of different compound of different alkaloid note that alkaloids derived from nicotinic acid can be termed as derived from aspartic acid because nicotinic acid originated from aspartic acid classical examples of nicotinic acid derived alkaloids : - - ricinine : is found in Ricinus communis family Euphorbiaceae (castor beans), but it does not contaminating in oil which is used as laxative. More important than castor beans is Tobacco alkaloids : We have nicotine and nor nicotine By which carboxylic grp eliminated and attached to ornithine originated pyrollidine ring Nicotine is possessing a methyl grp , methylation of the methyl grp obtains no nicotine 4 - - - Anabasine : we have pyridine we have pyridine and we have pipyridine The origin of pipyridine in tobacco alkaloids is the amino acid lysine , so we’ll get nicotinic acid decarboxylated , condensed with pipyridine (lysine originated ) Another alkaloid Anatabine : it is very similar in structure to anabasine , the difference is anatabine has mono unsaturated pipyridine ring , its heterocyclic ring is originated fron nicotinic acid while in anabasine originated from nicotinic acid and lysine Both of anatabine and anabasine occure in the same plant , similarity in the structure but different biogenetic origin . 5 - We’ll talk about the plant nictiana tobacum , nicotiana rusticam , nicotiana has 100 diffrenet species , family solanaceae - Originally it has been used by indian american(the origin is america) , later by frensh men , they took it overseas and cultrated it - Nicotine is one of the earliest alkaloids isolated (1920), indian amirican smooked it using a pipe so frensh men smooked it just like them until 1980 they develop new siggirate industry , in the begening in eurupe they used the pipes to smook - It didn’t remain in particular area , it has been brought from overseas - We have in jordan , in Madaba nicotiana tobacum plants - We don’t have just species of nicotiana , we also have varieties , even in some countries they said they didn’t culturate it , it is naturalize 6 - - - - - - Naturalize means in more than hundred years poeople culturated it , and people didn’t recognise that people brought it from overseas, the plant is adapted to the soroundings and it grows alone , so naturalized means the plant has been culturated after many years as it is endogenus plant. So tobacco has been cultrated and naturalized in many different countries Leaves is the site that contains alkaloids although the site of biosynthesis are the roots Many types of alkaloids have been isolated from nicotiana in the form of volatile liquids, non volatile liquids, solids, aromatics According to the species we have the major alkaloid , so nicotine is not always the major Nicotine and nor nicotine are liquids (don’t have oxygen in their structure) In cigarette Nicotine is classified as natural compound insecticide and it is available in the form of its salt because in salt form will be in crystal form , u can prepare easily a solution of it by solubilizing it by aqueous or semi hydroalkoholic solvent, and splitting the sulphate by adding often alkaline solution , if there is no alkaline sol we can add simple salt sol , this will be sufficiently to provide alkaline solution The insecticidal activity of free alkaloid is more compared to the salt. In past farmers used to powder the leaves and spread it over other plant, to protect them from insect attack (in record the dr said insecticidal attack!) Pure nicotine is used in fumigation of green house, by keeping a small amount of liquid nicotine in the green house, it will volatilize, and act as insecticide. It also used in stent Pharmacological activity of Nicotine in stimulation and internalization of peripheral, autonomic, brain, ganglia ,.. etc it is very well known in activity in pharmacology and toxicology The fatal dose of nicotine is : 40 mg ,it is not much diluted , u can find them in just 3 cigarette. Cigarette must not be opened to children , they may eat some of the tobacco so toxicity occur , it gives burn sensation , but some children will like thin burning and continue eating and this will cause a lot of irritation and toxicity , the anti dote is atropine It is reported in all references to pharmacology that burning sensation of cigarette develops more than 4000 cmpds , typical smoker apparatus is adjusted and attached to GCMS to predict theses cmpds The cmpds can be separated to : 1) gas phase 2) particular phase Nicotine is part of particular phase because it is found in the suspending on the tar , tar is more toxic than nicotine Cigarette producers are forced to write on the boxed the amount of nicotine and the amount of tar that will be produced during smoking process Tar contains the most carcinogenic which are polycyclic hydrocarbons ,polycyclic aromatic hydrocarbons, polycyclic aromatic hydrocarbons, metallic ions ,and radiating ions The gaseous phase contents: carbon mono oxide, carbon dioxide, volatile sulfur, nitrogen, compounds, aldehydes, ketons .. etc 7 - U can separate gaseous phase from particulate phase but u can’t make standard composition or exact composition because it depends on different factors like: 1) type of filter used , 2) quality of paper used in the formation of cigarette, how much this paper is bleached, what type of cellulose in this paper 3) how dense the cigarette column is , old people used to roll their own cigarette , and now is industrial produced , there is a big difference how dense the column of the cigarette .4) the length of the column and its diameter 5) The additional perfumes added 6) the percent of smoked cigarette (very important factor) : what kind of component will be produced is determined by temp at which these cmpds are burned (temp of pyrolysis ) What affect temp of pyrolysis :the strength of inhalation , if the person inhaled strongly the tem of pyrolysis will be higher and we get completely different constituent copared to aperson who is not inhaling very strongly Worldwide, it’s not classified as social drug any more , it is classified as non social , a drug to smoke in closed area in order to protect non smokers Alkaloids derived from aromatic amino acids : - We have 3 amino acids : 1) phenyl alanine 2) tyrosine 3)tryptophan Para hydroxyl phenyl alanine is tyrosine , so phenyl alanine and tyrosine are closely related The doctor made a little bit deviation from our text book , in the text book they discussed the alkaloids originated from a.a tyrosine then they discussed alkaloids from phenyl alanine , the doctor will put them together , because she consider a more logical attitude in discussing alkaloids ,to recognize similarities and differences 8 - - ( الفقرةالسابقة للناس اللي بتدرس من الكتاب:P Alkaloid derived from phenyl alanine and tyrosine have a basic difference in their structure which is phenyl alanine never contribute nitrogen to the terminal cmpd , so when phenyl alanine is the precursor it provides carbon skeleton and we need transamination , when tyrosine is the precursor it will provide carbon skeleton plus nitrogen. One of the classes to be discussed is phenyl alkyl amines (the name is indicative enough to know the structure aromatic ring +alkyl chain+nitrogen ) Amaryllidaceae alkaloids for example galanthamine : promising in the treatment of Parkinson disease and colchicine used in management of acute attacks of gout Here We have both amino incorporated , - We have in this grp isoquinoline alkaloids , opium alkaloid, curare alkaloids..etc The name phenyl alkyl amine indicates the formation ,we can obtain amine from a.a by synthetic carboxylase - Any amino acid can provide it’s biosynthetic amine by synthetic carboxylase , and this biogenic amine when we modify the structure, then it will never be considered as the true amine…(min 44:35) - And this phenyl alkyl amine depending on carbon no. of the side chain we can sub classify as benzyl amine derivatives , which means we have c6 aromatic and benzyl grp c1 , or we can elongate the side chain by 2 carbons for example , then we’ll have a phenyl ethyl amine derivative (so the side chain here is 2 carbons) - The third grp is very indicative Beta Amino phenyl propane derivatives u should be able to write down these structures based on this head line We’ll talk about capciasin alkaloid in the first grp . in the second grp very important adrenaline catecholamines (we will not discuss this is your homework :/),and we’ll discuss mescaline , in this grp we’ll talk about ephedrine Capsacinoids the pungent principle of the capcicums (piper), this the type is not of the black piper , we talk here about paprikas ( green, red, white sweet piper and شطة - It is very very pungent , these pungent principles are grouped as capsacinoids - U see aromatic ring originaly , benzyl amine , the amino is esterified within acid grp ang we obtain amide alkaloid . - Recognize the cmpd by amide grp, benzene must be benzyl amine and long fatty acid chain - hydroxy capcaisin are the basic principle of capsicum species especially found in hot chilli pipers of capsicum frutescens , it is very pungent that u feel the cmpd even if 1 part is in 11million part of water ! Imagine how much u have to dilute if u have 1 gm or 1 kilogram !! 9 - - this pungency is used for its rubefacient effect and skin irritant properties in form of (min 48:43but I think it is roimal ) plasters for treatment of rhumatiod pain of joints and muscles otherwise in stomach , its irritant activity will cause increase secretion of gastric juices , very recently they say secretion of gastric juices improve the appetite , dietitians recommend to take some pungent principle in breakfast , this will increase metabolism and by increasing the metabolism causing burning of more fat , then weight loss biogenetically origin capcaisin derived from phenyl alanine so we need to remove of the nitrogen - phenyl alanine will continue via cinnamic acid to hydroxyl cinnamic acid then methylation to get ferulic acid ,beta oxidation of ferulic acid and we’ll obtain vanillic acid , reduction to get vanillin . vanilline will be converted by changing the methyl to amino grp corresponding vanillin amine . this react with fatty acid to obtain capciasin - the strange that we have not pungent taste everywhere because we have the acid moeity malonyl coA, it is fatty acid with 9 carbons , in nature the majority of fatty acids biosynthesized are characterized by even numbers , but strange compound posses different activity ,this is bearing a methyl grp on position 8 and unsaturation between carbons 6and 7 , esterfication get vanillin amide - this process produces capsaicin , u can oxidize methyl grp to obtain hydroxycapsaicin - small modification will obtain series of cmpds different in substitution but possessing the pungent principle 10 - The end Done by: shuruq sallam 11