Minggu, 25 November 2012

Chemistry of Natural Products Mid Test

Chemistry of Natural Products

Name                         :  Lina Purwanti
Student number          :  RSA1C110009
Study Program           :  Chemistry Education of ISSTE

3.  Jelaskan kaidah-kaidah pokok dalam memilih pelarut  untuk isolasi dan purifikasi suatu senyawa bahan alam. Berikan dengan contoh untuk 4 golongan senyawa bahan alam : terpenoid, alkaloid, flavonoid dan steroid !
Answer :  The solvent selected for the extraction seen by the ability of interesting secondary metabolites from plants. As the fluid used to perform the extraction of water, ether, or a mixture of ethanol and water. Alcohol, however, is a versatile solvent for extraction.
            Methods of isolation steroid
Procedures for isolation of steroids differ according to the chemical nature of the steroids and the scale and purpose of the isolation. Steroids are isolated from natural sources by extraction with organic solvents, in which they usually dissolve more readily than in the aqueous fluids of tissues. The source material often is treated initially with an alcoholic solvent, which dehydrates it, denatures (renders insoluble) proteins associated with the steroids, and dissolves many steroids. Saponification either of whole tissues or of substances extracted from them by alcohol splits the molecules of sterol esters, triglycerides, and other fatty esters and permits the extraction of the sterols by means of water-immiscible solvents, such as hexane or ether, with considerable purification. Intact sterol esters or hormonal steroids and their metabolites (compounds produced by biological transformation) that are sensitive to strong acids or alkalies, however, require essentially neutral conditions for isolation, and, although some procedures for analysis of urinary steroids employ acid treatment, milder hydrolysis, as by enzymes, is preferred. The acidity of some steroids allows them to be held in alkaline solution, while nonacidic impurities are extracted with organic solvents.
Commercially, abundant steroids usually are purified by repeated crystallization from solvents. Small-scale laboratory isolations for investigative or assay purposes usually exploit differing polarities of the steroid and of its impurities, which may be separated by partitioning between solvents differing in polarity or by chromatography. Occasionally, special reagents may selectively precipitate or otherwise sequester the desired steroid. A classical example is the precipitation of 3β-hydroxy sterols such as cholesterol by the natural steroid derivative digitonin. New steroids of great physiological interest often are isolated from tissue only with extreme difficulty, because they are usually trace constituents. In one example, 500 kg (1,100 pounds) of silkworm pupae yielded 25 mg (0.0008 ounce) of pure molting hormone, the steroid ecdysone (i.e., 20 × 106-fold purification). In such cases each isolation step is followed by an assay for the relevant physiological activity to ensure that the desired material is being purified. The percentage recovery of known steroid hormones during their assay in small biological samples usually is assessed by adding a trace of the same steroid in radioactive form to the initial sample, followed by radioassay (analysis based on radioactivity) after purification is complete. The efficiency of recovery of the radioactive steroid is assumed to be the same as that of the natural substance.
extraction of Flavonoids
Flavonoid metabolites (mainly glycosides) can be degraded by the activity of enzymes in plant material has not been dried or fresh ingredients. Thus it is recommended to use dried, lyophilized or frozen samples. The use of dried botanicals commonly milled into powder first. In the solvent extraction process should choose the appropriate type of flavonoid required so should consider the polarity of the solvent. Types of non-polar flavonoids (eg, isoflavones, flavanones, flavones and flavonols alcohol) was extracted using chloroform, dichloromethane, diethyl ether, or ethyl acetate, while the flavonoid glycoside and aglycone would be more appropriate extracted with alcohol or alcohol-water mixture. To glycosides increased solubility if the water or alcohol-water mixture. Generally most of the extraction process materials containing flavonoids is done simply with the addition of direct solvent extraction.
Powdered plant material can also be extracted using a Soxhlet, initially with hexan, to remove lipids and then with ethyl acetate or ethanol to obtain phenolic compounds. This method is unsuitable for the content of compounds that are not heat resistant. The procedure is safe and commonly used sequential solvent extraction. The first phase, with dichloromethane, to extract flavonoid aglycone and content of non-polar. The next stage of the alcohol will extract and flavonoid glycoside content of polar compounds.
Chalcone glycosides specific flavanones and difficult to soluble in methanol, ethanol, or a mixture of alcohol and water. Flavanones solubility depends on the pH of the water as a solvent. Flavan-3-ol (like catechin, proanthocyanidin, and condensed tannins) can generally be extracted directly with water. However, the content of the compounds in the extract is not much different, either using water, methanol, ethanol, acetone, or ethyl acetate. In this case, can not be claimed that methanol is the best solvent for catechins and procyanidin acetone 70%, and so on.
Anthocyanins can be extracted with cold acidified methanol. The acid used is usually acetic acid (approximately 7%) or trifluoroacetic acid (TFA) (about 3%).

Anthocyanin extraction (include in flavonoid)
Using solvent extraction based on the solubility of the component to other components in the mixture. stating that polar solvents will dissolve polar solutes and non-polar solvents will dissolve the non-polar solute or so-called "like dissolve like".
In the fruit or vegetable, anthocyanin pigments are generally located in the cells near the surface. Extraction of anthocyanin pigments from plant materials commonly used solvent extractors HCl in ethanol. HCl in ethanol plants will denaturation of the cell membrane and then dissolving the pigment anthocyanin out of the cell. Anthocyanin pigments soluble in ethanol because both polar.
In research for the extraction of anthocyanins from flowers girlfriend water, the best solvent used is ethanol 95%. So is the research on the extraction of pigment from the skin of the fruit rambutan. This is due to the level of anthocyanin polarity similar to the 95% ethanol that can dissolve well in ethanol 95%. In addition to the solvent, the factors that can affect the outcome of anthocyanin extraction is the extraction time, pH and temperature extraction.
Methods Isolation of Compounds Alkaloids (Nicotine)
Alkaloids are usually isolated from the plant by using the method of extraction. Solvents are used when extracting the compound mixture is acidified water molecules. This solvent will be able to dissolve the alkaloid salts.
It also can alkalinize alkaloid-containing plant material by adding sodium carbonate. Bases are formed can then extraction by organic solvents such as chloroform or ether
For alkaloids that are not heat resistant, insulation can be done using techniques alkalinize the solution concentration by first. By using this technique the alkaloid will evaporate and then be purified by steam distillation method.
Each compound in the extract (extraction) based on the level of polarity (solubility)
Extraction is usually performed in stages ranging from non-polar compounds >> semi-polar polar >>
Polar compounds will tersari with polar solvents (eg, ethanol, methanol, water) as did so. examples of semi-polar solvent (ethyl acetate), an example of a non-polar solvent (n-hexane)
Compounds tersari with non-polar solvents >> Lipids, Steroids, Tannins
Compounds tersari the semi-polar solvents >> Alkaloids, Flavonoids, Glycosides
Compounds with a polar solvent tersari >> flavonoid Glycosides
Extractions are often used to separate organic compounds are liquid extraction, the separation of substances based on the comparison of the distribution of substances dissolved in the two solvents are not mutually dissolve.
It's best in a solvent in which the solubility is one greater than the concentration of solutes in the other solvents, the price of K should be larger or smaller than the short-term extraction process called pengorokan, whereas in the long-term use and the heating soxhlot.
Solvent selection criteria:
- Solvents dissolve easily extracted material
- The solvent does not mix with the juices extracted
- Solvent extract little or no impurities that exist
- Solvent easily separated from the solute
- The solvent does not react with the solute through any means

4.  jelaskan dasar titik tolak penentuan struktur suatu senyawa organic. Bila senyawa bahan alam tersebut adalah kafein misalnya. Kemukakan gagasan anda tentang hal-hal pokok apa saja yang diperlukan untuk menentukan struktur secara keseluruhan !
Answer :  I chose the determination structure of tobacco (nicotine).
            To know the strycture we should have solvent like methanol, and the tools for identification the structure.
We can identification structure based on some method like Using Column Chromatography, Using TLC, Infrared Spectrophotometer (IR), UV spectrophotometer, GC-MS.
Example in Results Identification of Compounds in Tobacco Leaf Extract Using TLC. in this method we can use developer solution of methanol. At this stage the results of the chromatography column (more concentrated solutions) that have been obtained and identified by thin layer chromatography using the solvent methanol developers.
From the analysis of thin-layer chromatography separation obtained only one peak each sample, it means that it has produced a compound perfectly separated.
Results Infrared Spectrophotometer (IR) in the Tobacco Leaf Extract Fraction Methanol. In this method we can use methanol as a solvent. Infrared spectrophotometer was used to analyze the functional group of chemical compounds found in tobacco leaves with the solvent methanol. results of Infrared Spectrophotometer (IR) was also determined from the use of solvent in column chromatography for example in one result of identification structure using infrared spectrophotometer produce The existence of absorption at 3398.3 wavenumber indicates the-OH group. This is because the use of methanol as column chromatography. So chromatography column was first performed will affect the outcome of the determination of the method used for the next.
Test results with a UV spectrophotometer Tobacco Leaf Extract Fraction methanol. UV spectrophotometry is used for organic compounds associated with electronic transitions in electron energy levels given. Usually measured compounds having conjugated double bonds. Nicotine has a conjugated double bond in the ring of piridin. Maximum absorption difference may be due to differences in the solvent used. In this method we can use different solvent and that will make difference absorption.
                The results of GC-MS Fraction Methanol Extracts of Tobacco Leaves.  The end of for identification is using GC-MS, from the first step until the end step have relationship like using the same solvent, from one to another will affect result for the next identification structure.

2.  jelaskan bagaimana idenya suatu senyawa bahan alam yang memiliki potensi biologis tinggi dan prospektif untuk kemaslahatan makhluk hidup dapat disintesis di labortorium !

Answer :  For this question I choose calkon (calkon synthesis of pyridine compounds as potential drug candidates)
calkon natural materials including compound flovonoid group, calkon compounds have a wide range of interesting activities such biolgi antioxidant, antitumor, anti-inflammatory, and others. calkon content at relatively low in extrack of plant with limited structural variation, because calkon an intermediate product in the process of formation of the biosynthesis of other flavonoid compounds. this is one of the factors to conduct molecular synthesis calkon well to study the physico-chemical properties and understand the relationship between structure and activity, and as an effort to find new bioactive compounds of potential used modern medicine. synthesis of compounds has been carried out in the presence of pyridine calkon various combinations of functional groups and pyridine core with several other heterocyclic core. calkon some synthesized compounds turned out to exhibit strong antibacterial activity.
calkon compound pyridine synthesis approach with combinatorial chemistry to produce a compound with a structure that varies in a relatively short time and using a simple method.

1-      synthesis of pyridine calkon compounds were calculated using grinding or mixing by using a simpler tool.
2-   synthesis of pyridine compounds calkon done by eliminating or minimizing the use of organic solvents.
3-      synthesis of pyridine calkon compounds can produce high redeman a relatively short time.
4-     some calkon pyridine compounds showed strong antibacterial activity.
5-      calkon pyridine compounds potentially have other activities such as antioxidant and anti-inflammatory.

From synthesis calkon can obtain potential new drugs and useful for life in the community, in addition to the method used is also simple, environmentally friendly, and the compound structure of the new calkon.
  

1. kemukakan gagasan anda bagaimana cara mengubah suatu senyawa bahan alam yang tidak punya potensi (tidak aktif) dapat dibuat menjadi senyawa unggul yang memiliki potensi aktifitas biologis tinggi. Berikan dengan contoh !
Answer :  the way to convert a compound of natural ingredients that do not have the potential (inactive) can be made into a superior compound that has the potential of high biological activity is activated by using pengaktifasi functional groups.
One example is an important alkaloid found in mengkudu  fruit is xeronine. Xeronine also produced by the human body in a limited number of functions to activate enzymes and regulate fungtion of  proteins in the cell.
            other than that to activate it can also be reacted with an enzyme that is sensitive to a reaction that takes place
 


Jumat, 23 November 2012

NICOTINE

Nicotine is an alkaloid with the chemical name 3 - (1-methyl-2-pirolidil) pyridine. When extracted from the leaves of tobacco, nicotine is colorless, but may be brown. Nicotine can evaporate and be purified by steam distillation from the basified solution. Nicotine is a substance that is toxic alkaloid tertiary amine compound, is a weak base with a pH of 8.0. At pH, as many as 31% of the nicotine in the form of ions and can not pass through the cell membrane. At this pH the nicotine is in the form of ions and can not pass through the membrane rapidly resulting in only a slight cheek mucosa absorption of nicotine from cigarette smoke. Nicotine is an alkaloid that is naturally in tobacco plants. Nicotine is also found in other plants of the family Solanaceae biological such as tomatoes, potatoes, eggplant and green pepper at very small compared to tobacco. Alkaloid substances are known to have pharmacological properties, such as the stimulant effects of caffeine increases blood pressure and heart rate. Alkaloid nicotine undergo metabolic processes, which is a process by which nicotine undergo structural changes due to the chemical compounds in the vicinity. Isolation of nicotine from tobacco leaves 1) 25 grams of chopped dried tobacco leaves that have been wrapped in filter paper inserted into the Soxhlet apparatus, extraction using 300 mL of methanol for 7 hours. The sample used is 100 grams so the extraction is done 4 times. 2) Extract / resulting filtrate evaporated until the resulting solution or filtrate concentrated with 10% of the original volume. 3) concentrated solution is poured into the erlenmeyer flask and acidified with 2 M H2SO4 at 25 mL. The solution was stirred with a magnetic stirer to be homogeneous. The solution was tested with litmus paper to red. Then the solution was extracted with chloroform 25 mL 3 times a separating funnel. 4) Extract the resulting bottom layer is tested with reagents Dragendorf, if there is a positive alkaloid orange precipitate. 5) The extract was neutralized again by adding NH4OH and then extracted again with 25 mL of chloroform 3 times. 6) The extract obtained was evaporated to aerate, then purified by column chromatography on silica gel 11.5 grams as the stationary phase, column length 10 cm, diameter 3 cm column and with eluent n hexane and chloroform, methanol with a ratio 1:0, 7:3, 5:5, 3:7 and 0:1 respectively - each as much as 10 mL. 7) The results of column chromatography followed by thin layer chromatography with a solution of methanol developers. 8) The extract was then tested by using GC-MS, UV-Vis spectrophotometer and IR spectrophotometer. The effect of nicotine in the body Nicotine found in tobacco, is one of the known additives. Nicotine is an inhibitor of the central nervous system (CNS) that upsets the balance nerve. Physical and psychological dependence on nicotine is growing very fast. Inhaling tobacco produces nicotine's effects on the CNS in less than ten seconds. If you chew tobacco, the effect on the CNS experienced within 3-5 minutes. Effects of nicotine in tobacco use by sucking, chew tobacco or breathe through a straw, causing constriction of blood vessels, increased heart rate and blood pressure, decreased appetite, partly eliminating the feeling of taste and smell as well as the lungs become painful. Tobacco use in the long term can cause damage to the lungs, heart, and blood vessels. Nicotine is addictive. That's why smokers continue to smoke tobacco regularly because they are addicted to nicotine. Addiction is marked by a passionate desire to always find and use, although aware of the negative health consequences. From natural dependency properties is discovered that nicotine activate the brain tissue that causes feelings of pleasure, calm, and relax. A chemical in the brain, including the desire to continue consuming intermediaries, ie neurotransmitters dopamine, the research shows that nicotine increases the levels of dopamine. Acute effects of nicotine in a few minutes causes the smoker to continue dosing frekuentif per day in an effort to maintain the effect of pleasures that arise and defend itself from the effects of addiction. Nicotine can act as a stimulant and a sedative or painkillers. Directly after the contact with nicotine stimulation of the adrenal glands arise which cause the release of the hormone adrenaline. The hormone adrenaline stimulates the body and causes a sudden release of glucose which eventually decreased blood sugar levels and blood pressure also increases. Similarly, the breathing and heart rate. The reaction is almost the same as that seen in the case of abuse of drugs such as cocaine and heroin are suspected to cause a sensation happy. But on the other hand nicotine may cause effects as sedatives or pain relievers, depending on levels consumed in the system and the dose used. Nicotine in metabolism may disappear from the body within a few hours, but if smokers continue to smoke and the longer growing strong that smoking just to get the desired stimulation. Unfortunately, if the stop input nicotine dependence typically diikuiti reactions (withdrawal syndrome), which may take about a month or so. This includes symptoms, which appear irritability angry, overly sensitive, addiction, reduced cognitive function body and focusing of attention, and sleep disturbances. The most harmful effects of consuming tobacco and nicotine are kertergantungan cause cancer and one-third of all cancer is the cancer of the lung. The disease was first killer in men and women and controls around 90% of all cases of lung cancer in smokers.

Jumat, 02 November 2012

STEROID

Biosynthesis Steroids Hormones
PRODUCTION LINE OF CHOLESTEROL and STEROIDS The raw material of steroid hormones is cholesterol. All steroid-producing organs (except placenta) can synthesize steroids from acetate, but most organs can not meet the needs of raw materials locally and require cholesterol in circulation. Major cholesterol carrier in the circulation is LDL - low density lipoprotein. LDL is taken out of circulation by the cells - steroidogenic cells using cell surface receptors that can recognize specific proteins on the surface of LDL (Apoprotein). Once in the cell, cholesterol is transported through a series of enzymatic changes for steroid hormones produce the final product: • Progestins • Androgens • Estrogen • Glucocorticoids (sugar) • mineralocorticoid (salt) All steroid producing tissues using molecular precursors and enzymes with a common sequence. Network specifications generated by the specific enzyme in the series. For example: different gonads adrenal glands because the ovaries and testes do not produce the enzyme 21-hydroxylase or 11β-hydroxylase required to produce corticosteroids that the gonads (ovaries and testes) produce only progestin, androgen and estrogen alone. During the conversion of cholesterol to steroid metabolites, the number of atoms C (carbon) decreased gradually. Progestins have 21 molecules of carbon (C-21); androgen carbon 19 (C-19) and estrogen carbon 18 (C-18). Progestins are obligatory precursors for the production of androgens and estrogens, whereas androgens are obligatory precursors to produce estrogen. Once formed pregnenolone, steroid production may continue to one of two paths, via the progesterone or 17 α-OH pregnonolon LOCATION PRODUCTION
OVARIUM Produce steroids in the ovary occurs in two cell systems. Theca cells produce androgens. Androgens diffuses into the granulosa cells and converted into estrogen. Theca cells respond to LH by increasing the number of LDL receptors and then insert cholesterol into cells. The presence of LH also causes increased production of androgens. When androgens diffuse into granulosa cells, androgen metabolized by aromatase to estrogen. FSH triggers aromatase activity in granulosa cells thereby increasing the conversion of androgens to estrogens. TESTIS in the testis, predominantly androgen production in the Leydig cells under the influence of LH. Androgens enter the circulation directly or perform diffusion into Sertoli cells nearby. Sertoli cells will convert androgens to estrogen. The mechanism of steroid production in the testis similar to that occurring in the ovarium. GLAND ADRENAL ProdUCE sex hormones by the adrenal is largely a product of the biosynthesis of corticosteroids. Contributions to the adrenal sex steroid total circulating sex steroids are generally very small except in certain circumstances. Ovary post-menopausal women no longer produce steroid hormones in sufficient quantity so that adrenal androgen production is clinically more meaningful. During pregnancy, the placenta can not synthesize cholesterol from acetate resulting in the formation of cholesterol from adrenal androgen dependent on the mother and the fetus. Low cortisol levels provide feedback to improve the production of adrenal glucocorticoids. When there is deficiency of 21 - hydroxylase occur in the female fetus, the increased production of androgens will cause masculinization of the external genitalia, known as congenital adrenal hyperplasia syndrome. Similarly, differentiation and sexual development disorders in men may be caused by genetic defects in androgen production.