Glycine is an amino acid that has a single hydrogen atom as its side chain. It is the simplest amino acid, with the chemical formula NH2‐CH2‐COOH. Glycine is one of the proteinogenic amino acids, it is encoded by all the codons starting with GG. Glycine is known as a "helix breaker", due to its ability to act as a hinge in the secondary structure of proteins. Glycine is a sweet-tasting crystalline solid, it is the only achiral proteinogenic amino acid. It can fit into hydrophilic or hydrophobic environments, due to its minimal side chain of only one hydrogen atom; the acyl radical is glycyl. Glycine was discovered in 1820 by the French chemist Henri Braconnot when he hydrolyzed gelatin by boiling it with sulfuric acid, he called it "sugar of gelatin", but the French chemist Jean-Baptiste Boussingault showed that it contained nitrogen. The American scientist Eben Norton Horsford a student of the German chemist Justus von Liebig, proposed the name "glycocoll"; the name comes from the Greek word γλυκύς "sweet tasting".
In 1858, the French chemist Auguste Cahours determined. Although glycine can be isolated from hydrolyzed protein, this is not used for industrial production, as it can be manufactured more conveniently by chemical synthesis; the two main processes are amination of chloroacetic acid with ammonia, giving glycine and ammonium chloride, the Strecker amino acid synthesis, the main synthetic method in the United States and Japan. About 15 thousand tonnes are produced annually in this way. Glycine is cogenerated as an impurity in the synthesis of EDTA, arising from reactions of the ammonia coproduct. In aqueous solution, glycine itself is amphoteric: at low pH the molecule can be protonated with a pKa of about 2.4 and at high pH it loses a proton with a pKa of about 9.6. Glycine is not essential to the human diet, as it is biosynthesized in the body from the amino acid serine, in turn derived from 3-phosphoglycerate, but the metabolic capacity for glycine biosynthesis does not satisfy the need for collagen synthesis.
In most organisms, the enzyme serine hydroxymethyltransferase catalyses this transformation via the cofactor pyridoxal phosphate: serine + tetrahydrofolate → glycine + N5,N10-Methylene tetrahydrofolate + H2OIn the liver of vertebrates, glycine synthesis is catalyzed by glycine synthase. This conversion is reversible: CO2 + NH+4 + N5,N10-Methylene tetrahydrofolate + NADH + H+ ⇌ Glycine + tetrahydrofolate + NAD+ Glycine is degraded via three pathways; the predominant pathway in animals and plants is the reverse of the glycine synthase pathway mentioned above. In this context, the enzyme system involved is called the glycine cleavage system: Glycine + tetrahydrofolate + NAD+ ⇌ CO2 + NH+4 + N5,N10-Methylene tetrahydrofolate + NADH + H+In the second pathway, glycine is degraded in two steps; the first step is the reverse of glycine biosynthesis from serine with serine hydroxymethyl transferase. Serine is converted to pyruvate by serine dehydratase. In the third pathway of glycine degradation, glycine is converted to glyoxylate by D-amino acid oxidase.
Glyoxylate is oxidized by hepatic lactate dehydrogenase to oxalate in an NAD+-dependent reaction. The half-life of glycine and its elimination from the body varies based on dose. In one study, the half-life varied between 4.0 hours. The principal function of glycine is as a precursor to proteins. Most proteins incorporate only small quantities of glycine, a notable exception being collagen, which contains about 35% glycine due to its periodically repeated role in the formation of collagen's helix structure in conjunction with hydroxyproline. In the genetic code, glycine is coded by all codons starting with GG, namely GGU, GGC, GGA and GGG. In higher eukaryotes, δ-aminolevulinic acid, the key precursor to porphyrins, is biosynthesized from glycine and succinyl-CoA by the enzyme ALA synthase. Glycine provides the central C2N subunit of all purines. Glycine is an inhibitory neurotransmitter in the central nervous system in the spinal cord and retina; when glycine receptors are activated, chloride enters the neuron via ionotropic receptors, causing an Inhibitory postsynaptic potential.
Strychnine is a strong antagonist at ionotropic glycine receptors, whereas bicuculline is a weak one. Glycine is a required co-agonist along with glutamate for NMDA receptors. In contrast to the inhibitory role of glycine in the spinal cord, this behaviour is facilitated at the glutamatergic receptors which are excitatory; the LD50 of glycine is 7930 mg/kg in rats, it causes death by hyperexcitability. In the US, glycine is sold in two grades: United States Pharmacopeia, technical grade. USP grade sales account for 80 to 85 percent of the U. S. market for glycine. If purity greater than the USP standard is needed, for example for intravenous injections, a more expensive pharmaceutical grade glycine can be used. Technical grade glycine, which may or may not meet USP grade standards, is sold at a lower price for use in industrial applications, e.g. as an agent in metal complexing and finishing. USP glycine has a wide variety of uses, including as an additive in pet food and animal feed, in foods and pharmaceuticals as a sweetener/taste enhancer, or as a component of food supplements and protein drinks.
Two glycine molecules in a dipeptide form are referred to as a diglycinate. Because they use a different s
In chemistry, a salt is an ionic compound that can be formed by the neutralization reaction of an acid and a base. Salts are composed of related numbers of cations and anions so that the product is electrically neutral; these component ions can be inorganic, such as organic, such as acetate. Salts can be classified in a variety of ways. Salts that produce hydroxide ions when dissolved in water are called alkali salts. Salts that produce acidic solutions are acidic salts. Neutral salts are those salts that are neither basic. Zwitterions contain an anionic and a cationic centres in the same molecule, but are not considered to be salts. Examples of zwitterions include amino acids, many metabolites and proteins. Solid salts tend to be transparent. In many cases, the apparent opacity or transparency are only related to the difference in size of the individual monocrystals. Since light reflects from the grain boundaries, larger crystals tend to be transparent, while the polycrystalline aggregates look like white powders.
Salts exist in many different colors, which arise either from the cations. For example: sodium chromate is yellow by virtue of the chromate ion potassium dichromate is orange by virtue of the dichromate ion cobalt nitrate is red owing to the chromophore of hydrated cobalt. copper sulfate is blue because of the copper chromophore potassium permanganate has the violet color of permanganate anion. Nickel chloride is green of sodium chloride, magnesium sulfate heptahydrate are colorless or white because the constituent cations and anions do not absorb in the visible part of the spectrumFew minerals are salts because they would be solubilized by water. Inorganic pigments tend not to be salts, because insolubility is required for fastness; some organic dyes are salts, but they are insoluble in water. Different salts can elicit all five basic tastes, e.g. salty, sour and umami or savory. Salts of strong acids and strong bases are non-volatile and odorless, whereas salts of either weak acids or weak bases may smell like the conjugate acid or the conjugate base of the component ions.
That slow, partial decomposition is accelerated by the presence of water, since hydrolysis is the other half of the reversible reaction equation of formation of weak salts. Many ionic compounds exhibit significant solubility in water or other polar solvents. Unlike molecular compounds, salts dissociate in solution into cationic components; the lattice energy, the cohesive forces between these ions within a solid, determines the solubility. The solubility is dependent on how well each ion interacts with the solvent, so certain patterns become apparent. For example, salts of sodium and ammonium are soluble in water. Notable exceptions include potassium cobaltinitrite. Most nitrates and many sulfates are water-soluble. Exceptions include barium sulfate, calcium sulfate, lead sulfate, where the 2+/2− pairing leads to high lattice energies. For similar reasons, most alkali metal carbonates are not soluble in water; some soluble carbonate salts are: potassium carbonate and ammonium carbonate. Salts are characteristically insulators.
Molten salts or solutions of salts conduct electricity. For this reason, liquified salts and solutions containing dissolved salts are called electrolytes. Salts characteristically have high melting points. For example, sodium chloride melts at 801 °C; some salts with low lattice energies are liquid near room temperature. These include molten salts, which are mixtures of salts, ionic liquids, which contain organic cations; these liquids exhibit unusual properties as solvents. The name of a salt starts with the name of the cation followed by the name of the anion. Salts are referred to only by the name of the cation or by the name of the anion. Common salt-forming cations include: Ammonium NH+4 Calcium Ca2+ Iron Fe2+ and Fe3+ Magnesium Mg2+ Potassium K+ Pyridinium C5H5NH+ Quaternary ammonium NR+4, R being an alkyl group or an aryl group Sodium Na+ Copper Cu2+Common salt-forming anions include: Acetate CH3COO− Carbonate CO2−3 Chloride Cl− Citrate HOC2 Cyanide C≡N− Fluoride F− Nitrate NO−3 Nitrite NO−2 Oxide O2− Phosphate PO3−4 Sulfate SO2−4 Salts with varying number of hydrogen atoms, with respect to the parent acid, replaced by cations can be referred to as monobasic, dibasic or tribasic salts: Sodium phosphate monobasic Sodium phosphate dibasic Sodium phosphate tribasic Salts are formed by a chemical reaction between: A base and an acid, e.g. NH3 + HCl → NH4Cl A metal and an acid, e.g. Mg + H2SO4 → MgSO4 + H2 A metal and a non-metal, e.g. Ca + Cl2 → CaCl2 A base and an a
European Chemicals Agency
The European Chemicals Agency is an agency of the European Union which manages the technical and administrative aspects of the implementation of the European Union regulation called Registration, Evaluation and Restriction of Chemicals. ECHA is the driving force among regulatory authorities in implementing the EU's chemicals legislation. ECHA helps companies to comply with the legislation, advances the safe use of chemicals, provides information on chemicals and addresses chemicals of concern, it is located in Finland. The agency headed by Executive Director Bjorn Hansen, started working on 1 June 2007; the REACH Regulation requires companies to provide information on the hazards and safe use of chemical substances that they manufacture or import. Companies register this information with ECHA and it is freely available on their website. So far, thousands of the most hazardous and the most used substances have been registered; the information is technical but gives detail on the impact of each chemical on people and the environment.
This gives European consumers the right to ask retailers whether the goods they buy contain dangerous substances. The Classification and Packaging Regulation introduces a globally harmonised system for classifying and labelling chemicals into the EU; this worldwide system makes it easier for workers and consumers to know the effects of chemicals and how to use products safely because the labels on products are now the same throughout the world. Companies need to notify ECHA of the labelling of their chemicals. So far, ECHA has received over 5 million notifications for more than 100 000 substances; the information is available on their website. Consumers can check chemicals in the products. Biocidal products include, for example, insect disinfectants used in hospitals; the Biocidal Products Regulation ensures that there is enough information about these products so that consumers can use them safely. ECHA is responsible for implementing the regulation; the law on Prior Informed Consent sets guidelines for the import of hazardous chemicals.
Through this mechanism, countries due to receive hazardous chemicals are informed in advance and have the possibility of rejecting their import. Substances that may have serious effects on human health and the environment are identified as Substances of Very High Concern 1; these are substances which cause cancer, mutation or are toxic to reproduction as well as substances which persist in the body or the environment and do not break down. Other substances considered. Companies manufacturing or importing articles containing these substances in a concentration above 0,1% weight of the article, have legal obligations, they are required to inform users about the presence of the substance and therefore how to use it safely. Consumers have the right to ask the retailer whether these substances are present in the products they buy. Once a substance has been identified in the EU as being of high concern, it will be added to a list; this list is available on ECHA's website and shows consumers and industry which chemicals are identified as SVHCs.
Substances placed on the Candidate List can move to another list. This means that, after a given date, companies will not be allowed to place the substance on the market or to use it, unless they have been given prior authorisation to do so by ECHA. One of the main aims of this listing process is to phase out SVHCs where possible. In its 2018 substance evaluation progress report, ECHA said chemical companies failed to provide “important safety information” in nearly three quarters of cases checked that year. "The numbers show a similar picture to previous years" the report said. The agency noted that member states need to develop risk management measures to control unsafe commercial use of chemicals in 71% of the substances checked. Executive Director Bjorn Hansen called non-compliance with REACH a "worry". Industry group CEFIC acknowledged the problem; the European Environmental Bureau called for faster enforcement to minimise chemical exposure. European Chemicals Bureau Official website
Fat is one of the three main macronutrients, along with carbohydrate and protein. Fats molecules consist of carbon and hydrogen atoms, thus they are all hydrocarbon molecules. Examples include cholesterol and triglycerides; the terms "lipid", "oil" and "fat" are confused. "Lipid" is the general term, though a lipid is not a triglyceride. "Oil" refers to a lipid with short or unsaturated fatty acid chains, liquid at room temperature, while "fat" refers to lipids that are solids at room temperature – however, "fat" may be used in food science as a synonym for lipid. Fats, like other lipids, are hydrophobic, are soluble in organic solvents and insoluble in water. Fat is an important foodstuff for many forms of life, fats serve both structural and metabolic functions, they are a necessary part of the diet of most heterotrophs and are the most energy dense, thus the most efficient form of energy storage. Some fatty acids that are set free by the digestion of fats are called essential because they cannot be synthesized in the body from simpler constituents.
There are two essential fatty acids in human nutrition: linoleic acid. Other lipids needed by the body can be synthesized from other fats. Fats and other lipids are broken down in the body by enzymes called lipases produced in the pancreas. Fats and oils are categorized according to the number and bonding of the carbon atoms in the aliphatic chain. Fats that are saturated fats have no double bonds between the carbons in the chain. Unsaturated fats have one or more double bonded carbons in the chain; the nomenclature is based on the non-acid end of the chain. This end is called the n-end, thus alpha-linolenic acid is called an omega-3 fatty acid because the 3rd carbon from that end is the first double bonded carbon in the chain counting from that end. Some oils and fats are therefore called polyunsaturated fats. Unsaturated fats can be further divided into cis fats, which are the most common in nature, trans fats, which are rare in nature. Unsaturated fats can be altered by reaction with hydrogen effected by a catalyst.
This action, called hydrogenation, tends to break all the double bonds and makes a saturated fat. To make vegetable shortening liquid cis-unsaturated fats such as vegetable oils are hydrogenated to produce saturated fats, which have more desirable physical properties e.g. they melt at a desirable temperature, store well, whereas polyunsaturated oils go rancid when they react with oxygen in the air. However, trans fats are generated during hydrogenation as contaminants created by an unwanted side reaction on the catalyst during partial hydrogenation. Saturated fats can stack themselves in a packed arrangement, so they can solidify and are solid at room temperature. For example, animal fats tallow and lard are solids. Olive and linseed oils on the other hand are liquid. Fats serve both as energy sources for the body, as stores for energy in excess of what the body needs immediately; each gram of fat when burned or metabolized releases about 9 food calories. Fats are broken down in the healthy body to release their constituents and fatty acids.
Glycerol itself can be converted to glucose by the liver and so become a source of energy. There are many different kinds of fats. All fats are derivatives of fatty acids and glycerol. Most fats are glycerides triglycerides. One chain of fatty acid is bonded to each of the three -OH groups of the glycerol by the reaction of the carboxyl end of the fatty acid with the alcohol. Water is eliminated and the carbons are linked by an -O- bond through dehydration synthesis; this process is called esterification and fats are therefore esters. As a simple visual illustration, if the kinks and angles of these chains were straightened out, the molecule would have the shape of a capital letter E; the fatty acids would each be a horizontal line. Fats therefore have "ester" bonds; the properties of any specific fat molecule depend on the particular fatty acids. Fatty acids form a family of compounds that are composed of increasing numbers of carbon atoms linked into a zig-zag chain; the more carbon atoms there are in any fatty acid, the longer its chain will be.
Long chains are more susceptible to intermolecular forces of attraction, so the longer ones melt at a higher temperature. Fatty acid chains may differ by length categorized as short to long. Short-chain fatty acids are fatty acids with aliphatic tails of fewer than six carbons. Medium-chain fatty acids are fatty acids with aliphatic tails of 6–12 carbons, which can form medium-chain triglycerides. Long-chain fatty acids are fatty acids with aliphatic tails of 13 to 21 carbons. Long chain fatty acids are fatty acids with aliphatic tails of 22 or more carbons. Any of these aliphatic fatty acid chains may be glycerated and the resultant fats may have tails of different lengths from short triformin to long, e.g. cerotic acid, or hexacosanoic acid, a 26-carbon long-chain saturated fatty acid. Long chain fats are exemplified by tallow. Most fats found in foo
Bile or gall is a dark green to yellowish brown fluid, produced by the liver of most vertebrates, that aids the digestion of lipids in the small intestine. In humans, bile is produced continuously by the liver, stored and concentrated in the gallbladder. After eating, this stored bile is discharged into the duodenum; the composition of hepatic bile is 97% water, 0.7% bile salts, 0.2% bilirubin, 0.51% fats, 200 meq/l inorganic salts. About 400 to 800 ml of bile is produced per day in adult human beings. Bile or gall acts to some extent as a surfactant, helping to emulsify the lipids in food. Bile salt anions are hydrophobic on the other side; the hydrophilic sides are negatively charged, this charge prevents fat droplets coated with bile from re-aggregating into larger fat particles. Ordinarily, the micelles in the duodenum have a diameter around 14–33 μm; the dispersion of food fat into micelles provides a increased surface area for the action of the enzyme pancreatic lipase, which digests the triglycerides, is able to reach the fatty core through gaps between the bile salts.
A triglyceride is broken down into two fatty acids and a monoglyceride, which are absorbed by the villi on the intestine walls. After being transferred across the intestinal membrane, the fatty acids reform into triglycerides, before being absorbed into the lymphatic system through lacteals. Without bile salts, most of the lipids in food would be excreted in faeces, undigested. Since bile increases the absorption of fats, it is an important part of the absorption of the fat-soluble substances, such as the vitamins A, D, E, K. Besides its digestive function, bile serves as the route of excretion for bilirubin, a byproduct of red blood cells recycled by the liver. Bilirubin derives from hemoglobin by glucuronidation. Bile tends to be alkali on average; the pH of common duct bile is higher than that of the corresponding gallbladder bile. Bile in the gallbladder becomes more acidic the longer a person goes without eating, though resting slows this fall in pH; as an alkali, it has the function of neutralizing excess stomach acid before it enters the duodenum, the first section of the small intestine.
Bile salts act as bactericides, destroying many of the microbes that may be present in the food. In the absence of bile, fats become indigestible and are instead excreted in feces, a condition called steatorrhea. Feces lack their characteristic brown color and instead are white or gray, greasy. Steatorrhea can lead to deficiencies in fat-soluble vitamins. In addition, past the small intestine the gastrointestinal tract and gut flora are not adapted to processing fats, leading to problems in the large intestine; the cholesterol contained in bile will accrete into lumps in the gallbladder, forming gallstones. Cholesterol gallstones are treated through surgical removal of the gallbladder. However, they can sometimes be dissolved by increasing the concentration of certain occurring bile acids, such as chenodeoxycholic acid and ursodeoxycholic acid. On an empty stomach – after repeated vomiting, for example – a person's vomit may be green or dark yellow, bitter; the bitter and greenish component may be bile or normal digestive juices originating in the stomach.
The color of bile is likened to "fresh-cut grass", unlike components in the stomach that look greenish yellow or dark yellow. Bile may be forced into the stomach secondary to a weakened valve, the presence of certain drugs including alcohol, or powerful muscular contractions and duodenal spasms. Biliary obstruction refers to a condition when bile ducts which deliver bile from the gallbladder or liver to the duodenum become obstructed; the blockage of bile might cause a build up of bilirubin in the bloodstream which can result in jaundice. There are several potential causes for biliary obstruction including gallstones, trauma, choledocal cysts, or other benign causes of bile duct narrowing; the most common cause of bile duct obstruction is when gallstone are dislodged from the gallbladder into the cystic duct or common bile duct resulting in a blockage. A blockage of the gallbladder or cystic duct may cause cholecystitis. If the blockage is beyond the confluence of the pancreatic duct, this may cause gallstone pancreatitis.
In some instances of biliary obstruction, the bile may become infected by bacteria resulting in ascending cholangitis. In medical theories prevalent in the West from Classical Antiquity to the Middle Ages, the body's health depended on the equilibrium of four "humors", or vital fluids, two of which related to bile: blood, phlegm, "yellow bile", "black bile"; these "humors" are believed to have its roots in the appearance of a blood sedimentation test made in open air, which exhibits a dark clot at the bottom, a layer of unclotted erythrocytes, a layer of white blood cells and a layer of clear yellow serum. Excesses of black bile and yellow bile were thought to produce depression and aggression and the Greek names for them gave rise to the English words cholera and melancholia. In the former of those senses, the same theories explain the derivation of the English word bilious from bile, the meaning of gall in English as "exasperation" or "impudence", the Latin word cholera, derived from the Greek kholé, passed along in
The melting point of a substance is the temperature at which it changes state from solid to liquid. At the melting point the solid and liquid phase exist in equilibrium; the melting point of a substance depends on pressure and is specified at a standard pressure such as 1 atmosphere or 100 kPa. When considered as the temperature of the reverse change from liquid to solid, it is referred to as the freezing point or crystallization point; because of the ability of some substances to supercool, the freezing point is not considered as a characteristic property of a substance. When the "characteristic freezing point" of a substance is determined, in fact the actual methodology is always "the principle of observing the disappearance rather than the formation of ice", that is, the melting point. For most substances and freezing points are equal. For example, the melting point and freezing point of mercury is 234.32 kelvins. However, certain substances possess differing solid-liquid transition temperatures.
For example, agar melts at 85 °C and solidifies from 31 °C. The melting point of ice at 1 atmosphere of pressure is close to 0 °C. In the presence of nucleating substances, the freezing point of water is not always the same as the melting point. In the absence of nucleators water can exist as a supercooled liquid down to −48.3 °C before freezing. The chemical element with the highest melting point is tungsten, at 3,414 °C; the often-cited carbon does not melt at ambient pressure but sublimes at about 3,726.85 °C. Tantalum hafnium carbide is a refractory compound with a high melting point of 4215 K. At the other end of the scale, helium does not freeze at all at normal pressure at temperatures arbitrarily close to absolute zero. Many laboratory techniques exist for the determination of melting points. A Kofler bench is a metal strip with a temperature gradient. Any substance can be placed on a section of the strip, revealing its thermal behaviour at the temperature at that point. Differential scanning calorimetry gives information on melting point together with its enthalpy of fusion.
A basic melting point apparatus for the analysis of crystalline solids consists of an oil bath with a transparent window and a simple magnifier. The several grains of a solid are placed in a thin glass tube and immersed in the oil bath; the oil bath is heated and with the aid of the magnifier melting of the individual crystals at a certain temperature can be observed. In large/small devices, the sample is placed in a heating block, optical detection is automated; the measurement can be made continuously with an operating process. For instance, oil refineries measure the freeze point of diesel fuel online, meaning that the sample is taken from the process and measured automatically; this allows for more frequent measurements as the sample does not have to be manually collected and taken to a remote laboratory. For refractory materials the high melting point may be determined by heating the material in a black body furnace and measuring the black-body temperature with an optical pyrometer. For the highest melting materials, this may require extrapolation by several hundred degrees.
The spectral radiance from an incandescent body is known to be a function of its temperature. An optical pyrometer matches the radiance of a body under study to the radiance of a source, calibrated as a function of temperature. In this way, the measurement of the absolute magnitude of the intensity of radiation is unnecessary. However, known temperatures must be used to determine the calibration of the pyrometer. For temperatures above the calibration range of the source, an extrapolation technique must be employed; this extrapolation is accomplished by using Planck's law of radiation. The constants in this equation are not known with sufficient accuracy, causing errors in the extrapolation to become larger at higher temperatures. However, standard techniques have been developed to perform this extrapolation. Consider the case of using gold as the source. In this technique, the current through the filament of the pyrometer is adjusted until the light intensity of the filament matches that of a black-body at the melting point of gold.
This establishes the primary calibration temperature and can be expressed in terms of current through the pyrometer lamp. With the same current setting, the pyrometer is sighted on another black-body at a higher temperature. An absorbing medium of known transmission is inserted between this black-body; the temperature of the black-body is adjusted until a match exists between its intensity and that of the pyrometer filament. The true higher temperature of the black-body is determined from Planck's Law; the absorbing medium is removed and the current through the filament is adjusted to match the filament intensity to that of the black-body. This establishes a second calibration point for the pyrometer; this step is repeated to carry the calibration to hi
The Jmol applet, among other abilities, offers an alternative to the Chime plug-in, no longer under active development. While Jmol has many features that Chime lacks, it does not claim to reproduce all Chime functions, most notably, the Sculpt mode. Chime requires plug-in installation and Internet Explorer 6.0 or Firefox 2.0 on Microsoft Windows, or Netscape Communicator 4.8 on Mac OS 9. Jmol operates on a wide variety of platforms. For example, Jmol is functional in Mozilla Firefox, Internet Explorer, Google Chrome, Safari. Chemistry Development Kit Comparison of software for molecular mechanics modeling Jmol extension for MediaWiki List of molecular graphics systems Molecular graphics Molecule editor Proteopedia PyMOL SAMSON Official website Wiki with listings of websites and moodles Willighagen, Egon. "Fast and Scriptable Molecular Graphics in Web Browsers without Java3D". Doi:10.1038/npre.2007.50.1