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CP 55,940
CP 55,940
CP 55,940
is a cannabinoid which mimics the effects of naturally occurring THC (one of the psychoactive compounds found in cannabis). CP 55,940
CP 55,940
was created by Pfizer
Pfizer
in 1974 but was never marketed
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Regulation Of Therapeutic Goods
The regulation of therapeutic goods, that is drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as is the case in Australia. The role of therapeutic goods regulation is designed mainly to protect the health and safety of the population. Regulation is aimed at ensuring the safety, quality, and efficacy of the therapeutic goods which are covered under the scope of the regulation. In most jurisdictions, therapeutic goods must be registered before they are allowed to be marketed
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N-Arachidonoyl Dopamine
Dopamine
Dopamine
(DA, a contraction of 3,4-dihydroxyphenethylamine) is an organic chemical of the catecholamine and phenethylamine families that plays several important roles in the brain and body. It is an amine synthesized by removing a carboxyl group from a molecule of its precursor chemical L-DOPA, which is synthesized in the brain and kidneys. Dopamine
Dopamine
is also synthesized in plants and most animals. In the brain, dopamine functions as a neurotransmitter—a chemical released by neurons (nerve cells) to send signals to other nerve cells. The brain includes several distinct dopamine pathways, one of which plays a major role in the motivational component of reward-motivated behavior. The anticipation of most types of rewards increase the level of dopamine in the brain,[2] and many addictive drugs increase dopamine neuronal activity
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IUPAC Nomenclature Of Chemistry
The International Union of Pure and Applied Chemistry
International Union of Pure and Applied Chemistry
(IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry
IUPAC nomenclature of inorganic chemistry
(Red Book) IUPAC nomenclature of organic chemistry
IUPAC nomenclature of organic chemistry
(Blue Book)This chemistry-related article is a stub
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Echinacea
Brauneria Necker ex T.C.Porter & Britton Helichroa Raf. Echinacea
Echinacea
/ˌɛkɪˈneɪʃiə/[1] is a genus, or group of herbaceous flowering plants in the daisy family. The Echinacea
Echinacea
genus has nine species, which are commonly called coneflowers. They are found only in eastern and central North America, where they grow in moist to dry prairies and open wooded areas. They have large, showy heads of composite flowers, blooming from early to late summer. The generic name is derived from the Greek word ἐχῖνος (ekhinos), meaning "hedgehog," due to the spiny central disk. These flowering plants and their parts have different uses. Some species are cultivated in gardens for their showy flowers. Echinacea purpurea
Echinacea purpurea
is used in folk medicine.[2] Two of the species, E. tennesseensis and E
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PubMed Identifier
PubMed
PubMed
is a free search engine accessing primarily the MEDLINE database of references and abstracts on life sciences and biomedical topics. The United States National Library of Medicine
United States National Library of Medicine
(NLM) at the National Institutes of Health
National Institutes of Health
maintains the database as part of the Entrez
Entrez
system of information retrieval. From 1971 to 1997, MEDLINE online access to the MEDLARS Online computerized database primarily had been through institutional facilities, such as university libraries
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PubMed Central
PubMed
PubMed
Central (PMC) is a free digital repository that archives publicly accessible full-text scholarly articles that have been published within the biomedical and life sciences journal literature. As one of the major research databases within the suite of resources that have been developed by the National Center for Biotechnology Information (NCBI), PubMed
PubMed
Central is much more than just a document repository
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Digital Object Identifier
In computing, a Digital Object Identifier or DOI is a persistent identifier or handle used to uniquely identify objects, standardized by the International Organization for Standardization
International Organization for Standardization
(ISO).[1] An implementation of the Handle System,[2][3] DOIs are in wide use mainly to identify academic, professional, and government information, such as journal articles, research reports and data sets, and official publications though they also have been used to identify other types of information resources, such as commercial videos. A DOI aims to be "resolvable", usually to some form of access to the information object to which the DOI refers. This is achieved by binding the DOI to metadata about the object, such as a URL, indicating where the object can be found. Thus, by being actionable and interoperable, a DOI differs from identifiers such as ISBNs and ISRCs which aim only to uniquely identify their referents
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Pfizer
Coordinates: 41°20′04″N 72°04′05″W / 41.3343429°N 72.06795°W / 41.3343429; -72.06795 Pfizer
Pfizer
Inc.Entrance to Pfizer
Pfizer
headquartersTypePublicTraded asNYSE: PFE DJIA Component S&P 100 Component S&P 500 ComponentIndustry PharmaceuticalFounded 1849; 169 years ago (1849)Founders Charles Pfizer Charles F. ErhartHeadquarters New York City, New York, U.S.Area servedWorldwideKey people Ian Read (Chairman & CEO)Products See listRevenue US$52.546 billion (2017)[1]Operating income US$13.620 billion (2017)[1]Net income US$21.308 billion (2017)[1]Total assets US$171.797 billion (2017)[2]Total equity US$71.308 billion (2017)[2]Number of employees96,500 (2016)[3]Subsidiaries Agouron Pharmaceuticals G.D. Searle Greenstone Hospira InnoPharma Parke-DavisWebsite www.pfizer.com Pfizer
Pfizer
Inc
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Epigallocatechin Gallate
Epigallocatechin
Epigallocatechin
gallate (EGCG), also known as epigallocatechin-3-gallate, is the ester of epigallocatechin and gallic acid, and is a type of catechin. EGCG, the most abundant catechin in tea, is a polyphenol under basic research for its potential to affect human health and disease
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International Chemical Identifier
The IUPAC
IUPAC
International Chemical Identifier
Identifier
(InChI /ˈɪntʃiː/ IN-chee or /ˈɪŋkiː/ ING-kee) is a textual identifier for chemical substances, designed to provide a standard way to encode molecular information and to facilitate the search for such information in databases and on the web
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Molar Mass
In chemistry, the molar mass M is a physical property defined as the mass of a given substance (chemical element or chemical compound) divided by the amount of substance.[1] The base SI unit
SI unit
for molar mass is kg/mol
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CAS Registry Number
A CAS Registry Number,[1] also referred to as CASRN or CAS Number, is a unique numerical identifier assigned by the Chemical Abstracts Service (CAS) to every chemical substance described in the open scientific literature (currently including all substances described from 1957 through the present, plus some substances from the early or mid 1900s), including organic and inorganic compounds, minerals, isotopes, alloys and nonstructurable materials (UVCBs, of unknown, variable composition, or biological origin).[2] The Registry maintained by CAS is an authoritative collection of disclosed chemical substance information. It currently identifies more than 129 million organic and inorganic substances and 67 million protein and DNA sequences,[3] plus additional information about each substance
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ChemSpider
ChemSpider
ChemSpider
is a database of chemicals. ChemSpider
ChemSpider
is owned by the Royal Society of Chemistry.[3][4][5][6][7][8][9][10][11][12][13]Contents1 Database 2 Crowdsourcing 3 Searching 4 Chemistry document mark-up 5 History 6 Services6.1 SyntheticPages 6.2 Open PHACTS7 See also 8 ReferencesDatabase[edit] The database contains information on more than 63 million molecules from over 280 data sources including:EPA DSSTox[14][15] U.S
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ChEMBL
Ch EMBL
EMBL
or ChEMBLdb is a manually curated chemical database of bioactive molecules with drug-like properties.[1] It is maintained by the European Bioinformatics Institute
European Bioinformatics Institute
(EBI), of the European Molecular Biology Laboratory
Laboratory
(EMBL), based at the Wellcome Trust
Wellcome Trust
Genome Campus, Hinxton, UK. The database, originally known as StARlite, was developed by a biotechnology company called Inpharmatica Ltd. later acquired by Galapagos NV
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Chemical Formula
A chemical formula is a way of information about the chemical proportions of atoms that constitute a particular chemical compound or molecule, using chemical element symbols, numbers, and sometimes also other symbols, such as parentheses, dashes, brackets, commas and plus (+) and minus (−) signs. These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a chemical name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulas can fully specify the structure of only the simplest of molecules and chemical substances, and are generally more limited in power than are chemical names and structural formulas. The simplest types of chemical formulas are called empirical formulas, which use letters and numbers indicating the numerical proportions of atoms of each type
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