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  2. Chlorphenamine - Wikipedia

    en.wikipedia.org/wiki/Chlorphenamine

    Chlorphenamine is the INN Tooltip International Nonproprietary Name while chlorpheniramine is the USAN Tooltip United States Adopted Name and former BAN Tooltip British Approved Name. Brand names include Chlor-Trimeton, Demazin, Allerest 12 Hour, Piriton, Chlorphen-12, Tylenol Cold/Allergy, and numerous others according to country.

  3. Coricidin - Wikipedia

    en.wikipedia.org/wiki/Coricidin

    Coricidin, Coricidin 'D' (decongestant), or Coricidin HBP (for high blood pressure), is the name of an over-the-counter cough and cold drug containing dextromethorphan (a cough suppressant) and chlorpheniramine maleate (an antihistamine). [1] Introduced by Schering-Plough in 1949 as one of the first antihistamines, it is now owned by Bayer.

  4. Chlorpheniramine - Wikipedia

    en.wikipedia.org/?title=Chlorpheniramine&redirect=no

    Download QR code; Print/export Download as PDF; Printable version; In other projects Appearance. move to sidebar hide. ... Chlorpheniramine. Add languages ...

  5. List of chemical databases - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_databases

    WURCS GlycoCT PubChem CID G "Glycan Repository". 122194 Gmelin Gmelin database: Elsevier: inorganic and organometallic compounds closed access 1,500,000 G-SRS Global Substance Registration System: CAS PubChem ChEMBL INN UNII "G-SRS". 109,260 GMD Golm Metabolome Database GC/MS of metabolites "GMD". Guide to PHARMACOLOGY IUPHAR: drugs and targets

  6. PubChem - Wikipedia

    en.wikipedia.org/wiki/PubChem

    PubChem is a database of chemical molecules and their activities against biological assays. The system is maintained by the National Center for Biotechnology Information (NCBI), a component of the National Library of Medicine , which is part of the United States National Institutes of Health (NIH).

  7. Dexchlorpheniramine - Wikipedia

    en.wikipedia.org/wiki/Dexchlorpheniramine

    Dexchlorpheniramine is an antihistamine, or an antagonist of the histamine H 1 receptor. A study found that dexchlorpheniramine had a K i value of 20 to 30 μM for the muscarinic acetylcholine receptors using rat brain tissue. [4]