{"Abbreviation":[],"Aliases":["Panthenol","panthenol","Pantothenol","Pantothenyl alcohol","Pantenol","Panthenolum","Panthenol, racemic","Pantenolo","2,4-Dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutyramide","Purple Toner","ELF Perm","Roota Re F Tonic","Roota Re V Tonic","Mannitol, Panthenol","AAPE Hair Ampoule","Eyelash Growth Serum","Roota Re F for men","Panthenol, Niacinamide","BREXTEM H","Roota Re V for women","Ngf 574h hair","Hyaluronic Acid Facial Serum","Shinmo saengbaleum hair","Ngf 574h hair tonic","Shinmo saengbaleum treatment"],"CAS":"16485-10-2","ChEMBL":"CHEMBL1371937","ChemicalClasses":[],"Chirality":"racemic","Classes":["Provitamin"],"Drug Indication":"Panthenol (containing a racemic mixture of dexpanthenol and levopanthenol) is not currently available in any FDA-approved products and therefore does not have an indication.  Please see [DB09357] for FDA-approved uses of the dextrorotatory form of Panthenol.","EINECS":"240-540-6","Erowid Experience Reports":null,"Esters":[],"European Community (EC) Number":"240-540-6","Formating":[],"HMDB ID":"HMDB0304820","HeavyAtomCount":14,"IUPACName":"2,4-dihydroxy-N-(3-hydroxypropyl)-3,3-dimethylbutanamide","InChI":"InChI=1S/C9H19NO4/c1-9(2,6-12)7(13)8(14)10-4-3-5-11/h7,11-13H,3-6H2,1-2H3,(H,10,14)","InChIKey":"SNPLKNRPJHDVJA-UHFFFAOYSA-N","LD50":[{"dosages":[{"amount":"10100 mg/kg","route":"intraperitoneal"}],"organism":"Mouse"}],"MolecularFormula":"C\u003csub\u003e9\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eNO\u003csub\u003e4\u003c/sub\u003e","MolecularWeight":"205.25 g/mol","Opticalactivity":"( + / - )","Pharmacodynamics":"Pantothenic acid is a precursor of coenzyme A, which serves as a cofactor for a variety of enzyme-catalyzed reactions involving transfer of acetyl groups. The final step in the synthesis of acetylcholine consists of the choline acetylase transfer of acetyl group from acetylcoenzyme A to choline. Acetylcholine is the neurohumoral transmitter in the parasympathetic system and as such maintains the normal functions of the intestine. Decrease in acetylcholine content would result in decreased peristalsis and in extreme cases adynamic ileus.","PubChemId":4678,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Panthenol","Name":"Panthenol","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB11204","Name":"Panthenol","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/4678","Name":"Panthenol","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1371937","Name":"Panthenol","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=16485-10-2","Name":"Panthenol","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0304820","Name":"Panthenol","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D03726","Name":"Panthenol","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/WV9CM0O67Z","Name":"Panthenol","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID3044598","Name":"Panthenol","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 4678, Panthenol. Accessed August 14, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/4678\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/4678\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Panthenol. UNII: WV9CM0O67Z. Global Substance Registration System. Accessed August 14, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/WV9CM0O67Z\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/WV9CM0O67Z\u003c/a\u003e"],"SMILES":"CC(C)(CO)C(C(=O)NCCCO)O","SaltData":[],"Salts":[],"Solubility":"\u003e30.8 [ug/mL] (The mean of the results at pH 7.4)","StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CC(C)(CO)[C@@H](O)C(=O)NCCCO","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 133.035 44.262\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h134v45H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m89.717 37.616 9.796-11.675M99.513 25.941l9.796 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