| 词条 | Biotin sulfoxide |
| 释义 | {{Orphan|date=December 2012}}{{unreferenced|date=February 2017}}{{Chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 423719739 | ImageFile = Biotin sulfoxide.png | ImageFile_Ref = {{chemboximage|correct|??}} | ImageSize = 200px | ImageName = Stereo, skeletal formula of biotin sulfoxide | IUPACName = 5-[(3aS,4S,6aR)-5-Oxido-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid | OtherNames = D-Biotin-d-sulfoxide |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|changed|??}} | CASNo = 10406-89-0 | UNII_Ref = {{fdacite|changed|FDA}} | UNII = 71ET0LK93W | PubChem = 83833 | ChemSpiderID = 75652 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | MeSHName = D-Biotin-d-sulfoxide | ChEMBL = 1231481 | ChEMBL_Ref = {{ebicite|changed|EBI}} | SMILES = C1[C@H]2[C@@H]([C@@H](S1=O)CCCCC(=O)O)NC(=O)N2 | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C10H16N2O4S/c13-8(14)4-2-1-3-7-9-6(5-17(7)16)11-10(15)12-9/h6-7,9H,1-5H2,(H,13,14)(H2,11,12,15)/t6-,7-,9-,17?/m0/s1 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = KCSKCIQYNAOBNQ-YBSFLMRUSA-N }} |Section2={{Chembox Properties | C=10 | H=16 | N=2 | O=4 | S=1 | LogP = -2.026 | pKa = 4.724 | pKb = 9.273 }} }} Biotin sulfoxide is the substance that is formed when biotin is exposed to ultraviolet light in the presence of oxygen. {{Heterocyclic-stub}} 5 : Nitrogen heterocycles|Sulfur heterocycles|Sulfoxides|Heterocyclic compounds (2 rings)|Carboxylic acids |
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