{{Chembox | Verifiedfields = changed | Watchedfields = changed | Name = Bacillomycin D | verifiedrevid = 459512784 | ImageFile = Bacillomycin.svg | ImageName = | IUPACName= 3-[3,9-Bis(2-amino-2-oxo-ethyl)-16-(1-hydroxyethyl)-19-(hydroxymethyl)-6-[(4-hydroxyphenyl)methyl]-13-octyl-2,5,8,11,15,18,21,24-octaoxo-1,4,7,10,14,17,20,23-octazabicyclo[23.3.0]octacosan-22-yl]propanoic acid | SystematicName = 3-[16,22-Bis(carbamoylmethyl)-9-(1-hydroxyethyl)-6-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-12-octyl-1,4,7,10,14,17,20,23-octaoxo-hexacosahydro-1''H''-pyrrolo[1,2-j]1,4,7,10,13,16,19,22-octaazacyclopentacosan-3-yl]propanoic acid | OtherNames = 3-[16,22-bis(carbamoylmethyl)-9-(1-hydroxyethyl)-6-(hydroxymethyl)-19-[(4-hydroxyphenyl)methyl]-12-octyl-1,4,7,10,14,17,20,23-octaoxo-octadecahydro-2''H''-pyrrolo[1,2-j]1,4,7,10,13,16,19,22-octaazacyclopentacosan-3-yl]propanoic acid |Section1={{Chembox Identifiers | CASNo = 1395-21-7 | CASNo_Ref = {{Cascite|changed|EPA}} | PubChem = 3086051 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 2342763 | SMILES = CCCCCCCCC1CC(=O)NC(CC(N)=O)C(=O)NC(CC2=CC=C(O)C=C2)C(=O)NC(CC(N)=O)C(=O)N2CCCC2C(=O)NC(CCC(O)=O)C(=O)NC(CO)C(=O)NC(C(C)O)C(=O)N1 | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C45H68N10O15/c1-3-4-5-6-7-8-10-26-20-36(61)49-30(21-34(46)59)41(66)51-29(19-25-12-14-27(58)15-13-25)40(65)52-31(22-35(47)60)45(70)55-18-9-11-33(55)43(68)50-28(16-17-37(62)63)39(64)53-32(23-56)42(67)54-38(24(2)57)44(69)48-26/h12-15,24,26,28-33,38,56-58H,3-11,16-23H2,1-2H3,(H2,46,59)(H2,47,60)(H,48,69)(H,49,61)(H,50,68)(H,51,66)(H,52,65)(H,53,64)(H,54,67)(H,62,63) | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = VLKSXJAPRDAENT-UHFFFAOYSA-N | MeSHName=}} |Section2={{Chembox Properties | C=45 | H=68 | N=10 | O=15 | Appearance= | Density= | Solubility= }} |Section3={{Chembox Hazards | FlashPtC = }} }}
'''Bacillomycins''' are a group of antifungal polypeptide antibiotics isolated from ''Bacillus subtilis''.
Examples include: * Bacillomycin A (fungosin, structure unknown)<ref>[https://www.uniprot.org/uniprot/G1FUQ9 Bacillomycin A]</ref><ref name=Buckingham >{{cite book | title = Dictionary of Natural Products | editor = John Buckingham | pages = 590–591}}</ref> * Bacillomycin C (structure unknown)<ref name=Buckingham/> * Bacillomycin D (C<sub>45</sub>H<sub>68</sub>N<sub>10</sub>O<sub>15</sub>)<ref>{{cite journal | pmid = 7285926| year = 1981| last1 = Peypoux| first1 = F| title = Structure of bacillomycin D, a new antibiotic of the iturin group| journal = European Journal of Biochemistry| volume = 118| issue = 2| pages = 323–7| last2 = Besson| first2 = F| last3 = Michel| first3 = G| last4 = Delcambe| first4 = L| doi=10.1111/j.1432-1033.1981.tb06405.x| doi-access = }}</ref> * Bacillomycin F (C<sub>52</sub>H<sub>84</sub>N<sub>12</sub>O<sub>14</sub>)<ref>{{PubChem|3086138}}</ref> * Bacillomycin Fc (C<sub>52</sub>H<sub>84</sub>N<sub>12</sub>O<sub>14</sub>)<ref>{{PubChem|3086563}}</ref> * Bacillomycin L (Landy substance)<ref name=Buckingham/><ref>{{cite journal | pmid = 24043450| year = 2013| last1 = Zhang| first1 = B| title = Purification and partial characterization of bacillomycin L produced by Bacillus amyloliquefaciens K103 from lemon| journal = Applied Biochemistry and Biotechnology| volume = 171| issue = 8| pages = 2262–72| last2 = Dong| first2 = C| last3 = Shang| first3 = Q| last4 = Cong| first4 = Y| last5 = Kong| first5 = W| last6 = Li| first6 = P| doi = 10.1007/s12010-013-0424-7| s2cid = 9380325}}</ref> * Bacillomycin S (structure unknown)<ref name=Buckingham/>
==References== {{reflist}}
Category:Polypeptide antibiotics Category:Antifungals
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