Leucomycin V; 4B-(3-Methylbutanoyl), 3-Ac 

AlkaPlorer ID: AK304289

Synonym: Josamycin, Leucomycin A3, Platenomycin A3, Turimycin A5, Iosalide, Jomybel, Josacine, Josalid, Josaxin, Proxacin, Yosaxin, X 7III, YL 704A3, Antibiotic X 7III, Antibiotic YL 704A3 

IUPAC Name: [6-[6-[[4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxan-3-yl] 3-methylbutanoate

Structure

SMILES: COC1C(OC(C)=O)CC(=O)OC(C)CC=CC=CC(O)C(C)CC(CC=O)C1OC1OC(C)C(OC2CC(C)(O)C(OC(=O)CC(C)C)C(C)O2)C(N(C)C)C1O

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InChI: InChI=1S/C42H69NO15/c1-23(2)19-32(47)56-40-27(6)53-34(22-42(40,8)50)57-37-26(5)54-41(36(49)35(37)43(9)10)58-38-29(17-18-44)20-24(3)30(46)16-14-12-13-15-25(4)52-33(48)21-31(39(38)51-11)55-28(7)45/h12-14,16,18,23-27,29-31,34-41,46,49-50H,15,17,19-22H2,1-11H3

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InChIKey: XJSFLOJWULLJQS-UHFFFAOYSA-N

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Reference

PubChem CID: 3804

CAS: 16846-24-5

COCONUT: CNP0209846.9

Properties Information

Molecule Weight: 828.0060000000001

TPSA: 206.05

MolLogP: 3.0134000000000056

Number of H-Donors: 3

Number of H-Acceptors: 16

RingCount: 3

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information