chalcomycin   Click here for help

GtoPdb Ligand ID: 11058

Comment: Chalcomycin is a 16-membered macrolide antibiotic, originally isolated from Streptomyces.
2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 14
Hydrogen bond donors 3
Rotatable bonds 8
Topological polar surface area 181.2
Molecular weight 700.37
XLogP 0.74
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
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Canonical SMILES CO[C@H]1C[C@@H](C)O[C@H]([C@@H]1O)O[C@H]1[C@@H](C)/C=C/C(=O)O[C@H](C)[C@@H](CO[C@@H]2O[C@H](C)[C@H]([C@H]([C@H]2OC)OC)O)[C@H]2[C@H](/C=C/C(=O)[C@@](C[C@@H]1C)(C)O)O2
Isomeric SMILES CO[C@H]1C[C@@H](C)O[C@H]([C@@H]1O)O[C@H]1[C@@H](C)/C=C/C(=O)O[C@H](C)[C@@H](CO[C@@H]2O[C@H](C)[C@H]([C@H]([C@H]2OC)OC)O)[C@H]2[C@H](/C=C/C(=O)[C@@](C[C@@H]1C)(C)O)O2
InChI InChI=1S/C35H56O14/c1-17-10-13-26(37)46-20(4)22(16-44-34-32(43-9)31(42-8)27(38)21(5)47-34)30-23(48-30)11-12-25(36)35(6,40)15-18(2)29(17)49-33-28(39)24(41-7)14-19(3)45-33/h10-13,17-24,27-34,38-40H,14-16H2,1-9H3/b12-11+,13-10+/t17-,18-,19+,20+,21+,22+,23-,24-,27+,28+,29-,30-,31+,32+,33-,34+,35-/m0/s1
InChI Key KLGADJPDTCIJLO-FCNIXBKESA-N
Classification Click here for help
Compound class Natural product or derivative
IUPAC Name Click here for help
(1S,2R,3R,6E,8S,9R,10S,12S,14E,16S)-12-hydroxy-2-[[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxymethyl]-9-[(2S,3R,4S,6R)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione
Database Links Click here for help
Specialist databases
Antibiotic DB Antibiotic DB Database logo 1143
Other databases
CAS Registry No. 20283-48-1 (source: Scifinder)
GtoPdb PubChem SID 405560499
PubChem CID 6436271
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