Compound ID | 1749

Update compound information

Caminoside A

Class: Glycolipid

Spectrum of activity: Gram-negative
Details of activity: Active against EPEC
Year first mentioned: 2020
Highest developmental phase: Preclinical
Chemical structure(s):
Click here for structure editor
Molecular weight: 1027.2
Iso. SMILES: CCCCCCCCC[C@H](CCCCCCCC(=O)C)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO[C@H]3[C@H]([C@H]([C@H]([C@H](O3)C)O)O)O)OC(=O)C)OC(=O)CCC)O[C@H]4[C@H]([C@@H]([C@H]([C@@H](O4)C)O)O)O
InChI Key: XTQWRNIJLVUYJY-ZFMPSFEPSA-N
Can. SMILES: CCCCCCCCC[C@H](CCCCCCCC(=O)C)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]3[C@H]([C@H]([C@H]([C@@H](C)O3)O)O)O)O2)OC(=O)C)OC(=O)CCC)O[C@H]4[C@H]([C@@H]([C@H]([C@H](C)O4)O)O)O
InChI: InChI=1S/C49H86O22/c1-7-9-10-11-12-15-18-22-30(23-19-16-13-14-17-21-26(3)51)66-48-43(39(59)36(56)31(24-50)67-48)70-49-45(71-47-41(61)38(58)35(55)28(5)64-47)44(69-33(53)20-8-2)42(65-29(6)52)32(68-49)25-62-46-40(60)37(57)34(54)27(4)63-46/h27-28,30-32,34-50,54-61H,7-25H2,1-6H3/t27-,28+,30-,31-,32-,34+,35+,36-,37+,38-,39+,40+,41+,42-,43-,44+,45-,46-,47+,48-,49+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/21777925
Citation: https://www.nature.com/articles/s41429-020-0344-z

AntibioticDB is supported by GARDP.

If you have feedback, experience problems, or are interested in a collaboration, please contact us. | Terms and conditions

The content of this site is intended for educational and scientific research purposes only and not as a source of medical advice or consultation.