Misplaced Pages

Cladinose: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 11:23, 5 May 2011 editOnegumas (talk | contribs)36 editsm pl← Previous edit Revision as of 12:38, 10 September 2012 edit undoThe chemistds (talk | contribs)Extended confirmed users5,761 edits added CSID, (Std)InChI and (Std)InChIKeyNext edit →
Line 9: Line 9:
| PubChem=443504 | PubChem=443504
| SMILES=C1((CC(O1)O)(C)OC)O | SMILES=C1((CC(O1)O)(C)OC)O
| ChemSpiderID = 391713
| InChI = 1/C8H16O4/c1-5-7(10)8(2,11-3)4-6(9)12-5/h5-7,9-10H,4H2,1-3H3/t5-,6?,7-,8+/m0/s1
| InChIKey = YHVUVJYEERGYNU-SBEGJHHSBA
| StdInChI = 1S/C8H16O4/c1-5-7(10)8(2,11-3)4-6(9)12-5/h5-7,9-10H,4H2,1-3H3/t5-,6?,7-,8+/m0/s1
| StdInChIKey = YHVUVJYEERGYNU-SBEGJHHSSA-N
}} }}
|Section2= {{Chembox Properties |Section2= {{Chembox Properties

Revision as of 12:38, 10 September 2012

Cladinose
Names
IUPAC name (4R,5S,6S)-4-Methoxy-4,6-dimethyl-tetrahydropyran-2,5-diol
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H16O4/c1-5-7(10)8(2,11-3)4-6(9)12-5/h5-7,9-10H,4H2,1-3H3/t5-,6?,7-,8+/m0/s1Key: YHVUVJYEERGYNU-SBEGJHHSSA-N
  • InChI=1/C8H16O4/c1-5-7(10)8(2,11-3)4-6(9)12-5/h5-7,9-10H,4H2,1-3H3/t5-,6?,7-,8+/m0/s1Key: YHVUVJYEERGYNU-SBEGJHHSBA
SMILES
  • C1((CC(O1)O)(C)OC)O
Properties
Chemical formula C8H16O4
Molar mass 176.21 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Cladinose is a hexose deoxy sugar that in several antibiotics (such as erythromycin) is attached to the macrolide ring.

In ketolides, a relatively new class of antibiotics, the cladinose is replaced with a keto group.

Erythromycin with cladinose visible at bottom


External links


Stub icon

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

Categories: