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Erythromycin C (Standard)

CAT: 0804-HY-125546RSize: 1 EachDry Ice: NoHazardous: No
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Description
Erythromycin C (Standard) is the analytical standard of Erythromycin C. This product is intended for research and analytical applications. Erythromycin C is an antibiotic. Erythromycin C could be isolated from the fermentation process of the penicillium Streptomyces erythreus[1].
CAS Number
1675-02-1
UNSPSC
12352005
Target
Antibiotic; Reference Standards
Type
Reference compound
Related Pathways
Anti-infection; Others
Field of Research
Infection
Assay Protocol
https://www.medchemexpress.com/erythromycin-c-standard.html
Smiles
C[C@H]1[C@@H]([C@@](C)(C[C@@]([H])(O1)O[C@@H]([C@@H]([C@H]([C@](O)(C[C@H](C2=O)C)C)O[C@]3([C@@H]([C@H](C[C@H](O3)C)N(C)C)O)[H])C)[C@H](C(O[C@@H]([C@](O)(C)[C@@H]([C@H]2C)O)CC)=O)C)O)O
Molecular Formula
C36H65NO13
Molecular Weight
719.90
References & Citations
[1]Peirú S, et, al. Production of the potent antibacterial polyketide erythromycin C in Escherichia coli. Appl Environ Microbiol. 2005 May;71 (5) :2539-47.
Shipping Conditions
Room temperature
Scientific Category
Reference Standards

Chemical Information

Erythromycin C

Erythromycin C is an erythromycin that consists of erythronolide A having 2,6-dideoxy-3-C-methyl-alpha-L-ribo-hexopyranosyl and 3,4,6-trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranosyl residues attahced at positions 4 and 6 respectively. It is functionally related to an erythronolide A. It is a conjugate base of an erythromycin C(1+).

CAS Number1675-02-1
PubChem CID83933
IUPAC Name(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-4-[(2R,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
Molecular FormulaC36H65NO13
Molecular Weight719.9
XLogP2.2
Topological Polar Surface Area205
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count14
Rotatable Bond Count6
Heavy Atom Count50
Formal Charge0
Complexity1160
SMILES
CC[C@@H]1[C@@]([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2C[C@@]([C@H]([C@@H](O2)C)O)(C)O)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)C)C)O)(C)O
InChI
InChI=1S/C36H65NO13/c1-13-24-36(10,45)29(40)19(4)26(38)17(2)15-35(9,44)31(50-33-27(39)23(37(11)12)14-18(3)46-33)20(5)28(21(6)32(42)48-24)49-25-16-34(8,43)30(41)22(7)47-25/h17-25,27-31,33,39-41,43-45H,13-16H2,1-12H3/t17-,18-,19+,20+,21-,22+,23+,24-,25+,27-,28+,29-,30+,31-,33+,34-,35-,36-/m1/s1
InChIKey
MWFRKHPRXPSWNT-QNPWSHAKSA-N
Chemical Structure
2D Structure
2D structure of Erythromycin C
CAS: 1675-02-1
CID: 83933
Formula: C36H65NO13
MW: 719.9
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight719.9
XLogP32.2
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count14
Rotatable Bond Count6
Exact Mass719.44559113
Monoisotopic Mass719.44559113
Topological Polar Surface Area205 Ų
Heavy Atom Count50
Formal Charge0
Complexity1160
Isotope Atom Count0
Defined Atom Stereocenter Count18
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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