Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H12N2O2 |
Molecular Weight | 288.3001 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 2 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C=C1)\C=C([N+]#[C-])\C([N+]#[C-])=C\C2=CC=C(O)C=C2
InChI
InChIKey=YBMVKDUTYAGKEW-WHYMJUELSA-N
InChI=1S/C18H12N2O2/c1-19-17(11-13-3-7-15(21)8-4-13)18(20-2)12-14-5-9-16(22)10-6-14/h3-12,21-22H/b17-11-,18-12-
Molecular Formula | C18H12N2O2 |
Molecular Weight | 288.3001 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 2 |
Optical Activity | NONE |
Xanthocillin is an antibiotic derived from Penicillium notatum. In vitro tests have shown that most of the common Gram-positive and Gram-negative pathogens, including Proteus and Pseudomonas pyocyanea, are sensitive to xanthocillin. Xanthocillin participated in the trial in patients with a variety of eczematous and intertriginous eruptions, in all of which bacterial infection was thought to be playing a part. Xanthocillin cream produced results, which were on par with other treatments. Information about the current use of this agent is not available.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Xanthocillin in dentistry]. | 1952 Aug |
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[Therapeutic possibilities in dentistry with xanthocillin, a new antibiotic]. | 1953 Feb 10 |
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[Structure of xanthocillin, a new antibiotic]. | 1956 Jun |
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Xanthocillin; experimental and clinical studies. | 1956-1957 |
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Xanthocillin cream for local treatment. | 1959 May 9 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13651693
xanthocillin cream was applied in the form of patch tests for 48 hours to the normal skin of 20 other subjects.
Route of Administration:
Topical
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:58:10 GMT 2023
by
admin
on
Fri Dec 15 15:58:10 GMT 2023
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Record UNII |
06Z55VZ40D
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Record Status |
Validated (UNII)
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