Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H3I2NO3 |
Molecular Weight | 390.9019 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(I)C=C(C=C1I)[N+]([O-])=O
InChI
InChIKey=UVGTXNPVQOQFQW-UHFFFAOYSA-N
InChI=1S/C6H3I2NO3/c7-4-1-3(9(11)12)2-5(8)6(4)10/h1-2,10H
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Ancylostoma caninum |
|||
Target ID: Uncinaria stenocephala |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | ANCYLOL Approved UseThe drug is used for the treatment of both dogs infested with hookworms (including Ancylostoma caninum, A. braziliense and
Uncinaria stenocephala) and cats infested with the hookworm A.
tubaeforme. Launch Date1964 |
PubMed
Title | Date | PubMed |
---|---|---|
2,6-Diiodo-4-nitrophenol, 2,6-diiodo-4-nitrophenyl acetate and 2,6-diiodo-4-nitroanisole: interplay of hydrogen bonds, iodo-nitro interactions and aromatic pi-pi-stacking interactions to give supramolecular structures in one, two and three dimensions. | 2002 Aug |
Patents
Sample Use Guides
Dogs and cats: Disophenol is administered subcutaneously
at a dosage level equivalent to 4.5 milligrams
of disophenol per pound of
body weight. A second treatment may
be indicated 21 days after the initial
treatment.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/588311
Disophenol produced contracture of the rat cardiac muscle at concentrations of 100 and 1000 ng/ml and at the latter dose diastolic tension after 60 min perfusion was approximately 300 per cent of its initial value.
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C250
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SUBSTANCE RECORD