Sulfamethoxypyridazine
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This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.
Identification
- Summary
Sulfamethoxypyridazine is a sulphonamide antibiotic indicated in the treatment of gonorrhea, inflammation, urinary tract ulcers, and bronchitis.
- Generic Name
- Sulfamethoxypyridazine
- DrugBank Accession Number
- DB13773
- Background
Not Available
- Type
- Small Molecule
- Groups
- Experimental
- Structure
- Weight
- Average: 280.3
Monoisotopic: 280.063011436 - Chemical Formula
- C11H12N4O3S
- Synonyms
- Sulfamethoxypyridazine
- sulfametoxipiridazina
- External IDs
- CL-13494
Pharmacology
- Indication
Not Available
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- Pharmacodynamics
Not Available
- Mechanism of action
- Not Available
- Absorption
Not Available
- Volume of distribution
Not Available
- Protein binding
Not Available
- Metabolism
- Not Available
- Route of elimination
Not Available
- Half-life
Not Available
- Clearance
Not Available
- Adverse Effects
- Improve decision support & research outcomesWith structured adverse effects data, including: blackbox warnings, adverse reactions, warning & precautions, & incidence rates. View sample adverse effects data in our new Data Library!Improve decision support & research outcomes with our structured adverse effects data.
- Toxicity
Not Available
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs Browse all" title="About SNP Mediated Effects/ADRs" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
- Not Available
Interactions
- Drug Interactions Learn More" title="About Drug Interactions" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAcarbose The therapeutic efficacy of Acarbose can be increased when used in combination with Sulfamethoxypyridazine. Acenocoumarol The risk or severity of bleeding can be increased when Sulfamethoxypyridazine is combined with Acenocoumarol. Acetohexamide The therapeutic efficacy of Acetohexamide can be increased when used in combination with Sulfamethoxypyridazine. Albiglutide The therapeutic efficacy of Albiglutide can be increased when used in combination with Sulfamethoxypyridazine. Alogliptin The therapeutic efficacy of Alogliptin can be increased when used in combination with Sulfamethoxypyridazine. - Food Interactions
- Not Available
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
Categories
- ATC Codes
- J01ED05 — Sulfamethoxypyridazine
- Drug Categories
- Amides
- Amines
- Aniline Compounds
- Anti-Bacterial Agents
- Anti-Infective Agents
- Antibacterials for Systemic Use
- Antiinfectives for Systemic Use
- Benzene Derivatives
- Benzenesulfonamides
- Long-Acting Antibacterial Sulfonamides
- Sulfanilamides
- Sulfonamide Antibacterial
- Sulfonamides
- Sulfonamides and trimethoprim
- Sulfones
- Sulfur Compounds
- Chemical TaxonomyProvided by Classyfire
- Description
- This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
- Kingdom
- Organic compounds
- Super Class
- Benzenoids
- Class
- Benzene and substituted derivatives
- Sub Class
- Benzenesulfonamides
- Direct Parent
- Aminobenzenesulfonamides
- Alternative Parents
- Benzenesulfonyl compounds / Aniline and substituted anilines / Alkyl aryl ethers / Pyridazines and derivatives / Organosulfonamides / Imidolactams / Heteroaromatic compounds / Aminosulfonyl compounds / Azacyclic compounds / Primary amines show 3 more
- Substituents
- Alkyl aryl ether / Amine / Aminobenzenesulfonamide / Aminosulfonyl compound / Aniline or substituted anilines / Aromatic heteromonocyclic compound / Azacycle / Benzenesulfonyl group / Ether / Heteroaromatic compound show 16 more
- Molecular Framework
- Aromatic heteromonocyclic compounds
- External Descriptors
- sulfonamide, pyridazines, sulfonamide antibiotic (CHEBI:102516)
- Affected organisms
- Not Available
Chemical Identifiers
- UNII
- T034E4NS2Z
- CAS number
- 80-35-3
- InChI Key
- VLYWMPOKSSWJAL-UHFFFAOYSA-N
- InChI
- InChI=1S/C11H12N4O3S/c1-18-11-7-6-10(13-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,15)
- IUPAC Name
- 4-amino-N-(6-methoxypyridazin-3-yl)benzene-1-sulfonamide
- SMILES
- COC1=NN=C(NS(=O)(=O)C2=CC=C(N)C=C2)C=C1
References
- General References
- FDA Thailand: Gana Tab (Sulfamethoxypyridazine) Oral Tablet [Link]
- External Links
- ChemSpider
- 5139
- 10181
- ChEBI
- 102516
- ChEMBL
- CHEMBL268869
- ZINC
- ZINC000000049141
- Wikipedia
- Sulfamethoxypyridazine
Clinical Trials
- Clinical Trials Learn More" title="About Clinical Trials" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
Phase Status Purpose Conditions Count
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Tablet 500 mg - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Not Available
- Experimental Properties
- Not Available
- Predicted Properties
Property Value Source Water Solubility 0.325 mg/mL ALOGPS logP 0.51 ALOGPS logP 0.47 Chemaxon logS -2.9 ALOGPS pKa (Strongest Acidic) 6.84 Chemaxon pKa (Strongest Basic) 2.02 Chemaxon Physiological Charge -1 Chemaxon Hydrogen Acceptor Count 6 Chemaxon Hydrogen Donor Count 2 Chemaxon Polar Surface Area 107.2 Å2 Chemaxon Rotatable Bond Count 3 Chemaxon Refractivity 72.39 m3·mol-1 Chemaxon Polarizability 26.19 Å3 Chemaxon Number of Rings 2 Chemaxon Bioavailability 1 Chemaxon Rule of Five Yes Chemaxon Ghose Filter Yes Chemaxon Veber's Rule No Chemaxon MDDR-like Rule No Chemaxon - Predicted ADMET Features
- Not Available
Spectra
- Mass Spec (NIST)
- Not Available
- Spectra
- Chromatographic Properties
Collision Cross Sections (CCS)
Adduct CCS Value (Å2) Source type Source [M-H]- 178.4626009 predictedDarkChem Lite v0.1.0 [M-H]- 164.60902 predictedDeepCCS 1.0 (2019) [M+H]+ 179.6326009 predictedDarkChem Lite v0.1.0 [M+H]+ 166.96704 predictedDeepCCS 1.0 (2019) [M+Na]+ 178.3423009 predictedDarkChem Lite v0.1.0 [M+Na]+ 173.06018 predictedDeepCCS 1.0 (2019)
Drug created at June 23, 2017 20:48 / Updated at May 22, 2021 06:01