Sulfametrole

This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.

Identification

Summary

Sulfametrole is an antibiotic indicated in combination intravenous products for various bacterial infections.

Generic Name
Sulfametrole
DrugBank Accession Number
DB15975
Background

Not Available

Type
Small Molecule
Groups
Experimental
Structure
Weight
Average: 286.32
Monoisotopic: 286.019432546
Chemical Formula
C9H10N4O3S2
Synonyms
  • Sulfametrole
External IDs
  • 251-288-1

Pharmacology

Indication

Not Available

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Associated Conditions
Indication TypeIndicationCombined Product DetailsApproval LevelAge GroupPatient CharacteristicsDose Form
Used in combination to treatBacterial urinary tract infectionsCombination Product in combination with: Trimethoprim (DB00440)••••••••••••••••••••
Used in combination to treatGastrointestinal bacterial infectionCombination Product in combination with: Trimethoprim (DB00440)••••••••••••••••••••
Used in combination to treatGenital infection bacterialCombination Product in combination with: Trimethoprim (DB00440)••••••••••••••••••••
Used in combination to treatKidney infection caused by susceptible bacteriaCombination Product in combination with: Trimethoprim (DB00440)••••••••••••••••••••
Used in combination to treatPneumonia, bacterialCombination Product in combination with: Trimethoprim (DB00440)••••••••••••••••••••
Contraindications & Blackbox Warnings
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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
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
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.
DrugInteraction
AcarboseThe therapeutic efficacy of Acarbose can be increased when used in combination with Sulfametrole.
AcetohexamideThe therapeutic efficacy of Acetohexamide can be increased when used in combination with Sulfametrole.
AlbiglutideThe therapeutic efficacy of Albiglutide can be increased when used in combination with Sulfametrole.
AlogliptinThe therapeutic efficacy of Alogliptin can be increased when used in combination with Sulfametrole.
BenzylpenicillinSulfametrole may decrease the excretion rate of Benzylpenicillin which could result in a higher serum level.
Food Interactions
Not Available

Products

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Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing EndRegionImage
Rokiprim InfusionslösungSulfametrole (800 mg/250ml) + Trimethoprim (160 mg/250ml)SolutionIntravenousRokitan Gmb H1979-10-30Not applicableAustria flag

Categories

ATC Codes
J01EE03 — Sulfametrole and trimethoprim
Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
F5AK41IPQG
CAS number
32909-92-5
InChI Key
IZOYMGQQVNAMHS-UHFFFAOYSA-N
InChI
InChI=1S/C9H10N4O3S2/c1-16-9-8(11-17-12-9)13-18(14,15)7-4-2-6(10)3-5-7/h2-5H,10H2,1H3,(H,11,13)
IUPAC Name
4-amino-N-(4-methoxy-1,2,5-thiadiazol-3-yl)benzene-1-sulfonamide
SMILES
COC1=NSN=C1NS(=O)(=O)C1=CC=C(N)C=C1

References

General References
  1. BASG: Rokiprim (Sulfametrol, Trimethoprim) Intravenous Injection [Link]
ChemSpider
58466
RxNav
37328
ChEBI
88258
ChEMBL
CHEMBL2105398
ZINC
ZINC000000002099
Wikipedia
Sulfametrole

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
FormRouteStrength
SolutionIntravenous
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.757 mg/mLALOGPS
logP1.04ALOGPS
logP1.05Chemaxon
logS-2.6ALOGPS
pKa (Strongest Acidic)5.51Chemaxon
pKa (Strongest Basic)1.9Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area107.2 Å2Chemaxon
Rotatable Bond Count3Chemaxon
Refractivity69.46 m3·mol-1Chemaxon
Polarizability26.36 Å3Chemaxon
Number of Rings2Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
Not Available

Spectra

Mass Spec (NIST)
Not Available
Spectra
SpectrumSpectrum TypeSplash Key
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-000i-0090000000-03b5f50001452bcc32d6
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-000i-0390000000-b7480b8ed1038ab2db79
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0a4r-0930000000-fa6503d7af6b526ae2be
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-0aba-0920000000-66a244859c45cc11eb3a
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-014i-9450000000-f7087b2dac4f8c83118d
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-0a4m-3900000000-3e9fffc7c3db79862ab8
Predicted 1H NMR Spectrum1D NMRNot Applicable
Predicted 13C NMR Spectrum1D NMRNot Applicable
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-160.00148
predicted
DeepCCS 1.0 (2019)
[M+H]+162.35948
predicted
DeepCCS 1.0 (2019)
[M+Na]+168.45264
predicted
DeepCCS 1.0 (2019)

Drug created at December 03, 2020 15:47 / Updated at May 07, 2021 21:09