Art. -Nr.: HY-19581

Baquiloprim

Name: Baquiloprim
Brand: MedChemExpress
SKU: HY-19581
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Baquiloprim is an orally active Antibiotic and selective inhibitor of Bacterial Dihydrofolate reductase (DHFR), with an IC₅₀ of 19 nM against E. coli and an IC₅₀ of 190 μM against rat liver dihydrofolate reductase. Baquiloprim is a bacteriostatic broad-spectrum antibacterial agent that acts against Gram-negative and Gram-positive bacteria. Baquiloprim inhibits glucuronidation in cultured hepatocytes. Baquiloprim can be used in research related to Pasteurella haemolytica infection, bacterial infection, Escherichia coli diarrhea, bacterial infection in pigs, and pneumonic pasteurellosis.

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Reinheit: 99.66%
CAS. Nr.: 102280-35-3
Formel: C₁₇H₂₀N₆
Molecular Weight:308.38

Speicherung:

-20°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Baquiloprim Chemical Structure

CAS. Nr.: 102280-35-3

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Biologische Aktivität
- Beschreibung
- In Vitro
- Parmacokinetics
- In Vivo
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

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In Vitro

Baquiloprim exerts in vitro bacteriostatic activity against Salmonella species (MIC₅₀ = 0.12 μg/mL), Streptococcus zooepidemicus (MIC₅₀ = 0.25 μg/mL), coagulase-positive Staphylococcus species (MIC₅₀ = 0.5 μg/mL), and Taylorella equigenitalis (MIC₅₀ = 2 μg/mL)^[1].
Baquiloprim (24 h) exhibits broad-spectrum in vitro antibacterial activity against cattle, sheep, and pig bacterial isolates, with geometric mean MIC₅₀ ranging from 0.03 mg litre^-1 to 0.18 mg litre^-1^[2].
Baquiloprim (1:100 ratio with sulphadimidine; 24 h) shows high synergistic in vitro antibacterial activity with sulphadimidine against most cattle bacterial pathogens, with FIC indices below 0.5 and reduced MICs for baquiloprim in the 1:100 mixture^[2].
Baquiloprim (<0.008-8.0 μg/mL alone; 0.004:0.4-0.5:50 μg/mL in 1:100 ratio with sulphadimidine) alone and in 1:100 combination with sulphadimidine inhibits growth of susceptible porcine bacterial pathogens^[4].
Baquiloprim potently inhibits Pasteurella haemolytica in vitro with a mean MIC of 0.09 mg/L, and its activity is synergistically enhanced by sulphadimidine, reducing its mean MIC to 0.02 mg/l^[6].
Baquiloprim (0.02-0.1 mM) potently inhibits glucuronidation in cultured rat and goat hepatocytes at 0.1 mM, but only weakly inhibits this pathway at the physiologically relevant concentration of 0.02 mM^[1].
Baquiloprim potently inhibits Escherichia coli DHFR with an I₅₀ of 1.9×10^-8 M, and shows ~10,000-fold lower affinity for rat liver DHFR with an I₅₀ of 1.9×10^-4 M^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Parmacokinetics

Species	Dose	Route	C_max	T_max	T_1/2	AUC
Pig^[4]	10 mg/kg	i.m.	0.55 μg/mL	2.50 h	6.3 h	6.3 μg·h/mL
Pig^[4]	30 mg/kg	i.m.	0.87 μg/mL	3.30 h	10.6 h	16.8 μg·h/mL

In Vivo

Baquiloprim (8 mg/kg; i.v.; single dose; intra-ruminal; single dose via nasogastric catheter) exhibits a two-compartment pharmacokinetic profile with rapid distribution, slow elimination, and moderate systemic bioavailability in healthy female dwarf goats^[1].
Baquiloprim (0.5 mg/kg; p.o.; at 1 and 6 hours post-infection) exhibits potent in vivo efficacy against E. coli infection in mice, with an average ED₅₀ of 0.5 mg/kg^[2].
Baquiloprim (10 mg/kg; i.m.; once daily; 3 days) achieves mean peak serum concentrations of 0.55 μg/mL and maintains concentrations above the assay limit for at least 24 hours post-dose, with an elimination half-life of 6.3 hours^[4].
Baquiloprim (30 mg/kg; i.m.; single dose) achieves a mean peak serum concentration of 0.87 μg/mL and maintains measurable concentrations in most pigs for at least 48 hours, with an extended elimination half-life of 10.6 hours^[4].
Baquiloprim (4 mg/kg; oral; single dose 6 hours pre-infection, second dose 48 hours post-infection) combined with sulphadimidine suppresses P. haemolytica-induced pneumonic pasteurellosis in calves, as evidenced by normal body temperatures, minimal signs, negligible lung lesions, and no bacterial recovery^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

Dwarf goats (female, healthy, mean bodyweight 30.6 kg)^[1]
Dosage:

8 mg/kg (i.v.); 8 mg/kg (intra-ruminal)
Administration:

i.v.; single dose; intra-ruminal; single dose via nasogastric catheter
Result:

Exhibited mean distribution half-life (t₁/₂α) of 0.89 hours, mean elimination half-life (t₁/₂β) of 14.0 hours, mean volume of distribution at steady-state (Vdss) of 14.1 litres/kg, mean AUC_0-48h of 9.6 μg hours/mL, and mean clearance (CI) of 0.77 litres/kg/hours after intravenous administration.
Reached mean maximum plasma concentration (Cmax) of 0.09 μg/mL, mean time to maximum concentration (Tmax) of 35 hours, mean AUC_0-48h of 3.2 μg hours/mL, and mean systemic oral bioavailability of 33.7 per cent after intra-ruminal administration.

Animal Model:

CD-1 (female, 18 to 20 g, Escherichia coli P855 infection model)^[2]
Dosage:

0.5 mg/kg
Administration:

p.o.; at 1 and 6 hours post-infection
Result:

Achieved an average ED50 of 0.5 mg/kg across three experiments.

Animal Model:

female hybrid (6 weeks old, 13-18 kg)^[4]
Dosage:

10 mg/kg (total formulation)
Administration:

i.m.; once daily; 3 days
Result:

Reached mean maximum serum concentration (Cmax) of 0.55 μg/mL at 2.5 hours after the first dose.
Had mean elimination half-life (t½) of 6.3 hours, area under the serum concentration-time curve (AUC∞) of 6.27 μg·mL^-1·hour, volume of distribution (Vd(area)/F) of 2.41 litre/kg, and clearance (Clp/F) of 273 mL·hour^-1·kg^-1.
Achieved mean baquiloprim concentrations of 0.05 μg/mL, 0.08 μg/mL, and 0.11 μg/mL at 24 hours after the first, second, and third doses, respectively.
Detected concentrations ≥0.02 μg/mL in all samples taken 24 hours after each injection.

Animal Model:

male hybrid (7 weeks old, 23-36 kg)^[4]
Dosage:

30 mg/kg (total formulation)
Administration:

i.m.; single dose
Result:

Reached mean maximum serum concentration (Cmax) of 0.87 μg/mL at 3.3 hours post-dose.
Had mean elimination half-life (t½) of 10.6 hours, area under the serum concentration-time curve (AUC∞) of 16.8 μg·mL^-1·hour, volume of distribution (Vd(area)/F) of 4.60 litre/kg, and clearance (Clp/F) of 308 mL·hour^-1·kg^-1.
Detected concentrations ≥0.02 μg/mL in all but two samples taken 48 hours post-dose.

Animal Model:

Friesian calves (female, 21 weeks old, mean bodyweights 117-121 kg, endobronchial inoculation with Pasteurella haemolytica type A1)^[6]
Dosage:

4 mg/kg (single dose 6 hours pre-infection); 4 mg/kg (second dose 48 hours post-infection)
Administration:

oral; single dose (6 hours pre-infection); second dose (48 hours post-infection)
Result:

Maintained mean rectal temperatures close to pre-infection levels (maximum individual temperature 39.3°C).
Achieved a mean score of 1.6 (single dose) or 1.5 (repeat dose), versus 8.6 in untreated controls.
Had post-mortem lung lesion scores of 0.2 (single dose) and 0.25 (repeat dose), compared to 2.4 in untreated controls.
Prevented isolation of P. haemolytica from all treated calves, whereas the organism was isolated from all 5 untreated controls.

Chemical Information

CAS. Nr. 102280-35-3
Appearance Solid
Molecular Weight 308.38
Formel C₁₇H₂₀N₆
Color White to yellow
SMILES

NC1=NC=C(CC2=C3C=CC=NC3=C(N(C)C)C(C)=C2)C(N)=N1
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

-20°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (284 KB)
SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Lewicki J, et al. Oral bioavailability and pharmacokinetics of baquiloprim in dwarf goats. Research in veterinary science. 1995 May;58(3):268-71. [Content Brief]

[2]. White G, et al. Baquiloprim, a new antifolate antibacterial: in vitro activity and pharmacokinetic properties in cattle. Research in veterinary science. 1993 May;54(3):372-8. [Content Brief]

[3]. White DG, et al. Comparison of danofloxacin with baquiloprim/sulphadimidine for the treatment of experimentally induced Escherichia coli diarrhoea in calves. The Veterinary record. 1998 Sep 05;143(10):273-6. [Content Brief]

[4]. Davies AM, et al. Pharmacokinetics of baquiloprim and sulphadimidine in pigs after intramuscular administration. Research in veterinary science. 1994 Jul;57(1):69-74. [Content Brief]

[5]. Sunderland SJ, et al. Efficacy of danofloxacin 18% injectable solution in the treatment of Escherichia coli diarrhoea in young calves in Europe. Research in veterinary science. 2003 Apr;74(2):171-8. [Content Brief]

[6]. Dassanayake L, et al. Administration of a bolus formulation of baquiloprim and sulphadimidine to calves: plasma concentration--time profiles and efficacy in suppressing experimental pneumonic pasteurellosis. Veterinary microbiology. 1994 Jan;38(3):255-62. [Content Brief]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Baquiloprim

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