Drug Standards
Med Vet International CISPLATIN INJECTION, 1 MG/ML, 50ML
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
CISPLATIN INJECTION, 1 MG/ML, 50ML
PHARMACEUTICAL BUYERS INTERNATIONAL INC LEUCOVORIN 500 MG SDV 50 ML
NC3779128 LEUCOVORIN 500 MG SDV 50 ML
HARWICK STANDARD DISTRIBUTION SYNPRO ZN STEARATE DLG-10-25LB
NC3781364 SYNPRO ZN STEARATE DLG-10-25LB
Med Vet International Ivermectin, Pour-on, 2.5 Liter
NOT FOR SALE IN CALIFORNIAIVERMAX Ivermectin Pour On for Cattle contains 5 mg ivermectin/ml. Itdelivers internal and external parasite control in one convenientlow-volume application. For the treatment and control ofgastrointestinal roundworms (including inhibited Ostertagia ostertagi)lungworms, grubs, horn flies, sucking and biting lice, and sarcopticmange mites in cattle. The dose is 1 ml for each 22 lb of body weight.Do not use in female dairy cattle of breeding age. Cattle must not betreated within 48 days of slaughter for human consumptionProducts are not always manufacturer specific. Actual product appearance may differ from website image.
U.S. Pharmacopeia Chloroxylenol, 88-04-0, MFCD00002324, 125mg
Molecular formula C8H9ClO, Molecular weight 156.61, Melting Point 239.9 °F (115.5 °C), Boiling Point 474.8 °F (246 °C), Synonyms: Parachlorometaxylenol, PCMX
Apexbio Technology LLC Diphenhydramine HCl 147-24-0 250mg
Diphenhydramine HCl is a small-molecule antagonist targeting histamine H1 receptors It is designed to competitively inhibit histamine binding to H1 receptors in peripheral tissues and the central nervous system thereby suppressing histamine-mediated hypersensitivity responses Diphenhydramine HCl exerts its biological activity primarily through antagonism of histamine H1 receptors and also exhibits anticholinergic activity within the central nervous system Based on these pharmacological properties Diphenhydramine HCl holds research potential in the study of allergic reactions sleep regulation sedation pathways motor disorders cognitive function memory processes and investigations of cholinergic and histaminergic neurotransmission
Medchemexpress LLC Enalaprilat (dihydrate) | 84680-54-6 | 99.6% | 1 ML
Enalaprilat dihydrate (MK-422), the active metabolite of the oral proagent Enalapril, is a potent, competitive, and long-acting angiotensin-converting enzyme (ACE) inhibitor with an IC50 of 1.94 nM. This product is intended for research on hypertension.
- Potent and long-acting ACE inhibitor
- Attenuates IGF-I induced neonatal rat cardiac fibroblast growth in vitro
- Shows significant intraocular pressure (IOP)-lowering effect in rabbits in vivo
Medchemexpress LLC Diclofenac epolamine | 119623-66-4 | 100.0% | 411.32 | 50 MG
Diclofenac epolamine is a non-steroidal anti-inflammatory drug (NSAID) used for relieving arthritis pain, acute pain, osteoarthritis, and actinic keratosis. It demonstrates good skin absorption characteristics without local adverse reactions or allergies.
- Relieves arthritis pain, acute pain, osteoarthritis, and actinic keratosis.
- Demonstrates good skin absorption characteristics.
- Does not cause local adverse reactions or allergies.
- Effective in treating inflammatory conditions.
- Increases partitioning into the skin.
- Enhances and sustains drug transport through the skin.
Medchemexpress LLC Naphazoline nitrate | 5144-52-5 | MFCD00014316 | 99.1% | 273.29 | 50 MG
Naphazoline nitrate is an α-adrenergic receptor agonist that reduces vascular hyperpermeability and promotes vasoconstriction. It is also known to reduce levels of inflammatory factors, cytokines, IgE, GMCSF, and NGF, making it suitable for non-bacterial conjunctivitis research.
- α-adrenergic receptor agonist
- Reduces vascular hyperpermeability
- Promotes vasoconstriction
- Reduces levels of inflammatory factors (TNF-α, IL-1β, IL-6)
- Reduces levels of cytokines (IFN-γ, IL-4)
- Reduces IgE, GMCSF, and NGF
- Can be used for non-bacterial conjunctivitis research
Medchemexpress LLC Naphazoline nitrate | 5144-52-5 | 99.1% | 273.29 | 100 MG
Naphazoline nitrate is an α-adrenergic receptor agonist that reduces vascular hyperpermeability and promotes vasoconstriction. It also reduces levels of inflammatory factors and can be used for non-bacterial conjunctivitis research.
- Targets α-adrenergic receptors
- Helps manage vascular issues
- Decreases levels of TNF-α, IL-1β, IL-6, IFN-γ, IL-4, IgE, GMCSF, and NGF
- Applicable for non-bacterial conjunctivitis research
- Solid, white to off-white appearance
- Solubility: 100 mg/mL in DMSO
Medchemexpress LLC Suplatast (Tosilate) | 94055-76-2 | 99.7% | 499.64 | 1 G
Suplatast Tosilate (IPD 1151T) is an orally active Th2 cytokine inhibitor that can inhibit both IL-4 and IL-5 production from Th2 cells and suppress IgE synthesis. It acts as an anti-allergic agent with antiasthmatic, anti-inflammatory, and antifibrotic activity.
- Orally active Th2 cytokine inhibitor
- Inhibits IL-4 and IL-5 production from Th2 cells
- Suppresses IgE synthesis
- Anti-allergic agent
- Antiasthmatic activity
- Anti-inflammatory activity
- Antifibrotic activity
Medchemexpress LLC Sulfamerazine | 127-79-7 | 99.8% | 1 G
Sulfamerazine (RP-2632) is a sulfonamide antibacterial, identified as the monomethyl derivative of sulfadiazine (2-sulfanilamido-4-methylpyrimidine). It acts as a bacteriostatic agent by inhibiting bacterial synthesis of dihydrofolic acid, competing with para-aminobenzoic acid (PABA) for binding to dihydropteroate synthesizes, which ultimately reduces the synthesis of bacterial nucleotides and DNA.
- Appearance: Solid
- Color: White to off-white
- Molecular weight: 264.30
- Formula: C11H12N4O2S
- Solubility in DMSO: ≥ 100 mg/mL (378.36 mM)
- Solubility in H2O: < 0.1 mg/mL (insoluble)
Medchemexpress LLC Oxytetracycline | 79-57-2 | MFCD00003700 | 99.2% | 10 G
Oxytetracycline is an antibiotic from the tetracycline class. It potently inhibits Gram-negative and Gram-positive bacteria. This antibiotic functions as a protein synthesis inhibitor by preventing the binding of aminoacyl-tRNA to the ribosomal RNA complex. It also exhibits anti-HSV-1 activity.
- Antibiotic from the tetracycline class
- Potently inhibits Gram-negative and Gram-positive bacteria
- Functions as a protein synthesis inhibitor
- Prevents binding of aminoacyl-tRNA to ribosomal RNA complex
- Exhibits anti-HSV-1 activity
- Member of the bacterial aromatic polyketide family
- Synthesized by a type II polyketide synthase
Medchemexpress LLC Detomidine hydrochloride | 90038-01-0 | 99.83% | 1 ML
Detomidine hydrochloride is an imidazole derivative and a potent α2-adrenergic agonist. It produces dose-dependent analgesic effects. This product is for research use only and not sold to patients.
- Potent α2-adrenergic agonist
- Produces dose-dependent analgesic effects
- Exhibits cardiac and respiratory effects
- Has an antidiuretic action
- Available in solid and solution forms
- For research use only