Drug Standards
Apexbio Technology LLC Econazole nitrate 24169-02-6 1g
Econazole nitrate (24169-02-6) is a small-molecule inhibitor targeting the enzyme 14 -demethylase It is designed to disrupt ergosterol synthesis in fungal membrane sterol biosynthesis thereby decreasing membrane integrity altering permeability and attenuating fungal cellular growth Econazole nitrate exerts its biological activity primarily through inhibition of 14 -demethylase In vitro studies demonstrate antifungal activity with reported IC50 values against various fungal isolates typically ranging from approximately 0 05 to 1 g/mL depending on experimental parameters and organism specificity Based on these pharmacological properties econazole nitrate holds research potential in antifungal susceptibility testing exploration of drug resistance mechanisms in fungal strains characterization of dermatopathogenic microorganisms and drug target identification studies
TARGETMOL CHEMICALS INC Lynestrenol 50MG
Also available in 5 mg, 10 mg, 25 mg, 100 mg and bulk. Please contact Fisher for quotes. Lynestrenol is a synthetic progestational hormone, is the progesterone receptor agonist Purity 99.47%
Selleck Chemical LLC Siponimod (BAF312) 5mg 1230487-00-9
BAF312 (Siponimod) is a next-generation S1P receptor agonist, selective for S1P1 and S1P5 receptors with EC50 of 0.39 nM and 0.98 nM, exhibits >1000-fold selectivity over S1P2, S1P3 and S1P4 receptors. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Norfloxacin | 70458-96-7 | MFCD00079532 | 98.3% | 319.33 | 500 MG
Norfloxacin (MK-0366) is a broad-spectrum antibiotic active against both Gram-positive and Gram-negative bacteria, functioning by inhibiting DNA gyrase. It is a synthetic chemotherapeutic antibacterial agent sometimes used for common and complicated urinary tract infections.
- Broad-spectrum antibiotic
- Active against Gram-positive bacteria
- Active against Gram-negative bacteria
- Inhibits DNA gyrase
- Synthetic chemotherapeutic antibacterial agent
- Used for urinary tract infections
Medchemexpress LLC Deacetyl Ganoderic Acid F | 100665-44-9 | 1 MG
Deacetyl Ganoderic Acid F is a 7-anostane triterpenoid from *Ganoderma lucidum*. It is presented as a white to off-white solid with a purity of 98.82%.
- Purity of 98.82%
- Molecular weight: 528.63
- Formula: C30H40O8
- Appearance: White to off-white solid
- Structure classification: Terpenoids, triterpenes
- Initial source: Plants, Polyporaceae
- For research use only
- Store at 4°C, sealed, away from moisture
Enzo Life Sciences Tamoxifen. citrate (1g). CAS: 54965-24-1
Antiestrogen with anti-cancer activity. Selective protein kinase C (PKC) inhibitor and induces PKC epsilon translocation. Induces apoptosis in estrogen receptor-negative human cancer cell lines. Alternative name: (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethyl-ethanamine . citrate. Purity: ≥99% (Assay). Appearance: White to off-white powder. Solubility: Soluble in methanol or ethanol; very slightly soluble in water or acetone. Long Term Storage: +4°C.
Sigma Aldrich Fine Chemicals Biosciences Nitrofural impurity B European Pharmacopoeia (EP) Reference Standard | 92-55-7 | MFCD00003244 |
Nitrofural impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 243.17 | 92-55-7 | MFCD00003244 |
Cayman Chemical Salbutamol-d9 1mg
An internal standard for the quantification of salbutamol by GC- or LC-MS
Medchemexpress LLC 1'-epi Gemcitabine hydrochloride | 122111-05-1 | C9H12ClF2N3O4 | 5 MG
1'-epi Gemcitabine hydrochloride is an isomer of Gemcitabine hydrochloride and can be used as an experimental control. It is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent that inhibits DNA synthesis and repair, resulting in autophagy and apoptosis.
- Isomer of Gemcitabine hydrochloride
- Can be used as an experimental control
- Pyrimidine nucleoside analog antimetabolite
- Antineoplastic agent
- Inhibits DNA synthesis and repair
- Results in autophagy and apoptosis
- For research use only
Medchemexpress LLC Cariprazine hydrochloride | 1083076-69-0 | 99.9% | 463.87 | 100 MG
Cariprazine hydrochloride is a novel antipsychotic agent candidate with high affinity for D3 (Ki=0.085 nM) and D2 (Ki=0.49 nM) receptors, and moderate affinity for the 5-HT1A receptor (Ki=2.6 nM).
- Demonstrates high potency in stimulating inositol phosphate (IP) formation.
- Exhibits approximately 10-fold higher affinity for human D3 versus human D2L and D2S receptors.
- Displays high affinity and pure antagonism at human serotonin (5-HT) type 2B receptors.
- More potent than Aripiprazole in inhibiting isoproterenol-induced cAMP production in HEK-293 cells.
- Achieves dose-dependent dopamine D2/D3 receptor occupancy.
- Significantly reduces ouabain-induced hyperactivity.
eMolecules 1228182-47-5 | Medchem Express | Fenbendazole-d3 | 1mg | 705861420 | HY-B0413S | 302.37 | C15H13N3O2S
Medchem Express | Aldoxorubicin | 5mg | 446267301 | HY-16261 | 1361644-26-9 | MFCD15146982 | 750.758 | C37H42N4O13
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