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Filtered Search Results
Med Vet International MED VET INTERNATIONAL
5000900733 MDM CP MLT-SYM 2MG/125MG 18CT
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Ambeed AMBEED
5000891180 COPPERII PIVALATE 250MG
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Ambeed AMBEED
5000891640 3-OXO CITALOPRAM 100MG
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Medchemexpress LLC CPD-1224 | 2891620-68-9 | C43H47ClN8O7S | 5 MG
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CPD-1224 is an orally effective ALK inhibitor that is a derivative of an ALK inhibitor connected to the cereblon ligand. It targets the EML4-ALK oncogenic fusion protein, degrading both ALK and its mutant forms L1196M/G1202R. This compound has the ability to slow down tumor growth.
- Orally effective ALK inhibitor.
- Targets and degrades the EML4-ALK oncogenic fusion protein.
- Degrades mutant forms L1196M/G1202R of ALK.
- Can slow down tumor growth.
- Significantly enhances kinase binding selectivity and exhibits good degradation selectivity.
- Has 28% oral bioavailability in mice.
- Inhibits tumor growth in mice at a dosage of 10 mg/kg, orally, twice daily for 15 days.
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Med Vet International MED VET INTERNATIONAL
5000898109 MECLIZINE HCL 25MG CHEWS 100CT
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Sigma Aldrich Fine Chemicals Biosciences Ibuprofen United States Ph50MG
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
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Medchemexpress LLC (±)-Naproxen | 23981-80-8 | MFCD00439456 | C14H14O3 | 5 G
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(±)-Naproxen is a racemate of Naproxen. It functions as a COX-1 and COX-2 inhibitor, with IC50 values of 8.72 and 5.15 μM, respectively.
- Racemate of naproxen
- Inhibits COX-1 and COX-2
- Purity of 99.79%
- Molecular weight: 230.26
- Solid appearance
- White to light yellow color
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Crescent Chemical Co Inc Pimaricin, 7681-93-8, MFCD00135085, 50mg
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Molecular Formula C33H47NO13, Molecular Weight 665.728, Pharma./veter. comp. (WS), Storage: +5°C
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Selleck Chemical LLC Celecoxib S1261-10mM/1mL
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Celecoxib is a selective COX-2 inhibitor with IC50 of 40 nM in Sf9 cells
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Apexbio Technology LLC Risperidone(Synonyms: Risperdal, Risperdal Consta, Belivon, Rispen, Risperin, Rispolept, Ridal, Risnia, Risperdone, Risperdaloro, Sequinan), 10mg, CAS: 106266-06-2.
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Risperidone (CAS 106266-06-2) is an atypical antipsychotic small molecule that functions predominantly as an antagonist at serotonin receptor subtype 5-HT2A and dopamine receptor D2 (D2DR) It exhibits high receptor binding affinity with inhibitory constants (Ki) of approximately 0 4 nM for 5-HT2A receptors and 3 13 nM for D2 receptors Due to these pharmacological properties risperidone serves as a valuable research tool to study neurotransmitter modulation and receptor signaling pathways associated with psychiatric disorders particularly schizophrenia and related psychoses
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Chemscene CHEMSCENE
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5000578045 CLOPIDOGREL-RELATED COMP 100MG
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Apexbio Technology LLC Zileuton 111406-87-2 10mM (in 1mL DMSO)
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Zileuton (CAS 111406-87-2) is a pharmacological inhibitor targeting the enzyme 5-lipoxygenase (5-LOX) It inhibits conversion of arachidonic acid to leukotriene precursors thereby attenuating formation of inflammatory leukotrienes (LTB4 LTC4 LTD4 LTE4) In rat leukocyte and basophilic leukemia assays Zileuton exhibits inhibition with reported IC50 values of 0 3 M and 0 5 M respectively Research demonstrates that Zileuton induces COX-2 expression and PGE2 synthesis via PKC -dependent activation of ERK1/2 and Akt suggesting cardioprotective potential against ischemia/reperfusion injury Additionally animal models indicate neuroprotective benefits by mitigating inflammatory responses after cerebral ischemia Clinically Zileuton is utilized for asthma management targeting leukotriene-mediated airway inflammation
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AdipoGen Diclofenac Impurity B
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Chemical. CAS 22121-58-0. Formula C13H9Cl2NO. MW 266.12. Diclofenac Impurity B is a degradation product of and a regulatory impurity in the drug Diclofenac which is a non-steroidal anti-inflammatory drug NSAID that is clinically used to treat inflammation associated with arthritis and gout as well as other pain or inflammatory disorders. This product can be used as a working standard or secondary analytical reference standard. It can also be used as an organic building block and intermediate for synthesis.
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U.S. Pharmacopeia LACOSAMIDE RELATED COMPOUND D
NC3812230 LACOSAMIDE RELATED COMPOUND D
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Cyclodextrin Technologies Development Hydroxypropyl BCD, 31g
Beta Cyclodextrin derivative for enhanced solubility >50g/100ml - meets USP/EP standards. Pharmaceutical Grade
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