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Filtered Search Results
Medchemexpress LLC Ganciclovir (sodium) | 107910-75-8 | 99.9% | 277.21 | 1 ML
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Ganciclovir (sodium) is a nucleoside analogue and an orally active antiviral agent effective against CMV. It exhibits in vitro activity against human herpes viruses (HSV 1 and 2, CMV) and various other DNA viruses, including several adenovirus serotypes. With an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1), this compound can also diffuse into the brain, making it a versatile tool for antiviral research.
- Nucleoside analogue antiviral agent
- Orally active and effective against CMV
- Active against herpes group and other DNA viruses
- Inhibits replication of human herpes viruses and adenovirus serotypes
- IC50 of 5.2 μM for feline herpesvirus type-1
- Capable of diffusing into the brain
- Superior activity against CMV compared to acyclovir
- Inhibits viral DNA replication through ganciclovir-5'-triphosphate
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Cayman Chemical MetoclopramIde-d3 1mg
An internal standard for the quantification of metoclopramide by GC- or LC-MS
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Sigma Aldrich Fine Chemicals Biosciences Azithromycin | 117772-70-0 | MFCD01862248 | 410mg
Azithromycin | Mol Wt: 785.02 | 117772-70-0 | MFCD01862248 | 410mg
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Sigma Aldrich Fine Chemicals Biosciences Cinchocaine hydrochloride European Pharmacopoeia (EP) Reference Standard | 61-12-1 | MFCD00012735 |
Cinchocaine hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 379.92 | 61-12-1 | MFCD00012735 |
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Sigma Aldrich Fine Chemicals Biosciences Dopamine hydrochloride British Pharmacopoeia (BP) Reference Standard | 62-31-7 | MFCD00012898 |
Dopamine hydrochloride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 189.64 | 62-31-7 | MFCD00012898 |
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Cayman Chemical R-CrIzotInIb 50mg
A dual inhibitor of c-Met and ALK (IC50s = 8 and 20 nM, respectively, in a cell-based assay); selective for c-Met and ALK over several other receptor and non-receptor tyrosine kinases, including Ron, Tie2, Abl, LCK, and VEGFR2 (IC50s = 0.08, 0.448, 1.159, 2.741, and >10 µM, respectively); selectively inhibits the proliferation of cancer cell lines with MET amplifications over cancer cell lines with MET or EGFR mutations (IC50s = 5-10, 472-1,284, and 767-787 nM, respectively); induces apoptosis in MET-amplified EBC-1 and NCI H1993 cells at 100 nM; reduces tumor volume in an EBC-1 mouse xenograft model at 25 mg/kg
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Sigma Aldrich Fine Chemicals Biosciences Naphazoline Related Compound A United States Pharmacopeia (USP) Reference Standard | 36321-43-4 | 30mg
Naphazoline Related Compound A United States Pharmacopeia (USP) Reference StandardPurity: | MW: 228.29 | 36321-43-4 | 30mg
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Sigma Aldrich Fine Chemicals Biosciences Anagrelide Related Compound C United States Pharmacopeia (USP) Reference Standard | 70381-75-8 | 25MG
Anagrelide Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 383.07 | 70381-75-8 | 25MG
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TARGETMOL CHEMICALS INC LODOXAMIDE TROMETHAMINE 5MG
Also available in 10 mg 25 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Lodoxamide tromethamine is a mast cell stabilizer with anti-allergic properties and can be used in studies about the treatment of asthma and allergic conjunctivitis. purity: 99%
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Selleck Chemical LLC Benzethonium Chloride S4162-50mg
Benzethonium chloride is a potent inhibitor of nAChRs it inhibits 4 2 nAChRs and 7 nAChRs with IC50 of 49 nM and 122 nM respectively
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Cerilliant Corporation CARISOPRODAL 1/MG PER ML
Carisoprodol, 1.0 mg/mL; 1 mL/ampoule
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Medchemexpress LLC Venlafaxine-d6 hydrochloride | 1062606-12-5 | 98.2% | 319.90 | C17H22D6ClNO2 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Venlafaxine-d6 hydrochloride is the deuterium-labeled hydrochloride salt of venlafaxine, provided as a high-purity analytical standard for bioanalytical and mass spectrometry applications. It is intended for use as an internal standard in quantitative assays to improve accuracy and precision. The substance has CAS 1062606-12-5 and molecular weight 319.90.
- Deuterium-labeled internal standard for LC-MS/MS quantitation
- High purity (98.2%) for reliable analytical performance
- Hydrochloride salt form, stable under typical storage conditions
- Suitable for pharmacokinetic and toxicology studies
- Supplied in verified small quantities for reference use
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Medchemexpress LLC Tofacitinib | 477600-75-2 | MFCD22628813 | 99.9% | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Tofacitinib (Standard) is an analytical reference standard of the JAK inhibitor tofacitinib supplied for research and analytical use. It is provided as a high-purity material suitable for method development, calibration, and quantitative analysis; not for human or clinical use.
- Analytical reference standard for HPLC and LC-MS method development.
- High purity suitable for quantitative assay calibration.
- Supplied in small pack sizes for laboratory testing.
- Applicable as an in vitro pharmacology reference compound.
- Not for human or clinical use; intended for research only.
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Med Vet International Voriconazole 200mg Tablet White Ovl 30 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Voriconazole 200mg Tablet White Ovl 30 Tablets.
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Medchemexpress LLC Imatinib | 152459-95-5 | MFCD05662257 | C29H31N7O | 10 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Imatinib is an orally bioavailable tyrosine kinase inhibitor that selectively inhibits BCR/ABL, v-Abl, PDGFR, and c-kit kinase activity. It functions by binding near the ATP binding site, locking it in a closed or self-inhibited conformation, thereby semicompetitively inhibiting the enzyme activity of the protein. It is also an inhibitor of SARS-CoV and MERS-CoV and acts as an antineoplastic agent.
- Orally bioavailable tyrosine kinase inhibitor
- Selectively inhibits BCR/ABL, v-Abl, PDGFR, and c-kit kinase activity
- Functions by binding close to the ATP binding site
- Inhibits SARS-CoV and MERS-CoV
- Acts as an antineoplastic agent
- Used for the treatment of chronic myelogenous leukemia and gastrointestinal stromal tumours
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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