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Filtered Search Results
Medchemexpress LLC Dacomitinib impurity 13 | 5mg
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Dacomitinib impurity 13 is an impurity of Dacomitinib (HY-13272)
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Matrix Scientific SULFAMIDE-25G
Sulfamide, 25g,H4N2O2S, MFCD00011606, mw 96.11, [7803-58-9]
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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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Apexbio Technology LLC Flurbiprofen 5104-49-4 100mg
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Flurbiprofen (CAS 5104-49-4) is a nonsteroidal anti-inflammatory compound that functions as an inhibitor of cyclooxygenase (COX) enzymes thereby reducing the synthesis of prostaglandins involved in inflammatory processes This small molecule is frequently employed in biomedical research to study the molecular mechanisms underlying inflammation and to assess potential therapeutic strategies for inflammatory conditions such as osteoarthritis and rheumatoid arthritis Its well-characterized pharmacological profile makes it a valuable tool for preclinical studies investigating pathways associated with pain and inflammation
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Sigma Aldrich Fine Chemicals Biosciences Letrozole European Pharmacopoeia (EP) Reference Standard | 112809-51-5 | MFCD00866241 |
Letrozole European Pharmacopoeia (EP) Reference Standard | Mol Wt: 285.3 | 112809-51-5 | MFCD00866241 |
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Cayman Chemical EscItalopram 25mg
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A selective serotonin reuptake inhibitor; selectively binds to SERT (Ki = 0.89 nM) over the norepinephrine and dopamine transporters (Kis = >10,000 and 8,150 nM, respectively); inhibits 5-HT reuptake in rat brain synaptosomes (IC50 = 2.1 nM); reduces immobility in the forced swim test in mice (ED50 = 12 mg/kg) and increases exploratory behavior in the black-and-white box test in mice (MED = 0.49 mg/kg); prevents acid sphingomyelinase activation and subsequent ceramide release induced by pp-VSV-SARS-CoV-2 infection in Vero cells at 20 µM
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Medchemexpress LLC (1R)-2-chloro-1-(3,4-difluorophenyl)-1-ethanol | 1212376-05-0 | MFCD09863591 | 1g
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Ticagrelor impurity 89 is an impurity of Ticagrelor (HY-10064)
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Sigma Aldrich Fine Chemicals Biosciences Paliperidone Related Compound A United States Pharmacopeia (USP) Reference Standard | 849903-79-3 | 20MG
Paliperidone Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 208.26 | 849903-79-3 | 20MG
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Sigma Aldrich Fine Chemicals Biosciences Penicillin G procaine United States Pharmacopeia (USP) Reference Standard | 6130-64-9 | 200MG
Penicillin G procaine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 588.72 | 6130-64-9 | 200MG
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Sigma Aldrich Fine Chemicals Biosciences Orphenadrine Related Compound B United States Pharmacopeia (USP) Reference Standard | 93940-17-1 | 20MG
Orphenadrine Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 333.9 | 93940-17-1 | 20MG
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![Medchemexpress LLC Ethyl 3-(1-methyl-2-oxo-N-(pyridin-2-yl)-2,3-dihydro-1H-benzo[d]imidazole-5-carboxamido)propanoate | 1642853-67-5 | MFCD30741307 | 50mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267749.png-250.jpg)
Medchemexpress LLC Ethyl 3-(1-methyl-2-oxo-N-(pyridin-2-yl)-2,3-dihydro-1H-benzo[d]imidazole-5-carboxamido)propanoate | 1642853-67-5 | MFCD30741307 | 50mg
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Dabigatran impurity 29 (Dabigatran impurity F) is an impurity of Dabigatran (HY-10163)
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Medchemexpress LLC Sulfamerazine | 127-79-7 | 99.8% | 1 ML
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Sulfamerazine (RP-2632) is a sulfonamide antibacterial. It is the monomethyl derivative of sulfadiazine, specifically 2-sulfanilamido-4-methylpyrimidine. This sulfonamide drug inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA) for binding to dihydropteroate synthesizes.
- Functions as a sulfonamide antibacterial.
- Inhibits bacterial synthesis of dihydrofolic acid.
- Competes with para-aminobenzoic acid (PABA) for binding.
- Monomethyl derivative of sulfadiazine.
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Medchemexpress LLC 3S 4S -Tivantinib | 100MG
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3S 4S -Tivantinib | 100MG
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Sigma Aldrich Fine Chemicals Biosciences Guaifenesin United States200mg
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 Tenofovir alafenamide hemifumarate | 1392275-56-7 | C21H29N6O5P.1/2 C4H4O4 | 50 MG
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Tenofovir alafenamide hemifumarate is an investigational oral prodrug of Tenofovir, an HIV-1 nucleotide reverse transcriptase inhibitor. It offers good oral bioavailability and increased plasma stability compared to Tenofovir disoproxil fumarate (TDF).
- Antiviral activities range from 5 to 7 nM across all cell types
- CC50 varies from 4.7 to 42 μM for MT-4 and MT-2 cells, respectively
- Effective against a panel of HIV-1 and HIV-2 isolates
- Mean EC50 for 29 primary HIV-1 isolates in PBMCs is 3.5 nM
- Mean EC50 for HIV-2 isolates is 1.8 nM
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