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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Schizandrin European Pharmacopoeia (EP) Reference Standard | 7432-28-2 | MFCD00905761 |
Schizandrin European Pharmacopoeia (EP) Reference Standard | Mol Wt: 432.51 | 7432-28-2 | MFCD00905761 |
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Cayman Chemical 4-hydroxy FlurbIprofen 10mg
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A major active metabolite of flurbiprofen, (R)-flurbiprofen, and (S)-flurbiprofen; inhibits COX-1 by 94% at 1,000 µM but does not inhibit oxygenation of arachidonic acid; completely inhibits cyclooxygenation of 2-AG at 300 µM; inhibits FAAH hydrolysis of anandamide in rat brain homogenates (IC50 = 84 µM at a pH of 6)
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Sigma Aldrich Fine Chemicals Biosciences Gemcitabine hydrochloride | 122111-03-9 | MFCD01735988 | 50mg
Gemcitabine hydrochloride | Purity: 98% | Mol Wt: 299.66 | 122111-03-9 | MFCD01735988 | 50mg
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Research Products International Corp Ketoconazole 100 MG
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Ketoconazole is an antifungal used for its ability to inhibit the growth of various fungi. It belongs to the azole class of antifungals and works by disrupting the synthesis of ergosterol, an essential component of fungal cell membranes. Without proper ergosterol production, the fungal cell membrane becomes weakened and permeable, leading to the death of the fungus.
Ketoconazole can be utilized to study the effects of inhibiting fungal growth and to explore potential antifungal treatments. Its mechanism of action and broad-spectrum antifungal activity make it a valuable tool in understanding fungal biology and developing strategies for controlling fungal infections.
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Medchemexpress LLC Butylated hydroxytoluene-d21 | 64502-99-4 | MFCD00209760 | 98.7% | 241.48 | C15H3D21O | 5mg
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Butylated hydroxytoluene-d21 is the deuterium labeled Butylated hydroxytoluene[1] Butylated hydroxytoluene is an antioxidant widely used in foods and in food-related products[2] Butylated hydroxytoluene is a Ferroptosis inhibitor[3]
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Sigma Aldrich Fine Chemicals Biosciences Reserpine, 50-55-5, MFCD00005091, 1 g
Empirical Formula (Hill Notation): C33H40N2O9, Molecular Weight: 608.68, crystallized, ≥99.0% (HPLC), mp: ~265 °C, Synonym: (3β, 16β, 17α, 18β, 20α)-11,17-Dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylic acid methyl ester.
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Sigma Aldrich Fine Chemicals Biosciences Thiamazole European Pharmacopoeia (EP) Reference Standard | 60-56-0 | MFCD00179321 |
Thiamazole European Pharmacopoeia (EP) Reference Standard | Mol Wt: 114.17 | 60-56-0 | MFCD00179321 |
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Sigma Aldrich Fine Chemicals Biosciences Captopril British Pharmacopoeia (BP) Reference Standard | 62571-86-2 | MFCD00168073 |
Captopril British Pharmacopoeia (BP) Reference Standard | Mol Wt: 217.29 | 62571-86-2 | MFCD00168073 |
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Sigma Aldrich Fine Chemicals Biosciences Paclitaxel from semisynthetic, >=97% | 33069-62-4 | MFCD00869953 | 5MG
Paclitaxel from semisynthetic, >=97% | Purity: >=97% | Mol Wt: 853.91 | 33069-62-4 | MFCD00869953 | 5MG
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Sigma Aldrich Fine Chemicals Biosciences Thioguanine United States Pharmacopeia (USP) Reference Standard | 154-42-7 | MFCD00233553 | 200MG
Thioguanine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 167.19 | 154-42-7 | MFCD00233553 | 200MG
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Medchemexpress LLC (R)-Ketorolac | 66635-93-6 | 99.7% | 10 MM 1 ML
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(R)-Ketorolac is an orally active inhibitor of Cdc42 and Rac1. It inhibits GTPase and modifies ovarian cancer cell behaviors crucial for invasion and metastasis. This compound also ameliorates cancer-associated cachexia.
- Inhibits Cdc42 and Rac1
- Inhibits GTPase activity
- Modifies ovarian cancer cell behaviors for invasion and metastasis
- Ameliorates cancer-associated cachexia
- Decreases filopodia number and length
- Reduces cell adherence to fibronectin and collagen
- Prolongs survival in C26 tumour-bearing mice
- Alleviates C26-induced weight loss
- Prevents C26-induced T-lymphopenia
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Apexbio Technology LLC Cefpodoxime Proxetil 87239-81-4 10mM (in 1mL DMSO)
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Cefpodoxime Proxetil is an oral prodrug belonging to the third-generation cephalosporin antibiotics After absorption it undergoes enzymatic hydrolysis in vivo converting to the active metabolite cefpodoxime Cefpodoxime exerts antibacterial activity by binding bacterial penicillin-binding proteins (PBPs) and inhibiting peptidoglycan synthesis thus preventing proper cell wall formation and ultimately leading to bacterial growth inhibition Cefpodoxime Proxetil is routinely employed in biomedical research studies to evaluate its antibacterial spectrum pharmacokinetics bioavailability and bacterial resistance mechanisms Additionally researchers utilize this compound for investigating antibacterial potential via in vitro and in vivo experiments with typical IC50 values varying based on bacterial strains and experimental conditions
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Sigma Aldrich Fine Chemicals Biosciences Irbesartan British Pharmacopoeia (BP) Reference Standard | 138402-11-6 | MFCD00864464 |
Irbesartan British Pharmacopoeia (BP) Reference Standard | Mol Wt: 428.53 | 138402-11-6 | MFCD00864464 |
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Cayman Chemical TemozolomIde AcId 25mg
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An active metabolite of temozolomide; cytotoxic to TLX5 murine lymphoma cells; a synthetic intermediate in the synthesis of temozolomide prodrugs with anticancer activity
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Medchemexpress LLC Meropenem trihydrate | 119478-56-7 | 99.9% | 437.51 | 25 MG
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Meropenem trihydrate is a carbapenem antibiotic with broad-spectrum antibacterial activity. It inhibits bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBPs).
- Intrinsically stable to dehydropeptidase-1 (DHP-1) degradation
- Broad-spectrum in vitro activity against many Gram-positive, Gram-negative, and anaerobic bacteria
- Targets β-lactam
- Active against susceptible and resistant N. gonorrhoeae, H. influenzae, and H. ducreyi
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