Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Cefadroxil European Pharmacopoeia (EP) Reference Standard | 66592-87-8 |
Cefadroxil European Pharmacopoeia (EP) Reference Standard | Mol Wt: 381.4 | 66592-87-8 |
Sigma Aldrich Fine Chemicals Biosciences Propafenone Related Compound B United States Pharmacopeia (USP) Reference Standard | 88308-22-9 | 50MG
Propafenone Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 339.43 | 88308-22-9 | 50MG
Sigma Aldrich Fine Chemicals Biosciences Isoprenaline impurity A European Pharmacopoeia (EP) Reference Standard | 16899-81-3 |
Isoprenaline impurity A European Pharmacopoeia (EP) Reference Standard | Mol Wt: 245.7 | 16899-81-3 |
Medchemexpress LLC Chloromethyl propyl carbonate | 35273-90-6 | MFCD19232313 | 5g
Tenofovir Impurity 54 (Chloromethyl Propyl Carbonate) is an impurity of Tenofovir (HY-13910)
Selleck Chemical LLC Idoxuridine S1883-1g
Idoxuridine (NSC 39661 SKF 14287 5-Iodo-2 -deoxyuridine 5-IUdR IdUrd) is an antiviral agent for feline herpesvirus type-1 with IC50 of 4 3 M
Sigma Aldrich Fine Chemicals Biosciences Ketorolac Related Compound A United States Pharmacopeia (USP) Reference Standard | 167105-80-8 | 20MG
Ketorolac Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 358.39 | 167105-80-8 | 20MG
Sigma Aldrich Fine Chemicals Biosciences Tolcapone Related Compound B United States Pharmacopeia (USP) Reference Standard | 134612-80-9 | 25MG
Tolcapone Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 287.27 | 134612-80-9 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Carboprost trometamol European Pharmacopoeia (EP) Reference Standard | 58551-69-2 | MFCD01694769 |
Carboprost trometamol European Pharmacopoeia (EP) Reference Standard | Mol Wt: 489.64 | 58551-69-2 | MFCD01694769 |
ILEX LIFE SCIENCES LLC PAN Biotech Nystatin Suspension 10000 U per ml in DPBS cell culture antifungal 600 ML 1/EA
PAN-Biotech Nystatin Suspension 10 000 U/ml in DPBS cell culture antifungal 6 x 100 ml DESCRIPTION PAN-Biotech Nystatin Suspension 10 000 U/ml in DPBS is a fungistatic and fungicidal polyene antibiotic commonly used as a cell culture media supplement to control fungal contamination Its mode of action is by increasing the permeability of the cell membrane of sensitive fungi by binding to sterols mainly ergosterol Its main action is against Candida species Nystatin is produced by Streptomyces noursei and Streptomyces aureus APPLICATION Nystatin solution is often used as a cell culture media supplement to prevent contamination with fungi it has no antibacterial activity LIQUID/POWDER liquid STERILE Yes STORAGE TEMP -20 C MANUFACTURER PAN-Biotech GmbH COUNTRY OF ORIGIN Germany USAGE This product is intended for Laboratory Research Use Only Not for use in diagnostic or therapeutic procedures
Medchemexpress LLC Sitagliptin impurity 4 | 486459-98-7 | 500mg
Sitagliptin impurity 4 is an impurity of Sitagliptin (HY-13749)
Medchemexpress LLC Tafamidis meglumine | 951395-08-7 | 99.8% | 503.33 | 5 MG
Tafamidis meglumine is a potent and selective transthyretin (TTR) stabilizer. It shows comparable potency and efficacy to the mutant homotetramers V30M-TTR, V122I-TTR, and wild type WT-TTR, with EC50s of 2.7-3.2 μM. Tafamidis meglumine inhibits amyloidogenesis.
- Potent and selective transthyretin (TTR) stabilizer
- Inhibits amyloidogenesis
- Comparable potency and efficacy to mutant homotetramers V30M-TTR, V122I-TTR, and wild type WT-TTR
- Binds selectively to thyroxine-binding sites of the tetramer
- Kinetically stabilizes TTR
Medchemexpress LLC Tivantinib (ARQ 197) | 905854-02-6 | 99.6% | 369.42 | 5 MG
Tivantinib is a highly selective c-Met tyrosine kinase inhibitor with a Ki of 355 nM. It is a low-molecular-weight compound and the first orally available selective inhibitor of c-Met. Tivantinib selectively inhibits c-Met activity in cell-free and cell-based assays, causing dose-dependent loss of proliferative capacity or caspase-dependent apoptosis in c-Met-expressing cancer cell lines.
- Highly selective c-Met tyrosine kinase inhibitor
- Ki of 355 nM
- Selectively inhibits c-Met activity in cell-free and cell-based assays
- First orally available selective inhibitor of c-Met
- Inhibits constitutive c-Met phosphorylation in HT29 and MKN-45 cells, and HGF-induced c-Met phosphorylation in MDA-MB-231 and NCI-H441 cells with an IC50 of 100 to 300 nM
- Strongly inhibits c-Met phosphorylation in human colon xenograft tumors (HT29)
Medchemexpress LLC Dabigatran impurity 9 | 211915-00-3 | MFCD27996082 | 25mg
Dabigatran impurity 9 is an impurity of Dabigatran (HY-10163)