Drug Standards
Cambridge Isotope Laboratories Nornicotine (unlabeled) 100 ug/mL in MTBE 1 2 mL
Nornicotine (unlabeled) 100 ug/mL in MTBE 1 2 mL
Selleck Chemical LLC Flurbiprofen S1679-50mg
Flurbiprofen is a member of the phenylalkanoic acid derivative family of non-steroidal anti-inflammatory drugs (NSAIDs)
Selleck Chemical LLC Mitotane S1732-1g
Mitotane (NCI-C04933) is an antineoplastic medication used in the treatment of adrenocortical carcinoma
Medchemexpress LLC Triamcinolone hexacetonide | 5611-51-8 | 532.64 | 25 MG
Triamcinolone hexacetonide is a commonly used, long-acting steroid for the treatment of subacute and chronic inflammatory joint diseases. This compound is intended for research use only.
- Used in the treatment of subacute and chronic inflammatory joint diseases.
- Shows a dose-dependent protective effect against chemically induced articular cartilage damage.
- Reduces chondrocyte cloning, osteophyte formation, and fibrillation in animal models.
- Local application may reduce mechanical sensitivity and enhance regeneration after nerve injury.
- High purity of 98.06%.
- Appears as a white to off-white solid.
- Soluble in DMSO for in vitro applications.
Selleck Chemical LLC Crizotinib S1068-1g
Crizotinib is a potent inhibitor of c-Met and ALK with IC50 of 11 nM and 24 nM in cell-based assays respectively It is also a potent ROS1 inhibitor with Ki value less than 0 025 nM Crizotinib induces autophagy through inhibition of the STAT3 pathway in multiple lung cancer cell lines
Selleck Chemical LLC Nilotinib S1033-100mg
Nilotinib is a selective Bcr-Abl inhibitor with IC50 less than 30 nM in Murine myeloid progenitor cells Nilotinib induces autophagy through AMPK activition
Selleck Chemical LLC Fenticonazole Nitrate S2031-10mg
Fenticonazole Nitrate(Lomexin REC 15-1476 Falvin) is an azole antifungal agent
Selleck Chemical LLC Imatinib Mesylate S1026-5g
Imatinib Mesylate is an orally bioavailability mesylate salt of Imatinib which is a multi-target inhibitor of v-Abl c-Kit and PDGFR with IC50 of 0 6 M 0 1 M and 0 1 M in cell-free or cell-based assays respectively Imatinib Mesylate (STI571) induces autophagy
Sigma Aldrich Fine Chemicals Biosciences Sulfafurazole European Pharmacopoeia (EP) Reference Standard | 127-69-5 | MFCD00003150 |
Sulfafurazole European Pharmacopoeia (EP) Reference Standard | Mol Wt: 267.3 | 127-69-5 | MFCD00003150 |
Medchemexpress LLC Fenofibrate | 49562-28-9 | 99.9% | 360.83 | 1 ML
Fenofibrate is a selective peroxisome proliferator-activated receptor alpha (PPARα) agonist with an EC50 of 30 μM. It also demonstrates inhibitory activity against various human cytochrome P450 isoforms. This compound is widely utilized in cardiovascular disease and cancer research.
- Selective PPARα agonist
- Inhibits human cytochrome P450 isoforms (CYP2C19, CYP2B6, CYP2C9, CYP2C8, CYP3A4)
- Useful in cardiovascular disease and cancer research
- Supplied as a 10 mM solution in 1 mL DMSO
- Appearance is a solid with a melting point of 80-81°C
- High purity of 99.92%
- Stable for 3 years as powder at -20°C or 1 year in solvent at -80°C
Selleck Chemical LLC Bromfenac Sodium S4248-1g
Bromfenac Sodium (AHR 10282R Bromsite Bromday Prolensa Xibrom) is a nonsteroidal anti-inflammatory drug (NSAID) which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2
Selleck Chemical LLC Enoxaparin sodium S5415-100mg
Enoxaparin sodium(PK 10169) is a low-molecular-weight heparin used to prevent and treat deep vein thrombosis or pulmonary embolism It binds to and accelerates the activity of antithrombin III
Enzo Life Sciences Amiloride hydrochloride dihydrate (1g). CAS: 17440-83-4
Selectively blocks low threshold (T-type) calcium channel (KD=30μM) with no effect on L-type channels or tetrodotoxin Na+ channels. Inhibits the epithelial tetrodotoxin insensitive Na+ channel (IC50 =1μM). Clinically useful K+ sparing diuretic. Alternative name: 3 5-Diamino-N-(aminoiminomethyl)-6-chloropyrazinecarboxamide HCl 2H2O. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO (25mg/ml) or water (1mg/ml warm). Long Term Storage: Ambient.
Selleck Chemical LLC Minocycline HCl S4226-1g
Minocycline HCl is the most lipid soluble and most active tetracycline antibiotic binds to the 30S ribosomal subunit preventing the binding of tRNA to the mRNA-ribosome complex and interfering with protein synthesis
Apexbio Technology LLC Escitalopram 128196-01-0 100mg
Escitalopram (CAS 128196-01-0) is the S-( )-enantiomer of citalopram and functions as a selective serotonin reuptake inhibitor (SSRI) It exhibits high affinity for the human serotonin transporter with a Ki of 6 6 nM for inhibition of [3H]-5-HT uptake in COS-1 cells expressing 5-HTT and 3 9 nM for inhibition of [125I]-RTI-55 binding In rat brain synaptosome assays escitalopram potently inhibits [3H]-5-HT uptake (IC50 2 1 nM) while showing significantly lower affinity for norepinephrine (IC50 2500 nM) and dopamine (IC50 40000 nM) transporters It also displays moderate binding to rat histamine H1 and 1 sites Escitalopram is widely used in neuropharmacological research and preclinical studies modeling antidepressant and anxiolytic activity