Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Valsartan European Pharmacopoeia (EP) Reference Standard | 137862-53-4 | MFCD00865840 |
Valsartan European Pharmacopoeia (EP) Reference Standard | Mol Wt: 435.52 | 137862-53-4 | MFCD00865840 |
Sigma Aldrich Fine Chemicals Biosciences Nitazoxanide | 55981-09-4 | MFCD00416599 | 10mg
Nitazoxanide | Purity: 98% | Mol Wt: 307.28 | 55981-09-4 | MFCD00416599 | 10mg
Sigma Aldrich Fine Chemicals Biosciences Metaxalone Related Compound C United States Pharmacopeia (USP) Reference Standard | 805972-34-3 | 25MG
Metaxalone Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 373.49 | 805972-34-3 | 25MG
Medchemexpress LLC Quetiapine impurity 1 | 1076199-40-0 | MFCD11977896 | 399.51 | C21H25N3O3S | 5 MG
Quetiapine impurity 1 is a synthetic impurity related to the antipsychotic quetiapine, supplied for analytical reference and synthetic intermediate applications. Identifiers provided by the manufacturer include CAS 1076199-40-0, molecular formula C21H25N3O3S, and molecular weight 399.51 g·mol⁻¹.
- Used as an analytical reference and drug intermediate
- Supplied as a powder for laboratory handling and storage
- Molecular formula C21H25N3O3S
- Molecular weight 399.51 g·mol⁻¹
- CAS number 1076199-40-0 for unambiguous identification
Medchemexpress LLC Idoxuridine | 54-42-2 | 99.8% | 1 ML
Idoxuridine is an iodinated thymidine analogue that acts as a competitive inhibitor of phosphorylases. It inhibits viral activity, particularly viral eye infections like herpes simplex keratitis, by inhibiting DNA polymerase and affecting viral replication. It demonstrates an IC50 value of 4.3 μM against feline herpesvirus and shows anti-orthopoxvirus activity.
- Inhibits viral activity
- Acts as a competitive inhibitor of phosphorylases
- Inhibits DNA polymerase
- Affects viral replication
- Shows anti-orthopoxvirus activity
Medchemexpress LLC Diphenhydramine | 58-73-1 | 99.6% | 250 MG
Diphenhydramine is a first-generation histamine H1-receptor antagonist with an anti-cholinergic effect. Diphenhydramine hydrochloride can cross the ovine blood-brain barrier (BBB).
- Histamine H1-receptor antagonist
- Anti-cholinergic effect
- Can cross the ovine blood-brain barrier (BBB)
- Molecular weight: 255.35
- Molecular formula: C17H21NO
- Liquid appearance
- Colorless to light yellow
- In vitro solubility in DMSO: 100 mg/mL
- Targets H1 receptor and NMDA receptor
- IC50 for NMDA receptor: 24.6 μM
Medchemexpress LLC Iopamidol | 60166-93-0 | 99.9% | 50 MG
Iopamidol is a nonionic, X-Ray iodinated contrast agent (CA) suitable for various diagnostic applications. It contains amide and hydroxyl functionalities that can be utilized for generating chemical exchange saturation transfer (CEST) contrast. This product is for research use only.
- Nonionic, X-Ray iodinated contrast agent
- Suitable for a wide variety of diagnostic applications
- Amide and hydroxyl functionalities can be exploited for generating chemical exchange saturation transfer (CEST) contrast
- Can be used as a responsive MRI-chemical exchange saturation transfer contrast agent for pH mapping of kidneys in vivo
Medchemexpress LLC Latanoprost acid | 41639-83-2 | 95.1% | 390.51 | 10 MG
Latanoprost acid, an analog of prostaglandin (PG) F2α, is a selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor. It inhibits RANKL-induced osteoclastogenesis and function by inhibiting the ERK, AKT, JNK, and p38 cascade, followed by the c-fos/NFATc1 pathway. Latanoprost acid is also a medication used to lower pressure inside the eyes.
- Selective prostanoid receptor (FP) agonist.
- Activates the FP-PG receptor.
- Inhibits RANKL-induced osteoclastogenesis and function.
- Lowers pressure inside the eyes.
- Inhibits ERK, AKT, JNK, and p38 cascade.
- Reduces protein expressions of c-fos and NFATc1 in bone marrow-derived macrophages cells (BMMs).
- Significantly inhibits mature osteoclast formation.
- Notably prevents LPS-induced bone destruction in 8-week-old C57BL/6J mice.
Medchemexpress LLC Triamcinolone hexacetonide | 5611-51-8 | MFCD00867440 | 532.64 | 100 MG
Triamcinolone hexacetonide | 5611-51-8 | MFCD00867440 | 532.64 | 100 MG
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 S4226-200mg
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
Sigma Aldrich Fine Chemicals Biosciences Allopurinol British Pharmacopoeia (BP) Reference Standard | 315-30-0 | MFCD00599413 |
Allopurinol British Pharmacopoeia (BP) Reference Standard | Mol Wt: 136.11 | 315-30-0 | MFCD00599413 |
Apexbio Technology LLC Robenidine hydrochloride 25875-50-7 200mg
Robenidine hydrochloride (CAS 25875-50-7) is a small-molecule antimicrobial agent with activity against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) It is designed to inhibit these bacterial pathogens thereby interfering with microbial survival Robenidine hydrochloride exerts its biological activity primarily through disruption of microbial cell membrane integrity In in vitro studies Robenidine hydrochloride demonstrates inhibitory activity with MIC50 values of 8 1 M for MRSA and 4 7 M for VRE Based on these pharmacological properties Robenidine hydrochloride holds research potential in the fields of microbial infection drug resistance and the development of novel anti-infective strategies
Apexbio Technology LLC Neostigmine Bromide 114-80-7 500mg
Neostigmine Bromide (CAS 114-80-7) is a synthetic quaternary ammonium compound that acts as a reversible inhibitor of acetylcholinesterase (AChE) By blocking AChE activity neostigmine bromide prolongs the action of acetylcholine at neuromuscular junctions and cholinergic synapses thereby enhancing muscarinic and nicotinic receptor-mediated effects This compound is frequently studied in contexts involving neuromuscular function and its use extends to research on disorders such as myasthenia gravis postoperative urinary retention paralytic ileus and primary open-angle glaucoma Additionally it is investigated as an adjuvant for local anesthetics and opioids in pain management following gynecological or abdominal surgery
Sigma Aldrich Fine Chemicals Biosciences Butane 13 diol United Stat
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.