Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Famotidine Related Compound F United States Pharmacopeia (USP) Reference Standard | 107880-74-0 | 25MG
Famotidine Related Compound F United States Pharmacopeia (USP) Reference Standard | Mol Wt: 260.34 | 107880-74-0 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Daunorubicinone United States Pharmacopeia (USP) Reference Standard | 21794-55-8 | 25MG
Daunorubicinone United States Pharmacopeia (USP) Reference Standard | Mol Wt: 398.36 | 21794-55-8 | 25MG
Medchemexpress LLC Naphazoline | 835-31-4 | 99.7% | 210.27 | 50 MG
Naphazoline is a potent α-adrenergic receptor agonist that reduces vascular hyperpermeability and promotes vasoconstriction. It also reduces the levels of inflammatory factors (TNF-α, IL-1β and IL-6), cytokines (IFN-γ and IL-4), IgE, GMCSF, and NGF. It can be used for non-bacterial conjunctivitis research.
- Reduces vascular hyperpermeability.
- Promotes vasoconstriction.
- Reduces inflammatory factors.
- Reduces cytokines.
- Reduces IgE, GMCSF, and NGF.
- Suitable for non-bacterial conjunctivitis research.
Medchemexpress LLC Talazoparib tosylate | 1373431-65-2 | 507274 | 99.9% | 552.55 | 50 MG
Talazoparib tosylate (BMN 673ts) is a novel, potent, and orally available PARP1/2 inhibitor with an IC50 of 0.57 nM for PARP1. It is for research use only and has not been fully validated for medical applications.
- Potent PARP1/2 inhibitor
- Orally available
- Suitable for research applications
TARGETMOL CHEMICALS INC DINOPROST TROMETHAMINE S 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Dinoprost tromethamine salt (PGF2(alpha) THAM) is a naturally occurring prostaglandin used in medicine to induce labor and as an abortifacient. purity: 99%
Medchemexpress LLC Naphazoline | 835-31-4 | 99.7% | 210.27 | 100 MG
Naphazoline (Naphthazoline) is a potent α-adrenergic receptor agonist that reduces vascular hyperpermeability and promotes vasoconstriction. It can also reduce levels of inflammatory factors, cytokines, IgE, GMCSF, and NGF, making it suitable for non-bacterial conjunctivitis research.
- Reduces vascular hyperpermeability
- Promotes vasoconstriction
- Reduces levels of inflammatory factors (TNF-α, IL-1β and IL-6)
- Reduces levels of cytokines (IFN-γ and IL-4)
- Reduces levels of IgE, GMCSF, and NGF
- Can be used for non-bacterial conjunctivitis research
Medchemexpress LLC Folic acid | 59-30-3 | 99.0% | 441.40 | 1 ML
Folic acid is an orally active essential nutrient from the B complex group of vitamins. It has shown antidepressant-like effects and can reduce the risk of neonatal neural tube defects. It can also be used in research for megaloblastic and macrocytic anemias due to its deficiency.
- An orally active essential nutrient from the B complex group of vitamins.
- Shows antidepressant-like effects.
- Reduces the risk of neonatal neural tube defects.
- Can be used to research megaloblastic and macrocytic anemias due to its deficiency.
Medchemexpress LLC Itacitinib adipate | 1334302-63-4 | 99.2% | 699.66 | 5 MG
Itacitinib adipate is an orally bioavailable and selective JAK1 inhibitor that has been tested for efficacy and safety in a phase II trial in myelofibrosis. It is suitable for research use only.
- Orally bioavailable
- Selective JAK1 inhibitor
- Tested in phase II trial for myelofibrosis
- Suitable for research use
Medchemexpress LLC Ranitidine | 66357-35-5 | MFCD00081180 | 99.9% | 25 MG
Ranitidine is a potent, selective, and orally active histamine H2-receptor antagonist that inhibits gastric secretion. It has been shown to inhibit breast tumor development and spread in mice, and also antagonizes histamine-induced effects in isolated rat tissues.
- Potent, selective, and orally active H2-receptor antagonist
- Inhibits gastric acid secretion
- Antagonizes histamine-induced effects in isolated rat atrium and uterine horn
- Inhibits breast tumor development and spread
- Reduces specific myeloid cell populations in mice
- Increases latency of breast tumorigenesis
Medchemexpress LLC Ketorolac (tromethamine salt) | 74103-07-4 | MFCD00887595 | 99.5% | 1 G
Ketorolac tromethamine salt is a non-steroidal anti-inflammatory agent that acts as a nonselective COX inhibitor. With IC50s of 20 nM for COX-1 and 120 nM for COX-2, this compound is intended for laboratory chemical use and substance manufacturing, and is for research use only.
- Non-steroidal anti-inflammatory agent
- Nonselective COX inhibitor
- Solid appearance
- Purity of 99.5%
- IC50 of 20 nM for COX-1
- IC50 of 120 nM for COX-2
Medchemexpress LLC Nitisinone | 104206-65-7 | 99.93% | 5 MG
Nitisinone is an orally active, competitive, and reversible 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) inhibitor. It promotes tyrosine accumulation in a dose-dependent manner and is utilized in studies of hereditary tyrosinemia type 1 (HT-1) and albinism.
- Orally active 4-HPPD inhibitor
- Promotes tyrosine accumulation
- Used in studies of hereditary tyrosinemia type 1 (HT-1)
- Applicable in albinism research
- Purity of 99.93%
Medchemexpress LLC Nitisinone | 104206-65-7 | 100 MG
Nitisinone is an orally active, competitive, and reversible 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) inhibitor with an IC50 of 173 nM. It promotes tyrosine accumulation in a dose-dependent manner and can be used in studies of hereditary tyrosinemia type 1 (HT-1) and albinism.
- Orally active and competitive 4-HPPD inhibitor
- Promotes tyrosine accumulation
- Useful in studies of hereditary tyrosinemia type 1 (HT-1)
- Applicable in studies of albinism
Selleck Chemical LLC Neratinib (HKI-272) 100mg 698387-09-6
Neratinib (HKI-272) is a highly selective HER2 and EGFR inhibitor with IC50 of 59 nM and 92 nM in cell-free assays; weakly inhibits KDR and Src, no significant inhibition to Akt, CDK1/2/4, IKK-2, MK-2, PDK1, c-Raf and c-Met. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Fluticasone propionate-d5 | 1093258-28-6 | 91.7% | 1 MG
Fluticasone propionate-d5 is a deuterium labeled form of Fluticasone propionate. It is a potent topical anti-inflammatory corticosteroid and a selective glucocorticoid receptor agonist with an absolute affinity (KD) of 0.5 nM. It exhibits little to no activity at other steroid receptors and possesses anti-viral activity.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC Amoxicillin | 26787-78-0 | 99.9% | 1 ML
Amoxicillin is an antibiotic characterized by good oral absorption and broad-spectrum antimicrobial activity. It functions by inhibiting the biosynthesis of polypeptides in the cell wall, which in turn inhibits cell growth. This product is intended for research use only.
- Antibiotic with good oral absorption
- Broad-spectrum antimicrobial activity
- Inhibits biosynthesis of polypeptides in the cell wall
- Inhibits cell growth
- For research use only