Drug Standards
Cayman Chemical Itraconazole 250mg
An antifungal agent and hedgehog pathway inhibitor; inhibits hedgehog signaling (IC50 = 0.8 μM); binds to 14-α sterol demethylase/CYP51 isoform B (Kd = 31 nM for A. fumigatus enzyme expressed in E. coli); inhibits ergosterol biosynthesis in C. neoformans (IC50 = 6 nM after 16 hours); inhibits C. neoformans growth by 50% at 3.2 nM; suppresses growth of medulloblastomas in a Ptch+/-p53-/- mouse allograft model at 100 mg/kg twice daily; reduces viral titers of several enteroviruses in infected cells from 1.25-100 µM
Sigma Aldrich Fine Chemicals Biosciences S-Nitroso-N-acetyl-DL-penicillamine | 67776-06-1 | MFCD00272624 | 25 mg
S-Nitroso-N-acetyl-DL-penicillamine | Purity: ≥97% | Mol Wt: 220.25 | 67776-06-1 | MFCD00272624 | 25 mg
TARGETMOL CHEMICALS INC N-desmethyl Enzalutamide 25MG
Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. N-desmethyl Enzalutamide (N-desmethyl MDV 3100) is the active Enzalutamide metabolite.It is the active metabolite of Enzalutamide. N-desmethyl Enzalutamide demonstrates primary and secondary pharmacodynamics of similar potency to Enzalutamide and circulates at approximately the same plasma concentrations as enzalutamide. Purity 99.74%
TARGETMOL CHEMICALS INC Bromfenac sodium hydrate 500MG
Also available in 1 mL, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Bromfenac sodium hydrate (Bromfenac monosodium salt sesquihydrate) is the sodium salt form of bromfenac, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and anti-inflammatory properties. Upon ophthalmic administration, bromfenac binds to and inhibits cyclooxygenase II (COX II), an enzyme that converts arachidonic acid to cyclic endoperoxides, which are prostaglandin (PG) precursors. By inhibiting PG formation, bromfenac prevents PG-induced inflammation, vasodilation, leukocytosis, disruption of the blood-aqueous humor barrier, increased vascular permeability, and elevated intraocular pressure (IOP). Purity 99.65%
TARGETMOL CHEMICALS INC Fexofenadine 100MG
Also available in 1 mL, 10 mg, 25 mg, 50 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Fexofenadine (Carboxyterfenadine), an antihistamine pharmaceutical drug, is used to treat allergy symptoms, such as nasal congestion, hay fever, and urticaria. Compared to first-generation antihistamines, Fexofenadine is less able to pass the blood-brain barrier and cause sedation. Purity 99.87%
Cayman Chemical Fluconazole 5g
A triazole antifungal agent that is effective against most Candida strains
Cayman Chemical HaloperIdol 500mg
A typical antipsychotic and dopamine D2-like receptor antagonist (Kis = 0.6, 0.2, and 22 nM, for D2, D3, and D4 receptors, respectively); An inverse agonist at D2 and D3 receptors (IC50s = 0.8 and 0.6 nM, respectively); binds to α1- and α2- adrenergic and histamine H1 receptors, as well as 5-HT receptor subtypes 5-HT1D and 5-HT2A (Kds = 17, 600, 260, 40, and 61 nM, respectively); inhibits stereotypic behavior induced by apomorphine and amphetamine in rats (ID50s = 0.532 and 0.101 μmol/kg, respectively); inhibits apomorphine-induced decreases in prepulse inhibition of the acoustic startle response in rats in a dose-dependent manner
Medchemexpress LLC Bumetanide | 28395-03-1 | 99.97% | 364.42 | 25 MG
Bumetanide (Standard) is the analytical standard of Bumetanide, intended for research and analytical applications. It is a highly potent loop diuretic and a Na+-K+-Cl+ cotransporter (NKCC) blocker. Bumetanide selectively inhibits NKCC1, and also inhibits NKCC2. This compound is used as a reference standard in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard for research and analytical applications.
- Highly potent loop diuretic.
- Na+-K+-Cl+ cotransporter (NKCC) blocker.
- Selective NKCC1 inhibitor, also inhibits NKCC2.
- Used in HPLC, GC, and MS research experiments.
Selleck Chemical LLC Zelavespib10mg
Zelavespib (PU-H71, NSC 750424) is a potent and selective inhibitor of HSP90 with IC50 of 51 nM. Phase 1. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Ranitidine
Ranitidine(AH-19065) is an H2 histamine receptor antagonist that works by blocking histamine and thus decreasing the amount of acid released by cells of the stomach
Selleck Chemical LLC Pantoprazole sodium hydrate
Pantoprazole (BY10232 SKF96022) sodium hydrate (Protonix) is a potent inhibitor of H /K( )-ATPase with IC50 of 6 8 M
Selleck Chemical LLC Estradiol dipropionate
Estradiol dipropionate (17-Beta-Estradiol-3 17-Dipropionate) is a semisynthetic steroidal estrogen which has been used in hormone therapy for menopausal symptoms and low estrogen levels in women and in the treatment of gynecological disorders
Selleck Chemical LLC Metoclopramide
Metoclopramide is a dopamine antagonist used for the treatment of nausea and vomiting