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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences GR 89696 fumarate salt solid | 126766-32-3 | MFCD00274044 | 25MG
GR 89696 fumarate salt solid | Mol Wt: 530.4 | 126766-32-3 | MFCD00274044 | 25MG
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Selleck Chemical LLC Cediranib Maleate S5242-10mg
Cediranib Maleate (AZD2171) is the maleate salt of Cediranib which is a potent inhibitor of VEGFR with IC50 of 1 nM and also inhibits Flt1/4 with IC50 of 5 nM/ 3 nM
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Medchemexpress LLC AZD9496 maleate | ≥95.0% | 2 MG
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AZD9496 maleate is a potent and selective estrogen receptor (ERα) antagonist. It acts as an orally bioavailable selective oestrogen receptor degrader (SERD).
- Potent and selective ERα antagonist
- Orally bioavailable selective oestrogen receptor degrader (SERD)
- IC50 of 0.28 nM
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eMolecules 103-60-6 | 2-Phenoxyethyl isobutyrate | Ambeed | MFCD00027363 | 208.257 | C12H16O3 | 98.000 | CC(C)C(=O)OCCOc1ccccc1 | 25g | 490489950
2-Phenoxyethyl isobutyrate | Ambeed | 103-60-6 | MFCD00027363 | 208.257 | C12H16O3 | 98.000 | CC(C)C(=O)OCCOc1ccccc1 | 25g | 490489950
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Selleck Chemical LLC Timolol Maleate S4123-50mg
Timolol Maleate (MK-950 (S)-Timolol Maleate) is a non-selective beta-adrenergic receptor antagonist for 1/ 2 with Ki of 1 97 nM/2 0 nM
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Selleck Chemical LLC Indacaterol Maleate S3083-1g
Indacaterol (QAB149) is an ultra-long-acting -adrenoceptor agonist with pKi of 7 36 for 1-adrenoceptor and pKi of 5 48 for 2-adrenoceptor
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Ambeed 2-BROMOETHYL METHACRYLATE -25G
2-Bromoethyl methacrylate | 4513-56-8 | MFCD00045051 |
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Selleck Chemical LLC Timolol Maleate S4123-1g
Timolol Maleate (MK-950 (S)-Timolol Maleate) is a non-selective beta-adrenergic receptor antagonist for 1/ 2 with Ki of 1 97 nM/2 0 nM
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Apexbio Technology LLC Cinepazide maleate 26328-04-1 10mM (in 1mL DMSO)
Cinepazide maleate (CAS 26328-04-1) is the maleate salt of cinepazide classified as a vasodilatory agent It exerts its effects primarily through inhibition of calcium influx in vascular smooth muscle cells leading to vessel relaxation and increased blood flow This mechanism is associated with reduced peripheral resistance and enhanced microcirculation Cinepazide maleate has been utilized in research exploring vascular tone modulation cerebral blood flow and ischemia models providing a tool for investigating mechanisms of vasodilation and circulatory disorders in preclinical settings
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eMolecules 4392-24-9 | 3-Phenyl-2-propenyl bromide | Ambeed197.075 | C9H9Br | 98.000 | BrCC=Cc1ccccc1 | 5g | 525881520
3-Phenyl-2-propenyl bromide | Ambeed | 4392-24-9197.075 | C9H9Br | 98.000 | BrCC=Cc1ccccc1 | 5g | 525881520
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Chemscene ChemScene | Benzyl propiolate | 250MG | CS-0109544 | 0.95 | 14447-01-9| MFCD11976128 | 160.17
ChemScene | Benzyl propiolate | 250MG | CS-0109544 | 0.95 | 14447-01-9| MFCD11976128 | 160.17
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1PLUSCHEM LLC Ingenol mebutate | 75567-37-2 | 430.5 g/mol | 1MG
Ingenol mebutate | 75567-37-2 | 430.5 g/mol | 1MG
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TARGETMOL CHEMICALS INC FLUPIRTINE MALEATE 200MG
Also available in 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Flupirtine maleate (Katadolon maleate) a centrally acting non-opioid analgesia is the salt form of Flupirtine. It is an NMDA receptor antagonist and also a specific neuronal potassium channel opener. purity: 99%
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Medchemexpress LLC Ciproxifan maleate | 184025-19-2 | C20H22N2O6 | 1 ML
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Ciproxifan maleate is a potent, selective, orally bioavailable, and competitive antagonist of the histamine H3-receptor, with an IC50 of 9.2 nM. It shows low apparent affinity at other receptor subtypes and can be used for the research of aging disorders and Alzheimer's disease.
- Inhibits [3H]HA release from synaptosomes of rat cerebral cortex (Ki: 0.5 nM).
- Inhibits binding of [125I]iodoproxyfan with rat striatal membranes (Ki: 0.7 nM).
- Increases t-MeHA level in mouse brain (ED50: 0.14 mg/kg).
- Improves accuracy of responding in five-choice tasks in rats.
- Induces neocortical electroencephalogram activation and waking state in cats.
- Decreases H3-receptor ligand concentration in serum in mice.
- Exhibits oral bioavailability (F=62%) and maximal concentration (Cmax=420 nM) in mice.
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Medchemexpress LLC U-99194 maleate (U-99194A) | 234757-41-6 | 99.2% | 50 MG
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U-99194 (PNU-99194) maleate is a selective and potent dopamine D3 receptor antagonist. It inhibits the activation of D3 receptors mediated by endogenously released dopamine or exogenous D3 agonists. This compound can be used for the study of dopamine D3 receptor-mediated motor disorders, particularly kinetic tremors.
- Selective, potent dopamine D3 receptor antagonist (Ki = 160 nM).
- Inhibits D3 receptor activation.
- Abrogates IPSC-suppressive effect of D3 agonist PD 128907 in rat hippocampal slices.
- Significantly suppresses nicotine-induced tremor in mice.
- Useful for studying dopamine D3 receptor-mediated motor disorders, especially kinetic tremors.
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