Phenoxy compounds
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Filtered Search Results
![eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148824.JPG-250.jpg)
eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
(S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | 58879-34-8 | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
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Medchemexpress LLC SRC INHIBITOR 1 5MG
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Src Inhibitor 1 is a potent, ATP-competitive and selective dual site Src tyrosine kinase inhibitor with IC50 values of 44 nM for Src and 88nM for Lck.CAS No. : 179248-59-0
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Medchemexpress LLC BMS-191095 | 166095-21-2 | 98.0% | C22H21ClN4O2 | 100 MG
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BMS-191095 is a selective activator of mitochondrial ATP-sensitive potassium (mitoKATP) channels, inhibiting human platelet aggregation by opening mitochondrial K(ATP) channels. It induces mitochondrial depolarization of vascular smooth muscle (VSM) cells and dose-dependently induces vasodilation in endothelium-denuded cerebral arteries. BMS-191095 also reduces neuronal damage in rats with transient focal cerebral ischemia.
- Induces mitochondrial depolarization of vascular smooth muscle (VSM) cells.
- Dose-dependently induces vasodilation in endothelium denuded cerebral arteries.
- Increases the frequency of calcium sparks in VSM cells.
- Inhibits human platelet aggregation induced by collagen and thrombin.
- Reduces neuronal damage in rats with transient focal cerebral ischemia.
- Reduces total infarct volume and induces rapid mitochondrial depolarization in rats with ischemia.
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Sigma Aldrich Fine Chemicals Biosciences Otilonium bromide >=98% (HPLC) | 26095-59-0 | MFCD00211142 | 5MG
Otilonium bromide >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 563.57 | 26095-59-0 | MFCD00211142 | 5MG
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![eMolecules 103188-94-9 | Benzyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-beta-D-glucopyranoside | Apollo Scientific488.580 | C30H32O6 | 0.000 | C=CCO[C@@H]1[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)O[C@@H]2COC(O[C@@H]12)c1ccccc1 | 500mg | 603091257](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502155404.JPG-250.jpg)
eMolecules 103188-94-9 | Benzyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-beta-D-glucopyranoside | Apollo Scientific488.580 | C30H32O6 | 0.000 | C=CCO[C@@H]1[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)O[C@@H]2COC(O[C@@H]12)c1ccccc1 | 500mg | 603091257
Benzyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-beta-D-glucopyranoside | Apollo Scientific | 103188-94-9488.580 | C30H32O6 | 0.000 | C=CCO[C@@H]1[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)O[C@@H]2COC(O[C@@H]12)c1ccccc1 | 500mg | 603091257
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Enzo Life Sciences Suberoyl bis-hydroxamic acid (100mg). CAS: 38937-66-5
Induces cellular differentiation. Inhibits histone deacetylation. Purity: ≥95% (TLC). Solubility: Soluble in DMSO. Long Term Storage: Ambient.
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eMolecules 173952-44-8 | Medchem Express | SYM2206 | 5mg | 446269307 | HY-18689 | MFCD00946571 | 366.421 | C20H22N4O3
Medchem Express | EST73502 (monohydrochloride) | 5mg | 569407474 | HY-134189A | 2535970-65-9 | 388.880 | C19H27ClF2N2O2
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Medchemexpress LLC HY-114091 5mg Medchemexpress, PF-00356231 (hydrochloride) CAS:820223-77-6 Purity:>98%
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Medchemexpress, HY-114091 5mg PF-00356231 (HCl) CAS:820223-77-6 PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). PF-00356231 hydrochloride binds to MMP-12 and forms PF-00356231/MMP-12 complex. PF-00356231 hydrochloride shows potency against MMP-13, MMP-8, MMP-9, MMP-3 with IC50s of 0.00065, 1.7, 0.98, 0.39 μM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Eltoprazine hydrochloride | 98206-09-8 | 99.3% | 256.73 | 5 MG
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Eltoprazine hydrochloride (DU 28853) is a 5-HT1A/5-HT1B receptors agonist and a 5-HT2C receptor antagonist. It shows antiaggressive and anxiogenic effects.
- Acts as a 5-HT1A/5-HT1B receptors agonist.
- Acts as a 5-HT2C receptor antagonist.
- Shows antiaggressive and anxiogenic effects.
- For research use only.
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eMolecules 2682097-49-8 | (S)-(1-Methylazetidin-2-yl)methanamine dihydrochloride | 100mg
Pharmablock | 4-chloro-8-methoxy-2-methylquinoline | 25mg | 794216359 | PB96024 | 64951-58-2 | MFCD00272401 | 207.660 | C11H10ClNO
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Selleck Chemical LLC AST-487
AST-487 (NVP-AST487) a N N -diphenyl urea is an ATP competitive inhibitor of Flt3 with ki of 0 12 M Besides FLT3 AST487 also inhibits RET KDR c-KIT and c-ABL kinase with IC50 values below 1 M
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eMolecules 103860-60-2 | 2,3-Dihydroxynaphthalene-1,4-dicarbaldehyde | MFCD09800457 | 100mg
Medchem Express | Terevalefim | 5mg | 665626281 | HY-137455 | 1070881-42-3 | 176.240 | C9H8N2S
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Sigma Aldrich Fine Chemicals Biosciences Otilonium bromide >=98% (HPLC) | 26095-59-0 | MFCD00211142 | 25MG
Otilonium bromide >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 563.57 | 26095-59-0 | MFCD00211142 | 25MG
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Medchemexpress LLC HY-107658 5mg Medchemexpress, SN 6 CAS:415697-08-4 Purity:>98%
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Medchemexpress, HY-107658 5mg SN 6 CAS:415697-08-4 SN 6 is a selective Na+/Ca2+ exchanger (NCX) inhibitor, and inhibits 45Ca2+ uptake by NCX1, NCX2, and NCX3, with IC50s of 2.9, 16, and 8.6 μM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Propoxycaine hydrochloride | 550-83-4 | 99.7% | 100 MG
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Propoxycaine hydrochloride inhibits voltage-gated sodium channels, and thereby inhibits the ionic flux required for the initiation and conduction of impulses. Propoxycaine hydrochloride application can lead to a loss of sensation.
- Sodium channel inhibitor
- Inhibits voltage-gated sodium channels
- Inhibits the ionic flux required for the initiation and conduction of impulses
- Can lead to a loss of sensation
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