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Filtered Search Results
Medchemexpress LLC HY-105917 5mg Medchemexpress, Endovion CAS:265646-85-3 Purity:>98%
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Medchemexpress, HY-105917 5mg Endovion CAS:265646-85-3 Endovion (NS3728) is a pharmacological anion channel inhibitor (like chloride channel) and the specific VRAC/VSOAC blocker. Endovion (NS3728) is also an Anoctamin-1 (ANO 1) channel inhibitor [1] [2] . 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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eMolecules 468747-17-3 | Medchem Express | mTOR inhibitor-1 | 5mg | 455326087 | HY-112914 | 363.211 | C16H15BrN2O3
Pharmablock | methyl 46-dichloropyridine-2-carboxylate | 25mg | 586143466 | PBGC022 | 98273-19-9 | MFCD12965121 | 206.020 | C7H5Cl2NO2
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![Medchemexpress LLC (2S)-2-[[3-cyclobutyl-5-(3,4,5-trifluorophenoxy)imidazo[4,5-b]pyridin-2-yl]methylamino]propanamide | 1233231-30-5 | 98.3% | 419.4 g/mol | C20H20F3N5O2 | 25MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000237969.png-250.jpg)
Medchemexpress LLC (2S)-2-[[3-cyclobutyl-5-(3,4,5-trifluorophenoxy)imidazo[4,5-b]pyridin-2-yl]methylamino]propanamide | 1233231-30-5 | 98.3% | 419.4 g/mol | C20H20F3N5O2 | 25MG
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DSP-2230 (ANP-230) is an orally active voltage-gated sodium channel inhibitor used in preclinical research to modulate Nav1.7, Nav1.8, and Nav1.9 activity and to evaluate approaches for neuropathic pain. The compound is supplied as a solid with characterized solubility profiles and storage recommendations for laboratory use only.
- Inhibits Nav1.7, Nav1.8, and Nav1.9 with reported IC50s of 7.1 μM, 11.4 μM, and 6.7 μM respectively.
- Reported purity 98.33%.
- Soluble in DMSO at ≥100 mg/mL; multiple in vivo formulation protocols with solubility ≥2.25 mg/mL are provided.
- Powder stability: -20°C for up to 3 years; solution stability conditions are reported.
- Intended for preclinical studies of sodium channel pharmacology and neuropathic pain models.
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eMolecules 1191908-14-1 | Medchem Express | ADRA1D receptor antagonist 1 | 5mg | 778475771 | HY-135270 | 337.2 | C15H14Cl2N4O
ChemScene | 3-Bromo-4-fluorobenzene-12-diamine | 100mg | 569145596 | CS-0098679 | 1257535-06-0 | MFCD18071059 | 205.030 | C6H6BrFN2
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Aobchem 2-Bromophenylboronic acid, AOBCHEM USA 10975-25G. 244205-40-1. MFCD01114672
2-Bromophenylboronic acid, AOBCHEM USA 10975-25G. 244205-40-1. MFCD01114672
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eMolecules 1114808-93-3 | 2-Benzyloxy-4-bromotoluene | Combi-Blocks | MFCD11520656 | 277.161 | C14H13BrO | 98.000 | Cc1ccc(Br)cc1OCc1ccccc1 | 1g | 117543435
2-Benzyloxy-4-bromotoluene | Combi-Blocks | 1114808-93-3 | MFCD11520656 | 277.161 | C14H13BrO | 98.000 | Cc1ccc(Br)cc1OCc1ccccc1 | 1g | 117543435
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![Medchemexpress LLC 3-[4-[(3S)-4-(4-Br-benzoyl)-3-(4-Cl-phenyl)piperazine-1-carbonyl]-5-methylpyrazol-1-yl]benzonitrile | 2095486-67-0 | 100.0% | 588.88 g/mol | C29H23BrClN5O2 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000246170.png-250.jpg)
Medchemexpress LLC 3-[4-[(3S)-4-(4-Br-benzoyl)-3-(4-Cl-phenyl)piperazine-1-carbonyl]-5-methylpyrazol-1-yl]benzonitrile | 2095486-67-0 | 100.0% | 588.88 g/mol | C29H23BrClN5O2 | 50 MG
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eIF4A3-IN-1 is a research-grade small-molecule inhibitor of the eukaryotic translation initiation factor eIF4A3, used in biochemical, cellular, and in vivo studies. It displays selective eIF4A3 inhibition with reported antitumor and analgesic activity in preclinical models. The compound is supplied as a high-purity solid or DMSO solution and is commonly formulated in DMSO for in vitro work.
- Selective inhibitor of eIF4A3 with demonstrated cellular activity.
- High purity suitable for analytical and biological assays.
- Available as solid and as 10 mM solution in DMSO for convenient dosing.
- Recommended solvent for in vitro use: DMSO; in vivo example: 10% DMSO in corn oil.
- Stable when stored frozen as powder or in solution under recommended conditions.
- Suitable for biochemical assays, cell-based studies, and in vivo preclinical models.
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eMolecules 119162-53-7 | 5-Amino-3-(4-bromophenyl)isoxazole | Chem-Impex | MFCD06199354 | 239.072 | C9H7BrN2O | 99.000 | Nc1cc(no1)-c1ccc(Br)cc1 | 1g | 112761107
5-Amino-3-(4-bromophenyl)isoxazole | Chem-Impex | 119162-53-7 | MFCD06199354 | 239.072 | C9H7BrN2O | 99.000 | Nc1cc(no1)-c1ccc(Br)cc1 | 1g | 112761107
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Medchemexpress LLC CP-547632 hydrochloride | 252003-71-7 | MFCD20268381 | 99.9% | C20H25BrClF2N5O3S | 10MG
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CP-547632 hydrochloride is the hydrochloride salt form of a potent, orally active ATP-competitive inhibitor of VEGFR-2 and FGF kinases, with reported IC50 values of 11 nM and 9 nM, respectively. It demonstrates selectivity versus EGFR and PDGFRβ and has shown antitumor efficacy in preclinical models.
- ATP-competitive VEGFR-2 and FGF kinase inhibition.
- Low-nanomolar potency (IC50s ≈11 nM and ≈9 nM).
- Selective profile versus related tyrosine kinases.
- Suitable for in vitro and in vivo preclinical studies.
- High supplied purity (~99.9%).
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eMolecules 70146-78-0 | DIETHYL 2-(4-BROMOBENZYL)MALONATE | AstaTech | MFCD00017852 | 329.190 | C14H17BrO4 | 95.000 | CCOC(=O)C(Cc1ccc(Br)cc1)C(=O)OCC | 1g | 432789531
DIETHYL 2-(4-BROMOBENZYL)MALONATE | AstaTech | 70146-78-0 | MFCD00017852 | 329.190 | C14H17BrO4 | 95.000 | CCOC(=O)C(Cc1ccc(Br)cc1)C(=O)OCC | 1g | 432789531
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eMolecules 1148050-30-9 | 3-(4-Bromophenyl)-1,1,1-trifluoro-2-propanol | Combi-Blocks, Inc. | MFCD16615965 | 269.061 | C9H8BrF3O | 97.000 | OC(Cc1ccc(Br)cc1)C(F)(F)F | 1g | 603154569
3-(4-Bromophenyl)-1,1,1-trifluoro-2-propanol | Combi-Blocks, Inc. | 1148050-30-9 | MFCD16615965 | 269.061 | C9H8BrF3O | 97.000 | OC(Cc1ccc(Br)cc1)C(F)(F)F | 1g | 603154569
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Sigma Aldrich Fine Chemicals Biosciences 3-Bromotoluene 98% | 591-17-3 | MFCD00000085 | 25G
3-Bromotoluene 98% | Purity: 98% | Mol Wt: 171.03 | 591-17-3 | MFCD00000085 | 25G
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eMolecules METHYL 3-((3-BROMOPHENOXY)METHYL)BENZOATE | 148255-19-0 | MFCD03290349 | 1g
AstaTech | METHYL 3-((3-BROMOPHENOXY)METHYL)BENZOATE | 1g | 432789545 | 20689 | 95.000 | 148255-19-0 | MFCD03290349 | 321.170 | C15H13BrO3
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eMolecules 17878-47-6 | (3-Bromophenyl)trimethylsilane | MFCD00093882 | 25g
Medchem Express | Emidurdar | 5mg | 455325932 | HY-105917 | 265646-85-3 | 495.183 | C16H9BrF6N6O
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Medchemexpress LLC HY-111798A 5mg Medchemexpress, HO-1-IN-1 hydrochloride CAS:1092851-70-1 Purity:>98%
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Medchemexpress, HY-111798A 5mg HO-1-IN-1 hydrochloride CAS:1092851-70-1 HO-1-IN-1 hydrochloride (Compound 2) is a heme oxygenase 1 ( HO-1 ) inhibitor with an IC 50 of 250 nM [1] . 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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