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Filtered Search Results
U S PHARMACOPEIA MENAQUINONE VITAMIN K2
NC2594584 MENAQUINONE VITAMIN K2
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eMolecules 1347815-21-7 | Naphthalene-1,4-dithiocarboxamide | Oakwood Chemicals | MFCD20265223 | 246.350 | C12H10N2S2 | 0.000 | NC(=S)c1ccc(C(N)=S)c2ccccc12 | 5g | 480147477
Naphthalene-1,4-dithiocarboxamide | Oakwood Chemicals | 1347815-21-7 | MFCD20265223 | 246.350 | C12H10N2S2 | 0.000 | NC(=S)c1ccc(C(N)=S)c2ccccc12 | 5g | 480147477
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eMolecules 92-44-4 | 2,3-Dihydroxynaphthalene | Ambeed | MFCD00004073 | 160.172 | C10H8O2 | 98.000 | Oc1cc2ccccc2cc1O | 25g | 552747162
2,3-Dihydroxynaphthalene | Ambeed | 92-44-4 | MFCD00004073 | 160.172 | C10H8O2 | 98.000 | Oc1cc2ccccc2cc1O | 25g | 552747162
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Medchemexpress LLC Octopamine hydrochloride | 770-05-8 | 99.9% | 1 G
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Octopamine hydrochloride is a biogenic monoamine structurally related to noradrenaline. It functions as a neurohormone, neuromodulator, and neurotransmitter in invertebrates, stimulating alpha2-adrenoceptors and increasing various metabolic processes. It mediates behaviors like learning and memory, regulates endocrine gland activity, and mobilizes lipids and carbohydrates through specific G protein-coupled receptors.
- Acts as a neurohormone, neuromodulator, and neurotransmitter
- Stimulates alpha2-adrenoceptors (ARs)
- Increases glycogenolysis, glycolysis, oxygen uptake, gluconeogenesis, and portal perfusion pressure
- Regulates sensory input desensitization, arousal, and rhythmic behaviors
- Involved in complex behaviors like learning and memory
- Regulates endocrine gland activity
- Induces lipid and carbohydrate mobilization
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Medchemexpress LLC Antazoline hydrochloride | 2508-72-7 | 99.6% | 500 MG
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Antazoline hydrochloride | 2508-72-7 | 99.6% | 500 MG
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Medchemexpress LLC (2S)-3-[3-[[3-cyano-4-(difluoromethyl)-6-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]pyridin-2-yl]amino | 3043939-18-7 | 97.8% | 489.58 g/mol | C24H29F2N5O2S | 10 MG
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BI-9787 is a potent, zwitterionic ketohexokinase (KHK) inhibitor provided for research use. It exhibits low-nanomolar potency against human KHK isoforms, shows good metabolic stability, and has been characterized in preclinical pharmacokinetic studies.
- Potent KHK inhibitor with reported IC50 values of 12 nM (hKHK-A) and 12.8 nM (hKHK-C).
- Zwitterionic structure supporting permeability and oral exposure in preclinical models.
- Demonstrated metabolic stability and favorable pharmacokinetic properties in rat studies.
- High chemical purity (~97.8%) suitable for research applications.
- Molecular weight 489.58 g/mol; formula C24H29F2N5O2S.
- Available in small pack sizes for dosing and in vivo work.
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Medchemexpress LLC Paroxetine hydrochloride hemihydrate | 110429-35-1 | 100.0% | 1 ML
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Paroxetine hydrochloride hemihydrate | 110429-35-1 | 100.0% | 1 ML
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Medchemexpress LLC Mk-571 | 115104-28-4 | 98.85% | 515.09 | 50 MG
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MK-571 is an orally active, potent, and selective competitive leukotriene D4 (LTD4) receptor antagonist. It demonstrates Ki values of 0.22 nM in guinea pig lung and 2.1 nM in human lung membranes. This compound also functions as an MRP4 and ABCC1 (MRP1) inhibitor, effectively inhibiting constitutive and antigen-stimulated S1P (sphingosine-1-phosphate) release.
- Orally active
- Potent and selective competitive leukotriene D4 (LTD4) receptor antagonist
- Acts as an MRP4 and ABCC1 (MRP1) inhibitor
- Inhibits constitutive and antigen-stimulated S1P release
- Recommended storage at 4°C, protected from light
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Medchemexpress LLC Buflomedil (hydrochloride) | 35543-24-9 | 99.8% | 10 G
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Buflomedil hydrochloride is a vasodilator agent and an orally active α1A-adrenoceptor antagonist. It is primarily used for the study of peripheral circulatory disorders and exhibits specific Ki values for α1A-AR and α1B-AR.
- Vasodilator agent
- Orally active α1A-adrenoceptor antagonist
- Used in the study of peripheral circulatory disorders
- Ki of 4.06 μM for rat α1A-adrenergic receptor
- Ki of 6.84 μM for α1B-adrenergic receptor
- Purity of 99.8%
- Molecular formula: C17H26ClNO4
- Molecular weight: 343.85
- Appearance: white to off-white solid
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Medchemexpress LLC BI-4020 | 2664214-60-0 | 99.3% | 1 ML
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BI-4020 is a fourth-generation, orally active, and non-covalent EGFR tyrosine kinase inhibitor. It shows activity against various EGFR variants, including the triple mutant EGFR del19 T790M C797S, the double mutant EGFR del19 T790M, and primary mutant EGFR del19. It also exhibits activity against EGFR wt.
- Inhibits EGFR del19 T790M C797S variant with an IC50 of 0.2 nM
- Inhibits EGFR del19 T790M and EGFR del19 with an IC50 of 1 nM
- Exhibits high kinome selectivity
- Possesses good DMPK properties
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Medchemexpress LLC 2-naphthalen-1,3,4,5,6,7,8-d7-amine | 93951-94-1 | MFCD00142864 | 99.0% | 150.23 g/mol | C10H2ND7 | 5 MG
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2-Naphthalen-1,3,4,5,6,7,8-d7-amine is the deuterium-labeled form of 2-aminonaphthalene supplied for laboratory research use as an isotopically labeled reference standard. It is intended for analytical applications such as mass spectrometry, tracer experiments, and metabolic studies; handle and store according to the product SDS and supplier recommendations.
- Deuterium-labeled internal standard for mass spectrometry.
- High isotopic enrichment suitable for quantitative analysis.
- Available in small milligram pack sizes for analytical workflows.
- Stable as a powder under low-temperature storage when handled per SDS instructions.
- Commonly used in tracer, metabolic, and pharmacokinetic studies.
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eMolecules 90-13-1 | 1-Chloronaphthalene | Combi-Blocks | MFCD00003874 | 162.620 | C10H7Cl | 85.000 | Clc1cccc2ccccc12 | 25g | 485192721
1-Chloronaphthalene | Combi-Blocks | 90-13-1 | MFCD00003874 | 162.620 | C10H7Cl | 85.000 | Clc1cccc2ccccc12 | 25g | 485192721
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Medchemexpress LLC Quinpirole hydrochloride | 85798-08-9 | 100.0% | 1 ML
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Quinpirole hydrochloride (LY 171555 hydrochloride) is a high-affinity agonist of dopamine D2/D3 receptor. This chemical is provided as a white to light yellow solid with a high purity of 99.97%, and is intended for research use only.
- High-affinity agonist of dopamine D2/D3 receptor
- Purity: 99.97%
- Molecular Weight: 255.79
- Appearance: White to light yellow solid
- Shipping: Room temperature in continental US
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month.
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eMolecules 113826-06-5 | (2R)-(-)-Glycidyl tosylate | Ambeed | MFCD00010834 | 228.260 | C10H12O4S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@H]1CO1 | 1g | 552609531
(2R)-(-)-Glycidyl tosylate | Ambeed | 113826-06-5 | MFCD00010834 | 228.260 | C10H12O4S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@H]1CO1 | 1g | 552609531
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TARGETMOL CHEMICALS INC BI-2493 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. BI-2493 is a highly selective pan-KRAS inhibitor and structural analog of BI-2865.BI-2493 exhibits antitumor activity and inhibits tumor cell growth and can be used in the study of cancerous diseases.BI-2493 is a highly selective pan-KRAS inhibitor and structural analog of BI-2865. purity: 99%
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