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Filtered Search Results
Medchemexpress LLC Mpt0b390 | 1817802-18-8 | 98.8% | C17H17N3O5S | 100 MG
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MPT0B390 is an arylsulfonamide-based derivative that exhibits potent HDAC inhibitory ability. It acts as a TIMP3 inducer and is shown to inhibit tumor growth, metastasis, and angiogenesis. This compound demonstrates antiproliferative activity against the human colon cancer cell line HCT116 with a GI50 of 0.03 μM.
- Exhibits potent HDAC inhibitory ability
- Acts as a TIMP3 inducer
- Inhibits tumor growth, metastasis, and angiogenesis
- Demonstrates antiproliferative activity against human colon cancer cell line HCT116 with a GI50 of 0.03 μM
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Cay10614 10Mg | HY-135042:10MG
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Cay10614 10Mg
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Medchemexpress LLC 5-Amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid | 61348-28-5 | 98.0% | 246.26 | 100 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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5-Amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid is a glutamine derivative. It is for research use only and not sold to patients. Amino acids and amino acid derivatives, such as this product, have been commercially used as ergogenic supplements due to their influence on anabolic hormone secretion, fuel supply during exercise, mental performance under stress, and prevention of exercise-induced muscle damage. They are recognized as beneficial ergogenic dietary substances.
- For research use only
- Glutamine derivative
- Influences anabolic hormone secretion
- Supplies fuel during exercise
- Enhances mental performance under stress
- Prevents exercise-induced muscle damage
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Fitusiran | 1499251-18-1 | 94.7% | C78H139N11O30 | 10MG
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Fitusiran is a small interfering RNA (siRNA) that targets antithrombin (AT) messenger RNA in the liver to lower AT production and thereby increase thrombin generation. It is supplied as a research-grade, chemically modified oligonucleotide for preclinical and biochemical studies in coagulation and hemophilia research.
- Targets antithrombin mRNA to reduce antithrombin levels.
- Increases thrombin generation for coagulation studies.
- Contains chemically modified nucleotides for enhanced stability.
- Provided with reported purity suitable for research use.
- Supplied in small pack sizes for preclinical and in vitro experiments.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Tris(2,4-di-tert-butylphenyl)phosphate | 95906-11-9 | MFCD29918884 | 99.8% | 662.92 | 250 MG
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Tris(2,4-di-tert-butylphenyl)phosphate is an active compound derived from the leaves of Vitex negundo L. It exhibits anti-inflammatory activity, demonstrated by its inhibition of secretory Phospholipase A2 (sPLA2) through molecular docking.
- Derived from the leaves of Vitex negundo L.
- Exhibits anti-inflammatory activity.
- Inhibits secretory Phospholipase A2 (sPLA2) through molecular docking.
- Reduces paw edema volume in a carrageenan-induced paw edema model.
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Medchemexpress LLC Chlorogenic acid butyl ester | 132741-56-1 | 410.42 | 50 MG
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Chlorogenic acid butyl ester, a caffeoylquinic acid, is a potent melanogenesis inhibitor. It inhibits the expression of microphtalmia-associated transcription factor (MITF), tyrosinase, tyrosinerelated protein 1 (TRP-1), and TRP-2. This compound also demonstrates antioxidant activity.
- Caffeoylquinic acid
- Exhibits inhibitory activities with 33-62% reduction of melanin content at 100 μM concentration on a-MSH-stimulated B16 melanoma cells
- Potent melanogenesis inhibitor
- Inhibits expression of MITF, tyrosinase, TRP-1, and TRP-2
- Shows antioxidant activity
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Pfaltz & Bauer VALEROPHENONE 99% 5G
Valerophenone 99% 5G CAS# 1009-14-9
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Medchemexpress LLC Pyrano[2,3-c]pyrazole-5-carbonitrile, 6-amino-4-cyclobutyl-4-(3,5-dichlorophenyl)-1,4-dihydro-3-meth | 1508286-18-7 | 99.9% | 50 MG
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SHMT-IN-1 is a potent inhibitor of plasmodial serine hydroxymethyltransferase (SHMT) and exhibits antitumor activity.
- Potent inhibitor of SHMT
- Exhibits antitumor activity
- Target: SHMT
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Medchemexpress LLC O-Nornuciferine | 3153-55-7 | 5 MG
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O-Nornuciferine is an aporphine-type alkaloid derived from lotus leaf. It acts as a potent hERG channel inhibitor, exhibiting an IC50 of 7.91 μM in vitro hERG blockages in HEK293 cells. This compound is intended for research use only.
- Potent hERG channel inhibitor
- 99.85% purity
- White to off-white solid appearance
- Store at 4°C, sealed, away from moisture and light
- Soluble in DMSO at 50 mg/mL
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Medchemexpress LLC (Z-LL)2 ketone | 313664-40-3 | >99.6% | 809.00 | 10 MG
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(Z-LL)2 ketone is an inhibitor of ketone with an IC50 value of 50 nM. It inhibits the processing of the p-Prl signal peptide. This product is intended for research use only and is not sold to patients.
- Inhibitor of ketone
- Inhibits processing of p-Prl signal peptide
- Purity: >99.6%
- CAS number: 313664-40-3
- Molecular weight: 809.00
- White to off-white solid appearance
- Soluble in DMSO
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Medchemexpress LLC Arecaidine but-2-yny 10mg | 119630-77-2 | 10MG
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Arecaidine but-2-ynyl ester tosylate (ABET) is a selective mAChR M2 agonist that dose-dependently decreases mean arterial pressure and heart rate in rats Arecaidine but-2-ynyl ester tosylate can be used for cardiovascular disease research[1 [2 Arecaidine but-2-ynyl ester (tosylate) is a click chemistry reagent it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups
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Medchemexpress LLC Delsoline | 509-18-2 | MFCD00274545 | 99.1% | 467.6 | C25H41NO7 | 10 MG
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Delsoline is a naturally occurring alkaloid isolated from Delphinium anthriscifolium Hance. It exhibits curare-like and ganglion-blocking activity and is supplied as a research reagent for studies of neuromuscular pharmacology and biochemical effects. Typical attributes include high purity and a defined molecular weight.
- High purity (99.06%).
- Molecular formula C25H41NO7.
- Molecular weight 467.6 g/mol.
- Supplied as a 10 mg solid.
- Used for neuromuscular and ganglionic activity studies.
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Medchemexpress LLC LUF6096 | 1116652-18-6 | 99.16% | 414.33 | 100 MG
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LUF6096 is a potent allosteric enhancer of the adenosine A3 receptor, capable of enhancing agonist binding. It exhibits low orthosteric affinity for any of the adenosine receptors and demonstrates protective effects in myocardial ischemia/reperfusion injury.
- Enhances agonist binding of the adenosine A3 receptor.
- Exhibits low orthosteric affinity for adenosine receptors.
- Shows protective effects in myocardial ischemia/reperfusion injury.
- Available in various sizes for research needs.
- High purity for reliable experimental results.
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eMolecules 111043-06-2 | 4-Acetyl-3-bromopyridine | Apollo Scientific | MFCD00128861 | 200.035 | C7H6BrNO | 97.000 | CC(=O)c1ccncc1Br | 1g | 562459326
4-Acetyl-3-bromopyridine | Apollo Scientific | 111043-06-2 | MFCD00128861 | 200.035 | C7H6BrNO | 97.000 | CC(=O)c1ccncc1Br | 1g | 562459326
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Medchemexpress LLC SNX-0723 | 1073969-18-2 | 99.1% | 399.46 g·mol^-1 | C22H26FN3O3 | 50 MG
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SNX-0723 is a brain-permeable small-molecule Hsp90 inhibitor reported to have anti-Plasmodium and antitumor activity. It is supplied for research use in high-purity solid and solution formats for in vitro and in vivo studies.
- Potent Hsp90 inhibitor with reported biological activity.
- Reported purity ~99.1% suitable for research applications.
- Molecular weight 399.46 g·mol⁻¹ and formula C22H26FN3O3.
- Available as solid powder and as DMSO solution for flexibility.
- Stored under recommended low-temperature conditions for stability.
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