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Filtered Search Results
![Aobchem 1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Aobchem 1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 1g
1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 1g
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Aobchem 1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 500mg
1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 500mg
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Aobchem 1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 250mg
1-[3-(Cyclohexylmethoxy)phenyl]ethanone | 95% | CAS 1019368-02-5 | C15H20O2 | 250mg
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Medchemexpress LLC Minocycline (hydrochloride) (standard) | 13614-98-7 | 99.5% | 493.94 | 100 MG
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Minocycline (hydrochloride) (standard) | 13614-98-7 | 99.5% | 493.94 | 100 MG
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eMolecules 17609-80-2 | 4-Amino-3-chlorophenol | MFCD00801116 | 1g
Medchem Express | Xanthosine 5-monophosphate (sodium salt) | 50mg | 642185150 | HY-W008990 | 25899-70-1 | 408.170 | C10H11N4Na2O9P
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Medchemexpress LLC Benzenecarboximidamide, hydrochloride, hydrate | 206752-36-5 | 99.6% | C7H8N2·ClH·xH2O | 5 G
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Benzamidine hydrochloride hydrate is a reversible competitive inhibitor of trypsin-like serine proteases used in enzymatic assays and protease inhibition studies. It is supplied as a white to light-yellow solid with high purity for biochemical research.
- Reversible competitive inhibitor of trypsin-like serine proteases.
- High purity: 99.58%.
- White to light-yellow solid physical form.
- Available in common lab pack sizes, including 5 g.
- Intended for research use in enzymology and protease inhibition assays.
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Medchemexpress LLC Cycloguanil hydrochloride | 152-53-4 | 99.9% | 25 MG
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Cycloguanil hydrochloride is a dihydrofolate reductase (DHFR) inhibitor with an IC50 of 10.8 μM against human DHFR. It functions by blocking the folate metabolic pathway, which affects nucleotide synthesis and interferes with DNA replication. It inhibits DHFR in Plasmodium, making it relevant for malaria research. Additionally, it exhibits anticancer activity by potently inhibiting DHFR in human cancer cells and blocking the transcriptional activity of STAT3.
- Inhibits dihydrofolate reductase (DHFR)
- Blocks the folate metabolic pathway
- Interferes with DNA replication and nucleotide synthesis
- Relevant for malaria research through Plasmodium DHFR inhibition
- Exhibits anticancer activity in human cancer cells
- Blocks transcriptional activity of STAT3
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Medchemexpress LLC Tracazolate hydrochloride | 1135210-68-2 | MFCD03791317 | 99.2% | 340.85 g/mol | C16H25ClN4O2 | 10 MG
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Tracazolate hydrochloride is the hydrochloride salt of tracazolate (ICI 136753), a potent positive allosteric modulator of GABAA receptors with reported subtype selectivity. It is supplied as a research reagent for in vitro and in vivo studies of GABAA receptor pharmacology, anxiolytic effects, and anticonvulsant activity.
- Potent GABAA receptor positive allosteric modulator.
- Reported selectivity for the β3 subunit.
- High purity (99.2%).
- Off-white to light yellow solid appearance.
- Recommended storage: -20°C, sealed, protect from moisture.
- Available in small research pack sizes such as 10 MG.
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Medchemexpress LLC Trihexyphenidyl hydrochloride | 52-49-3 | MFCD00058212 | 99.9% | 100 MG
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Trihexyphenidyl hydrochloride | 52-49-3 | MFCD00058212 | 99.9% | 100 MG
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Medchemexpress LLC PF-07038124 hydrochloride | 2415317-57-4 | 99.3% | C18H23BClNO4 | 1 MG
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PF-07038124 hydrochloride is a potent PDE4 inhibitor with an IC50 of 0.5 nM for PDE4B2. It demonstrates immunomodulatory effects by inhibiting IL-13, IL4, and IFNγ, making it suitable for research related to atopic dermatitis and plaque psoriasis. This compound has been investigated in Phase 1 and Phase 2 clinical trials for these conditions. It is supplied as an off-white to light yellow solid.
- Specifically targets PDE4B2 with high potency
- Shows inhibitory activity against IL-13, IL4, and IFNγ
- Used in the study of atopic dermatitis and plaque psoriasis
- Investigated in Phase 1 and Phase 2 clinical trials
- Soluble in DMSO at 100 mg/mL
- Recommended storage is 4°C sealed, away from moisture
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Medchemexpress LLC Ractopamine hydrochloride | 90274-24-1 | 99.2% | 100 MG
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Ractopamine (LY031537) hydrochloride is a potent β-adrenergic receptor (βAR) agonist with a Kd value of approximately 25 nM for pig β1AR and β2AR. It is linked to protein metabolism and can be used for researching to increase lean tissue growth and improve production efficiency in pigs. It is for research use only and not sold to patients.
- Potent β-adrenergic receptor (βAR) agonist.
- Kd value of ~25 nM for pig β1AR and β2AR.
- Linked to protein metabolism.
- Can be used to research increased lean tissue growth and improved production efficiency in pigs.
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Medchemexpress LLC Vernakalant hydrochloride | 748810-28-8 | MFCD09833303 | ≥98.0% | 385.93 g·mol⁻¹ | C20H32ClNO4 | 5 MG
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Vernakalant hydrochloride is a research-grade antiarrhythmic compound that acts as a mixed voltage- and frequency-dependent sodium channel blocker and an atria-preferred potassium channel blocker. It is used in electrophysiology and cardiac ion-channel studies to investigate mechanisms of atrial fibrillation and to evaluate potential therapeutic effects. Consult the manufacturer datasheet and SDS for purity, handling, and storage details.
- Mixed voltage- and frequency-dependent sodium channel blocker and atria-preferred potassium channel blocker.
- Useful for studies of atrial fibrillation and cardiac electrophysiology.
- Suitable for in vitro pharmacology and ion-channel assays.
- Supplied in small research quantities for preclinical experiments.
- Refer to the product datasheet and safety data sheet for purity, storage, and handling information.
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Medchemexpress LLC CARM1-IN-3 dihydrochloride | 912970-67-3 | C24H34Cl2N4O2 | 50 MG
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CARM1-IN-3 dihydrochloride (compound 17b) is a potent and selective co-activator associated arginine methyltransferase (CARM1) inhibitor.
- Potent and selective CARM1 inhibitor
- IC50 value of 0.07 μM for CARM1
- IC50 value of >25 μM for CARM3
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Medchemexpress LLC Dexmedetomidine hydrochloride | 145108-58-3 | 99.9% | 236.74 | 25 MG
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Dexmedetomidine hydrochloride is a potent, selective, and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. It exhibits anxiolysis, sedation, and modest analgesia effects. This product is an analytical standard intended for research and analytical applications.
- Potent, selective, and orally active agonist of α2-adrenoceptor
- Shows 1620-fold selectivity against α1-adrenoceptor
- Exhibits anxiolysis, sedation, and modest analgesia effects
- Intended for research and analytical applications
- Analytical standard
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Medchemexpress LLC Dapiprazole hydrochloride | 72822-13-0 | 99.3% | C19H28ClN5 | 50 MG
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Dapiprazole hydrochloride is a potent, selective, and orally active alpha-1 adrenoceptor antagonist.
- Suppresses opioid withdrawal symptoms.
- Used as eye drops for reversing mydriasis.
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