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Filtered Search Results
Medchemexpress LLC Tamsulosin (hydrochloride) | 106463-17-6 | 99.8% | 25 MG
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Tamsulosin hydrochloride is an orally active antagonist of the α1-adrenergic receptor. It induces apoptosis and is used for research related to prostatic hyperplasia. It also attenuates abdominal aortic aneurysm growth and inhibits inflammation in animal models.
- Orally active α1-adrenergic receptor antagonist
- Induces apoptosis
- Used for research of prostatic hyperplasia
- Attenuates abdominal aortic aneurysm growth
- Inhibits inflammation in animal models
- Stable under recommended storage conditions
- White to off-white solid appearance
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Medchemexpress LLC G4RGDSP, integrin-binding peptide | 774577-43-4 | 99.6% | 758.74 | 25 MG
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G4RGDSP, Integrin-binding peptide is a cell integrin-binding peptide that targets integrin receptors. It is coupled to alginate to increase the viability of cells in the scaffold. It can be used as an extrudable carrier for chondrocyte delivery for the study of 3D printing technology.
- Targets integrin receptors.
- Can be coupled to alginate to increase cell viability in scaffolds.
- Usable as an extrudable carrier for chondrocyte delivery for 3D printing technology.
- Can increase the expression of aggregin, collagen type II, and sox9 genes in HAC cells.
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Medchemexpress LLC CRA-026440 hydrochloride | 847459-98-7 | 98.1% | 456.92 | 100 MG
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CRA-026440 hydrochloride is a potent, broad-spectrum HDAC inhibitor. It shows antitumor and antiangiogenic activities. This compound is also a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent, broad-spectrum HDAC inhibitor
- Shows antitumor and antiangiogenic activities
- Click chemistry reagent
- Contains an alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc)
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Medchemexpress LLC Tricyclo[3.3.1.13,7]decan-1-amine, hydrochloride (1:1) | 665-66-7 | MFCD00074723 | 98.0% | 25 MG
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Tricyclo[3.3.1.13,7]decan-1-amine, hydrochloride (1:1) | 665-66-7 | MFCD00074723 | 98.0% | 25 MG
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Medchemexpress LLC Amorolfine hydrochloride (Standard) | 78613-38-4 | 99.6% | 25 MG
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Amorolfine hydrochloride (Standard) is an analytical standard and a potent anti-fungal agent that inhibits ergosterol biosynthesis. This product is intended for research and analytical applications, and has potential for the study of *Neoscytalidium dimidiatum* onychomycosis. It acts primarily by inhibiting ergosterol biosynthesis, a component of fungal cell membranes, and and possesses both fungistatic and fungicidal activity.
- Analytical standard for reference assays
- Used in qualitative research experiments
- Used in quantitative research experiments
- Used in methodological research experiments
- Suitable for HPLC applications
- Suitable for GC applications
- Suitable for MS applications
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Medchemexpress LLC Loperamide (hydrochloride) | 34552-83-5 | 99.8% | 25 MG
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Loperamide hydrochloride is an opioid receptor agonist and a selective and competitive human intestinal carboxylesterases (hiCE) inhibitor. It exhibits an anti-diarrheal effect and is for research use only.
- Opioid receptor agonist
- Selective and competitive human intestinal carboxylesterases (hiCE) inhibitor
- Exhibits anti-diarrheal effect
- Induces hallmarks of ER stress and autophagy in GBM cells and MEFs (in vitro)
- Decreases LC3B and GABARAP lipidation levels in ATF4 KO cells compared to WT cells (in vitro)
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Medchemexpress LLC Aceclidine hydrochloride | 6109-70-2 | 98.0% | 205.68 | 1 ML
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Aceclidine hydrochloride is a modulator of the M3 muscarinic acetylcholine receptor and acts as an M1 receptor agonist with an EC50 of 40 μM. It functions as a cycloplegic agent, a surfactant, a tonicity adjustor, and can optionally serve as a viscosity enhancer and an antioxidant. This compound holds potential for research into various disorders, including refractive errors of the eye, xerostomia, Sjogren's syndrome, glaucoma, conjunctivitis, lacrimal gland disease, and esotropia.
- Modulator of M3 muscarinic acetylcholine receptor.
- M1 receptor agonist (EC50: 40 μM).
- Functions as a cycloplegic agent.
- Acts as a surfactant.
- Serves as a tonicity adjustor.
- Can optionally be a viscosity enhancer and an antioxidant.
- Potential for research in disorders such as refractive errors of the eye, xerostomia, Sjogren's syndrome, glaucoma, conjunctivitis, lacrimal gland disease, and esotropia.
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Medchemexpress LLC Aceclidine hydrochloride | 6109-70-2 | 98.0% | 205.68 | 500 MG
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Aceclidine hydrochloride is identified as a modulator of the M3 muscarinic acetylcholine receptor and an M1 receptor agonist, with an EC50 of 40 μM. It functions as a cycloplegic agent, a surfactant, a tonicity adjustor, and can optionally act as a viscosity enhancer and an antioxidant. This product holds potential for research into various disorders, including refractive errors of the eye, xerostomia, Sjogren's syndrome, glaucoma, conjunctivitis, lacrimal gland disease, and esotropia.
- Modulator of M3 muscarinic acetylcholine receptor and an M1 receptor agonist (EC50: 40 μM).
- Acts as a cycloplegic agent.
- Functions as a surfactant.
- Serves as a tonicity adjustor.
- Can be used as a viscosity enhancer.
- Possesses antioxidant properties.
- Potential for research in eye-related conditions and disorders such as xerostomia and Sjogren's syndrome.
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Synnovator Inc 3- 2-AMINO-5- NAPHTHALEN-2-YL
3-(2-Amino-5-(naphthalen-2-yl)pyridin-3-yl)acrylic acid
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Medchemexpress LLC Fomepizole (hydrochloride) | 56010-88-9 | 99.9% | 25 MG
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Fomepizole hydrochloride (4-Methylpyrazole hydrochloride) is a potent and orally active cytochrome P450 (CYP2E1) inhibitor. It acts as a competitive inhibitor of the enzyme alcohol dehydrogenase, preventing the conversion of methanol and ethylene glycol into toxic metabolites. It is considered a potential antidote for ethylene glycol or methanol poisoning.
- Potent and orally active cytochrome P450 (CYP2E1) inhibitor.
- Competitive inhibitor of alcohol dehydrogenase.
- Blocks conversion of methanol and ethylene glycol to toxic metabolites.
- Potential antidote for ethylene glycol or methanol poisoning.
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Medchemexpress LLC Vardenafil (hydrochloride) | 224785-91-5 | 99.8% | 25 MG
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Vardenafil hydrochloride is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. It competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis, thereby increasing cGMP levels.
- Selective and orally active inhibitor of PDE5 (IC50 of 0.7 nM)
- Inhibits PDE1 (IC50 of 180 nM) and PDE6 (IC50 of 11 nM)
- Increases cGMP levels
- Used in research for erectile dysfunction, hepatitis, and diabetes
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Cayman Chemical Naphthol AS-BI-Phosphate, Purity: ≥95%, CAS: 1919-91-1, 500 mg
A fluorogenic substrate for acid and alkaline phosphatases; is converted to N-ASBI which displays ex/em spectra of 405/515 nm, respectively; fluorescence is a quantitative marker of acid and alkaline phosphatase activity
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Chemscene CHEMSCENE
5000575391 S-1- NAPHTHALEN-1-YL ETHAN 25G
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Ambeed DIISOPROPYL DIAZENE-12-DICARB
NC3368068 DIISOPROPYL DIAZENE-12-DICARB
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eMolecules 3886-70-2 | (1R)-1-(naphthalen-1-yl)ethan-1-amine | Pharmablock | MFCD00064114 | 171.243 | C12H13N | 97.000 | C[C@@H](N)c1cccc2ccccc12 | 50g | 551090446
(1R)-1-(naphthalen-1-yl)ethan-1-amine | Pharmablock | 3886-70-2 | MFCD00064114 | 171.243 | C12H13N | 97.000 | C[C@@H](N)c1cccc2ccccc12 | 50g | 551090446
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