Laboratory Surfactants and Wetting Agents
Medchemexpress LLC Stearamide | 124-26-5 | MFCD00008038 | 97.0% | 283.49 g/mol | C18H37NO | 500 MG
Stearamide is a primary fatty acid amide (octadecanamide) supplied as a research-grade reagent. It has reported cytotoxic and ichthyotoxic activity and is used in chemical research, materials studies, and analytical applications. Available in small laboratory pack sizes for experimental work.
- Primary fatty acid amide (octadecanamide).
- CAS number 124-26-5.
- Molecular formula C18H37NO; molecular weight 283.49 g/mol.
- Typical purity around 97.0%.
- Available in laboratory pack sizes including 500 mg.
- Suitable for research and material testing applications.
Medchemexpress LLC L-803087 | 217480-26-7 | 99.7% | 485.53 | 1 MG
L-803087 is a potent and selective somatostatin sst4 receptor agonist with a Ki of 0.7 nM. It is >280-fold higher than other somatostatin receptors. L-803087 facilitates AMPA-mediated hippocampal synaptic responses in vitro and increases kainate-induced seizures in mice.
- Potent and selective somatostatin sst4 receptor agonist.
- Facilitates AMPA-mediated hippocampal synaptic responses in vitro.
- Increases kainate-induced seizures in mice.
Medchemexpress LLC L-803,087 trifluoroacetate | 217480-26-7 | MFCD09037334 | 99.7% | 485.53 g/mol | C25H29F2N5O3 | 5 MG
L-803087 is a potent, selective somatostatin sst4 receptor agonist used in receptor pharmacology and preclinical research. It demonstrates subnanomolar affinity and high selectivity, and is supplied as a stable solid suitable for in vitro formulation and testing.
- Potent somatostatin sst4 receptor agonist (Ki = 0.7 nM) with >280-fold selectivity versus other somatostatin receptors.
- High purity (99.7%) suitable for research applications.
- White to light yellow solid; molecular weight 485.53 g/mol.
- Soluble in DMSO (250 mg/mL); ultrasonic assistance recommended.
- Stable as powder at -20°C for up to 3 years; in solvent: -80°C for 6 months or -20°C for 1 month.
- Available in milligram packages, including 5 mg, and as a 10 mM solution in DMSO for reconstitution.
Medchemexpress LLC Taurocholic acid sodium salt hydrate | 345909-26-4 | 98.5% | 500 MG
Taurocholic acid sodium salt hydrate is a chemical compound with a molecular formula of C26H46NNaO8S and a molecular weight of 555.70. It is typically supplied as a white to yellow solid.
- Consistent with structure based on 1H NMR spectrum
- High purity of 98.51% confirmed by HPLC
- Complies with given specifications
Medchemexpress LLC CHAPS | 75621-03-3 | C32H58N2O7S | 10 MM 1 ML
CHAPS | 75621-03-3 | C32H58N2O7S | 10 MM 1 ML
eMolecules 511-26-2 | Medchem Express | MAP4343 | 5mg | 572596436 | HY-107116 | 330.512 | C22H34O2
Medchem Express | MAP4343 | 5mg | 572596436 | HY-107116 | 511-26-2 | 330.512 | C22H34O2
Cambridge Isotope Laboratories TAUROCHOLIC ACID, SODIUM SALT HYDRATE UNLABELED 97% CHEMICAL PURITY, 50 MG
TAUROCHOLIC ACID, SODIUM SALT HYDRATE UNLABELED 97% CHEMICAL PURITY, 50 MG
Medchemexpress LLC Methanone, [(2S,3aS,7aS)-octahydro-1-[[(1R,2R)-2-phenylcyclopropyl]carbonyl]-1H-indol-2-yl]-3-thiazolidinyl- | 176797-26-5 | C22H28N2O2S | 50 MG
S 17092 (S 17092-1) is an orally active cerebral prolyl-endopeptidase (PEP) inhibitor with an IC50 of 1.2 nM. It inhibits cell apoptosis by slowing down the degradation of neuroactive peptides, thereby enhancing memory function. It is suitable for research on memory impairment and cognitive disorders associated with cerebral aging.
- Orally active cerebral prolyl-endopeptidase (PEP) inhibitor
- Inhibits cell apoptosis
- Enhances memory function
- Useful for research on memory impairment and cognitive disorders
- Long-acting PEP inhibitor with a half-life of over 9 hours
Medchemexpress LLC Cid44216842 (Cdc42-IN-1) | 1222513-26-9 | 99.8% | C22H20BrN3O3S | 10MG
CID44216842 (Cdc42-IN-1) is a potent, selective small-molecule inhibitor of the Rho GTPase Cdc42 that blocks GTP and GDP binding to both wild-type and Q61L mutant forms. Supplied as a solid white to off-white powder with high purity, it is intended for use as a molecular probe in biochemical and cellular research.
- Selective inhibition of Cdc42 over other GTPases.
- Low-micromolar potency in GTP and GDP binding assays.
- High chemical purity suitable for research applications.
- Stable solid form with defined storage conditions.
- Useful as a molecular probe for studying Cdc42-mediated signaling.
Medchemexpress LLC Serpin A8/Angiotensi 500ug
Serpin A8 (or angiotensinogen) is an important regulator in the renin-angiotensin system fine-tuning blood pressure and electrolyte balance This multifunctional protein acts as a potent vasoconstrictor affecting vascular smooth muscle and affecting cardiac function via the sympathetic nervous system Serpin A8/Angiotensinogen Protein Mouse (HEK293 His) is the recombinant mouse-derived Serpin A8/Angiotensinogen protein expressed by HEK293 with C-His labeled tag
eMolecules 26530-26-7 | Medchem Express | KM04416 | 5mg | 779715174 | HY-148685 | MFCD00097921 | 249.28 | C12H11NO3S
Ambeed | (E)-4455-Tetramethyl-2-(3-((tetrahydro-2H-pyran-2-yl)oxy)prop-1-en-1-yl)-132-dioxaborolane | 250mg | 660584824 | A630869 | 642066-70-4 | 268.160 | C14H25BO4
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Medchemexpress LLC Cdc42-IN-1 | 1222513-26-9 | 99.8% | 486.38 | 50 MG
CID44216842 (Cdc42-IN-1) is a potent and selective guanine nucleotide binding lead inhibitor targeting Cdc42. It functions as a molecular probe, specifically inhibiting GTP binding to both Cdc42 and its mutant in a dose-dependent manner. This inhibition is specific toward Cdc42 with no effects on other GTPases including Rac and Rho in the same family.
- Potent Cdc42-selective guanine nucleotide binding lead inhibitor
- EC50s for Cdc42 WT and Cdc42Q61L mutant are 1.0 and 1.2 μM in GTP binding assay
- EC50s for Cdc42 WT and Cdc42Q61L mutant are 0.3 and 0.5 μM in GDP binding assay
- Used as a molecular probe
- Specific inhibition of Cdc42 without affecting other GTPases like Rac and Rho