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Filtered Search Results
Chem-Impex International, Inc. 4-Chloro-2,6-diaminopyrimidine | MFCD00006097 | 5G
4-Chloro-2,6-diaminopyrimidine, MFCD00006097, 5G
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Chem-Impex International, Inc. 4-Chloro-2,6-diaminopyrimidine | MFCD00006097 | 25G
4-Chloro-2,6-diaminopyrimidine, MFCD00006097, 25G
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Medchemexpress LLC Methyl 2,5-dihydroxycinnamate | 63177-57-1 | MFCD00132932 | 99.8% | 194.18 | C10H10O4 | 10 MG
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Methyl 2,5-dihydroxycinnamate is a small-molecule research chemical described as an erbstatin analog that potently inhibits epidermal growth factor receptor (EGFR) kinase activity. It is supplied as a solid and as DMSO solutions for laboratory research and biochemical assays. Intended for research use only; not for human or clinical applications.
- Potent inhibitor of EGFR kinase activity.
- Erbstatin analog small-molecule structure.
- Available as solid and as 10 mM solution in DMSO.
- High purity suitable for analytical and biological assays.
- Documented identifiers and physicochemical data for compound tracking.
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Medchemexpress LLC Pepsin | 9001-75-6 | 250 MG
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Pepsin is the major pig and human gastric protease and a minor pepsin-like gastric proteolytic enzyme. It contributes to the proteolysis of food proteins in the vertebrate stomach.
- Optimal pH for activity is 1.0-3.0.
- Activated by hydrochloric acid (HCl) and trifluoroacetic acid (TFA).
- Inactivated by pH greater than 6.0.
- To reconstitute, resuspend in double-distilled water (pH 5.5 or lower) to 1 mg/mL.
- Reconstituted Pepsin can be stored at 4 °C for up to one month.
- Cleavage specificity for Phenylalanine (Phe) and Leucine (Leu) is best at pH 1.0 and decreased above pH 2.0.
- Irreversibly inactivates above pH 6.0.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431272 HELICID 250MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000430470 D- -GLUCONO-1 5-LA 250MG
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Sigma Aldrich Fine Chemicals Biosciences Pyrimethamine United States Pharmacopeia (USP) Reference Standard | 58-14-0 | MFCD00057350 | 200MG
Pyrimethamine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 248.71 | 58-14-0 | MFCD00057350 | 200MG
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Medchemexpress LLC (E)-2-Hydroxycinnamaldehyde | 60125-23-7 | 250 MG
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(E)-2-Hydroxycinnamaldehyde is an aldehyde that can be isolated from the stem bark of cinnamon. It functions by inhibiting cell proliferation and inducing apoptosis through the suppression of STAT3 signal transduction and reactive oxygen species production. This compound exhibits antitumor activity.
- Inhibits cell proliferation
- Induces apoptosis by suppressing STAT3 signal transduction
- Induces apoptosis by suppressing reactive oxygen species production
- Exhibits antitumor activity
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Medchemexpress LLC (5-Methyl-1-Tritylimidazol-4-yl)Methanol | 106147-84-6 | 99.4% | C24H22N2O | 5 G
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(5-Methyl-1-Tritylimidazol-4-yl)Methanol, catalog number HY-75329 from MedChemExpress, is a high-purity laboratory chemical with a CAS number of 106147-84-6. It has a molecular formula of C24H22N2O and a molecular weight of 354.44. This solid compound is intended for research use only by experienced personnel.
- Identified as a laboratory chemical
- For research use only
- Stable under recommended storage conditions
- High purity (99.35%)
- Molecular formula C24H22N2O
- Solid appearance
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![eMolecules ChemScene / (R)-4-Isopropyl-2-(pyrimidin-2-yl)-45-dihydrooxazole / 100mg / 632337594 / CS-0179438 / 0.000 / 2757082-66-7 / [null] / 191.234 / C10H13N3O](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502443136.PNG-250.jpg)
eMolecules ChemScene / (R)-4-Isopropyl-2-(pyrimidin-2-yl)-45-dihydrooxazole / 100mg / 632337594 / CS-0179438 / 0.000 / 2757082-66-7 / [null] / 191.234 / C10H13N3O
ChemScene / (R)-4-Isopropyl-2-(pyrimidin-2-yl)-45-dihydrooxazole / 100mg / 632337594 / CS-0179438 / 0.000 / 2757082-66-7 / [null] / 191.234 / C10H13N3O
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Medchemexpress LLC Bevenopran | 676500-67-7 | MFCD26967979 | 99.8% | 386.44 g/mol | C20H26N4O4 | 10 MG
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Bevenopran is a peripherally acting μ-opioid receptor antagonist supplied for research use. It has been investigated for the treatment of opioid-induced bowel dysfunction and is provided as a solid or as a DMSO solution for laboratory studies.
- Peripherally selective μ-opioid receptor antagonist.
- High purity (>99.8%).
- White to off-white solid appearance.
- Available as multiple solid quantities and as a 10 mM solution in DMSO.
- Molecular weight 386.44 g/mol; formula C20H26N4O4.
- Recommended storage: powder at -20°C; solution at -80°C for long-term stability.
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Medchemexpress LLC Bevenopran | 676500-67-7 | MFCD26967979 | 99.8% | 386.44 g/mol | C20H26N4O4 | 50 MG
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Bevenopran is a peripherally acting μ-opioid receptor antagonist, with additional activity at δ-opioid receptors, investigated for treatment of opioid-induced bowel dysfunction. It is supplied as a high-purity research compound for use in in vitro and in vivo pharmacology studies.
- Peripherally acting μ-opioid receptor antagonist with δ-opioid receptor activity.
- Intended for research use in studies of opioid-induced bowel dysfunction and related pharmacology.
- High purity (99.82%) suitable for in vitro and in vivo experiments.
- Molecular weight 386.44 g/mol; chemical formula C20H26N4O4.
- CAS number 676500-67-7 for unambiguous substance identification.
- Available as solid quantities (5 mg-200 mg) and as 10 mM solution in DMSO.
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Medchemexpress LLC TTHA | 869-52-3 | 98.0% | 494.45 | 250 MG
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TTHA is a complexonate that exhibits high affinity for light rare earth elements (LREE), particularly for La3+ in ternary mixtures and Y3+ in quinary mixtures. It is intended for research use only.
- High affinity for light rare earth elements (LREE)
- Specifically effective for La3+ in ternary mixtures
- Specifically effective for Y3+ in quinary mixtures
- Intended for research use only
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Apexbio Technology LLC Ro 61-8048 199666-03-0 50mg
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Ro 61-8048 is a small-molecule inhibitor targeting kynurenine 3-hydroxylase (KMO) It is designed to selectively inhibit the catalytic conversion of kynurenine into 3-hydroxykynurenine thereby modulating the kynurenine pathway of tryptophan metabolism Ro 61-8048 exerts its biological activity primarily through selective KMO inhibition In in vitro studies Ro 61-8048 demonstrates inhibitory potency with an IC50 value of approximately 37 nM Based on these pharmacological properties Ro 61-8048 holds research potential in investigations of neurodegenerative and central nervous system immune-related disorders
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eMolecules 4-CHLORO-2-METHYL-PYRIMIDIN 1G
5000216297 4-CHLORO-2-METHYL-PYRIMIDIN 1G
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