Phenols
Medchemexpress LLC Cefotiam hexetil hydrochloride | 95789-30-3 | MFCD00897074 | 95.1% | 768.76 | C27H39Cl2N9O7S3 | 10 MG
Cefotiam hexetil hydrochloride is the hydrochloride salt of cefotiam hexetil, an oral prodrug of the third-generation cephalosporin cefotiam. Intended for research and analytical use, the compound is used in prodrug, formulation, and pharmacology studies and is inactive as an antibacterial until converted to cefotiam.
- Hydrochloride salt with reported purity 95.1%
- Molecular formula C27H39Cl2N9O7S3 and molecular weight 768.76
- Soluble in DMSO (250 mg/mL); ultrasonic agitation recommended
- Appearance: solid, off-white to light yellow
- Storage: store sealed at 4°C, protect from moisture and light
- Supplied in small research sizes such as 10 mg
eMolecules 1107-00-2 | 5,5'-(Perfluoropropane-2,2-diyl)bis(isobenzofuran-1,3-dione) | Ambeed | MFCD00039143 | 444.241 | C19H6F6O6 | 98.000 | FC(F)(F)C(c1ccc2C(=O)OC(=O)c2c1)(c1ccc2C(=O)OC(=O)c2c1)C(F)(F)F | 1g | 490493560
5,5'-(Perfluoropropane-2,2-diyl)bis(isobenzofuran-1,3-dione) | Ambeed | 1107-00-2 | MFCD00039143 | 444.241 | C19H6F6O6 | 98.000 | FC(F)(F)C(c1ccc2C(=O)OC(=O)c2c1)(c1ccc2C(=O)OC(=O)c2c1)C(F)(F)F | 1g | 490493560
Matrix Scientific 4-FLUORO-2-METHYLPHENOL-25G
4-Fluoro-2-methylphenol, 99%; 25g,C7H7FO, MFCD00075088, mw 126.13, [452-72-2]
Medchemexpress LLC 2,3-Bis(3-indolylmethyl)indole | 138250-72-3 | 375.47 | 1 ML
2,3-Bis(3-indolylmethyl)indole significantly suppresses RANKL-induced osteoclast formation, actin ring formation, and bone resorption in a concentration-dependent manner.
- Significantly suppresses RANKL-induced osteoclast formation
- Inhibits actin ring formation
- Reduces bone resorption
- High purity (99.53%)
- Light yellow to light brown solid appearance
- Soluble in DMSO
Medchemexpress LLC Cresol red | 1733-12-6 | 99.3% | 100 MG
Cresol red, 97% is an anionic dye utilized as a pH indicator. It changes from orange to yellow at pH 1.8-2.0 and from yellow to purple at pH 7.0-8.8.
- Anionic dye
- Functions as a pH indicator
- Changes color based on pH: orange to yellow at pH 1.8-2.0; yellow to purple at pH 7.0-8.8
- For research use only; not sold to patients
Medchemexpress LLC Thiethylperazine dimaleate | 1179-69-7 | 100.0% | 1 ML
Thiethylperazine dimaleate is a phenothiazine derivative that acts as an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. It is also a selective ABCC1 activator that reduces amyloid-β (Aβ) load in mice. This compound exhibits anti-emetic, antipsychotic, and antimicrobial effects.
- Phenothiazine derivative
- Orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist
- Selective ABCC1 activator
- Reduces amyloid-β (Aβ) load in mice
- Exhibits anti-emetic, antipsychotic, and antimicrobial effects
Medchemexpress LLC 5-O-(E)-p-Coumaroylquinic acid | 5746-55-4 | 338.31 | 5 MG
5-O-(E)-p-Coumaroylquinic acid, a quinic acid derivative, is a potent phytochemical agent against hepatitis B virus. For research use only; not for sale to patients.
- Reduces HBV DNA level in the release of mature HBV particles from HepG2.2.15 cultivation.
- Purity: 99.86%.
- Molecular weight: 338.31.
- Formula: C16H18O8.
- CAS No.: 5746-55-4.
- Appearance: Solid.
- Color: White to off-white.
- Initial source: Plants (Leguminosae Spatholobus suberectus Dunn, Compositae).
Medchemexpress LLC Triacetonamine (2,2,6,6-tetramethyl-4-piperidone) | 826-36-8 | MFCD00005975 | 155.24 | 1000 G
Triacetonamine is utilized as an intermediate in the synthesis of pharmaceutical products, pesticides, and photostabilizers for polymers. It exhibits oral activity and can induce acute liver failure (ALF) in rats.
- Used as an intermediate for the synthesis of pharmaceutical products, pesticides, and photostabilizers for polymers
- Has oral activity
- Can induce acute liver failure (ALF) in rats
Medchemexpress LLC Trimethyloctylammoni 25g
Trimethyloctylammonium bromide (TOAB) is used as a surfactant and phase transfer catalyst in various chemical reactions TOAB can be used in the synthesis of nanomaterials due to its ability to selectively transfer ions across interfaces and as a surfactant in the production of emulsions and foams It is valued for its amphiphilic properties which allow it to interact with water and oils stabilizing and dispersing mixtures
Medchemexpress LLC Methenamine hippurate | 5714-73-8 | MFCD00072147 | >95.0% | 319.36 g/mol | C15H21N5O3 | 10 MG
Methenamine hippurate is the analytical reference standard of methenamine hippurate supplied for research and analytical use. The compound is the hippurate salt of methenamine, an orally active urinary antiseptic that releases formaldehyde under acidic conditions; supplied as a dry solid and handled per SDS storage recommendations.
- Analytical reference standard suitable for research and quality control.
- CAS number 5714-73-8; molecular weight 319.36 g/mol.
- Purity reported by suppliers as ≥95% (HPLC) to ≥98%; check lot-specific certificate.
- Recommended storage: 4°C sealed and dry; in solution -80°C (6 months) or -20°C (1 month).
- Provided as a solid for analytical preparation and formulation testing.
Medchemexpress LLC YIL781 hydrochloride | 1640226-17-0 | 99.48% | 445.96 | 25 MG
YIL781 hydrochloride is a potent, orally active ghrelin receptor (GHSR) antagonist. It has been shown to improve glucose homeostasis in rats and effectively inhibits the calcium response induced by ghrelin.
- Potent and orally active ghrelin receptor (GHSR) antagonist.
- Produces a greater improvement in glucose homeostasis in rats.
- Inhibits the calcium response induced by ghrelin with pIC50 values of 7.90 and 8.27.
- For research use only.
Medchemexpress LLC 1H-1,2,4-Triazol-3-amine, 5-[4-[(2S,5S)-5-[(4-chlorophenyl)methyl]-2-methyl-4-morpholinyl]... | 2088453-21-6 | 99.9% | 390.91 | 1 ML
OATD-01 is a highly potent, first-in-class, orally active, and selective chitinase inhibitor. It demonstrates low nanomolar activity towards CHIT1 and exhibits an excellent pharmacokinetic profile across multiple species. This compound shows significant antifibrotic efficacy in vivo and is being investigated for pulmonary fibrosis (IPF) research.
- Highly potent and selective chitinase inhibitor
- Low nanomolar activity towards CHIT1 (hCHIT1, IC50=23 nM)
- Excellent pharmacokinetic profile across multiple species
- Selective against a panel of off-targets
- Significant antifibrotic efficacy in vivo
- Suitable for pulmonary fibrosis (IPF) research
- Exhibits high affinity toward h/mCHIT1 and h/mAMCase
- Reduced lung fibrosis in animal models
- Clinical trials are underway for pulmonary sarcoidosis (Phase 2)