Phenols
eMolecules 3-Chloro-N-(4-hydroxyphenyl)propanamide | 19314-10-4 | MFCD09878796 | 1g
Ambeed | 3-Chloro-N-(4-hydroxyphenyl)propanamide | 1g | 600837883 | A336498 | | 19314-10-4 | MFCD09878796 | 199.630 | C9H10ClNO2
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Medchemexpress LLC ML-00253764 hydrochloride | 1706524-94-8 | 99.3% | 413.71 | 25 MG
ML-00253764 hydrochloride is a brain-penetrant, nonpeptidic melanocortin receptor 4 (MC4R) antagonist. This compound exhibits a Kᵢ of 0.16 μM and an IC₅₀ of 0.103 μM, and is capable of crossing the blood-brain barrier. It is intended for research use only.
- Brain-penetrant compound
- Nonpeptidic melanocortin receptor 4 (MC4R) antagonist
- Kᵢ of 0.16 μM
- IC₅₀ of 0.103 μM
- Capable of crossing the blood-brain barrier
- Intended for research use only
Cayman Chemical 3-Methoxycatechol 10g
A lignan-derived phenol; a GPR35 agonist (EC50 = 147 µM in a DMR assay) using HT-29 cells; promotes esophageal carcinogenesis in rats at 2% in the diet either alone or in a multiorgan model of nitrosamine-induced carcinogenesis; has been used as a precursor in the enzymatic synthesis of pyrogallol and purpurogallin; has been used as a precursor in the electro-organic synthesis of coumestan derivatives
Medchemexpress LLC Olopatadine hydrochloride | 5 MG
Olopatadine hydrochloride is a second-generation selective histamine H1-receptor antagonist and a potent anti-allergic drug with mast cell stabilizing and anti-histamine properties. It is primarily used for the treatment of allergic conjunctivitis and allergic rhinitis. It significantly inhibits ear swelling and the production of several interleukins (IL-4, IL-1beta, IL-6), GM-CSF, and NGF in lesioned ears. It is rapidly absorbed and inhibits histamine release from human conjunctival mast cells in vitro.
- Second-generation selective histamine H1-receptor antagonist
- Potent anti-allergic drug
- Mast cell stabilizing and anti-histamine properties
- Used to treat allergic conjunctivitis and allergic rhinitis
- Inhibits ear swelling and production of IL-4, IL-1beta, IL-6, GM-CSF, and NGF
- Rapidly absorbed in healthy human volunteers
- Inhibits histamine release from human conjunctival mast cell preparations in vitro
Medchemexpress LLC Nizatidine | 76963-41-2 | 98.7% | 25 G
Nizatidine is a potent and orally active histamine H2 receptor antagonist. It is used in research for stomach and intestine ulcers, functioning by decreasing gastric acid secretion and preventing ulcer recurrence in animal models.
- Potent and orally active histamine H2 receptor antagonist
- Decreases gastric acid secretion
- Prevents ulcer recurrence after healing in animal models
- Molecular weight: 331.46
- Formula: C12H21N5O2S2
- Appearance: Solid
- Color: White to off-white
- Recommended storage for powder: -20°C for 3 years, 4°C for 2 years
- Recommended storage in solvent: -80°C for 2 years, -20°C for 1 year
- Melting/freezing point: 130–132°C