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Home > Biochemical Engineering > Inhibitors (Find 41 items)

Biochemical Engineering

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Inhibitors

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Inhibitors

Donepezil hydrochloride

(120011-70-3)
1. A nootropic. An inhibitor of acetylcholinesterase
2. A labelled nootropic. An inhibitor of acetylcholinesterase.
3. Antialzheimer
4. Labeled Donepezil, intended for use as an internal standard for the quantification of Donepezilby GC- or LC-mass spectrometry.

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Doxycycline hydrochloride

(10592-13-9)
Doxycycline hydrochloride is a salt prepared from doxycycline taking advantage of the basic dimethylamino group which protonates and readily forms a salt in hydrochloric acid solutions. The hydrochloride is the preferred formulation for pharmaceutical applications. Like all tetracyclines, doxycycline shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis.

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Duloxetine hydrochloride

(136434-34-9)
solubility H2O: soluble5 mg/mL (clear solution, warmed)

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Dorzolamide hydrochloride

(130693-82-2)
An inhibitor of carbonic anhydrase.

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Dydrogesterone

(152-62-5)
A synthetic progestin largely used in hormone therapy, on the central nervous system by studying two markers of the neuroendocrine function: the neurosteroid allopregnanolone and the opioid .beta.-endorphin. Progestogen.

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Desonide

(638-94-8)
Anti-inflammatory

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Darifenacin hydrobromide

(133099-07-7)
acute lymphoblastic leukemia therapeutic

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Dexmedetomidine hydrochloride

(145108-58-3)
highly selective, potent α2-adrenoceptor agonist, analgesic, anxiolytic, bradycardic, hypotensive, sedative, hypothermic

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Dienogest

(65928-58-7)
Dienogest is an orally active synthetic progesterone (or progestin). It is available for use as an oral contraceptive in combination with ethinylestradiol. It has antiandrogenic activity and as a result can improve androgenic symptoms. It is a non-ethinyl

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Dexmedetomidine

(113775-47-6)
α2-Adrenergic agonist; (+)-isomer of Medetomidine; sedative; analgesic.

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Small molecule inhibitors are a type of molecules that can interact with proteins and reduce the biological activity of target proteins, including enzyme inhibitors, transcription factor inhibitors, and ion channel blockers. It acts on popular signaling pathways, popular targets and popular research fields: MAPK, PI3K, JAK / STAT and other signaling pathways, HDAC, Aurora kinase, CDK and cell cycle regulators, integrase / protease, etc. Research fields such as epigenetics, CNS, GPCR, anti-virus, antibacterial / anti-inflammatory. It is an effective tool for cell biology research.

Source Inhibitors Raw Materials by Region

South Korea

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