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Home > Biochemical Engineering > Inhibitors (Find 1044 items)

Inhibitors

Tacrolimus

(104987-11-3)
For use after allogenic organ transplant to reduce the activity of the patient's immune system and so the risk of organ rejection. It was first approved by the FDA in 1994 for use in liver transplantation, this has been extended to include kidney, heart,

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Venlafaxine hydrochloride

(99300-78-4)
Venlaxafine is an inhibitor of reuptake of both serotonin (IC50 = 0.21 μM) and norepinephrine (IC50 = 0.64 μM). It is effective in vitro and in vivo and against human as well as rat receptors. As an antidepressant, it is properly placed in the serotonin-norepinephrine reuptake inhibitor class.[Cayman Chemical]

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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.

Isophosphamide

(3778-73-2)
A cytostatic agent, related structurally to cyclophosphamide

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Apixaban

(503612-47-3)
Apixaban, sold under the tradename Eliquis, is an anticoagulant for the treatment of venous thromboembolic events. It is taken by mouth. It is a direct factor Xa inhibitor.Apixaban was approved in Europe in 2012. It was approved in the U.S. in 2014 for treatment and secondary prophylaxis of deep vein thrombosis (DVT) and pulmonary embolism (PE). It is being developed in a joint venture by Pfizer and Bristol-Myers Squibb.

Tianeptine Salt

(30123-17-2)
1. Tricyclic compound with psychostimulant, anti-ulcer and anti-emetic properties. Antidepressant
2. Tianeptine (INN) (Stablon, Coaxil, Tatinol) is a selective serotonin reuptake enhancer (SSRE) drug used for treating major depressive episodes (mild, moderate, or severe). Unlike conventional tricyclic antidepressants, tianeptine enhances the reuptake of

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XYLAZINE HYDROCHLORIDE

(23076-35-9)
Xylazine is used as a sedative, analgesic, muscle relaxant.
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.
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