12 Results for "

Ucp2

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "Ucp2" in MCE Product Catalog:

22
22 Publications Verification
Art. -Nr.: HY-17389
CAS. Nr.: 6902-77-8
Synonyms: (+)-Genipin
Genipin ((+)-Genipin) is a natural crosslinking reagent derived from Gardenia jasminoides Ellis fruits. Genipin inhibits UCP2 (uncoupling protein 2) in cells. Genipin has a variety of bioactivities, including modulation on proteins, antitumor, anti-inflammation, immunosuppression, antithrombosis, and protection of hippocampal neurons. Genipin also can be used for type 2 diabetes research [2].
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2
2 Cited Publications
Art. -Nr.: HY-138830
CAS. Nr.: 1818252-53-7
Reinheit:  99.81%
Target:  

Histone Demethylase

Forschungsgebiete:  

Neurological Disease

TAK-418 is an orally active, blood-brain barrier-penetrant LSD1 inhibitor with a human IC50 of 2.9 nM. TAK-418 irreversibly inhibits LSD1 by forming a compact flavin-FAD adduct with the catalytic domain FAD, blocking the demethylation of H3K4me1/2 and H3K9me1/2 without disrupting the LSD1-GFI1B interaction. TAK-418 restores normally dysregulated brain gene expression and DNA methylation, increases H3K4me1/2/3 and H3K9me2 at the Ucp2 locus, and induces Ucp2 mRNA expression. TAK-418 rescues defective H3K4 histone modifications, normalizes adult neurogenesis, and improves recognition memory, social behavior, and cognition in rodent models. TAK-418 can be used in research related to neurodevelopmental disorders, Alzheimer's disease, and autism spectrum disorders [2] .
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Art. -Nr.: HY-P5534
CAS. Nr.: 524060-93-3
Synonyms: Ucp2
Target:  

Inhibitory Antibodies

Forschungsgebiete:  

Cancer

Enavermotide (UCP2) is an immunological agent for active immunization (antineoplastic) .
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Art. -Nr.: HY-17389R
CAS. Nr.: 6902-77-8
Synonyms: (+)-Genipin (Standard)
Genipin (Standard) is the analytical standard of Genipin. This product is intended for research and analytical applications. Genipin ((+)-Genipin) is a natural crosslinking reagent derived from Gardenia jasminoides Ellis fruits. Genipin inhibits UCP2 (uncoupling protein 2) in cells. Genipin has a variety of bioactivities, including modulation on proteins, antitumor, anti-inflammation, immunosuppression, antithrombosis, and protection of hippocampal neurons. Genipin also can be used for type 2 diabetes research [2].
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Art. -Nr.: HY-RS15411
Forschungsgebiete:  

Others

UCP2 Human Pre-designed siRNA Set A contains three designed siRNAs for UCP2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-RS24369
Forschungsgebiete:  

Others

Ucp2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Ucp2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-RS17900
Forschungsgebiete:  

Others

Ucp2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ucp2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-101824
CAS. Nr.: 179068-64-5
Target:  

PPAR

Forschungsgebiete:  

Metabolic Disease

NC-2100 is a PPAR activator. NC-2100 can effectively reduce the plasma glucose and triglyceride levels of obese KKAy mice. NC-2100 can induce UCP1 and UCP2 expression in mesenteric and subcutaneous WAT of mice. NC-2100 can be used in research related to type 2 diabetes .
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Art. -Nr.: HY-P84407
Synonyms: UcpH; BMIQ4; SLC25A8

Host:  

Mouse

Application:  

ICC/IF, FC, ELISA

Reactivity:  

Human

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Art. -Nr.: HY-P84407A
Synonyms: UcpH; BMIQ4; SLC25A8

Host:  

Mouse

Application:  

ICC/IF, FC, ELISA

Reactivity:  

Human

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Art. -Nr.: HY-189057
Anethole trithione derivative-1 is a derivative of Anethole trithione (HY-B1223), and also a regulator of sulfide:quinone oxidoreductase (SQR) and uncoupling protein 2 (UCP2), with mitochondrial uncoupling-inducing activity and neuroprotective activity. Anethole trithione derivative-1 mediates mitochondrial uncoupling via SQR-dependent reverse electron transport of complex I, ROS-dependent UCP2 activation, and reduction of mitochondrial membrane potential. Anethole trithione derivative-1 reduces brain damage and improves function in mouse models of ischemic and hemorrhagic stroke. Anethole trithione derivative-1 can be used in stroke research .
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Art. -Nr.: HY-138830B
CAS. Nr.: 1818252-52-6
Target:  

Histone Demethylase

Forschungsgebiete:  

Neurological Disease

TAK-418 free base is an orally active, blood-brain barrier-penetrant LSD1 inhibitor with a human IC50 of 2.9 nM. TAK-418 free base irreversibly inhibits LSD1 by forming a compact flavin-FAD adduct with the catalytic domain FAD, blocking the demethylation of H3K4me1/2 and H3K9me1/2 without disrupting the LSD1-GFI1B interaction. TAK-418 free base restores normally dysregulated brain gene expression and DNA methylation, increases H3K4me1/2/3 and H3K9me2 at the Ucp2 locus, and induces Ucp2 mRNA expression. TAK-418 free base rescues defective H3K4 histone modifications, normalizes adult neurogenesis, and improves recognition memory, social behavior, and cognition in rodent models. TAK-418 free base can be used in research related to neurodevelopmental disorders, Alzheimer's disease, and autism spectrum disorders [2] .
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