20 Results for "

Mn-SOD

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "Mn-SOD" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-B0124
CAS No.: 68291-97-4
Synonyms: AD 810; CI 912
Research Areas:  

Neurological Disease

Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy .
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2
2 Cited Publications
Cat. No.: HY-13336
CAS No.: 218791-21-0
Purity:  98.15%
Synonyms: M40403; GC4403
Target:  

SOD

Research Areas:  

Cancer

Imisopasem manganese (M40403) is a stable non-peptidyl mimetic of manganese superoxide MnSOD.
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1
1 Cited Publications
Cat. No.: HY-P71073
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SOD2; Manganese-Containing Superoxide Dismutase; Superoxide Dismutase 2; Gastric Cancer–Associated LncRNA 1; Superoxide Dismutase [Mn], Mitochondrial; Gastric Cancer-Associated LncRNA 1; LncRNA-GC1; Mangano-Superoxide Dismutase; GClnc1; Mn Superoxide Dism
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-B0124A
CAS No.: 68291-98-5
Synonyms: AD 810 SODium; CI 912 SODium
Zonisamide (AD 810) sodium is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide sodium exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide sodium also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide sodium can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy .
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Cat. No.: HY-124665
CAS No.: 473870-63-2
LMP-420 is a selective tumor necrosis factor-α (TNF-α) inhibitor. LMP-420 reduces the release of pro-inflammatory cytokines (e.g., IL-1β, IL-2), inducing the expression of anti-inflammatory cytokine IL-10 and anti-apoptotic molecules SOCS-1 and Mn-SOD. LMP-420 also downregulates chemokines (e.g., IP-10, MCP-1) to reduce immune cell infiltration. LMP-420 is promising for research of type 1 diabetes mellitus, inflammatory diseases (e.g., colitis), and HIV-Mycobacterium tuberculosis coinfection .
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Cat. No.: HY-P83938
Synonyms: IPOB; IPO-B; MnSOD; MVCD6; Mn-SOD

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P83938A
Synonyms: IPOB; IPO-B; MnSOD; MVCD6; Mn-SOD

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P80898
Synonyms: IPOB; IPO-B; MnSOD; MVCD6; Mn-SOD; SOD2

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-P80898A
Synonyms: IPOB; IPO-B; MnSOD; MVCD6; Mn-SOD; SOD2

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-P810660
Synonyms: IPOB; IPO-B; MnSOD; MVCD6; Mn-SOD; SOD2

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-RS23382
Research Areas:  

Others

Sod2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Sod2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS13560
Research Areas:  

Others

SOD2 Human Pre-designed siRNA Set A contains three designed siRNAs for SOD2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-B0124R
CAS No.: 68291-97-4
Synonyms: AD 810 (Standard); CI 912 (Standard)
Zonisamide (Standard) is the analytical standard of Zonisamide. This product is intended for research and analytical applications. Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy .
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Cat. No.: HY-B0124S2
Synonyms: AD 810-13C6; CI 912-13C6
Zonisamide- 13C6 (AD 810- 13C6) is 13C labeled Zonisamide. Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy .
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Cat. No.: HY-RS16939
Research Areas:  

Others

Sod2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sod2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P74538
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SOD2; Manganese-Containing Superoxide Dismutase; Superoxide Dismutase 2; Gastric Cancer–Associated LncRNA 1; Superoxide Dismutase [Mn], Mitochondrial; Gastric Cancer-Associated LncRNA 1; LncRNA-GC1; Mangano-Superoxide Dismutase; GClnc1; Mn Superoxide Dism
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-179151
Research Areas:  

Cancer

CDK4/6-IN-26 is a carbamate derivative that targets CDK4/CDK6. CDK4/6-IN-26 reduces CDK4/CDK6 levels, resulting in cell cycle arrest in the G0/G1 phase and in the S phase. CDK4/6-IN-26 exhibits high potency against SW480 cells (IC50 = 6.3 μM). CDK4/6-IN-26 affects ROS levels by increasing the expression of SOD2/MnSOD. CDK4/6-IN-26 establishes several interactions with the amino acids of the CDK6 active site. CDK4/6-IN-26 can be used for the research of colorectal cancer .
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Cat. No.: HY-B0124S3
CAS No.: 2308764-57-8
Zonisamide- 15N,d4 is the 15N- and deuterium labeled Zonisamide (HY-B0124). Zonisamide (AD 810) is an orally active carbonic anhydrase inhibitor, with Kis of 35.2 and 20.6 nM for hCA II and hCA V, respectively. Zonisamide exerts neuroprotective effects through anti-apoptosis and upregulating MnSOD levels. Zonisamide also increases the expression of Hrd1, thereby improving cardiac function in AAC rats. Zonisamide can be used in studies of seizure, parkinson’s disease and cardiac hypertrophy .
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Cat. No.: HY-183853
CAS No.: 35516-99-5
Arecaidine-propargyl ester is a selective M2 muscarinic receptor agonist with blood-brain barrier permeability, with a pKi of 5.91 for hm1, 7.06 for hm2, 6.07 for hm3, 6.01 for hm4, and 6.03 for hm5. Arecaidine-propargyl ester stimulates central and peripheral muscarinic receptors. Arecaidine-propargyl ester increases intracellular ROS, induces DNA damage and Apoptosis, and upregulates the expression of MnSOD and SIRT1. Arecaidine-propargyl ester reduces sympathetic nerve outflow, induces dose-dependent hypotension, and triggers negative chronotropic effects at high peripheral doses. Arecaidine-propargyl ester can be used in research related to Alzheimer's disease and glioblastoma .
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Cat. No.: HY-119590
CAS No.: 31501-55-0
Synonyms: Lonchocarpine
Lonchocarpin (Lonchocarpine) is a Wnt/β-catenin signaling pathway inhibitor. The IC50 of Lonchocarpin in SW480 pBAR/Renilla cells is 4 μM. Acting downstream of β-catenin stabilization, Lonchocarpin inhibits β-catenin nuclear localization and TCF-mediated transcription, as well as the proliferation and migration of colorectal cancer cells. Lonchocarpin enhances Nrf2/ARE-mediated antioxidant responses in primary astrocytes via AMPK and JNK-related signaling, reduces H2O2-induced ROS production, and increases the expression of HO-1, NQO1 and MnSOD. Lonchocarpin can be used in research on colorectal cancer and oxidative stress .
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