335 Results for "

AA

" in MedChemExpress (MCE) Product Catalog:
Products (335)

335 Results for "AA" in MCE Product Catalog:

28
28 Publications Verification
Cat. No.: HY-B0713
CAS No.: 68302-57-8
Synonyms: AA673; Amoxanox; CHX3673
Target:  

IKK

Research Areas:  

Metabolic Disease

Amlexanox (AA673; Amoxanox; CHX3673) is a specific inhibitor of IKKε and TBK1, and inhibits the IKKε and TBK1 activity determined by MBP phosphorylation with an IC50 of approximately 1-2 μM.
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19
19 Cited Publications
Cat. No.: HY-P7110A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VEGF-AA; rHuVEGF165; VPF; Folliculostellate cell-derived growth factor; Glioma-derived endothelial cell mitogen
Species:  
Source:  
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11
11 Cited Publications
Cat. No.: HY-15414
CAS No.: 508233-74-7
Purity:  98.61%
Synonyms: Lu AA 21004
Vortioxetine (Lu AA 21004) is an antagonist of 5-HT3A and 5-HT7 receptors (Ki: 3.7 nM, 19 nM) and an inhibitor of serotonin transporter (SERT) (Ki: 1.6 nM), as well as a 5-HT1A agonist and a partial agonist of 5-HT1B (Ki: 15 nM, 33 nM) .
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11
11 Cited Publications
Cat. No.: HY-15414A
CAS No.: 960203-27-4
Purity:  99.87%
Synonyms: Lu AA21004 hydrobromide
Vortioxetine (Lu AA 21004) hydrobromide is an antagonist of 5-HT3A and 5-HT7 receptors (Ki: 3.7 nM, 19 nM) and an inhibitor of 5-hydroxytryptamine transporter (SERT) (Ki: 1.6 nM), as well as a 5-HT1A agonist and a partial 5-HT1B agonist (Ki: 15 nM, 33 nM) .
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10
10 Cited Publications
Cat. No.: HY-P2565
Research Areas:  

Inflammation/Immunology

Pepinh-TRIF (TFA) is a 30 aa peptide that blocks TIR-domain-containing adapter-inducing interferon-β (TRIF) signaling by interfering with TLR-TRIF interaction .
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9
9 Cited Publications
Cat. No.: HY-P7312
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: VEGF-AA; rMuVEGF164; VPF
Species:  
Source:  
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9
9 Cited Publications
Cat. No.: HY-153169
CAS No.: 2754428-18-5
Purity:  99.30%
Synonyms: 6PPD-Quinone
6PPD-Q (6PPD-Quinone) is an environmental pollutant that can be detected in human urine and is widely present in the environment. 6PPD-Q targets and binds to CNR2, CNR1, AA2AR, LCAT, and TRPA1, with CNR2 exhibiting the highest binding affinity, potentially acting as a CNR2 receptor agonist to activate cannabinoid receptors. 6PPD-Q induces intestinal inflammation and barrier damage by disrupting mitochondrial function, reducing neuronal glycolysis metabolites and TCA cycle intermediates, and exacerbating α-synuclein (α-syn) aggregation. 6PPD-Q is applicable in research on environmental toxicology, neurodegenerative diseases, and inflammation-related disorders .
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8
8 Cited Publications
Cat. No.: HY-P1388
CAS No.: 166090-74-0
Synonyms: Amyloid β-peptide (1-42) (rat/mouse)
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

β-Amyloid (1-42), (rat/mouse) is a 42-aa peptide, shows cytotoxic effect on acute hippocampal slices, and used in the research of Alzheimer's disease.
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8
8 Cited Publications
Cat. No.: HY-P1388A
Synonyms: Amyloid β-peptide (1-42) (rat/mouse) TFA
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

β-Amyloid (1-42), (rat/mouse) TFA is a 42-aa peptide, shows cytotoxic effect on acute hippocampal slices, and used in the research of Alzheimer's disease.
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4
4 Cited Publications
Cat. No.: HY-124293
CAS No.: 393121-74-9
Purity:  99.81%
AA147 is a endoplasmic reticulum (ER) proteostasis regulator. AA147 promotes protection against oxidative damage in neuronal cells and prevents endothelial barrier dysfunction by activating ATF6 arm (selectively) of the unfolded protein response (UPR) and the NRF2 oxidative stress response. AA147 can rebalances XBP1s expression in vivo, and also induces survival motor neuron (SMN) expression and spinal motorneuron (MN) protection .
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4
4 Cited Publications
Cat. No.: HY-101518
CAS No.: 1818393-16-6
Purity:  98.67%
Synonyms: APG-115; AA-115
Research Areas:  

Cancer

Alrizomadlin (APG-115) is an orally active MDM2 protein inhibitor binding to MDM2 protein with IC50 and Ki values of 3.8 nM and 1 nM, respectively . Alrizomadlin blocks the interaction of MDM2 and p53 and induces cell-cycle arrest and apoptosis in a p53-dependent manner .
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4
4 Cited Publications
Cat. No.: HY-B0774
CAS No.: 112665-43-7
Synonyms: AA 2414
Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
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4
4 Cited Publications
Cat. No.: HY-P72238
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Heat shock 86 kDa; Heat shock protein 90kDa alpha cytosolic class A member 1; Heat shock protein 90kDa alpha cytosolic class B member 1; Heat shock protein HSP 90 alpha ; Heat shock protein HSP 90 beta; Heat shock protein HSP 90-alpha; HS90A_HUMAN; HSP 84; HSP 86; Hsp 90; HSP86; HSP90A; HSP90AA1; HSP90AB1; HSP90B; HSPC1; HSPC2; HSPCAL1 ; HSPCAL4; Renal carcinoma antigen NY-REN-38
Species:  
Source:  
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3
3 Cited Publications
Cat. No.: HY-P7311
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rRtVEGF164; VEGF-AA; VPF
Species:  
Rat
Source:  
CHO
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3
3 Cited Publications
Cat. No.: HY-P1569
CAS No.: 151705-84-9
Synonyms: LCMV GP(33-41) M-peptide; gp33 epitope
Target:  

Arenavirus

Research Areas:  

Infection Inflammation/Immunology

LCMV gp33-41, the carboxyl-extended 9-aa-long peptide, is an lymphocytic choriomeningitis virus sequence restricted by MHC class I H-2Db molecules and presented to cytotoxic T lymphocytes .
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3
3 Cited Publications
Cat. No.: HY-P1569A
Synonyms: LCMV GP(33-41) M-peptide TFA; gp33 epitope TFA
Target:  

Arenavirus

Research Areas:  

Inflammation/Immunology

LCMV gp33-41 (TFA), the carboxyl-extended 9-aa-long peptide, is an lymphocytic choriomeningitis virus sequence restricted by MHC class I H-2Db molecules and presented to cytotoxic T lymphocytes .
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2
2 Cited Publications
Cat. No.: HY-110111
CAS No.: 1380782-27-3
Purity:  99.04%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

T2AA is a monoubiquitinated proliferating cell nuclear antigen (PCNA) inhibitor that prevents DNA repair, increases double-strand break (DSB) formation and promotes necroptosis and cell cycle arrest in G1 phase .
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2
2 Cited Publications
Cat. No.: HY-125145
CAS No.: 457961-34-1
Purity:  99.94%
Target:  

Melanopsin Receptor

Research Areas:  

Metabolic Disease Cancer

AA92593 is a selective and competitive melanopsin OPN4 antagonist .
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2
2 Cited Publications
Cat. No.: HY-N0026
CAS No.: 94492-24-7
Synonyms: 2'-AA
2'-Acetylacteoside (2'-AA) is a natural compound with oral activity and blood-brain barrier permeability. 2'-Acetylacteosideexhibits MAO‑B inhibitory activity (IC50 = 17.71 μM, Ki = 13.81 μM). 2'-Acetylacteoside downregulates the expression of RANK, TRAF6, NF‑κB, NFATc1 and IKKβ, disrupts the RANKL/RANK interaction, blocks downstream signaling pathways, and increases the level of phosphorylated Akt. 2'-Acetylacteoside possesses potent anti-osteoclastogenic, anti-bone resorptive, pro-neurogenic, neuroprotective and antioxidant activities. 2'-Acetylacteoside can be used in the research of osteoporosis, ischemic stroke and Parkinson's disease .
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2
2 Cited Publications
Cat. No.: HY-P70598
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PDGFAA; PDGF-AA
Species:  
Source:  
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