348 Results for "

AA

" in MedChemExpress (MCE) Product Catalog:
Products (348)

348 Results for "AA" in MCE Product Catalog:

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1 Cited Publications
Cat. No.: HY-N6958
CAS No.: 562043-82-7
Synonyms: AA-2βG
2-O-β-D-Glucopyranosyl-L-ascorbic acid (AA-2βG) is an orally active vitamin C derivative. 2-O-β-D-Glucopyranosyl-L-ascorbic acid exhibits multiple activities including antioxidant, anti-tumor and immunomodulatory effects. 2-O-β-D-Glucopyranosyl-L-ascorbic acid mediates tumor cell apoptosis, induces cell cycle arrest, scavenges free radicals and eliminates oxidative stress. 2-O-β-D-Glucopyranosyl-L-ascorbic acid can be used in studies related to cancer, inflammation and immunity .
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1 Cited Publications
Cat. No.: HY-N3027
CAS No.: 117230-33-8
Soyasaponin Aa is a soyasaponin that can be found in soy. Soyasaponin Aa suppresses PPARγ transcriptional activity, reduces PPARγ and C/EBPα expression, inhibits adipocyte differentiation and lipid accumulation, and reduces adipogenic marker gene expression. Soyasaponin Aa reduces hydrogen peroxide-induced reactive oxygen species (ROS) production and malondialdehyde levels. Soyasaponin Aa exhibits cellular antioxidant activity. Soyasaponin Aa can be used for the research of obesity .
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1 Cited Publications
Cat. No.: HY-Y0641
CAS No.: 39515-51-0
Synonyms: m-Phenoxybenzaldehyde
Target:  

Drug Intermediate

Research Areas:  

Others

3-Phenoxybenzaldehyde (m-Phenoxybenzaldehyde) is the major product of CYP6AA3-mediated deltamethrin metabolism, generated by oxidative cleavage of deltamethrin. 3-Phenoxybenzaldehyde often serves as an intermediate .
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1 Cited Publications
Cat. No.: HY-P1045
CAS No.: 380488-27-7
Target:  

Arp2/3 Complex

Research Areas:  

Others

187-1, N-WASP inhibitor, a 14-aa cyclic peptide, is an allosteric neural Wiskott-Aldrich syndrome protein (N-WASP) inhibitor. 187-1, N-WASP inhibitor potently inhibits actin assembly induced by phosphatidylinositol 4,5-bisphosphate (PIP2) with an IC50 of 2 μM. 187-1, N-WASP inhibitor prevents the activation of Arp2/3 complex by N-WASP by stabilizing the autoinhibited state of the protein .
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1 Cited Publications
Cat. No.: HY-148088
CAS No.: 3027658-65-4
Purity:  98.04%
Target:  

Adenosine Receptor

Research Areas:  

Cancer

M1069 is a selective and orall active, dual A2A/A2B adenosine receptor antagonist with a selectivity of >100 fold against the A1 and A3 receptors. M1069 counteracts immune-suppressive mechanisms of adenosine, and exhibits anti-tumor activity .
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1 Cited Publications
Cat. No.: HY-N0511
CAS No.: 475-80-9
Synonyms: Aristolochic acid II
Aristolochic acid B (Aristolochic Acid II) is an orally active major component of aristolochic acid (AA). Aristolochic acid B can be isolated from plants of the genus Aristolochica. Aristolochic acid B forms DNA adducts. Aristolochic acid B is mutagenic. Aristolochic acid B exhibits a greater carcinogenic risk in vivo than Aristolochic acid I (HY-N0510) .
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1 Cited Publications
Cat. No.: HY-P0323A
Synonyms: LCMV GP(33-41) C-peptide TFA
Target:  

Arenavirus

Research Areas:  

Infection

GP(33-41) TFA, a 9-aa-long peptide, is the optimal sequence of the GP1 epitope of lymphocytic choriomeningitis virus. GP(33-41) TFA can upregulate H-2D b molecules at the RMA-S (Db Kb) cell surface with a SC50 of 344 nM .
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1 Cited Publications
Cat. No.: HY-148088A
CAS No.: 2459881-03-7
Purity:  98.92%
Target:  

Adenosine Receptor

Research Areas:  

Cancer

M1069 (free base) is a selective and orall active, dual A2A/A2B adenosine receptor antagonist with a selectivity of >100 fold against the A1 and A3 receptors. M1069 (free base) counteracts immune-suppressive mechanisms of adenosine, and exhibits anti-tumor activity .
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1 Cited Publications
Cat. No.: HY-P3029
CAS No.: 9001-84-7
Synonyms: PLA2
Phospholipase A2 (PLA2) is a calcium-dependent, heat-stable enzyme that catalyzes the hydrolysis of glycerophospholipids at the sn-2 position of cellular membranes, thereby releasing Arachidonic Acid (AA) (HY-109590). Phospholipase A2 is a key mediator in the biosynthesis of pro-inflammatory lipid mediators, critically involved in inflammatory processes. Phospholipase A2 can be used for cardiovascular and inflammatory diseases research .
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1 Cited Publications
Cat. No.: HY-P1585
CAS No.: 212370-40-6
Synonyms: Hgp100 (25-33)
Target:  

MHC

Research Areas:  

Cancer

Gp100 (25-33), human (Hgp100 (25-33)) is the amino acids 25-33 fragment of the human melanoma antigen. Gp100 (25-33), human is a 9-amino acid (AA) epitope restricted by MHC class I H-2D b and recognized by the T cells. Gp100 (25-33), human has immunogenicity and induces specific T cells. Gp100 (25-33), human can be used for the cancer research, such as melanoma .
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1 Cited Publications
Cat. No.: HY-P1585A
Synonyms: Hgp100 (25-33) TFA
Target:  

MHC

Research Areas:  

Cancer

Gp100 (25-33), human TFA (Hgp100 (25-33) (TFA)) is the amino acids 25-33 fragment of the human melanoma antigen. Gp100 (25-33), human TFA is a 9-amino acid (AA) epitope restricted by MHC class I H-2D b and recognized by the T cells. Gp100 (25-33), human TFA has immunogenicity and induces specific T cells. Gp100 (25-33), human TFA can be used for the cancer research, such as melanoma .
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Cat. No.: HY-107729
CAS No.: 304008-29-5
Purity:  98.3%
Research Areas:  

Neurological Disease

Lu AA33810 is a selective, orally active and brain-penetrant antagonist of neuropeptide Y5 receptor with a Ki of 1.5 nM for the rat receptor. Lu AA33810 exhibts antianxiolytic-like and antidepressant-like effects .
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Cat. No.: HY-18522
CAS No.: 1312782-34-5
Target:  

Phospholipase

Research Areas:  

Metabolic Disease

AA26-9 is a potent and broad spectrum serine hydrolase inhibitor. AA26-9 targets included serine peptidases, lipases, amidases, esterases, and thioesterases. AA26-9 shows inhibitory activity against approximately 1/3 of the 40+ serine hydrolases detected in immortalized T cell lines .
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Cat. No.: HY-12886
CAS No.: 80809-81-0
Purity:  99.31%
Synonyms: AA 861
Research Areas:  

Inflammation/Immunology

Docebenone (AA 861) is a potent, selective and orally active 5-LO (5-lipoxygenase) inhibitor.
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Cat. No.: HY-159700
CAS No.: 3027565-91-6
Research Areas:  

Infection Cancer

AA3-DLin is a biodegradable ionizable cationic lipid (pKa = 5.8). AA3-DLin is used to combine mRNA with lipid nanoparticles (LNPs) for delivery, thereby achieving endosomal escape and cytoplasmic release. AA3-DLin can be used in research on type 2 diabetes, steroid-resistant asthma, lung cancer, ischemic stroke, breast cancer, melanoma, and COVID-19 .
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Cat. No.: HY-125928
CAS No.: 354812-16-1
Purity:  ≥98.0%
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

AA43279 is an in gamma-aminobutyric acid (GABA) fast-firing interneurons located activator for Nav1.1 channel (SCN1A) with an EC50 of 9.5 μM. AA43279 enhances specific neuronal firing activity in vitro, and exhibits anticonvulsant activity in rat MEST model .
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Cat. No.: HY-18544
CAS No.: 65815-76-1
Target:  

MAGL FAAH

Research Areas:  

Metabolic Disease

AA38-3 is a serine hydrolase (SH) inhibitor. AA38-3 can inhibit three SHs, ABHD6, ABHD11, and FAAH .
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Cat. No.: HY-D1021
CAS No.: 936327-10-5
Synonyms: Aminoallyl-dUTP sodium
AA-dUTP (Aminoallyl-dUTP) sodium salt is a reverse transcriptase and DNA polymerase I substrate with probe precursor activity. AA-dUTP sodium salt undergoes enzymatic incorporation into DNA during cDNA synthesis and nick translation. AA-dUTP sodium salt generates amine-modified DNA, which can be used for labeling with amine-reactive fluorescent dyes .
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Cat. No.: HY-119390
CAS No.: 1869921-96-9
Target:  

DNA Methyltransferase

Research Areas:  

Cancer

AA-CW236 is a MGMT (O6-methylguanine DNA methyltransferase) inhibitor. AA-CW236 targets MGMT active site Cys145 for covalent modification .
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Cat. No.: HY-168969
Target:  

PROTACs

Research Areas:  

Neurological Disease Cancer

AA-BR-157 is a metallothionein 2A (MT2A) PROTAC degrader, DC50 is 200 nM (MT2A overexpressed in MDA-MB-231 cells). AA-BR-157 increases intracellular zinc levels, downregulates DIAPH3, disrupts cytoskeleton remodeling, and reduces the migration and invasion abilities of cancer cells. AA-BR-157 can be used for research on triple-negative breast cancer and glioblastoma .
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