94 Results for "

MR

" in MedChemExpress (MCE) Product Catalog:
Products (94)

94 Results for "MR" in MCE Product Catalog:

11
11 Publications Verification
Cat. No.: HY-113313
CAS No.: 52-39-1
Purity:  98.93%
Aldosterone is the primary mineralocorticoid. Aldosterone is a steroid hormone, and it is synthesized and secreted in response to renin-angiotensin system activation (RAS) or high dietary potassium by the zona glomerulosa (ZG) of the adrenal cortex. Aldosterone activity is dependent by the binding and activation of the cytoplasmic/nuclear mineralocorticoid receptor (MR) at cellular level .
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9
9 Cited Publications
Cat. No.: HY-111372
CAS No.: 1050477-31-0
Purity:  99.66%
Synonyms: BAY 94-8862
Finerenone (BAY 94-8862) is a third-generation, selective, and orally active nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50 = 18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (> 500-fold). Finerenone has the potential for cardiorenal diseases research, such as type 2 diabetes mellitus and chronic kidney disease .
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3
3 Cited Publications
Cat. No.: HY-12206
CAS No.: 106243-16-7
Purity:  99.91%
Synonyms: MR-12842
Target:  

Histamine Receptor

Research Areas:  

Neurological Disease

Thioperamide (MR-12842) is a potent, orally available, brain penetrant and selective H3 receptor antagonist with a Ki of 4.3 nM for inhibition of [ 3H]histamine release. Thioperamide inhibits [ 3H]histamine synthesis with a Ki of 31 nM .
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3
3 Cited Publications
Cat. No.: HY-12206A
CAS No.: 148440-81-7
Purity:  98.26%
Synonyms: MR-12842 maleate
Target:  

Histamine Receptor

Research Areas:  

Neurological Disease

Thioperamide maleate (MR-12842 maleate) is a potent, orally available, brain penetrant and selective H3 receptor antagonist with a Ki of 4.3 nM for inhibition of [ 3H]histamine release. Thioperamide maleate inhibits [ 3H]histamine synthesis with a Ki of 31 nM .
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3
3 Cited Publications
Cat. No.: HY-P702520
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: A2MR; Alpha-2-Macroglobulin Receptor; APOER; APR; CD91; LRP1 Cluster II; LRP-1 Cluster II; LRP1; TGFBR5
Species:  
Source:  
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2
2 Cited Publications
Cat. No.: HY-N0471
CAS No.: 101-31-5
Synonyms: Hyoscyamine
L-Hyoscyamine (Daturine), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine is a levo-isomer to Atropine (HY-B1205) .
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2
2 Cited Publications
Cat. No.: HY-128358
CAS No.: 2374703-19-0
Purity:  98.37%
Research Areas:  

Neurological Disease

MR-L2 is a reversible and noncompetitive allosteric activator of long-isoform phosphodiesterase-4 (PDE4), activates representative PDE4 long-isoform variants (PDE4A4, PDE4B1, PDE4C3, PDE4D5). MR-L2 suppresses PGE2-induced MDCK cell cyst formation with an EC50 of 1.2 μM .
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2
2 Cited Publications
Cat. No.: HY-N0471A
CAS No.: 620-61-1
Synonyms: Daturine sulfate
L-Hyoscyamine sulfate (Daturine sulfate), a natural plant tropane alkaloid, is a potent and competitive muscarinic receptor (MR) antagonist. L-Hyoscyamine sulfate is a levo-isomer to Atropine (HY-B1205) .
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1
1 Cited Publications
Cat. No.: HY-W145667
CAS No.: 9036-88-8
Mannan is an orally active polysaccharide compound that binds to the mannose receptor (MR). Mannan promotes bacterial uptake and endosomal degradation by binding to MR, thereby enhancing the production of IL-12 in immune cells. Mannan enhances ROS production. Mannan modulates immunity, inhibits Aflatoxin B1 (HY-N6615)-induced toxicity, and reduces lipid .
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1
1 Cited Publications
Cat. No.: HY-126855
CAS No.: 60320-05-0
Purity:  99.92%
Synonyms: 7-Sulfocholic acid
Cholic acid 7-sulfate (7-Sulfocholic acid) is a selective agonist targeting TGR5 (EC50=0.17 μM) and a ligand for MHC class I-related protein (MR1). As a gut-restricted TGR5 agonist, cholic acid 7-sulfate binds to TGR5 on enteroendocrine L cells, induces GLP-1 secretion, and improves glucose tolerance in a TGR5-dependent manner. Cholic acid 7-sulfate also acts as an endogenous ligand for MR1, promoting the survival of mucosal-associated invariant T cells MAIT and the expression of homeostatic gene signatures, affecting MAIT cell development and function. Cholic acid 7-sulfate is mainly used in the research of diabetes and MAIT cell-related immune regulation .
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1
1 Cited Publications
Cat. No.: HY-N0179
CAS No.: 3604-87-3
Synonyms: α-Ecdysone
Ecdysone (α-Ecdysone), a major steroid hormone in insects and herbs, triggers mineralocorticoid receptor (MR) activation and induces cellular apoptosis. Ecdysone plays essential roles in coordinating developmental transitions and homeostatic sleep regulation through its active metabolite 20-hydroxyecdysone (Crustecdysone; 20E; HY-N6979) .
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1
1 Cited Publications
Cat. No.: HY-138283
CAS No.: 1210906-48-1
Purity:  99.82%
Research Areas:  

Cancer

MR837 is an inhibitor of NSD2-PWWP1. MR837 can bind with human nuclear receptor binding SET domain protein 2 (PWWP domain) .
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1
1 Cited Publications
Cat. No.: HY-14234
CAS No.: 1245526-82-2
Purity:  99.06%
Glucocorticoid receptor agonist is a Glucocorticoid receptor agonist that acts on Glucocorticoid receptor (GR), progesterone receptor (PR) and mineralocorticoid receptor (MR) with the IC50 values of 2.1 , 1200 and 210 nM, respectively. Glucocorticoid receptor agonist has steroid-like anti-inflammatory properties and may be used to improve metabolism and reduce increased levels of body fat and serum insulin .
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1
1 Cited Publications
Cat. No.: HY-12527
CAS No.: 1651890-44-6
Purity:  99.95%
Synonyms: MR-29072
Target:  

Bcl-2 Family

Research Areas:  

Cancer

Pyridoclax is a potential Mcl-1 inhibitor.
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1
1 Cited Publications
Cat. No.: HY-111372S1
Synonyms: BAY 94-8862-d5
Finerenone-d5 (BAY 94-8862-d5) is deuterium labeled Finerenone. Finerenone (BAY 94-8862) is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50=18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (>500-fold). Finerenone has the potential for cardiorenal diseases research, such as type 2 diabetes mellitus and chronic kidney disease .
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1
1 Cited Publications
Cat. No.: HY-107631
CAS No.: 76676-34-1
Purity:  ≥98.0%
Synonyms: RU 28318
Research Areas:  

Endocrinology

Oxprenoate potassium is a potent mineralocorticoid (MR) antagonist. Oxprenoate potassium accentuates DEX (dexamethasone)-induced apoptosis .
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1
1 Cited Publications
Cat. No.: HY-P83714M
Synonyms: MMR; MR; MRC1; macrophage mannose receptor; mannose receptor

Host:  

Rat

Application:  

FC

Reactivity:  

Mouse

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1
1 Cited Publications
Cat. No.: HY-P80746
Synonyms: A2MR; alpha 2MR; Alpha 2 macroglobulin receptor; CD91; APR; LRP1; LRP85; TGFBR5

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-P71133
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Plasminogen activator inhibitor 1; Endothelial plasminogen activator inhibitor; Serpin E1; MR1; Pai1; Planh1;
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P704765
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: A2MR; Alpha-2-Macroglobulin Receptor; APOER; APR; CD91; LRP1 Cluster II; LRP-1 Cluster II; LRP1; TGFBR5
Species:  
Source:  
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