152 Results for "

LP

" in MedChemExpress (MCE) Product Catalog:
Products (152)

152 Results for "LP" in MCE Product Catalog:

17
17 Publications Verification
Cat. No.: HY-15516
CAS No.: 1018899-04-1
Purity:  99.63%
Synonyms: LX-4211; LP-802034
Target:  

SGLT

Research Areas:  

Metabolic Disease

Sotagliflozin (LX-4211) is a potent dual SGLT2/1 inhibitor. Antidiabetic agents.
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8
8 Cited Publications
Cat. No.: HY-10521
CAS No.: 356057-34-6
Purity:  99.94%
Synonyms: SB-480848
Target:  

Phospholipase Apoptosis

Research Areas:  

Cardiovascular Disease Cancer

Darapladib (SB-480848) is an orally active, selective and reversible Lp-PLA2 inhibitor (IC50=0.25 nM). Darapladib can trigger irreversible actions on glioma cell apoptosis and induce cycle arrest. Darapladib can be used in the study of atherosclerosis and cancer .
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7
7 Cited Publications
Cat. No.: HY-15849
CAS No.: 945976-43-2
Purity:  98.02%
LP-533401 is a Tryptophan hydroxylase 1 inhibitor that regulates serotonin production in the gut.
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7
7 Cited Publications
Cat. No.: HY-15849A
CAS No.: 1040526-12-2
Purity:  98.02%
LP-533401 hydrochloride is a tryptophan hydroxylase 1 inhibitor that regulates serotonin production in the gut.
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3
3 Cited Publications
Cat. No.: HY-P3400
CAS No.: 887255-16-5
Synonyms: LQVTDSGLYRCVIYHPP
Target:  

Inhibitory Antibodies

Research Areas:  

Neurological Disease

LP17 (LQVTDSGLYRCVIYHPP) is a BBB-penetrable triggering receptor expressed on myeloid cells (TREM-1) inhibitory peptide. LP17 substantially alleviates ischemia-induced infarction and neuronal injury. LP17 can get access into brain and block TREM-1 .
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3
3 Cited Publications
Cat. No.: HY-P3400A
Synonyms: LQVTDSGLYRCVIYHPP TFA
Target:  

Inhibitory Antibodies

Research Areas:  

Neurological Disease

LP17 (LQVTDSGLYRCVIYHPP) TFA is a BBB-penetrable triggering receptor expressed on myeloid cells (TREM-1) inhibitory peptide. LP17 TFA substantially alleviates ischemia-induced infarction and neuronal injury. LP17 TFA can get access into brain and block TREM-1 .
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3
3 Cited Publications
Cat. No.: HY-102004
CAS No.: 412950-08-4
Purity:  99.44%
Synonyms: SB 659032
Rilapladib (SB 659032) is a selective Lp-PLA2 (lipoprotein-associated phospholipase A2) inhibitor with an IC50 of 230 pM . Rilapladib (SB 659032) is also a PAFR (Platelet Activating Factor Receptor) antagonist .
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2
2 Cited Publications
Cat. No.: HY-46760
CAS No.: 1799316-64-5
Target:  

Liposome

Research Areas:  

Others

LP01 (Example 13) is a cationic lipid used in the delivery of biologically active agents to cells and tissues .
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2
2 Cited Publications
Cat. No.: HY-117626
CAS No.: 1454555-29-3
Purity:  99.74%
LP-935509 is an orally active, potent, selective, ATP-competitive and brain-penetrant inhibitor of adaptor protein-2 associated kinase 1 (AAK1) with an IC50 of 3.3 nM and a Ki of 0.9 nM, respectively. LP-935509 is also a potent inhibitor of BIKE (IC50=14 nM) and a modest inhibitor of GAK (IC50=320 nM). LP-935509 shows antinociceptive activity. LP-935509 can be used for neuropathic pain and SARS-CoV-2 research .
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2
2 Cited Publications
Cat. No.: HY-111455
CAS No.: 1052147-86-0
Purity:  99.87%
Target:  

5-HT Receptor

LP-211 is a selective and blood brain barrier penetrant 5-HT7 receptor agonist, with a Ki of 0.58 nM, with high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).
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1
1 Cited Publications
Cat. No.: HY-145588
CAS No.: 1637677-22-5
Purity:  99.00%
Synonyms: INCB54707
Target:  

JAK

Research Areas:  

Inflammation/Immunology

Povorcitinib (INCB54707) is a potent and selective JAK1 inhibitor that effectively reduces abscesses and inflammatory nodules. Povorcitinib is used to study cutaneous lupus erythematosus (CLE) and lichen planus (LP) .
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1
1 Cited Publications
Cat. No.: HY-131034
CAS No.: 1365060-22-5
Purity:  99.63%
Target:  

Wnt

Research Areas:  

Others

LP-922056 is an orally active, highly potent Notum Pectinacetylesterase inhibitor with EC50s of 21 nM, 55 nM in human and mouse cellular assay, respectively. LP-922056 significantly increases midshaft femur cortical bone thickness in mice and rats .
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1
1 Cited Publications
Cat. No.: HY-120179
CAS No.: 1454808-95-7
Purity:  99.73%
Target:  

AAK1

Research Areas:  

Neurological Disease

LP-922761 is a potent, selective and orally active adapter protein-2 associated kinase 1 (AAK1) inhibitor with IC50s of 4.8 nM and 7.6 nM in enzyme and cell assays, respectively. LP-922761 also inhibits BMP-2-inducible protein kinase (BIKE) with an IC50 of 24 nM. LP-922761 exhibits no significant activity at cyclin G-associated kinase (GAK), opioid, adrenergic α2 or GABAa receptors .
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1
1 Cited Publications
Cat. No.: HY-P3460A
TDSRCVIGLYHPPLQVY TFA is a disordered control peptide. TDSRCVIGLYHPPLQVY TFA is a peptide containing the same amino acids as LP17 (HY-P3400) but in a different sequence order .
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1
1 Cited Publications
Cat. No.: HY-P3460
CAS No.: 887973-01-5
TDSRCVIGLYHPPLQVY is a disordered control peptide. TDSRCVIGLYHPPLQVY is a peptide containing the same amino acids as LP17 (HY-P3400) but in a different sequence order .
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1
1 Cited Publications
Cat. No.: HY-145588A
CAS No.: 1637677-33-8
Purity:  98.82%
Synonyms: INCB54707 phosphate
Target:  

JAK

Research Areas:  

Inflammation/Immunology

Povorcitinib (INCB54707) phosphate is a potent and selective JAK1 inhibitor that effectively reduces abscesses and inflammatory nodules. Povorcitinib phosphate can be used to study cutaneous lupus erythematosus (CLE) and lichen planus (LP) (information extracted from patent WO2021076124A1) .
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1
1 Cited Publications
Cat. No.: HY-18778
CAS No.: 866399-87-3
Synonyms: TA-8995; DEZ-001; AMG-899
Research Areas:  

Cardiovascular Disease

Obicetrapib (TA-8995; DEZ-001) is an orally active cholesteryl ester transfer protein (CETP) inhibitor. Obicetrapib potently reduces atherogenic lipoproteins (such as LDL-C, ApoB, Lp (a)) and increases HDL-C. Obicetrapib can be used for the research of dyslipidemia and atherosclerotic cardiovascular disease (ASCVD) .
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1
1 Cited Publications
Cat. No.: HY-P3496
CAS No.: 1322711-38-5
Target:  

Pyroptosis

Research Areas:  

Inflammation/Immunology

Pep19-2.5 is an synthetic and antitoxin peptide, blocks the intracellular endotoxin signaling cascade. Pep19-2.5 inhibits signaling of lipopeptides (LP) and lipopolysaccharides (LPS) mediated by transmembrane and cytosolic pattern recognition receptors (PRRs). The signaling cascades lead to inflammation and cell pyroptosis .
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Cat. No.: HY-152857
CAS No.: 2565656-70-2
Purity:  99.96%
Synonyms: LY3473329
Target:  

Apolipoprotein

Research Areas:  

Cardiovascular Disease

Muvalaplin (LY3473329) is an orally active small molecule apolipoprotein a (apolipoprotein a) inhibitor that binds to the KIV8 domain (Kd = 22 nM) and kringle IV domains 7 and 8, blocks the non-covalent interaction between apo (a) and apoB-100, and prevents Lp (a) assembly, thereby lowering circulating Lp (a) levels. Muvalaplin can be used in research on atherosclerotic cardiovascular disease .
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Cat. No.: HY-156601
CAS No.: 2035818-24-5
Purity:  99.96%
Synonyms: LP352
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Bexicaserin (LP352) is a 5-HT2C receptor agonist with potential for studying obesity and psychiatric-related disorders (such as epilepsy) .
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