161 Results for "

COPD

" in MedChemExpress (MCE) Product Catalog:
Products (161)

161 Results for "COPD" in MCE Product Catalog:

1
1 Cited Publications
Art. -Nr.: HY-19519A
CAS. Nr.: 865625-56-5
Synonyms: DF 2156A
Target:  

CXCR

Forschungsgebiete:  

Infection Inflammation/Immunology Cancer

Ladarixin sodium (DF 2156A) is an orally active, allosteric non-competitive and dual CXCR1 and CXCR2 antagonist. Ladarixin sodium can be used for the research of COPD and asthma .
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1
1 Cited Publications
Art. -Nr.: HY-19519
CAS. Nr.: 849776-05-2
Synonyms: DF 2156A free base
Target:  

CXCR

Forschungsgebiete:  

Inflammation/Immunology Cancer

Ladarixin (DF 2156A free base) is an orally active, allosteric non-competitive and dual CXCR1 and CXCR2 antagonist. Ladarixin can be used for the research of COPD and asthma .
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1
1 Cited Publications
Art. -Nr.: HY-136239
CAS. Nr.: 5534-18-9
Reinheit:  99.76%
Synonyms: Beclomethasone-17-monopropionate; 17-BMP
Beclomethasone 17-propionate (Beclomethasone-17-monopropionate), an active metabolite of Beclomethasone dipropionate (HY-13571), is a glucocorticoid receptor (GR) agonist. Beclomethasone 17-propionate exhibits greater affinity for GR than Beclomethasone dipropionate. Beclomethasone 17-propionate effectively suppresses cytokine production in chronic obstructive pulmonary disease (COPD) lung macrophages .
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1
1 Cited Publications
Art. -Nr.: HY-137976
CAS. Nr.: 151937-76-7
Reinheit:  99.2%
Synonyms: Penequinine hydrochloride
Penehyclidine (Penequinine) hydrochloride, a anticholinergic agent, is a selective antagonist of M1 and M3 receptors. Penehyclidine hydrochloride activates NF-kβ in lung tissue and inhibits the release of inflammatory factors. Penehyclidine hydrochloride can alleviate the pulmonary inflammatory response in rats with chronic obstructive pulmonary disease (COPD) undergoing mechanical ventilation .
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1
1 Cited Publications
Art. -Nr.: HY-B0010D
CAS. Nr.: 200815-49-2
Synonyms: (R,R)-Formoterol tartrate
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Inflammation/Immunology

Arformoterol ((R,R)-Formoterol) tartrate, the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol tartrate can be used for the research of chronic obstructive pulmonary disease (COPD) .
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1
1 Cited Publications
Art. -Nr.: HY-B0010A
CAS. Nr.: 67346-49-0
Synonyms: (R,R)-Formoterol
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Inflammation/Immunology

Arformoterol ((R,R)-Formoterol), the (R,R)-enantiomer of Formoterol, is a long-acting β2-adrenergic receptor (β2-AR) agonist, with a Kd of 2.9 nM. Arformoterol can be used for the research of chronic obstructive pulmonary disease (COPD) .
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1
1 Cited Publications
Art. -Nr.: HY-119708
CAS. Nr.: 1884461-72-6
Reinheit:  99.70%
Synonyms: RPL-554
Ensifentrine (RPL-554) is an inhaled dual inhibitor of PDE3 and PDE4 with IC50s of 0.4 nM and 1479 nM, respectively. Ensifentrine blocks PDE3 and PDE4 enzymes, thereby increasing the levels of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) in lung cells, dilating the bronchi, and inhibiting the activation and migration of inflammatory cells. Ensifentrine can be used in the research of chronic obstructive pulmonary disease (COPD) .
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1
1 Cited Publications
Art. -Nr.: HY-121246
CAS. Nr.: 848353-85-5
Reinheit:  99.78%
Synonyms: AKF-PD
Forschungsgebiete:  

Inflammation/Immunology Cancer

Fluorofenidone (AKF-PD) is an orally active compound with anti-fibrotic, antioxidant, and anti-inflammatory pharmacological effects. Fluorofenidone downregulates the expression of ACSL4, upregulates GPX4 expression and inhibits the NF-κB signaling pathway to alleviate inflammation and fibrosis. Fluorofenidone ameliorates cholestasis and fibrosis by inhibiting hepatic Erk/-Egr-1 signaling and Tgfβ1/Smad pathway in mice. Fluorofenidone demonstrates protective effects against chronic lung injury in mice. Fluorofenidone can be used for the study of chronic obstructive pulmonary disease (COPD), pulmonary interstitial fibrosis (PIF) and non-small cell lung cancer (NSCLC) .
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1
1 Cited Publications
Art. -Nr.: HY-14180
CAS. Nr.: 503555-55-3
Reinheit:  99.40%
PHA-408 is a highly selective, orally active and ATP-competitive IKK-2 inhibitor with an IC50 of 40 nM. PHA-408 blocks NF-κB signaling by suppressing IκBα phosphorylation and degradation, p65 phosphorylation, and pro-inflammatory cytokine production, and prevents TNF-α-induced premature senescence in HUVECs. PHA-408 alleviates LPS-and cigarette smoke-triggered pulmonary inflammation, reduces LPS-stimulated serum TNF-α release, and ameliorates joint damage in SCW-induced arthritis in rats. PHA-408 is applicable for the research of rheumatoid arthritis, chronic obstructive pulmonary disease (COPD), and Duchenne muscular dystrophy .
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Art. -Nr.: HY-12463
CAS. Nr.: 137888-11-0
Reinheit:  98.73%
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Inflammation/Immunology

Carmoterol hydrochloride is a highly potent, selective and long-acting β2-adrenoceptor agonist with the pEC50 of 10.19. Carmoterol has 53 times higher affinity for the β2-adrenoceptors than for the β1-adrenoceptors. Carmoterol hydrochloride can be used for the research of asthma and chronic obstructive pulmonary disease (COPD) .
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Art. -Nr.: HY-15545
CAS. Nr.: 1003566-93-5
Reinheit:  99.10%
Target:  

CCR

Forschungsgebiete:  

Inflammation/Immunology

AZD-4818 is a potent, orally active antagonist of chemokine CCR1. AZD-4818 can be used for researching chronic obstructive pulmonary disease (COPD) .
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Art. -Nr.: HY-B1675A
CAS. Nr.: 50293-90-8
Synonyms: (R)-Albuterol hydrochloride; (R)-Salbutamol hydrochloride; Levosalbutamol hydrochloride
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Inflammation/Immunology

Levalbuterol ((R)-Albuterol) hydrochloride is a short-acting β2-adrenergic receptor agonist and the active (R)-enantiomer of Salbutamol. Levalbuterol hydrochloride is a more potent bronchodilator than Salbutamol and has the potential for the treatment of COPD .
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Art. -Nr.: HY-105092
CAS. Nr.: 145739-56-6
Reinheit:  ≥98.0%
Synonyms: OPC-6535
Forschungsgebiete:  

Inflammation/Immunology

Tetomilast (OPC-6535) is a PDE4 inhibitor with potential for the research of inflammatory bowel disease (IBD) and chronic obstructive pulmonary disease (COPD).
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Art. -Nr.: HY-109177
CAS. Nr.: 1334546-77-8
Reinheit:  99.87%
Synonyms: QBW251
Target:  

CFTR

Forschungsgebiete:  

Inflammation/Immunology

Icenticaftor (QBW251) is an orally active CFTR channel potentiator, with EC50s of 79 nM and 497 nM for F508del and G551D CFTR, respectively. Icenticaftor can be used for chronic obstructive pulmonary disease (COPD) and cystic fibrosis research .
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Art. -Nr.: HY-107046
CAS. Nr.: 380221-63-6
Target:  

Adenosine Receptor

Forschungsgebiete:  

Inflammation/Immunology

UK-432097 is a highly potent and selective A2AAR agonist with a pKi of 8.4 for human A2AAR. UK-432097 has anti-inflammatory and anti-aggregatory properties. UK-432097 has the potential for COPD (Chronic Obstructive Pulmonary Disease) research .
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Art. -Nr.: HY-111144
CAS. Nr.: 915133-65-2
Synonyms: AZD0548; LAS100977
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Inflammation/Immunology

Abediterol (LAS100977) is an inhaled long-acting β2-adrenoceptor agonist (LABA) and can be used for the research of asthma and chronic obstructive pulmonary disease (COPD) .
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Art. -Nr.: HY-168973
CAS. Nr.: 1285607-08-0
Synonyms: AER-01; MUC-031
Target:  

Mucin

Forschungsgebiete:  

Inflammation/Immunology

Fexlamose (AER-01) is a thiol-modified carbohydrate agent with mucolytic property. Fexlamose cleaves disulfides to cause mucolysis. Fexlamose can be used for researchs of chronic obstructive pulmonary disease (COPD) and muco-obstructive lung diseases (MOLD) .
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Art. -Nr.: HY-14190
CAS. Nr.: 220847-86-9
Reinheit:  98.57%
Synonyms: R-411 free base
Target:  

Integrin

Forschungsgebiete:  

Inflammation/Immunology

Valategrast (R-411 free base) is a potent and orally active integrin α4β1 (VLA-4) and α4β7 dual antagonist. Valategrast has the potential for Chronic obstructive pulmonary disease (COPD) and asthma treatment .
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Art. -Nr.: HY-120595
CAS. Nr.: 1220626-82-3
Reinheit:  99.85%
Synonyms: RV568
Target:  

p38 MAPK Src

Forschungsgebiete:  

Inflammation/Immunology

JNJ-49095397 (RV568) is an inhaled narrow-spectrum kinase inhibitor (NSKI) against both the α and γ isoforms of p38 MAPK. JNJ-49095397 also inhibits SRC kinase family, specifically haematopoietic kinase (HCK) JNJ-49095397 shows potent anti-inflammatory effects and can be used for the research of chronic obstructive pulmonary disease (COPD) and asthma .
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Art. -Nr.: HY-131910A
CAS. Nr.: 2429889-62-1
Reinheit:  99.75%
Target:  

PI3K

Forschungsgebiete:  

Inflammation/Immunology

(R)-IHMT-PI3Kδ-372 (R-18) is a potent and selective PI3Kδ inhibitor with an IC50 of 19 nM. (R)-IHMT-PI3Kδ-372 (R-18) can be used in chronic obstructive pulmonary disease (COPD) research .
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