261 Results for "

5R

" in MedChemExpress (MCE) Product Catalog:
Products (261)

261 Results for "5R" in MCE Product Catalog:

3
3 Cited Publications
Art. -Nr.: HY-P0227
CAS. Nr.: 168482-23-3
Target:  

Melanocortin Receptor

Forschungsgebiete:  

Metabolic Disease

SHU 9119 is a potent human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist; with IC50 values of 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively.
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1
1 Cited Publications
Art. -Nr.: HY-19969
CAS. Nr.: 163769-88-8
Target:  

Interleukin Related

Forschungsgebiete:  

Inflammation/Immunology

YM-90709 is a novel IL-5 inhibitor which selectively blocks the binding of IL-5 to the IL-5 receptor (IL-5R).YM-90709 potently inhibits the binding of [ 125I]-IL-5 to IL-5R on human peripheral eosinophils and eosinophilic HL-60 clone 15 cells with IC50 values of 1.0 and 0.57 μM .
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1
1 Cited Publications
Art. -Nr.: HY-P9923
CAS. Nr.: 1044511-01-4
Synonyms: MEDI-563; BIW-8405; KHK4563

Forschungsgebiete:  

Inflammation/Immunology Cancer

Benralizumab (MEDI-563) is an interleukin-5 receptor α (IL-5Rα)-directed cytolytic monoclonal antibody that induces direct, rapid and nearly complete depletion of eosinophils via enhanced antibody-dependent cell-mediated cytotoxicity. Benralizumab can be used for severe eosinophilic asthma .
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1
1 Cited Publications
Art. -Nr.: HY-W021425
CAS. Nr.: 5505-63-5
Synonyms: (2S,3R,4S,5R)-2-Amino-3,4,5,6-tetrahydroxyhexanal hydrochloride
D-Mannosamine ((2S,3R,4S,5R)-2-Amino-3,4,5,6-tetrahydroxyhexanal) hydrochloride is a six-carbon amino sugar and an amino derivative of D-mannose. D-Mannosamine hydrochloride can block mannose receptors .
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1
1 Cited Publications
Art. -Nr.: HY-76948
CAS. Nr.: 865479-71-6
Target:  

Factor Xa

Forschungsgebiete:  

Cardiovascular Disease

5-R-Rivaroxaban is (R)-enantiomer of Rivaroxaban. Rivaroxaban (BAY 59-7939) is a highly potent and selective, direct Factor Xa (FXa) inhibitor, achieving a strong gain in anti-FXa potency (IC50 0.7 nM; Ki 0.4 nM).
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1
1 Cited Publications
Art. -Nr.: HY-N2185
CAS. Nr.: 87095-74-7
Synonyms: (5R)-trans-1,7-diphenyl-5-hydroxy-6-hepten-3-one
(5R,6E)-5-Hydroxy-1,7-diphenyl-6-hepten-3-one is the methylene chloride extract of Alpinia nutans, has antioxidant activity .
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1
1 Cited Publications
Art. -Nr.: HY-P9923A
CAS. Nr.: 1044511-01-4
Synonyms: MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA )

Forschungsgebiete:  

Inflammation/Immunology Cancer

Benralizumab (anti-IL5RA ) (MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA)) is an interleukin-5 receptor α (IL-5Rα)-directed cytolytic monoclonal antibody that induces direct, rapid and nearly complete depletion of eosinophils via enhanced antibody-dependent cell-mediated cytotoxicity. Benralizumab can be used for severe eosinophilic asthma study .
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1
1 Cited Publications
Art. -Nr.: HY-152223
CAS. Nr.: 2882035-56-3
Reinheit:  99.66%
Target:  

PCSK9

Forschungsgebiete:  

Cardiovascular Disease

PCSK9-IN-11 (compound 5r) is a potent and orally active PCSK9 inhibitor. PCSK9-IN-11 exhibits PCSK9 transcriptional inhibitory activity in HepG2 cells, with an IC50 of 5.7 μM. PCSK9-IN-11 increases LDL receptor (LDLR) protein level. PCSK9-IN-11 can be used for atherosclerosis research .
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1
1 Cited Publications
Art. -Nr.: HY-153100
CAS. Nr.: 89665-84-9
Reinheit:  99.43%
Target:  

Drug Isomer

Forschungsgebiete:  

Others

(R)-mchm5U is a diastereomer of (S)-mchm5U (HY-153100A) .
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1
1 Cited Publications
Art. -Nr.: HY-108495
CAS. Nr.: 1345858-76-5
Reinheit:  ≥98.0%
Synonyms: ML248
Target:  

LPL Receptor

Forschungsgebiete:  

Cardiovascular Disease

CYM50308 (ML248) is a potent, selective and high affinity sphingosine-1-phosphate receptor 4 (S1P4-R) agonist with an EC50 of 56 nM. CYM50308 displays 37-fold more selective for S1P4-R than S1P5-R. CYM50308 has no activity at S1P1-R, S1P2-R and S1P3-R subtypes at concentrations up to 25 μM .
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1
1 Cited Publications
Art. -Nr.: HY-10624
CAS. Nr.: 312637-48-2
Reinheit:  98.28%
Target:  

Melanocortin Receptor

Forschungsgebiete:  

Metabolic Disease

THIQ is the first selective agonist of the melanocortin-4 receptor (MC4R), with high affinity and potency for hMC4R (IC50=1.2 nM, EC50=2.1 nM) and rMC4R (IC50=0.6 nM, EC50=2.9 nM). THIQ maintains low potency at MC1R, MC3R and MC5R. THIQ plays a role in eliciting erectile activity in rodents. THIQ acts as a pharmacoperone of the MC4R rescuing the cell surface expression and signaling of some intracellularly retained MC4R mutants .
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1
1 Cited Publications
Art. -Nr.: HY-134851
CAS. Nr.: 1821309-39-0
Reinheit:  99.10%
Target:  

HIV

Forschungsgebiete:  

Infection

HIV-1 inhibitor-6 (compound 9), a diheteroarylamide-based compound, is a potent HIV-1 pre-mRNA alternative splicing inhibitor. HIV-1 inhibitor-6 blocks HIV replication. HIV-1 inhibitor-6 is active against wild-type HIV-1IIIB (subtype B, X4-tropic) and HIV-1 97USSN54 (subtype A, R5-tropic) with EC50s of 0.6 μM and 0.9 μM, respectively. HIV-1 inhibitor-6 inhibits HIV strains resistant to agents targeting HIV reverse transcriptase, protease, integrase, and coreceptor CCR5 with EC50s ranging from 0.9 to 1.5 μM .
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Art. -Nr.: HY-B1175
CAS. Nr.: 4697-14-7
Target:  

Antibiotic Bacterial

Forschungsgebiete:  

Infection

(2S,5R,6R)-Ticarcillin disodium is a semisynthetic antibiotic with bactericidal activities. (2S,5R,6R)-Ticarcillin disodium is the (2S,5R,6R)-enantiomer of Ticarcillin (HY-139805) .
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Art. -Nr.: HY-115644
CAS. Nr.: 2341796-82-3
Reinheit:  99.85%
Target:  

Melanocortin Receptor

Forschungsgebiete:  

Inflammation/Immunology

BMS-470539 dihydrochloride is a highly potent and selective melanocortin-1 receptor (MC-1R) agonist with an IC50 of 120 nM, an EC50 of 28 nM. BMS-470539 dihydrochloride does not activate MC-3R and is a very weak partial agonist at MC-4R and MC-5R. BMS-470539 dihydrochloride has potently anti-inflammatory properties .
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Art. -Nr.: HY-34550A
CAS. Nr.: 1932042-59-5
Target:  

Drug Intermediate

Forschungsgebiete:  

Others

tert-Butyl (1S,4S,5R)-5-hydroxy-2-azabicyclo[2.2.1]heptane-2-carboxylate is a pharmaceutical intermediate used to synthesize various active compounds, such as FXR receptor agonists.
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Art. -Nr.: HY-107101
CAS. Nr.: 583028-68-6
Reinheit:  99.67%
Synonyms: PG 701; LLDT-8; 5α-Hydroxytriptolide
(5R)-5-Hydroxytriptolide is an extracted compound from Tripterygium, and shows lower cell cytotoxicity and higher immunosuppressive activity. (5R)-5-Hydroxytriptolide can be used for study of rheumatoid arthritis .
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Art. -Nr.: HY-79858
CAS. Nr.: 1192651-49-2
Synonyms: Avibactam sodium intermediate
Target:  

Drug Intermediate

Forschungsgebiete:  

Others

(2S,5R)-6-(Benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamide (Avibactam sodium intermediate) is a drug intermediate for synthesis of various active compounds.
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Art. -Nr.: HY-I0909
CAS. Nr.: 170985-86-1
Synonyms: 4-[4-[4-[4-[[(3r,5R)-5-(2,4-Difluorophenyl)-5-(1,2,4-triazol-1-ylmethyl)oxolan-3-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-2-[(2s,3s)-2-phenylmethoxypentan-3-yl]-1,2,4-triazol-3-one
Target:  

Drug Intermediate

Forschungsgebiete:  

Others

O-Benzyl posaconazole (4-[4-[4-[4-[[(3r,5r)-5-(2,4-Difluorophenyl)-5-(1,2,4-triazol-1-ylmethyl)oxolan-3-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-2-[(2s,3s)-2-phenylmethoxypentan-3-yl]-1,2,4-triazol-3-one) is a drug intermediate for synthesis of various active compounds.
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Art. -Nr.: HY-113025A
CAS. Nr.: 172213-74-0
Synonyms: (2S,5R)-5-Hydroxylysine dihydrochloride
L-hydroxylysine dihydrochloride ((2S,5R)-5-Hydroxylysine dihydrochloride), an amino acid, is exclusive to collagen protein, which is formed by posttranslational hydroxylation of some lysine residues .
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Art. -Nr.: HY-135383A
CAS. Nr.: 254452-88-5
Forschungsgebiete:  

Metabolic Disease

(3S,5R)-Pitavastatin calcium is the enantiomer of Pitavastatin Calcium (HY-B0144). Pitavastatin is a potent HMG-CoA reductase inhibitor .
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