15 Results for "

57547

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "57547" in MCE Product Catalog:

Cat. No.: HY-14277A
CAS No.: 79547-78-7
Purity:  99.3%
Synonyms: R 50547 hydrochloride
Levocabastine (R 50547) hydrochloride is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a Ki of 17 nM for mNTR2. Levocabastine hydrochloride can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC) .
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Cat. No.: HY-P99593
CAS No.: 1418200-58-4
Synonyms: DMUC5754A

Research Areas:  

Cancer

Sofituzumab vedotin (DMUC5754A) is a MMAE-containing anti-MUC16 antibody-drug conjugate (ADC) with a protease-cleavable linker. Sofituzumab vedotin can be used for the research of cancer .
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Cat. No.: HY-14157
CAS No.: 850176-30-6
Purity:  99.82%
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

ADL-5747 is a selective and orally active agonist of the δ-opioid receptor (DOR). By binding to the δ-opioid receptors, ADL-5747 activates these receptors, thereby playing a role in pain management pathways. ADL-5747 can be used for research into pain management mechanisms .
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Cat. No.: HY-14277
CAS No.: 79516-68-0
Synonyms: R 50547
Levocabastine (R 50547) is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a Ki of 17 nM for mNTR2. Levocabastine can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC) .
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Cat. No.: HY-129316
CAS No.: 143209-04-5
Synonyms: CGP 52547
Research Areas:  

Infection

(S)-Dihydroaeruginoic acid is an antibiotic originally isolated from P. fluorescens. It has antimicrobial activity in a disc assay against R. solani, P. ultimum, B. cinera, S. rolfsii, C. gloeosporioide, F. oxysporum, and S. tritici fungi as well as B. subtilis, E. herbicola, and S. albus bacteria when used at a concentration of 200 μg/disc.
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Cat. No.: HY-14124
CAS No.: 919482-44-3
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

MK-5757 is a Nociceptin/Orphanin FQ Peptide Receptor antagonist. ORL1 antagonist 3 can improve cerebral blood flow disorders and ischemic damage, and alleviate abnormal neurological symptoms. ORL1 antagonist 3can be used for the research of neurological disease, such as traumatic brain injury .
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Cat. No.: HY-14277AR
CAS No.: 79547-78-7
Synonyms: R 50547 hydrochloride (Standard)
Levocabastine (hydrochloride) (Standard) is the analytical standard of Levocabastine (hydrochloride). This product is intended for research and analytical applications. Levocabastine (R 50547) hydrochloride is a potent and selective histamine H1-receptor antagonist. Levocabastine hydrochloride is also a selective, high affinity neurotensin receptor subtype 2 (NTR2) antagonist, with a Ki of 17 nM for mNTR2. Levocabastine hydrochloride can act as a VLA-4 antagonist, interferes with conjunctival eosinophil infiltration in allergic conjunctivitis (AC) .
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Cat. No.: HY-14157A
CAS No.: 1187653-56-0
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

ADL-5747 hydrochloride is a selective and orally active agonist of the δ-opioid receptor (DOR). By binding to the δ-opioid receptors, ADL-5747 hydrochloride activates these receptors, thereby playing a role in pain management pathways. ADL-5747 hydrochloride can be used for research into pain management mechanisms .
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Cat. No.: HY-W718262
CAS No.: 49608-51-7
Synonyms: (Rac)-CGP 52547
Research Areas:  

Infection Cancer

Dihydroaeruginoic acid ((Rac)-CGP 52547), an antifungal antibiotic, is a thiazoline iron chelator. Dihydroaeruginoic acid is the condensation product of salicylate and one cysteine residue. Dihydroaeruginoic acid chelates Fe(III), inhibits DNA replication via ribonucleotide reductase, induces G1/S cell cycle block, reduces leukemia cell clonogenic viability. Dihydroaeruginoic acid inhibits phytopathogenic fungi and bacteria, suppresses Candida albicans development, and inhibits Agrobacterium tumefaciens biofilm formation via extracellular iron sequestration. Dihydroaeruginoic acid can be used for the research of phytopathogenic fungal and bacterial infections, and leukemia .
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Cat. No.: HY-P86065

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Species independent

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Cat. No.: HY-P85855

Host:  

Mouse

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human

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Cat. No.: HY-P87862

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P75817
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Human respiratory syncytial virus (RSV) Fusion protein / RSV-F Protein
Species:  
Source:  
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Cat. No.: HY-P86062
Synonyms: Prelamin-A/C [Cleaved into: Lamin-A/C; 70 kDa lamin; Renal carcinoma antigen NY-REN-32; ]

Host:  

Mouse

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat, Monkey

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Cat. No.: HY-P86055
Synonyms: ABC20; ABCB1; ATP binding cassette, sub family B; MDR/TAP; , member 1; ATP-binding cassette sub-family B member 1; CD243; CLCS; Colchicin sensitivity; Doxorubicin resistance; GP170; MDR1; MDR1_HUMAN; Multidrug resistance 1; Multidrug resistance protein 1; P glycoprotein 1; P gp; P-glycoprotein 1; PGY1

Host:  

Mouse

Application:  

IHC-P, ELISA

Reactivity:  

Human, Mouse

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