27 Results for "

H1R

" in MedChemExpress (MCE) Product Catalog:
Products (27)

27 Results for "H1R" in MCE Product Catalog:

11
11 Cited Publications
Cat. No.: HY-N0328
CAS No.: 6147-11-1
Synonyms: α-Mangostin
alpha-Mangostin (α-Mangostin) is a dietary xanthone with broad biological activities, such as antioxidant, anti-allergic, antiviral, antibacterial, anti-inflammatory and anticancer effects. It is an inhibitor of mutant IDH1 (IDH1-R132H) with a Ki of 2.85 μM.
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Cat. No.: HY-B1808
CAS No.: 486-12-4
Target:  

Histamine Receptor

Research Areas:  

Infection

Triprolidine is an orally active H1R Antagonist antagonist. Triprolidine has the function of spinal cord motor and sensory block. Triprolidine can be used for the research of allergic rhinitis [1] .
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Cat. No.: HY-B1177
CAS No.: 483-63-6
Research Areas:  

Infection

Crotamiton is a TRPV4 inhibitor. Crotamiton inhibits TRPV4 currents. Crotamiton inhibits TRPV4 selective agonist-induced pruritus-related behaviors in mice. Crotamiton inhibits Histamine- and Chloroquine-induced calcium influx via the H1R/TRPV1, MRGPRA3/TRPA1 pathways, and also suppresses calcium influx in primary mouse dorsal root ganglion neurons. Crotamiton is applicable to research related to pruritus, scabies, and non-scabietic pruritus [1] .
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Cat. No.: HY-100657
CAS No.: 479035-75-1
Purity:  98.63%
Synonyms: meta-MDL-16455; meta-Terfenadine carboxylate
Target:  

Drug Metabolite

Research Areas:  

Inflammation/Immunology

meta-Fexofenadine (meta-MDL-16455) is an impurity of Fexofenadine [1]. Fexofenadine, a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial .
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Cat. No.: HY-101063
CAS No.: 142457-00-9
Purity:  99.64%
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

Amthamine is a histamine receptor (H1R-H4R) agonist. Amthamine can produce liver congestion and necrosis of liver cells. Amthamine can be used to study the induction effect of H1R-H4 agonist on hepatotoxicity [1].
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Cat. No.: HY-107565
CAS No.: 3343-39-3
Purity:  99.86%
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

2-Pyridylethylamine is a histamine-1 (H1R) receptor agonist. 2-Pyridylethylamine can reduce the joint injury induced by formalin in rats. 2-Pyridylethylamine can be used to study the spinal cord release of neuropeptide (NPY) [1].
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Cat. No.: HY-N0328R
CAS No.: 6147-11-1
Synonyms: α-Mangostin (Standard)
alpha-Mangostin (Standard) is the analytical standard of alpha-Mangostin. This product is intended for research and analytical applications. alpha-Mangostin (α-Mangostin) is a dietary xanthone with broad biological activities, such as antioxidant, anti-allergic, antiviral, antibacterial, anti-inflammatory and anticancer effects. It is an inhibitor of mutant IDH1 (IDH1-R132H) with a Ki of 2.85 μM.
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Cat. No.: HY-170789
CAS No.: 19642-70-7
Target:  

Histamine Receptor

Research Areas:  

Neurological Disease

H1R ligand-1 (Compound fragment 1) is a high-affinity ligand for the human histamine H1 receptor (H1R). H1R ligand-1 can be used as a scaffold to design and synthesize a set of derivatives to explore H1R binding kinetics [1].
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Cat. No.: HY-111501
CAS No.: 1429375-54-1
Purity:  99.82%
Target:  

Histamine Receptor

H4R antagonist 1 is a potent and highly selective histamine H4 receptor (H4R) antagonist with an IC50 of 27 nM. H4R antagonist 1 does not show any noticeable binding affinity to other subtypes of histamine receptors, H1R, H2R, and H3R [1].
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Cat. No.: HY-129508
CAS No.: 142437-67-0
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

Amthamine is a histamine receptor (H1R-H4R) agonist. Amthamine can produce liver congestion and necrosis of liver cells. Amthamine can be used to study the induction effect of H1R-H4 agonist on hepatotoxicity [1].
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Cat. No.: HY-12752
CAS No.: 84-96-8
Synonyms: Trimeprazine
Alimemazine is a phenothiazine derivative that is generally used as an antipruritic agent and also a hemagglutinin (HA)-receptor antagonist.Alimemazine (Trimeprazine) is also acts as a partial agonist against the histamine H1 receptor (H1R) and other GPCRs. Alimemazine displays antiserotonin, antispasmodic, and antiemetic properties [1] .
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Cat. No.: HY-131274
CAS No.: 185066-33-5
Target:  

Drug Metabolite

Research Areas:  

Others

Fexofenadine Impurity F is the impurity of Fexofenadine. Fexofenadine, a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial [1].
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Cat. No.: HY-122166
CAS No.: 744270-00-6
Target:  

STAT

Research Areas:  

Others

Histamine receptors inhibitor 1 (compound 303) is an inhibitor of H1R or H4R that can be used in the research of inflammatory, autoimmune, allergic, and ocular [1].
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Cat. No.: HY-B0462C
CAS No.: 153408-28-7
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

(R)-Azelastine hydrochloride, an antihistamine, has been demonstrated to down-regulate the levels of H1R, M1R, and M3R, while also inhibiting the proliferation of HNEpC.
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Cat. No.: HY-B0801AS
CAS No.: 1215821-44-5
Synonyms: MDL-16455-d10 hydrochloride; Terfenadine carboxylate-d10 hydrochloride
Fexofenadine-d10 (hydrochloride) is deuterium labeled Fexofenadine (hydrochloride). Fexofenadine hydrochloride (MDL-16455 hydrochloride), a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial (person aged ≥16 years) [1].
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Cat. No.: HY-Z12728
CAS No.: 143228-84-6
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

(R)-Azelastine is an antihistamine compound with antiallergic activity. (R)-Azelastine can downregulate the levels of H1R, M1R, and M3R. (R)-Azelastine has also been shown to inhibit the proliferation of HNEpC [1].
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Cat. No.: HY-B0462D
CAS No.: 143228-85-7
Synonyms: (+)-Azelastine
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

(S)-Azelastine ((+)-Azelastine) is an antihistamine with antiallergic and antiasthmatic activity. (S)-Azelastine has been shown to downregulate H1R, M1R, and M3R levels. (S)-Azelastine also has the property of inhibiting HNEpC proliferation [1].
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Cat. No.: HY-100657S
Synonyms: meta-MDL-16455-d6; meta-Terfenadine carboxylate-d6
Meta-Fexofenadine-d6 is the deuterium labeled meta-Fexofenadine. meta-Fexofenadine (meta-MDL-16455) is an impurity of Fexofenadine [1]. Fexofenadine, a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial .
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Cat. No.: HY-100657R
CAS No.: 479035-75-1
Synonyms: meta-MDL-16455 (Standard); meta-Terfenadine carboxylate (Standard)
meta-Fexofenadine (Standard) is the analytical standard of meta-Fexofenadine. This product is intended for research and analytical applications. meta-Fexofenadine (meta-MDL-16455) is an impurity of Fexofenadine [1]. Fexofenadine, a H1R antagonist, is an anti-allergic agent used in seasonal allergic rhinitis and chronic idiopathic urticarial .
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Cat. No.: HY-P702580
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Histamine H1 receptor; H1R; HH1R
Species:  
Source:  
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