156 Results for "

FP

" in MedChemExpress (MCE) Product Catalog:
Products (156)

156 Results for "FP" in MCE Product Catalog:

  • Isoforms Recommended:
13
13 Publications Verification
Art. -Nr.: HY-50901
CAS. Nr.: 402473-54-5
Synonyms: AE 3-208
Forschungsgebiete:  

Endocrinology Cancer

ONO-AE3-208 is a selective and orally active EP4 receptor antagonist with a Ki of 1.3 nM. ONO-AE3-208 shows less potently affects EP3, FP, and TP receptors (Ki of 30 nM, 790 nM, and 2400 nM, respectively). ONO-AE3-208 suppresses cell invasion, migration, and metastasis of prostate cancer .
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10
10 Cited Publications
Art. -Nr.: HY-12956
CAS. Nr.: 551-11-1
Reinheit:  99.63%
Synonyms: Prostaglandin F2α; PGF2α
Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour .
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10
10 Cited Publications
Art. -Nr.: HY-12956A
CAS. Nr.: 38562-01-5
Reinheit:  ≥98.0%
Synonyms: Prostaglandin F2α tromethamine salt; PGF2α THAM; Prostaglandin F2α THAM
Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour .
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6
6 Cited Publications
Art. -Nr.: HY-117468
CAS. Nr.: 2609-88-3
Reinheit:  98.00%
Target:  

Fluorescent Dye

Forschungsgebiete:  

Others

Lissamine rhodamine B is a red-fluorescent dye, it is a derivative of rhodamine. Lissamine rhodamine B can be used as a fluorescent probe to develop competitive aptamer fluorescence anisotropy/polarization (FA/FP) assays .
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5
5 Cited Publications
Art. -Nr.: HY-B0577
CAS. Nr.: 130209-82-4
Synonyms: PHXA41
Forschungsgebiete:  

Cardiovascular Disease Others

Latanoprost (PHXA41) is a prostaglandin F2α analogue and can be used for glaucoma research. Latanoprost can effectively pass through cornea and be hydrolyzed by esterase to latanoprost acid. latanoprost acid is an F-prostaglandin (FP) receptor agonist, and can effectively reduce intraocular pressure (IOP) by increasing the outflow of aqueous humor through uvea .
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4
4 Cited Publications
Art. -Nr.: HY-10858
CAS. Nr.: 915759-45-4
Reinheit:  99.24%
Target:  

sFRP-1 Wnt

Forschungsgebiete:  

Cancer

WAY 316606 is an inhibitor of the secreted protein sFRP-1, an endogenous antagonist of the secreted glycoprotein Wnt. The affinity of WAY-316606 for sFRP-1 is determined using the FP binding assay with IC50 of 0.5 μM .
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4
4 Cited Publications
Art. -Nr.: HY-10858A
CAS. Nr.: 1781835-02-6
Target:  

sFRP-1 Wnt

Forschungsgebiete:  

Cancer

WAY 316606 hydrochloride is an inhibitor of the secreted protein sFRP-1, an endogenous antagonist of the secreted glycoprotein Wnt. The affinity of WAY-316606 for sFRP-1 is determined using the FP binding assay with IC50 of 0.5 μM .
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3
3 Cited Publications
Art. -Nr.: HY-B0584
CAS. Nr.: 157283-68-6
Synonyms: Fluprostenol isopropyl ester; AL6221; Flu-Ipr
Forschungsgebiete:  

Cardiovascular Disease Endocrinology

Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension .
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3
3 Cited Publications
Art. -Nr.: HY-108563
CAS. Nr.: 146033-02-5
Forschungsgebiete:  

Neurological Disease

SC 51089 is a selective antagonist of prostaglandin E2 EP1 receptor, with Kis of 1.3, 11.2, 17.5, and 61.1 μM for EP1, TP, EP3, and FP receptors, respectively. SC 51089 exhibits neuroprotective activity .
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3
3 Cited Publications
Art. -Nr.: HY-108563A
CAS. Nr.: 146033-03-6
Reinheit:  98.64%
Forschungsgebiete:  

Neurological Disease

SC 51089 free base is a selective antagonist of prostaglandin E2 EP1 receptor, with Kis of 1.3, 11.2, 17.5, and 61.1 μM for EP1, TP, EP3, and FP receptors, respectively. SC 51089 free base exhibits neuroprotective activity .
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3
3 Cited Publications
Art. -Nr.: HY-125837A
CAS. Nr.: 2748239-18-9
Reinheit:  ≥98.0%
Forschungsgebiete:  

Cancer

MS31 trihydrochloride is a potent, highly affinity and selective fragment-like methyllysine reader protein spindlin 1 (SPIN1) inhibitor. MS31 trihydrochloride potently inhibits the interactions between SPIN1 and H3K4me3 (IC50=77 nM, AlphaLISA; 243 nM, FP). MS31 trihydrochloride selectively binds Tudor domain II of SPIN1 (Kd=91 nM). MS31 trihydrochloride potently inhibits binding of trimethyllysine-containing peptides to SPIN1, and is not toxic to nontumorigenic cells .
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2
2 Cited Publications
Art. -Nr.: HY-100449
CAS. Nr.: 246246-19-5
Reinheit:  99.00%
AL-8810 is a potent and selective antagonist of the PGF receptor (FP receptor). AL-8810 is an activator of MAPK and ERK1/2. The Ki of the FP receptor of mouse 3T3 cells and rat A7r5 cells are 0.2±0.06 μM and 0.4±0.1 μM, respectively. AL-8810 can be used in the study of elevated intraocular pressure (OHT) and primary open-angle glaucoma (POAG) .
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2
2 Cited Publications
Art. -Nr.: HY-112284
CAS. Nr.: 2005486-31-5
Reinheit:  98.65%
Synonyms: OBE022
Forschungsgebiete:  

Endocrinology

Ebopiprant (OBE022) is an oral and selective prostaglandin F (PGF) receptor antagonist, with Kis of 1 nM, 26 nM for human and rat FP receptors, respectively.
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2
2 Cited Publications
Art. -Nr.: HY-B0813
CAS. Nr.: 830354-48-8
Synonyms: UT-15C
Forschungsgebiete:  

Endocrinology

Treprostinil (UT-15C) diethanolamine is a potent EP2, DP1 and IP agonist with Ki values of 3.6, 4.4, 32.1, 212, 826, 2505 and 4680 nM for EP2, DP1, IP, EP1, EP4, EP3 and FP, respectively. Treprostinil (UT-15C) diethanolamine increases upregulation of cAMP toward maintaining homeostasis within the vasculature. Treprostinil (UT-15C) diethanolamine can result in vasodilatation of human pulmonary arteries .
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1
1 Cited Publications
Art. -Nr.: HY-B0601
CAS. Nr.: 209860-88-8
Synonyms: AFP-172
Tafluprost acid (AFP-172), an active metabolic form of Tafluprost, is a selective prostanoid FP receptor agonist. Tafluprost acid shows a high affinity for human prostanoid FP receptor with Ki and EC50 values of 0.4 nM and 0.53 nM, respectively. Tafluprost acid has 126 times weaker binding affinity for prostanoid EP3 receptor (IC50=67 nM) than for the prostanoid FP receptor. Tafluprost acid can be used in the research of glaucoma .
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1
1 Cited Publications
Art. -Nr.: HY-113756A
CAS. Nr.: 41639-83-2
Reinheit:  99.62%
Forschungsgebiete:  

Inflammation/Immunology

Latanoprost acid, an analog of prostaglandin (PG) F2α, is an selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor . Latanoprost acid inhibits RANKL-induced osteoclastgenesis and function by inhibiting ERK, AKT, JNK, and p38 cascade, following by the c-fos/NFATc1 pathway. Latanoprost acid is a medication which works to lower pressure inside the eyes .
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1
1 Cited Publications
Art. -Nr.: HY-P99236
CAS. Nr.: 2259301-27-2
Synonyms: FP-1305

Forschungsgebiete:  

Inflammation/Immunology Cancer

Bexmarilimab (FP-1305) is a potent humanized anti-CLEVER-1 IgG4 antibody with an IC50 value of 4.51 nM. Bexmarilimab is capable of inducing a phenotypic M2 to M1 immune switch of tumor-associated macrophages. Bexmarilimab can promote antigen presentation and pro-inflammatory cytokine secretion. Bexmarilimab can induce B-cell and T-cell activation. Bexmarilimab can be used in researches of immunology and cancer, such as colorectal carcinoma .
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1
1 Cited Publications
Art. -Nr.: HY-117233
CAS. Nr.: 1500080-17-0
Reinheit:  99.63%
Target:  

β-catenin Wnt

Forschungsgebiete:  

Metabolic Disease Cancer

UU-T02 is a novel potent, selective small-molecule inhibitor of β-Catenin/T-cell factor protein-protein interaction (β-catenin/Tcf PPI) with a Ki of 1.36 μM . UU-T02 inhibits canonical Wnt signaling and the growth of colorectal cancer cells .
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Art. -Nr.: HY-136924
CAS. Nr.: 259270-28-5
Reinheit:  99.84%
Target:  

FAAH

Forschungsgebiete:  

Others

FP-biotin is a potent organophosphorus toxicant, well-suited for searching for new biomarkers of organophosphorus toxicants exposure. FP-Biotin quantifies FAAH, ABHD6, and MAG-lipase activity. FP-biotin is used for studies with plasma because biotinylated peptides are readily purified by binding to immobilized avidin beads .
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Art. -Nr.: HY-156963
CAS. Nr.: 877176-23-3
Reinheit:  98.16%
Synonyms: FP-025
Target:  

MMP

Forschungsgebiete:  

Inflammation/Immunology

Aderamastat (FP-025) is an orally active, selective MMP-12 inhibitor. Aderamastat provides protection against house dust mite (HDM)-sensitized allergic asthma. Aderamastat can be used in the research of respiratory diseases, including chronic inflammatory airway diseases and pulmonary fibrosis .
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