Diphenylmethanes
Tamoxifen, 98%
CAS: 10540-29-1 Molecular Formula: C26H29NO Molecular Weight (g/mol): 371.52 MDL Number: MFCD00010454 InChI Key: NKANXQFJJICGDU-QPLCGJKRSA-N Synonym: tamoxifen,trans-tamoxifen,crisafeno,soltamox,tamoxifene,diemon,tamoxifeno,tamoxifenum,citofen,istubol PubChem CID: 2733526 ChEBI: CHEBI:41774 IUPAC Name: (2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethyl)dimethylamine SMILES: CC\C(=C(/C1=CC=CC=C1)C1=CC=C(OCCN(C)C)C=C1)C1=CC=CC=C1
Medchemexpress LLC 6-hydroxy-7-methoxycoumarin | 776-86-3 | 192.17 | 5 MG
Isoscopoletin is an active constituent found in Artemisia argyi leaves. It demonstrates inhibitory activity against HBV replication and exhibits anti-inflammatory effects by inhibiting the MAPK/NF-κB/STAT/AKT signaling pathway. It also significantly inhibits cell proliferation.
- Significantly inhibits cell proliferation in human CCRF-CEM leukaemia cells and multidrug-resistant subline CEM/ADR5000 cells.
- Demonstrates inhibitory activity against HBV replication.
- Exhibits anti-inflammatory effects by inhibiting the MAPK/NF-κB/STAT/AKT signaling pathway.
- Inhibits intracellular glucose consumption and lactate production in tumor cells.
- Downregulates levels of TARC, MDC, MCP-1, IL-8, and IL-1β in HaCaT cells.
Apexbio Technology LLC Epinastine HCl 108929-04-0 50mg
Epinastine hydrochloride (CAS 108929-04-0) is a small molecule antagonist of the histamine H1 receptor and a mast cell stabilizer By inhibiting H1 receptor-mediated signaling and preventing the degranulation of mast cells epinastine suppresses the release of pro-inflammatory mediators such as histamine It is commonly applied in ophthalmic research models to investigate mechanisms underlying allergic conjunctival inflammation and to evaluate antiallergic therapies Epinastine hydrochloride is used to study the modulation of allergic responses at the cellular and molecular levels particularly within ocular tissues
Apexbio Technology LLC BADGE 1675-54-3 10mg
BADGE (CAS nan) is a small-molecule antagonist targeting peroxisome proliferator-activated receptor gamma (PPAR ) It is designed to inhibit PPAR activity thereby modulating receptor-mediated signaling pathways involved in immune regulation BADGE exerts its biological activity primarily by antagonizing PPAR resulting in altered immune responses such as increased histamine secretion from immune cells and changes in cell-mediated immune mechanisms Based on these pharmacological properties BADGE holds research potential in investigating immune-related biological pathways allergic reactions and chemical sensitization mechanisms at the molecular and cellular levels
Medchemexpress LLC FH1 (NSC 12407) | 2719-05-3 | MFCD00027653 | 99.2% | 282.34 | C17H18N2O2 | 100MG
FH1 (NSC 12407) is a small-molecule hepatocyte function enhancer used in cell-based research to promote hepatocyte differentiation and improve liver cell function. Supplied as a solid (yellow to orange), it is characterized by high purity and defined storage conditions for reliable experimental use.
- Promotes hepatocyte differentiation and maturation in vitro.
- Modulates quinone reductase (NQO2) pathway relevant to liver function.
- High purity (99.2%) suitable for biological assays.
- Chemical formula C17H18N2O2; molecular weight 282.34.
- Available in multiple package sizes for experimental flexibility.
- Stable when stored as powder at -20 °C for long-term storage.
Medchemexpress LLC Epinastine hydrochloride | 108929-04-0 | 99.9% | 100 MG
Epinastine hydrochloride is a selective and orally active histamine H1 receptor antagonist, CD96/PVR inhibitor, and mast cell stabilizer. It exhibits high affinity for neuronal octapamine receptors in locusts (Ki = 2 nM) and honeybees (Ki = 1.1 nM) and is used in the research of allergic diseases.
- Selective and orally active histamine H1 receptor antagonist
- CD96/PVR inhibitor
- Mast cell stabilizer
- High affinity for neuronal octapamine receptors
- Inhibits TARC, IL-8, and IL-4
- Activates anti-colon cancer immunity
- Inhibits Substance P-induced scratching behavior and increased vascular permeability
Echelon Biosciences Research Labs DPPE 250 mg
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) is a water soluble derivative of phosphatidylethanolamine with (16:0) palmitoyl acyl chains. Phosphatidylethanolamine (PE) is formed primarily in the reaction of CDP-ethanolamine and diacylglycerol. PE is one of the major components of cell membranes in bacteria and in nervous system. This item is non returnable
Selleck Chemical LLC Letrozole CGS 20267-25mg
Letrozole is a third generation inhibitor of aromatase with IC50 of 0.07-20 nM in cell-free assays.It has no effect on the plasma levels of 17α-OH progesterone, thyroid-stimulating hormone (TSH), luteinizing hormone (LH), follicle-stimulating hormone (FSH), or androstenedione and does not affect normal urine electrolyte excretion or thyroid function in clinical studies. Letrozole induces autophagy.
Medchemexpress LLC Epinastine hydrochloride | 108929-04-0 | 99.86% | 50 MG
Epinastine hydrochloride is a selective and orally active histamine H1 receptor antagonist, a CD96/PVR inhibitor, and a mast cell stabilizer. It demonstrates high affinity for neuronal octopamine receptors and inhibits TARC, IL-8, and IL-4. It can activate anti-colon cancer immunity and inhibit Substance P-induced scratching behavior and increased vascular permeability. Epinastine hydrochloride is utilized in the research of allergic diseases.
- Selective and orally active histamine H1 receptor antagonist
- CD96/PVR inhibitor
- Mast cell stabilizer
- Demonstrates high affinity for neuronal octopamine receptors
- Inhibits TARC, IL-8, and IL-4
- Activates anti-colon cancer immunity
- Inhibits Substance P-induced scratching behavior and increased vascular permeability
- Utilized in the research of allergic diseases
Medchemexpress LLC Epinastine hydrochloride | 108929-04-0 | 99.9% | 500 MG
Epinastine hydrochloride is a selective and orally active histamine H1 receptor antagonist, CD96/PVR inhibitor, and mast cell stabilizer. This compound has high affinity for neuronal octapamine receptors in locusts (Ki = 2 nM) and honeybees (Ki = 1.1 nM). It is capable of inhibiting TARC, IL-8, and IL-4, activating anti-colon cancer immunity, and inhibiting Substance P-induced scratching behavior and increased vascular permeability. Epinastine hydrochloride is suitable for research into allergic diseases.
- Selective and orally active histamine H1 receptor antagonist
- CD96/PVR inhibitor and mast cell stabilizer
- Exhibits high affinity for neuronal octapamine receptors
- Inhibits TARC, IL-8, and IL-4
- Activates anti-colon cancer immunity
- Inhibits Substance P-induced scratching behavior and increased vascular permeability
- Applicable for research into allergic diseases
Medchemexpress LLC HY-B0640 50mg Medchemexpress, Epinastine CAS:80012-43-7 Purity:>98%
Medchemexpress, HY-B0640 50mg Epinastine CAS:80012-43-7 Epinastine (WAL801) is an antihistamine and mast cell stabilizer. Epinastine is a potent, selective and orally-active histamine H1 receptor antagonist. Epinastine also inhibits IL-8 release and has an antiallergic action[4]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Echelon Biosciences Research Labs N-PALMITOYL-DPPE 10mg
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-palmitoyl (N-palmitoyl-DPPE) is a type of N-acylphosphatidylethanolamine (NAPE) which as a group includes substrates in the endocannabinoid biosynthesis pathway. Fatty acid amides are formed by hydrolysis of NAPEs by a specific phospholiase D, and N-palmitoyl-ethanolamine (PEA) is found in significant concentrations in the mammalian circulation and central nervous systems. PEA is recognized for its anti-inflammatory and analgesic properties in cells and in vivo animal models of neuropathic and inflammatory diseases. Further, PEA-containing products are licensed for use in humans typically as an analgesic or anti-inflammatory with demonstrated high safety and tolerability. This item is non returnable
Echelon Biosciences Research Labs N-PALMITOYL-DPPE 5mg
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-palmitoyl (N-palmitoyl-DPPE) is a type of N-acylphosphatidylethanolamine (NAPE) which as a group includes substrates in the endocannabinoid biosynthesis pathway. Fatty acid amides are formed by hydrolysis of NAPEs by a specific phospholiase D, and N-palmitoyl-ethanolamine (PEA) is found in significant concentrations in the mammalian circulation and central nervous systems. PEA is recognized for its anti-inflammatory and analgesic properties in cells and in vivo animal models of neuropathic and inflammatory diseases. Further, PEA-containing products are licensed for use in humans typically as an analgesic or anti-inflammatory with demonstrated high safety and tolerability. This item is non returnable
Echelon Biosciences Research Labs N-PALMITOYL-DPPE 50mg
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-palmitoyl (N-palmitoyl-DPPE) is a type of N-acylphosphatidylethanolamine (NAPE) which as a group includes substrates in the endocannabinoid biosynthesis pathway. Fatty acid amides are formed by hydrolysis of NAPEs by a specific phospholiase D, and N-palmitoyl-ethanolamine (PEA) is found in significant concentrations in the mammalian circulation and central nervous systems. PEA is recognized for its anti-inflammatory and analgesic properties in cells and in vivo animal models of neuropathic and inflammatory diseases. Further, PEA-containing products are licensed for use in humans typically as an analgesic or anti-inflammatory with demonstrated high safety and tolerability. This item is non returnable