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Filtered Search Results
Medchemexpress LLC Epinastine hydrochloride | 108929-04-0 | 99.86% | 50 MG
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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
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eMolecules 138876-39-8 | (2R,3S)-1-(diphenylmethyl)-2-methylazetidin-3-ol | 1g
Medchem Express | Tyk2-IN-5 | 5mg | 482203984 | HY-111745 | 1797432-62-2 | 434.435 | C21H19FN8O2
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eMolecules 76300-15-7 | N-Methoxyadamantan-2-imine | Synthonix - Stock179.263 | C11H17NO | 95.000 | CON=C1C2CC3CC(C2)CC1C3 | 1g | 499993936
N-Methoxyadamantan-2-imine | Synthonix - Stock | 76300-15-7179.263 | C11H17NO | 95.000 | CON=C1C2CC3CC(C2)CC1C3 | 1g | 499993936
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eMolecules 41332-24-5 | 1-[4-(DIPHENYLMETHYL)-1-PIPERAZINYL]-3,3-DIPHENYL-1-PROPANONE | AstaTech | MFCD03387795 | 460.621 | C32H32N2O | 95.000 | O=C(CC(c1ccccc1)c1ccccc1)N1CCN(CC1)C(c1ccccc1)c1ccccc1 | 0.25g | 323612546
1-[4-(DIPHENYLMETHYL)-1-PIPERAZINYL]-3,3-DIPHENYL-1-PROPANONE | AstaTech | 41332-24-5 | MFCD03387795 | 460.621 | C32H32N2O | 95.000 | O=C(CC(c1ccccc1)c1ccccc1)N1CCN(CC1)C(c1ccccc1)c1ccccc1 | 0.25g | 323612546
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eMolecules 2304-98-5 | Ambeed | (S)-2-(((Benzyloxy)carbonyl)amino)-5-(3-nitroguanidino)pentanoic acid | 1g | 596568615 | A388098 | 353.335 | C14H19N5O6
Medchem Express | QX-222 (chloride) | 5mg | 705859928 | HY-101362 | 5369-00-6 | MFCD01459898 | 256.770 | C13H21ClN2O
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eMolecules 1817-77-2 | 4-Nitrodiphenylmethane | Combi-Blocks | MFCD00024783 | 213.236 | C13H11NO2 | 98.000 | [O-][N+](=O)c1ccc(Cc2ccccc2)cc1 | 5g | 342866093
4-Nitrodiphenylmethane | Combi-Blocks | 1817-77-2 | MFCD00024783 | 213.236 | C13H11NO2 | 98.000 | [O-][N+](=O)c1ccc(Cc2ccccc2)cc1 | 5g | 342866093
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Medchemexpress LLC HY-109092 5mg Medchemexpress, Licogliflozin CAS:1291094-73-9 Purity:>98%
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Medchemexpress, HY-109092 5mg Licogliflozin CAS:1291094-73-9 Licogliflozin is a sodium glucose cotransporter (SGLT1 and SGLT2) inhibitor. 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.
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Medchemexpress LLC Epinastine hydrochloride | 108929-04-0 | 99.9% | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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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
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 1104-22-9 | Meclizine dihydrochloride | Combi-Blocks | MFCD00058199 | 463.870 | C25H29Cl3N2 | 98.000 | Cl.Cl.Cc1cccc(CN2CCN(CC2)C(c2ccccc2)c2ccc(Cl)cc2)c1 | 25g | 205398444
Meclizine dihydrochloride | Combi-Blocks | 1104-22-9 | MFCD00058199 | 463.870 | C25H29Cl3N2 | 98.000 | Cl.Cl.Cc1cccc(CN2CCN(CC2)C(c2ccccc2)c2ccc(Cl)cc2)c1 | 25g | 205398444
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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.
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Electron Microscopy Sciences Auramine O, Certified, C.I. DcAu-4 25 GR
(Pyoctanunum aureum; Basic Yellow 2; Pyoktanin Yellow; Canary Yellow)
CAS #2465-27-2 C₁₇H₂₁N₃HCl·H₂O F.W. 321.86
Solubility: 1.0% Water; 4.0% Alcohol; 1.2% Cellosolve; 1.75% Glycol; 0.05% Xylene
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Medchemexpress LLC N-methyl-N-[3-[4-(phenylmethyl)phenoxy]propyl β-alanine hydrochloride | 423169-68-0 | MFCD00951253 | 99.9% | 363.88 | C20H26ClNO3 | 5 MG
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SC-57461A is a selective leukotriene A4 hydrolase (LTA4H) inhibitor supplied as the hydrochloride salt for research use. It is provided as a crystalline solid with high stated purity and is used in biochemical and pharmacological assays to probe inflammatory pathways.
- Selective LTA4 hydrolase inhibition for mechanistic studies.
- High purity suitable for analytical and pharmacological assays.
- Available as a solid hydrochloride salt and as a DMSO solution.
- Molecular weight and formula support accurate dosing and calculations.
- Stable when stored desiccated at recommended temperatures.
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Sigma Aldrich Fine Chemicals Biosciences Levocetirizine dihydrochloride >=98% (HPLC) | 130018-87-0 | MFCD07366507 | 50MG
Levocetirizine dihydrochloride >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 461.81 | 130018-87-0 | MFCD07366507 | 50MG
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Medchemexpress LLC N-methyl-n-[3-[4-(phenylmethyl)phenoxy]propyl β-alanine hydrochloride | 423169-68-0 | MFCD00951253 | 99.9% | 363.88 | C20H26ClNO3 | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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SC-57461A is a potent, orally active, nonpeptide inhibitor of leukotriene A4 (LTA4) hydrolase used in research to inhibit leukotriene B4 (LTB4) synthesis and study inflammatory pathways.
- Potent LTA4 hydrolase inhibition (human recombinant IC50 = 2.5 nM).
- Cellular activity in whole-blood assays (IC50 ≈ 49 nM).
- Demonstrated oral efficacy in rodent models.
- High purity (≈99.9%) and solid, white to off-white appearance.
- Formula C20H26ClNO3 and molecular weight 363.88 g/mol.
- Soluble in DMSO (~250 mg/mL); store sealed at 4°C; in solvent store at -80°C for long-term stability.
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eMolecules 83881-54-3 | Medchem Express | Deschloro Cetirizine (dihydrochloride) | 5mg | 758391341 | HY-131579 | 427.37 | C21H28Cl2N2O3
Medchem Express | Deschloro Cetirizine (dihydrochloride) | 5mg | 758391341 | HY-131579 | 83881-54-3 | 427.370 | C21H28Cl2N2O3
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