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Filtered Search Results
eMolecules Diphenyl[1-(prop-2-en-1-yl)-1H-1,2,4-triazol-5-yl]methanol | 209970-00-3 | MFCD00971583 | 10mg
Oakwood Chemical | Diphenyl[1-(prop-2-en-1-yl)-1H-1,2,4-triazol-5-yl]methanol | 10mg | 537708310 | 101413 | | 209970-00-3 | MFCD00971583 | 291.354 | C18H17N3O
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Accela Chembio Inc (s)-(-)-2-amino-3-methyl-1 | 1-diphenyl-1-butanol | 5g | 78603-95-9 | MFCD01318248 | 97+% | Shelf Life: 1620 Days | Moissanite Sensitive/+4
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(s)-(-)-2-amino-3-methyl-1 | 1-diphenyl-1-butanol | 5g | 78603-95-9 | MFCD01318248 | 97+% | Shelf Life: 1620 Days | Moissanite Sensitive/+4
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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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Sigma Aldrich Fine Chemicals Biosciences SC-57461A >=98% (HPLC) | 423169-68-0 | MFCD00951253 | 5MG
SC-57461A >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 363.88 | 423169-68-0 | MFCD00951253 | 5MG
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Medchemexpress LLC 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid HCl | 423169-68-0 | MFCD00951253 | 99.9% | 363.88 | C20H26ClNO3 | 50 MG
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SC-57461A is a potent, orally active, nonpeptide inhibitor of leukotriene A4 (LTA4) hydrolase used for research. It shows low-nanomolar inhibitory activity against human, mouse, and rat LTA4 hydrolase and is supplied as a purified solid for laboratory studies.
- Potent LTA4 hydrolase inhibition with low-nanomolar IC50s.
- Intended for research use only, not for human or veterinary use.
- High purity (≈99.9%).
- White to off-white solid appearance.
- Molecular weight 363.88; formula C20H26ClNO3.
- Supplied as a 50 mg vial suitable for bench-scale experiments.
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eMolecules 3-Methoxybenzhydrol | 13391-45-2 | MFCD06201261 | 1g
Oakwood Chemical | 3-Methoxybenzhydrol | 1g | 537680169 | 022430 | | 13391-45-2 | MFCD06201261 | 214.264 | C14H14O2
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eMolecules 1-(diphenylmethyl)-2,2-dimethylazetidin-3-ol | 159556-73-7 | MFCD11848691 | 1g
Pharmablock | 1-(diphenylmethyl)-2,2-dimethylazetidin-3-ol | 1g | 551256166 | PBLLA075 | | 159556-73-7 | MFCD11848691 | 267.372 | C18H21NO
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Chem-Impex International, Inc. 4,4'-Methylenebis(2,6-diethylaniline) | MFCD00071552 | 250G
4,4'-Methylenebis(2,6-diethylaniline), MFCD00071552, 250G
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Medchemexpress LLC HY-100852 1mg Medchemexpress, ER-000444793 CAS:792957-74-5 Purity:>98%
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Medchemexpress, HY-100852 1mg ER-000444793 CAS:792957-74-5 ER-000444793 is a potent inhibitor of mitochondrial permeability transition pore ( mPTP ) opening. ER-000444793 inhibits mPTP with an IC 50 of 2.8 μM. 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 HY-128723 5mg Medchemexpress, Dapagliflozin impurity CAS:960404-86-8 Purity:>98%
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Medchemexpress, HY-128723 5mg Dapagliflozin impurity CAS:960404-86-8 Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 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 2-(1H-indol-3-yl)-N-(2-oxo-1,2-dihydroquinolin-4-yl)acetamide | 792957-74-5 | 98.0% | 354.40 | C23H18N2O2 | 25 MG
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This small-molecule inhibitor blocks mitochondrial permeability transition pore (mPTP) opening and is intended for in vitro research. It shows inhibitory activity with an IC50 of 2.8 μM and is supplied as a solid, high-purity research reagent.
- Inhibits mPTP opening (IC50 2.8 μM).
- For in vitro research use only.
- Purity 98.0%.
- Solid, off-white to light yellow.
- Soluble in DMSO (50 mg/mL); ultrasonic agitation recommended.
- Molecular weight 354.40; formula C23H18N2O2.
- CAS number 792957-74-5.
- Storage: powder -20°C (3 years), 4°C (2 years).
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eMolecules Ambeed / (S)-2-(((Benzyloxy)carbonyl)amino)-5-(3-nitroguanidino)pentanoic acid / 1g / 596568615 / A388098 / / 2304-98-5 / [null] / 353.335 / C14H19N5O6
Ambeed / (S)-2-(((Benzyloxy)carbonyl)amino)-5-(3-nitroguanidino)pentanoic acid / 1g / 596568615 / A388098 / / 2304-98-5 / [null] / 353.335 / C14H19N5O6
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eMolecules 4-Nitrodiphenylmethane | 1817-77-2 | 5G | Purity: 95%
Combi-Blocks | 4-Nitrodiphenylmethane | 5G | 1817-77-2 | MFCD00024783
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Sigma Aldrich Fine Chemicals Biosciences Ospemifene >=98% (HPLC) | 128607-22-7 | 50MG
Ospemifene >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 378.89 | 128607-22-7 | 50MG
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Sigma Aldrich Fine Chemicals Biosciences Diphenylfulvene 98% | 2175-90-8 | MFCD00001419 | 10G
Diphenylfulvene 98% | Purity: 98% | Mol Wt: 230.3 | 2175-90-8 | MFCD00001419 | 10G
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