Naphthalenes
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000700927 A-NAPHTHOLBENZEIN 500MG
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5000737791 BENZOCAINE HYDROCHL 1G
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5000738091 NAPHTHOL AS-BI PHOSP 100MG
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5000741698 BI-655064 1MG
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Medchemexpress LLC Gallopamil hydrochloride | 16662-46-7 | 99.15% | C28H41ClN2O5 | 1 ML
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Gallopamil hydrochloride (Methoxyverapamil hydrochloride), a methoxy derivative of Verapamil, is a phenylalkylamine calcium antagonist. It inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM. It is also a potent antiarrhythmic and vasodilator agent.
- Also known as: Methoxyverapamil hydrochloride
- Methoxy derivative of Verapamil
- Phenylalkylamine calcium antagonist
- Inhibits acid secretion in a concentration-dependent manner with an IC50 of 10.9 μM
- Potent antiarrhythmic and vasodilator agent
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eMolecules 2135683-40-6 | [(3R)-1-tert-butoxycarbonylpyrrolidin-3-yl]methylzinc iodide, 0.5M in THF | Synthonix - Stock | MFCD31536791 | 376.540 | C10H18INO2Zn | 0.000 | [I-].CC(C)(C)OC(=O)N1CC[C@@H](C[Zn+])C1 | 50ml | 353003201
[(3R)-1-tert-butoxycarbonylpyrrolidin-3-yl]methylzinc iodide, 0.5M in THF | Synthonix - Stock | 2135683-40-6 | MFCD31536791 | 376.540 | C10H18INO2Zn | 0.000 | [I-].CC(C)(C)OC(=O)N1CC[C@@H](C[Zn+])C1 | 50ml | 353003201
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eMolecules 2089286-94-0 | 6-Fluoropyridin-3-ylzinc iodide, 0.50 M in THF | Synthonix288.370 | C5H3FINZn | 0.000 | [I-].Fc1ccc([Zn+])cn1 | 100ml | 532652856
6-Fluoropyridin-3-ylzinc iodide, 0.50 M in THF | Synthonix | 2089286-94-0288.370 | C5H3FINZn | 0.000 | [I-].Fc1ccc([Zn+])cn1 | 100ml | 532652856
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000784070 6-BROMO-2-NAPHTHOL 500G
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Medchemexpress LLC Rolapitant hydrochloride hydrate | 914462-92-3 | 98.36% | 554.95 | 1 ML
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Rolapitant hydrochloride hydrate | 914462-92-3 | 98.36% | 554.95 | 1 ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770702 1 1 -BI-2-NAPHTHOL 5G
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5000693377 SPERMIDINE HYDROCHL 1G
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Medchemexpress LLC Higenamine hydrochloride | 11041-94-4 | 307.77 | 500 MG
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Higenamine hydrochloride is a selective inhibitor of LSD1 with an IC50 of 1.47 μM, naturally sourced from aconite. It exhibits anti-inflammatory and antibacterial properties and can mitigate IL-1β-induced apoptosis via the ROS-mediated PI3K/Akt signaling pathway. Additionally, it offers protective effects for brain cells against oxygen deprivation and stimulates bone formation in osteoporosis through the SMAD2/3 pathway. It is utilized in research for various conditions, including cancer, inflammation, and cardiorenal syndrome.
- Selective LSD1 inhibitor (IC50=1.47 μM)
- Derived from aconite
- Possesses anti-inflammatory activity
- Exhibits antibacterial activity
- Attenuates IL-1β-induced apoptosis
- Protects brain cells from oxygen deprivation
- Promotes bone formation in osteoporosis
- Relevant for studying cancer, inflammation, and cardiorenal syndrome
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TARGETMOL CHEMICALS INC BI-1408 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. BI-1408 is a modulator potent of (gamma) secretase (IC50 0.04 uM for A(beta)42). purity: 98%
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eMolecules 109669-45-6 | Tributyl(5,6-dihydro-4H-pyran-2-yl)stannane | Synthonix - Stock373.168 | C17H34OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)C1=CCCCO1 | 5g | 525924751
Tributyl(5,6-dihydro-4H-pyran-2-yl)stannane | Synthonix - Stock | 109669-45-6373.168 | C17H34OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)C1=CCCCO1 | 5g | 525924751
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695238 CEVIMELINE HYDROCHL 25MG
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