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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770702 1 1 -BI-2-NAPHTHOL 5G
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![eMolecules 126403-68-7 | Cyclopropylzinc bromide, 0.50 M in THF | Synthonix | MFCD08741505 | 186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]C1CC1 | 100ml | 627353805](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695212.jpg-250.jpg)
eMolecules 126403-68-7 | Cyclopropylzinc bromide, 0.50 M in THF | Synthonix | MFCD08741505 | 186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]C1CC1 | 100ml | 627353805
Cyclopropylzinc bromide, 0.50 M in THF | Synthonix | 126403-68-7 | MFCD08741505 | 186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]C1CC1 | 100ml | 627353805
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000291709 B7-2/CD86 HUMAN BI 20UG
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Medchemexpress LLC L-5,6,7,8-tetrahydrofolic acid | 135-16-0 | 96.8% | C19H23N7O6 | 10MG
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Tetrahydrofolic acid (L-5,6,7,8-tetrahydrofolic acid) is a biologically active folate derivative that functions as a donor of one-carbon units in amino acid, nucleic acid, and lipid metabolism. It is used in biochemical and pharmaceutical research involving folate-mediated one-carbon transfer. The compound is unstable in solution and is stored frozen, protected from light; DMSO is a suitable solvent.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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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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(CCCC)C1=CCCCO1 | 5g | 525924751](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696451.jpg-250.jpg)
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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Selleck Chemical LLC BI-D1870 S2843-50mg
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BI-D1870 is an ATP-competitive inhibitor of S6 ribosome for RSK1/2/3/4 with IC50 of 31 nM/24 nM/18 nM/15 nM in cell-free assays respectively 10- to 100-fold selectivity for RSK than MST2 GSK-3 MARK3 CK1 and Aurora B BI-D1870 exhibits anticancer attributes including the generation of reactive oxygen species (ROS) and increases in endoplasmic reticulum (ER) stress and autophagy
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eMolecules 57381-59-6 | 5-Bromo-2-fluorobenzoic acid methyl ester | ChemScene | MFCD06203710 | 233.036 | C8H6BrFO2 | 95.000 | COC(=O)c1cc(Br)ccc1F | 10g | 602865991
5-Bromo-2-fluorobenzoic acid methyl ester | ChemScene | 57381-59-6 | MFCD06203710 | 233.036 | C8H6BrFO2 | 95.000 | COC(=O)c1cc(Br)ccc1F | 10g | 602865991
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000703225 BI-2852 5MG
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![Medchemexpress LLC (2S)-tert-butoxy[4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-2-methylquinolin-3-yl]acetic acid | 1155419-89-8 | 99.7% | 442.51 g/mol | C27H26N2O4 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000295050.png-250.jpg)
Medchemexpress LLC (2S)-tert-butoxy[4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-2-methylquinolin-3-yl]acetic acid | 1155419-89-8 | 99.7% | 442.51 g/mol | C27H26N2O4 | 10 MG
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BI 224436 is a research-grade small-molecule noncatalytic site integrase inhibitor for HIV-1, intended for in vitro antiviral and biochemical studies. It demonstrates potent activity against laboratory strains and is supplied as a solid with defined storage requirements.
- Potent noncatalytic site integrase inhibitor with EC50 <15 nM.
- High purity, 99.7%.
- Molecular weight 442.51 g/mol.
- Chemical formula C27H26N2O4.
- Solid, white to yellow appearance.
- Store at -20°C and protect from light.
- Suitable for in vitro antiviral and biochemical assays.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695238 CEVIMELINE HYDROCHL 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695509 2-METHYL-1-NAPHTHOL 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000697446 PF-4455242 HYDROCHL 25MG
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