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Filtered Search Results
eMolecules Medchem Express | Seladelpar sodium salt | 5mg | 446269888 | HY-19522A | 466.45 | C21H22F3NaO5S
Medchem Express | Seladelpar sodium salt | 5mg | 446269888 | HY-19522A | | 466.450 | C21H22F3NaO5S
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Medchemexpress LLC HY-12335 5mg Medchemexpress, UNC0379 CAS:1620401-82-2 Purity:>98%
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Medchemexpress, HY-12335 5mg UNC0379 CAS:1620401-82-2 UNC0379 is a selective, substrate-competitive inhibitor of lysine methyltransferase SETD8 (KMT5A) with an IC50 of 7.3 μM; selective over 15 other methyltransferases. 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-15485 5mg Medchemexpress, Zardaverine CAS:101975-10-4 Purity:>98%
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Medchemexpress, HY-15485 5mg Zardaverine CAS:101975-10-4 0 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 BRD4 Inhibitor-24 | 309951-18-6 | 99.27% | 262.26 | 50 MG
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BRD4 Inhibitor-24 (compound 3U) is a potent BRD4 inhibitor that has demonstrated antitumor activity. It shows IC50 values of 33.7 μM against MCF7 cells and 45.9 μM against K652 cells. This compound has been extracted from patent CN107721975A.
- Potent BRD4 inhibitor.
- Exhibits antitumor activity against MCF7 (IC50: 33.7 μM) and K652 (IC50: 45.9 μM) cells.
- Derived from patent CN107721975A.
- For research use only.
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Medchemexpress LLC HY-B0290 100mg Medchemexpress, Pranlukast CAS:103177-37-3 Purity:>98%
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Medchemexpress, HY-B0290 100mg Pranlukast CAS:103177-37-3 Pranlukast is a highly potent, selective and competitive antagonist of peptide leukotrienes. Pranlukast inhibits [3H]LTE4, [3H]LTD4, and [3H]LTC4 bindings to lung membranes with Kis of 0.63±0.11, 0.99±0.19, and 5640±680 nM, respectively. 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-N6631 100mg Medchemexpress, 7-Methoxyisoflavone CAS:1621-56-3 Purity:>98%
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Medchemexpress, HY-N6631 100mg 7-Methoxyisoflavone CAS:1621-56-3 7-Methoxyisoflavone is an isoflavone derivative and also an activator of adenosine monophosphate-activated protein kinase ( AMPK ). 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 Lucitanib | 1058137-23-7 | C26H25N3O4 | 100 MG
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Lucitanib (E-3810) is a novel dual inhibitor of VEGFR and FGFR, potently and selectively inhibiting multiple receptors. It is suitable for use in various laboratory applications, including the manufacture of substances.
- Inhibits VEGFR1 with an IC50 of 7 nM
- Inhibits VEGFR2 with an IC50 of 25 nM
- Inhibits VEGFR3 with an IC50 of 10 nM
- Inhibits FGFR1 with an IC50 of 17.5 nM
- Inhibits FGFR2 with an IC50 of 82.5 nM
- Targeted for cancer research
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![Medchemexpress LLC 2,4-Pyrimidinediamine, N2-[4-[(3-aminopropyl)amino]phenyl]-N4-(5-cyclopropyl-1H-pyrazol-3-yl) HCl | 2700435-52-3 | 99.5% | 400.91 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000387884-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2,4-Pyrimidinediamine, N2-[4-[(3-aminopropyl)amino]phenyl]-N4-(5-cyclopropyl-1H-pyrazol-3-yl) HCl | 2700435-52-3 | 99.5% | 400.91 | 50 MG
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VEGFR-2-IN-5 hydrochloride is an off-white to light yellow solid. It is identified as a VEGFR2 inhibitor, extracted from patent WO2013055780A1. This compound targets VEGFR, demonstrating activity against VEGFR2.
- Acts as a VEGFR2 inhibitor.
- Appearance: off-white to light yellow solid.
- Complies with given specifications.
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Medchemexpress LLC Epertinib hydrochloride | 2071195-74-7 | 98.2% | 596.48 g/mol | C30H28Cl2FN5O3 | 100 MG
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Epertinib hydrochloride is the hydrochloride salt of epertinib, a potent, orally active, reversible, and selective inhibitor of EGFR, HER2, and HER4. It is provided for preclinical research to evaluate signaling pathways and antitumor efficacy and is compatible with click-chemistry applications because of an alkyne functional group.
- Potent, selective tyrosine kinase inhibitor of EGFR, HER2, and HER4.
- Used in preclinical antitumor and signaling research.
- Contains an alkyne moiety compatible with copper-catalyzed azide-alkyne cycloaddition (CuAAC).
- Supplied as a light yellow to yellow solid with high purity.
- Stable under recommended storage: 4°C sealed; in solvent -80°C (6 months), -20°C (1 month).
- Molecular weight 596.48 g/mol; molecular formula C30H28Cl2FN5O3.
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eMolecules 1644543-95-2 | Medchem Express | S65487 (hydrochloride) | 5mg | 694125052 | HY-138697B | 753.73 | C41H42Cl2N6O4
Ambeed | 1-Boc-4-(Hydroxymethyl)-4-methylpiperidine | 1g | 525022997 | A123210 | 236406-21-6 | MFCD08062516 | 229.320 | C12H23NO3
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Selleck Chemical LLC RS-102895 Hydrochloride
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RS-102895 hydrochloride (HCl) is a potent antagonist of Chemokine (C-C motif) receptor 2 (CCR2) with IC50 of 360 nM and shows no effect on CCR1 RS-102895 hydrochloride also inhibits human 1a and 1d receptors rat brain cortex 5-HT1a receptor in cells with IC50s of 130 nM 320 nM 470 nM respectively
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Medchemexpress LLC AMTB hydrochloride | 926023-82-7 | 99.2% | 430.99 | C23H27ClN2O2S | 5 MG
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AMTB hydrochloride is a research-grade small molecule that selectively blocks TRPM8 ion channels and also inhibits voltage-gated sodium channels. Supplied as a white to off-white solid with high chemical purity, it is intended for in-vitro and in-vivo research applications investigating TRPM8-mediated physiology and pharmacology.
- Selective TRPM8 channel blocker and non-selective voltage-gated sodium channel inhibitor.
- High purity: 99.18%.
- White to off-white solid form suitable for formulation.
- Soluble in DMSO (up to 100 mg/mL) with sonication.
- In vivo formulation protocols available for concentrations ≥ 2.5 mg/mL.
- Supplied in small research pack sizes, including 5 mg.
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eMolecules 63019-39-6 | 3-Hydroxychrysene | Toronto Research Chemicals | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
3-Hydroxychrysene | Toronto Research Chemicals | 63019-39-6 | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
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Medchemexpress LLC 5-O-Methylvisammioside | 84272-85-5 | 452.45 | 50 MG
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5-O-Methylvisammioside is a natural compound isolated from Saposhnikovia divaricata.
- Natural compound
- Isolated from Saposhnikovia divaricata
- Purity: 99.90%
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Medchemexpress LLC HY-12001 5mg Medchemexpress, WZ-3146 CAS:1214265-56-1 Purity:>98%
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Medchemexpress, HY-12001 5mg WZ-3146 CAS:1214265-56-1 WZ3146 is a mutant selective EGFR inhibitor with IC 50 s of 2, 2, 5, 14 and 66 nM for EGFR L858R , EGFR L858R/T790M , EGFR E746_A750 , EGFR E746_A750/T790M and EGFR, respectively. 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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