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Filtered Search Results
Medchemexpress LLC Lonafarnib 10 Mm 1 Ml In Dmso | HY-15136
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Lonafarnib 10 Mm 1 Ml In Dmso
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Medchemexpress LLC Way-213613 hydrochloride | 2450268-84-3 | 99.8% | 451.65 g/mol | C16H14BrClF2N2O4 | 25 MG
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WAY-213613 hydrochloride is a potent, selective inhibitor of the excitatory amino acid transporter 2 (EAAT2) used in biochemical and pharmacological research to study glutamate uptake and transporter-mediated signaling. The compound is supplied as a hydrochloride salt with well-defined chemical properties and high purity suitable for in vitro assays and mechanistic studies.
- Potent and selective EAAT2 inhibition at nanomolar concentrations.
- High purity appropriate for biochemical and cell-based assays.
- Supplied as a hydrochloride salt to enhance stability and solubility.
- Includes molecular weight and formula information for experimental planning.
- Available in small-scale quantities for research workflows.
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Medchemexpress LLC Selumetinib (sulfate) | 943332-08-9 | 99.6% | C17H17BrClFN4O7S | 500 MG
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Selumetinib sulfate is a selective, non-ATP-competitive oral MEK1/2 inhibitor, with an IC50 of 14 nM for MEK1. It inhibits ERK1/2 phosphorylation and can penetrate the blood-brain barrier (BBB).
- Selective, non-ATP-competitive oral MEK1/2 inhibitor
- Inhibits ERK1/2 phosphorylation
- Can penetrate the blood-brain barrier (BBB)
- Causes time- and dose-dependent reduction in DNA synthesis and cell viability
- Induces growth arrest and apoptosis by inactivating ERK in primary cells
- Shows anti-proliferative effects through G0/G1 arrest on H-441 and H-1437 cells
- Inhibits growth of several cell lines with B-Raf and Ras mutations
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Medchemexpress LLC Selumetinib (sulfate) | 943332-08-9 | C17H17BrClFN4O7S | 200 MG
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Selumetinib (AZD6244) sulfate is a selective, non-ATP-competitive oral MEK1/2 inhibitor, with an IC50 of 14 nM for MEK1. It inhibits ERK1/2 phosphorylation and can penetrate the blood-brain barrier (BBB).
- Inhibits ERK1/2 phosphorylation
- Penetrates the blood-brain barrier
- Reduces DNA synthesis and cell viability
- Induces growth arrest and apoptosis
- Shows anti-proliferative effects through G0/G1 arrest
- Inhibits growth of cell lines with B-Raf and Ras mutations
- Decreases growth rate of xenografts
- Causes tumor regressions in xenograft models
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eMolecules 4-Amino-3-bromo-5-nitrobenzonitrile | 1239720-33-2 | MFCD22383659 | 1g
Ambeed | 4-Amino-3-bromo-5-nitrobenzonitrile | 1g | 600836923 | A302000 | | 1239720-33-2 | MFCD22383659 | 242.032 | C7H4BrN3O2
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eMolecules 3-Bromo-4-(trifluoromethoxy)benzeneboronic acid | 2304634-32-8 | MFCD22580724 | 1g
Apollo Scientific | 3-Bromo-4-(trifluoromethoxy)benzeneboronic acid | 1g | 562428627 | PC49293 | | 2304634-32-8 | MFCD22580724 | 284.820 | C7H5BBrF3O3
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eMolecules 2-Bromo-4-(trifluoromethoxy)phenol | 200956-13-4 | MFCD07778431 | 1g
Apollo Scientific | 2-Bromo-4-(trifluoromethoxy)phenol | 1g | 562440425 | PC3121 | 97.000 | 200956-13-4 | MFCD07778431 | 257.006 | C7H4BrF3O2
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eMolecules Medchem Express / WHI-P97 / 5mg / 446259841 / HY-11067 / / 211555-05-4 / MFCD02683947 / 455.106 / C16H13Br2N3O3
Medchem Express / WHI-P97 / 5mg / 446259841 / HY-11067 / / 211555-05-4 / MFCD02683947 / 455.106 / C16H13Br2N3O3
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eMolecules [1-(4-Amino-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl ester | 264916-40-7 | MFCD28536084 | 5g
J & W PharmLab LLC | [1-(4-Amino-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl ester | 5g | 347416492 | 20R1677 | 96.000 | 264916-40-7 | MFCD28536084 | 250.342 | C14H22N2O2
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eMolecules Medchem Express / P7C3-OMe / 5mg / 495800373 / HY-128856 / / 313268-18-7 / MFCD00689264 / 504.222 / C22H20Br2N2O2
Medchem Express / P7C3-OMe / 5mg / 495800373 / HY-128856 / / 313268-18-7 / MFCD00689264 / 504.222 / C22H20Br2N2O2
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eMolecules Medchem Express / P2Y2R/GPR17 antagonist 1 / 10mg / 742367727 / HY-146486 / / 2395016-49-4 / [null] / 432.830 / C19H13ClN2O6S
Medchem Express / P2Y2R/GPR17 antagonist 1 / 10mg / 742367727 / HY-146486 / / 2395016-49-4 / [null] / 432.830 / C19H13ClN2O6S
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eMolecules N-(1-(4-bromophenyl)ethylidene)-4-methylbenzenesulfonohydrazide | 75230-51-2 | | 1g
WuXi ChemSupply | N-(1-(4-bromophenyl)ethylidene)-4-methylbenzenesulfonohydrazide | 1g | 599171522 | LN04540342 | 95.000 | 75230-51-2 | | 367.260 | C15H15BrN2O2S
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Medchemexpress LLC Bcl-xL antagonist 2 | 1235032-75-3 | 98.86% | 10 MG
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Bcl-xL antagonist 2 is a potent, selective, and orally active antagonist of BCL-XL, exhibiting IC50 and Ki values of 0.091 μM and 65 nM, respectively. This compound promotes the apoptosis of cancer cells and is being researched for its potential applications in chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma (NHL).
- Potent and selective BCL-XL antagonist
- Orally active
- Promotes apoptosis in cancer cells
- Potential for chronic lymphocytic leukemia (CLL) research
- Potential for non-Hodgkin's lymphoma (NHL) research
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eMolecules N-[1-(4-Bromophenyl)ethyl]prop-2-yn-1-amine hydrochloride | 2387695-90-9 | | 1g
Apollo Scientific | N-[1-(4-Bromophenyl)ethyl]prop-2-yn-1-amine hydrochloride | 1g | 562460590 | OR475108 | | 2387695-90-9 | | 274.590 | C11H13BrClN
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Medchemexpress LLC HY-112777 10mg Medchemexpress, Kinesore CAS:363571-83-9 Purity:>98%
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Medchemexpress, HY-112777 10mg Kinesore CAS:363571-83-9 Kinesore is an inhibitor of the KLC2-SKIP Interaction. 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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