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Filtered Search Results
eMolecules 138786-67-1 | Medchem Express | Pantoprazole (sodium) | 100mg | 446268552 | HY-17507A | MFCD09852812 | 405.35 | C16H14F2N3NaO4S
Pharmablock | tert-butyl N-(2-oxoazepan-3-yl)carbamate | 25mg | 778477209 | PBTEN15225 | 179686-45-4 | MFCD02183574 | 228.292 | C11H20N2O3
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Medchemexpress LLC HY-Y0202 100mg Medchemexpress, Pyrocatechuic acid CAS:303-38-8 Purity:>98%
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Medchemexpress, HY-Y0202 100mg Pyrocatechuic acid CAS:303-38-8 Pyrocatechuic acid is a normal human benzoic acid metabolite found in plasma, and has increased levels after aspirin ingestion. 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 Unc0224 | HY-10929
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Unc0224
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Medchemexpress LLC N4-(4-(dimethylamino)phenyl)-2-(pyridin-4-yl)-5,6,7,8-tetrahydroquinazoline-4,6-diamine | 2230854-93-8 | 98.1% | C21H24N6 | 10MG
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ARN-21934 is a selective small-molecule inhibitor of human topoisomerase IIα with reported blood-brain barrier penetration and favorable in vivo pharmacokinetics. It inhibits DNA relaxation (IC50 = 2 μM versus etoposide 120 μM) and is supplied for research use only.
- Selective topoisomerase IIα inhibition (IC50 = 2 μM).
- Reported blood-brain barrier penetration and favorable in vivo profile.
- Molecular formula C21H24N6; molecular weight 360.46 g·mol⁻¹.
- High purity, 98.1%.
- Available as solid (5-100 mg) and 10 mM solution in DMSO (1 mL).
- Intended for laboratory research use; not for human use.
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Medchemexpress LLC HY-108599A 10mg Medchemexpress, DCPLA-ME CAS:56687-67-3 Purity:>98%
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Medchemexpress, HY-108599A 10mg DCPLA-ME CAS:56687-67-3 DCPLA-ME, the methyl ester form of DCPLA, is a potent PKCε activator for use in the treatment of neurodegenerative diseases. 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-N0129 100mg Medchemexpress, Sclareolide CAS:564-20-5 Purity:>98%
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Medchemexpress, HY-N0129 100mg Sclareolide CAS:564-20-5 Sclareolide is isolated from the flower of Salvia sclarea with antibacterial and cytotoxic activities. 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-12420 5mg Medchemexpress, JNJ-47117096 hydrochloride CAS:1610536-69-0 Purity:>98%
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Medchemexpress, HY-12420 5mg JNJ-47117096 hydrochloride CAS:1610536-69-0 JNJ-47117096 hydrochloride is potent and selective MELK inhibitor, with an IC50 of 23 nM, also effectively inhibits Flt3, with an IC50 of 18 nM. 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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Selleck Chemical LLC BLU9931-5mg
BLU9931 is a potent, selective, and irreversible FGFR4 inhibitor with IC50 of 3 nM, about 297-, 184-, and 50-fold selectivity over FGFR1/2/3, respectively.
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Medchemexpress LLC KRAS inhibitor-9 | 300809-71-6 | 99.9% | 292.81 | 100 MG
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KRAS inhibitor-9 is a potent inhibitor of KRAS (Kd=92 μM) that blocks the formation of GTP-KRAS and downstream activation of KRAS signaling pathways. It binds to KRAS G12D, KRAS G12C, and KRAS Q61H proteins with moderate binding affinities. This product is intended for research use only.
- Causes G2/M cell cycle arrest and induces apoptosis in non-small cell lung cancer (NSCLC) cells
- Selectively inhibits the proliferation of NSCLC cells with KRAS mutation but does not affect normal lung cells
- Inhibits the activation of the KRAS downstream signaling pathway
- Blocks GTP-KRAS formation
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Medchemexpress LLC HY-N4277 5mg Medchemexpress, Methyl protogracillin CAS:54522-53-1 Purity:>98%
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Medchemexpress, HY-N4277 5mg Methyl protogracillin CAS:54522-53-1 Methyl protogracillin (NSC-698793), isolated from the roots of Dioscorea opposite Thunb, exhibits strong anti-cancer activity. 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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eMolecules 38363-41-6 | Medchem Express | ()-Penbutolol | 5mg | 441681964 | HY-116790A | 291.435 | C18H29NO2
ChemScene | 6-Bromo-4-methyl-1H-indazole | 100mg | 536833872 | CS-D0158 | 885520-98-9 | MFCD07781476 | 211.062 | C8H7BrN2
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Sigma Aldrich Fine Chemicals Biosciences Neostigmine bromide >=98% (HPLC and titration), powder | 114-80-7 | MFCD00011795 | 10G
Neostigmine bromide >=98% (HPLC and titration), powder | Purity: >=98% (HPLC and titration) | Mol Wt: 303.2 | 114-80-7 | MFCD00011795 | 10G
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Medchemexpress LLC HY-19792 2mg Medchemexpress, Mertansine CAS:139504-50-0 Purity:>98%
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Medchemexpress, HY-19792 2mg Mertansine CAS:139504-50-0 Mertansine (DM1) is a microtubulin inhibitor and is an antibody-conjugatable maytansinoid that is developed to overcome systemic toxicity associated with maytansine and to enhance tumor-specific delivery. Mertansine can be attached to a monoclonal antibody with a linker to create an antibody-drug conjugate (ADC)[2]. 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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Sigma Aldrich Fine Chemicals Biosciences Neostigmine methyl sulfate | 51-60-5 | MFCD00011796 | 500MG
Neostigmine methyl sulfate | Mol Wt: 334.39 | 51-60-5 | MFCD00011796 | 500MG
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Medchemexpress LLC V-9302 hydrochloride | 2416138-42-4 | 99.10% | 575.14 | 100 MG
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V-9302 hydrochloride is a competitive antagonist of transmembrane glutamine flux. It selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) but not ASCT1. It inhibits ASCT2-mediated glutamine uptake (IC50=9.6 μM) in HEK-293 cells.
- Competitive antagonist of transmembrane glutamine flux.
- Selectively targets amino acid transporter ASCT2 (SLC1A5).
- Potently inhibits ASCT2-mediated glutamine uptake.
- Attenuates cancer cell growth and proliferation.
- Increases cell death and oxidative stress.
- Prevents tumor growth in xenograft models.
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