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Filtered Search Results
GRAINGER INC L-LEUCINAMIDE HYDROCHLORIDE 1G
502781434 L-LEUCINAMIDE HYDROCHLORIDE 1G
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AMBEED OXAZOLIDIN 2 ONE
NC2867241 OXAZOLIDIN 2 ONE
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AA BLOCKS LLC 2-ETHOXYPYRIDINE-4-BO 250MG
NC3308920 2-ETHOXYPYRIDINE-4-BO 250MG
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AMBEED S-3 3-DIMETHYLBUTAN-2-AMINE 5G
NC2888176 S-3 3-DIMETHYLBUTAN-2-AMINE 5G
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Medchemexpress LLC Aa26-9 50Mg | SE6054
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Aa26-9 50Mg
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eMolecules 2-(Hydroxy(4-Phenoxyphenyl)Methylene)Malononitrile | 330792-68-2 | MFCD20270362 | 250mg
WuXi AppTec | 2-(Hydroxy(4-Phenoxyphenyl)Methylene)Malononitrile | 250mg | 583187405 | LN01347852 | | 330792-68-2 | MFCD20270362 | 262.268 | C16H10N2O2
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eMolecules Building Block Tool
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eMolecules S S-BN-PYBOX 5G
5000159052 S S-BN-PYBOX 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371366 S -P-SCN-BN-DOTA 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383241 P-SCN-BN-DEFEROXAMIN 50MG
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eMolecules EMOLECULES INC
5000470534 R R-BN-PYBOX 5G
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eMolecules EMOLECULES INC
5000471545 BENZYLTRIETHYLAMMONIUM CH 10G
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eMolecules EMOLECULES INC
5000471007 BENZYLTRIETHYLAMMONIUM CHL 5G
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Medchemexpress LLC 8-Azaadenine | 1123-54-2 | 99.9% | 136.12 | 250 MG
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8-Azaadenine is an inhibitor of Xanthine Oxidase with an IC50 of 0.54 μM and a Ki of 0.66 μM. It is produced via the metabolism of 8-Azaadenosine and can be incorporated into polynucleotide chains alongside 8-Azaguanine to impact purine metabolism. This product is used in cancer studies and can also be synthesized into various derivatives through alkylation reactions, which demonstrate antiviral activity.
- Inhibits Xanthine Oxidase with an IC50 of 0.54 μM and a Kᵢ of 0.66 μM
- Produced via the metabolism of 8-Azaadenosine
- Incorporated into polynucleotide chains to affect purine metabolism
- Used in the study of cancer
- Can be synthesized into derivatives with antiviral activity
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Medchemexpress LLC Febrifugine dihydrochloride | 32434-42-7 | 5 MG
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Febrifugine dihydrochloride is a quinazolinone alkaloid with demonstrated antimalarial activity against P. falciparum. It also exhibits anti-cancer properties by inhibiting DNA synthesis, inducing apoptosis, and reducing steroids in bladder cancer cells.
- Quinazolinone alkaloid with antimalarial activity
- Inhibits P. falciparum
- Demonstrates anti-cancer properties
- Inhibits DNA synthesis
- Induces apoptosis
- Reduces steroids in bladder cancer cells
- Increases eIF2α phosphorylation
- Inhibits asexual blood stage of P. falciparum 3D7 parasite strain
- Inhibits proliferation growth of bladder cancer cells
- Increases cells in G1 phase and decreases cells in G2 phase
- Reduces mortality and parasitemia in Plasmodium berghei infected mice
- Inhibits bladder cancer xenograft proliferation in nude mice
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TARGETMOL CHEMICALS INC Ezurpimtrostat hydrochloride
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Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Ezurpimtrostat hydrochloride (GNS561 hydrochloride) is an orally available palmitoyl protein thioesterase-1 inhibitor with antifibrotic, antiviral, and anticancer effects that blocks cancer cell proliferation by interacting with palmitoyl protein thioesterase to inhibit late autophagy and dose-dependently increase lysosomal accumulation. Purity 99.84%
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