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Filtered Search Results
Aobchem AOBCHEM
5000972007 5- 2 6-DICHLORO-4-METHYLPHENYL
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Aobchem AOBCHEM
5000958971 2 2-DICHLORO-1- 3 5-DICHLOROPH
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Aobchem AOBCHEM
5000958973 2 2-DICHLORO-1- 2 4-DIFLUOROPH
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Aobchem AOBCHEM
5000975331 3 4-DICHLORO- -PROPYLBENZENEME
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Aobchem AOBCHEM
5001052149 2 4-DICHLORO-1- 3-CHLOROPROPOX
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Aobchem AOBCHEM
5001053327 3 6-DICHLORO-2-METHOXYBENZALDE
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Aobchem AOBCHEM
5001053221 3 6-DICHLORO-2-METHOXYBENZALDE
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Aobchem AOBCHEM
5000983573 2 3-DICHLORO-4-ETHOXYPHENYLBOR
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Aobchem AOBCHEM
5001054239 1- 3 4-DICHLORO-2-METHYLPHENYL
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Aobchem AOBCHEM
5001054158 2- 3 5-DICHLORO-2-METHYLPHENYL
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Aobchem AOBCHEM
5001054975 2 2-DICHLORO-1- 6-METHOXYNAPHT
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Medchemexpress LLC Leu-AMS R enantiomer | 459.48 | 10 MG
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Leu-AMS R enantiomer is the R enantiomer of Leu-AMS. Leu-AMS is a potent inhibitor of leucyl-tRNA synthetase (LRS) and inhibits the growth of bacteria. For research use only.
- Potent inhibitor of leucyl-tRNA synthetase (LRS).
- Inhibits the growth of bacteria.
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Medchemexpress LLC SGC-CK2-1 | 2470424-39-4 | 99.7% | 375.43 | 50 MG
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SGC-CK2-1 is a highly potent, ATP-competitive, and cell-active CK2 chemical probe. It shows exclusive selectivity for both human CK2 isoforms, with IC50s of 36 nM for CK2α and 16 nM for CK2α′ in the nanoBRET assay. This compound can be utilized for research into neurodegenerative diseases.
- Highly potent, ATP-competitive, and cell-active
- Exclusive selectivity for human CK2 isoforms
- Useful for neurodegenerative disease research
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Medchemexpress LLC 2-Pyrimidinamine, 5-[8-methyl-9-(1-methylethyl)-2-(4-morpholinyl)-9H-purin-6-yl]- | 1246560-33-7 | 98.7% | 354.41 | 100 MG
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VS-5584 is a pan-PI3K/mTOR kinase inhibitor that simultaneously blocks both mTORC2 and mTORC1. This ATP-competitive inhibitor selectively targets PI3K/mTOR signaling with low nanomolar potency against all human Class I PI3K isoforms and mTOR kinase. It preferentially inhibits cancer stem cells in HMLE breast cancer cells, reducing Aldefluor-positive cancer stem cells. In vivo, it reduces cancer stem cells in breast cancer tumors and induces tumor regression in Docetaxel-resistant models. Rapidly absorbed with a tmax of 0.9 hours and an elimination half-life of 10 hours, it leads to significant tumor growth inhibition.
- Pan-PI3K/mTOR kinase inhibitor
- Blocks mTORC2 and mTORC1
- Selectively inhibits PI3K/mTOR signaling
- Inhibits cancer stem cells
- Induces tumor regression
- Rapidly absorbed, long half-life
- Leads to tumor growth inhibition
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eMolecules 6160-65-2 | Thiocarbonyldiimidazole | ChemScene | MFCD00005289 | 178.210 | C7H6N4S | 98.000 | S=C(n1ccnc1)n1ccnc1 | 20g | 894453299
Thiocarbonyldiimidazole | ChemScene | 6160-65-2 | MFCD00005289 | 178.210 | C7H6N4S | 98.000 | S=C(n1ccnc1)n1ccnc1 | 20g | 894453299
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