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Filtered Search Results
eMolecules 1-Methyl-1h-imidazole-5-carbonitrile | 66121-66-2 | MFCD06200859 | 1g
Combi-Blocks | 1-Methyl-1h-imidazole-5-carbonitrile | 1g | 517032619 | QJ-1530 | 96.000 | 66121-66-2 | MFCD06200859 | 107.116 | C5H5N3
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000382086 BENDAMUSTINE 100MG
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Medchemexpress LLC HY-128671 10mg Medchemexpress, 6-Thioinosine CAS:574-25-4 Purity:>98%
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Medchemexpress, HY-128671 10mg 6-Thioinosine CAS:574-25-4 6-Thioinosine (6TI) is a purine antimetabolite , acts as an anti-adipogenesis agent, downregulates mRNA levels of PPAR γ and C/EBPα , as well as PPAR γ target protein such as LPL, CD36, aP2, and LXRα [1] [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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![eMolecules 1H-BENZO[D]IMIDAZOLE-2-CARBOXAMIDE | 5805-52-7 | MFCD05723975 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502179989.JPG-250.jpg)
eMolecules 1H-BENZO[D]IMIDAZOLE-2-CARBOXAMIDE | 5805-52-7 | MFCD05723975 | 1g
AstaTech | 1H-BENZO[D]IMIDAZOLE-2-CARBOXAMIDE | 1g | 573027209 | 27762 | 95.000 | 5805-52-7 | MFCD05723975 | 161.164 | C8H7N3O
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Medchemexpress LLC HY-113008A 10mg Medchemexpress, cis-Urocanic acid CAS:7699-35-6 Purity:>98%
Medchemexpress, HY-113008A 10mg cis-Urocanic acid CAS:7699-35-6 cis-Urocanic acid is a 5-HT2A receptor agonist. cis-Urocanic acid binds to 5-HT receptor with relatively high affinity (Kd=4.6 nM). cis-Urocanic acid is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor. 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 MEDCHEMEXPRESS LLC
5000449967 METHYL 4-HYDROXYPHEN 250MG
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Accela Chembio Inc 1-hexyl-3-methylimidazolium Tetrafluoroborate | 100g | 244193-50-8 | MFCD03095459 | 97+% | D: 1.149 | Shelf Life: 1440 Days | Moisture Sensitive/n2
1-hexyl-3-methylimidazolium Tetrafluoroborate | 100g | 244193-50-8 | MFCD03095459 | 97+% | D: 1.149 | Shelf Life: 1440 Days | Moisture Sensitive/n2
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000419654 METHYL ELAIDATE 500UL
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eMolecules 2 4-DICHLORO-5-NITROPYRIM 100G
5000188328 2 4-DICHLORO-5-NITROPYRIM 100G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000410655 METHYL GREEN 10MM 1ML
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Apexbio Technology LLC WM-2474 5mg
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WM-2474 is a negative control compound structurally related to the histone acetyltransferase (HAT) inhibitor WM-8014 with minimal activity against the KAT6A/B enzymes It exhibits negligible inhibitory activity with a reported IC value exceeding 125 M WM-2474 does not alter cellular proliferation underscoring its lack of significant impact on KAT6A/B-mediated processes Based on these pharmacological properties WM-2474 is used as a control in research involving epigenetic regulation and tumor cell biology particularly to assess non-specific effects linked to the compound s structural features rather than active HAT inhibition
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eMolecules 2 4-DICHLORO-8-METHOXYQUINA 1G
5000218570 2 4-DICHLORO-8-METHOXYQUINA 1G
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eMolecules 6-Methylbenzimidazole-5-carboxylic acid hydrochloride | 10351-76-5 | MFCD09909565 | 1g
Combi-Blocks | 6-Methylbenzimidazole-5-carboxylic acid hydrochloride | 1g | 537623346 | QF-6950 | 95.000 | 10351-76-5 | MFCD09909565 | 212.630 | C9H9ClN2O2
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Chem-Impex International, Inc. 4-Imidazolecarboxaldehyde | MFCD00173726 | 25G
4-Imidazolecarboxaldehyde, MFCD00173726, 25G
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![Medchemexpress LLC N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]propanamide | 2470424-39-4 | 99.7% | C20H21N7O | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259288.png-250.jpg)
Medchemexpress LLC N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]propanamide | 2470424-39-4 | 99.7% | C20H21N7O | 10MG
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SGC-CK2-1 is a selective, cell-active ATP-competitive chemical probe for casein kinase 2 (CK2) used in research to investigate CK2 signaling and neurodegenerative disease-related pathways. It shows low-nanomolar potency in cellular assays and is suitable for mechanistic and cell-based studies.
- Low-nanomolar cellular potency against CK2 isoforms.
- High selectivity for CK2 over other kinases.
- Cell-permeable and active in cell-based assays.
- Suitable for mechanistic studies of CK2 signaling and neurodegeneration.
- Stable solid form with recommended cold storage for long-term retention.
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