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Filtered Search Results
eMolecules 4,5-Dibromo-1H-imidazole | 2302-30-9 | MFCD00091826 | 1g
WuXi ChemSupply | 4,5-Dibromo-1H-imidazole | 1g | 599167353 | LN01263341 | 95.000 | 2302-30-9 | MFCD00091826 | 225.871 | C3H2Br2N2
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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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![Medchemexpress LLC 5-[(E)-2-thiophen-2-ylethenyl]-1H-pyrazole | 1070881-42-3 | 99.9% | C9H8N2S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000258416.png-250.jpg)
Medchemexpress LLC 5-[(E)-2-thiophen-2-ylethenyl]-1H-pyrazole | 1070881-42-3 | 99.9% | C9H8N2S | 10MG
Terevalefim (ANG-3777) is a small-molecule hepatocyte growth factor (HGF) mimetic that selectively activates the c-Met receptor. It has been used in preclinical studies to decrease apoptosis, increase cellular proliferation, and promote organ repair and function. For research use only; not for clinical use or sale to patients.
- Selectively activates the c-Met receptor in cellular assays.
- Demonstrated to decrease apoptosis and promote proliferation in preclinical models.
- High chemical purity suitable for research applications.
- Solid, white to light brown appearance for convenient handling and storage.
- Soluble in DMSO at high concentration; ultrasonic agitation recommended.
- Stable when stored under recommended cryogenic conditions.
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Selleck Chemical LLC BAY 1436032
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BAY-1436032 is a highly selective potent and orally available inhibitor of mutant Isocitrate Dehydrogenase 1 (mIDH1) It is a double-digit nanomolar and selective pan-inhibitor of the enzymatic activity of various IDH1-R132X mutants in vitro and displays potent inhibition of 2-HG release (nanomolar range) in patient derived and engineered cell lines expressing different IDH1 mutants
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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 MEDCHEMEXPRESS LLC
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5000344285 DELAMANID-D4 1MG
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Accela Chembio Inc 4-imidazolecarboxaldehyde | 25g | 3034-50-2 | MFCD00173726 | 97+% | Shelf Life: 1440 Days | Light Sensitive/n2/+4
4-imidazolecarboxaldehyde | 25g | 3034-50-2 | MFCD00173726 | 97+% | Shelf Life: 1440 Days | Light Sensitive/n2/+4
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Boston Bioproducts Inc Krebs-Henseleit w/o Ca 500ml
Krebs-Henseleit Solution (without Calcium) - 500ml (For Research Use and Further Manufacturing Only)
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Medchemexpress LLC HY-19740 5mg Medchemexpress, BIA 10-2474 CAS:1233855-46-3 Purity:>98%
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Medchemexpress, HY-19740 5mg BIA 10-2474 CAS:1233855-46-3 BIA 10-2474 is an inhibitor of fatty acid amide hydrolase (FAAH) with IC50 values of 50 to 70mg/kg in various rat brain regions. 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 ETHYL 4 6-DICHLORO-1 5-NA 2.5G
5000170548 ETHYL 4 6-DICHLORO-1 5-NA 2.5G
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Ambeed AMBEED
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NC3906642 1-VINYLIMIDAZOLE
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eMolecules 1-Methylimidazole-2-carboxylic acid, lithium salt | 684242-85-1 | MFCD03789111 | 10g
Oakwood Chemical | 1-Methylimidazole-2-carboxylic acid, lithium salt | 10g | 537677390 | 018814 | | 684242-85-1 | MFCD03789111 | 132.050 | C5H5LiN2O2
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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 LINSITINIB 5MG
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501871919 LINSITINIB 5MG
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Medchemexpress LLC KINETIN RIBOSIDE 100MG
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501871781 KINETIN RIBOSIDE 100MG
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