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Filtered Search Results
Aobchem Naphthalen-2-yl sulfofluoridate | ≥97% | CAS 141694-39-5 | C10H7FO3S | 1g
Naphthalen-2-yl sulfofluoridate | ≥97% | CAS 141694-39-5 | C10H7FO3S | 1g
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Aobchem 5-Chloro-2-naphthalenol | ≥97% | CAS 116668-72-5 | C10H7ClO | 5g
5-Chloro-2-naphthalenol | ≥97% | CAS 116668-72-5 | C10H7ClO | 5g
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000429175 8-AMINO-2-NAPHTHOL 10G
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Aobchem AOBCHEM
5000926076 2- 4- BENZYLOXY -1-NAPHTHYL -4
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Aobchem 1-(3-Bromophenyl)-2 2-difluoroethanone | ≥95% | CAS 1002356-02-6 | C8H5BrF2O | 250mg
1-(3-Bromophenyl)-2 2-difluoroethanone | ≥95% | CAS 1002356-02-6 | C8H5BrF2O | 250mg
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Aobchem 8-Bromo-1-naphthoic acid | ≥95% | CAS 1729-99-3 | C11H7BrO2 | 5g
8-Bromo-1-naphthoic acid | ≥95% | CAS 1729-99-3 | C11H7BrO2 | 5g
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Aobchem AOBCHEM
5001012095 BENZYL 3-BROMOPHENYL SULFANE 2
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5000369773 DELTARASIN HYDROCHL 10MM 1ML
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Aobchem AOBCHEM
5001016909 2-METHYL-1- NAPHTHALEN-1-YL PR
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Selleck Chemical LLC BI-9564
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BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM and 3 4 M respectively
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Medchemexpress LLC BI-0474 | 2750570-55-7 | 99.8% | 587.74 | 100 MG
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BI-0474 is a potent KRASG12C inhibitor with an IC50 value of 7.0 nM for the GDP-KRAS::SOS1 protein-protein interaction. It demonstrates significant anti-proliferative activity against NCI-H358 cells carrying the G12C mutation and shows favorable anti-tumor activity in non-small cell lung cancer xenograft models.
- Potent KRASG12C inhibitor
- Inhibits GDP-KRAS::SOS1 protein-protein interaction with an IC50 of 7.0 nM
- Exhibits anti-proliferative activity against NCI-H358 cells with G12C mutation
- Shows anti-tumor activity in non-small cell lung cancer xenograft models
- Induces programmed cell death in xenograft models
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Aobchem AOBCHEM
5000875940 1-BENZYL-4- 4-BROMOPHENYL -4-P
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Medchemexpress LLC 4-[4-[(dimethylamino)methyl]-3,5-dimethoxyphenyl]-2-methyl-2,7-naphthyridin-1-one | 1883429-21-7 | MFCD30489736 | >98.0% | 353.4 Da | C20H23N3O3 | 10 MM x 1 ML
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BI-7273 is a selective, cell-permeable bromodomain inhibitor primarily targeting BRD9 with secondary activity against BRD7. It has been characterized in biochemical, structural, and cellular assays and is supplied for research use in both concentrated DMSO solution and solid formats.
- High affinity for BRD9 (KD ≈ 15 nM) and low-nanomolar biochemical potency.
- Reduced activity against BRD7 (IC50 ≈ 117 nM), enabling differential target studies.
- High selectivity versus BET bromodomains (no measurable activity up to 100 μM).
- Supplied as a 10 mM solution in DMSO or as solid quantities for reconstitution.
- Typical purity ≥98% and molecular weight 353.4 Da.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701166 BENZYL 2-NAPHTHYL ET 100G
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TARGETMOL CHEMICALS INC BI-78D3 25MG
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Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. BI-78D3, a competitive JNK inhibitor. IC50 of BI-78D3 is 280 nM that displays > 100 fold selectivity over p38alpha, and have no activity at mTOR and PI-3K. Purity 97.89%
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