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Filtered Search Results
Aobchem AOBCHEM
5000930043 2 3-DIMETHOXY-5-PROPYLPHENYL
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Aobchem AOBCHEM
5000930279 ETHYL 4 5-DIMETHOXY-2-METHYLBE
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Aobchem AOBCHEM
5000930443 2- CYCLOHEXYLOXY -5- TRIMETHYL
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Aobchem AOBCHEM
5000931578 2 3-DIMETHOXY-5-PROPYLPHENYL
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Aobchem AOBCHEM
5000931579 2 3-DIMETHOXY-5-PROPYLPHENYL
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Aobchem AOBCHEM
5000931737 2- 2 3-DIMETHOXY-6- METHOXYMET
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Aobchem AOBCHEM
5000931835 2- 2 3-DIMETHOXY-6- METHOXYMET
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Aobchem AOBCHEM
5000932255 2- 2 3-DIMETHOXY-6- METHOXYMET
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Medchemexpress LLC 1-tert-Butyl-3-ethoxybenzene | 133073-81-1 | 95.0% | C12H18O | 500 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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1-tert-Butyl-3-ethoxybenzene is a drug intermediate for the synthesis of various active compounds. This product is intended for research use only and is not for human or medical applications.
- A drug intermediate for the synthesis of various active compounds.
- For research use only.
- Appearance: Liquid.
- Color: Light yellow to light brown.
- Chemically stable under recommended storage conditions.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC TL02-59 | 1315330-17-6 | 99.9% | 609.64 | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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TL02-59 is an orally active, selective Src-family kinase Fgr inhibitor with an IC50 of 0.03 nM. It also inhibits Lyn and Hck with IC50s of 0.1 nM and 160 nM, respectively. This compound potently suppresses the growth of acute myelogenous leukemia (AML) cells.
- Selectively targets the Src-family kinase Fgr with high potency (IC50 of 0.03 nM).
- Also shows inhibitory activity against Lyn (IC50 of 0.1 nM) and Hck (IC50 of 160 nM).
- Potently suppresses acute myelogenous leukemia (AML) cell growth.
- Induces growth arrest and apoptosis of AML cell lines at single-digit nM potency and induces growth arrest in primary AML bone marrow samples.
- Completely eliminates AML cells from the spleen and peripheral blood, and dramatically suppresses bone marrow involvement in a mouse model of AML.
- Has good oral bioavailability with a t1/2 of 5.7 h by i.v injection and 6.5 h by p.o. administration.
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Medchemexpress LLC 6 7-Dichloroquinolin 10g
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6 7-Dichloroquinoline-5 8-dione (compound DA3002) is a potent CDC25B2 inhibitor with an IC50 value of 4 6 M 6 7-Dichloroquinoline-5 8-dione has the potential for the research of cancer[1]
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TARGETMOL CHEMICALS INC ABBV-318 5MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ABBV-318 can be used as small molecule Nav1.7/Nav1.8 blockers for the treatment of pain with IC50 values of 2.8 uM for hNav1.7 and 3.8 uM for hNav1.8. ABBV-318 can be used to study pain-related disorders. purity: 99%
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Ambeed 1R 2S 1Amino2 3dihydro1Hinden
(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol, 136030-00-7, 98%
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Ambeed 3 2 9HFluoren9yl methoxy ca
3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)propanoic acid, 1654740-73-4, 97%
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Ambeed S 4 9HFluoren9yl methoxy c
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid, 84793-07-7, 98%
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