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Filtered Search Results
Aobchem AOBCHEM
5000865945 2-CHLORO-6-METHOXYNAPHTHALENE
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Aobchem AOBCHEM
5000874483 1-BENZYL-4- 4-BROMOPHENYL -4-P
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TARGETMOL CHEMICALS INC BI-882370 10MG
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Also available in 1 mg, 2 mg, 5 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. BI-882370 is a specific RAF kinase inhibitor. BI-882370 inhibits the oncogenic BRAFV600E-mutant, the WT BRAF and CRAF kinases (IC50s 0.4, 0.8 and 0.6 nM). BI-882370 also inhibits SRC family kinases. Purity 99.07%
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eMolecules 455-26-5 | 4-(Fluorosulfonyl)benzoic acid | Combi-Blocks, Inc. | MFCD00007420 | 204.170 | C7H5FO4S | 97.000 | OC(=O)c1ccc(cc1)S(F)(=O)=O | 25g | 603130477
4-(Fluorosulfonyl)benzoic acid | Combi-Blocks, Inc. | 455-26-5 | MFCD00007420 | 204.170 | C7H5FO4S | 97.000 | OC(=O)c1ccc(cc1)S(F)(=O)=O | 25g | 603130477
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000700880 ROMIFIDINE HYDROCHL 25MG
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eMolecules 51285-26-8 | Picolinimidamide hydrochloride | Ambeed | MFCD00052271 | 157.600 | C6H8ClN3 | 97.000 | Cl.NC(=N)c1ccccn1 | 100g | 490512025
Picolinimidamide hydrochloride | Ambeed | 51285-26-8 | MFCD00052271 | 157.600 | C6H8ClN3 | 97.000 | Cl.NC(=N)c1ccccn1 | 100g | 490512025
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eMolecules AstaTech / (S)-N-BOC-2-AMINOCYCLOHEXANONE / 0.25g / 411875461 / AC2588 / 95.000 / 145106-47-4 / MFCD09838825 / 213.277 / C11H19NO3
AstaTech / (S)-N-BOC-2-AMINOCYCLOHEXANONE / 0.25g / 411875461 / AC2588 / 95.000 / 145106-47-4 / MFCD09838825 / 213.277 / C11H19NO3
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380618 ARZOXIFENE HYDROCHL 1MG
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Medchemexpress LLC 5-hydroxy-4H-1,4-benzoxazin-3-one derivative (substituted amine) | 1202235-68-4 | 99.6% | 25 MG
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BI-167107 is a high-affinity full agonist of the β2 adrenergic receptor (β2AR) with a reported dissociation constant of approximately 84 pM. Supplied as a high-purity solid for research use, it is commonly used as a pharmacology and structural biology tool because of its slow dissociation rate and strong receptor affinity.
- High-affinity β2AR full agonist with Kd ≈ 84 pM.
- High purity solid suitable for biochemical assays and structural studies.
- Available in small milligram pack sizes for research use.
- Soluble in DMSO; available as a 10 mM solution format for assay preparation.
- Molecular weight 370.4 g/mol; formula C21H26N2O4.
- Used as a tool compound for receptor pharmacology and crystallography due to very slow off-rate.
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Medchemexpress LLC BI-2865 | 2937327-93-8 | C23H27N7O2S | 25 MG
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BI-2865 is a non-covalent pan-KRAS inhibitor that binds to wild-type and various mutant KRAS proteins. It effectively inhibits the proliferation of KRAS-expressing cells, making it suitable for research into KRAS-driven cancers and related pathways.
- Non-covalent pan-KRAS inhibitor
- Binds to WT, G12C, G12D, G12V, and G13D mutant KRAS
- Inhibits proliferation of G12C, G12D, or G12V mutant KRAS expressing BaF3 cells
- High purity (99.65%)
- Molecular weight: 465.57
- Derivative with a prolinol substituent and a pyrimidine linker
- Exhibits direct ionic interaction with E62
- Forms a water-mediated hydrogen bond network with R68 and Q61
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eMolecules 1141-38-4 | Naphthalene-2,6-dicarboxylic acid | Apollo Scientific US - Building Blocks | MFCD00004105 | 216.192 | C12H8O4 | 98.000 | OC(=O)c1ccc2cc(ccc2c1)C(O)=O | 5g | 397996059
Naphthalene-2,6-dicarboxylic acid | Apollo Scientific US - Building Blocks | 1141-38-4 | MFCD00004105 | 216.192 | C12H8O4 | 98.000 | OC(=O)c1ccc2cc(ccc2c1)C(O)=O | 5g | 397996059
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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(CCCC)c1ncncc1Br | 250mg | 525910903](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502446253.PNG-250.jpg)
eMolecules 1416437-21-2 | 5-Bromo-4-(tributylstannyl)pyrimidine | Synthonix - Stock | MFCD16170450 | 448.036 | C16H29BrN2Sn | 94.000 | CCCC[Sn](CCCC)(CCCC)c1ncncc1Br | 250mg | 525910903
5-Bromo-4-(tributylstannyl)pyrimidine | Synthonix - Stock | 1416437-21-2 | MFCD16170450 | 448.036 | C16H29BrN2Sn | 94.000 | CCCC[Sn](CCCC)(CCCC)c1ncncc1Br | 250mg | 525910903
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TARGETMOL CHEMICALS INC BI-69A11 25MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Also available in 1 mL, 1 mg, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. BI-69A11 ((E)-3-(1H-Benzo[d]imidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one) is a dual AKT and NFkB pathway inhibitor. It enhances the susceptibility of colon cancer cells to mda-7/IL-24-induced growth inhibition by targeting Akt. Purity 96.97%
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Aobchem AOBCHEM
5000862451 2- 4-BROMOPHENYL METHOXY -1 3
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Medchemexpress LLC Adapalene (CD271) | 106685-40-9 | 99.9% | C28H28O3 | 500 MG
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Adapalene (CD271) is a third-generation synthetic retinoid primarily used for acne research. It functions as a potent RAR agonist and non-competitively inhibits GOT1 enzymatic activity, also demonstrating anti-tumor properties.
- Acts as a potent RAR agonist with varying AC50s for RAR subtypes.
- Inhibits viability of various cancer cell lines.
- Induces apoptosis and inhibits proliferation in ES-2 cells.
- Increases G1-phase population in LoVo or DLD1 cells.
- Inhibits GOT1 activity.
- Inhibits expression of plasma membrane-associated enzyme transglutaminase Type I.
- Inhibits growth of DLD1 cell-derived xenograft tumors in BALB/C nude mice, reducing tumor weight and volume.
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