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Filtered Search Results
Ambeed Dicyclohexyl 2 6 diisopropoxy
Dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphine, 787618-22-8, 97%
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eMolecules 3-Hydroxyquinoline-2-carboxylic acid | 15462-45-0 | MFCD08705721 | 250mg
Ambeed | 3-Hydroxyquinoline-2-carboxylic acid | 250mg | 602849783 | A247110 | | 15462-45-0 | MFCD08705721 | 189.170 | C10H7NO3
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Medchemexpress LLC Idramantone | 20098-14-0 | 99.94% | 200 MG
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Idramantone is an Adamantane derivative and an immunostimulant. It serves as a versatile starting material for synthesizing various adamantine derivatives. It can be produced using P450cam monooxygenase coupled with NADH regeneration as an oxidation biocatalyst and can be studied in research on bronchial pathology.
- Adamantane derivative
- Immunostimulant
- Versatile starting material for synthesizing various derivatives
- Can be produced using P450cam monooxygenase
- Suitable for research on bronchial pathology
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Medchemexpress LLC Amino-PEG9-amine | 474082-35-4 | >98% | C20H44N2O9 | 100 MG
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Amino-PEG9-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based linker
- Used in the synthesis of PROTACs
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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Ambeed 11bR 2R 5R 1 Dinaphtho 2 1d
(11bR)-(2R,5R)-1-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2,5-diphenylpyrrolidine, 444667-33-8, 98%
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Ambeed OC614 2 3Butanedione 2 3di
(OC-6-14)-[[2,3-Butanedione 2,3-di(oximato-κN)](1-)][2,3-butanedione 2,3-di(oxime-κN)]dichlorocobalt, 23638-66-6, 98%
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Medchemexpress LLC Mal-amido-PEG10-C2-NHS ester | 1137109-22-8 | MFCD20226950 | 777.81 g/mol | C34H55N3O17 | 250 MG
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Mal-amido-PEG10-C2-NHS ester is a PEG-based, non-cleavable linker containing a maleimide group and an N-hydroxysuccinimide (NHS) ester. The NHS ester enables conjugation to primary amines on proteins, amine-modified oligonucleotides, and other amine-containing molecules, while the maleimide allows thiol-selective coupling. This reagent is supplied for research use only.
- Non-cleavable PEG-based linker with maleimide and NHS ester functionality.
- Enables amine and thiol bioconjugation for protein and oligonucleotide labeling.
- Molecular weight approximately 777.8 g/mol for predictable mass additions.
- Provided as a small-molecule reagent suitable for research applications.
- Store in a tightly closed container in a cool, dry, well-ventilated place.
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Ambeed Palladium II acetate
Palladium(II) acetate, 3375-31-3, 99.9%
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Ambeed 11bR 2R 5R 1 Dinaphtho 2 1d
(11bR)-(2R,5R)-1-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2,5-diphenylpyrrolidine, 444667-33-8, 98%
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Medchemexpress LLC Romaciclib monohydrochloride | 2443816-41-7 | 99.29% | 450.60 | 10 MG
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Romaciclib monohydrochloride (SEL120-34A monohydrochloride) is an ATP-competitive and selective inhibitor of Cyclin-Dependent Kinase 8 (CDK8). It demonstrates potent inhibitory activity against the kinase complexes of CDK8/CycC and CDK19/CycC, with IC50 values of 4.4 nM and 10.4 nM, respectively, and a Kd of 3 nM for CDK8. While it weakly inhibits CDK9, it shows no significant activity against other CDKs such as CDK1, 2, 4, 6, 5, and 7. The compound effectively inhibits the phosphorylation of STAT1 S727 and STAT5 S726 and has demonstrated anti-tumor activity.
- Selective inhibition of specific cyclin-dependent kinases.
- ATP-competitive mechanism of action.
- Impacts key signaling pathways by inhibiting STAT1 S727 and STAT5 S726 phosphorylation.
- Demonstrated efficacy in anti-tumor applications.
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Ambeed 7Bromo3 4dihydroquinolin2 1H o
7-Bromo-3,4-dihydroquinolin-2(1H)-one, 14548-51-7, 97%
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TARGETMOL CHEMICALS INC LEMINOPRAZOLE 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Leminoprazole is an orally available H+K(+)-ATPase inhibitor that protects gastric mucosal cells from various cellular damages. purity: 99%
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Medchemexpress LLC SRI 6409-94 | 127697-58-9 | 99.25% | 379.49 | 5 MG
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SRI 6409-94 is an orally active Ro 13-6298 analogue that is teratogenic. It serves as a molecular tool to study the effect of the three-dimensional configuration of retinol on teratogenic activity.
- Orally active compound.
- Aids in the study of retinol's three-dimensional configuration and its effect on teratogenic activity.
- Induces deformed offspring in a dose-dependent manner in virgin female outbred Syrian golden hamsters.
- Leads to significant reductions in mean fetal body weight and the number of ossified skeletal districts in studies.
- Purity of 99.25%.
- Available in solid form with a light yellow to brown color.
- Stable for 3 years at -20°C as a powder, and 2 years at 4°C as a powder.
- In solvent, stable for 6 months at -80°C and 1 month at -20°C.
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Medchemexpress LLC Amine-PEG3-Lys(PEG3-N3)-PEG3-N3 | 2244602-35-3 | 98.0% | 750.84 g·mol⁻¹ | C30H58N10O12 | 25 MG
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Amine-PEG3-Lys(PEG3-N3)-PEG3-N3 is a branched polyethylene glycol (PEG) linker intended for the construction of antibody-drug conjugates (ADCs). It features a primary amine handle and two azide (N3) termini to enable click chemistry and payload attachment, with high purity and defined molecular weight for controlled bioconjugation.
- Branched PEG linker with amine and azide functional groups.
- High purity: 98.0%.
- Molecular weight: 750.84 g·mol⁻¹.
- Soluble in DMSO at approximately 100 mg/mL; ultrasonic assistance may be required.
- Storage: pure form -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (up to 6 months).
- Suitable for click chemistry and payload attachment in ADC construction.
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Ambeed 1HImidazole2carbaldehyde
1H-Imidazole-2-carbaldehyde, 10111-08-7, 95%
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