Organo-Metalloid Compounds
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- (253)
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- (1)
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- (1)
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- (115)
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Filtered Search Results
eMolecules S-2-METHYL-MORPHOLINE 5G
5000166014 S-2-METHYL-MORPHOLINE 5G
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AARON CHEMICALS LLC
NC3926688 TRIPHENYLMETHYLTHIONYL IMIDE
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Chemscene CHEMSCENE
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NC3974138 TRIPHENYLMETHYLTHIONYL IMIDE
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Medchemexpress LLC PS-1145 | 431898-65-6 | 99.9% | 322.75 | 1 ML
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PS-1145 | 431898-65-6 | 99.9% | 322.75 | 1 ML
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TARGETMOL CHEMICALS INC NVR 3-778 5MG
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Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. NVR 3-778 is a first-in-class, orally bioavailable HBV CAM belonging to the SBA class, exhibiting anti-HBV activity. Purity 99.74%
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TARGETMOL CHEMICALS INC L-796 778 1MG
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Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. L-796,778 is an SST3 agonist and a selective ligand of SST3, which can increase the level of cAMP in the body.
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(OC)c1ccccc1 | 10g | 525102076](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC2039302.JPG-250.jpg)
eMolecules 3027-21-2 | Dimethoxy(methyl)(phenyl)silane | Ambeed | MFCD00008343 | 182.294 | C9H14O2Si | 98 | CO[Si](C)(OC)c1ccccc1 | 10g | 525102076
Ambeed | (S)-2-((2R3R)-3-((S)-1-((3R4S5S)-4-((S)-N3-Dimethyl-2-((S)-3-methyl-2-(methylamino)butanamido)butanamido)-3-methoxy-5-methylheptanoyl)pyrrolidin-2-yl)-3-methoxy-2-methylpropanamido)-3-phenylpropanoic acid | 2mg | 491171472 | A309085 | 745017-94-1 | MFCD25976742 | 731.976 | C39H65N5O8
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Accela Chembio Inc 2 | 2'-bis(trifluoromethyl)benzidine | 100g | 341-58-2 | MFCD00190155 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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2 | 2'-bis(trifluoromethyl)benzidine | 100g | 341-58-2 | MFCD00190155 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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Medchemexpress LLC AK-778-XXMU | 1227045-76-2 | 99.9% | C22H17ClN2O3 | 50 MG
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AK-778-XXMU is a potent DNA binding inhibitor 2 (ID2) antagonist with a KD of 129 nM, used for the study of glioma. It inhibits the ID2-KDR signaling axis, leading to the downregulation of downstream angiogenic factors and invasion-related proteins, and the upregulation of the tumor suppressor factor PTEN. This compound demonstrates significant cancer-suppressing potency by inhibiting cell migration and invasion of glioma cell lines and inducing apoptosis.
- Potent ID2 antagonist with a KD of 129 nM
- Inhibits cell migration and invasion of glioma cell lines
- Induces apoptosis
- Inhibits ID2-KDR signaling axis
- Downregulates angiogenic factors (VEGFA) and invasion-related proteins (MMP2/9)
- Upregulates tumor suppressor factor (PTEN)
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Accela Chembio Inc 2 | 2'-bis(trifluoromethyl)benzidine | 25g | 341-58-2 | MFCD00190155 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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2 | 2'-bis(trifluoromethyl)benzidine | 25g | 341-58-2 | MFCD00190155 | 97+% | Shelf Life: 1260 Days | Light Sensitive
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Medchemexpress LLC Ps-1145 | 431898-65-6 | MFCD08705411 | 99.9% | 322.75 | C17H11ClN4O | 10 MG
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PS-1145 is a small-molecule inhibitor of IκB kinase (IKK) used in research to block NF-κB signaling and induce apoptosis in cell models. It is supplied as a powder with documented solubility and storage recommendations for experimental use.
- Potent IKK inhibitor with IC50 of 88 nM.
- High chemical purity (99.88%).
- Provided as a powder for convenient handling and formulation.
- Soluble in DMSO at 20.83 mg/mL; multiple in vitro formulations available.
- Stable under recommended storage conditions for long-term use.
- Suitable for in vitro studies of NF-κB signaling and apoptosis pathways.
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eMolecules 1503378-02-6 | ChemScene | 7-Methoxy-23-dihydrobenzofuran-3-carboxylic acid | 100mg | 712840997 | CS-0438340 | MFCD26129953 | 194.186 | C10H10O4
Ambeed | 4-Bromo-2-(26-dioxopiperidin-3-yl)isoindoline-13-dione | 250mg | 633418021 | A1215363 | 2093536-12-8 | 337.129 | C13H9BrN2O4
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Medchemexpress LLC DNP-PEG3-azide | 951671-87-7 | 99.2% | C14H20N6O7 | 25 MG
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DNP-PEG3-azide is a PEG-based PROTAC linker crucial for the synthesis of PROTACs. It acts as a click chemistry reagent, featuring an azide group that enables both copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne groups and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups. It is a light yellow to yellow viscous liquid with a high purity of 99.18%.
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Medchemexpress LLC Nh-bis(peg3-boc) | 1814901-03-5 | 98.0% | C26H51NO10 | 100 MG
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This compound serves as a PEG-based linker for assembling Proteolysis Targeting Chimeras (PROTACs). PROTACs are designed with two distinct ligands connected by such a linker: one targets an E3 ubiquitin ligase, and the other binds to a specific target protein. This design enables PROTACs to leverage the cell's ubiquitin-proteasome system for the targeted degradation of proteins.
- Functions as a linker for PROTACs.
- Utilizes the ubiquitin-proteasome system.
- Enables targeted protein degradation.
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Medchemexpress LLC N-(Amino-PEG3)-N-bis(PEG4-Boc) | 2353409-57-9 | 98.0% | C38H76N2O15 | 100 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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N-(Amino-PEG3)-N-bis(PEG4-Boc) is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. PROTACs consist of two different ligands connected by a linker; one ligand targets an E3 ubiquitin ligase, and the other targets the protein of interest. These molecules exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Utilized in PROTAC synthesis
- Applicable in cancer-programmed cell death research
- Connects two different ligands for PROTAC formation
- Targets E3 ubiquitin ligase and protein of interest
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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