Organo-Metalloid Compounds
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- (21)
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- (9)
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- (1)
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- (1)
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Filtered Search Results
Aobchem AOBCHEM
5000930791 2-BROMO-5- ETHYLTHIO -3-METHYL
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Aobchem AOBCHEM
5000930915 ETHYL 2- 2- ETHYLTHIO PHENYL -
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Apexbio Technology LLC OSI-930 728033-96-3 5mg
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OSI-930 (CAS 728033-96-3) is a small molecule inhibitor targeting multiple receptor tyrosine kinases including Flt1 (IC 8 nM) KDR/VEGFR2 (IC 9 nM) CSF-1R (IC 15 nM) Lck c-Raf and Kit (IC 80 nM) In cellular studies OSI-930 inhibits proliferation and induces apoptosis in HMC-1 cells whose survival is dependent on Kit signaling while exhibiting minimal effects on COLO-205 cells under standard conditions Additionally OSI-930 inactivates cytochrome P450 3A4 in a time- and concentration-dependent manner and alters its spectral properties These characteristics make OSI-930 a valuable tool compound for investigating receptor tyrosine kinase signaling pathways and related cellular processes in cancer research
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eMolecules 1256354-94-5 | 3-(t-Butyldimethylsilyloxy)-4-chloro-2-fluorophenylboronic acid | Combi-Blocks | MFCD17015761 | 304.620 | C12H19BClFO3Si | 95.000 | CC(C)(C)[Si](C)(C)Oc1c(Cl)ccc(B(O)O)c1F | 1g | 117524740
3-(t-Butyldimethylsilyloxy)-4-chloro-2-fluorophenylboronic acid | Combi-Blocks | 1256354-94-5 | MFCD17015761 | 304.620 | C12H19BClFO3Si | 95.000 | CC(C)(C)[Si](C)(C)Oc1c(Cl)ccc(B(O)O)c1F | 1g | 117524740
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Medchemexpress LLC Tri(Amino-PEG5-amide)-amine | 2055013-52-8 | 99.9% | C45H93N7O18 | 50 MG
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Tri(Amino-PEG5-amide)-amine is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. PROTACs are compounds that leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins. They consist of two different ligands connected by a linker: one ligand binds to an E3 ubiquitin ligase, and the other to the target protein. This mechanism allows PROTACs to effectively degrade specific proteins.
- PEG-based PROTAC linker
- Can be used in the synthesis of PROTACs
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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Medchemexpress LLC Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate | 632-93-9 | MFCD00005950 | 99.5% | 267.32 g/mol | C14H21NO4 | 10 G
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Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate is a diethyl ester of a 1,4-dihydropyridine used as a small-molecule reagent or synthetic intermediate in research laboratories.
- White to off-white solid suitable for laboratory use.
- Molecular formula C14H21NO4; molecular weight 267.32 g/mol.
- High purity (99.5% assay) appropriate for analytical and synthetic work.
- Stable as powder at -20°C (up to 3 years) or 4°C (up to 2 years).
- In solvent recommended storage -80°C (6 months) or -20°C (1 month).
- Available in multiple sizes, including 10 G, for flexibility in experiments.
- Used as a dihydropyridine ester intermediate or reagent in chemical research.
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eMolecules 122296-00-8 | 1-[(Trimethylsilyl)methyl]benzotriazole | Combi-Blocks | MFCD00956443 | 205.336 | C10H15N3Si | 96.000 | C[Si](C)(C)Cn1nnc2ccccc12 | 25g | 335374987
1-[(Trimethylsilyl)methyl]benzotriazole | Combi-Blocks | 122296-00-8 | MFCD00956443 | 205.336 | C10H15N3Si | 96.000 | C[Si](C)(C)Cn1nnc2ccccc12 | 25g | 335374987
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Medchemexpress LLC LL-37 amide | 597562-32-8 | 99.9% | 4492.28 | 5 MG
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LL-37 amide is a selective agonist of formyl peptide receptor-like FPRL1. It effectively inhibits periodontal pathogens by activating FPRL1-mediated immune cell chemotaxis and disrupting bacterial cell membrane integrity. This compound also regulates inflammatory responses and promotes angiogenesis. The amidation modification reduces its sensitivity to serum inhibition and improves its stability. It is primarily used in research on infection-related diseases and wound healing due to its key activities in bactericidal action, immunomodulation, and wound healing.
- Selective FPRL1 agonist
- Effectively inhibits periodontal pathogens
- Disrupts bacterial cell membranes
- Regulates inflammation and promotes angiogenesis
- Amidation enhances stability and reduces serum inhibition
- Used in research for infection and wound healing
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eMolecules 1825-61-2 | Ambeed | Methoxytrimethylsilane | 25g | 596329927 | A407382 | MFCD00008344 | 104.224 | C4H12OSi
Ambeed | (4-(Methoxycarbonyl)-1H-indol-6-yl)boronic acid | 100mg | 714083998 | A1536411 | 2828439-69-4 | 219.000 | C10H10BNO4
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Aobchem AOBCHEM
5001011744 2 2 2-TRICHLORO-N-METHOXY-N-ME
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Aobchem AOBCHEM
5001011747 2 2 2-TRICHLORO-N-METHOXY-N-ME
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Aobchem AOBCHEM
5001059840 TRIMETHYL P-TOLYL SILANE 25G
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Aobchem AOBCHEM
5000937871 TRIETHYL 4-PROPYLPHENYL SILANE
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Medchemexpress LLC Silane, [[(1a,3b,5E,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraene-1,3-diyl]bis(oxy)]bis[(1,1-dimethyl- | 111594-58-2 | 99.6% | C40H72O2Si2 | 100 MG
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Silane, [[(1a,3b,5E,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraene-1,3-diyl]bis(oxy)]bis[(1,1-dimethylethyl)dimethyl- is a drug intermediate used for the synthesis of various active compounds. This product is for research use only and appears as a white to off-white solid.
- Used as a drug intermediate
- For synthesis of various active compounds
- Appears as a white to off-white solid
- For research use only
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Medchemexpress LLC (S)-S007-1558 | 1327156-14-8 | ≥98.0% | 339.35 g/mol | C17H17N5O3 | 5 MG
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(S)-S007-1558 is a small-molecule glycoprotein VI (GPVI) platelet receptor antagonist for research use. It inhibits collagen-induced platelet aggregation with a reported IC50 of 0.17 μM in human platelets and is supplied at high purity for biochemical and cellular studies. Recommended cold storage preserves compound stability.
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