Aryl iodides
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Filtered Search Results
eMolecules AstaTech / 4-IODO-N-(2-METHYLBUT-3-YN-2-YL)BENZENESULFONAMIDE / 0.1g / 718056181 / AR3704 / 95.000 / 1009101-88-5 / MFCD11501889 / 349.190 / C11H12INO2S
AstaTech / 4-IODO-N-(2-METHYLBUT-3-YN-2-YL)BENZENESULFONAMIDE / 0.1g / 718056181 / AR3704 / 95.000 / 1009101-88-5 / MFCD11501889 / 349.190 / C11H12INO2S
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Cayman Chemical 5-Iodo-2-deoxycytIdIn 5g
A nucleoside analog; inhibits the growth of P815 cells (IC50 = 14 µM), as well as sensitizes P815 cells to irradiation when used at a concentration of 1 µM
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eMolecules Pharmablock tert-butyl 6-iodo-2-azaspiro[3 3]heptane-2-carboxylate 500mg 713714201 PBXH381 0 000 2059140-61-1 323 174 C11H18INO2
Pharmablock tert-butyl 6-iodo-2-azaspiro[3 3]heptane-2-carboxylate 500mg 713714201 PBXH381 0 000 2059140-61-1 323 174 C11H18INO2
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Frontier Specialty Chemicals 5G 3,5-DIMETHYL-4-IODOISOXAZOL
This item has a minimum qty of 9 per supplier requirements.
3,5-Dimethyl-4-iodoisoxazole; CAS No: 10557-85-4
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Accela Chembio Inc 3 | 5-dimethyl-4-iodoisoxazole | 25g | 10557-85-4 | MFCD00173743 | 97+% | Shelf Life: 1800 Days | Light Sensitive
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3 | 5-dimethyl-4-iodoisoxazole | 25g | 10557-85-4 | MFCD00173743 | 97+% | Shelf Life: 1800 Days | Light Sensitive
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Medchemexpress LLC Methylcbi-azaindole-benzamide-mom-boc-ethylenediamine-d | 2222445-87-4 | 99.7% | 859.36 | C44H51ClN6O10 | 1 MG
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MethylCBI-azaindole-benzamide-MOM-Boc-ethylenediamine-D is a cleavable ADC linker used in the synthesis of antibody-drug conjugates and supplied as a high-purity research reagent for conjugation and synthetic workflows.
- Cleavable linker for intracellular release
- High purity (99.7%)
- Molecular weight 859.36 g/mol
- Available in small research quantities (1 mg and larger)
- Storage: powder at -20°C; in solvent at -80°C (6 months) or -20°C (1 month)
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Medchemexpress LLC MyoMed 205 | 2614161-13-4 | 98.0% | 491.56 g/mol | C26H25N3O5S | 10 MG
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MyoMed 205 is a small-molecule inhibitor of MuRF1 supplied as a white to off-white solid for research use. It reduces ubiquitination and proteasomal degradation of muscle proteins and has been used in preclinical studies to prevent early diaphragmatic systolic dysfunction and muscle atrophy. Recommended handling includes storage of the powder at low temperature and preparation of solutions in DMSO with warming as needed.
- Small-molecule MuRF1 inhibitor for research use.
- White to off-white solid with high reported purity.
- Soluble in DMSO at up to 25 mg/mL with sonication and warming.
- Formulatable for in vivo dosing in 10% DMSO/90% corn oil at ≥ 2.5 mg/mL.
- Store powder at -20°C for long-term stability.
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Medchemexpress LLC AG-205 | 00-00-0 | 99.0% | 454.98 | C22H23ClN6OS | 5 MG
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AG-205 is a small-molecule inhibitor of progesterone receptor membrane component-1 (PGRMC1) provided for research use. It displays anti-mitotic, anti-migratory, and anti-invasive activity, modulates apoptosis and cell-cycle regulation, and influences expression of genes involved in cholesterol biosynthesis and steroidogenesis.
- PGRMC1 inhibitor activity relevant for cell-signaling studies.
- Anti-mitotic, anti-migratory, and anti-invasive effects in cancer cell models.
- Modulates apoptosis and cell-cycle regulatory pathways.
- Alters expression of genes involved in cholesterol biosynthesis and steroidogenesis.
- High purity (99%) suitable for research applications.
- Stable as a powder under recommended cold storage conditions.
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Chem-Impex International, Inc. 3-Iodopyridine | 1120-90-7 | MFCD00023553 | 25G
3-Iodopyridine, 1120-90-7, MFCD00023553, 25G
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Apexbio Technology LLC 4-iodo-SAHA 1219807-87-0 500mg
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4-iodo-SAHA (CAS 1219807-87-0) is a hydrophobic analog of suberoylanilide hydroxamic acid (SAHA) that functions as a histone deacetylase (HDAC) inhibitor targeting both class I and II HDACs By blocking HDAC activity 4-iodo-SAHA modulates the reversible acetylation of lysine residues on histone and non-histone proteins affecting transcriptional regulation In cellular assays 4-iodo-SAHA demonstrated antiproliferative effects with EC50 values of 1 1 M in SKBR3 breast cancer cells and 0 95 0 12 0 24 0 85 and 1 3 M in HT29 U937 JA16 HL60 and K562 tumor cell lines respectively Notably it exhibited greater potency than SAHA in inhibiting proliferation of U937 leukemia cells These properties make 4-iodo-SAHA valuable for investigating HDAC-related cellular processes and cancer models
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eMolecules 4-Iodo-3-methyl-5-phenylisoxazole | 16114-53-7 | 5G
Chem-Impex | 4-Iodo-3-methyl-5-phenylisoxazole | 5G | 16114-53-7 | MFCD11040185 | MW:279.15
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eMolecules Ambeed / 25-Dichloro-4-iodopyridine / 1g / 490506282 / A133886 / / 796851-03-1 / MFCD13185538 / 273.880 / C5H2Cl2IN
Ambeed / 25-Dichloro-4-iodopyridine / 1g / 490506282 / A133886 / / 796851-03-1 / MFCD13185538 / 273.880 / C5H2Cl2IN
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eMolecules Synthonix (3 5-Dimethylisoxazol-4-yl)methanamine 100mg 649425704 D41432 0 000 131052-47-6 MFCD06213033 126 159 C6H10N2O
Synthonix (3 5-Dimethylisoxazol-4-yl)methanamine 100mg 649425704 D41432 0 000 131052-47-6 MFCD06213033 126 159 C6H10N2O
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eMolecules 5-Iodopyrimidine-4,6-diamine | 214907-09-2 | 1G | Purity: 98%
Combi-Blocks | 5-Iodopyrimidine-4,6-diamine | 1G | 214907-09-2 | MFCD20040099
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eMolecules 5-Iodoisoquinoline | 58142-99-7 | MFCD11226893 | 1g
Ambeed | 5-Iodoisoquinoline | 1g | 552568456 | A134703 | | 58142-99-7 | MFCD11226893 | 255.058 | C9H6IN
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