Aryl iodides
3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole, 95%
CAS: 887144-97-0 Molecular Formula: C10H10F3IO Molecular Weight (g/mol): 330.09 InChI Key: HVAPLSNCVYXFDQ-UHFFFAOYSA-N Synonym: 3,3-dimethyl-1-trifluoromethyl-1,2-benziodoxole,1-trifluoromethyl-3,3-dimethyl-1,2-benziodoxole,togni's reagent,togni reagent,unii-3ok0e02mt6,1,2-benziodoxole, 3,3-dimethyl-1-trifluoromethyl,1,3-dihydro-3,3-dimethyl-1-trifluoromethyl-1,2-benziodoxole,3,3-dimethyl-1-trifluoromethyl-1,3-dihydro-1lambda3,2-benziodoxole,3,3-dimethyl-1-trifluoromethyl-1? 3 ,2-benziodaoxole,togni's reagents dimethyl compound mi PubChem CID: 16043572 IUPAC Name: 3,3-dimethyl-1-(trifluoromethyl)-1$l^{3},2-benziodoxole SMILES: CC1(C2=CC=CC=C2I(O1)C(F)(F)F)C
5-Iodo-2-phenoxypyridine, ≥95%, Thermo Scientific™
CAS: 352018-92-9 Molecular Formula: C11H8INO Molecular Weight (g/mol): 297.095 MDL Number: MFCD02681952 InChI Key: JCEXQQNAXWYXRX-UHFFFAOYSA-N Synonym: 5-iodo-2-phenoxy-pyridine,pyridine,5-iodo-2-phenoxy PubChem CID: 2776503 IUPAC Name: 5-iodo-2-phenoxypyridine SMILES: C1=CC=C(C=C1)OC2=NC=C(C=C2)I
2-Cyano-3-iodopyridine, 95%
CAS: 827616-52-4 Molecular Formula: C6H3IN2 Molecular Weight (g/mol): 230.008 MDL Number: MFCD09037451 InChI Key: MZZGCCSFZCRVAF-UHFFFAOYSA-N Synonym: 3-iodopicolinonitrile,2-cyano-3-iodopyridine,2-pyridinecarbonitrile,3-iodo,pubchem15743 PubChem CID: 12180890 IUPAC Name: 3-iodopyridine-2-carbonitrile SMILES: C1=CC(=C(N=C1)C#N)I
2-Chloro-5-iodopyrimidine, 95%
CAS: 32779-38-7 Molecular Formula: C4H2ClIN2 Molecular Weight (g/mol): 240.43 MDL Number: MFCD06200210 InChI Key: WSZRCNZXKKTLQE-UHFFFAOYSA-N PubChem CID: 1714223 IUPAC Name: 2-chloro-5-iodopyrimidine SMILES: ClC1=NC=C(I)C=N1
2-Iodopyrazine, 95%
CAS: 32111-21-0 Molecular Formula: C4H3IN2 Molecular Weight (g/mol): 205.986 MDL Number: MFCD01319019 InChI Key: OYWPFIUVDKHHGQ-UHFFFAOYSA-N Synonym: iodopyrazine,2-iodo-pyrazine,2-iodo-1,3-diazine,iodo-pyrazine,2-iodo pyrazine,pyrazine, 2-iodo,acmc-1ad2s PubChem CID: 642841 IUPAC Name: 2-iodopyrazine SMILES: C1=CN=C(C=N1)I
Sigma Aldrich Fine Chemicals Biosciences 3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole 95% | Purity: 95% | Mol Wt: 330.09 | 887144-97-0 | MFCD10567056 | 250MG
3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole 95% | Purity: 95% | Mol Wt: 330.09 | 887144-97-0 | MFCD10567056 | 250MG
eMolecules 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid | 75092-30-7 | 1G | Purity: 95%
ChemBridge - BB | 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid | 1G | 75092-30-7 | MFCD00461121
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Sigma Aldrich 2,4-Dichloro-5-iodopyrimidine
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Apexbio Technology LLC 4-iodo-SAHA 1219807-87-0 100mg
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
Apexbio Technology LLC 4-iodo-SAHA 1219807-87-0 500mg
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
Apexbio Technology LLC 4-iodo-SAHA 1219807-87-0 250mg
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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