Alpha-halocarboxylic acids and derivatives
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Sodium iodoacetate, 305-53-3, MFCD00002686, 25 g
Linear Formula: ICH2COONa, Molecular Weight: 207.93, ≥98%, Synonym: Iodoacetic acid sodium salt. Reagent for the modification of cysteine residues in proteins. Used in protein sequencing (including by Sanger in sequencing bovine insulin) to prevent oxidation of -SH sidechains. Reagent for the modification of cysteine residues in proteins. Used to induce animal osteoarthritis model system, which mimics both symptoms and histopathology of the human disease.
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AdipoGen Rhodamine 6G p-DAX amide bis
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Chemical. CAS 591742-78-8. Formula C34H36N4O2 . C4H2F6O4. MW 760.72. Synthetic. Fluorescent labelling.
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eMolecules Ambeed / tert-Butyl 5-bromovalerate / 1g / 490515401 / A153912 / / 88987-42-2 / MFCD26398445 / 237.137 / C9H17BrO2
Ambeed / tert-Butyl 5-bromovalerate / 1g / 490515401 / A153912 / / 88987-42-2 / MFCD26398445 / 237.137 / C9H17BrO2
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Medchemexpress LLC Sodium iodoacetate | 305-53-3 | MFCD00002686 | 99.9% | 1 G
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Sodium iodoacetate is identified as a specific inhibitor of GAPDH, exhibiting glycolysis inhibitory activity. It is also known to induce osteoarthritis and related pain models in experimental animals.
- Specific inhibitor of GAPDH.
- Exhibits glycolysis inhibitory activity.
- Induces osteoarthritis and related pain models in experimental animals.
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Chem-Impex International, Inc. Bromoacetic acid | MFCD00002678 | 1KG
Bromoacetic acid, MFCD00002678, 1KG
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Medchemexpress LLC Acetic acid, 2-iodo-, sodium salt | 305-53-3 | 99.9% | 10 G
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Sodium iodoacetate is a specific inhibitor of GAPDH and exhibits glycolysis inhibitory activity. It can also induce osteoarthritis and related pain models in experimental animals.
- Specific inhibitor of GAPDH.
- Has glycolysis inhibitory activity.
- Can induce osteoarthritis and related pain models in experimental animals.
- Useful for research involving GAPDH inhibition.
- Applicable in studies related to glycolysis inhibition.
- Can be used to establish osteoarthritis and pain models in experimental animals.
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Cayman Chemical Indolicidin trifluoroacetate
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An antimicrobial peptide; active against MDR-EAEC (MICs = 32 µM for all); active against S. cerevisiae, T. beigelii, and C. albicans (MICs = 5-10, 2.5-5, and 5-10 µM, respectively); reduces viral replication of HIV-1 in MT-2 cells from 67-100 UG/ml; increases survival of MDR-EAEC-infected G. mellonella larvae
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Sigma Aldrich Fine Chemicals Biosciences Ethyl alpha-bromoisobutyrate 98% | 600-00-0 | MFCD00000123 | 500G
Ethyl alpha-bromoisobutyrate 98% | Purity: 98% | Mol Wt: 195.05 | 600-00-0 | MFCD00000123 | 500G
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Sigma Aldrich Fine Chemicals Biosciences Ethyl 2-bromopropionate 99% | 535-11-5 | MFCD00000144 | 100G
Ethyl 2-bromopropionate 99% | Purity: 99% | Mol Wt: 181.03 | 535-11-5 | MFCD00000144 | 100G
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Sigma Aldrich Fine Chemicals Biosciences Benzyl bromoacetate 96% | 5437-45-6 | MFCD00000190 | 250G
Benzyl bromoacetate 96% | Purity: 96% | Mol Wt: 229.07 | 5437-45-6 | MFCD00000190 | 250G
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Sigma Aldrich Fine Chemicals Biosciences Sodium iodoacetate BioUltra, >=99.5% (NT) | 305-53-3 | MFCD00002686 | 25G
Sodium iodoacetate BioUltra, >=99.5% (NT) | Purity: >=99.5% (NT) | Mol Wt: 207.93 | 305-53-3 | MFCD00002686 | 25G
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Sigma Aldrich Fine Chemicals Biosciences tert-Butyl chloroacetate 97% | 107-59-5 | MFCD00000930 | 25G
tert-Butyl chloroacetate 97% | Purity: 97% | Mol Wt: 150.6 | 107-59-5 | MFCD00000930 | 25G
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Sigma Aldrich Fine Chemicals Biosciences Ethyl chloroacetate 99% | 105-39-5 | MFCD00000932 | 1L
Ethyl chloroacetate 99% | Purity: 99% | Mol Wt: 122.55 | 105-39-5 | MFCD00000932 | 1L
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AdipoGen Saquayamycin B1
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Chemical. CAS 99260-68-1. Formula C31H32O12. MW 596.6. Isolated from Streptomyces nodosus. Angucycline antibiotic. Antibacterial. Antitumor compound. Active against Gram-positive bacteria and P388 leukaemia cells. Farnesyl-protein transferase inhibitor. Inhibitor of nitric oxide synthase NOS shown for Saquayamycin A1.
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AdipoGen Rhodamine 6G bis AEA amide bis
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Chemical. CAS 1173097-37-4. Formula C30H37N5O2 . C4H2F6O4. MW 727.69. Synthetic. Fluorescent labelling.
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