Tricarboxylic acids and derivatives
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Filtered Search Results
Molecular Dimensions 2.5M AMMONIUM CITRATE DIBASIC
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2.5M Ammonium citrate dibasic 100ml
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Bioss Citrate synthetase Polyclonal
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Citrate synthetase Polyclonal Antibody
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TARGETMOL CHEMICALS INC Zoledronic acid monohydrate
Also available in 10 mg, 25 mg, 50 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Zoledronic acid monohydrate (CGP 42446) is a synthetic imidazole bisphosphonate analog with anti-bone-resorption activity. Purity ≥95%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379762 FMOC-NH-PEG5-CH2COOH 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000357938 DIMAL-O-CH2COOH 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000436673 METHADP TRIAMMONIUM 10MM 1ML
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Sigma Aldrich Fine Chemicals Biosciences Triethyl citrate >=99%, FCC, FG | 77-93-0 | MFCD00009201 |
Triethyl citrate >=99%, FCC, FG | Purity: >=99% | Mol Wt: 276.28 | 77-93-0 | MFCD00009201 |
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Selleck Chemical LLC Ixazomib Citrate (MLN9708) Analogue S2181-10mM/1mL
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Ixazomib Citrate (MLN9708) Analogue is the analogue of Ixazomib Citrate (MLN9708) from WO2016165677A1 Ixazomib Citrate (MLN9708) immediately hydrolyzed to Ixazomib (MLN2238) the biologically active form on exposure to aqueous solutions or plasma Ixazomib (MLN2238) inhibits the chymotrypsin-like proteolytic ( 5) site of the 20S proteasome with IC50/Ki of 3 4 nM/0 93 nM in cell-free assays less potent to 1 and little activity to 2 Ixazomib (MLN2238) induces autophagy Phase 3
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Apexbio Technology LLC Amfenac Sodium Monohydrate 61618-27-7 10mM (in 1mL DMSO)
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Amfenac Sodium Monohydrate (CAS 61618-27-7) is a synthetic non-steroidal anti-inflammatory compound structurally characterized by an acetic acid moiety It functions by inhibiting cyclooxygenase (COX) enzymes consequently suppressing prostaglandin synthesis and mitigating inflammatory processes and pain signaling Amfenac Sodium Monohydrate is utilized in biomedical research to investigate inflammatory pathways and to evaluate non-steroidal analgesic drug effects in cellular and animal models of inflammation Its well-defined inhibitory mechanism makes it a valuable tool for elucidating COX-mediated physiological and pathological responses
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000402286 BOC-NH-PEG3-CH2COOH 250MG
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Selleck Chemical LLC Clomifene citrate S2561-1g
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Clomifene citrate (NSC 35770 Clomiphene citrate) is a selective estrogen receptor modulator used in the treatment of ovulation induction
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Apexbio Technology LLC Clomiphene citrate 50-41-9 10mM (in 1mL DMSO)
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Clomiphene citrate (CAS 50-41-9) is a small-molecule modulator targeting estrogen receptors (ER) It is designed to selectively modulate ER-mediated signaling thereby influencing estrogen-dependent cellular pathways Clomiphene citrate exerts its biological activity primarily through competitive inhibition at estrogen receptors It demonstrates both antiestrogenic and estrogenic activities depending on tissue context Based on these pharmacological properties clomiphene citrate holds research potential in the investigation of estrogen receptor-mediated transcriptional regulation cellular proliferation and differentiation as well as hypothalamic-pituitary-gonadal axis regulation and ovarian follicular maturation in reproductive biology studies
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Medchemexpress LLC 5,8,11,14,17,20-hexaoxa-2-azadocosanedioic acid, 1-(9H-fluoren-9-ylmethyl) ester | 437655-96-4 | 99.4% | 561.62 | C29H39NO10 | 250 MG
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Fmoc-NH-PEG6-CH2COOH is an Fmoc-protected polyethylene glycol (PEG6) linker with a terminal carboxylic acid, supplied for research use as a cleavable linker for antibody-drug conjugates and as a PEG-based PROTAC linker in targeted protein degradation research.
- Fmoc-protected amine with terminal carboxylic acid functionality.
- Suitable for ADC and PROTAC linker synthesis.
- Reported purity 99.4% and molecular weight 561.62.
- Molecular formula C29H39NO10.
- Available in small-scale pack sizes including 250 MG.
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Medchemexpress LLC Fmoc-NH-PEG1-CH2COOH | 260367-12-2 | 99.5% | 341.36 g/mol | C19H19NO5 | 1 G
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Fmoc-NH-PEG1-CH2COOH is an Fmoc-protected PEG-based linker with a terminal carboxylic acid, designed for installation of linkers in medicinal chemistry workflows such as ADC and PROTAC synthesis.
- Used in antibody-drug conjugate linker synthesis.
- Used in proteolysis-targeting chimera (PROTAC) synthesis.
- Contains an Fmoc-protected amine and a terminal carboxylic acid for conjugation.
- White to off-white solid with good purity for research applications.
- Available in multiple sizes, including 1 g, for flexible laboratory use.
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Sigma Aldrich Fine Chemicals Biosciences Tris(2-carboxyethyl)phosphine hydrochloride BioUltra, >=98% (NMR) | 51805-45-9 | MFCD00145469 | 10G
Tris(2-carboxyethyl)phosphine hydrochloride BioUltra, >=98% (NMR) | Purity: >=98% (NMR) | Mol Wt: 286.65 | 51805-45-9 | MFCD00145469 | 10G
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