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Organic compounds with acidic properties, organic acids are generally weak acids incapable of complete dissociation in water. Available in a range of chemical compositions and acid strengths, they can be used for various industrial and everyday applications.
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VLX600 is a small-molecule research compound that acts as an iron-chelating inhibitor of oxidative phosphorylation (OXPHOS). It induces mitochondrial dysfunction, shifts cells toward glycolysis, and shows selective cytotoxicity against quiescent cancer cells. The material is supplied as a light yellow solid with high purity for laboratory research.
Iron-chelating inhibitor of oxidative phosphorylation.
Selective cytotoxicity toward quiescent cancer cells.
High purity: 99.8%.
Molecular formula C17H15N7; molecular weight 317.35 g·mol⁻¹.
Light yellow solid appearance.
Stable as powder: store at -20°C for long term or 4°C for short term.
Available in small research pack sizes starting at 5 mg.
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(S)-Malic acid ((S)-2-Hydroxysuccinic acid) is a dicarboxylic acid in naturally occurring form contributes to the pleasantly sour taste of fruits and is used as a food additive
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SN-38-CO-DMEDA TFA is a research-grade carbamate intermediate (trifluoroacetate salt) used in the synthesis of antibody-drug conjugates such as LND1035. Supplied as a 10 mM solution in DMSO (1 mL), it has CAS number 1224601-17-5, chemical formula C29H31F3N4O8, molecular weight 620.57 g/mol, and reported purity 98.07%.
10 mM solution in DMSO, 1 mL
Intended for use as a chemical synthesis intermediate
Reported purity 98.07%
CAS number 1224601-17-5
Available as solid quantities in multiple sizes
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CL2E-SN-38 TFA is an antibody-drug conjugate (ADC) drug-linker consisting of an SN-38 payload attached via a CL2E linker in the trifluoroacetate (TFA) salt form. It is intended for preclinical research into ADCs, where SN-38 functions as a topoisomerase I inhibitor.
Highly releasable and structurally stable antibody-SN-38 conjugate.
Contains SN-38 payload, a topoisomerase I inhibitor.
TFA salt form for improved solubility and handling.
Available in small research quantities (5 MG).
High purity suitable for preclinical ADC development.
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Lafadofensine (D-(-)-mandelic acid) is a research-grade monoamine reuptake inhibitor provided as the D-(-)-mandelic acid salt for preclinical pharmacology and transporter studies. It is supplied in small milligram-scale quantities and is suitable for in vitro and in vivo experiments; reported molecular data include formula C32H32F2N2O6 and molecular weight 578.60 g·mol⁻¹.
Monoamine reuptake inhibitor activity for transporter research.
Supplied as D-(-)-mandelic acid salt, suitable for formulation work.
High reported purity (99.95%) for experimental consistency.
Available in small mg pack sizes for preclinical studies.
Molecular formula and weight provided for dosing and calculations.
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MTvkPABC-P5 TFA is the trifluoroacetic acid (TFA) salt of a synthetic Toll-like receptor 7 (TLR7) agonist. It functions as an immune stimulant used in research applications, including the synthesis of immune-stimulating antibody conjugates (ISACs).
Acts as a TLR7 agonist and immune stimulant.
Suitable for synthesis of immune-stimulating antibody conjugates (ISACs).
Provided as a solid TFA salt.
High purity, 98.8%.
Molecular weight 1190.22, formula C54H74F3N11O16.
Available as 25 MG quantity.
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Tigulixostat is an orally active, non-purine selective xanthine oxidase inhibitor used in preclinical research to reduce serum uric acid in studies of gout and hyperuricemia. It is supplied as a powder and is suitable for solution preparation for biochemical and cellular assays.
Selective xanthine oxidase inhibition with low-nanomolar potency.
Supplied as a powder for laboratory use.
Molecular formula C16H14N4O2; molecular weight 294.31 g·mol⁻¹.
Pack size provided as 5 MG with solution concentration preparations noted.
Storage: powder -20°C; in solvent -80°C up to 6 months, -20°C up to 1 month.
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