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Organic compounds that contain three carboxyl groups; carboxyl groups consist of a carbonyl group bonded to a hydroxy group. Includes compounds that are derived from tricarboxylic acids.
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DMAPP (Dimethylallyl diphosphate) triammonium is an isoprenoid precursor found in virtually all life forms. It is an isomer of isopentenyl pyrophosphate (IPP) and plays a role in both the mevalonate and MEP pathways of isoprenoid precursor biosynthesis. The enzyme isopentenyl pyrophosphate isomerase catalyzes the isomerization between DMAPP and IPP.
Isoprenoid precursor
Isomer of isopentenyl pyrophosphate (IPP)
Found in virtually all life forms
Product of mevalonate and MEP pathways
Involved in isoprenoid precursor biosynthesis
Isomerization catalyzed by isopentenyl pyrophosphate isomerase
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Clomiphene citrate is an orally active estrogen-receptor modulator. It has anti-cancer activity, induces perturbations during meiotic maturation and cytogenetic abnormalities, and aids in managing psychiatric and cognitive impairment.
Inhibits viability of PC3 human prostate cancer cells
Induces chromosome abnormalities in mouse oocytes
Demonstrates anxiolytic potential
Improves cognitive functions in letrozole-induced polycystic ovary syndrome (PCOS) rats
Raises NRF-2 gene expression
Down-regulates acetylcholine esterase expression
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Fmoc-NH-PEG6-CH2COOH is an Fmoc-protected PEG6 linker bearing a terminal carboxylic acid and an Fmoc-protected amine. It is used as a hydrophilic spacer in the synthesis of proteolysis targeting chimeras (PROTACs) and antibody-drug conjugates (ADCs), providing solubility and a reactive handle for amide coupling.
Fmoc-protected amine for orthogonal protection in synthesis.
Terminal carboxylic acid suitable for amide coupling.
PEG6 spacer increases hydrophilicity and solubility.
High reported purity (≈99.4%).
Available in multiple package sizes for milligram to gram scale work.
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Sparfosic acid trisodium is a DNA antimetabolite agent and a potent inhibitor of aspartate transcarbamoyl transferase, an enzyme that catalyzes the second step of de novo pyrimidine biosynthesis. It synergistically enhances the cytotoxicity of a combination of 5-fluorouracil (5-FU) and interferon-alpha (IFN) against human colon cancer cell lines. It is for research use only.
DNA antimetabolite agent
Potent inhibitor of aspartate transcarbamoyl transferase
Synergistically enhances the cytotoxicity of 5-fluorouracil (5-FU) and interferon-alpha (IFN) against human colon cancer cell lines
Causes apoptosis in resistant Br1 cells
Leads to progressive accumulation of cells in S phase and activation of an apoptotic pathway at 300 μM
Increases lifespan in mice bearing B16 melanoma
Curative in 50% of mice with Lewis lung carcinoma when treated on days 1, 5, and 9 following s.c. implantation
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