9月
Lynamicin B；Lynamicin BLynamicin B (2024/9/8)
簡(jiǎn)介：lynamicin b, a promising pesticide, functions as a selective chitinase inhibitor exclusive to lepidoptera. it exhibits a ki value of 8.76 μm, indicating its potential efficacy.
Fibronectin；粘連蛋白Fibronectin (2024/9/8)
簡(jiǎn)介：fibronectin is a macromolecular glycoprotein found in blood, connective tissue, and cell surfaces that serves as a biomarker for tissue damage.fibronectin is recognized by the integrin family of surface receptors.fibronectin is used in the study of primary open-angle glaucoma.fibronectin is used in the study of primary open-angle glaucoma.fibronectin is used in the study of metastatic prostat
Quinolinic acid；喹啉酸pyridine-2,3-dicarboxylic acid|||QUIN；喹啉酸|||pyridine-2,3-dicarboxylic acid|||QUIN (2024/9/8)
簡(jiǎn)介：quinolinic acid (quin) is an endogenous n-methyl-d-aspartate (nmda) receptor agonist synthesized from l-tryptophan via the kynurenine pathway.
T0467T0467T0467 (2024/9/8)
簡(jiǎn)介：t0467 is a chemical compound that activates the translocation of parkin to the mitochondria in a pink1-dependent manner in vitro. however, t0467 does not induce the accumulation of pink1 in the mitochondria of dopaminergic neurons. as a result, t0467 shows promise as a potential compound for activating the pink1-parkin signaling pathway and can be utilized in research related to parkinson´s disease and related disorders.
Milategrast；MilategrastE6007；E6007 (2024/9/8)
簡(jiǎn)介：milategrast is a chemical compound that functions as a potent cell adhesion inhibitor and cell infiltration inhibitor. in vitro studies have demonstrated its ability to effectively inhibit the adhesion of jurkat cells to human fibronectin, with an ic50 value of less than 5 μm.
Adeninobananin；AdeninobananinAdeninobananin (2024/9/8)
簡(jiǎn)介：adeninobananin, a negative control tool, exhibits no inhibitory activity against the sars coronavirus helicase.
Eubananin；EubananinEubananin (2024/9/8)
簡(jiǎn)介：eubananin effectively inhibits the atpase activity of the sars coronavirus helicase, displaying an ic50 value of 2.8 μm.
Vanillinbananin；VanillinbananinVanillinbananin (2024/9/8)
簡(jiǎn)介：vanillinbananin is a potent inhibitor of sars coronavirus helicase atpase activity, displaying an ic50 value of 0.68 μm.
Iodobananin；IodobananinIodobananin (2024/9/8)
簡(jiǎn)介：iodobananin effectively inhibits the atpase activity of the sars coronavirus helicase, displaying an ic 50 value of 0.54 μm.
Karrikinolide；KarrikinolideKarrikinolide (2024/9/8)
簡(jiǎn)介：karrikinolide, a phytoreactive compound derived from smoke, holds potential in horticulture, ecological restoration, and agriculture. this compound exhibits regulatory properties by influencing endogenous cytokinin concentrations and stimulating plant growth.
Dibromochloroacetamide；二溴一氯乙酰胺Dibromochloroacetamide (2024/9/8)
簡(jiǎn)介：dibromochloroacetamide, belonging to the haloacetamides class, is a disinfection byproduct (dbp) commonly found in drinking water.
ABT-107；ABT-107ABT-107 (2024/9/8)
簡(jiǎn)介：abt-107, a selective α7 neuronal nicotinic receptor agonist, demonstrates neuroprotective effects against nigrostriatal damage in rats with unilateral 6-hydroxydopamine lesions.
A3334；A3334A3334 (2024/9/8)
簡(jiǎn)介：a3051, is a robust and orally active inhibitor of cxxc5-dvl with an ic 50 of 63.06 nm. its applications include research into phenotypes associated with obesity, diabetes, and nash that are induced by high fat diet (hfd) and methionine-choline deficient diet (mcd).
ZINC00881524；化合物ZINC00881524ROCK inhibitor；ROCK inhibitor (2024/9/8)
簡(jiǎn)介：zinc00881524 (rock inhibitor) is an effective and specific rock inhibitor.
KMG-104；KMG-104KMG-104 (2024/9/8)
簡(jiǎn)介：kmg-104 is a fluorescent magnesium (mg2+) probe known for its exceptional selectivity. it has been extensively utilized to investigate the mobilization of mg2+ in the cytoplasm across different cell types.
PR-104 sodium；PR-104 sodiumPR-104 sodium (2024/9/8)
簡(jiǎn)介：pr-104 sodium is a hypoxia-activated dna cross-linking agent used in the research of tumor xenograft models. it functions as a nitrogen mustard pre-prodrug and efficiently transforms into the more lipophilic dinitrobenzamide mustards alcohol pr-104a.
Seph-PAO；Seph-PAOSeph-PAO (2024/9/8)
簡(jiǎn)介：seph-pao, a modified form of polyalphaolefin (pao) compound, is created by coupling a sepharose fluorophore. its primary application lies in the detection of thioredoxin reductase (trxr).
Phospho-Glycogen Synthase Peptide-2(substrate)；Phospho-Glycogen Synthase Peptide-2(substrate)Phospho (2024/9/8)
簡(jiǎn)介：phospho-glycogen synthase peptide-2, a substrate for glycogen synthase kinase-3 (gsk-3), serves as a peptide substrate effective in the affinity purification of protein-serine kinases.
Bis-acrylate-PEG6；Bis-acrylate-PEG6Bis-acrylate-PEG6；Bis-acrylate-PEG6 (2024/9/8)
簡(jiǎn)介：bis-acrylate-peg6 is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
EMD527040；EMD527040EMD527040 (2024/9/8)
簡(jiǎn)介：emd527040 is a powerful and highly specific αvβ6 antagonist, exhibiting notable antifibrotic properties. it is suitable for conducting research on carcinoma and liver fibrosis.
(R)-(4′-Hydroxy)-5,7-dihydroxy-4-chromanone；(R)-(4′-Hydroxy)-5,7-dihydroxy-4-chromanone(R)-(4′-Hydro (2024/9/8)
簡(jiǎn)介：(r)-(4′-hydroxy)-5,7-dihydroxy-4-chromanone, an antiangiogenic homoisoflavonoid, exhibits activity against human retinal microvascular endothelial cells.
Olmesartan lactone impurity；Olmesartan lactone impurityOlmesartan lactone impurity (2024/9/8)
簡(jiǎn)介：olmesartan lactone impurity is a cyclic ester impurity derived from olmesartan, which is an angiotensin ii receptor (at1r) antagonist with potential applications in the study of high blood pressure.
7,3′,5′-Trihydroxyflavanone；7,3′,5′-Trihydroxyflavanone7,3′,5′-Trihydroxyflavanone (2024/9/8)
簡(jiǎn)介：7,3′,5′-trihydroxyflavanone, a flavanoid derivative, promotes apoptotic cell death in mcf-7 cells by augmenting bax expression. additionally, this compound demonstrates antioxidant properties.
Ginger extract；Ginger extractGinger extract (2024/9/8)
簡(jiǎn)介：ginger extract demonstrates (exhibits) anti-cancer, anti-inflammatory, and chemotherapeutic properties in living organisms (in vivo).
Wilforlide B；Wilforlide BWilforlide B (2024/9/8)
簡(jiǎn)介：wilforlide b, a naturally occurring norditerpenoid, exhibits anti-tumor effects in human cancer cells.
Quinclorac；二氯喹啉酸Quinclorac (2024/9/8)
簡(jiǎn)介：quinclorac, a commonly used agricultural herbicide, elicits oxidative stress by triggering the production of free radicals and altering the antioxidant defense system.
CH2COOH-PEG6-CH2COOHCH2COOH-PEG6-CH2COOHCH2COOH-PEG6-CH2COOH (2024/9/8)
簡(jiǎn)介：ch2cooh-peg6-ch2cooh is a peg-based linker for protacs which joins two essential ligands, crucial for forming protac molecules. this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
Ginsenoside C-Y；Ginsenoside C-YGinsenoside C-Y|||Ginsenoside Y；Ginsenoside C-Y|||Ginsenoside Y (2024/9/8)
簡(jiǎn)介：ginsenoside c-y, a natural antioxidant, exhibits antiphotoaging and antimelanogenesis properties.
Bromochloroacetonitrile；溴代氯乙腈Bromochloroacetonitrile (2024/9/8)
簡(jiǎn)介：bromochloroacetonitrile is a chemical compound that is formed as a by-product during the chlorine disinfection process of water that contains natural organic material. this compound exhibits direct mutagenic activity and can induce dna strand breakage.
Benzylacyclouridine；Benzylacyclouridine5-Benzylacyclouridine|||BAU；5-Benzylacyclouridine|||BAU (2024/9/8)
簡(jiǎn)介：benzylacyclouridine (bau) is a powerful and selective inhibitor of uridine phosphorylase, the initial enzyme involved in uridine catabolism. additionally, it can regulate the cytotoxic adverse effects of 5-fluorouracil (5-fu) and its derivatives.
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