Imazamox is an imidazolinone (IMI) herbicides, inhibition of the biosynthesis of acetohydroxyacid synthase, which would then inhibit plant growth and ultimately lead to plant death.increase the GST (The glutathione-S-transferase) activity.in vivo: Half-life of imazamox in the soil ranges from 1 to 3 months exhibit low mammalian toxicity. [1] plants are treated with imazamox (250 μM) in the nutrient solution and harvested 7 days after. Imazamox is mainly accumulated inV. sativa, six fold higher than those detected in P.vulgaris. [2]
LTβR-IN-1 is a potent, selective lymphotoxin β receptor (LTβR) inhibitor with an IC50 of 10 μM. LTβR-IN-1 is potent in TWEAK-stimulated p52 translocation assays with an IC50 of 10 μM and did not alter TNF-α–induced p65 nuclear translocation[1].
Indigo carmine is an efficient reagent for the determination of ozone by chemlluminescence (CL)[1].
Ac-Phe-Phe-OH is a negatively charged analogue of the diphenylalanine peptide that forms large aggregates when combined with the NH2-Phe-Phe-OH peptide[1].
Fmoc-D-Ala-OH is an alanine derivative[1].
Ozanezumab (GSK1223249) is an anti-Nogo-A (neurite outgrowth inhibitor A) monoclonal antibody. Ozanezumab can be used in amyotrophic lateral sclerosis (ALS) and multiple sclerosis research[1].
Glucosylsphingosine-d7 is deuterium labeled Glucosylsphingosine.
UCPH-102 is a highly selective EAAT1 inhibitor with an IC50 of 0.43 µM. UCPH-102 exhibits a specific anti-proliferative effect on T-ALL cells. UCPH-102 also shows good blood-brain permeability, which can be used in studies of amyotrophic lateral sclerosis, Alzheimer’s disease, chronic pain and obsessive compulsive disorder[1][2][3][4].
SLSLSPG can be obtained from the C-end of the heavy chain of human Igγ-1. SLSLSPG is a common variant in IgG[1].
Boc-β-iodo-D-Ala-OBzl is an alanine derivative[1].
Elpamotide is an epitope peptide derived from VEGFR2. Elpamotide induces cytotoxic T lymphocytes (CTLs) to kill VEGFR2-expressing endothelial cells. Elpamotide has potential immunostimulatory and antineoplastic activities. Elpamotide can be used in the research of cancer, such as pancreatic cancer[1][2].
Desmethylsildenafil-d8 (citrate) is the deuterium labeled Desmethylsildenafil citrate[1].
2,5-Di-(tert-butyl)-4-methoxyphenol-3,6-d20 is the deuterium labeled 2,5-Di-tert-butyl-4-methoxyphenol[1].
Cixutumumab (IMC-A12) is a humanized anti-IGF-1R monoclonal antibody with high affinity that inhibits ligand-dependent receptor activation and downstream signaling. Cixutumumab also mediates the internalization and degradation of IGF-IR. Cixutumumab shows broad-spectrum anti-tumour activity and can be used in studies of cancers such as lung cancer, malignancies, leukaemia, non-small cell lung cancer and prostate cancer[1].
4-Methylumbelliferyl β-D-galactopyranoside is a fluorescent substrate for β-galactosidase which, when cleaved, produces a water-soluble blue fluorescent coumarin fluorophore that can be detected using a fluoroenzymeter or fluorometer[1].
4-Methyl-5,6,7,8-tetrahydroquinoline, a tetrahydroquinoline alkaloid, is isolated from the roots of Glycyrrhiza uralensis Fisch[1].
1-Deoxynojirimycin (DNJ, Duvoglustat) is a potent α-glucosidase inhibitor, suppresses postprandial blood glucose, thereby possibly preventing diabetes mellitus. Target: α-glucosidase1-Deoxynojirimycin is an alpha-glucosidase inhibitor, most commonly found in mulberry leaves. Although it can be obtained in small quantities by brewing an herbal tea from mulberry leaves, interest in commercial production has led to research on developing mulberry tea higher in DNJ, and on alternate routes of production, such as via Bacillusspecies.
1-Methoxyindole-3-carboxylic acid (compound 5) is synthetic from a phytoalexin nucleophilic substitution reaction selectively at the 2-position[1].
Choline-d13 (sulfate) is the deuterium labeled Choline sulfate[1].
Lavandoside is an active compound found from Lavandula spica flowers[1].
D-Cysteine hydrochloride is a cysteine derivative[1].
Cimiside B, a glycoside alkaloid, isolated from the rhizome of Cimicifuga dahurica.
Hydrazine sulfate-15N2 is the 15N labeled Hydrazine sulfate[1].
N3Ac-OPhOMe is a click chemistry reagent containing an azide group. N3Ac-OPhOMe can be used for the research of various biochemical[1].
Fmoc-Cpa-OH is a compound containing both an amino group and a carboxyl group.
Fmoc-Glu(ODmab)-OH is a glutamic acid derivative[1].
Combretastatin A1 phosphate (Oxi4503; CA1P; Combretastatin A1 diphosphate) is a potent vascular disruptive agent. Combretastatin A1 phosphate exerts anti-angiogenic effects on tumors. Combretastatin A1 phosphate has the potential for the research of pancreatic neuroendocrine tumors[1][2].
Uvaol diacetate (Compound 5) is a type of triterpenoids derived from Nerium oleunder L. leaves [1].
Mca-Pro-Leu-Gly-Leu-Glu-Glu-Ala-Dap(Dnp)-NH2 is highly selective substrate for matrix metalloproteases 12 (MMP12) substrate with a kcat/Km value of 1.85*105 M-1s-1, and poor substrate of other MMPs with the exception of MMP13 (kcat/Km = 0.53*105 M-1s-1) and MMP9 (0.33*105 M-1s-1)[1].
Kaempferol tetraacetate (AF33) is a natural product. Kaempferol tetraacetate shows cytotoxicity[1][2].