|Description||Imidazolidinyl urea is an antimicrobial preservative acts as a formaldehyde releaser.|
|Synonyms||Imidurea; N,N'-Methylenebis[N'-(3-hydroxymethyl-2,5-dioxo-4-imidazolidinyl)urea]; 1-[3-(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl]-3-[[[3-(hydroxymethyl)-2,5-dioxoimidazolidin-4-yl]carbamoylamino]methyl]urea;|
|Solubility||Soluble in DMSO|
|Storage||Store at 2-8 °C|
|Application||An antimicrobial preservative used in cosmetics|
|Quality Standard||Enterprise Standard|
|Shelf Life||As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly|
The deacetylated of BMS-202 which is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50= 18 nM).
NVS-PAK1-1 is potent and specific allosteric PAK1 inhibitor (IC50= 5 nM) with selective over PAK2 and a panel of 442 kinases.
Benzoylhypacoitine is extracted from the roots of Aconitum carmichaeli Debx. It might be the principal active components which affect mitochondrial growth by Fu...
Hematoxylin (Hydroxybrazilin) is a compound that forms strongly colored complexes with certain metal ions, notably Fe(III) and Al(III) salts and a kind of stain...
SB290157 trifluoroacetate is selective, high affinity, competitive C3areceptor antagonist (IC50= 200 nM) suitable for use in animal models of inflammation.
N-Desmethyl Regorafenib is a metabolite of Regorafenib. Regorafenib is useful for the treatment of inflammation and as an anti-proliferative agent.
Protein degrader 1 hydrochloride
Protein degrader 1, also called as MDK7526, is used in the synthesis of HaloPROTACs and a potent and selective protein degrader.
D-Glucosamine (Free Base)
An amino sugar, part of the structure of the polysaccharides chitosan and chitin, is made naturally in the form of glucosamine-6-phosphate, and is the biochemic...
Cardamonin is a naturally occuring chalcone initially isolated from the seeds of Amomum subulatum and subsequently from other zingiberous plant species. Cardamo...
(Z)-MDL 105519 is the inactive isoform of MDL 105519 which is a high affinity NMDA glutamate receptor antagonist at the glycine site.
HLM 006474 acts as an E2F transcription factor inhibitor, preventing DNA binding activity. This results in the induction of apoptosis in breast cancer cells.
PYR-9588 is an intermediate used in the chemical synthesis of a series of anaplastic lymphoma kinase (ALK) inhibitors.
Sodium gluconate is the sodium salt of gluconic acid widely used in food and pharmaceutical industry.
5(acute)-GTP trisodium salt
Guanosine 5'-(tetrahydrogen triphosphate) Trisodium Salt, is the salt form of GTP, which is a substrate for the synthesis of RNA during the transcription proces...
Fenoxaprop-P-ethyl is a post-emergent phenoxy herbicide for control of postemergence annual grasses in crop fields.
JPH203 is a potent and selective L-type amino acid transporter 1 (LAT1) inhibitor. It inhibits 14C-leucine uptake and cell growth in human colon cancer-derived ...
Ligustilide not only has an active dilatory effect on myometrium but also an effective role in reducing the neurogenic and inflammatory pain, thus having the po...
BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression.
2-Ethoxybenzamide is a common analgesic and anti-inflammatory drug. It is used to reduce the fever, headaches, and other minor aches and pains. It is an ingredi...
Carbidopa is an aromatic-L-amino-acid decarboxylase inhibitor with an IC50 of 29 ± 2 μM.