Chemicals & Small Molecules

Pantoprazole-d6 is a deuterated compound of Pantoprazole. Pantoprazole has a CAS number of 102625-70-7. Pantoprazole is a proton pump inhibitor used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.

Sudan 4-d6 (naphthyl-d6) is a deuterated compound of Sudan 4.Sudan 4 has a CAS number of 85-83-6.

Pentanoic-d9 Acid is a deuterated compound of Pentanoic Acid. Pentanoic Acid has a CAS number of 109-52-4. Valeric acid, or pentanoic acid, is a straight chain alkyl carboxylic acid with the chemical formula CH3(CH2)3COOH. Like other low molecular weight carboxylic acids, it has a very unpleasant odor. It is found naturally in the perennial flowering plant valerian (Valeriana officinalis), from which it gets its name.

IL-32 Protein, Human, Recombinant (isoform beta, GST & His) is expressed in E. coli. The accession number is P24001-2. Note: For testing in cell culture applications, please filter before use.

Corn starch is a natural product.

Deoxynivalenol-3-β-D-glucoside (DON-3-β-D-glucoside) is a plant metabolite of the Fusarium mycotoxin Deoxynivalenol, exhibiting lower toxicity than Deoxynivalenol in vitro and in vivo [1][2].

Kuwanon U (4'-methoxykuwanon E), a compound from Morus alba, is a cholinesterase inhibitor with antimicrobial activity, inhibits acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), and exerts its inhibitory effect by preventing ATP binding in the cytoplasmic domain of SERCA1, which can be used in the study of diabetes mellitus and bacterial infections.

T-Cadinol (Cedrelanol) is a sesquiterpene compound isolated from C. sylvestris that exhibits anti-Trypanosoma cruzi activity and potential anticancer activity, inhibits trypanosomes and flagellomorphs, induces dendritic cells and drives Th1 polarization in human monocytes.T-Cadinol is a calcium antagonist that relaxes the contraction of 60 mM K+ induced by T-Cadinol in a concentration-dependent manner. 60 mM K+-induced contraction.

T-Muurolol (epi-α-Muurolol), a sesquiterpene compound derived from Streptomyces sp. M491, possesses antimicrobial, antioxidant, and anti-inflammatory activities, and exhibits strong binding interactions with Flavin Adenine Dinucleotide (FAD)-dependent Nicotinamide Adenine Dinucleotide Phosphate (NAD(P)H) Oxidase and Cyclooxygenase-2. binding interactions.