6rk73

6RK73 is a covalent, irreversible, and specific UCHL1 inhibitor (IC50: 0.23 µM) with almost no inhibition of UCHL3 (IC50: 236 µM).

Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6 15 2 3 3000 nM) against PKC, PKA, c-Fgr, phosphorylase kinase and TAOK2. Staurosporine also induces apoptosis.

Alginic acid (Snow acid algin G) is a natural polysaccharide extracted from brown seaweeds with anti-anaphylactic and anti-inflammatory activities. Alginic acid inhibits histamine release and can be used in the food industry.

Stachybotrin F is a useful organic compound for research related to life sciences. The catalog number is T125774 and the CAS number is 1510813-73-6.

AChE-IN-73 (compound 6), an insecticide, exhibits potent mosquito inhibitory capabilities, particularly against C. pipiens with an LC 50 of 78.0 mg L. It demonstrates high affinity for acetylcholinesterase (AChE) and nicotinic acetylcholine receptors (nAChR), with respective binding energies of -8.11 kcal mol and -6.27 kcal mol.

TAS-103 is a dual inhibitor of DNA topoisomerase I II, utilized in cancer research.

10-hydroxy Warfarin is a metabolite of (R)-warfarin .1It is formed from (R)-warfarin by the cytochrome P450 (CYP) isoform CYP3A4. 10-hydroxy Warfarin is an inhibitor of CYP2C9 (IC50= 1.6 μM), the enzyme that converts (S)-warfarin to its 6-hydroxy warfarin and 7-hydroxy warfarin metabolites.2 1.Kaminsky, L.S., and Zhang, Z.-Y.Human P450 metabolism of warfarinPharmacol. Ther.73(1)67-74(1997) 2.Jones, D.R., Kim, S.-Y., Guderyon, M., et al.Hydroxywarfarin metabolites potently inhibit CYP2C9 metabolism of S-warfarinChem. Res. Toxicol.23(5)939-945(2010)

AZ876 is a potent, highly selective LXR agonist with Ki EC50 of 7 6 nM and 11 73 nM for hLXRα and hLXRβ respectively.

Aurantiamide has anti-cancer, anti-inflammatory and antinociceptive activities, it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the

SARS-CoV-2-IN-6 is an inhibitor of SARS-CoV-2 3CLpro with an IC50 value of 73 nM.

Methanesulfonato(2-dicyclohexylphosphino-2',6'-bis(dimethylamino)-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II) is a useful organic compound for research related to life sciences. The catalog number is T64712 and the CAS number is 1447963-73-6.

(S)-2-(2-Aminoacetamido)propanoic acid is a useful organic compound for research related to life sciences. The catalog number is T65215 and the CAS number is 3695-73-6.

Methyl (tert-butoxycarbonyl)-L-phenylalaninate is a useful organic compound for research related to life sciences. The catalog number is T65542 and the CAS number is 51987-73-6.

2-(Fluoromethyl)-6-nitro-3-(o-tolyl)quinazolin-4(3H)-one is a useful organic compound for research related to life sciences. The catalog number is T67189 and the CAS number is 56287-73-1.

(4-Amino-2-methyl-5-pyrimidinyl)methanol is a useful organic compound for research related to life sciences. The catalog number is T67640 and the CAS number is 73-67-6.

Fucosterol is isolated from E. stolonifera with anti-diabetic, anti-adipogenic and anti-cancer activities. It regulates adipogenesis via modulation of PPARα and C EBPα expression.

MELATONIN(ACETYL-d3) is a deuterated compound of MELATONIN. MELATONIN has a CAS number of 73-31-4. Melatonin is a biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.

5-Hydroxy-canthin-6-one is a natural product for research related to life sciences. The catalog number is TN3122 and the CAS number is 64118-73-6.

Amooracetal is a natural product for research related to life sciences. The catalog number is TN3407 and the CAS number is 1351617-73-6.

Y16 acetate(429653-73-6 free base) is a G-protein–coupled Rho GEFs inhibitor; works synergistically with Rhosin G04 in inhibiting LARG-RhoA interaction, RhoA activation, and RhoA-mediated signaling functions.

Angiotensin amide acetate is a derivative of Angiotensin amide, an octapeptide amide that increases blood pressure through vasoconstriction.