The PyrR binding site is an RNA element that is found upstream of a variety of genes involved in pyrimidine biosynthesis and transport. The RNA structure...

Pseudomon-groES RNA motif Pseudomonas rnk leader Pseudomonas rpsL leader PyrG leader PyrR binding site R2 RNA element RbcL 5′ UTR RNA stabilising element Red clover...

beta-glucan-transporting ATPase - beta2-adaptin C-terminal domain - binding site - biological organisation - biological process - Biomolecular gradient...

stain Microscopy Romanowsky stain Wright's stain Zipfel, E.; Grezes, J. -R.; Naujok, A.; Seiffert, W.; Wittekind, D. H.; Zimmermann, H. W. (1984). "Über...

measure of fivefold (5×) discrepancy in the entropy of binding at their presumed shared target binding site, which may account for the higher abuse potential...

5-MeO-pyr-T, also known as 5-methoxy-N,N-tetramethylenetryptamine or as 5-methoxy-3-(2-pyrrolidinoethyl)indole, is a serotonin receptor modulator and...

(December 2011). "Trace amine-associated receptor 1 is a stereoselective binding site for compounds in the amphetamine class". Bioorg Med Chem. 19 (23): 7044–7048...

it is hypothesized that AMPT competes with tyrosine at the tyrosine-binding site, causing inhibition of tyrosine hydroxylase. It has been used in the...

high-affinity, extracellular, and allosteric Zn2+ (zinc ion) binding site which, upon zinc binding, inhibits dopamine reuptake, inhibits amphetamine-induced...

funnel that is suggested to serve as the insertion site for ubiquinone, in conjunction with the FMN binding cavity at the C-terminal. The two terminal domains...

given during migraine attacks decreases brain serotonin 5-HT1B receptor binding in humans, with a corresponding receptor occupancy of 16%. However, this...

transporter contains a high affinity extracellular zinc binding site which, upon zinc binding, inhibits dopamine reuptake and amplifies amphetamine-induced...

receptor indicates binding site structure". Medicinal Chemistry Research. 3: 52–66. Shahar O, Botvinnik A, Esh-Zuntz N, Brownstien M, Wolf R, Lotan A, et al...

steric interactions between the ring structure and the binding site. Nichols DE, Snyder SE, Oberlender R, Johnson MP, Huang XM (January 1991). "2,3-Dihydrobenzofuran...

Table II. Affinities of Selected Phenalkylamines for 5-HT1 and 5-HT2 Binding Sites Cerletti A, Taeschler M, Weidmann H (1968). Pharmacologic studies on...

of non-binding sites on the DAT molecule to exert its own binding, as well as the potential of augmented affinity for NET if its binding site is otherwise...

family. It is a benzodiazepine site agonist selective for certain subunits. TCS 1205 acts at the benzodiazepine binding site, it is selective for the α1...

Phenalkylamines for 5-HT1 and 5-HT2 Binding Sites [...] Shannon M, Battaglia G, Glennon RA, Titeler M (June 1984). "5-HT1 and 5-HT2 binding properties of derivatives...

concentrations of 50-100 μmol/L. Its efficacies at the other receptor binding sites are unclear. It has also been shown in vitro to be a substrate for the...

tryptamine Tetrahydropyridinylindole VU6067416 RS134-49 (R)-69 RU-24,969 EMD-386088 SN-22 MPMI Pyr-T Pip-T Kitson SL (2007). "5-hydroxytryptamine (5-HT)...

ibogaine and its principal metabolite (12-hydroxyibogamine) at the MK-801 binding site of the NMDA receptor complex". Neurosci Lett. 192 (1): 53–56. doi:10...

the active site cavity when the mobile ‘flap’ (which allows for the entrance of urea into the active site) is open. Stability of the binding of urea to...

the chemical structure of the site of binding (sulfhydryl, phosphinyl, carboxyl) to the active center of ACE. Kumar R, Chaudhary K, Sharma M, Nagpal...

of the trimethylsilyl group in 1S-LSD is thought to slightly alter its binding affinity and metabolic profile, although empirical data is still needed...

Phenalkylamines for 5-HT1 and 5-HT2 Binding Sites Shannon M, Battaglia G, Glennon RA, Titeler M (June 1984). "5-HT1 and 5-HT2 binding properties of derivatives...

Phenalkylamines for 5-HT1 and 5-HT2 Binding Sites Shannon M, Battaglia G, Glennon RA, Titeler M (June 1984). "5-HT1 and 5-HT2 binding properties of derivatives...

reported to have an IC50 of about 50 nM for the inhibition of [3H]5-HT binding, which is at least 5 times less potent than typical reported values for...

Erasmus University Repository. Retrieved 19 June 2025. Table 1.2 Receptor binding properties (pKi values) of sumatriptan and second-generation triptans at...

5-HT2C binding of phenylalkyl- and indolylalkylamines". Journal of Medicinal Chemistry. 37 (13): 1929–35. doi:10.1021/jm00039a004. PMID 8027974. Heim R (March...

"Angiotensin-Converting Enzyme 2 Metabolizes and Partially Inactivates Pyr-Apelin-13 and Apelin-17: Physiological Effects in the Cardiovascular System"...