A group of TETRAHYDRONAPHTHALENES containing a keto oxygen.
A plant family of the order Magnoliales, subclass Magnoliidae, class Magnoliopsida. The wood lacks water-conducting cells but has acrid sap. The leaves are gland-dotted, leathery, and smooth-margined. The flowers are small, in clusters, with two to six sepals, petals in two or more series, several stamens, and one to several carpels.

Naftopidil, a novel alpha1-adrenoceptor antagonist, displays selective inhibition of canine prostatic pressure and high affinity binding to cloned human alpha1-adrenoceptors. (1/40)

The pharmacological profiles of the alpha1-adrenoceptor antagonists naftopidil, tamsulosin and prazosin were studied in an anesthetized dog model that allowed the simultaneous assessment of their antagonist potency against phenylephrine-mediated increases in prostatic pressure and mean blood pressure. The intravenous administration of each of these compounds dose-dependently inhibited phenylephrine-induced increases in prostatic pressure and mean blood pressure. To further assess the ability of the three compounds to inhibit phenylephrine-induced responses, the doses required to produce a 50% inhibition of the phenylephrine-induced increases in prostatic and mean blood pressure and the selectivity index obtained from the ratio of those two doses were determined for each test compound. Forty minutes after the intravenous administration of naftopidil, the selectivity index was 3.76, and those of tamsulosin and prazosin were 1.23 and 0.61, respectively. These findings demonstrated that naftopidil selectively inhibited the phenylephrine-induced increase in prostatic pressure compared with mean blood pressure in the anesthetized dog model. The selectivity of naftopidil for prostatic pressure was the most potent among the test compounds. In addition, using cloned human alpha1-adrenoceptor subtypes, naftopidil was selective for the alpha1d-adrenoceptor with approximately 3- and 17-fold higher affinity than for the alpha1a- and alpha1b-adrenoceptor subtypes, respectively. The selectivity of naftopidil for prostatic pressure may be attributable to its high binding affinity for alpha1a- and alpha1d-adrenoceptor subtypes.  (+info)

Alpha(1)-adrenoceptor subtypes mediating inotropic responses in rat heart. (2/40)

We studied the distribution of alpha(1)-adrenoceptor subtypes by radioligand binding assays using (125)I-labeled 2-beta(4-hydroxyphenyl)-ethylaminomethyl)-tetralone (BE2254) and RNase protection assays, and determined the role of each subtype in mediating the inotropic response in rat heart. Chlorethylclonidine preincubation causes a approximately 72% decrease in the maximal binding capacity (B(max)). On the other hand, protection from phenoxybenzamine alkylation by 5-methyl-urapidil or BMY7378 decreased B(max) by 59 and 70%. By competitive inhibition, we have identified 19 to 28% and 30% high-affinity binding sites for the alpha(1A)- and alpha(1D)-selective antagonists in rat ventricles, with the alpha(1B)-adrenoceptor estimated as 45%. Consistent with the receptor-binding result, a similar distribution of mRNAs encoding alpha(1A), alpha(1B,) and alpha(1D) (22, 39, and 39%), based on RNase protection assays, was observed. In addition, we demonstrated that the noradrenaline response through alpha(1)-adrenoceptor was antagonisted by 5-methyl-urapidil, RS-17053, BMY7378, and WB4101 in contraction functional experiments. K(I) values for the above compounds were defined for all three alpha(1)-adrenoceptor subtypes expressed in the human embryonic kidney 293 cell stably, and were further compared with the corresponding pA(2) values. Interestingly, the correlation was significantly higher for alpha(1A) (r(2) = 0.73) and alpha(1B) (r(2) = 0.66) than alpha(1D) (r(2) = 0.35) in these experiments. Because the potential of alpha(1D) measured to be 21% based on protection from phenoxybenzamine-caused inhibition by BMY7378, the combined potential of alpha(1A) and alpha(1B) can be estimated as approximately 80%. Taken together, these results suggest that the three alpha(1)-adrenoceptor subtypes coexist in rat heart, with alpha(1A) and alpha(1B) playing a more prominent role in the positive inotropic response to noradrenaline.  (+info)

Both alpha(1A)- and alpha(1B)-adrenergic receptor subtypes couple to the transient outward current (I(To)) in rat ventricular myocytes. (3/40)

1. Regulation of transient outward current (I(To)) by alpha(1)-adrenergic (alpha(1)AR) plays a key role in cardiac repolarization. alpha(1)ARs comprise a heterogeneous family; two natively expressed subtypes (alpha(1A) and alpha(1B)) and three cloned subtypes (alpha(1a), alpha(1b) and alpha(1d)) can be distinguished. We have examined the electrophysiological role of each alpha(1)AR subtype in regulating I(To) in isolated rat ventricular myocytes. 2. Reverse transcription-PCR study revealed the presence of three subtype mRNAs (alpha(1a), alpha(1b) and alpha(1d)) in rat myocytes. 3. Radioligand binding assay using [(125)I]-HEAT showed that the inhibition curves for alpha(1A)AR-selective antagonists (WB4101, 5-methylurapidil, (+)-niguldipine and KMD-3213) in rat ventricles best fit a two-site model, with 30% high and 70% low affinity binding sites. The high affinity sites were resistant to 100 microM chloroethylclonidine (CEC), while the low affinity sites were highly inactivated by CEC. 4. Whole cell voltage clamp study revealed that methoxamine reduced a 4-aminopyridine(4-AP)-sensitive component of I(To) in the isolated rat ventricle myocytes. Lower concentrations of KMD-3213 (1 nM) or 5-MU (10 nM) did not affect the methoxamine-induced reduction of I(To). On the other hand, CEC treatment (100 microM) of isolated myocytes reduced the methoxamine-induced reduction of I(To) by 46%, and the remaining response was abolished by lower concentrations of KMD-3213 or 5-MU. 5. The results indicate that rat ventricular myocytes express transcripts of the three alpha(1)AR subtypes (alpha(1a), alpha(1b) and alpha(1d)); however, two pharmacologically distinct alpha(1)AR subtypes (alpha(1A) and alpha(1B)) are predominating in receptor populations, with approximately 30% alpha(1A)AR and 70% alpha(1B)AR. Although both alpha(1A) and alpha(1B)AR subtypes are coupled to the cardiac I(To), alpha(1B)ARs predominantly mediate alpha(1)AR-induced effect.  (+info)

Human ejaculatory duct: parameters of smooth muscle motor activity and modulatory role of autonomic drugs. (4/40)

The contractile behaviour and effects of several autonomic drugs on the motor activity of human isolated ejaculatory ducts were investigated. Ejaculatory ducts exhibited spontaneous contractions characterised by an amplitude of 2.35 +/- 0.28 mN, a duration of 62. 9 +/- 3.72 s and a frequency of 0.64 +/- 0.014 waves min-1. Acetylcholine (10-5-10-4 m) induced a slight increase in basal tone and in the frequency of the contraction waves. These effects were suppressed by atropine (10-4 m). Noradrenaline (norepinephrine) increased the basal tone and frequency of spontaneous contractions in a dose-dependent manner. These responses were competitively inhibited by HEAT, a selective a1-adrenoceptor antagonist. These preliminary functional findings, indicating the presence of spontaneous motor activity of human ejaculatory ducts and its possible control by adrenergic agonists, suggests a physiological role for human ejaculatory duct in the propulsion of semen from the seminal vesicle towards the urethra.  (+info)

Constitutive activation of the alpha 1B-adrenergic receptor by all amino acid substitutions at a single site. Evidence for a region which constrains receptor activation. (5/40)

Mutations in an intracellular region of the alpha 1B-adrenergic receptor constitutively activate the receptor, resulting in G protein coupling in the absence of agonist, as evidenced by elevated levels of polyphosphoinositide hydrolysis. Remarkably, all 19 possible amino acid substitutions at a single site in this region (alanine 293) confer constitutive activity. This set of mutated receptors exhibits a graded range of elevated biological activities, apparently representing a spectrum of receptor conformations which mimic the "active" state of the wild type receptor. In addition to their constitutive activities, these mutated receptors all demonstrate a higher affinity for agonists, another primary characteristic of the "active" conformation of G protein-coupled receptors. The fact that all possible mutations at this particular site result in increased activity suggests that this region may function to constrain the G protein coupling of the receptor, a constraint which is normally relieved by agonist occupancy.  (+info)

Studies on the constituents of Juglans species. I. Structural determination of (4S)- and (4R)-4-hydroxy-alpha-tetralone derivatives from the fruit of Juglans mandshurica MAXIM. var. sieboldiana MAKINO. (6/40)

Four enantiomerically pure new alpha-tetralones, (4S)- and (4R)-5-hydroxy-4-methoxy-alpha-tetralones and (4S)- and (4R)-5,8-dihydroxy-4-methoxy-alpha-tetralones were isolated, together with five known ones, (4S)- and (4R)-4,8-dihydroxy-alpha-tetralones, (4S)-4,8-dihydroxy-5-methoxy-alpha-tetralone and (4S)- and (4R)-4-hydroxy-alpha-tetralones, from the fruit of Juglans mandshurica MAXIM. var. sieboldiana MAKINO. Their structures were established on the basis of spectral analysis. To the best of our knowledge, this is the first isolation of the (4R)-4-hydroxy-alpha-tetralone derivative from Juglans species.  (+info)

Sub- and supercritical chiral separation of racemic compounds on columns with stationary phases having different functional groups. (7/40)

Separation of the enantiomers of each of three different racemates, neutral rac-alpha-tetralol, acidic rac-2-phenylpropionic acid, and basic rac-1-phenylethylamine, using subcritical and supercritical fluid chromatography with two different chiral stationary phases, heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (Sumichiral OA-7500 column) and tris(3,5-dimethylphenylcarbamate) of amylose (Chiralpak AD-H column), was compared. The elution order of the enantiomers of the three racemates was determined, and the effects of the type of alcohol modifier, column oven temperature, mobile phase composition, flow rate, and pressure were examined. The most appropriate column oven temperature depended on both the type of alcohol modifier and the compound analyzed. Lower alcohol content improved the peak separation of both rac-alpha-tetralol on the Sumichiral OA-7500 column and rac-1-phenylethylamine on the Chiralpak AD-H column, while the same phenomenon was not observed with either rac-alpha-tetralol or rac-2-phenylpropionic acid on the Chiralpak AD-H column. Decreasing outlet pressure improved the peak separation obtained with rac-2-phenylpropionic acid, but had little effect on either rac-alpha-tetralol or rac-1-phenylethylamine.  (+info)

Compensatory changes in the noradrenergic nervous system in the locus ceruleus and hippocampus of postmortem subjects with Alzheimer's disease and dementia with Lewy bodies. (8/40)

In Alzheimer's disease (AD), there is a significant loss of locus ceruleus (LC) noradrenergic neurons. However, functional and anatomical evidence indicates that the remaining noradrenergic neurons may be compensating for the loss. Because the noradrenergic system plays an important role in learning and memory, it is important to determine whether compensation occurs in noradrenergic neurons in the LC and hippocampus of subjects with AD or a related dementing disorder, dementia with Lewy bodies (DLB). We observed profound neuronal loss in the LC in AD and DLB subjects with three major changes in the noradrenergic system consistent with compensation: (1) an increase in tyrosine hydroxylase (TH) mRNA expression in the remaining neurons; (2) sprouting of dendrites into peri-LC dendritic zone, as determined by alpha2-adrenoreceptors (ARs) and norepinephrine transporter binding sites; and (3) sprouting of axonal projections to the hippocampus as determined by alpha2-ARs. In AD and DLB subjects, the postsynaptic alpha1-ARs were normal to elevated. Expression of alpha1A- and alpha2A-AR mRNA in the hippocampus of AD and DLB subjects were not altered, but expression of alpha1D- and alpha2C-AR mRNA was significantly reduced in the hippocampus of AD and DLB subjects. Therefore, in AD and DLB subjects, there is compensation occurring in the remaining noradrenergic neurons, but there does appear to be a loss of specific AR in the hippocampus. Because changes in these noradrenergic markers in AD versus DLB subjects were similar (except neuronal loss and the increase in TH mRNA were somewhat greater in DLB subjects), the presence of Lewy bodies in addition to plaques and tangles in DLB subjects does not appear to further affect the noradrenergic compensatory changes.  (+info)

Tetralones are not a medical term, but rather a chemical classification. They refer to a class of organic compounds that contain a tetralone ring structure, which is a cyclohexanone fused to a benzene ring. These compounds have various applications in the pharmaceutical industry as intermediates in the synthesis of drugs. Some tetralones have been studied for their potential medicinal properties, such as anti-inflammatory and analgesic effects, but they are not themselves approved medical treatments.

I apologize for any confusion, but "Winteraceae" is not a medical term. It is actually the name of a family of flowering plants, also known as the winter's bark family. This family includes around 80 species of evergreen trees and shrubs, mostly native to tropical regions in the Southern Hemisphere, particularly in Australasia, Southeast Asia, and Central America.

If you have any medical terms or concepts that you would like me to define or explain, please let me know!

... may refer to either of two chemical isomers: 1-Tetralone 2-Tetralone This set index article lists chemical compounds ...
A related compound is 1-tetralone. 2-Tetralone is prepared by reductive cleavage of 2-naphthyl ethers. 2-Tetralone is an ... 2-Tetralone is an organic chemical compound with the molecular formula C10H10O. This colourless oil is an intermediate in ... M. D. Soffer, M. P. Bellis, Hilda E. Gellerson, and Roberta A. Stewart "β-Tetralone" Org. Synth. 1952, 32, 97 doi:10.15227/ ...
"1-Tetralone". pubchem.ncbi.nlm.nih.gov. H.R. Snyder, F.X. Werber (1940). "α-Tetralone". Org. Synth. 20: 94. doi:10.15227/orgsyn ... The carbon skeleton of 1-tetralone is found in natural products such as Aristelegone A (4,7-dimethyl-6-methoxy-1-tetralone) ... The AlCl3-catalyzed acylation of benzene with γ-butyrolactone produces 1-tetralone. 1-Tetralone can be reduced via a Birch ... catalyzed arylation of 1-tetralone using phenyl boronic acid neopentyl glycol ester gives 8-phenyl-1-tetralone in up to 86% ...
Examples of such procedures are described for benzaldehyde, 2-tetralone, citral, the ethyl ester of pyruvic acid and glyoxal. ... 5, p. 437 Soffer, M. D.; Bellis, M. P.; Gellerson, Hilda E.; Stewart, Roberta A. (1963). "β-Tetralone". Organic Syntheses.; ...
A variant of the Friedel-Crafts alkylation, the Haworth reaction, is named after him (1932). It creates 1-tetralone. The ...
14) Tetralones complexed to chromium may be deprotonated without side reactions. Alkylation of the resulting enolate proceeds ...
It can also be obtained by oxidations of 5,8-dihydroxy-1-tetralone with silver oxide (Ag2O), manganese dioxide (MnO2), or 2,3- ... J. Khalafy; J.M. Bruce (2002). "Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and α- ...
Khalafy, Jabbar; Bruce, J.M. (2002-06-01). "Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and ...
"Oxidative Dehydrogenation of 1-Tetralones: Synthesis of Juglone, Naphthazarin, and α-Hydroxyanthraquinones" (pdf). Journal of ...
Khalafy, J.; Bruce, J. M. (2002). "Oxidative Dehydrogenation of 1-Tetralones: Synthesis of Juglone, Naphthazarin, and α- ...
Talapatra, Sunil K.; Karmacharya, Bimala; De, Shambhu C.; Talapatra, Bani (January 1988). "(−)-Regiolone, an α-tetralone from ...
Gu W, Ding H. (2008). "Two new tetralone derivatives from the culture of Xylaria hypoxylon AT-028." Chinese Chemical Letters 19 ...
... leading to the inclusion of traditionally difficult substrates like t-butyl ketones and 1-tetralones as viable substrates for ... Complexes for Efficient Asymmetric Hydrogenation of 1-Tetralones and Analogues". Organic Letters. 6 (16): 2681-2683. doi: ...
... the pharmaceutical Norgestrel begins from methoxy-1-tetralone, a petrochemical derived from phenol. A number of Nobel Prizes ...
Naphtharazin can also be obtained by oxidation of 5,8-dihydroxy-1-tetralone with manganese dioxide (MnO2). Thomson R.H. ... J. Khalafy and J.M. Bruce (2002), Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and α- ...
When the side chain is homologated by the Arndt-Eistert reaction, subsequent cyclization affords 2-tetralone, derivatives. ...
Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and [alpha]-hydroxyanthraquinones. Journal of ...
This results in the formation of 3a which tautomerizes to the more stable 3b to the sulfonic acid of tetralone. A nucleophilic ...
V. Kinetics of the bromide ion promoted elimination reaction of 2-benzyl-2-bromo-4,4-dimethyl-1-tetralone in solvent ...
10) With the lone exception of methylidene tetralone substrates, no general methods are available for the asymmetric ...
The Haworth reaction is a classic method for the synthesis of 1-tetralone. In this reaction, benzene is reacted with succinic ...
This yields 1-(5-bromopentyl)-1-methyl-7-methoxy-2-tetralone, which is then cyclized with NaH to produce 5-methyl-3-methoxy-5,6 ... The synthesis of dezocine begins with the condensation of 1-methyl-7-methoxy-2-tetralone with 1,5-dibromopentane through use of ...
Benzylideneacetone Tetralones 1-Tetralone 2-Tetralone This set index page lists chemical structure articles associated with the ...
Tetralones, Ophthalmology drugs). ...
Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and α-hydroxyanthraquinones. Journal of Sciences ...
... tetralones MeSH D04.615.638.975 - tolnaftate MeSH D04.615.680.500 - perylene MeSH D04.615.723.089 - aristolochic acids MeSH ...
... and 1-tetralone. Other oxidation reagents like potassium permanganate or potassium dichromate oxidize to the more stable ...
... for certain substrates like α-tetralone, the group that migrates can sometimes change, depending on the conditions used, to ...
... which is oxidized to 1-tetralone, which undergoes dehydrogenation. Some reactions of 1-naphthol are explicable with reference ...
Tetralone may refer to either of two chemical isomers: 1-Tetralone 2-Tetralone This set index article lists chemical compounds ...
Sertrakine Tetralone Impurity .. We also perform custom synthesis and purification of impurity from mg to gm scale, isolation ... We have manufacture Sertrakine Tetralone Impurity . It is fully characterized using HPLC, LC-MS, 1H NMR spectra and COA and is ... Rxn Chemicals is manufacturer and supplier of unknown Sertrakine Tetralone Impurity . which can be used for ANDA filing/DMF ...
6-Methoxy-1-tetralone supplier, 6-Methoxy-1-tetralone distributor, CAS 1078-19-9 , 6-Methoxy-1-tetralone manufacturer, 6- ... 6-Methoxy-a-tetralone; 6-Methoxy-1-tetralone; 6-Methoxy-1,2,3,4-tetrahydro-1-naphthalenone; 6-Methoxy-3,4-dihydro-1(2H)- ... 6-Methoxy-a-tetralone; 6-Methoxy-1-tetralone; 6-Methoxy-1,2,3,4-tetrahydro-1-naphthalenone; 6-Methoxy-3,4-dihydro-1(2H)- ... 6-Methoxy-1-tetralone; 6-Methoxy-3,4-dihydro-1(2H)-naphthalenone; 6-Methoxy-alpha-tetralone; EC 214-078-0; EINECS 214-078-0; ...
Tetralone CAS:79560-19-3,What is 4-(3,4-Dichloro Phenyl)-Tetralone?Where can buy 4-(3,4-Dichloro Phenyl)-Tetralone or what is ... Tetralone supplier,Welcome to contact us for 4-(3,4-Dichlorophenyl)-1-tetralone COA or MSDS., China and India manufacturer of 4 ... Tetralone producer, 4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenone factory and 4-(3,4-Dichloro Phenyl)- ... 4-(3,4-Dichloro Phenyl)-Tetralone. *CAS:. 79560-19-3. *Synonym:. 4-(3,4-Dichloro Phenyl)-Tetralone. 4-(3,4-Dichlorophenyl)-1- ...
Tetralone® Advanced Hop Acid. If a more intense hop profile is what youre after, our proprietary Tetralone products provide 50 ... Tetralone is light stable and can be added post-fermentation or into the fermenter. ...
EC number: 444-830-5 , CAS number: 124379-29-9 S EDIN; S TETRALONE ...
5,6-Dimethoxy-2-tetralone sodium bisulfite adduct. 0 out of 5 ...
5,6-Dimethoxy-2-tetralone sodium bisulfite adduct. 0 out of 5 ...
The reaction of 4-phenyl-α-chloroacetophenone, 2-chloro-1-tetralone, and 2-chloro-1-indanone with various aroma... ...
6 grams of an allylated tetralone from commercially available materials. Furthermore, use of non-racemic PHOX ligands allows ...
The ligands were synthesized from 1-tetralone and different aromatic amines in refluxing toluene. The cyclometalated Ir(III)- ...
farnesyl diphosphate + 2-carboxy-4-hydroxy-alpha-tetralone = demethylmenaquinone-3 + phosphate + CO2 ...
1(2H)-Naphthalenone, 3,4-dihydro-5,7-dimethyl- is a tetralone derivative and has the binding affinity of -8.3 kcal/mol. ... Tetralone derivatives are also known for action on serotonin and dopamine[16]. ... and antibacterial activities of novel tetralone-based 1,4-benzothiazepine derivatives, J. Biochem. Mol. Toxicol. 31 (2017) 1-11 ...
... tetralones, and chinones (Figure 2) (Joseph and Priya, 2011; Godstime et al., 2014). Many factors have been reported to affect ...
3-Benzyl-2-tetralones (3a-c) were prepared in two different ways from 2-tetralone and 6-methoxy-2-tetralone. Regioselective ... Demethoxycarbonylation using lithium iodide afforded the desired 3-benzyl-2-tetralones (3a-c), which furnished the lactams (4a- ...
Sertraline 2,3-Dichloro Tetralone Methanamine. Price : CAS No. : 340830-05-9. ...
The reaction carried out on α-cyanocyclohexanone and 2-cyano-α-tetralone afforded the corresponding adipic acid and 2- ...
ALPHA-(SPIROCYANOCYCLOPROPYL)-ALPHA-TETRALONE (2 suppliers). IUPAC Name: 4-oxospiro[1,2-dihydronaphthalene-3,2-cyclopropane]-1 ... Synonyms: alpha-(Spirocyanocyclopropyl)-alpha-tetralone, 4-oxospiro[1,2-dihydronaphthalene-3,2-cyclopropane]-1-carbonitrile, ...
TETRALONE (BE 2254) USING REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY JOURNAL OF CHROMATOGRAPHY Riemer, R. K., Kuhn, ...
2-tetralone with CAS 530-93-8. /*! elementor - v3.13.3 - 22-05-2023 */ .elementor-widget-image{text-align:center}.elementor- ...
Talapatra, S. K., Karmacharya, B., and Talabatra, B. (1988). "Levoregiolone an alpha-tetralone from Juglans regia; Structure, ...
Asymmetric phase-transfer catalytic (PTC) sulfanylation of 2-methylsulfinyl-1-tetralone  Paiva, Derisvaldo Rosa [UNIFESP]; ...
Dive into the research topics where Ho-Cheng Wu is active. These topic labels come from the works of this person. Together they form a unique fingerprint ...
1-Tetralone. 529-34-0 P. Pinacolone. 75-97-8. P. 4,4-Dimethoxybenzophenone. 90-96-0. C. ...
Alpha-Tetralone * 2-Methyl-4-isothiazolin-3-one ( MIT ) * 2446-83-5 synthesis ...
EC number: 444-830-5 , CAS number: 124379-29-9 S EDIN; S TETRALONE ...
2-diazo-1-tetralone. dichloromethane. N Parameter: 3.51. sN Parameter: 0.86. Eur. J. Org. Chem. 2023, 26, e202300005. DOI: ...
  • 3. P. H. Tran, V. H. Huynh, P. E. Hansen, D. K. N. Chau, T. N. Le, An efficient and green synthesis of 1-indanone and 1-tetralone via intramolecular Friedel-Crafts acylation reaction, Asian Journal of Organic Chemistry , 2015 , 4 (5), 482-486. (edu.vn)
  • China 4-(3,4-Dichloro Phenyl)-Tetralone CAS:79560-19-3 manufacturer supplier producer and factory-NINGBO INNO PHARMCHEM CO.,LTD. (nbinno.com)
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  • If a more intense hop profile is what you're after, our proprietary Tetralone products provide 50-70% more bitterness than iso-alpha acids, making for a sharp bitterness at the back of the tongue. (kalsec.com)
  • Where can buy 4-(3,4-Dichloro Phenyl)-Tetralone or if you want to know the price market of 4-(3,4-Dichlorophenyl)-1-tetralone? (nbinno.com)
  • Previous studies explored 2-benzylidine-1-tetralone derivatives as innovative adenosine A 1 and A 2A receptor antagonists for alternative non-dopaminergic treatment of Parkinson's disease. (thieme-connect.com)
  • 13 Legoabe LJ, Van der Walt MM, Terre'Blanche G. Evaluation of 2-benzylidene-1-tetralone derivatives as antagonists of A 1 and A 2A adenosine receptors of hydroxy-substituted 2-benzylidene-1-tetralones as antagonist of A 1 and A 2A adenosine receptors. (thieme-connect.com)
  • Stereoselective annulations on Cr(CO) 3 complexed tetralone and benzosuberone § derivatives have been achieved. (johnshopkins.edu)
  • Used with a dendrimeric supported L-pyrrolidinol in the asymmetric reduction of indanones and tetralones. (thomassci.com)
  • In this paper new cellulose tribenzoate/gypsum layers in the ratio up to 8/1 (w/w) were investigated for the chiral resolution of closely related aromatic ketones (e.g. tetralones and indanones), alcohols (e.g. benzhydrols) and racemates or enantiomers of other compound classes (e.g. dinitrophenyl amino acids). (unifi.it)
  • Tetralone may refer to either of two chemical isomers: 1-Tetralone 2-Tetralone This set index article lists chemical compounds articles associated with the same name. (wikipedia.org)
  • CH-activating oxidative hydroxylation of 1-tetralones and related compounds with high regio- and stereoselectivity. (mpg.de)
  • The catalytic Cys145 subsequently binds covalently in a Michael addition to the methylene carbon atom of 2-methylene-1-tetralone. (bvsalud.org)