• 제목/요약/키워드: A1

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A Novel 3-(8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-yl)phenyl Acetate Skeleton and Pharmacophore Model as Glucagon-like Peptide 1 Receptor Agonists

  • Gong, Young-Dae;Cheon, Hyae-Gyeong;Lee, Tae-Ho;Kang, Nam-Sook
    • Bulletin of the Korean Chemical Society
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    • 제31권12호
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    • pp.3760-3764
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    • 2010
  • We screened 10,000 heterocyclic small molecules and identified a novel hit core skeleton of 3-(8-chloro-6-(trifluoromethyl) imidazo[1,2-a]pyridine-2-yl)phenyl acetate derivatives. It has been selected as a potential glucagon-like peptide 1 receptor (GLP-1R) activator and demonstrated its effects in increasing GLP-1 secretion, and thereby increasing the glucose responsiveness in both in vitro and pharmacology analyses. Further studies are currently underway to optimize the potency and selectivity of 3-(8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-yl)phenyl acetate derivatives (hit compounds 2 and 8), and address their in vivo efficacy and therapeutic potential. These molecules may serve as useful evidence showing that compounds with a 3-(8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-yl)phenyl acetate moiety are selective GLP-1R agonists, and have potential as anti-diabetic treatment agents.

CAUCHY-RASSIAS STABILITY OF A GENERALIZED ADDITIVE MAPPING IN BANACH MODULES AND ISOMORPHISMS IN C*-ALGEBRAS

  • Shin, Dong Yun;Park, Choonkil
    • 충청수학회지
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    • 제24권4호
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    • pp.617-630
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    • 2011
  • Let X, Y be vector spaces, and let r be 2 or 4. It is shown that if an odd mapping $f:X{\rightarrow}Y$ satisfies the functional equation $${\hspace{50}}rf(\frac{\sum_{j=1}^{d}\;x_j} {r})+\;{\sum\limits_{\iota(j)=0,1 \atop {\sum_{j=1}^{d}}\;{\iota}(j)=l}}\;rf(\frac{\sum_{j=1}^{d}{(-1)^{\iota(j)}x_j}}{r}) \\({\ddag}){\hspace{160}}=(_{d-1}C_l-_{d-1}C_{l-1}+1)\;{\sum\limits_{j=1}^{d}\;f(x_j)}$$ then the odd mapping $f:X{\rightarrow}Y$ is additive, and we prove the Cauchy-Rassias stability of the functional equation in Banach modules over a unital $C^*$-algebra. As an application, we show that every almost linear bijection $h:{\mathcal{A}}{\rightarrow}{\mathcal{B}}$ of a unital $C^*$-algebra ${\mathcal{A}}$ onto a unital $C^*$-algebra ${\mathcal{B}}$ is a $C^*$-algebra isomorphism when $h(2^nuy)=h(2^nu)h(y)$ for all unitaries $u{\in}{\mathcal{A}}$, all $y{\in}{\mathcal{A}}$, and $n=0,1,2,{\cdots}$.

PAIR MEAN CORDIAL LABELING OF SOME UNION OF GRAPHS

  • R. PONRAJ;S. PRABHU
    • Journal of Applied and Pure Mathematics
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    • 제6권1_2호
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    • pp.55-69
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    • 2024
  • Let a graph G = (V, E) be a (p, q) graph. Define $${\rho}=\{\array{{\frac{p}{2}} && p\;\text{is even} \\ {\frac{p-1}{2}} && p\;\text{is odd,}}$$ and M = {±1, ±2, … ± 𝜌} called the set of labels. Consider a mapping λ : V → M by assigning different labels in M to the different elements of V when p is even and different labels in M to p - 1 elements of V and repeating a label for the remaining one vertex when p is odd. The labeling as defined above is said to be a pair mean cordial labeling if for each edge uv of G, there exists a labeling $\frac{{\lambda}(u)+{\lambda}(v)}{2}$ if λ(u) + λ(v) is even and $\frac{{\lambda}(u)+{\lambda}(v)+1}{2}$ if λ(u) + λ(v) is odd such that ${\mid}\bar{\mathbb{s}}_{{\lambda}_1}-\bar{\mathbb{s}}_{{\lambda}^c_1}{\mid}\,{\leq}\,1$ where $\bar{\mathbb{s}}_{{\lambda}_1}$ and $\bar{\mathbb{s}}_{{\lambda}^c_1}$ respectively denote the number of edges labeled with 1 and the number of edges not labeled with 1. A graph G with a pair mean cordial labeling is called a pair mean cordial graph. In this paper, we investigate the pair mean cordial labeling behavior of some union of graphs.

PAIR DIFFERENCE CORDIALITY OF CERTAIN SUBDIVISION GRAPHS

  • R. PONRAJ;A. GAYATHRI;S. SOMASUNDARAM
    • Journal of applied mathematics & informatics
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    • 제42권1호
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    • pp.1-14
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    • 2024
  • Let G = (V, E) be a (p, q) graph. Define $$\begin{cases}\frac{p}{2},\:if\:p\:is\:even\\\frac{p-1}{2},\:if\:p\:is\:odd\end{cases}$$ and L = {±1, ±2, ±3, ···, ±ρ} called the set of labels. Consider a mapping f : V → L by assigning different labels in L to the different elements of V when p is even and different labels in L to p - 1 elements of V and repeating a label for the remaining one vertex when p is odd.The labeling as defined above is said to be a pair difference cordial labeling if for each edge uv of G there exists a labeling |f(u) - f(v)| such that |Δf1 - Δfc1| ≤ 1, where Δf1 and Δfc1 respectively denote the number of edges labeled with 1 and number of edges not labeled with 1. A graph G for which there exists a pair difference cordial labeling is called a pair difference cordial graph. In this paper we investigate the pair difference cordial labeling behavior of subdivision of some graphs.

A kinematic study of young stars in Monoceros OB1 and R1 associations

  • Lim, Beomdu;Naze, Yael;Hong, Jongsuk;Yoon, Sungyong;Lee, Jinhee;Hwang, Narae;Park, Byeong-Gon;Lee, Jeong-Eun
    • 천문학회보
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    • 제46권2호
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    • pp.50.1-50.1
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    • 2021
  • The Gaia mission opens a new window to study the kinematics and dynamics of young stellar systems in detail. The kinematic properties of young stars provide vital constraints on the formation process of their host systems. Here, we present a kinematic study of the two associations Monoceros OB1 (Mon OB1) and R1 (Mon R1). Member candidates are first selected from the published list of member candidates, a compilation of OB star catalogues, and the classification of young stellar objects with the AllWISE data. According to the conventional wisdom, we selected a total of 728 members with similar proper motions at almost the same distance. Mon OB1 and Mon R1 have high levels of substructures that are also kinematically distinct. We identify six stellar groups in these associations, of which five show a pattern of expansion. In addition, the signature of rotation is found in two stellar groups of Mon OB1. Star formation history is inferred from a color-magnitude diagram. As a result, star formation in Mon OB1 has been sustained for several million years, while Mon R1 formed at almost the same epoch as the recent star formation in Mon OB1. Some old members in the outskirt of Mon OB1 have outward motions, which rules out the previously proposed outside-in star formation scenario. Star-forming regions including Mon OB1 and Mon R1 are found along a large arc-like gas structure. Hence, the formation of these two associations may originate from the hierarchical star formation along filaments in a turbulent molecular cloud.

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A Genetic Marker Associated with the A1 Mating Type Locus in Phytophthora infestans

  • KIM KWON-JONG;EOM SEUNG-HEE;LEE SANG-PYO;JUNG HEE-SUN;KAMOUN SOPHIEN;LEE YOUN SU
    • Journal of Microbiology and Biotechnology
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    • 제15권3호
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    • pp.502-509
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    • 2005
  • Sexual reproduction plays an important role in the biology and epidemiology of oomycete plant pathogens such as the heterothallic species Phytophthora infestans. Recent worldwide dispersal of A2 mating type strains of P. infestans resulted in increased virulence, gene transfer, and genetic variation, creating new challenges for disease management. To develop a genetic assay for mating type identification in P. infestans, we used the Amplified Fragment Length Polymorphism (AFLP) technique. The primer combination E+AT/M+CTA detected a fragment specific to A1 mating type (Mat-A1) of P. infestans. This fragment was cloned and sequenced, and a pair of primers (INF-1, INF-2) were designed and used to differentiate P. infestans Mat-A1 from Mat-A2 strains. The Mat A1-specific fragment was detected using Southern blot analysis of PCR products amplified with primers INF-1 and INF-2 from genomic DNA of 14 P. infestans Mat-A1 strains, but not 13 P. infestans Mat-A2 strains or 8 other isolates representing several Phytophthora spp. Southern blot analysis of genomic DNAs of P. infestans isolates revealed a 1.6 kb restriction enzyme (EcoRI, BamHI, AvaI)-fragment only in Mat-A1 strains. The A1 mating type-specific primers amplified a unique band under stringent annealing temperatures of $63^{\circ}C-64^{\circ}C$, suggesting that this PCR assay could be developed into a useful method for mating type determination of P. infestans in field material.

점화식 an=an-1+an-3, a1=a2=a3=1의 일반항에 대하여 (On the general terms of the recurrence relation an=an-1+an-3, a1=a2=a3=1)

  • 노문기;정재훈;강정기
    • 한국수학교육학회지시리즈E:수학교육논문집
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    • 제27권4호
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    • pp.357-367
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    • 2013
  • 교사 위주의 수업보다 학생 중심의 탐구 활동이 지속적으로 강조되고 있지만, 이를 실행하기란 쉽지 않은 것이 현실이다. 학생들의 지적 호기심은 주관적이며, 지적 호기심을 충족해주는 것은 교육 과정에 충실한 교육 못지않게 중요하다. 본 연구는 문제를 해결하는 과정에서 얻은 수열로부터 시작되었다. 이 수열은 점화식 $a_n=a_{n-1}+a_{n-3}$ ($n{\geq}4$), $a_1=a_2=a_3=1$으로 표현되었는데, 우리는 이 수열의 일반항을 찾아보고자 시도하였다. 주어진 문제의 점화식은 피보나치 수열의 점화식과 형태는 비슷해 보이지만 일반항을 구하는 과정은 결코 비슷하지 만은 않았다. 각고의 노력 끝에 우리는 같지만 서로 다르게 표현되는 두 개의 아름다운 일반항을 얻을 수 있었다. 본 연구와 같은 탐구과정이 교육 현장에 활력을 불어 넣는 데 일조할 수 있기를 기대한다.

Phosphorylation of SAV1 by mammalian ste20-like kinase promotes cell death

  • Park, Byoung-Hee;Lee, Yong-Hee
    • BMB Reports
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    • 제44권9호
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    • pp.584-589
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    • 2011
  • The mammalian ste20-like kinase (MST) pathway is important in the regulation of apoptosis and cell cycle and emerges as a novel tumor suppressor pathway. MST-induced phosphorylation of Salvador homolog 1 (SAV1), which is a scaffold protein, has not been evaluated in detail. We performed a mass spectrometric analysis of the SAV1 protein that was co-expressed with MST2. Phosphorylation was detected at Thr-26, Ser-27, Ser-36 and Ser-269. Although single or double mutations had little effects, the mutation of all four residues in SAV1 to Ala (SAV1-4A) had inhibitory effects on the MST pathway. MST2-mediated induction of SAV1-4A protein levels, SAV1-4A interaction with MST2 and the self-dimerization of SAV1-4A were weaker compared to those of wild-type SAV1. SAV1-4A inhibited MST2- and K-RasG12V-induced cell death of MCF7 cells. These results suggest that MST-mediated phosphorylation of four residues within SAV1 may be important in the induction of cell death by the MST pathway.

인체 간 조직의 Cytochrome P450 3A4의 활성에 대한 Troleandomycin의 작용기전 (Reaction Mechanism of Troleandomycin on the Activity of Human Liver Microsomal Cytochrome P450 3A4)

  • 김복량;오현숙;김혜정
    • Toxicological Research
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    • 제11권2호
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    • pp.329-335
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    • 1995
  • Incubation of aflatoxin $B_1$ $(AFB_1)$ with microsomes isolated from human liver number 110 yielded two metabolite peaks which were aflatoxin $Q_1$ $(AFQ_1)$ and $(AFB_1)$-exo-8, 9-epoxide (exo-epoxide) in high performance liquid chromatography. Production ratio of $AFQ_1$ to exo-epoxide was 2.43$\pm $0.04. Metabolism of $(AFB_1)$ to $(AFQ_1)$ and exo-epoxide was inhibited by troleandomycin in a same degree although troleandomycin was not activated as a mechanism-based inhibitor. The inhibitory effect was dependent upon either the incubation time with $(AFB_1)$ or the preincubation time before the addition of $(AFB_1)$. Incubation of troleandomycin and NADPH by the microsomes resulted in the formation of a cytochrome P 450 (P450)-metabollc intermediate (MI) complex and the level was approximately 80% of total P450 3A4 in the microsomes. This figure was similar to that of the inhibitory effect of troleandomycin on $AFB_1$ metabolism. Glutathione which was reported that it prevented the formation of MI complex in rat liver microsomes did not inhibit the formation of MI complex in human liver microsomes. These results suggested that the inhibitory effect of troleandomycin on $AFB_1$ metabolism is due to the formation of MI complex with P450 3A4. And the reaction mechanism of troleandomycin by human liver microsomes might be dlfferent from that one by rat liver microsomes.

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바나하 공간에서의 완전 수렴성 (Complete Convergence in a Banach Space)

  • 성수학
    • 자연과학논문집
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    • 제9권1호
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    • pp.57-60
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    • 1997
  • {$X_{ni}$,1$\leq$i$\leq$,n$\geq$1}은 2p차 적률을 갖는 적당한 확률변수 X에 의해서 유계된 바나하 공간상의 값을 갖는 확률변수 열이다. 상수 열 {$a_{ni}$,1$\leq$i$\leq$,n$\geq$1}에 적당한 조건을 부여할 때 $sum_{i=1}^n a_{ni}X_{ni}$가 0에 확률적으로 수렴할 조건과 완전수렴할 조건은 서로 동치이다.

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