• Animal Systematics, Evolution and Diversity
• /
• nspc6호
• /
• pp.1-126
• /
• 2007

Thirty new species consisting of 24 poecilostomatoid and six siphonostomatoid copepods are described as associates of marine invertebrates from the Moluccas. New taxa in the order Poecilostomatoida are Amarda curvus n. sp., Anchimolgus gracilipes n. sp., A. partenuipes n. sp., A. parangensis n. sp., A. hastatus n. sp., Andrianellus papillipes n. sp., Exodontomolgus communis n. gen. n. sp., Jamescookina moluccensis n. sp., Odontomolgus flammeus n. sp., O. parvus n. sp., O. pavonus n. sp., Paranchimolgus parallelus n. gen. n. sp., and Scyphuliger karangmiensis n. sp. in the family Anchimolgidae; Enalcyonium circulatum n. sp. and E. ceramensis n. sp. in the family Lamippidae; Parastericola rimosus n. gen. n. sp. in the family Lichomolgidae; Pseudanthessius truncus n. sp. and P. planus n. sp. in the family Pseudanthessiidae; Acanthomolgus gomumuensis n. sp., A. dispadactylus n. sp., A. bandaensis n. sp., A. ambonensis n. sp., Kombia avitus n. sp. and Pionomolgus moluccensis n. sp. in the family Rhynchomolgiae. New taxa in the order Siphonostomatoida are Cryptopontius acutus n. sp. in the family Artotrogidae; Asteropontius fungicola n. sp., A. gonioporae n. sp., Collocheres humesi n. sp. and C. amicus n. sp. in the family Asterocheridae; and Molucomes ovatus n. gen. n. sp. in the family Stellicomitidae. Species new to the Moluccas and new host records are also included. Lists of 263 species of associated copepods known from the Moluccas and their 135 species of invertebrate hosts are provided.

• 약학회지
• /
• 제13권2_3호
• /
• pp.62-66
• /
• 1969

Ten new N$^{4}$-furoylsulfonamides were synthesized such as N$^{4}$-furoyl-N$^{1}$-(4,6-dimethyl-2-pyrimidinyl) sulfanilamide (I), N$^{4}$-furoylsulfanilamide (II), N$^{4}$-furoyl-N$^{1}$-(2,6-dimethoxy-4-pyrimidinyl) sulfanilamide (III), N$^{4}$-furoyl-N$^{1}$-(4-methyl-2-pyrimidinyl) sulfanilamide (IV), N$^{4}$-furoyl-N$^{1}$-(6-methoxy-3-pyridazinyl) sulfanilamide (V), N$^{4}$-furoyl-N$^{1}$-2-pyrimidinylsulfanilamide (VI), N$^{4}$-furoyl-N$^{1}$-(3,4-dimethyl-5-isoxazolyl) sulfanilamide (VII), N$^{4}$-furoyl-N$^{1}$-2-thiazoilysulfanilamide (VIII), N$^{4}$-furoyl-N$^{1}$-(5-methoxy-2-pyrimidinyl) sulfanilamide (IX) and N$^{4}$-furoyl-N$^{1}$-(2,6-dimethyl-4-pyrimidinyl) sulfanilamide (X). They were obtained by the action of N$^{1}$-(4,6-dimethyl-2-pyrimidinyl) sulfanilamide, N$^{1}$-(2,6-dimethoxy-4-pyrimidinyl) sulfanilamide, N$^{1}$-(4-methyl-2-pyrimidinyl) sulfanilamide, N$^{1}$-(6-methoxy-3-pyridazinyl) sulfanilamide, N-2-pyrimidinyl sulfanilamide, N$^{1}$-(3,4-dimethyl-5-isoxazolyl) sulfanilamide, N$^{1}$-2-(thiazolysulfanilamide), N$^{1}$-(5-methoxy-2-pyrimidinyl) sulfanilamide and N$^{1}$-(2,6-dimethyl-4-pyrimidinyl) sulfanilamide with furoyl chloride in 4% NaOH solution. Of the above ten compounds, N$^{4}$-furoylsulfathiazole exhibited a good antibacterial action against Staphylococeus aureus and Escherichia coli.

• 식물분류학회지
• /
• 제39권4호
• /
• pp.247-253
• /
• 2009

한국산 쑥속 20분류군의 분류를 위하여 체세포 염색체수를 조사하였다. 본 연구에서 취급된 분류군들의 체세포 염색체수는 2n = 16, 18, 34, 36, 50, 52, 54로서 기본 염색체수는 x=8, 9, 10, 13, 17이었으며, 실제비쑥(A. japonica var. angustissima 2n = 36)의 체세포염색체수는 본 연구에서 처음으로 밝혀졌다. 사철쑥 (A. capillaris 2n = 18), 섬쑥(A. japonica var. hallaisanensis 2n = 36), 갯제비쑥(A. japonica subsp. littoricola 2n = 36), 개똥쑥(A. annua 2n = 18), 개사철쑥(A. carvifolia 2n = 18), 큰비쑥(A. fukudo 2n = 16), 맑은대쑥(A. keiskeana 2n = 18), 넓은잎외잎쑥(A. stolonifera 2n = 36), 그늘쑥(A. sylvatica 2n = 16), 물쑥(A. selengensis 2n = 36), 산쑥 (A. montana 2n = 52), 뺑쑥(A. lancea 2n = 16), 산흰쑥(A. sieversiana 2n = 18) 등의 13분류군의 염색체수는 기존 보고와 일치하였으며, 기존 보고와 다르게 파악된 종류는 제비쑥(A. japonica var. japonica 2n = 18, 36 vs 2n = 36), 더위지기(A. sacrorum 2n = 18, 54 vs 2n = 54), 덤불쑥(A. rubripes 2n = 16, 34 vs 2n = 16), 쑥(A. indica 2n = 34, 36 vs 2n = 34), 참쑥(A. codonocephala 2n = 18, 50, 54 vs 2n = 50), 황해쑥(A. argyi 2n = 34, 36, 50 vs 2n = 34)의 6분류군이었다. 한국산 쑥속의 체세포 염색체수는 제비쑥, 더위지기, 참쑥, 황해쑥, 산쑥, 그늘쑥의 분류에 매우 유용한 형질이었다.

• Journal of applied mathematics & informatics
• /
• 제5권3호
• /
• pp.859-866
• /
• 1998

In this paper we shall prove weak(or strong) convergence of the iterates ${\chi_n} \;and \;{y_n}$ defined by $\chi-{n+1}= \alpha_nTy_n+(1-\alpha_n)S\chi_n , y_n=\beta_nT\chi_n+(1-\beta_n)\chi_n$ for all n$\geq$1, where $\alpha_n$ and $\beta_n$ satisfy 0$\leq\alpha_n,\beta_n\leq$b<1.

• 대한화학회지
• /
• 제53권5호
• /
• pp.512-520
• /
• 2009

본 연구에서는 반응성이 큰 황이 산소와 결합하여 산화황이 되고 이것들이 클러스터를 이루었 을 때의 구조와 결합에너지에 대하여 조사하였다. $S_{n}O_{n},\;S_{n}O_{2n},\;S_{n}O_{3n}\;(n\;=\;1{\sim}4)$까지의 여러 가능한 분자 구조를 B3LYP/6-311G** 이론수준까지 최적화 하였으며, 단량체($SO,\;SO_2,\;SO_3$)가 증가할 때의 결합에너지를 MP2/6-311G** 수준까지 계산하였다. $SnOn\;(n\;=\;1{\sim}4)$의 경우 S-O 단량체 증가에 따라 상대적으로 안정화되는 경향이 강하게 나타났으며, 약 20-25 kcal/mol 정도 증가하는 것으로 예측 되었다. 반면 $S_nO_{2n},\;S_nO_{3n} \;(n\;=\;1{\sim}4)$의 경우에는 $SO_2$ 나 $SO_3$ 의 증가에 따른 열역학적 안정성이 상대적으로 덜 안정화 되는 것으로 나타났으며, SO2 단량체가 증가함에 따른 결합에너지 변화는 2.2 kcal/mol, 그리고 $SO_3$ 단량체가 증가함에 따라 흡열반응으로 나타나 열역학적으로 더욱 불안정해질 것으로 예상된다.

• 대한화학회지
• /
• 제48권6호
• /
• pp.577-582
• /
• 2004

새로운 아자크라운 화합물인, 1,4-dioxa-7,10,13-triazacyclopentadecane-N,N',N''-triacetic acid, $N-ac_3[15]aneN_3O_2(II_a)$과 1,4-dioxa-7,10,13-triazacyclopentadecane-N,N',N''-tripropioc acid, $N-pr_3$[15]ane$N_3O_2(II_b)$는 이와 유사한 화합물의 합성방법을 수정하여 합성하였다. 합성된 이 아자크라운 화합물, $N-ac_3[15]aneN_3O_2와\;N-pr_3[15]aneN_3O_2$의 양성자화 상수값은 전위차법을 이용하여 PKAS 프로그램으로부터 측정되어졌다. 그리고 0.1 M $NaClO_4$수용액으로 이온강도를 조절하고, $25{\pm}0.1^{\circ}C$에서 란탄족금속인, $Ce^{3+},\;Eu^{3+},\;Gd^{3+}$ 및 $Yb^{3+}$과 리간드인 $N-ac_3[15]$ane$N_3O_2$와 $N-pr_3[15]aneN_3O_2$의 착물의 안정도상수를 전위차법을 이용하여 BEST 프로그램으로부터 구하였고, 또한 위와 같은 조건에서 전이금속인 $Co^{2+}$, $Ni^{2+}$, $Cu^{2+}$및 $Zn^{2+}$와 리간드인, $N-ac_3[15]aneN_3O_2$와 $N-pr_3[15]aneN_3O_2$의 착물의 안정도상수 값도 전위차법을 이용하여 BEST 프로그램으로부터 측정하였다. 합성된 아자크라운 화합물과 골격구조가 유사하고 아세트산과 프로피온산기를 포함하는, 1,7-dioxa-4,10,13-triazacyclopentadecane-N,N',N''-triacetic acid과 1,7-dioxa-4,10,13-triazacyclopentadecane-N,N',N''-tripropioc acid의 착물의 안정도를 비교분석하였다.

• 대한화학회지
• /
• 제35권6호
• /
• pp.707-712
• /
• 1991

수은 pool 전해조를 사용하여 (5:3) EtOH/4N-HCl 용액계에서 선택적인 -N-N=O기의 전기화학적 환원에 의해 N'-phenyl-N-(2-chloroethyl)-N-nitrosourea로부터 N'-phenyl-N-(2-chloroethyl)-N-aminourea를 합성하였다. 전기화학적 환원에 앞서 반응의 최적조건을 검토하기 위하여 몇 가지 N'-aryl-N-(2-chloroethyl)-N-nitrosourea 유사체에 대하여 pH변화에 따른 환원전위를 순환전압전류법으로 조사한 결과 pH에 따라 $E_p$값이 "-"쪽으로 이동하였으며 aryl기의 치환기 효과는 -N-N=O기의 환원 전위에 크게 영향을 미치지 않는 것으로 나타났다. 용액계의 pH에 따른 반응성을 조사한 결과 강산성 용액(pH<1)에서 반응이 가장 잘 진행되며 -0.7 V vs. Ag/AgCl/4 N-HCl에서 N-N=O기의 선택적인 4전자 환원반응에 의해 N-N$H_2$가 생성됨을 확인하였다.

• Animal Systematics, Evolution and Diversity
• /
• nspc7호
• /
• pp.1-90
• /
• 2009

Twenty-two new species of poecilostome copepods associated with marine invertebrates are described from the West Indies, Madagascar, and Pacific coast of Panama. They are Anthessius nosybensis n. sp. and Discanthessius solitarius n. gen. n. sp. in the Anthessiidae; Cemihyclops tenuis n. sp., Hemicyclops tripartitus n. sp., H. humesi n. sp., H. magnus n. sp., and Leptinogaster minuta n. sp. in the Clausidiidae; Schedomolgus crenulatus n. sp. and S. parvipediger n. sp. in the Anchimolgidae; Kelleria multiovigera n. sp. in the Kelleridae; Lichomolgus angustus n. sp. and L. fusiformis n. sp. in the Lichomolgidae; Pseudanthessius acutus n. sp., P. asper n. sp., and Tubiporicola pediger n. gen. n. sp. in the Pseudanthessiidae; Acanthomolgus tenuispinatus n. sp. and Notoxynus lokobensis n. sp. in the Rhynchomolgidae; Eupolymniphilus occidentalis n. sp. and E. brevicaudatus n. sp. in the Sabellephilidae; Enalcyonium robustum n. sp. and E. grandisetigerum n. sp. in the Lamippidae; and O. binoviger n. sp. in the Myicolidae. Hemicyclops geminus Stock is synonymized with H. columnaris Humes which is now known as a species of amphi-American distribution. Hemicyclops columnaris Humes, Modiolicola trabalis Humes, and Ostrincola breviseti Ho and Kim are redescribed.

• 약학회지
• /
• 제17권4호
• /
• pp.223-234
• /
• 1973

Sixteen compounds of N-aroyl-N'-(4'-alkoxyphenyl) thiourea derivative, twenty one compounds of N-aeryl-N'(3'-hydroxy-4'-alkoxycar-bonylphenyl) thiourea derivative, three compounds of N-aeroyl-N'-.alpha.-naphthyiourea derivative and three compounds of N-cyanoacetyl-N'-aroyl thiosemicarbazide derivative were syntrhesized as potential antitubercular agent and were subjected to screening test for antitubercular activity against Mycobacterium turberculosis H/sub 37/Rv by tube dilution method in vitro. Of the fourty three eompounds, N-p-cyanobenzoyl-N'-(4'-iso-butoxyphenyl) thiourea, N-p-cyanobenzoyl-N'-(4-n-amoxyphenyl)thiourea, N-furoyl-N'-(3'-hydroxy-4'-ethoxycarbonylphenyl)thiourea, N-p-cyanobenzoyl-N'-(3'-hydroxy-4'-n-butoxycarbonylphenyl)thiourea, N-p-cyanobenzoyl-N'-(3'-hydroxy-4'-n-amoxycarbonylphenyl)thiourea, and N-5-nitrofuroyl-N'(3'-hydroxy-4"-n-amoxycarbonylphrnyl)thiourea showed the growth inhibition of M. tuberculosis H/sub 37/Rv at the coccentraction og 10.mu.g/ml, respectively.

• Bulletin of the Korean Chemical Society
• /
• 제15권9호
• /
• pp.743-748
• /
• 1994

Photochemical reactions of saccharin with tertiary amines were explored. Saccharin was found to undergo an acid-base reaction with N-trimethylsilylmethyl-N,N-diethyl amine to form N-trimethylsilylmethyl-N,N-diethyl ammonium saccharin salt which is in equilibrium with free saccharin and N-trimethylsilylmethyl-N,N-diethyl amine insolution. Photoreaction of N-trimethylsilylmethyl-N,N-diethyl ammonium saccharin in $CH_3OH\;or\;CH_3CN$ results in the generation of desilylmethylated product, N,N-diethyl ammonium saccharin mainly along with benzamide. Photoreaction of N-methylsaccharin with N-trimethylsilylmethyl-N,N-diethyl amine in $CH_3OH$ leads to the production of o-(N-methylcarbamoyl)-N-ethylbenzenesulfonamid e as the major product along with N-methylbenzamide as the minor product. On the other hand, photoreaction of N,N,N-triethyl ammonium saccharin, generated from saccharin and triethylamine, produces N-methylbenzamide as the exclusive product. These photoreactions are quenched by oxygen indicating that triplets of saccharin and N-methylsaccharin are the reactive excited states. Based on the consideration of the redox potentials of saccharin and N-trimethylsilylmethyl-N,N-diethyl amine, and the nature of photoproducts, pathways involving initial triplet state single electron transfer are proposed for photoreactions of the saccharins with the ${\alpha}$-silylamine.