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"hsin l w"的相关文件
显示项目 36-60 / 60 (共2页)
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| 臺大學術典藏 |
2018-09-10T05:11:14Z |
Stereoselective synthesis of morphine fragments trans- and cis-octahydro-1H-benzo[4,5]furo[3,2-e]isoquinolines
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Hsin, L.-W.;Chang, L.-T.;Chen, C.-W.;Hsu, C.-H.;Chen, H.-W.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T05:11:14Z |
The effects of CRF antagonists, antalarmin, CP154,526, LWH234, and R121919, in the forced swim test and on swim-induced increases in adrenocorticotropin in rats
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Jutkiewicz, E.M.;Wood, S.K.;Houshyar, H.;Hsin, L.-W.;Rice, K.C.;Woods, J.H.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T05:11:13Z |
Asymmetric total synthesis of (-)-octahydro-1H-benzofuro[3,2-e] isoquinoline, a partial structure of morphine
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Hsin, L.-W.;Chen, C.-W.;Chang, L.-T.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:42:54Z |
Synthesis of 3-[4-acyl-2-(1-methoxy-1-methylethyl)morpholin-3-yl]- benzonitriles as novel potassium channel openers
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Lin, M.-S.;Hsin, L.-W.;Cheng, C.-Y.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:42:54Z |
Synthesis and opioid activity of 7-oxygenated 2,3,4,4a,5,6,7,7a-octahydro-1H-benzofuro[3,2-e]isoquinolin-9-ols
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Cheng, C.-Y.;Hsin, L.-W.;Tsai, M.-C.;Schmidt, W.K.;Smith, C.;William Tam, S.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:37:18Z |
Synthesis of galanthamine analogs as acetylcholinesterase inhibitors via intramolecular heck cvclization
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Liang, P.-H.;Hsin, L.-W.;Pong, S.-L.;Hsu, C.-H.;Cheng, C.-Y.; PI-HUI LIANG |
| 臺大學術典藏 |
2018-09-10T04:24:43Z |
A concise synthesis of (S)-(+)-1-(4-{2-[bis-(4-fluorophenyl)methoxy]-ethyl} piperazin-1-yl)-2-phenylpropan-2-ol dimaleate
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Prisinzano, T.;Hsin, L.-W.;Folk, J.E.;Flippen-Anderson, J.L.;George, C.;Jacobson, A.E.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:24:43Z |
Synthesis and dopamine transporter affinity of chiral 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(2-hydroxypropyl)piperazines as potential cocaine abuse therapeutic agents
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Hsin, L.-W.;Prisinzano, T.;Wilkerson, C.R.;Dersch, C.M.;Horel, R.;Jacobson, A.E.;Rothman, R.B.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:24:43Z |
Synthesis of galanthamine analogs as acetylcholinesterase inhibitors via intramolecular heck cvclization
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Liang, P.-H.;Hsin, L.-W.;Pong, S.-L.;Hsu, C.-H.;Cheng, C.-Y.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:04:49Z |
Selective reversible and irreversible ligands for the κ opioid receptor
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Cheng, C.-Y.;Wu, S.-C.;Hsin, L.-W.;William Tam, S.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:04:48Z |
CRHR1 Receptor binding and lipophilicity of pyrrolopyrimidines, potential nonpeptide corticotropin-releasing hormone type 1 receptor antagonists
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Hsin, L.-W.;Tian, X.;Webster, E.L.;Coop, A.;Caldwell, T.M.;Jacobson, A.E.;Chrousos, G.P.;Gold, P.W.;Habib, K.E.;Ayala, A.;Eckelman, W.C.;Contoreggi, C.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:04:48Z |
Development of long-acting dopamine transporter ligands as potential cocaine-abuse therapeutic agents: Chiral hydroxyl-containing derivatives of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy) ethyl]-4-(3-phenylpropyl)piperazine
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Hsin, L.-W.;Dersch, C.M.;Baumann, M.H.;Stafford, D.;Glowa, J.R.;Rothman, R.B.;Jacobson, A.E.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T04:04:48Z |
N-Arylated pyrrolidin-2-ones and morpholin-3-ones as potassium channel openers
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Liang, P.-H.;Hsin, L.-W.;Cheng, C.-Y.; LING-WEI HSIN; PI-HUI LIANG |
| 臺大學術典藏 |
2018-09-10T04:04:48Z |
Synthesis of 1,4-dihydro-2-phenyl-4,4-bis(4-pyridinylmethyl)-2H-isoquinolin-3-one and related compounds as acetylcholine release enhancers
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Lin, M.-S.;Hsin, L.-W.;Tsai, H.-B.;Tsai, M.-C.;Cheng, C.-Y.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T03:41:21Z |
The development of a potential single photon emission computed tomography (SPECT) imaging agent for the corticotropin-releasing hormone receptor type 1
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Tian, X.;Hsin, L.-W.;Webster, E.L.;Contoreggi, C.;Chrousos, G.P.;Gold, P.W.;Habib, K.;Ayala, A.;Eckelman, W.C.;Jacobson, A.E.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2018-09-10T03:23:36Z |
Synthesis and biological activity of fluoro-substituted pyrrolo[2,3-d]pyrimidines: The development of potential positron emission tomography imaging agents for the corticotropin-releasing hormone type 1 receptor
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Hsin, L.-W.;Webster, E.L.;Chrousos, G.P.;Gold, P.W.;Eckelman, W.C.;Contoreggi, C.;Rice, K.C.; LING-WEI HSIN |
| 國立臺灣大學 |
2008-09 |
A Practical Asymmetric Synthesis of the ACNO Fragment of Morphine Alkaloids.
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Hsin, L.-W.; Chang, L.-T.; Liou, H.-L. |
| 國立臺灣大學 |
2008-05 |
Design and Synthesis of 2- and 3-Substituted-3-phenylpropyl Analogs of 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(Diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine: Role of Amino, Fluoro, Hydroxyl, Meth
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Hsin, L.-W.; Chang, L.-T.; Rothman, R. B.; Dersch, C. M.; Jacobson, A. E.; Rice, K. C. |
| 國立臺灣大學 |
2008-02 |
WRC-213, an L-Methionine-conjugated Mitoxantrone Derivative, Displays Anticancer Activity with Reduced Cardiotoxicity and Drug Resistance: Identification of Topoisomerase II Inhibition and Apoptotic Machinery in Prostate Cancers
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Hsiao, C.-J.; Li, T.-K.; Chan, Y.-L.; Hsin, L.-W.; Liao, C.-H.; Lee, C.-H.; Lyu, P.-C.; Guh, J.-H. |
| 國立臺灣大學 |
2008-01 |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone–amino acid conjugates
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Hsin, L.-W.; Wang, H.-P.; Kao, P.-H.; Lee, O.; Chen, W.-R.; Chen, H.-W.; Guh, J.-H.; Chan, Y.-L.; His, C.-P.; Yang, M.-S.; Li, T.-K.; Lee, C.-H. |
| 國立臺灣大學 |
2004-12 |
Total synthesis of lycoramine: an intramolecular Heck reaction to the galanthamine skeleton.
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Liang, P. -H.; Liou, J. -P.; Hsin, L. -W.; Cheng, C. -Y. |
| 臺大學術典藏 |
2004 |
Intramolecular Heck cyclization to the galanthamine-type alkaloids: Total synthesis of (±)-lycoramine
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Liang, P.-H.;Liu, J.-P.;Hsin, L.-W.;Cheng, C.-Y.; LING-WEI HSIN; PI-HUI LIANG |
| 國立臺灣大學 |
2003-06 |
Synthesis of galanthamine analogs as acetylcholinesterase inhibitors via intra-molecular Heck cyclization.
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Liang, P. -H.; Hsin, L. -W.; Pong, S. -L.; Hsu, C. -H.; Cheng, C. -Y. |
| 國立臺灣大學 |
2002-12 |
N-Arylated Pyrrolidin-2-ones and Morpholin-3-ones as Potassium Channel Openers.
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Liang, P. -H.; Hsin, L. -W.; Cheng, C. -Y. |
| 臺大學術典藏 |
2000 |
Synthesis of [3H](4-fluorobutyl)propyl[2,5,6-trimethyl-7-(2,4,6-trimethylphenyl)pyrrolo[2,3-d]pyrimidin-4-yl]amine: A potent radioligand for corticotropin-releasing hormone type 1 receptor
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LING-WEI HSIN; Hsin, L.-W.;Webster, E.L.;Chrousos, G.P.;Gold, P.W.;Eckelman, W.C.;Contoreggi, C.;Rice, K.C. |
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