Search Results - "Dagnino, Raymond"

1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities by CHEN CHEN, DAGNINO, Raymond JR, HUANG, Charles Q, MCCARTHY, James R, GRIGORIADIS, Dimitri E

“…Cyclizations of alkylhydrazines with N-acyl-S-methylisothioureas, readily synthesized from acyl chlorides, sodium thioisocyanate, dialkylamines then methyl…”
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Design and Synthesis of a Series of Non-Peptide High-Affinity Human Corticotropin-Releasing Factor1 Receptor Antagonists by Chen, Dagnino, Raymond, De Souza, Errol B, Grigoriadis, Dimitri E, Huang, Charles Q, Kim, Kyung-Il, Liu, Zhengyu, Moran, Terry, Webb, Thomas R, Whitten, Jeffrey P, Xie, Yun Feng, McCarthy, James R

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Automated synthesis of peptide C-terminal aldehydes by Murphy, Aileen M, Dagnino, Raymond, Vallar, Pureza L, Trippe, Anthony J, Sherman, Shannon L, Lumpkin, Richard H, Tamura, Susan Y, Webb, Thomas R

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Corrigendum to “1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities” [Bioorg. Med. Chem. Lett. 11 (2001) 3165–3168] by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

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Corrigendum to “1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: Novel synthesis via cyclization of N-acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF1) receptor antagonist activities” [Bioorg. Med. Chem. Lett. 11 (2001) 3165–3168] by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

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A Convenient Synthetic Method for Trisubstituted s-Triazines by Chen, Chen, Dagnino, Raymond, McCarthy, James R

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1-Alkyl-3-amino-5-aryl-1 H-[1,2,4]triazoles: novel synthesis via cyclization of N-Acyl- S-methylisothioureas with alkylhydrazines and their potent corticotropin-Releasing factor-1 (CRF 1) receptor antagonist activities by Chen, Chen, Dagnino, Raymond, Huang, Charles Q., McCarthy, James R., Grigoriadis, Dimitri E.

“…Cyclizations of alkylhydrazines with N-acyl- S-methylisothioureas, readily synthesized from acyl chlorides, sodium thioisocyanate, dialkylamines then methyl…”
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Design and Synthesis of a Series of Non-Peptide High-Affinity Human Corticotropin-Releasing Factor 1 Receptor Antagonists by Chen, Dagnino, Raymond, De Souza, Errol B., Grigoriadis, Dimitri E., Huang, Charles Q., Kim, Kyung-Il, Liu, Zhengyu, Moran, Terry, Webb, Thomas R., Whitten, Jeffrey P., Xie, Yun Feng, McCarthy, James R.

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Environment-selective synergism using self-assembling cytotoxic and antimicrobial agents by Rideout, D, Jaworski, J, Dagnino, Jr, R

“…Environment-selective synergistic toxicity using combinations of aldehydes and hydrazine derivatives was demonstrated in two different model systems in vitro…”
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