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[Studies on the evaporation of thermolabile drugs].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Müller F, Herrmann G.
PMID: 5276819
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):10-5.

No abstract available.

Cite
Müller F, Herrmann G. Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):10-5
Müller, F., & Herrmann, G. (1971). Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 10-5.
Müller, F, and Herrmann, G. "Untersuchungen über das Eindampfen thermolabiler Stoffe." [Studies on the evaporation of thermolabile drugs]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 10-5.
Müller F, Herrmann G. Untersuchungen über das Eindampfen thermolabiler Stoffe. [Studies on the evaporation of thermolabile drugs]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):10-5. German. PMID: 5276819.
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[Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Fenner H.
PMID: 5276827
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):47-51. doi: 10.1002/ardp.19713040110.

No abstract available.

Cite
Fenner H. Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):47-51doi: 10.1002/ardp.19713040110.
Fenner, H. (1971). Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 47-51. https://doi.org/10.1002/ardp.19713040110
Fenner, H. "Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten." [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 47-51. doi: https://doi.org/10.1002/ardp.19713040110
Fenner H. Substituenteneffekte bei Phenothiazin-Radikalen. 3. Radikalkationen aus Phenothiazin-Derivaten mit Elektronen-Donator-Substituenten. [Substitution effects in phenothiazine radicals. 3. Cation radicals from phenothiazine derivatives with electron donor substituents]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):47-51. doi: 10.1002/ardp.19713040110. German. PMID: 5276827.
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[Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen].

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft

Knabe J, Powilleit H.
PMID: 5276828
Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):52-7. doi: 10.1002/ardp.19713040111.

No abstract available.

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Knabe J, Powilleit H. Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Arch Pharm Ber Dtsch Pharm Ges. 1971;304(1):52-7doi: 10.1002/ardp.19713040111.
Knabe, J., & Powilleit, H. (1971). Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft, 304(1), 52-7. https://doi.org/10.1002/ardp.19713040111
Knabe, J, and Powilleit, H. "Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff." [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft vol. 304,1 (1971): 52-7. doi: https://doi.org/10.1002/ardp.19713040111
Knabe J, Powilleit H. Dihydroisochinolin-Umlagerung. 14. Uber den Eifluss einiger Substituenten am Stickstoff. [Dihydroisoquinoline rearrangement. 14. Influence of some substituents on nitrogen]. Arch Pharm Ber Dtsch Pharm Ges. 1971 Jan;304(1):52-7. doi: 10.1002/ardp.19713040111. PMID: 5276828.
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CHEMICAL SYNTHESIS. Going with the flow.

Science (New York, N.Y.)

Martin RE.
PMID: 27034365
Science. 2016 Apr 01;352(6281):44-5. doi: 10.1126/science.aaf3065.

No abstract available.

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Martin RE. CHEMICAL SYNTHESIS. Going with the flow. Science. 2016;352(6281):44-5doi: 10.1126/science.aaf3065.
Martin, R. E. (2016). CHEMICAL SYNTHESIS. Going with the flow. Science (New York, N.Y.), 352(6281), 44-5. https://doi.org/10.1126/science.aaf3065
Martin, Rainer E. "CHEMICAL SYNTHESIS. Going with the flow." Science (New York, N.Y.) vol. 352,6281 (2016): 44-5. doi: https://doi.org/10.1126/science.aaf3065
Martin RE. CHEMICAL SYNTHESIS. Going with the flow. Science. 2016 Apr 01;352(6281):44-5. doi: 10.1126/science.aaf3065. PMID: 27034365.
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Editorial.

Bioorganic & medicinal chemistry letters

Boger DL.
PMID: 26343827
Bioorg Med Chem Lett. 2015 Nov 01;25(21):4713. doi: 10.1016/j.bmcl.2015.08.082. Epub 2015 Sep 01.

No abstract available.

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Boger DL. Editorial. Bioorg Med Chem Lett. 2015;25(21):4713doi: 10.1016/j.bmcl.2015.08.082.
Boger, D. L. (2015). Editorial. Bioorganic & medicinal chemistry letters, 25(21), 4713. https://doi.org/10.1016/j.bmcl.2015.08.082
Boger, Dale L. "Editorial." Bioorganic & medicinal chemistry letters vol. 25,21 (2015): 4713. doi: https://doi.org/10.1016/j.bmcl.2015.08.082
Boger DL. Editorial. Bioorg Med Chem Lett. 2015 Nov 01;25(21):4713. doi: 10.1016/j.bmcl.2015.08.082. Epub 2015 Sep 01. PMID: 26343827.
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No Denying It: Medicinal Chemistry Training Is in Big Trouble.

Journal of medicinal chemistry

Rafferty MF.
PMID: 27668824
J Med Chem. 2016 Dec 22;59(24):10859-10864. doi: 10.1021/acs.jmedchem.6b00741. Epub 2016 Oct 07.

There has been little consensus between the pharmaceutical industry and academic communities concerning the best approach to train medicinal chemists for drug discovery. For decades the pharmaceutical industry has shown preference for synthetic organic graduates over candidates with degrees...

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Rafferty MF. No Denying It: Medicinal Chemistry Training Is in Big Trouble. J Med Chem. 2016;59(24):10859-10864doi: 10.1021/acs.jmedchem.6b00741.
Rafferty, M. F. (2016). No Denying It: Medicinal Chemistry Training Is in Big Trouble. Journal of medicinal chemistry, 59(24), 10859-10864. https://doi.org/10.1021/acs.jmedchem.6b00741
Rafferty, Michael F. "No Denying It: Medicinal Chemistry Training Is in Big Trouble." Journal of medicinal chemistry vol. 59,24 (2016): 10859-10864. doi: https://doi.org/10.1021/acs.jmedchem.6b00741
Rafferty MF. No Denying It: Medicinal Chemistry Training Is in Big Trouble. J Med Chem. 2016 Dec 22;59(24):10859-10864. doi: 10.1021/acs.jmedchem.6b00741. Epub 2016 Oct 07. PMID: 27668824.
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Medicinal Chemists of the 21(st) Century--Who Are We and Where to Go?.

ChemMedChem

Nussbaumer P.
PMID: 25924977
ChemMedChem. 2015 Jul;10(7):1133-9. doi: 10.1002/cmdc.201500133. Epub 2015 Apr 29.

Many recent articles have dealt with the future challenges in medicinal chemistry. Here, I discuss my concerns over the future of medicinal chemists, who have to be skilled and knowledgeable in many different fields, particularly in the context of...

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Nussbaumer P. Medicinal Chemists of the 21(st) Century--Who Are We and Where to Go?. ChemMedChem. 2015;10(7):1133-9doi: 10.1002/cmdc.201500133.
Nussbaumer, P. (2015). Medicinal Chemists of the 21(st) Century--Who Are We and Where to Go?. ChemMedChem, 10(7), 1133-9. https://doi.org/10.1002/cmdc.201500133
Nussbaumer, Peter. "Medicinal Chemists of the 21(st) Century--Who Are We and Where to Go?." ChemMedChem vol. 10,7 (2015): 1133-9. doi: https://doi.org/10.1002/cmdc.201500133
Nussbaumer P. Medicinal Chemists of the 21(st) Century--Who Are We and Where to Go?. ChemMedChem. 2015 Jul;10(7):1133-9. doi: 10.1002/cmdc.201500133. Epub 2015 Apr 29. PMID: 25924977.
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Self-assembled organic nanostructures in medicinal chemistry: advances and applications.

Current topics in medicinal chemistry

Rodrigues J, Rathi B.
PMID: 25930062
Curr Top Med Chem. 2015;15(13):1161. doi: 10.2174/1568026615666150330105539.

No abstract available.

Cite
Rodrigues J, Rathi B. Self-assembled organic nanostructures in medicinal chemistry: advances and applications. Curr Top Med Chem. 2015;15(13):1161doi: 10.2174/1568026615666150330105539.
Rodrigues, J., & Rathi, B. (2015). Self-assembled organic nanostructures in medicinal chemistry: advances and applications. Current topics in medicinal chemistry, 15(13), 1161. https://doi.org/10.2174/1568026615666150330105539
Rodrigues, Joao, and Rathi, Brijesh. "Self-assembled organic nanostructures in medicinal chemistry: advances and applications." Current topics in medicinal chemistry vol. 15,13 (2015): 1161. doi: https://doi.org/10.2174/1568026615666150330105539
Rodrigues J, Rathi B. Self-assembled organic nanostructures in medicinal chemistry: advances and applications. Curr Top Med Chem. 2015;15(13):1161. doi: 10.2174/1568026615666150330105539. PMID: 25930062.
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Pierre-Joseph Macquer: Chemistry in the French Enlightenment.

Osiris

Lehman C.
PMID: 26103758
Osiris. 2014;29:245-61. doi: 10.1086/678106.

Despite recent studies of chemistry courses and of academic research at the beginning of the eighteenth century, the perception of chemistry in the French Enlightenment has often been overshadowed by Lavoisier's works. This article proposes three specific case studies...

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Lehman C. Pierre-Joseph Macquer: Chemistry in the French Enlightenment. Osiris. 2014;29:245-61doi: 10.1086/678106.
Lehman, C. (2014). Pierre-Joseph Macquer: Chemistry in the French Enlightenment. Osiris, 29245-61. https://doi.org/10.1086/678106
Lehman, Christine. "Pierre-Joseph Macquer: Chemistry in the French Enlightenment." Osiris vol. 29 (2014): 245-61. doi: https://doi.org/10.1086/678106
Lehman C. Pierre-Joseph Macquer: Chemistry in the French Enlightenment. Osiris. 2014;29:245-61. doi: 10.1086/678106. PMID: 26103758.
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[Formulation Optimization of Zuojin Floating-Bioadhesive Pellets by Central Composite Design-Response Surface Methodology].

Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials

Xu F, Wang LL, Shi ZQ, Chen F, Sun DM.
PMID: 26930991
Zhong Yao Cai. 2015 Sep;38(9):1969-73.

OBJECTIVE: To optimize the formulation of Zuojin floating-bioadhesive pellets by the central composite design-response surface methodology (CCD-RSM).METHODS: In the formulation design using CCD-RSM, independent variables were the amounts of sodium bicarbonate (X1), HPMC (X2) and MCC (X3) as factors....

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Xu F, Wang LL, Shi ZQ, et al. [Formulation Optimization of Zuojin Floating-Bioadhesive Pellets by Central Composite Design-Response Surface Methodology]. Zhong Yao Cai. 2015;38(9):1969-73
Xu, F., Wang, L. L., Shi, Z. Q., Chen, F., & Sun, D. M. (2015). [Formulation Optimization of Zuojin Floating-Bioadhesive Pellets by Central Composite Design-Response Surface Methodology]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 38(9), 1969-73.
Xu, Feng, et al. "[Formulation Optimization of Zuojin Floating-Bioadhesive Pellets by Central Composite Design-Response Surface Methodology]." Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials vol. 38,9 (2015): 1969-73.
Xu F, Wang LL, Shi ZQ, Chen F, Sun DM. [Formulation Optimization of Zuojin Floating-Bioadhesive Pellets by Central Composite Design-Response Surface Methodology]. Zhong Yao Cai. 2015 Sep;38(9):1969-73. Chinese. PMID: 26930991.
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Preface.

Current drug delivery

Toth I.
PMID: 27447004
Curr Drug Deliv. 2016;13(1):3. doi: 10.2174/156720181301160314153150.

No abstract available.

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Toth I. Preface. Curr Drug Deliv. 2016;13(1):3doi: 10.2174/156720181301160314153150.
Toth, I. (2016). Preface. Current drug delivery, 13(1), 3. https://doi.org/10.2174/156720181301160314153150
Toth, Istvan. "Preface." Current drug delivery vol. 13,1 (2016): 3. doi: https://doi.org/10.2174/156720181301160314153150
Toth I. Preface. Curr Drug Deliv. 2016;13(1):3. doi: 10.2174/156720181301160314153150. PMID: 27447004.
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Neonatal Formulations: The Need for a Tailored, Knowledge Driven Approach.

Current pharmaceutical design

Allegaert K, Cosaert K, van den Anker JN.
PMID: 26323412
Curr Pharm Des. 2015;21(39):5674-9. doi: 10.2174/1381612821666150901110207.

To attain effective and safe pharmacotherapy in neonates, caregivers have to consider both the clinical characteristics of the newborn and the pharmacokinetic estimates of a given compound during prescription and administration. Overall, clearance in neonates is low when compared...

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Allegaert K, Cosaert K, van den Anker JN. Neonatal Formulations: The Need for a Tailored, Knowledge Driven Approach. Curr Pharm Des. 2015;21(39):5674-9doi: 10.2174/1381612821666150901110207.
Allegaert, K., Cosaert, K., & van den Anker, J. N. (2015). Neonatal Formulations: The Need for a Tailored, Knowledge Driven Approach. Current pharmaceutical design, 21(39), 5674-9. https://doi.org/10.2174/1381612821666150901110207
Allegaert, Karel, et al. "Neonatal Formulations: The Need for a Tailored, Knowledge Driven Approach." Current pharmaceutical design vol. 21,39 (2015): 5674-9. doi: https://doi.org/10.2174/1381612821666150901110207
Allegaert K, Cosaert K, van den Anker JN. Neonatal Formulations: The Need for a Tailored, Knowledge Driven Approach. Curr Pharm Des. 2015;21(39):5674-9. doi: 10.2174/1381612821666150901110207. PMID: 26323412.
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Showing 13 to 24 of 236 entries