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1
Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors
Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors
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Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors

V J Hruby D Lu; S D Sharma; Ana Maria de Lauro Castrucci; R A Kesterson; F A Al-Obeidi; M E Hadley; R D Cone

Easton v.38, n.18, p.3454-61, 1995 Journal of Medicinal Chemistry

Easton 1995

Item não circula. Consulte sua biblioteca.(Acessar)

2
Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors
Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cyclic lactam 'ALFA'-melanotropin analogues of ac-nle4-cyclo [asp5,d-phe7, lys10] 'ALFA'-melanocyte-stimulating hormone- (4-10)-nh2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors

V J Hruby D Lu; S D Sharma; Ana Maria de Lauro Castrucci; R A Kesterson; F A Al-Obeidi; M E Hadley; R D Cone

Easton v.38, n.18, p.3454-61, 1995 Journal of Medicinal Chemistry

Easton 1995

Item não circula. Consulte sua biblioteca.(Acessar)

3
The Design, Synthesis, and Characterizations of Spore Germination Inhibitors Effective against an Epidemic Strain of Clostridium difficile
The Design, Synthesis, and Characterizations of Spore Germination Inhibitors Effective against an Epidemic Strain of Clostridium difficile
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The Design, Synthesis, and Characterizations of Spore Germination Inhibitors Effective against an Epidemic Strain of Clostridium difficile

Sharma, Shiv K ; Yip, Christopher ; Esposito, Emilio Xavier ; Sharma, Prateek V ; Simon, Matthew P ; Abel-Santos, Ernesto ; Firestine, Steven M

Journal of medicinal chemistry, 2018-08, Vol.61 (15), p.6759-6778 [Periódico revisado por pares]

United States: American Chemical Society

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4
(Bis)urea and (Bis)thiourea Inhibitors of Lysine-Specific Demethylase 1 as Epigenetic Modulators
(Bis)urea and (Bis)thiourea Inhibitors of Lysine-Specific Demethylase 1 as Epigenetic Modulators
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(Bis)urea and (Bis)thiourea Inhibitors of Lysine-Specific Demethylase 1 as Epigenetic Modulators

Sharma, Shiv K ; Wu, Yu ; Steinbergs, Nora ; Crowley, Michael L ; Hanson, Allison S ; Casero, Robert A ; Woster, Patrick M

Journal of medicinal chemistry, 2010-07, Vol.53 (14), p.5197-5212 [Periódico revisado por pares]

United States: American Chemical Society

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5
Discovery and Structure-Based Optimization of 2‑Ureidothiophene-3-carboxylic Acids as Dual Bacterial RNA Polymerase and Viral Reverse Transcriptase Inhibitors
Discovery and Structure-Based Optimization of 2‑Ureidothiophene-3-carboxylic Acids as Dual Bacterial RNA Polymerase and Viral Reverse Transcriptase Inhibitors
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Discovery and Structure-Based Optimization of 2‑Ureidothiophene-3-carboxylic Acids as Dual Bacterial RNA Polymerase and Viral Reverse Transcriptase Inhibitors

Elgaher, Walid A. M ; Sharma, Kamal K ; Haupenthal, Jörg ; Saladini, Francesco ; Pires, Manuel ; Real, Eleonore ; Mély, Yves ; Hartmann, Rolf W

Journal of medicinal chemistry, 2016-08, Vol.59 (15), p.7212-7222 [Periódico revisado por pares]

United States: American Chemical Society

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6
Novel N‑Linked Aminopiperidine-Based Gyrase Inhibitors with Improved hERG and in Vivo Efficacy against Mycobacterium tuberculosis
Novel N‑Linked Aminopiperidine-Based Gyrase Inhibitors with Improved hERG and in Vivo Efficacy against Mycobacterium tuberculosis
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Novel N‑Linked Aminopiperidine-Based Gyrase Inhibitors with Improved hERG and in Vivo Efficacy against Mycobacterium tuberculosis

Hameed P, Shahul ; Patil, Vikas ; Solapure, Suresh ; Sharma, Umender ; Madhavapeddi, Prashanti ; Raichurkar, Anandkumar ; Chinnapattu, Murugan ; Manjrekar, Praveena ; Shanbhag, Gajanan ; Puttur, Jayashree ; Shinde, Vikas ; Menasinakai, Sreenivasaiah ; Rudrapatana, Suresh ; Achar, Vijayashree ; Awasthy, Disha ; Nandishaiah, Radha ; Humnabadkar, Vaishali ; Ghosh, Anirban ; Narayan, Chandan ; Ramya, V. K ; Kaur, Parvinder ; Sharma, Sreevalli ; Werngren, Jim ; Hoffner, Sven ; Panduga, Vijender ; Kumar, C. N. Naveen ; Reddy, Jitendar ; Kumar KN, Mahesh ; Ganguly, Samit ; Bharath, Sowmya ; Bheemarao, Ugarkar ; Mukherjee, Kakoli ; Arora, Uma ; Gaonkar, Sheshagiri ; Coulson, Michelle ; Waterson, David ; Sambandamurthy, Vasan K ; de Sousa, Sunita M

Journal of medicinal chemistry, 2014-06, Vol.57 (11), p.4889-4905 [Periódico revisado por pares]

United States: American Chemical Society

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7
Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents
Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents
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Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents

Sharma, Moni ; Chauhan, Kuldeep ; Shivahare, Rahul ; Vishwakarma, Preeti ; Suthar, Manish K ; Sharma, Abhisheak ; Gupta, Suman ; Saxena, Jitendra K ; Lal, Jawahar ; Chandra, Preeti ; Kumar, Brijesh ; Chauhan, Prem M. S

Journal of medicinal chemistry, 2013-06, Vol.56 (11), p.4374-4392 [Periódico revisado por pares]

United States: American Chemical Society

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8
Nonclassical Phenyl Bioisosteres as Effective Replacements in a Series of Novel Open-Source Antimalarials
Nonclassical Phenyl Bioisosteres as Effective Replacements in a Series of Novel Open-Source Antimalarials
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Nonclassical Phenyl Bioisosteres as Effective Replacements in a Series of Novel Open-Source Antimalarials

Tse, Edwin G ; Houston, Sevan D ; Williams, Craig M ; Savage, G. Paul ; Rendina, Louis M ; Hallyburton, Irene ; Anderson, Mark ; Sharma, Raman ; Walker, Gregory S ; Obach, R. Scott ; Todd, Matthew H

Journal of medicinal chemistry, 2020-10, Vol.63 (20), p.11585-11601 [Periódico revisado por pares]

United States: American Chemical Society

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9
Non-steroidal CYP17A1 Inhibitors: Discovery and Assessment
Non-steroidal CYP17A1 Inhibitors: Discovery and Assessment
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Non-steroidal CYP17A1 Inhibitors: Discovery and Assessment

Wróbel, Tomasz M. ; Jørgensen, Flemming Steen ; Pandey, Amit V. ; Grudzińska, Angelika ; Sharma, Katyayani ; Yakubu, Jibira ; Björkling, Fredrik

Journal of medicinal chemistry, 2023-05, Vol.66 (10), p.6542-6566 [Periódico revisado por pares]

United States: American Chemical Society

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10
Discovery of Novel Alkylated (bis)Urea and (bis)Thiourea Polyamine Analogues with Potent Antimalarial Activities
Discovery of Novel Alkylated (bis)Urea and (bis)Thiourea Polyamine Analogues with Potent Antimalarial Activities
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Discovery of Novel Alkylated (bis)Urea and (bis)Thiourea Polyamine Analogues with Potent Antimalarial Activities

Verlinden, Bianca K ; Niemand, Jandeli ; Snyman, Janette ; Sharma, Shiv K ; Beattie, Ross J ; Woster, Patrick M ; Birkholtz, Lyn-Marie

Journal of medicinal chemistry, 2011-10, Vol.54 (19), p.6624-6633 [Periódico revisado por pares]

United States: American Chemical Society

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Deste Autor:

  1. Al-Obeidi, F
  2. Castrucci, A
  3. Hadley, M
  4. Sharma, S
  5. Cone, R

Neste Assunto:

  1. Life Sciences & Biomedicine
  2. Pharmacology & Pharmacy
  3. Science & Technology
  4. Chemistry, Medicinal
  5. Animals

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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