Synthesis and Biological Activity of the Functional Derivatives of 3- and 4-(Dimethyl-aminomethyl)-1,2-dithiolanes

1992 ◽  
Vol 56 (10) ◽  
pp. 1623-1631 ◽  
Author(s):  
Hideki Uneme ◽  
Hiroyuki Mitsudera ◽  
Junji Yamada ◽  
Toshiya Kamikado ◽  
Yoshiaki Kono ◽  
...  
Keyword(s):  
Biological Activity ◽  
Functional Derivatives ◽  
Derivatives Of

Functional derivatives of thiophene. XIX. Synthesis and biological activity of some esters of 2-benzoylaminothiophene-3-carboxylic acids

1980 ◽  
Vol 14 (12) ◽  
pp. 861-863
Author(s):  
I. A. Kharizomenova ◽  
A. N. Grinev ◽  
N. V. Samsonova ◽  
N. V. Kaplina ◽  
M. V. Kapustina ◽  
...  
Keyword(s):  
Biological Activity ◽  
Carboxylic Acids ◽  
Functional Derivatives ◽  
Derivatives Of

Struktur-Wirkungsbeziehungen von Analogen und Homologen von Blepharisma, dem niedermolekularem Konjugationshormon von Blepharisma japonicum / Structure-Activity-Relation of Analogues and Homologues of Blepharismone, the Low-Molecular Conjugation Hormone of Blepharisma japonicum

1982 ◽  
Vol 37 (11-12) ◽  
pp. 1136-1140 ◽  
Author(s):  
Michael Entzeroth ◽  
Lothar Jaenicke
Keyword(s):  
Biological Activity ◽  
Structural Relationship ◽  
Aromatic System ◽  
Structure Activity ◽  
Functional Derivatives ◽  
Blepharisma Japonicum ◽  
Derivatives Of

Abstract Some functional derivatives of blepharismone, the low-molecular conjugation hormone of Blepharisma japonicum, were synthesised and tested for their biological activity. The lipophilicity constant of the substituent in 5-position of the aromatic system directly correlates with the conjugation-inducing effect of this substance. Any change in the N-formyl-position leads to compounds less active than blepharismone, non-active or even inhibitory. Blepharismone-related kynurenine derivatives are inhibitors of the gamone activity depending on structural relationship.

ChemInform Abstract: FUNCTIONAL DERIVATIVES OF THIOPHENE. XIX. SYNTHESIS AND BIOLOGICAL ACTIVITY OF ESTERS OF 2-BENZOYLAMINOTHIOPHENE-3-CARBOXYLIC ACIDS

1981 ◽  
Vol 12 (21) ◽  
Author(s):  
I. A. KHARIZOMENOVA ◽  
A. N. GRINEV ◽  
N. V. SAMSONOVA ◽  
N. V. KAPLINA ◽  
M. V. KAPUSTINA ◽  
...  
Keyword(s):  
Biological Activity ◽  
Carboxylic Acids ◽  
Functional Derivatives ◽  
Derivatives Of

Synthesis and Biological Potentials of Quinoline Analogues: A Review of Literature

2019 ◽  
Vol 16 (7) ◽  
pp. 653-688 ◽  
Author(s):  
Leena Kumari ◽  
Salahuddin ◽  
Avijit Mazumder ◽  
Daman Pandey ◽  
Mohammad Shahar Yar ◽  
...  
Keyword(s):  
Biological Activity ◽  
Heterocyclic Compounds ◽  
Building Blocks ◽  
Vital Role ◽  
Review Of Literature ◽  
Drug Discovery Process ◽  
Active Compounds ◽  
Lead Compounds ◽  
Synthetic Approaches ◽  
Derivatives Of

Heterocyclic compounds are well known for their different biological activity. The heterocyclic analogs are the building blocks for synthesis of the pharmaceutical active compounds in the organic chemistry. These derivatives show various type of biological activity like anticancer, antiinflammatory, anti-microbial, anti-convulsant, anti-malarial, anti-hypertensive, etc. From the last decade research showed that the quinoline analogs plays a vital role in the development of newer medicinal active compounds for treating various type of disease. Quinoline reported for their antiviral, anticancer, anti-microbial and anti-inflammatory activity. This review will summarize the various synthetic approaches for synthesis of quinoline derivatives and to check their biological activity. Derivatives of quinoline moiety plays very important role in the development of various types of newer drugs and it can be used as lead compounds for future investigation in the field of drug discovery process.

Synthesis and Biological Activity of 28-Amide Derivatives of 23-Hydroxy Betulinic Acid as Antitumor Agent Candidates

2013 ◽  
Vol 9 (7) ◽  
pp. 920-925 ◽  
Author(s):  
Yi Bi ◽  
Jinyi Xu ◽  
Fei Sun ◽  
Xiaoming Wu ◽  
Wencai Ye ◽  
...  
Keyword(s):  
Biological Activity ◽  
Betulinic Acid ◽  
Antitumor Agent ◽  
Amide Derivatives ◽  
Derivatives Of

The melanocyte stimulating activity of N-nitroso-2-chloroethyl-carbamoyl derivatives of α-melanotropin fragments

1988 ◽  
Vol 53 (11) ◽  
pp. 2574-2582 ◽  
Author(s):  
Hedvig Medzihradszky-Schweiger ◽  
Helga Süli-Vargha ◽  
József Bódi ◽  
Kálmán Medzihradszky
Keyword(s):  
Biological Activity ◽  
Active Site ◽  
Frog Skin ◽  
Terminal Sequence ◽  
Subsequent Reaction ◽  
Affinity Labels ◽  
Derivatives Of

A number of N-nitroso-2-chloroethyl-carbamoyl (Q(NO)) derivatives of α-melanotropin fragments have been synthesized and their effect on the frog skin melanocytes studied. Peptides substituted in this way possess the biological activity of the parent compounds, indicating that they preserved their receptor recognizing ability. These compounds can therefore serve as affinity labels. Some of these derivatives, related to the C-terminal sequence of α-melanotropin show prolonged darkening reaction, which does not influence the subsequent reaction of melanocytes with α-melanotropin. The Q(NO)-derivative of a fragment derived from the classical active site of the hormone shows, however, inhibition of the effect of α-melanotropin. It can be concluded that the latter peptide acts through the melanotropin receptor, while others, related to the C-terminal sequence of the hormone through another mechanism.

ChemInform Abstract: BROMINATION OF FUNCTIONAL DERIVATIVES OF SOME VINYLACETYLENE HYDROCARBONS AND SILICON HYDROCARBONS

1976 ◽  
Vol 7 (44) ◽  
pp. no-no
Author(s):  
T. R. BORONOEVA ◽  
N. N. BELYAEV ◽  
M. D. STADNICHUK ◽  
A. A. PETROV
Keyword(s):  
Functional Derivatives ◽  
Derivatives Of
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