1999
DOI: 10.1016/s0960-894x(99)00088-8
|View full text |Cite
|
Sign up to set email alerts
|

Cytotoxic effects of NSL-1406, a new thienopyrimidine derivative, on leukocytes and osteoclasts

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
23
0

Year Published

1999
1999
2020
2020

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 34 publications
(23 citation statements)
references
References 21 publications
0
23
0
Order By: Relevance
“…Due to the similarity of reported pyrimidine as potential cancer chemotherapeutic agents [4]. Pyrimidine derivative showed a higher and faster peak of brain uptake and a faster washout from the brain in the normal mice.…”
Section: Biological Studymentioning
confidence: 96%
See 1 more Smart Citation
“…Due to the similarity of reported pyrimidine as potential cancer chemotherapeutic agents [4]. Pyrimidine derivative showed a higher and faster peak of brain uptake and a faster washout from the brain in the normal mice.…”
Section: Biological Studymentioning
confidence: 96%
“…Therefore, many methods for the synthesis of substituted Pyrroles have been described in the literature (1,2). Design and synthesis of thieno [2, 3-d] pyrimidine as potential cancer chemotherapeutic agents have been extensively studied (4)(5)(6)(7)(8)(9)(10).Recently, some new pyridine, pyrimidine and their derivatives have been synthesized and used as analgesic, anticonvulsant and anti-parkinsonian agents (11)(12)(13)(14). Catalysts are used to improve the radiochemical yield and decrease the reaction time in isotopic exchange reaction especially in radioiodination reactions with the short lived 321 I isotope.…”
Section: Introductionmentioning
confidence: 99%
“…11) Literature screening revealed that many thienopyrimidine derivatives A, B and C have been developed and showed pronounced cytotoxic activity. [12][13][14][15][16][17][18][19][20] In particular, they are currently an important group of compounds that have anticancer activity especially against solid tumors (e.g., breast and ovarian). [21][22][23][24] Several mechanisms have been reported for the cytotoxic activity of thienopyrimidines including: inhibition of protein kinases (PKs) either as competitive or noncompetitive inhibitors.…”
Section: -7)mentioning
confidence: 99%
“…Among these heterocyclic compounds, multisubstituted 2-aminothiophenes are privileged structures as they have attracted considerable attention in designing of bioactive molecules and found in several biologically active and natural compounds[1-4] due to their broad spectrum of biological activities, such as antioxidant [5], antibacterial [6], antifungal [7], antitumor [8], antiinflammatory [9], antianxiety [10] and antitubercular activities. Additionally, Nfunctionalized morpholines have found to possess diverse pharmacological activities.…”
Section: Introductionmentioning
confidence: 99%