Occurrence, biogenesis, and synthesis of biologically active carbazole alkaloids

AW Schmidt, KR Reddy, HJ Knölker - Chemical reviews, 2012 - ACS Publications
Since our previous review, 1 there has been a tremendous development in the field of
carbazole alkaloids. New synthetic methodologies have been developed, existing …

Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids

K Nepali, S Sharma, M Sharma, PMS Bedi… - European journal of …, 2014 - Elsevier
A Hybrid drug which comprises the incorporation of two drug pharmacophores in one single
molecule are basically designed to interact with multiple targets or to amplify its effect …

Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts

DW Fry, PJ Harvey, PR Keller, WL Elliott… - Molecular cancer …, 2004 - AACR
PD 0332991 is a highly specific inhibitor of cyclin-dependent kinase 4 (Cdk4)(IC50, 0.011
μmol/L) and Cdk6 (IC50, 0.016 μmol/L), having no activity against a panel of 36 additional …

The cervicovaginal microbiota-host interaction modulates Chlamydia trachomatis infection

VL Edwards, SB Smith, EJ McComb, J Tamarelle, B Ma… - MBio, 2019 - Am Soc Microbiol
The mechanism (s) by which Lactobacillus-dominated cervicovaginal microbiota provide a
barrier to Chlamydia trachomatis infection remain (s) unknown. Here we evaluate the impact …

Predicting stem cell fate changes by differential cell cycle progression patterns

M Roccio, D Schmitter, M Knobloch, Y Okawa… - …, 2013 - journals.biologists.com
Stem cell self-renewal, commitment and reprogramming rely on a poorly understood
coordination of cell cycle progression and execution of cell fate choices. Using existing …

Targeting the cell division cycle in cancer: CDK and cell cycle checkpoint kinase inhibitors

I Collins, MD Garrett - Current opinion in pharmacology, 2005 - Elsevier
The cyclin-dependent kinase (CDK) family of serine/threonine kinases regulate progression
through each stage of the cell division cycle and as such are major targets for deregulation …

Design, synthesis, molecular docking and biological activity evaluation of some novel indole derivatives as potent anticancer active agents and apoptosis inducers

AMS El-Sharief, YA Ammar, A Belal… - Bioorganic …, 2019 - Elsevier
Abstract Reaction of 5-morphilinosulfonylisatin (1) with acetophenones (2a–e) afforded 3-
hydroxy-3-substituted-2-oxoindoles 3a-e, when treated with acetic acid the expected 3 …

Metabolic regulation of pluripotency and germ cell fate through α‐ketoglutarate

J Tischler, WH Gruhn, J Reid, E Allgeyer… - The EMBO …, 2019 - embopress.org
An intricate link is becoming apparent between metabolism and cellular identities. Here, we
explore the basis for such a link in an in vitro model for early mouse embryonic …

Pyrido[2,3-d]pyrimidin-7-ones as Specific Inhibitors of Cyclin-Dependent Kinase 4

SN VanderWel, PJ Harvey, DJ McNamara… - Journal of medicinal …, 2005 - ACS Publications
Inhibition of the cell cycle kinase, cyclin-dependent kinase-4 (Cdk4), is expected to provide
an effective method for the treatment of proliferative diseases such as cancer. The pyrido [2 …

Mitigation of hematologic radiation toxicity in mice through pharmacological quiescence induced by CDK4/6 inhibition

SM Johnson, CD Torrice, JF Bell… - The Journal of …, 2010 - Am Soc Clin Investig
Total body irradiation (TBI) can induce lethal myelosuppression, due to the sensitivity of
proliferating hematopoietic stem/progenitor cells (HSPCs) to ionizing radiation (IR). No …