Anticancer steroids: linking natural and semi-synthetic compounds

JAR Salvador, JFS Carvalho, MAC Neves… - Natural product …, 2013 - pubs.rsc.org
Covering: up to 2012 Steroids, a widespread class of natural organic compounds occurring
in animals, plants and fungi, have shown great therapeutic value for a broad array of …

Various treatment options for benign prostatic hyperplasia: A current update

A Shrivastava, VB Gupta - Journal of mid-life health, 2012 - journals.lww.com
In benign prostatic hyperplasia (BPH) there will be a sudden impact on overall quality of life
of patient. This disease occurs normally at the age of 40 or above and also is associated …

Steroidal 5α-reductase and 17α-hydroxylase/17, 20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases

JAR Salvador, RMA Pinto, SM Silvestre - The Journal of steroid …, 2013 - Elsevier
The role of steroidal inhibitors of androgen biosynthesis as potential weapons in the
treatment of prostatic diseases, such as benign prostatic hyperplasia and prostatic cancer …

Molecular docking assisted 3D-QSAR study of benzylidene-2, 4-thiazolidinedione derivatives as PTP-1B inhibitors for the management of Type-2 diabetes mellitus

SK Verma, S Thareja - RSC advances, 2016 - pubs.rsc.org
Insulin resistance is the pathophysiological factor behind the etiology and progression of
Type 2 diabetes mellitus (T2DM), a metabolic syndrome that is continuously increasing in …

Steroidal 5α-reductase inhibitors: a comparative 3D-QSAR study review

S Thareja - Chemical Reviews, 2015 - ACS Publications
Benign prostatic hyperplasia (BPH) is the noncancerous growth of the prostate gland due to
overproliferation of the stromal and glandular elements of the prostate, resulting in the …

A review on steroidal 5α-reductase inhibitors for treatment of benign prostatic hyperplasia

J Sun, H Xiang, LL Yang… - Current medicinal …, 2011 - ingentaconnect.com
Benign prostatic hyperplasia (BPH) is a kind of common noncancerous prostate gland
enlargement with growing tendency in recent years. 5α-reductase is the key enzyme …

Self-organizing molecular field analysis of 2, 4-thiazolidinediones: A 3D-QSAR model for the development of human PTP1B inhibitors

S Thareja, S Aggarwal, TR Bhardwaj… - European journal of …, 2010 - Elsevier
Thiazolidinediones (TZDs) have been recently developed to treat diabetic patients that can
reverse insulin resistance by activation of gamma isoform of peroxisome proliferator …

Formylchromone derivatives as novel and selective PTP-1B inhibitors: a drug design aspect using molecular docking-based self-organizing molecular field analysis

SK Verma, S Thareja - Medicinal Chemistry Research, 2016 - Springer
Protein tyrosine phosphatase-1B (PTP-1B) acts as a negative regulator of the insulin
signaling pathway. It is evident from the literature that formylchromone derivatives exhibit …

3D-QSAR studies on unsaturated 4-azasteroids as human 5α-reductase inhibitors: a self organizing molecular field analysis approach

S Aggarwal, S Thareja, TR Bhardwaj… - European journal of …, 2010 - Elsevier
Azasteroids have been reported as inhibitors of human 5α-reductase enzyme. These were
designed by substitution of one carbon atom of steroidal A ring by heteroatom nitrogen. Due …

Synthesis and biological evaluation of novel unsaturated carboxysteroids as human 5α-reductase inhibitors: a legitimate approach

S Aggarwal, S Thareja, TR Bhardwaj… - European journal of …, 2012 - Elsevier
In the present study, novel steroidal 17a-substituted 3-cyano-17a-aza-D-homo-3, 5-
androstadien-17-ones (12–19) and 17a-substituted 17-oxo-17a-aza-D-homo-3, 5 …