<?xml version="1.0" encoding="utf-8"?>
<Journal>
<Journal-Info>
<name>International Journal of Pharma and Bio Sciences</name>
<website>ijpbs.net</website>
<email>editorijpbs@rediffmail.com (or) editorofijpbs@yahoo.com (or) prasmol@rediffmail.com</email>
</Journal-Info>
<article>
<article-id pub-id-type='other'>10.22376/ijpbs.2019.10.1.p1-12</article-id>
<issue_number>Volume 3 Issue 2</issue_number>
<issue_period>2012 (April - June)</issue_period>
<title>Cytotoxity Of Marine Algal Steroids In Hela Cells – 2d &amp; 3d Qsar Approach </title>
<abstract>The steroids of the brown alga  lessThan i greaterThan Turbinaria conoides lessThan /i greaterThan  were recognized as having mild-to-moderate cytotoxicity in HeLa cell, as it is being investigated towards determination of toxicity with various drugs. The cytotoxicity in HeLa cells was expressed in terms of 50% cytotoxic concentration (CC lessThan sub greaterThan 50 lessThan /sub greaterThan ). These oxygenated steroids exhibited cytotoxicity against HeLa cells with CC lessThan sub greaterThan 50 lessThan /sub greaterThan  values ranging from 60.9 µg/mL to  greaterThan 100 µg/mL. To analyse for their cytotoxicity, Quantitative structure activity relationship (QSAR) study was performed. It was done by multiple regression analysis with simulated annealing method of partial least square (PLS) model. A PLS model (r lessThan sup greaterThan 2 lessThan /sup greaterThan  = 0.90, q lessThan sup greaterThan 2 lessThan /sup greaterThan  = 0.80, pred_r lessThan sup greaterThan 2 lessThan /sup greaterThan  = 0.96) was used as a base of consensus prediction of cytotoxicity. QSAR studies indicated the carbon atom (T_C_O_4: 12%) and any atom (T_2_2_7: 15%) away from the oxygen and double bond respectively, atomic valence connectivity index-order 0 (chiV0: 50%) and distance between most hydrophobic and hydrophilic point on the VanderWaals surface (XAMostHydrophobicHydrophilic distance: 20%) correlating well with mild cytotoxicity while the partial charges of the molecules (dipole moment: 25%) contributing moderate cytotoxicity. The 3D QSAR model further described that less bulkier substituent is required at steric site S_2441. Thus it can be concluded from the present study that cytotoxicity can be achieved by modifying the aromatic ring and preferring less bulky group to reduce steric hindrance.</abstract>
<authors>S.Sadish Kumar And Jayendra</authors>
<keywords>Turbinaria conoides, oxygenated steroids, cytotoxicity, QSAR</keywords>
<pages>204-212</pages>
</article>
</Journal>
