DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair,With death on the horizon, This will not stop me, Gods call only..........
DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 29Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK PHARMA at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contributio
n

Monday, 11 April 2016

Donna L. Romero

 

Donna Romero

Pharmaceuticals Professional




Donna L. Romero currently owns her own consulting company, Pharma-Vation Consulting, LLC. She received her Ph.D. from the University of Wisconsin-Madison from Professor Barry Trost. She has many years of experience in the pharmaceutical industry working for The Upjohn Company, Pharmacia, and Pfizer and consulting for the NIH Blueprint program and a variety of biotechnology companies such as Nimbus Discovery..
 

Donna Romero is the Head of IRAK4 Program at Nimbus Therapeutics and has more than 20 years of experience in drug discovery and development and pharmaceutical research management. She began her career at the Upjohn Company where she was the inventor of the non-nucleoside reverse transcriptase inhibitor Rescriptor® marketed for the treatment of HIV. Subsequently, Dr. Romero held project team leadership positions on the Cell Cycle and Bacterial Genomics Teams. She has broad experience leading and supervising cross-disciplinary drug discovery teams in multiple therapeutic areas in the Upjohn, Pharmacia, and Pfizer pharmaceutical companies. Since leaving Pfizer in 2007, where she was a Senior Director in Medicinal Chemistry, Dr. Romero has been an independent consultant working with a broad array of biotechnology companies and with the Spinal Muscular Atrophy Lead Development team for the NINDS and the NIH Blueprint project

 links
 
 https://www.linkedin.com/in/donna-romero-0a98a23

*E-mail: dlromero@nimbusdiscovery.com. Phone: 636-579-6870.
 http://www.nimbustx.com/about-us/leadership

Summary

Specialties:Drug Discovery Project Leadership
Medicinal chemistry Strategy
Analog design and management of synthetic chemistry

Experience

Owner

Pharma-Vation Consulting, LLC
– Present (8 years 10 months)
Pharma-Vation Consulting provides drug discovery, medicinal chemistry, computational and synthetic chemistry consulting services. Clients include NIH, BioEnergenics, AzoRx, Michigan High Throughput Screening Center, Xenon, Reaction Biology, and SW Michigan Life Sciences Venture Fund.

Director

Nimbus Discovery
(3 years)

Vice President of Chemical Sciences and Pharmaceutical Development

Emiliem, Inc.
(6 months)
Emiliem, Inc. is a privately-held biopharmaceutical company focused on the discovery and development of molecular targeted cancer therapies with offices in the San Francisco Bay area and Kalamazoo, Michigan.

Senior Director

Pfizer Inc
(3 years 11 months)
• Supervising ~35-45 medicinal chemists in the three therapeutic areas (resourcing projects, mentoring, performance assessment, salary administration, recruiting).
• Chemistry Leadership Team, Discovery Leadership Team, CVMED Therapeutic Area Chemistry Liason, CVMED Global Management Team, Hypertension and Thrombosis New Target Teams, Management consultant/mentor to program teams.
• Leading the “Improving Project Success” initiative - a Global cross-site, cross-functional team that is analyzing causes of project/target attrition in Discovery and recommending strategies to improve project survival
• St. Louis Point of Contact for the Global Pfizer Closed Loop (CLD) Project
• Led a cross-functional team to define and implement processes and infrastructure that improves the output of the drug discovery pipeline
• Built high-throughput autopurification & centralized sample logistics capabilities in StL

Director

Pharmacia
(5 years)
Supervised and mentored ~50 medicinal chemists in the Infectious Diseases and CNS therapeutic areas.
Bacterial Genome Team Leader. Led a multidisciplinary group of ~50 scientists in identifying essentail targets, developing screening strategies, triaging hits, and optimizing novel antibacterial lead templates.
Identified 5 novel inhibitors of 4 distinct antibacterial targets that proceeded to the chemistry optimization stage.
Devised "reverse genomics" strategy of mining the compound collection that led to the identification of a novel inhibitor of a well-established target (gyrase).
Managed external research collaborations with Cetek and NeoGenesis. Managed external CRO chemistry (Albany Molecular, and Pharmeco).

Scientist

Upjohn
(10 years)

Additional Info

  • Advice for Contacting Donna

    I am interested in starting or becoming involved in existing biotech business opportunities in the St. Louis area. I am available for virtual Drug Discovery Project Leadership opportunities, i.e. leading and managing drug discovery projects. I am also interested in general medicinal chemistry and synthetic organic chemistry consulting opportunities. Inquiries regarding potential career opportunities are welcomed.






  • Publication number: 20160068543
    Abstract: The present invention provides compounds, compositions thereof, and methods of using the same.
    Type: Application
    Filed: September 17, 2015
    Publication date: March 10, 2016
    Inventors: Jeremy Robert Greenwood, Geraldine C. Harriman, Rosana Kapeller-Libermann, Craig E. Masse, Shaughnessy Robinson, Donna L. Romero, Mee Shelley, Ronald T. Wester
    Patent number: 9278973
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Grant
    Filed: October 25, 2013
    Date of Patent: March 8, 2016
    Assignee: BIOENERGENIX LLC
    Inventors: John McCall, Robert C. Kelly, Donna L. Romero
    Publication number: 20160002256
    Abstract: The present invention provides thienopyridine compounds, compositions thereof, and methods of using the same.
    Type: Application
    Filed: June 17, 2015
    Publication date: January 7, 2016
    Inventors: Geraldine C. Harriman, Ronald T. Wester, Donna L. Romero, Craig E. Masse, Shaughnessy Robinson, Jeremy R. Greenwood
    Publication number: 20160002257
    Abstract: The present invention provides arylo-fused thienopyrimidine compounds, compositions thereof, and methods of using the same.
    Type: Application
    Filed: June 17, 2015
    Publication date: January 7, 2016
    Inventors: Donna L. Romero, Shaughnessy Robinson, Matthew David Wessel, Jeremy Robert Greenwood
    Patent number: 9221843
    Abstract: The present invention relates to compounds and methods useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of disease.
    Type: Grant
    Filed: October 24, 2013
    Date of Patent: December 29, 2015
    Assignee: Tetra Discovery Partners, LLC
    Inventors: Mark E. Gurney, Timothy J. Hagen, Xuesheng Mo, A. Samuel Vellekoop, Donna L. Romero, Robert F. Campbell, Joel R. Walker, Lei Zhu
    Patent number: 9212190
    Abstract: The present invention provides compounds, compositions thereof, and methods of using the same.
    Type: Grant
    Filed: January 10, 2013
    Date of Patent: December 15, 2015
    Assignee: Nimbus Iris, Inc.
    Inventors: Geraldine C. Harriman, Ronald T. Wester, Donna L. Romero, Shaughnessy Robinson, Mee Shelley, Matthew David Wessel, Jeremy Robert Greenwood, Craig E. Masse, Rosana Kapeller-Libermann
    Patent number: 9193693
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Grant
    Filed: September 29, 2014
    Date of Patent: November 24, 2015
    Assignee: BioEnergenix LLC
    Inventors: John M. McCall, Donna L. Romero, John McKearn, Michael Clare
    Publication number: 20150329498
    Abstract: The present invention provides quinazoline and quinoline compounds, compositions thereof, and methods of using the same. Also disclosed is the activity of such compounds as inhibitors of IRAK enzymes.
    Type: Application
    Filed: April 21, 2015
    Publication date: November 19, 2015
    Inventors: Donna L. Romero, Shaughnessy Robinson, Jeremy Robert Greenwood, Mee Shelley, Craig E. Masse, Geraldine C. Harriman
    Patent number: 9175007
    Abstract: The present invention provides compounds, compositions thereof, and methods of using the same.
    Type: Grant
    Filed: January 8, 2014
    Date of Patent: November 3, 2015
    Assignee: Nimbus Iris, Inc.
    Inventors: Jeremy Robert Greenwood, Geraldine C. Harriman, Rosana Kapeller-Libermann, Craig E. Masse, Shaughnessy Robinson, Donna L. Romero, Mee Shelley, Ronald T. Wester
    Publication number: 20150290169
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Application
    Filed: March 19, 2015
    Publication date: October 15, 2015
    Inventors: John M. McCall, Donna L. Romero, Michael Clare
    Publication number: 20150284395
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Application
    Filed: October 25, 2013
    Publication date: October 8, 2015
    Inventors: John McCall, Robert C. Kelly, Donna L. Romero
    Publication number: 20150274740
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Application
    Filed: October 25, 2013
    Publication date: October 1, 2015
    Inventors: John McCall, Robert C. Kelly, Donna L. Romero
    Publication number: 20150266875
    Abstract: The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.
    Type: Application
    Filed: February 27, 2015
    Publication date: September 24, 2015
    Inventors: Craig E. MASSE, Jeremy Robert GREENWOOD, Donna L. ROMERO, Geraldine C. HARRIMAN, Ronald T. WESTER, Mee SHELLEY, Joshua Jahmil KENNEDY-SMITH, Markus DAHLGREN
    Patent number: 9085586
    Abstract: The present invention provides arylo-fused thienopyrimidine compounds, compositions thereof, and methods of using the same.
    Type: Grant
    Filed: July 11, 2013
    Date of Patent: July 21, 2015
    Assignee: Nimbus Iris, Inc.
    Inventors: Donna L. Romero, Shaughnessy Robinson, Matthew David Wessel, Jeremy Robert Greenwood
    Patent number: 9073902
    Abstract: Disclosed herein are substituted quinoxaline carboxylic acids of Formula (I): and compositions thereof, which may be useful as inhibitors of PAS Kinase (PASK) activity in a human or animal for the treatment of diseases such as diabetes mellitus.
    Type: Grant
    Filed: January 5, 2012
    Date of Patent: July 7, 2015
    Assignee: BioEnergenix, LLC
    Inventors: John M. McCall, Donna L. Romero
    Patent number: 9067948
    Abstract: The present invention provides thienopyridine compounds, compositions thereof, and methods of using the same.
    Type: Grant
    Filed: July 11, 2013
    Date of Patent: June 30, 2015
    Assignee: Nimbus Iris, Inc.
    Inventors: Geraldine C. Harriman, Ronald T. Wester, Donna L. Romero, Craig E. Masse, Shaughnessy Robinson, Jeremy Robert Greenwood
    Publication number: 20150141422
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Application
    Filed: January 26, 2015
    Publication date: May 21, 2015
    Inventors: John M. McCall, Donna L. Romero, Michael Clare
    Publication number: 20150119362
    Abstract: The present invention relates to compounds and methods useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of disease.
    Type: Application
    Filed: October 24, 2013
    Publication date: April 30, 2015
    Inventors: Mark E. Gurney, Timothy J. Hagen, Joel R. Walker, Xuesheng Mo, A. Samuel Vellekoop, Robert Campbell, Lei Zhu, Donna L. Romero
    Patent number: 9012637
    Abstract: Disclosed herein are substituted pyrazinyl acrylic acids of Formula (IV): and compositions thereof, which may be useful as inhibitors of PAS Kinase (PASK) activity in a human or animal for the treatment of diseases such as diabetes mellitus.
    Type: Grant
    Filed: April 28, 2014
    Date of Patent: April 21, 2015
    Assignee: BioEnergenix, LLC
    Inventors: John M. McCall, Donna L. Romero, Michael Clare
    Publication number: 20150031679
    Abstract: Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibiting PAS Kinase (PASK) activity in a human or animal subject are also provided for the treatment of diseases such as diabetes mellitus.
    Type: Application
    Filed: September 29, 2014
    Publication date: January 29, 2015
    Inventors: John M. McCall, Donna L. Romero, John McKearn, Michael Clare 
     
     
     
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    see all...........................



    *E-mail: dlromero@nimbusdiscovery.com. Phone: 636-579-6870.


    Recent Advances in the Discovery of Small Molecule Inhibitors of Interleukin-1 Receptor-Associated Kinase 4 (IRAK4) as a Therapeutic Target for Inflammation and Oncology Disorders

    Miniperspective

     Nimbus Discovery, 25 First Street, Suite 404, Cambridge, Massachusetts 02141, United States
     Schrödinger Inc., 120 West Forty-Fifth Street, New York, New York 10036, United States
    J. Med. Chem.201558 (1), pp 96–110
    DOI: 10.1021/jm5016044
    http://pubs.acs.org/doi/full/10.1021/jm5016044






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     à¤¸ुकून उतना ही देना प्रभू, जितने से जिंदगी चल जाये। औकात बस इतनी देना, कि औरों का भला हो जाये।
    DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO …..FOR BLOG HOME CLICK HERE



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    Anthony Melvin Crasto Dr.

      amcrasto@gmail.com

    09b37-misc2b027LIONEL MY SON
    He was only in first standard in school when I was hit by a deadly one in a million spine stroke called acute transverse mylitis, it made me 90% paralysed and bound to a wheel chair, Now I keep him as my source of inspiration and helping millions, thanks to millions of my readers who keep me going and help me to keep my son happy

    सुकून उतना ही देना प्रभू, जितने से
    जिंदगी चल जाये।
    औकात बस इतनी देना,
    कि औरों का भला हो जाये।
    Read all about Organic Spectroscopy on ORGANIC SPECTROSCOPY INTERNATIONAL  
     

    Saturday, 9 April 2016

    Susanta Samajdar Research Director at Aurigene Discovery Technologies


    Susanta Samajdar

    Susanta Samajdar

    Research Director at Aurigene Discovery Technologies



    Aurigene Discovery Technologies Limited
    39-40, KIADB Industrial Area Electronic City Ph II, Hosur Road
    Bangalore , Karnataka 560100
    India



    Susanta Samajdar, Ph.D., Research Director, Medicinal Chemistry, Aurigene Discovery Technologies Limited Susanta Samajdar received his Ph.D. in Synthetic Organic Chemistry from Indian Association for the Cultivation of Science (IACS), Kolkata and subsequently moved to MD Anderson Cancer Center for a Post-Doctoral training on anti-cancer drug discovery. He has over 12 years of synthetic and Medicinal Chemistry research experience in Indian Industries. Susanta has experience in leading multi-disciplinary drug discovery teams that successfully delivered several preclinical development candidates. He has elaborate experience in working with Kinases and other target classes like GPCRs, Ion channels, Proteases and NHRs, across different therapeutic areas like Oncology, Pain and Inflammation and Neurosciences.

     Susanta Samajdar
    links
    https://www.facebook.com/susanta.samajdar
    https://www.researchgate.net/profile/Susanta_Samajdar
    https://profiles.google.com/114544433547394350208/about
    https://in.linkedin.com/in/susanta-samajdar-b6025821
    http://selectbioindia.net/proceedings/Report%20MCI2015.pdf

    Susanta Samajdar, Research Director, Aurigene Discovery Technologies Limited

    Dr. Susanta Samajdar received his PhD in Synthetic Organic Chemistry from Indian Association for the Cultivation of Science (IACS), Kolkata and subsequently moved to MD Anderson Cancer Center for a Post-Doctoral Research on anti-cancer drug discovery. He has over 15 years of synthetic and Medicinal Chemistry research experience in Indian Industries. Susanta has experience in leading multi-disciplinary drug discovery teams that successfully delivered several preclinical development candidates. He has experience in working with various target classes including GPCRs, Ion channels, Proteases, Kinases, NHRs, Epigenetics etc across different therapeutic areas like Oncology, Pain and Inflammation, Metabolic Disorders and Neurosciences. He has more than 20 publications and several patents to his credit.

    Experience


    Research Director in Medicinal Chemistry

    Aurigene Discovery Technologies
    – Present (4 years 2 months)Bangalore

    Director

    Jubilant Biosys
    (9 months)Bangalore

    Associate Director

    Jubilant Biosys
    (4 years 11 months)Bangalore
    Drug Discovery Medicinal Chemistry

    Scientific Manager

    Syngene International
    (4 years)





    Education


    Kandi Raj College

    BSc, Chemistry



     

     Abstract Image


    Simple Synthesis of Substituted Pyrroles

    The University of Texas, M. D. Anderson Cancer Center, Department of Molecular Pathology, Box 89, 1515 Holcombe Boulevard, Houston, Texas 77030 %bbanik@mail.mdanderson.org
    J. Org. Chem., 2004, 69 (1), pp 213–216



    Journal: Australian Journal of Chemistry - AUST J CHEM , vol. 63, no. 1, 2010





    Abstract C190: Potent and selective inhibition of CDK7 by novel covalent inhibitors

    Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; November 5-9, 2015; Boston, MA

    Abstract

    Cyclin-dependent kinase 7 (CDK7) is an important constituent of the cellular transcriptional machinery, where it phosphorylates the C-terminal domain (CTD) of RNAP polymerase II (RNAPII). Because many tumor types are critically dependent on transcription for maintenance of their oncogenic state, pharmacological modulation of CDK7 kinase activity is considered as an approach to treat cancer. Multiple series of CDK7 inhibitors were identified by iterative medicinal chemistry efforts and SAR based approach. Early compounds were optimized towards attaining good physicochemical properties, high potency, good selectivity and desirable pharmacokinetic profile to achieve anti-tumor activity. We have identified compounds from two distinct chemical series that are highly potent in inhibiting CDK7 in biochemical assays. These inhibitors demonstrate time-dependent inhibition of CDK7 indicating covalent nature of binding. The compounds showed potent anti-proliferative activity in cell lines derived from various tumor types and this was accompanied by CDK7 modulation in cells as monitored by pS5RNAPII levels. They have excellent drug-like characteristics including solubility, permeability, metabolic stability and good oral bioavailability. In a broad panel of kinases (332 kinase), selected compounds from both series showed good selectivity profile. Tolerability and efficacy studies are ongoing with selected early leads to test their impact on tumor growth inhibition in xenograft models. We have identified novel and selective CDK7 covalent inhibitors from two series with desirable drug-like properties, which are being evauated for anti-tumor activity in xenograft models.
    Citation Format: Ramulu Poddutoori, Leena K. Satyam, Girish Daginakatte, Subhendu Mukherjee, Sivapriya Marappan, Sreevalsam Gopinath, Raghuveer Ramachandra, Anirudha Lakshminarasimhan, Manoj Pothuganti, Shilpa Nayak, Nandish C, Chandranath Naik, Ravindra MV, Madhu Dabbeeru, Thomas Antony, Chetan Pandit, Murali Ramachandra, Shekar Chelur, Susanta Samajdar. Potent and selective inhibition of CDK7 by novel covalent inhibitors. [abstract]. In: Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2015 Nov 5-9; Boston, MA. Philadelphia (PA): AACR; Mol Cancer Ther 2015;14(12 Suppl 2):Abstract nr C190.




     

    Event Abstract

    Discovery of potent and selective retinoid related orphan receptor gamma (RORγ) inverse agonists for the treatment of Th17 mediated diseases

    • 1 Aurigene Discovery Technologies Ltd., India
    Background: Th17 cells play a key pro-inflammatory role in a variety of autoimmune diseases. The nuclear hormone receptor RORγ controls the differentiation of Th17 cells and expression of IL-17.
    Methods: Novel RORγ inverse agonists were designed using structure and knowledge based methods. Compounds were screened in a RORγ radio-ligand binding assay using 3H 25- Hydroxycholesterol, as well as in a cell based reporter assay to demonstrate inverse agonism. Selected compounds were screened against RORα to evaluate selectivity. Crystal structure of RORγ in complex with known inverse agonists as well as novel compounds, were solved. Th17 differentiation assay was developed using primary mouse CD4+ve T-cells to determine functional effect of the compounds. Pharmacokinetic profile in mice was determined for selected compounds.
    Results: Novel hits from multiple structural classes have been identified, with IC50 in the range of 5 – 500 nM in binding assay. Compounds from the lead series demonstrated good activity (< 1 μM) in reporter assay. Co-crystal structure of novel compounds clearly showed the mode of binding. Several compounds demonstrated > 10 fold selectivity against RORα in a reporter assay. Compounds from multiple series have shown significant inhibition of IL-17 release from differentiated Th17 cells. Lead compounds have shown good pharmacokinetic properties in mice.
    Conclusions: We have identified novel and structurally diverse small molecule inverse agonists of
    RORγ. Selectivity against RORα and cell based activity has been demonstrated for compounds from multiple series. Relevant efficacy models have been established and profiling of lead compounds in these models in on-going.
    Keywords: RORγ, Autoimmune Diseases, Th17 Cells, IL-17, Psoriasis
    Conference: 15th International Congress of Immunology (ICI), Milan, Italy, 22 Aug - 27 Aug, 2013.
    Presentation Type: Abstract
    Topic: Immune-mediated disease pathogenesis
    Citation: Nellore K, Bejugam M, Ramanathan A, Mukherjee S, Lakshminarasimhan A, Dodheri SS, Rao N, Damarla R, Samajdar S and Subramanya H (2013). Discovery of potent and selective retinoid related orphan receptor gamma (RORγ) inverse agonists for the treatment of Th17 mediated diseases. Front. Immunol. Conference Abstract: 15th International Congress of Immunology (ICI). doi: 10.3389/conf.fimmu.2013.02.00678
    Received: 13 Jun 2013; Published Online: 22 Aug 2013.
    * Correspondence: Dr. Hosahalli Subramanya, Aurigene Discovery Technologies Ltd., Bangalore, India, hosahalli_s@aurigene.com


    Asymmetric synthesis of anticancer β-lactams via Staudinger reaction

    • Authors:
      • Bimal K. Banik
      • Susanta Samajdar
      • Frederick F. Becker
    • View Affiliations
    • Published online on: Monday, March 1, 2010
    • Pages: 319-321 DOI: 10.3892/mmr_00000259

    Abstract

    This study describes the symmetric synthesis of novel β-lactams derived from chrysene directed towards their SAR, as well as their biological activities against several cancer cell lines in vitro. To our knowledge, this is the first report on the synthesis and biological evaluation of optically active anticancer β-lactams. That these anticancer effects are not uniform against all tumor lines suggests that the target of the action of these compounds is highly specific.


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     à¤¸ुकून उतना ही देना प्रभू, जितने से जिंदगी चल जाये। औकात बस इतनी देना, कि औरों का भला हो जाये।
    DRUG APPROVALS BY DR ANTHONY MELVIN CRASTO …..FOR BLOG HOME CLICK HERE



    Join me on Linkedin

    View Anthony Melvin Crasto Ph.D's profile on LinkedIn

    Join me on Facebook FACEBOOK
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    Anthony Melvin Crasto Dr.

      amcrasto@gmail.com

    09b37-misc2b027LIONEL MY SON
    He was only in first standard in school when I was hit by a deadly one in a million spine stroke called acute transverse mylitis, it made me 90% paralysed and bound to a wheel chair, Now I keep him as my source of inspiration and helping millions, thanks to millions of my readers who keep me going and help me to keep my son happy

    सुकून उतना ही देना प्रभू, जितने से
    जिंदगी चल जाये।
    औकात बस इतनी देना,
    कि औरों का भला हो जाये।
    Read all about Organic Spectroscopy on ORGANIC SPECTROSCOPY INTERNATIONAL