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Ravi S Vinayak

from Mountain View, CA
Age ~66
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Also known as:
Ravi Dr Vinayak, Ravi Shankar Vinayak, Ravi Shankar Te Vinayak, Rabi S Vinayak, Raui S Vinayak, Shashi Vinayak, Vinayak Ravi, Ravi K
Phone and address:
781 San Carlos Ave, Mountain View, CA 94043
(650) 968-7027
Related to:
Vijay Ravi VinayakVivek R Vinayak, 31Shashi Vinayak, 59
Connected to:
Ajeet G Vinayak, 53Arjun Vinayak, 35Pooja G Vinayak, 34Vishal Vinayak, 48Vivek R Vinayak, 31Argetim Vinca, 41Barry J Vince, 59Cassandra M Vince, 36Christine E Vince, 54Dawna D Vince, 58

Ravi Vinayak Phones & Addresses

  • 781 San Carlos Ave, Mountain View, CA 94043 (650) 968-7027
  • 777 Lincoln Centre Dr, San Mateo, CA 94404 (650) 730-6346
  • 850 Lincoln Centre Dr, San Mateo, CA 94404 (650) 730-6346
  • 839 Catamaran St #1, San Mateo, CA 94404 (415) 571-1028
  • Foster City, CA
  • Santa Clara, CA
  • Pasadena, CA
  • 850 Lincoln Centre Dr, Foster City, CA 94404

Work

Company: CORE Specialities: leadership, business development, team building, problem solving skills

Education

School / High School: Science

Emails

r***[email protected]

Resumes

Resumes

Ravi Vinayak Photo 1

General Manager, Global Channel Distribution

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Location:
San Francisco, CA
Industry:
Biotechnology
Work:
New Trail Consulting - Mountain View, Ca since Jun 2005
President
Biomed Diagnostics - White City, Oregon since Dec 2012
Strategic Partnerships Consultant
LiteCure LLC since Mar 2012
Consultant
Rapator - San Francisco Bay Area Aug 2012 - Nov 2012
Co-Founder
Sutro Biopharma, Inc. Feb 2012 - Nov 2012
Biz Dev Consultant
Education:
California Institute of Technology
Post-doctoral fellow, Chemical Biology University of Alberta
Ph.D., Chemistry University of Mumbai
M.Sc., Organic Chemistry
Skills:
Biotechnology
Technology Transfer
Lifesciences
Commercialization
Medical Devices
Molecular Biology
R&D
Genomics
Pcr
Pharmaceutical Industry
Life Sciences
New Business Development
Product Development
Biopharmaceuticals
Infectious Diseases
Hardware Diagnostics
Strategy
Start Ups
Protein Chemistry
Biochemistry
Molecular Diagnostics
Drug Discovery
Immunology
Chemistry
International Sales
Qpcr
Cell
Oncology
Chromatography
Drug Development
Laboratory
Cancer
Microbiology
Medical Diagnostics
Hplc
Product Launch
Validation
Business Development
Goal Oriented
Science
Clinical Development
Fda
Genetics
Cell Biology
Bioinformatics
Laboratory Automation
Proteomics
Diagnostics
Glp
Results Oriented
Languages:
English
Hindi
Japanese
Ravi Vinayak Photo 2

Ravi Vinayak

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Skills:
Microsoft Excel
English
Documaker
Ravi Vinayak Photo 3

Ravi Vinayak

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Ravi Vinayak Photo 4

Ravi Vinayak

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Ravi Vinayak Photo 5

Ravi Vinayak

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Business Records

Name / Title
Company / Classification
Phones & Addresses
Ravi Vinayak
Owner
New Trail Consulting
Business Consulting Services
781 San Carlos Ave, Mountain View, CA 94043

Publications

Us Patents

Multiple-Labelled Oligonucleotides Synthesized On Solid-Supports

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US Patent:
6525183, Feb 25, 2003
Filed:
Nov 7, 2001
Appl. No.:
10/010717
Inventors:
Ravi S. Vinayak - San Carlos CA
Linda G. Lee - Palo Alto CA
Khairuzzaman B. Mullah - Union City CA
Barnett B. Rosenblum - San Jose CA
Assignee:
PE Corporation (NY) - Foster City CA
International Classification:
C07H 1900
US Classification:
536 221, 536 231, 536 241, 536 243, 536 2433, 536 2432, 536 253, 536 2532, 435 6
Abstract:
Methods and compositions to label oligonucleotides and analogs directly on a solid-support having the structure where S is a solid-support, A is a cleavable linker, X is a moiety with three or more attachment sites, L is a label, Y is a nucleophile, i. e. O, NH, NR or S, and P is an acid cleavable protecting group are provided. The labelled solid-support is reacted in a cyclical fashion to synthesize a labelled oligonucleotide on a solid-support in the 5â to 3â direction, having the structure: Labelled oligonucleotides are also synthesized by reacting: (i) a label reagent bearing functionality consisting of carboxylic acid, sulfonic acid, phosphonic acid, or phosphoric acid, (ii) an oligonucleotide on solid support with nucleophilic functionality, and (iii) a coupling reagent, whereby an ester, amide, thioester, sulfonamide, sulfonate, phosphonate, phosphoramidate, phosphorothioate, or phosphate bond is formed. The labelling reaction may be conducted at label sites including the 5â terminus, the 3â terminus, a nucleobase, an internucleotide linkage, a sugar, amino, sulfide, hydroxyl, and carboxyl.

Labelled Oligonucleotides Synthesized On Solid-Supports

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US Patent:
6835827, Dec 28, 2004
Filed:
Feb 20, 2003
Appl. No.:
10/371985
Inventors:
Ravi S. Vinayak - Mountain View CA
Linda G. Lee - Palo Alto CA
Khairuzzaman B. Mullah - Union City CA
Barnett B. Rosenblum - San Jose CA
Assignee:
Applera Corporation - Foster City CA
International Classification:
C07H 2100
US Classification:
536 253, 536 221, 536 231, 536 241, 536 243, 536 2431, 536 2432, 536 2433, 536 2532, 435 6, 436501
Abstract:
Methods and compositions to label oligonucleotides and analogs directly on a solid-support having the structure where S is a solid-support, A is a cleavable linker, X is a moiety with three or more attachment sites, L is a label, Y is a nucleophile, i. e. O, NH, NR or S, and P is an acid cleavable protecting group are provided. The labelled solid-support is reacted in a cyclical fashion to synthesize a labelled oligonucleotide on a solid-support in the 5â to 3â direction, having the structure: Labelled oligonucleotides are also synthesized by reacting: (i) a label reagent bearing functionality consisting of carboxylic acid, sulfonic acid, phosphonic acid, or phosphoric acid, (ii) an oligonucleotide on solid support with nucleophilic functionality, and (iii) a coupling reagent, whereby an ester, amide, thioester, sulfonamide, sulfonate, phosphonate, phosphoramidate, phosphorothioate, or phosphate bond is formed. The labelling reaction may be conducted at label sites including the 5â terminus, the 3â terminus, a nucleobase, an internucleotide linkage, a sugar, amino, sulfide, hydroxyl, and carboxyl.

Heteroconfigurational Polynucleotides And Methods Of Use

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US Patent:
20030198980, Oct 23, 2003
Filed:
Dec 23, 2002
Appl. No.:
10/328307
Inventors:
I. Greenfield - San Mateo CA, US
Stefan Matysiak - Montara CA, US
Benjamin Schroeder - San Mateo CA, US
Ravi Vinayak - Mountain View CA, US
Assignee:
Applera Corporation - Foster City CA
International Classification:
C12Q001/68
C07H021/02
C12M001/34
C07K014/00
US Classification:
435/006000, 435/287200, 530/350000, 536/023100
Abstract:
Methods, compositions and kits are disclosed that utilize heteroconfigurational polynucleotide comprising a D-form polynucleotide sequence portion and an L-form polynucleotide sequence portion that is covalently linked to the D-form polynucleotide sequence portion.

Labelled Oligonucleotides Synthesized On Solid-Supports

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US Patent:
20050191660, Sep 1, 2005
Filed:
Dec 6, 2004
Appl. No.:
11/006467
Inventors:
Ravi Vinayak - Mountain View CA, US
Linda Lee - Palo Alto CA, US
Khairuzzaman Mullah - Union City CA, US
Barnett Rosenblum - San Jose CA, US
Assignee:
Applera Corporation - Foster City CA
International Classification:
C12Q001/68
C07H021/04
C07H019/04
US Classification:
435006000, 536025320, 525054200, 536026600
Abstract:
Methods and compositions to label oligonucleotides and analogs directly on a solid-support having the structure where S is a solid-support, A is a cleavable linker, X is a moiety with three or more attachment sites, L is a label, Y is a nucleophile, i.e. O, NH, NR or S, and Pis an acid cleavable protecting group are provided. The labelled solid-support is reacted in a cyclical fashion to synthesize a labelled oligonucleotide on a solid-support in the 5′ to 3′ direction, having the structure: Labelled oligonucleotides are also synthesized by reacting: (i) a label reagent bearing functionality consisting of carboxylic acid, sulfonic acid, phosphonic acid, or phosphoric acid, (ii) an oligonucleotide on solid support with nucleophilic functionality, and (iii) a coupling reagent, whereby an ester, amide, thioester, sulfonamide, sulfonate, phosphonate, phosphoramidate, phosphorothioate, or phosphate bond is formed. The labelling reaction may be conducted at label sites including the 5′ terminus, the 3′ terminus, a nucleobase, an internucleotide linkage, a sugar, amino, sulfide, hydroxyl, and carboxyl.

Heteroconfigurational Polynucleotides And Methods Of Use

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US Patent:
20060286581, Dec 21, 2006
Filed:
Jun 22, 2006
Appl. No.:
11/425788
Inventors:
Stefan Matysiak - El Granada CA, US
Benjamin Schroeder - San Mateo CA, US
Ravi Vinayak - San Carlos CA, US
I. Greenfield - Eugene OR, US
Assignee:
APPLERA CORPORATION; APPLIED BIOSYSTEMS GROUP - Foster City CA
International Classification:
C12Q 1/68
C07K 14/47
C07H 21/02
C12M 1/34
C07H 21/04
US Classification:
435006000, 530350000, 536023100, 435287200, 977924000
Abstract:
Methods, compositions and kits are disclosed that utilize heteroconfigurational polynucleotide comprising a D-form polynucleotide sequence portion and an L-form polynucleotide sequence portion that is covalently linked to the D-form polynucleotide sequence portion.

Methods And Compositions For Synthesis Of Labelled Oligonucleotides And Analogs On Solid-Supports

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US Patent:
6255476, Jul 3, 2001
Filed:
Feb 22, 1999
Appl. No.:
9/256340
Inventors:
Ravi S. Vinayak - Mountain View CA
Linda G. Lee - Palo Alto CA
Khairuzzaman B. Mullah - Union City CA
Barnett B. Rosenblum - San Jose CA
Assignee:
PE Corporation (NY) - Foster City CA
International Classification:
C12Q 168
C07H 1900
C07H 2100
C07H 2102
C07H 2104
US Classification:
536 2532
Abstract:
Methods and compositions to label oligonucleotides and analogs directly on a solid-support having the structure ##STR1## where S is a solid-support, A is a cleavable linker, X is a moiety with three or more attachment sites, L is a label, Y is a nucleophile, i. e. O, NH, NR or S, and P. sub. 1 is an acid cleavable protecting group are provided. The labelled solid-support is reacted in a cyclical fashion to synthesize a labelled oligonucleotide on a solid-support in the 5' to 3' direction, having the structure: ##STR2## Labelled oligonucleotides are also synthesized by reacting: (i) a label reagent bearing functionality consisting of carboxylic acid, sulfonic acid, phosphonic acid, or phosphoric acid, (ii) an oligonucleotide on solid support with nucleophilic functionality, and (iii) a coupling reagent, whereby an ester, amide, thioester, sulfonamide, sulfonate, phosphonate, phosphoramidate, phosphorothioate, or phosphate bond is formed. The labelling reaction may be conducted at label sites including the 5' terminus, the 3' terminus, a nucleobase, an internucleotide linkage, a sugar, amino, sulfide, hydroxyl, and carboxyl.

Process And Compounds For Rna Synthesis

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US Patent:
52817016, Jan 25, 1994
Filed:
Jul 12, 1991
Appl. No.:
7/729492
Inventors:
Ravi S. Vinayak - Foster City CA
Assignee:
Applied Biosystems, Inc. - Foster City CA
International Classification:
C07H 19067
C07H 19167
C07H 2102
US Classification:
536 2534
Abstract:
A method and compositions are provided for synthesizing polynucleotides wherein the exocyclic amino groups of 5'-O-protected-2'O-alkylsilyl-adenosine phosphoramidite and 5'-O-protected-2'-O-alkylsilylguanosine phosphoramidite monomers are protected with dialkylformamidine. In a preferred embodiment, the ribonucleoside phosphoramidite monomers are activated with ethylthiotetrazole.
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Ravi S Vinayak from Mountain View, CA, age ~66 Get Report