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self evaluation report - Universitatea de Ştiinţe Agricole şi Medicină ...

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Crt. Product/patent/<br />

No. technology<br />

1 ERISOL - Antidiarrhea<br />

and rehydration oral<br />

medicine.<br />

Patent No.<br />

149003/2010, OSIM<br />

Bucuresti.<br />

2 Administration<br />

protocol (technique)<br />

of a naftalendionic<br />

<strong>de</strong>rivative used to<br />

control tumor growth.<br />

Patent granting in<br />

process; Application<br />

No.<br />

A/01250/30.11.2010.<br />

3 Naftalendionic<br />

<strong>de</strong>rivative used to<br />

control tumor growth.<br />

Patent granting in<br />

process; Application<br />

No.<br />

A/01251/30.11.2010<br />

VETERINARY MEDICINE<br />

Appendix – Technology transfer<br />

Authors Domain Beneficiary Description<br />

Roman<br />

Morar,<br />

Nicolae<br />

Miu, Emilia<br />

Morar,<br />

Corina<br />

Roman,<br />

Dana Pusta<br />

Radu<br />

Tamaian<br />

Ioan<br />

Marcus<br />

Bogdan<br />

Sevastre<br />

Iulia<br />

Prodan<br />

Niculescu<br />

Violeta<br />

Carolina<br />

Radu<br />

Tamaian<br />

Ioan<br />

Marcus<br />

Bogdan<br />

Sevastre<br />

Iulia<br />

Prodan<br />

Medicină<br />

Veterinară<br />

Veterinary<br />

oncology<br />

Veterinary<br />

oncology<br />

SC<br />

Plantarom<br />

ICSI Rm.<br />

Valcea<br />

ICSI Rm.<br />

Valcea<br />

Antidiarrhea and<br />

rehydration oral medicine<br />

The invention relates to a<br />

new 2.3-<strong>de</strong>rived<br />

naftalendionic disubstituit,<br />

chlorinated, with the<br />

formula C16H9 ClN2O3: N-<br />

(3- chloro- 1, 4- dioxo-1, 4dihidronaftalen<br />

-2-yl)<br />

pyridine-3-carboxymi<strong>de</strong>, at<br />

an injectable product, and<br />

also to its use in controlling<br />

tumor growth.<br />

The invention refers to a<br />

new <strong>de</strong>rived naphthaendionic<br />

2.3 - disubstituit,<br />

thiols, with the formula<br />

C16H10N2O3S: N-(1,4dioxo-3-sulphanilic-1,4dihidronaftalen-2-yl)<br />

pyridine-3-carboxami<strong>de</strong>, at<br />

two types of<br />

immunoconjugates<br />

(antigenic <strong>de</strong>terminants<br />

chosen as specific targets<br />

for monoclonal antibodies<br />

or for antigen binding<br />

fragments <strong>de</strong>rived from the<br />

monoclonal antibodies, are<br />

DNA topoisomerase II α<br />

chain and Tenascina C)<br />

polispecifics (with specific<br />

reactivity to Mus musculus<br />

and / or Rattus norvegicus<br />

and Homo sapiens), that<br />

have as load cytotoxic N-<br />

(1,4 - dioxo-3-sulphanilic -<br />

1,4-dihidronaftalen-2-yl)<br />

pyridine-3-carboxami<strong>de</strong>,<br />

and to the combined use of<br />

these immuno-conjugates<br />

as targeted antipro-<br />

Page 180 SELF-EVALUATION REPORT, March, 2012

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