108620-55-9Relevant articles and documents
METHOD OF TREATMENT AND DEVICE
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Paragraph 0046; 0054, (2020/07/25)
A method and an angioplasty balloon catheter used in a method of preventing or minimizing incidence of neointimal hyperplasia (NIH) in a blood vessel of an animal following angioplasty treatment. The method comprising locating the angioplasty balloon cath
Suzuki-Miyaura reaction catalyzed by graphene oxide supported palladium nanoparticles
Shang, Ningzhao,Feng, Cheng,Zhang, Haiyan,Gao, Shutao,Tang, Ranxiao,Wang, Chun,Wang, Zhi
, p. 111 - 115 (2013/07/26)
Pd supported on polyamine modified graphene oxide (GO-NH 2-Pd2 +) was fabricated for the first time. The prepared catalyst was characterized by transmission electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy and infrared spectroscopy. The catalytic activity of the prepared catalyst was investigated by employing Suzuki-Miyaura coupling reaction as a model reaction. A series of biphenyl compounds were synthesized through the Suzuki-Miyaura reaction using GO-NH2-Pd2 + as catalyst. The yields of the products were in the range from 71% to 95%. The catalyst can be readily recovered and reused at least 10 consecutive cycles without significant loss its catalytic activity.
Conformational analogues of Oxamflatin as histone deacetylase inhibitors
Dear, Anthony E.,Liu, Hong B.,Mayes, Penelope A.,Perlmutter, Patrick
, p. 3778 - 3784 (2008/09/18)
Conformational analogues of the hydroxamic acid Oxamflatin 1 - compounds 3a, 3b and 4 - have been synthesised to enable evaluation of the impact of varying the linking section on histone deacetylase inhibition. Preliminary testing indicates treatment of l
Derivatives of aminobenzoic and aminobiphenylcarboxylic acids useful as anti-cancer agents
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, (2008/06/13)
The present invention provides compounds having the formula: wherein n is0or1; R is —NH2or wherein R1and R2are independently selected from the group consisting of H, alkyl, aralkyl, heteroaralkyl, carboxy, carboxyalkyl, and carbamoyl; Q is R3C(O)— or wherein R5is selected from the group consisting of H, alkyl, aralkyl, heteroaralkyl, and carbamoylalkyl, and R3and R4are selected from the group consisting of H, alkyl, alkoxy, arylalkoxy, aralkyl, heteroaralkyl, and carbamoylalkyl; the Q—NH—(CH2)n— and the —C(O)R substituents of the compound of formula I are independently positioned ortho, meta, orpara relative to the carbon atoms that form the bond between the two phenyl groups to which said substituents are bound, with the proviso that said substituents are not both positioned ortho; and the Q—NH—(CH2)nand the —C(O)R substituents of the compound of formula II are positioned meta orpara to each other; or a biolabile ester thereof, or a pharmaceutically acceptable salt thereof. The compounds are useful for treating uPA- or uPAR-mediated disorders, e.g., tumor metastasis, tumor angiogenesis, restenosis, chronic inflammation, or corneal angiogenesis.