摘要:
Embodiments of the disclosure include elastomeric stretch fibers containing an anti-tack agent, methods of preparing the fiber, methods of using this fiber, articles including this fiber, and the like.
摘要:
An article comprising a yarn comprising an elastomeric propylene-based polymer composition; said polymer composition comprising at least one elastomeric propylene-based polymer, wherein said yarn has a draft greater than 200%; wherein said article is a fabric or a garment.
摘要:
A sensor chip comprising: a micro/nanofluidic channel; at least one nanostructure provided in said channel along an optical path for the transmission of a light beam; a light transparent element disposed along the optical path and arranged to allow transmission of light onto said nanostructure; and a non-transparent element surrounding at least a portion of said optical path to at least partially reduce light scatter from the optical path.
摘要:
A method and system for selecting a gateway and a gateway selection execution node in the mobile packet domain are disclosed. The method includes: encapsulating, by a gateway selection execution node upon reception of a bearer setup request transmitted from a User Equipment, an operator domain name corresponding to the bearer setup request into a DNS parse request when creating the DNS parse request, and transmitting the DNS parse request to a DNS server; parsing by the DNS server for obtaining the address of an access gateway; returning by the DNS server, to the gateway selection execution node, a DNS parse result containing the address information of the access gateway corresponding to the operator domain name; selecting by the gateway selection execution node according to the address information the access gateway corresponding to the operator domain name as the access gateway corresponding to the bearer setup request.
摘要:
The present invention is directed to a composition comprising i) a microencapsulated pesticide, ii) a dispersant selected from the group consisting of a lignin, b) a lignosulfonate salt and c) a lignosulfonate salt combined with the sodium salt of substituted naphthalene sulfonate formaldehyde polymer, iii) a salt selected from the group consisting of magnesium sulfate, sodium chloride, sodium nitrate and calcium chloride, and iv) a non-encapsulated pesticide. The present invention is also directed to methods of making and using the compositions of the present invention.
摘要:
The present invention is directed to an insecticidal water based suspension concentrate formulation comprising a water-soluble insecticide selected from the group consisting of N-cyanomethyl-4-(trifluoromethyl)nicotinamide and (EZ)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylidineamine and at least one water-soluble salt selected from the group consisting of magnesium sulfate (hydrated and anhydrous forms) and sodium sulfate, wherein the water-soluble insecticide is present in an insecticidally effective amount and methods of use.
摘要:
This invention relates to novel lactams of Formula (I): having drug and bio-affecting properties, their pharmaceutical compositions and methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.
摘要:
The present invention discloses 3D-structure of SARS-CoV Viral 3CL Protease obtained through molecular simulation. The 3D-structure is used as a drug target for screening the existing medical database CMC (Comprehensive Medicinal Chemistry, MDL Information System, Inc.), and a group of compounds which have the activity of inhibiting SARS-CoV virus 3CL Protease are found. Cinanserin was tested at molecular and viral levels, and it was found to be able to inhibit the SARS-CoV viral 3CL protease and SARS-CoV viruses. Cinanserin analogs were synthesized and tested at molecular and viral levels, they were found to be able to inhibit the SARS-CoV virus 3CL Protease and SARS-CoV viruses, and may be used for treating and/or preventing SARS-CoV virus infection.
摘要翻译:本发明公开了通过分子模拟获得的SARS-CoV病毒3CL蛋白酶的三维结构。 使用3D结构作为筛选现有医学数据库CMC(Comprehensive Medicinal Chemistry,MDL Information System,Inc。)的药物靶点,并发现一组具有抑制SARS-CoV病毒3CL蛋白酶活性的化合物。 在分子和病毒水平测试了Cinanserin,发现能够抑制SARS-CoV病毒3CL蛋白酶和SARS-CoV病毒。 合成Cinanserin类似物并在分子和病毒水平进行测试,发现它们能够抑制SARS-CoV病毒3CL蛋白酶和SARS-CoV病毒,可用于治疗和/或预防SARS-CoV病毒感染。
摘要:
The present invention relates to compounds and pharmaceutically acceptable salts, esters and prodrugs of Formula (I) or (II): which are useful as AMPK modulators effective in treating diabetes, obesity and cancer in a subject.
摘要:
The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of Cannabinoid Receptor 1 (CB1).