Abstract:
The present invention relates to uses of small molecule mimetics of hematopoietic growth factors. In particular the present invention relates to uses of small molecule mimetics of erythropoietin.
Abstract:
The present application provides a method and system for Cross Domain Single Sign On. The method comprises: receiving a request from a user to a service provider; processing the user request prior to relaying the request to the service provider; forwarding the processed request to the corresponding service provider according to the type of request; in response to receiving a response to the request from the service provider, processing the response, and forwarding the processed response to the user. By adopting the method and system of the present application, a Single Sign On management proxy is introduced as a united management system for a session lifetime of the user. The SSO management proxy manages operations of logging in, checking a session expiration and recovering, logging out, URL mapping, error processing, and access control, and effectively improves the availability, security, functional continuity of the service as well as the user's experience.
Abstract:
Methods of using compounds which are progesterone receptor agonists for contraception and the treatment of progesterone-related maladies alone or in combination with an estrogen receptor agonist or progesterone receptor antagonist are provided. These compounds have the structure: wherein R1, R2, R3, R4, R5, and Q1 are defined herein.
Abstract:
This invention relates to non-steroidal tricyclic compounds that are modulators of androgen receptors and to methods for making and using such compounds.
Abstract:
Methods of using compounds which are progesterone receptor agonists for contraception and the treatment of progesterone-related maladies alone or in combination with an estrogen receptor agonist or progesterone receptor antagonist are provided. These compounds have the structure: wherein R1, R2, R3, R4, R5, and Q1 are defined herein.
Abstract:
Non-steroidal tricyclic quinolinone and tricyclic quinoline compounds and compositions that are agonists, partial agonists and/or antagonists for androgen receptors (AR), their preparation and their uses are described.
Abstract:
This invention relates to non-steroidal tricyclic compounds that are modulators of androgen receptors and to methods for making and using such compounds.
Abstract:
This invention relates to compounds that bind to mineralocorticoid receptors and/or modulate activity of mineralocorticoid receptors, and to methods for making and using such compounds.
Abstract:
This invention relates to compounds that bind to mineralocorticoid receptors and/or modulate activity of mineralocorticoid receptors, and to methods for making and using such compounds.
Abstract:
This invention relates to substituted indoline derivative compounds which are antagonists of the progesterone receptor, their preparation and pharmaceutical utility, particularly including contraception and treatment of benign or malignant neoplastic diseases, having the general structure: wherein R1 and R2 may be single substituents or fused to form spirocyclic rings.
Abstract translation:本发明涉及作为孕酮受体拮抗剂的取代二氢吲哚衍生物化合物,其制备方法和药物应用,特别是包括具有以下一般结构的良性或恶性肿瘤疾病的避孕和治疗:其中R 1和 R 2可以是单个取代基或稠合形成螺环。