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10-Aryl-11h-benzo[b]fluorene derivatives and analogs for medicinal use

Patent 6756375 Issued on June 29, 2004. Estimated Expiration Date: Icon_subject August 17, 2021. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Inventors

Assignee

Application

No. 10362555 filed on 08/17/2001

US Classes:

514/238.8, Chalcogen attached indirectly to the morpholine ring by acyclic nonionic bonding514/730, Benzene ring containing514/765, Polycyclo ring system544/154, Polycyclo-carbocyclic ring system having at least three cyclos544/294, Polycyclo-carbocyclic ring system having at least three cyclos544/357, Plural diazine rings546/195, The additional ring is one of the cyclos in a polycyclo ring system546/285, Polycyclo-carbocyclic ring system having at least three cyclos548/528, Polycyclo carbocyclic ring system having at least three cyclos548/160, Polycyclo-carbocyclic ring system having at least three cyclos568/812, Halogen containing568/817, Polycyclo ring system568/719, Polycyclo ring system568/633, Polyoxy549/365, The ring oxygens are in the 1,2- or 1,3-positions of the hetero ring564/280Phenol or thiophenol addition salts

Examiners

Primary: Ramsuer, Robert W.
Assistant: Small, Andrea D.

Attorney, Agent or Firm

Foreign Patent References

  • 0733620 EP 09/01/1996
  • 0832881 EP 04/01/1998
  • 0873992 EP 10/01/1998
  • 9619458 WO 06/01/1996
  • 01 72713 WO 10/01/2001

International Classes

C07C32128
C07C 4323
A61K 3105
A61P 506
C07D29508

Abstract

The invention provides for a non-steroidal compound having the formula wherein Re and ′Re are OH, optionally independently etherified or esterified; Z is —CH2— or —CH2CH2—; R1 is H, halogen, CF3, or (1C-4C)alkyl; R2, R3 and R4 are independently H, halogen, —CF3, —OCF3, (1C-8C)Alkyl, hydroxy, (1C-8C)alkyloxy, aryloxy, aryl(1C-8C)alkyl, halo(1C-8C)alkyl, —O(CH2)mX, wherein X is halogen or phenyl and m=2-4; —O(CH2)mNRaRb, —S(CH2)mNRaRb or —(CH2)mNRaRb, wherein m=2-4 and Ra, Rb are independently (1C-8C)alkyl, (2C-8C)alkenyl, (2C-8C)alkynyl, or aryl, optionally substituted with halogen, —CF3, —OCF3, —CN, —NO2, —OH, (1C-8C)alkoxy, aryloxy, carboxyl, (1C-8C)alkylthio, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl or Ra and Rb form a 3-8 membered ring structure, optionally substituted with halogen, —CF3, —OCF3, —CN, —NO2, hydroxy, hydroxy(1C-4C)alkyl, (1C-8C)alkoxy, aryloxy, (1C-8C)alkylthio, carboxyl, carboxylate, (1C-8C)alkyl, aryl, aryl(1C-8C)alkyl, halo(1C-8C)alkyl. The compounds can be used for the preparation of a medicine, in particular for use in estrogen-receptor-related treatments.

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