2-substituted indane-2-mercaptoacetylamide derivatives...

C - Chemistry – Metallurgy – 07 – D

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C07D 471/04 (2006.01) A61K 31/55 (2006.01) C07D 487/04 (2006.01) C07D 491/147 (2006.01) C07D 498/04 (2006.01) C07D 513/04 (2006.01) C07K 5/078 (2006.01) A61K 38/00 (2006.01)

Patent

CA 2078758

The present invention relates to novel 2-substituted indane-2-mercaptoacetylamide derivatives of the formula (See formula I) wherein B1 and B2 are each independently hydrogen, hydroxy, -OR2 wherein R2 is a C1-C4 alkyl or an Ar-Y group wherein Ar is aryl and Y is a hydrogen or C1-C4 alkyl, or, where B1 and B2 are attached to adjacent carbon atoms, B1 and B2 can be taken together with said adjacent carbons to form a benzene ring or methyl- enedioxy; A is a bond, methylene, oxygen, sulfur, NR4 or NCOR5 wherein R4 is hydrogen, a C1-C4 alkyl or an Ar-Y- group and R5 is -CF3, a C1-C10 alkyl or an Ar-Y- group; R1 is hydrogen, acetyl, -CH2OC(O)C(CH3)3 or benzoyl; R3 is hydrogen or -CH2OC(O)C(CH3)3; n is an integer 0 to 3; and Q is a group of the formula (See formulas I,II,III,IV, and V) wherein Z is O, NH or S; and m is an integer 1 to 5; which are useful as inhibitors of enkephalinase and ACE.

LandOfFree

Say what you really think

Search LandOfFree.com for Canadian inventors and patents. Rate them and share your experience with other people.

Rating

2-substituted indane-2-mercaptoacetylamide derivatives... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with 2-substituted indane-2-mercaptoacetylamide derivatives..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and 2-substituted indane-2-mercaptoacetylamide derivatives... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFCA-PAI-O-1431762

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.