Abstract
A series of novel five- and six-membered ring urea derivatives have been described as potent and selective NK1 receptor antagonists. Several compounds in this series exhibited good oral activity and brain penetration. Syntheses of these compounds are also described herein.
Original language | English (US) |
---|---|
Pages (from-to) | 3896-3899 |
Number of pages | 4 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 15 |
Issue number | 17 |
DOIs | |
State | Published - Sep 1 2005 |
Fingerprint
All Science Journal Classification (ASJC) codes
- Drug Discovery
- Molecular Medicine
- Molecular Biology
- Biochemistry
- Clinical Biochemistry
- Pharmaceutical Science
- Organic Chemistry
Cite this
}
Cyclic urea derivatives as potent NK1 selective antagonists. / Shue, Ho Jane; Chen, Xiao; Shih, Neng Yang; Blythin, David J.; Paliwal, Sunil; Lin, Ling; Gu, Danlin; Schwerdt, John H.; Shah, Sapna; Reichard, Gregory A.; Piwinski, John J.; Duffy, Ruth A.; Lachowicz, Jean E.; Coffin, Vicki L.; Liu, Fei; Nomeir, Amin A.; Morgan, Cynthia A.; Varty, Geoffrey B.
In: Bioorganic and Medicinal Chemistry Letters, Vol. 15, No. 17, 01.09.2005, p. 3896-3899.Research output: Contribution to journal › Article
TY - JOUR
T1 - Cyclic urea derivatives as potent NK1 selective antagonists
AU - Shue, Ho Jane
AU - Chen, Xiao
AU - Shih, Neng Yang
AU - Blythin, David J.
AU - Paliwal, Sunil
AU - Lin, Ling
AU - Gu, Danlin
AU - Schwerdt, John H.
AU - Shah, Sapna
AU - Reichard, Gregory A.
AU - Piwinski, John J.
AU - Duffy, Ruth A.
AU - Lachowicz, Jean E.
AU - Coffin, Vicki L.
AU - Liu, Fei
AU - Nomeir, Amin A.
AU - Morgan, Cynthia A.
AU - Varty, Geoffrey B.
PY - 2005/9/1
Y1 - 2005/9/1
N2 - A series of novel five- and six-membered ring urea derivatives have been described as potent and selective NK1 receptor antagonists. Several compounds in this series exhibited good oral activity and brain penetration. Syntheses of these compounds are also described herein.
AB - A series of novel five- and six-membered ring urea derivatives have been described as potent and selective NK1 receptor antagonists. Several compounds in this series exhibited good oral activity and brain penetration. Syntheses of these compounds are also described herein.
UR - http://www.scopus.com/inward/record.url?scp=23244466620&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=23244466620&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.bmcl.2005.05.111
DO - https://doi.org/10.1016/j.bmcl.2005.05.111
M3 - Article
C2 - 16019209
VL - 15
SP - 3896
EP - 3899
JO - Bioorganic and Medicinal Chemistry Letters
JF - Bioorganic and Medicinal Chemistry Letters
SN - 0960-894X
IS - 17
ER -