Abstract
| Original language | English |
|---|---|
| Pages (from-to) | 4264-4276 |
| Journal | Journal of Medicinal Chemistry |
| Volume | 2013 |
| Issue number | 56 |
| DOIs | |
| Publication status | Published - 2013 |
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Bispyrimidines as potent histamine H4 receptor ligands: delineation of structure activity relationships and detailed H4 receptor binding mode. / Engelhardt, H.; Schultes, S.; de Graaf, C.; Nijmeijer, S.; Vischer, H.F.; Zuiderveld, O.B.; Dobler, J.; Stachurski, K.; Mayer, M.; Arnhof, H.; Scharn, D.; Haaksma, E.J.J.; de Esch, I.J.P.; Leurs, R.
In: Journal of Medicinal Chemistry, Vol. 2013, No. 56, 2013, p. 4264-4276.Research output: Contribution to Journal › Article › Academic › peer-review
TY - JOUR
T1 - Bispyrimidines as potent histamine H4 receptor ligands: delineation of structure activity relationships and detailed H4 receptor binding mode
AU - Engelhardt, H.
AU - Schultes, S.
AU - de Graaf, C.
AU - Nijmeijer, S.
AU - Vischer, H.F.
AU - Zuiderveld, O.B.
AU - Dobler, J.
AU - Stachurski, K.
AU - Mayer, M.
AU - Arnhof, H.
AU - Scharn, D.
AU - Haaksma, E.J.J.
AU - de Esch, I.J.P.
AU - Leurs, R.
PY - 2013
Y1 - 2013
N2 - The basic methylpiperazine moiety is considered a necessary substructure for high histamine H
AB - The basic methylpiperazine moiety is considered a necessary substructure for high histamine H
U2 - 10.1021/jm301886t
DO - 10.1021/jm301886t
M3 - Article
VL - 2013
SP - 4264
EP - 4276
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
SN - 0022-2623
IS - 56
ER -