olanzapine [Ligand Id: 47] activity data from GtoPdb

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  • 5-HT1A receptor in Human [GtoPdb: 1] [UniProtKB: P08908]
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  • 5-HT1B receptor in Human [GtoPdb: 2] [UniProtKB: P28222]
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  • 5-HT1D receptor in Human [GtoPdb: 3] [UniProtKB: P28221]
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  • 5-ht1e receptor in Human [GtoPdb: 4] [UniProtKB: P28566]
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  • 5-HT1F receptor in Human [GtoPdb: 5] [UniProtKB: P30939]
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  • 5-HT2A receptor in Human [GtoPdb: 6] [UniProtKB: P28223]
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  • 5-HT2C receptor in Human [GtoPdb: 8] [UniProtKB: P28335]
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  • 5-HT6 receptor in Human [GtoPdb: 11] [UniProtKB: P50406]
  • 5-HT6 receptor in Rat [GtoPdb: 11] [UniProtKB: P31388]
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  • 5-HT7 receptor in Human [GtoPdb: 12] [UniProtKB: P34969]
  • 5-HT7 receptor in Rat [GtoPdb: 12] [UniProtKB: P32305]
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  • α1A-adrenoceptor in Rat [GtoPdb: 22] [UniProtKB: P43140]
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  • α1D-adrenoceptor in Rat [GtoPdb: 24] [UniProtKB: P23944]
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  • D2 receptor in Human [GtoPdb: 215] [UniProtKB: P14416]
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  • H1 receptor in Human [GtoPdb: 262] [UniProtKB: P35367]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
5-HT1A receptor in Human [GtoPdb: 1] [UniProtKB: P08908]
GtoPdb - - 5.8 pKi - - - Eur J Pharmacol (1998) 355: 245-56 [PMID:9760039];
Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801]
5-HT1B receptor in Human [GtoPdb: 2] [UniProtKB: P28222]
GtoPdb - - 6.3 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801]
5-HT1D receptor in Human [GtoPdb: 3] [UniProtKB: P28221]
GtoPdb - - 6.2 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801]
5-ht1e receptor in Human [GtoPdb: 4] [UniProtKB: P28566]
GtoPdb - - 5.7 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801]
5-HT1F receptor in Human [GtoPdb: 5] [UniProtKB: P30939]
GtoPdb - - 6.5 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801]
5-HT2A receptor in Human [GtoPdb: 6] [UniProtKB: P28223]
GtoPdb - - 8.9 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801];
Neuropsychopharmacology (2003) 28: 519-26 [PMID:12629531];
Eur J Pharmacol (2002) 450: 37-41 [PMID:12176106];
J Psychopharmacol (Oxford) (2009) 23: 65-73 [PMID:18308814]
5-HT2C receptor in Human [GtoPdb: 8] [UniProtKB: P28335]
GtoPdb - - 8.4 pKi - - - Neuropsychopharmacology (2003) 28: 519-26 [PMID:12629531];
J Pharmacol Exp Ther (2000) 295: 226-32 [PMID:10991983];
J Psychopharmacol (Oxford) (2009) 23: 65-73 [PMID:18308814]
5-HT6 receptor in Human [GtoPdb: 11] [UniProtKB: P50406]
GtoPdb - - 8 pKi - - - J Neurochem (1996) 66: 47-56 [PMID:8522988];
Psychopharmacology (Berl.) (2005) 179: 461-9 [PMID:15821958]
5-HT6 receptor in Rat [GtoPdb: 11] [UniProtKB: P31388]
GtoPdb - - 8.6 pKi - - - Eur J Pharmacol (1996) 317: 417-23 [PMID:8997630];
J Pharmacol Exp Ther (1994) 268: 1403-10 [PMID:7908055]
5-HT7 receptor in Human [GtoPdb: 12] [UniProtKB: P34969]
GtoPdb - - 6.5 pKi - - - Br J Pharmacol (1998) 124: 1300-6 [PMID:9720804]
5-HT7 receptor in Rat [GtoPdb: 12] [UniProtKB: P32305]
GtoPdb - - 7 pKi - - - Eur J Pharmacol (1996) 317: 417-23 [PMID:8997630];
J Pharmacol Exp Ther (1994) 268: 1403-10 [PMID:7908055]
α1A-adrenoceptor in Rat [GtoPdb: 22] [UniProtKB: P43140]
GtoPdb Measured as antagonism of phenylephrine-induced contraction of endothelium-denuded rat small mesenteric artery. - 7.4 pA2 - - - Psychopharmacology (Berl.) (2008) 199: 15-27 [PMID:18542932]
α1D-adrenoceptor in Rat [GtoPdb: 24] [UniProtKB: P23944]
GtoPdb Measured as antagonism of phenylephrine-induced contraction of endothelium-denuded rat aorta. - 6.4 pA2 - - - Psychopharmacology (Berl.) (2008) 199: 15-27 [PMID:18542932]
D2 receptor in Human [GtoPdb: 215] [UniProtKB: P14416]
GtoPdb - - 8.68 pKi 2.1 nM Ki Neuropsychopharmacology (1998) 18: 63-101 [PMID:9430133]
H1 receptor in Human [GtoPdb: 262] [UniProtKB: P35367]
GtoPdb - - 9.2 pKi - - - Psychopharmacology (Berl.) (1996) 124: 57-73 [PMID:8935801];
Neuropsychopharmacology (2003) 28: 519-26 [PMID:12629531]

Our curators have not yet identified this ligand in ChEMBL, but you may find additional data by searching on the ChEMBL site using the ligand's name or structure.