PACAP-38 [Ligand Id: 2258] activity data from GtoPdb

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  • PAC1 receptor in Human [GtoPdb: 370] [UniProtKB: P41586]
  • PAC1 receptor in Rat [GtoPdb: 370] [UniProtKB: P32215]
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  • VPAC1 receptor in Human [GtoPdb: 371] [UniProtKB: P32241]
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  • VPAC2 receptor in Human [GtoPdb: 372] [UniProtKB: P41587]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
PAC1 receptor in Human [GtoPdb: 370] [UniProtKB: P41586]
GtoPdb inhibition of [125I]-PACAP-27 binding to membranes from HEK293 cells stably expressing the PAC1 very short receptor - 6.9 pKi 121 nM Ki J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb inhibition of [125I]-PACAP-27 binding to membranes from HEK293 cells stably expressing the PAC1 short receptor (ENST00000409363) - 8.8 pKi 1.7 nM Ki J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb inhibition of [125I]-PACAP-27 binding to membranes from HEK293 cells stably expressing the full length receptor (ENST00000304166) - 9 pKi 1.1 nM Ki J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb stimulation of cyclic AMP formation in HEK293 cells stably expressing the PAC1 very short receptor - 7.5 pEC50 29 nM EC50 J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb calcium influx in CHO cells stably expressing recombinant receptor - 8.3 pEC50 5.1 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]
GtoPdb stimulation of cyclic AMP formation in HEK293 cells stably expressing the PAC1 short receptor (ENST00000409363) - 9.2 pEC50 0.7 nM EC50 J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb stimulation of cyclic AMP formation in HEK293 cells stably expressing the full length receptor (ENST00000304166) - 9.2 pEC50 0.6 nM EC50 J Neuroendocrinol (1999) 11: 941-9 [PMID:10583729]
GtoPdb cyclic AMP formation in CHO cells stably expressing recombinant receptor - 10.3 pEC50 0.05 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]
PAC1 receptor in Rat [GtoPdb: 370] [UniProtKB: P32215]
GtoPdb inhibition of [125I]-[Ac-His1]PACAP-27 binding to membranes from CHO cells stably expressing the rat PAC1 receptor isoform lacking the hip and hop exons - 8.4 pKi 4 nM Ki Eur J Pharmacol (1995) 288: 259-67 [PMID:7774670]
GtoPdb inhibition of [125I]-[Ac-His1]PACAP-27 binding to membranes from CHO cells stably expressing the rat PAC1 receptor isoform including the hop1 exon - 8.8 pKi 1.5 nM Ki Eur J Pharmacol (1995) 288: 259-67 [PMID:7774670]
GtoPdb stimulation of adenylate cyclase in COS cells transiently expressing recombinant receptor - 9.5 pEC50 0.34 nM EC50 J Biol Chem (1997) 272: 966-70 [PMID:8995389]
GtoPdb stimulation of adenylate cyclase in CHO cells stably expressing the rat PAC1 receptor isoform including the hop1 exon - 10 pEC50 0.1 nM EC50 Eur J Pharmacol (1995) 288: 259-67 [PMID:7774670]
GtoPdb stimulation of adenylate cyclase in CHO cells stably expressing the rat PAC1 receptor isoform lacking the hip and hop exons - 10 pEC50 0.1 nM EC50 Eur J Pharmacol (1995) 288: 259-67 [PMID:7774670]
VPAC1 receptor in Human [GtoPdb: 371] [UniProtKB: P32241]
GtoPdb inhibition of [125I]-VIP binding to membranes from CHO cells stably expressing the recombinant receptor - 8.2 pKi 6.8 nM Ki Eur J Pharmacol (1996) 302: 207-14 [PMID:8791009]
GtoPdb calcium influx in CHO cells stably expressing recombinant receptor - 7.4 pEC50 37.4 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]
GtoPdb cyclic AMP formation in CHO cells stably expressing recombinant receptor - 9.7 pEC50 0.22 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]
VPAC2 receptor in Human [GtoPdb: 372] [UniProtKB: P41587]
GtoPdb calcium influx in CHO cells stably expressing recombinant receptor - 7.7 pEC50 19.4 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]
GtoPdb cyclic AMP formation in CHO cells stably expressing recombinant receptor - 9.3 pEC50 0.53 nM EC50 Neuropharmacology (2006) 51: 1086-98 [PMID:16930633]

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.