Drug Information
Drug General Information | |||||
---|---|---|---|---|---|
Drug ID |
D02UWB
|
||||
Former ID |
DIB018642
|
||||
Drug Name |
5-CT
|
||||
Synonyms |
5-CT; 5-carboxamidotryptamine
|
||||
Drug Type |
Small molecular drug
|
||||
Indication | Discovery agent | Investigative | [540614] | ||
Structure |
Download2D MOL |
||||
Formula |
C11H13N3O
|
||||
InChI |
InChI=1S/C11H13N3O/c12-4-3-8-6-14-10-2-1-7(11(13)15)5-9(8)10/h1-2,5-6,14H,3-4,12H2,(H2,13,15)
|
||||
InChIKey |
WKZLNEWVIAGNAW-UHFFFAOYSA-N
|
||||
PubChem Compound ID | |||||
PubChem Substance ID |
4829303, 7978607, 8151296, 11110879, 11113509, 15244333, 26751726, 29221008, 46530749, 47216985, 47515530, 47589185, 48110665, 48334714, 49689464, 49983500, 50104421, 53787336, 57321033, 80484291, 81054984, 85208924, 90341410, 103122975, 103183384, 104298785, 117562347, 124749645, 124879478, 124879479, 124879480, 126407200, 126730181, 129596750, 135066550, 135649828, 137005038, 139296926, 162908950, 179235696, 198944795, 204422531, 224826810, 228766706, 241134527
|
||||
Target and Pathway | |||||
Target(s) | 5-hydroxytryptamine 2C receptor | Target Info | Agonist | [525661] | |
5-hydroxytryptamine 1B receptor | Target Info | Agonist | [527317] | ||
5-hydroxytryptamine 1E receptor | Target Info | Agonist | [526943] | ||
5-hydroxytryptamine 1F receptor | Target Info | Agonist | [534427] | ||
5-hydroxytryptamine 5A receptor | Target Info | Agonist | [534080] | ||
5-hydroxytryptamine 1D receptor | Target Info | Agonist | [528072] | ||
5-hydroxytryptamine 7 receptor | Target Info | Agonist | [534022] | ||
5-hydroxytryptamine 2A receptor | Target Info | Agonist | [527178] | ||
5-hydroxytryptamine 1A receptor | Target Info | Agonist | [534412] | ||
5-hydroxytryptamine 6 receptor | Target Info | Agonist | [534065] | ||
5-hydroxytryptamine 2B receptor | Target Info | Agonist | [534042] | ||
KEGG Pathway | Calcium signaling pathway | ||||
Neuroactive ligand-receptor interaction | |||||
Gap junction | |||||
Serotonergic synapse | |||||
Inflammatory mediator regulation of TRP channelshsa04024:cAMP signaling pathway | |||||
Serotonergic synapsehsa04024:cAMP signaling pathway | |||||
Serotonergic synapsehsa04020:Calcium signaling pathway | |||||
Serotonergic synapsehsa04014:Ras signaling pathway | |||||
cAMP signaling pathway | |||||
Inflammatory mediator regulation of TRP channels | |||||
PANTHER Pathway | 5HT2 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | ||||
5HT1 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||||
5HT1 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||||
5HT1 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathwayP04374:5HT2 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||||
5HT1 type receptor mediated signaling pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathwayP04374:5HT2 type receptor mediated signaling pathway | |||||
WikiPathways | Serotonin Receptor 2 and ELK-SRF/GATA4 signaling | ||||
Monoamine GPCRs | |||||
GPCRs, Class A Rhodopsin-like | |||||
Gastrin-CREB signalling pathway via PKC and MAPK | |||||
GPCR ligand binding | |||||
GPCR downstream signalingWP722:Serotonin HTR1 Group and FOS Pathway | |||||
GPCR downstream signaling | |||||
GPCRs, OtherWP58:Monoamine GPCRs | |||||
GPCR downstream signalingWP734:Serotonin Receptor 4/6/7 and NR3C Signaling | |||||
GPCRs, OtherWP733:Serotonin Receptor 2 and STAT3 Signaling | |||||
SIDS Susceptibility Pathways | |||||
GPCRs, OtherWP722:Serotonin HTR1 Group and FOS Pathway | |||||
GPCR downstream signalingWP732:Serotonin Receptor 2 and ELK-SRF/GATA4 signaling | |||||
References | |||||
Ref 525661 | Agonist high and low affinity state ratios predict drug intrinsic activity and a revised ternary complex mechanism at serotonin 5-HT(2A) and 5-HT(2C) receptors. Synapse. 2000 Feb;35(2):144-50. | ||||
Ref 526943 | Molecular cloning and pharmacological characterization of the guinea pig 5-HT1E receptor. Eur J Pharmacol. 2004 Jan 26;484(2-3):127-39. | ||||
Ref 527178 | Pharmacological characterisation of the agonist radioligand binding site of 5-HT(2A), 5-HT(2B) and 5-HT(2C) receptors. Naunyn Schmiedebergs Arch Pharmacol. 2004 Aug;370(2):114-23. Epub 2004 Jul 30. | ||||
Ref 527317 | Mouse 5HT1B serotonin receptor: cloning, functional expression, and localization in motor control centers. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):3020-4. | ||||
Ref 528072 | Primary structure and functional characterization of a human 5-HT1D-type serotonin receptor. Mol Pharmacol. 1991 Aug;40(2):143-8. | ||||
Ref 534022 | Molecular cloning of a mammalian serotonin receptor that activates adenylate cyclase. Mol Pharmacol. 1993 Aug;44(2):229-36. | ||||
Ref 534042 | Pharmacological characteristics of the newly cloned rat 5-hydroxytryptamine2F receptor. Mol Pharmacol. 1993 Mar;43(3):419-26. | ||||
Ref 534065 | Cloning, characterization, and chromosomal localization of a human 5-HT6 serotonin receptor. J Neurochem. 1996 Jan;66(1):47-56. | ||||
Ref 534080 | Expression of functional mouse 5-HT5A serotonin receptor in the methylotrophic yeast Pichia pastoris: pharmacological characterization and localization. FEBS Lett. 1995 Dec 27;377(3):451-6. | ||||
Ref 534412 | Agonist activity of antimigraine drugs at recombinant human 5-HT1A receptors: potential implications for prophylactic and acute therapy. Naunyn Schmiedebergs Arch Pharmacol. 1997 Jun;355(6):682-8. | ||||
Ref 534427 | Cloning and characterization of the guinea pig 5-HT1F receptor subtype: a comparison of the pharmacological profile to the human species homolog. Neuropharmacology. 1997 Apr-May;36(4-5):569-76. |
If You Find Any Error in Data or Bug in Web Service, Please Kindly Report It to Dr. Zhou and Dr. Zhang.