Drug General Information
Drug ID	D0B2BO
Former ID	DNC012491
Drug Name	6,7,8,9-Tetrahydro-5-thia-8-aza-benzocycloheptene
Drug Type	Small molecular drug
Indication	Discovery agent		Investigative	[534195]
Structure		Download 2D MOL 3D MOL
Formula	C9H11NS
Canonical SMILES	C1CSC2=CC=CC=C2CN1
InChI	1S/C9H11NS/c1-2-4-9-8(3-1)7-10-5-6-11-9/h1-4,10H,5-7H2
InChIKey	SUBDEKBXSIKCSA-UHFFFAOYSA-N
PubChem Compound ID	12269106
Target and Pathway
Target(s)	Alpha-2C adrenergic receptor	Target Info	Inhibitor	[534195]
	Alpha-2A adrenergic receptor	Target Info	Inhibitor	[534195]
	Alpha-2B adrenergic receptor	Target Info	Inhibitor	[534195]
KEGG Pathway	cGMP-PKG signaling pathway
	Neuroactive ligand-receptor interactionhsa04022:cGMP-PKG signaling pathway
	Neuroactive ligand-receptor interaction
PANTHER Pathway	Alpha adrenergic receptor signaling pathway
	Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathwayP00002:Alpha adrenergic receptor signaling pathwayP00002:Alpha adrenergic receptor signaling pathway
	Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
Reactome	Adrenoceptors
	Adrenaline signalling through Alpha-2 adrenergic receptor
	Adrenaline,noradrenaline inhibits insulin secretion
	G alpha (i) signalling events
	G alpha (z) signalling events
	Surfactant metabolismR-HSA-390696:Adrenoceptors
WikiPathways	Monoamine GPCRs
	GPCRs, Class A Rhodopsin-like
	Platelet Aggregation (Plug Formation)
	Integration of energy metabolism
	GPCR ligand binding
	GPCR downstream signalingWP58:Monoamine GPCRs
	GPCR downstream signaling
References
Ref 534195	J Med Chem. 1996 Aug 30;39(18):3539-46.Effect of ring size or an additional heteroatom on the potency and selectivity of bicyclic benzylamine-type inhibitors of phenylethanolamine N-methyltransferase.
Ref 534195	J Med Chem. 1996 Aug 30;39(18):3539-46.Effect of ring size or an additional heteroatom on the potency and selectivity of bicyclic benzylamine-type inhibitors of phenylethanolamine N-methyltransferase.

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