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9-Aminomethyl-9,10-dihydroanthracene

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
9-Aminomethyl-9,10-dihydroanthracene
Identifiers
  • 1-(9,10-Dihydroanthracen-9-yl)methanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H15N
Molar mass209.292 g·mol−1
3D model (JSmol)
  • c3cccc1c3Cc2ccccc2C1CN
  • InChI=1S/C15H15N/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-8,15H,9-10,16H2 checkY
  • Key:GEICAQNIOJFRQN-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

AMDA (9-Aminomethyl-9,10-dihydroanthracene) is atricyclic compound andcyclized phenethylamine which acts as a potent and selectiveantagonist for the5-HT2Areceptor.[1][2] It has been used to help study the shape of the 5-HT2A protein,[3] and develop a large family of related derivatives with even higher potency and selectivity.[4][5][6][7][8]

See also

[edit]

References

[edit]
  1. ^Trachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 79,275–286,500–502.ISBN 978-3-03788-700-4.OCLC 858805226.
  2. ^Westkaemper RB, Runyon SP, Bondarev ML, Savage JE,Roth BL, Glennon RA (September 1999). "9-(Aminomethyl)-9,10-dihydroanthracene is a novel and unlikely 5-HT2A receptor antagonist".European Journal of Pharmacology.380 (1):R5 –R7.doi:10.1016/S0014-2999(99)00525-7.PMID 10513561.
  3. ^Runyon SP, Peddi S, Savage JE, Roth BL, Glennon RA, Westkaemper RB (April 2002). "Geometry-affinity relationships of the selective serotonin receptor ligand 9-(aminomethyl)-9,10-dihydroanthracene".Journal of Medicinal Chemistry.45 (8):1656–1664.doi:10.1021/jm010354g.PMID 11931619.
  4. ^Peddi S, Roth BL, Glennon RA, Westkaemper RB (December 2003). "Spiro[9,10-dihydroanthracene]-9,3'-pyrrolidine-a structurally unique tetracyclic 5-HT2A receptor antagonist".European Journal of Pharmacology.482 (1–3):335–337.doi:10.1016/j.ejphar.2003.09.059.PMID 14660041.
  5. ^Peddi S, Roth BL, Glennon RA, Westkaemper RB (May 2004). "Structural determinants for high 5-HT(2A) receptor affinity of spiro[9,10-dihydroanthracene]-9,3(')-pyrrolidine (SpAMDA)".Bioorganic & Medicinal Chemistry Letters.14 (9):2279–2283.doi:10.1016/j.bmcl.2004.02.014.PMID 15081025.
  6. ^Dewkar GK, Peddi S, Mosier PD, Roth BL, Westkaemper RB (October 2008)."Methoxy-substituted 9-aminomethyl-9,10-dihydroanthracene (AMDA) derivatives exhibit differential binding affinities at the 5-HT(2A) receptor".Bioorganic & Medicinal Chemistry Letters.18 (19):5268–5271.doi:10.1016/j.bmcl.2008.08.059.PMC 3082371.PMID 18774714.
  7. ^Runyon SP, Mosier PD, Roth BL, Glennon RA, Westkaemper RB (November 2008)."Potential modes of interaction of 9-aminomethyl-9,10-dihydroanthracene (AMDA) derivatives with the 5-HT2A receptor: a ligand structure-affinity relationship, receptor mutagenesis and receptor modeling investigation".Journal of Medicinal Chemistry.51 (21):6808–6828.doi:10.1021/jm800771x.PMC 3088499.PMID 18847250.
  8. ^Shah JR, Mosier PD, Peddi S, Roth BL, Westkaemper RB (February 2010)."9-Aminomethyl-9,10-dihydroanthracene (AMDA) analogs as structural probes for steric tolerance in 5-HT2A and H1 receptor binding sites".Bioorganic & Medicinal Chemistry Letters.20 (3):935–938.doi:10.1016/j.bmcl.2009.12.064.PMC 3252747.PMID 20045641.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others
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