Granted Patent
B2
US 12,415,804 · App. 19/002,520 · Granted Sep 16, 2025
Compounds for activating a serotonin receptor
Inventors:
Samuel Banister (Sydney, AU); William Jorgensen (Sydney, AU); Jinlong Tan (Sydney, AU); Lachlan Whish (Sydney, AU)
Assignee:
PSYLO PTY LTD
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Abstract
The present disclosure relates generally to compounds, their methods of synthesis, and their use in the treatment of mental illness or central nervous system disorders.
Claims (75)
1. A compound, selected from:
Com-
pound
No.
Structure
S1
S2
S3
S4
S5
S6
S7
S8
S9
S11
S12
S13
S14
S15
S16
S17
S18
S19
S20
S21
S22
S23
S24
S25
S26
S27
S28
S30
S31
S32
S33
S34
S35
S36
S37
S38
S39
S40
S41
S42
S43
S44
S45
S46
S47
S48
S49
S50
S51
S56
S57
S58
S59
S60
S61
S62
S63
S64
S65
S66
S67
S68
S69
S70
S71
S72
S73
S74
S75
or a pharmaceutically acceptable salt, solvate, tautomer, N-oxide, or stereoisomer thereof.
Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST
Recorded May 22, 2025
From: BANISTER, SAMUEL; JORGENSEN, WILLIAM; TAN, JINLONG; WHISH, LACHLAN
To: PSYLO PTY LTD
Reel/Frame 071198/0833 →
Priority Claims (1)
AU 2023902053
· Jun 28, 2023
· national
Continuity (2)
Continuation
PCTAU2024050706
· Jun 28, 2024
References Cited (37)
US 5364866A
· Strupczewski et al.
· 1994
[cited by applicant]
US 20100029629A1
· Conticello et al.
· 2010
[cited by applicant]
EP 0737685B1
· 2000
[cited by applicant]
EP 0870768B1
· 2002
[cited by applicant]
WO WO1995010513A1
· 1995
[cited by applicant]
WO 2008004117A1
· 2008
[cited by applicant]
WO WO2008003736A1
· 2008
[cited by applicant]
WO 2009102805A1
· 2009
[cited by applicant]
WO 2010011546A1
· 2010
[cited by applicant]
WO 2013063492A1
· 2013
[cited by applicant]
WO WO2018106907A1
· 2018
[cited by applicant]
WO WO2021041539A2
· 2021
[cited by applicant]
WO 2021076572A1
· 2021
[cited by applicant]
WO 2021155468A1
· 2021
[cited by applicant]
WO 2021155470A1
· 2021
[cited by applicant]
WO 2021168082A1
· 2021
[cited by applicant]
WO 2021179091A1
· 2021
[cited by applicant]
WO 2021226416A1
· 2021
[cited by applicant]
WO WO2022120181A1
· 2022
[cited by applicant]
WO 2023018864A1
· 2023
[cited by applicant]
WO WO2023115165A1
· 2023
[cited by applicant]
WO WO2024026359A1
· 2024
[cited by applicant]
WO WO2025000051A1
· 2025
[cited by examiner]
Berge et al.; “Pharmaceuticals Salts”; Journal of Pharmaceutical Sciences; vol. 66 No. 1; Jan. 1977; 19 pages.
[cited by applicant]
Whelligan et al.; “Two-Step Synthesis of Aza- and Diazaindoles from Chloroamino-N-heterocycles Using Ethoxyvinylborolane”; The Journal of Organic Chemistry; vol. 75; 2010; p. 11-15.
[cited by applicant]
CAS Registry No. 784079-60-3; dated Nov. 18, 2024; 1 page.
[cited by applicant]
CAS Registry No. 1337205-20-5; dated Oct. 18, 2011; 1 page.
[cited by applicant]
CAS Registry No. 2172589-79-4; dated Feb. 1, 2018; 1 page.
[cited by applicant]
CAS Registry No. 2025497-87-2; dated Nov. 6, 2016; 1 page.
[cited by applicant]
Blache et al.; “Application of the mercuric acetate-edetic acid oxidation method to the synthesis of 11-aza-1, 2, 3, 4, 5, 6, 7, 12b-octahydroindolo [2, 3-a] quinolizines”; Heterocycles; vol. 45 No. 1; 1997; p. 57-69.
[cited by applicant]
Fukuya et al.; “Practical Synthesis of 7-Azaserotonin and 7-Azamelatonin”; Synlett; vol. 33; 2022; p. 2033-2037.
[cited by applicant]
Bertaccini et al., The relative potency of 5-hydroxytryptamine like substances, Arch Int Pharmacodyn Ther., 133:138-56, 1961.
[cited by applicant]
Communication pursuant to Rule 114(2) EPC, Third Party Observations Regarding European Application No. 22908927.1, mailed Mar. 21, 2025, 27 pages.
[cited by applicant]
Klein et al., Toward selective drug development for the human 5-hydroxytryptamine 1E receptor: a comparison of 5-hydroxytryptamine 1E and 1F receptor structure-affinity relationships, Journal of Pharmacology and Experim…
[cited by applicant]
Pigini et al., Analogs with a 1,2-benzisoxazole nucleus of biologically active indole derivatives. IV. 5-Hydroxytryptamine isosteres, Eur J Med Chem, 10:33-6, 1975.
[cited by applicant]
Rao et al., Synthesis and radioprotective activity of beta-(3-indazolyl)-ethylamine derivatives , Yao Xue Xue Bao 22 (6): 426-432, 1987.
[cited by applicant]