Atomoxetine

Atomoxetine

SCHEMBL341802

CNCCC(Oc1ccccc1C)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2

The experimentally established mechanism targets of Atomoxetine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 9/20 1.00
SLC6A4 P31645 14/20 1.00
CYP1A2 P05177 4/20 1.00
CYP3A4 P08684 4/20 1.00
CYP2D6 P10635 4/20 1.00
TSHR P16473 3/20 1.00
SLC6A3 Q01959 3/20 1.00
CHRM1 P11229 2/20 1.00
ADRA2B P18089 2/20 1.00
HTR2A P28223 2/20 1.00
HTR2C P28335 2/20 1.00
HRH1 P35367 2/20 1.00
OPRM1 P35372 2/20 1.00
DRD3 P35462 2/20 1.00
OPRK1 P41145 2/20 1.00
HTR2B P41595 2/20 1.00
KCNH2 Q12809 2/20 1.00
KLF10 Q13118 2/20 1.00
HRH3 Q9Y5N1 2/20 1.00
KMT2A Q03164 2/20 1.00

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Atomoxetine SCHEMBL2209541 1.00 SLC6A4 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL34268 1.00 SLC6A4 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL5783906 1.00 SLC6A4 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL29440242 1.00 SLC6A4 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL12047445 1.00 SLC6A4 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL1560986 0.98 SLC6A2 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL29528186 0.98 SLC6A2 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL2206798 0.98 SLC6A2 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL649168 0.98 SLC6A2 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL122111 0.98 SLC6A2 (1.00) SLC6A4SLC6A2CYP1A2CYP3A4CYP2D6

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 350 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111302958-A Preparation method of optically pure (R) -N-methyl-3-phenyl-3- (o-tolyloxy) -propylamine hydrochloride 合肥医工医药股份有限公司 2020-06-19 CN claimed
US-8299305-B2 Method for preparing atomoxetine SCI PHARMTECH, INC. (TW) 2012-10-30 US claimed
US-20110319664-A1 METHOD FOR PREPARING ATOMOXETINE SCI PHARMTECH, INC. (TW) 2011-12-29 US claimed
US-7485754-B2 Efficient method for preparing 3-aryloxy-3-arylpropylamines and their optical stereoisomers APOTEX PHARMACHEM INC. (CA) 2009-02-03 US claimed
US-20070270483-A1 PROCESS FOR THE PREPARATION OF ARYLOXYPROPYLAMINES DIPHARMA FRANCIS S.R.L. (IT) 2007-11-22 US claimed
EP-1857435-A2 A process for the preparation of aryloxypropylamines Dipharma Francis S.r.l. (IT) 2007-11-21 EP claimed
WO-2007006132-A1 AN EFFICIENT METHOD FOR PREPARING 3-ARYLOXY-3- ARYLPROPYLAMINES AND THEIR OPTICAL STEREOISOMERS APOTEX PHARMACHEM INC. (CA) 2007-01-18 WO claimed
US-20070010678-A1 Efficient method for preparing 3-aryloxy-3-arylpropylamines and their optical stereoisomers APOTEX PHARMACHEM INC. 2007-01-11 US claimed
EP-1171417-B1 METHODS FOR PREPARING 3-ARYLOXY-3-ARYLPROPYLAMINES AND INTERMEDIATES THEREOF LILLY CO ELI (US) 2005-11-09 EP claimed
EP-0831799-B1 COMPOUNDS ACTIVE AT A NOVEL SITE ON RECEPTOR-OPERATED CALCIUM CHANNELS USEFUL FOR TREATMENT OF NEUROLOGICAL DISORDERS NPS PHARMA INC (US) 2003-05-02 EP claimed
US-6541668-B1 Using nucleophilic aromatic displacement in 1,3-dimethyl-2-imidazolidinone or N-methylpyrrolidinone ELI LILLY AND COMPANY 2003-04-01 US claimed
EP-1171417-A1 METHODS FOR PREPARING 3-ARYLOXY-3-ARYLPROPYLAMINES AND INTERMEDIATES THEREOF ELI LILLY AND COMPANY (US) 2002-01-16 EP claimed
WO-2000061540-A1 METHODS FOR PREPARING 3-ARYLOXY-3-ARYLPROPYLAMINES AND INTERMEDIATES THEREOF ELI LILLY AND COMPANY (US) 2000-10-19 WO claimed
EP-0193405-B1 RACEMIZATION PROCESS ELI LILLY AND COMPANY (US) 1989-03-08 EP claimed
US-4777291-A USING N-METHYL-3-(2-METHYLPHENOXY)-3-PHENYLPROPYLAMINE ELI LILLY AND COMPANY (US) 1988-10-11 US claimed
US-4626549-A Treatment of obesity with aryloxyphenylpropylamines ELI LILLY AND COMPANY (US) 1986-12-02 US claimed
EP-0193405-A1 Racemization process ELI LILLY AND COMPANY (US) 1986-09-03 EP claimed
EP-0052492-A1 3-Aryloxy-3-phenylpropylamines ELI LILLY AND COMPANY (US) 1982-05-26 EP claimed
JP-5070343-A None JP disclosed
EP-0052492-A1 3-Aryloxy-3-phenylpropylamines ELI LILLY AND COMPANY (US) 1982-05-26 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070270483-A1 PROCESS FOR THE PREPARATION OF ARYLOXYPROPYLAMINES NAT1, C1S, PAH SLC6A2 104/4885SLC6A4 310/4885CYP1A2 22/4885
US-20110319664-A1 METHOD FOR PREPARING ATOMOXETINE TPH2, HTR1A, HTR2B SLC6A2 30/4885SLC6A4 43/4885CYP1A2 6/4885
US-20070010678-A1 Efficient method for preparing 3-aryloxy-3-arylpropylamines and their optical stereoisomers SLC6A4, HTR3A, TPH2 SLC6A2 13/4885SLC6A4 1/4885CYP1A2 48/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.