Atomoxetine

Atomoxetine

SCHEMBL649168

CNCCC(Oc1ccccc1C)c1ccccc1.Cl

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 0.97
CYP1A2 P05177 4/20 0.97
CYP3A4 P08684 4/20 0.97
CYP2D6 P10635 4/20 0.97
TSHR P16473 3/20 0.97
SLC6A3 Q01959 3/20 0.97
CHRM1 P11229 2/20 0.97
ADRA2B P18089 2/20 0.97
HTR2A P28223 2/20 0.97
HTR2C P28335 2/20 0.97
HRH1 P35367 2/20 0.97
OPRM1 P35372 2/20 0.97
DRD3 P35462 2/20 0.97
OPRK1 P41145 2/20 0.97
HTR2B P41595 2/20 0.97
KCNH2 Q12809 2/20 0.97
KLF10 Q13118 2/20 0.97
HRH3 Q9Y5N1 2/20 0.97
PMP22 Q01453 2/20 0.97

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 SCHEMBL2206798 1.00 SLC6A2 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL1560986 1.00 SLC6A2 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL122111 1.00 SLC6A2 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL29528186 1.00 SLC6A2 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL627231 1.00 SLC6A2 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL5783906 0.98 SLC6A4 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL29440242 0.98 SLC6A4 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL341802 0.98 SLC6A4 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL12047445 0.98 SLC6A4 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6
Atomoxetine SCHEMBL2209541 0.98 SLC6A4 (1.00) SLC6A2SLC6A4CYP1A2CYP3A4CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111302958-B 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 2023-05-02 CN claimed
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-4626549-A Treatment of obesity with aryloxyphenylpropylamines ELI LILLY AND COMPANY (US) 1986-12-02 US claimed
US-12508315-B2 Use of vitamin E TPGS as a taste masking agent for bitter drugs HYLORIS DEVELOPMENTS SA (BE) 2025-12-30 US disclosed
EP-4654949-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS Hyloris Developments SA (BE) 2025-12-03 EP disclosed
US-20250345436-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS HYLORIS DEV SA (BE) 2025-11-13 US disclosed
US-20250049925-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS HYLORIS DEVELOPMENTS SA (BE) 2025-02-13 US disclosed
WO-2024156799-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS HYLORIS DEVELOPMENTS SA (BE) 2024-08-02 WO disclosed
CN-114790146-B Preparation method of 3- (methylamino) -1-aryl acetone 河南省科学院高新技术研究中心 2024-03-29 CN disclosed
CN-117024288-A Synthesis method of tomoxetine 迪嘉药业集团股份有限公司 2023-11-10 CN disclosed
CN-116396176-A Preparation method of small-granularity tomoxetine hydrochloride crystals 山东达因海洋生物制药股份有限公司 2023-07-07 CN disclosed
CN-1038644-A Nuclear substituted 2-amino-1,2,3,4-tetralin class LILLY CO ELI (US) 1990-01-10 CN disclosed
EP-0343830-A2 Ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes ELI LILLY AND COMPANY (US) 1989-11-29 EP disclosed
US-4876282-A ANTIDEPRESSANT, DIETETICS, ANTIALCOHOLISM AGENT ELI LILLY AND COMPANY (US) 1989-10-24 US disclosed
US-4868344-A OPTICALLY PURE HALOALCOHOLS ALDRICH-BORANES, INC. (US) 1989-09-19 US disclosed
US-4847092-A GELATIN CAPSULES ELI LILLY AND COMPANY (US) 1989-07-11 US disclosed
EP-0318233-A2 Improvements in or relating to serotonin and norepinephrine uptake inhibitors ELI LILLY AND COMPANY (US) 1989-05-31 EP disclosed
US-4797286-A GELATIN CAPSULES FOR DRUGS ELI LILLY AND COMPANY (US) 1989-01-10 US disclosed
EP-0288188-A1 1-Phenyl-3-naphthalenyloxy-propanamines ELI LILLY AND COMPANY (US) 1988-10-26 EP disclosed
CN-88102018-A 1-Phenyl-3-naphthyloxypropylamine 1988-10-26 CN 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-20250345436-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS TAS2R5, TAS2R10, TAS2R50 SLC6A2 20/4885SLC6A4 12/4885CYP1A2 326/4885
US-12508315-B2 Use of vitamin E TPGS as a taste masking agent for bitter drugs SLC6A4, SLC6A3, CHRM5 SLC6A2 4/4885SLC6A4 1/4885CYP1A2 1143/4885
US-20250049925-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS TAS2R5, TAS2R10, TAS2R50 SLC6A2 20/4885SLC6A4 12/4885CYP1A2 326/4885

“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.