Atomoxetine

Atomoxetine

SCHEMBL4730438

CNCC[C@@H](Oc1ccccc1C)c1ccccc1.O=C(O)C(O)c1ccccc1

nearest known ligand 0.78

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 11/20 0.78
SLC6A4 P31645 12/20 0.78
CYP2D6 P10635 5/20 0.78
CYP1A2 P05177 4/20 0.78
CYP3A4 P08684 4/20 0.78
TSHR P16473 3/20 0.78
SLC6A3 Q01959 3/20 0.78
CHRM1 P11229 2/20 0.78
ADRA2B P18089 2/20 0.78
HTR2A P28223 2/20 0.78
HTR2C P28335 2/20 0.78
HRH1 P35367 2/20 0.78
OPRM1 P35372 2/20 0.78
DRD3 P35462 2/20 0.78
OPRK1 P41145 2/20 0.78
HTR2B P41595 2/20 0.78
KCNH2 Q12809 2/20 0.78
KLF10 Q13118 2/20 0.78
HRH3 Q9Y5N1 2/20 0.78
KMT2A Q03164 2/20 0.78

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 SCHEMBL4943829 1.00 SLC6A4 (0.78) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL10523421 1.00 SLC6A4 (0.78) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL5011175 0.90 SLC6A4 (0.86) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL4730875 0.90 SLC6A4 (0.86) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL4082557 0.90 SLC6A4 (0.86) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL12047445 0.88 SLC6A4 (1.00) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL341802 0.88 SLC6A4 (1.00) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL5783906 0.88 SLC6A4 (1.00) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL29440242 0.88 SLC6A4 (1.00) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4
Atomoxetine SCHEMBL2209541 0.88 SLC6A4 (1.00) SLC6A4SLC6A2CYP2D6CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110294680-A A kind of preparation method in levels Moses spit of fland 北京深蓝海生物医药科技有限公司 2019-10-01 CN claimed
CN-110051657-A The purposes of mandelic acid 上海市计划生育科学研究所 2019-07-26 CN claimed
CN-104434890-A Application of mandelic acid SHANGHAI INST PLANNED PARENTHOOD RES 2015-03-25 CN claimed
CN-110194719-B Preparation method of R- (-) -atomoxetine hydrochloride 山东大学 2020-05-15 CN disclosed
CN-110294680-A A kind of preparation method in levels Moses spit of fland 北京深蓝海生物医药科技有限公司 2019-10-01 CN disclosed
CN-110194719-A A kind of preparation method in R- (-)-levels Moses spit of fland 山东大学 2019-09-03 CN disclosed
CN-110051657-A The purposes of mandelic acid 上海市计划生育科学研究所 2019-07-26 CN disclosed
CN-104434890-A Application of mandelic acid SHANGHAI INST PLANNED PARENTHOOD RES 2015-03-25 CN disclosed
US-7439398-B2 Enantiomerically pure atomoxetine and tomoxetine mandelate TEVA PHARMACEUTICAL FINE CHEMICALS S.R.L. (IT) 2008-10-21 US disclosed
US-7439398-B2 Enantiomerically pure atomoxetine and tomoxetine mandelate TEVA PHARMACEUTICAL FINE CHEMICALS S.R.L. (IT) 2008-10-21 US disclosed
WO-2008062473-A1 PROCESS FOR PREPARING ATOMOXETINE HYDROCHLORIDE CADILA HEALTHCARE LIMITED (IN) 2008-05-29 WO disclosed
EP-1682485-A2 ENANTIOMERICALLY PURE ATOMOXETINE AND TOMOXETINE MANDELATE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2006-07-26 EP disclosed
EP-1682485-A2 ENANTIOMERICALLY PURE ATOMOXETINE AND TOMOXETINE MANDELATE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2006-07-26 EP disclosed
WO-2006004923-A3 ENANTIOMERICALLY PURE ATOMOXETINE AND TOMOXETINE MANDELATE TEVA PHARM FINE CHEMICALS SRL (IT) 2006-04-20 WO disclosed
WO-2006037055-A1 SYNTHESIS OF ATOMOXETINE HYDROCHLORIDE DR. REDDY'S LABORATORIES LTD. (IN) 2006-04-06 WO disclosed
WO-2006009884-A1 3-ARYLOXY-3-ARYLPROPYLAMINE SYNTHESIS DR. REDDY'S LABORATORIES LTD. (IN) 2006-01-26 WO disclosed
WO-2006004923-A2 ENANTIOMERICALLY PURE ATOMOXETINE AND TOMOXETINE MANDELATE TEVA PHARMACEUTICAL FINE CHEMICALS S.R.L. (IT) 2006-01-12 WO disclosed
WO-2006004923-A2 ENANTIOMERICALLY PURE ATOMOXETINE AND TOMOXETINE MANDELATE TEVA PHARMACEUTICAL FINE CHEMICALS S.R.L. (IT) 2006-01-12 WO disclosed
US-20060009490-A1 Enantiomerically pure atomoxetine and tomoxetine mandelate TEVA PHARMACEUTICALS USA, INC. 2006-01-12 US disclosed
US-20060009490-A1 Enantiomerically pure atomoxetine and tomoxetine mandelate TEVA PHARMACEUTICALS USA, INC. 2006-01-12 US 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 (1 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-20060009490-A1 Enantiomerically pure atomoxetine and tomoxetine mandelate SLC6A4, HTR5A, SLC6A2 SLC6A2 3/4885SLC6A4 1/4885CYP2D6 32/4885

“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.