R-Fluoxetine

R-Fluoxetine

SCHEMBL1200433

CNCC[C@@H](Oc1ccc(C(F)(F)F)cc1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A4

The experimentally established mechanism targets of R-Fluoxetine. 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
SLC6A4 known ✓ P31645 11/20 1.00
MEN1 O00255 4/20 1.00
KMT2A Q03164 4/20 1.00
LMNA P02545 4/20 1.00
SLC6A2 P23975 4/20 1.00
SLC6A3 Q01959 4/20 1.00
NPC1 O15118 2/20 1.00
CYP2D6 P10635 2/20 1.00
CYP2C19 P33261 2/20 1.00
MTOR P42345 2/20 1.00
RAB9A P51151 2/20 1.00
CYP3A4 P08684 2/20 1.00
HTR2C P28335 2/20 1.00
KCNK2 O95069 2/20 1.00
KCNH2 Q12809 2/20 1.00
CACNA1C Q13936 2/20 1.00
HRH3 Q9Y5N1 2/20 1.00
KDM4E B2RXH2 1/20 1.00
TP53 P04637 1/20 1.00
CYP1A2 P05177 1/20 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
Fluoxetine SCHEMBL8467346 1.00 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL570572 1.00 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL8353 1.00 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL33947 1.00 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
R-Fluoxetine SCHEMBL3905325 0.99 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL7081402 0.99 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL8911991 0.99 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL17436534 0.99 SLC6A4 (0.97) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL3399076 0.99 SLC6A4 (1.00) SLC6A4MEN1KMT2ALMNASLC6A2
Fluoxetine SCHEMBL7902048 0.99 SLC6A4 (0.97) SLC6A4MEN1KMT2ALMNASLC6A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4623932-A1 AGENT FOR ALLEVIATING CLOZAPINE-INDUCED SIALORRHEA National University Corporation Chiba University (JP) 2025-10-01 EP claimed
WO-2024111636-A1 AGENT FOR ALLEVIATING CLOZAPINE-INDUCED SIALORRHEA 国立大学法人千葉大学 2024-05-30 WO claimed
US-20230355553-A1 COMPOSITIONS AND METHODS FOR TREATING AND/OR PREVENTING OCULAR DISORDERS UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2023-11-09 US claimed
CN-117007693-A 23 antidepressants and 17 metabolites detection method 河南中医药大学第一附属医院 2023-11-07 CN claimed
CN-114605272-B Preparation method of (R) -fluoxetine and derivatives thereof 中国科学技术大学 2023-09-08 CN claimed
US-20220249404-A1 COMPOSITION CONTAINING FLUOXETINE AND VITAMIN D3 OR ITS DERIVATIVES, AND APPLICATION THEREOF NANJING RUIYING RUNZE BIOPHARMACEUTICAL TECHNOLOGY CO., INC. (CN) 2022-08-11 US claimed
CN-114605272-A Preparation method of (R) -fluoxetine and derivative thereof 中国科学技术大学 2022-06-10 CN claimed
CN-112007039-B A pharmaceutical composition containing fluoxetine and vitamin D3Or derivatives thereof, and uses thereof 南京睿鹰润泽生物医药科技有限公司 2022-05-27 CN 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
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
US-6028224-A Fluoxetine process from benzoylpropionic acid SEPRACOR INC. (US) 2000-02-22 US claimed
US-5936124-A Fluoxetine process from benzoylpropionic acid SEPACOR INC. (US) 1999-08-10 US claimed
US-5068432-A Amination and etherification of a halo alcohol and resolution of a racemic mixture ALDRICH CHEMICAL COMPANY, INC. (US) 1991-11-26 US claimed
EP-4623932-A1 AGENT FOR ALLEVIATING CLOZAPINE-INDUCED SIALORRHEA National University Corporation Chiba University (JP) 2025-10-01 EP disclosed
EP-4577246-A1 DENDRIMER CONJUGATES OF ANTIDEPRESSANT AND ANTIPSYCHOTIC AGENTS AND THEIR METHODS OF USE The Johns Hopkins University (US) 2025-07-02 EP disclosed
US-20250177770-A1 SUBSTANCE USE DISORDER PREVENTION OR TREATMENT WITH LOW INTENSITY AND HIGH FREQUENCY MAGNETIC STIMULATION ACTIPULSE NEUROSCIENCE INC (US) 2025-06-05 US disclosed
EP-0909754-A1 Process to make chiral compounds ELI LILLY AND COMPANY (US) 1999-04-21 EP disclosed
EP-0612242-A4 METHODS AND COMPOSITIONS UTILIZING PURE S(+) ISOMER FLUOXETINE. SEPRACOR INC (US) 1997-01-15 EP disclosed
EP-0612242-A1 METHODS AND COMPOSITIONS UTILIZING PURE S(+) ISOMER FLUOXETINE SEPRACOR, INC. (US) 1994-08-31 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 (2 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-20230355553-A1 COMPOSITIONS AND METHODS FOR TREATING AND/OR PREVENTING OCULAR DISORDERS NLRP3, PYCARD, HTRA1 SLC6A4 345/4885MEN1 4205/4885KMT2A 2339/4885
US-20070010678-A1 Efficient method for preparing 3-aryloxy-3-arylpropylamines and their optical stereoisomers SLC6A4, HTR3A, TPH2 SLC6A4 1/4885MEN1 4831/4885KMT2A 1971/4885

“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.