Faxeladol

Faxeladol

SCHEMBL149508

CN(C)C[C@@H]1CCCC[C@H]1c1cccc(O)c1

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1SLC6A2SLC6A4

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SLC6A4 known ✓ P31645 9/20 0.50
SLC6A2 known ✓ P23975 6/20 0.50
OPRM1 known ✓ P35372 6/20 0.50
MEN1 O00255 1/20 0.50
OPRD1 P41143 1/20 0.50
OPRK1 P41145 1/20 0.50
KMT2A Q03164 1/20 0.50
HTR2A P28223 1/20 0.47
HTR2C P28335 1/20 0.47
HTR2B P41595 1/20 0.47

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
Faxeladol SCHEMBL5686250 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL354208 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL30616185 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL149507 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL616828 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL12027609 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL28793358 1.00 SLC6A4 (0.50) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL7893759 0.99 SLC6A4 (0.49) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL619079 0.99 SLC6A4 (0.49) SLC6A4SLC6A2OPRM1MEN1OPRD1
Faxeladol SCHEMBL465057 0.99 SLC6A4 (0.49) SLC6A4SLC6A2OPRM1MEN1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1765303-B2 ORAL TABLET SAFEGUARDED AGAINST ABUSE GRUENENTHAL GMBH (DE) 2022-11-23 EP claimed
EP-3560484-A1 ABUSE-DETERRENT PHARMACEUTICAL COMPOSITION G.L. Pharma GmbH (AT) 2019-10-30 EP claimed
EP-3423034-B1 ABUSE-DETERRENT PHARMACEUTICAL COMPOSITION G L PHARMA GMBH (AT) 2019-07-10 EP claimed
EP-3423034-A1 ABUSE-DETERRENT PHARMACEUTICAL COMPOSITION G.L. Pharma GmbH (AT) 2019-01-09 EP claimed
US-10160719-B2 Pharmaceutical salts GRUNENTHAL GMBH (DE) 2018-12-25 US claimed
CN-109069419-A Abuse resistant drugs composition G.L.制药有限责任公司 2018-12-21 CN claimed
EP-3210596-A1 ABUSE-DETERRENT PHARMACEUTICAL COMPOSITION G.L. Pharma GmbH (AT) 2017-08-30 EP claimed
US-20170137370-A1 PHARMACEUTICAL SALTS Grünenthal GmbH (DE) 2017-05-18 US claimed
US-9642801-B2 And potent tapentadol dosage forms GRUENENTHAL GMBH (DE) 2017-05-09 US claimed
US-20170119663-A1 NOVEL GASTRO-RETENTIVE DOSAGE FORMS Grünenthal GmbH (DE) 2017-05-04 US claimed
EP-1429754-A1 COMBINATION OF SELECTED OPIOIDS WITH MUSCARINE ANTAGONISTS FOR TREATING URINARY INCONTINENCE Grünenthal GmbH (DE) 2004-06-23 EP claimed
WO-2004047823-A1 COMBINATION OF SELECTED ANALGESICS AND COX-II INHIBITORS Grünenthal GmbH (DE) 2004-06-10 WO claimed
US-20040043968-A1 Use of 6-dimethylaminomethyl-1-phenyl-cyclohexane compounds for treatment of urinary incontinence GRUENENTHAL GMBH (DE) 2004-03-04 US claimed
EP-1390023-A2 PHARMACEUTICAL SALTS Grünenthal GmbH (DE) 2004-02-25 EP claimed
WO-2003099268-A1 COMBINATION OF SELECTED OPIOIDS WITH OTHER ACTIVE SUBSTANCES FOR USE IN THE THERAPY OF URINARY INCONTINENCE Grünenthal GmbH (DE) 2003-12-04 WO claimed
EP-1337246-A2 USE OF 6-DIMETHYLAMINOMETHYL-1-PHENYL-CYCLOHEXANE COMPOUNDS FOR TREATING URINARY INCONTINENCE Grünenthal GmbH (DE) 2003-08-27 EP claimed
WO-2003024444-A1 COMBINATION OF SELECTED OPIOIDS WITH MUSCARINE ANTAGONISTS FOR TREATING URINARY INCONTINENCE Grünenthal GmbH (DE) 2003-03-27 WO claimed
WO-2002067651-A2 PHARMACEUTICAL SALTS Grünenthal GmbH (DE) 2002-09-06 WO claimed
WO-2002067916-A2 PHARMACEUTICAL SALTS Grünenthal GmbH (DE) 2002-09-06 WO claimed
WO-2002043712-A2 USE OF 6-DIMETHYLAMINOMETHYL-1-PHENYL-CYCLOHEXANE COMPOUNDS FOR TREATING URINARY INCONTINENCE Grünenthal GmbH (DE) 2002-06-06 WO claimed

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-10160719-B2 Pharmaceutical salts SLC5A1, SLC5A2, SLC35A1 SLC6A4 83/4885SLC6A2 164/4885OPRM1 2283/4885
US-20170137370-A1 PHARMACEUTICAL SALTS SLC5A1, SLC5A2, SLC35A1 SLC6A4 83/4885SLC6A2 164/4885OPRM1 2283/4885
US-20040043968-A1 Use of 6-dimethylaminomethyl-1-phenyl-cyclohexane compounds for treatment of urinary incontinence UROD, DDC, ODC1 SLC6A4 4036/4885SLC6A2 2371/4885OPRM1 110/4885

“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.