Tapentadol

Tapentadol

SCHEMBL3841350

CCC(c1cccc(O)c1)[C@@H](C)CN(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1SLC6A2

The experimentally established mechanism targets of Tapentadol. 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
OPRM1 known ✓ P35372 3/20 1.00
SLC6A2 known ✓ P23975 6/20 0.38
SLC22A1 O15245 1/20 1.00
ADRA1A P35348 3/20 0.42
ADRB1 P08588 2/20 0.42
HTR2A P28223 2/20 0.42
MIF P14174 1/20 0.42
HTR2B P41595 1/20 0.42
HIF1A Q16665 3/20 0.42
LMNA P02545 3/20 0.42
GALR3 O60755 1/20 0.42
SLC6A3 Q01959 8/20 0.41
DRD1 P21728 2/20 0.41
DRD3 P35462 2/20 0.41
ADRB2 P07550 1/20 0.41
HTR1A P08908 1/20 0.41
ADRA2A P08913 1/20 0.41
ADRB3 P13945 1/20 0.41
TSHR P16473 1/20 0.41
ADRA2B P18089 1/20 0.41

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
Tapentadol SCHEMBL29447436 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL146800 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL1425181 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL116924 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL16267561 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL147058 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL16266162 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL416917 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL16267909 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A
Tapentadol SCHEMBL29611116 1.00 OPRM1 (1.00) OPRM1SLC22A1ADRA1AADRB1HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140356314-A1 3-[3-(DIMETHYLAMINO)-1-ETHYL-2-METHYLPROPYL]PHENOL RESIN COMPLEX AREVIPHARMA GMBH (DE) 2014-12-04 US claimed
US-11739049-B2 Process for the preparation of (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol Grünenthal GmbH (DE) 2023-08-29 US disclosed
US-20220177413-A1 PROCESS FOR THE PREPARATION OF TAPENTADOL AND ANALOGS THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2022-06-09 US disclosed
US-20170233330-A1 Process for the preparation of 3-[(1R,2R)-3-(Dimethylamino)-1-ethyl-2-methylpropyl]-phenol SANDOZ AG (CH) 2017-08-17 US disclosed
EP-2507203-B1 NEW PROCESS FOR THE PREPARATION OF TAPENTADOL AND INTERMEDIATES THEREOF EUTICALS SPA (IT) 2017-07-05 EP disclosed
US-9670200-B2 Quaternary ammonium salt prodrugs ALKERMES PHARMA IRELAND LIMITED (IE) 2017-06-06 US disclosed
EP-2792668-B1 Process for the preparation of substituted 3-(1-amino-2-methyl-pentane-3-yl)phenyl compounds GRUENENTHAL GMBH (DE) 2017-05-31 EP disclosed
EP-2519100-B1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF TAPENTADOL AND RELATED COMPOUNDS MAPI PHARMA LTD (IL) 2017-03-15 EP disclosed
US-20160361276-A1 Pharmaceutical Combination GRUENENTHAL GMBH (DE) 2016-12-15 US disclosed
EP-2992877-A1 PHARMACEUTICAL COMBINATION FOR THE TREATMENT OF PAIN Grünenthal GmbH (DE) 2016-03-09 EP disclosed
US-20120232306-A1 PROCESS FOR THE PREPARATION OF TAPENTADOL AND INTERMEDIATES THEREOF EUTICALS S.P.A. (IT) 2012-09-13 US disclosed
WO-2012001571-A1 NEW PROCESS FOR THE SYNTHESIS OF TAPENTADOL AND INTERMEDIATES THEREOF ARCHIMICA SRL (IT) 2012-01-05 WO disclosed
WO-2011080756-A1 PROCESS FOR THE PREPARATION OF 1-PHENYL-3-DIMETHYLAMINOPROPANE DERIVATIVES IND-SWIFT LABORATORIES LIMITED (IN) 2011-07-07 WO disclosed
WO-2011080736-A1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF TAPENTADOL AND RELATED COMPOUNDS MAPI PHARMA HK LIMITED (CN) 2011-07-07 WO disclosed
WO-2011067714-A1 NEW PROCESS FOR THE PREPARATION OF TAPENTADOL AND INTERMEDIATES THEREOF ARCHIMICA SRL (IT) 2011-06-09 WO disclosed
EP-1699440-B1 METHOD FOR THE PRODUCTION OF AN ADMINISTRATION FORM WHICH IS SECURED AGAINST MISUSE GRUENENTHAL GMBH (DE) 2009-11-11 EP disclosed
US-20090099138-A1 NSAIDs and tapentadol; synergistic pain relief GRUENENTHAL GMBH (DE) 2009-04-16 US disclosed
EP-2012763-A1 PHARMACEUTICAL COMBINATION COMPRISING 3- (3-DIMETHYLAMIN0-1-ETHYL-2-METHYL-PR0PYL) -PHENOL AND AN NSAID Grünenthal GmbH (DE) 2009-01-14 EP disclosed
WO-2007128412-A1 PHARMACEUTICAL COMBINATION COMPRISING 3- (3-DIMETHYLAMIN0-1-ETHYL-2-METHYL-PR0PYL) -PHENOL AND AN NSAID Grünenthal GmbH (DE) 2007-11-15 WO disclosed
EP-1612203-B1 Crystalline forms of (-)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride GRUENENTHAL GMBH (DE) 2007-08-01 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 (6 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-20120232306-A1 PROCESS FOR THE PREPARATION OF TAPENTADOL AND INTERMEDIATES THEREOF OPRK1, OPRD1, OPRL1 OPRM1 4/4885SLC6A2 282/4885SLC22A1 3207/4885
US-20160361276-A1 Pharmaceutical Combination MC2R, PTGER2, PTGER1 OPRM1 21/4885SLC6A2 743/4885SLC22A1 2078/4885
US-20170233330-A1 Process for the preparation of 3-[(1R,2R)-3-(Dimethylamino)-1-ethyl-2-methylpropyl]-phenol AGTR1, SAT1, TMT1A OPRM1 1153/4885SLC6A2 1382/4885SLC22A1 1704/4885
US-11739049-B2 Process for the preparation of (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol COMT, CYP1A1, CYP2E1 OPRM1 201/4885SLC6A2 3218/4885SLC22A1 4825/4885
US-20220177413-A1 PROCESS FOR THE PREPARATION OF TAPENTADOL AND ANALOGS THEREOF CYP1A1, CYP1B1, OPRL1 OPRM1 11/4885SLC6A2 310/4885SLC22A1 1725/4885
US-20090099138-A1 NSAIDs and tapentadol; synergistic pain relief PTGS1, OPRL1, PTGES3 OPRM1 29/4885SLC6A2 96/4885SLC22A1 1301/4885

“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.