(R,R)-Tramadol

(R,R)-Tramadol

SCHEMBL730723

COc1cccc([C@]2(O)CCCC[C@H]2CN(C)C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

The experimentally established mechanism targets of (R,R)-Tramadol. 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
OPRM1 known ✓ P35372 11/20 1.00
SLC6A2 P23975 13/20 1.00
SLC6A4 P31645 13/20 1.00
OPRD1 P41143 6/20 1.00
OPRK1 P41145 4/20 1.00
SLC22A1 O15245 3/20 1.00
MEN1 O00255 2/20 1.00
KMT2A Q03164 2/20 1.00
CHRM2 P08172 1/20 1.00
CHRM1 P11229 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
(R,R)-Tramadol SCHEMBL14579837 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL7464 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL12831358 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL6543836 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL1593740 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL3265792 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL5318670 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL11984200 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL57495 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1
Tramadol SCHEMBL57496 1.00 SLC6A2 (1.00) SLC6A2SLC6A4OPRM1OPRD1OPRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160039742-A1 EXTRACTION OF TRAMADOL FROM NAUCLEA LATIFOLIA SMITH UNIVERSITE JOSEPH FOURIER - GRENOBLE 1 (FR) 2016-02-11 US claimed
US-20140296262-A1 Method to Treat Premature Ejaculation in Humans TRINITY LABORATORIES, INC. (US) 2014-10-02 US claimed
US-20100120780-A1 TREATMENTS FOR PREMATURE EJACULATION IN HUMANS TRINITY LABORATORIES INC. 2010-05-13 US claimed
US-7470816-B2 Tramadol recovery process IPAC LABORATORIES LIMITED (IN) 2008-12-30 US claimed
EP-1363872-B1 METHOD FOR ISOLATING AND PURIFYING (1RS,2RS)-2- (DIMETHYLAMINO)METHYL -1-(3-METHOXYPHENYL)-CYCLOHEXANOL GRUENENTHAL GMBH (DE) 2008-08-20 EP claimed
US-20080176873-A1 Novel Pharmaceutical Compositions for Treating Acquired Chronic Pain and Associated Dysphoria TRINITY LABORATORIES, INC. (US) 2008-07-24 US claimed
US-20080058362-A1 Novel pharmaceutical compositions for treating chronic pain and pain associated with neuropathy JEFFERSON BANK 2008-03-06 US claimed
US-6909017-B2 Method for isolating and purifying (1RS,2RS)-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol GRUNENTHAL GMBH (DE) 2005-06-21 US claimed
EP-1210118-B1 COMPOSITION COMPRISING A TRAMADOL MATERIAL AND AN ANTICONVULSANT DRUG ORTHO MCNEIL PHARM INC (US) 2004-12-08 EP claimed
US-20040225154-A1 Method for isolating and purifying (1RS,2RS)-2-[ (dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol GRUNENTHAL GMBH (DE) 2004-11-11 US claimed
EP-1363872-A1 METHOD FOR ISOLATING AND PURIFYING (1RS,2RS)-2- (DIMETHYLAMINO)METHYL]-1-(3-METHOXYPHENYL)-CYCLOHEXANOL Grünenthal GmbH (DE) 2003-11-26 EP claimed
US-6562865-B1 Pharmaceutical composition comprising a synergistic combination of a tramadol material and topiramate, wherein the tramadol material and topiramate are present in a ratio based on a fraction of their respective ED50 values ORTHO-MCNEIL PHARMACEUTICAL, INC. 2003-05-13 US claimed
WO-2002066414-A1 METHOD FOR ISOLATING AND PURIFYING (1RS,2RS)-2-[(DIMETHYLAMINO)METHYL]-1-(3-METHOXYPHENYL)-CYCLOHEXANOL Grünenthal GmbH (DE) 2002-08-29 WO claimed
EP-1210118-A2 COMPOSITION COMPRISING A TRAMADOL MATERIAL AND AN ANTICONVULSANT DRUG Ortho-McNeil Pharmaceutical, Inc. (US) 2002-06-05 EP claimed
WO-2001013904-A2 COMPOSITION COMPRISING A TRAMADOL MATERIAL AND AN ANTICONVULSANT DRUG ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2001-03-01 WO claimed
JP-6157301-A None JP disclosed
JP-6107540-A None JP disclosed
EP-0009076-B1 METHOD FOR THE QUANTITATIVE ENZYMATIC DETERMINATION OF ADP AND REAGENT FOR THIS METHOD Roche Diagnostics GmbH (DE) 1981-07-29 EP disclosed
EP-0009076-A1 Method for the quantitative enzymatic determination of ADP and reagent for this method Roche Diagnostics GmbH (DE) 1980-04-02 EP disclosed
EP-0008342-A1 Method and reagent for the determination of glutamic oxalacetic transaminase and glutamic pyruvic transaminase Roche Diagnostics GmbH (DE) 1980-03-05 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-20040225154-A1 Method for isolating and purifying (1RS,2RS)-2-[ (dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol MRPS27, MAN1B1, MCRS1 OPRM1 470/4885SLC6A2 2496/4885SLC6A4 2629/4885
US-20160039742-A1 EXTRACTION OF TRAMADOL FROM NAUCLEA LATIFOLIA SMITH OPRK1, OPRD1, OPRM1 OPRM1 3/4885SLC6A2 15/4885SLC6A4 405/4885

“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.