(R,R)-Tramadol

(R,R)-Tramadol

SCHEMBL429520

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

nearest known ligand 0.98

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 0.98
SLC6A2 P23975 13/20 0.98
SLC6A4 P31645 13/20 0.98
OPRD1 P41143 6/20 0.98
OPRK1 P41145 4/20 0.98
SLC22A1 O15245 3/20 0.98
MEN1 O00255 2/20 0.98
KMT2A Q03164 2/20 0.98
CHRM2 P08172 1/20 0.98
CHRM1 P11229 1/20 0.98

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 SCHEMBL29625842 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL405854 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL41748 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL7141021 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL1377516 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL405853 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL7137387 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
Tramadol SCHEMBL6052999 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
Tramadol SCHEMBL405855 1.00 SLC6A2 (0.98) SLC6A2SLC6A4OPRM1OPRD1OPRK1
(R,R)-Tramadol SCHEMBL6543502 1.00 SLC6A2 (0.98) 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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210137835-A1 Tramadol Hydrochloride Solution ROSEMONT PHARMACEUTICALS LLC 2021-05-13 US disclosed
US-9427435-B2 Narcotic emulsion formulations for treatment of cancer pain TEIKOKU PHARMA USA, INC. (US) 2016-08-30 US disclosed
US-20150141461-A1 Narcotic Emulsion Formulations for Treatment of Cancer Pain TEIKOKU PHARMA USA, INC. 2015-05-21 US disclosed
US-8871791-B2 Narcotic emulsion formulations for treatment of cancer pain TEIKOKU PHARMA USA, INC. (US) 2014-10-28 US disclosed
US-20130338166-A1 REDUCING SIDE EFFECTS OF TRAMADOL DMI BIOSCIENCES, INC. (US) 2013-12-19 US disclosed
EP-2114147-B9 REDUCING SIDE EFFECTS OF TRAMADOL DMI BIOSCIENCES INC (US) 2013-04-10 EP disclosed
EP-2486921-A1 Reducing Side Effects of Tramadol DMI Biosciences, Inc. (US) 2012-08-15 EP disclosed
EP-2114147-B1 REDUCING SIDE EFFECTS OF TRAMADOL DMI BIOSCIENCES INC (US) 2012-05-16 EP disclosed
US-20120018333-A1 Reducing Side Effects of Tramadol ROSEWIND CORPORATION 2012-01-26 US disclosed
WO-2010098897-A1 NARCOTIC EMULSION FORMULATIONS FOR TREATMENT OF CANCER PAIN TEIKOKU PHARMA USA, INC. (US) 2010-09-02 WO disclosed
US-20100216842-A1 Narcotic Emulsion Formulations for Treatment of Cancer Pain TEIKOKU PHARMA USA INC. 2010-08-26 US disclosed
EP-2114147-A2 REDUCING SIDE EFFECTS OF TRAMADOL DMI Biosciences, Inc. (US) 2009-11-11 EP disclosed
US-20080261991-A1 comprising coadministering an effective amount of a phosphodiesterase inhibitor (PDE); reducing the incidence of newly-discovered side effects related to sexual function in human males DMI BIOSCIENCES, INC. (US) 2008-10-23 US disclosed
WO-2008100933-A2 REDUCING SIDE EFFECTS OF TRAMADOL DMI BIOSCIENCES, INC. (US) 2008-08-21 WO disclosed