Oxycodone

Oxycodone

SCHEMBL4104773

COc1ccc2c3c1O[C@H]1C(=O)CC[C@@]4(O)C(C2)N(C)CC[C@]314

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 Oxycodone. 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 8/20 1.00
▸ OPRD1 P41143 7/20 1.00
▸ OPRK1 P41145 6/20 1.00
▸ ALDH1A1 P00352 1/20 0.75
▸ CYP3A4 P08684 1/20 0.75
▸ CYP2D6 P10635 1/20 0.75
▸ TSHR P16473 1/20 0.75
▸ HSD17B10 Q99714 1/20 0.75
▸ LMNA P02545 1/20 0.74
▸ BLM P54132 1/20 0.74

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
Oxycodone SCHEMBL3121359 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL12945207 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL12960967 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL618773 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL14394071 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL8386507 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL18410410 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL22058352 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL22163723 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4
Oxycodone SCHEMBL16015666 1.00 OPRM1 (1.00) OPRM1OPRD1OPRK1ALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11529340-B2 Combination for treating pain REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2022-12-20 — — US disclosed
US-20200289489-A1 COMBINATION FOR TREATING PAIN REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2020-09-17 — — US disclosed
US-10760090-B2 Papaver somniferum strain with high concentration of thebaine TASMANIAN ALKALOIDS PTY. LTD. (AU) 2020-09-01 — — US disclosed
US-10227354-B2 Conversion of oxycodone base to oxycodone hydrochloride CODY LABORATORIES, INC. (US) 2019-03-12 — — US disclosed
US-9909137-B2 Papaver somniferum strain with high concentration of thebaine TASMANIAN ALKALOIDS PTY. LTD. (AU) 2018-03-06 — — US disclosed
US-9776971-B2 Opioid and opioid-like compounds and uses thereof TAIWANJ PHARMACEUTICALS CO., LTD. (TW) 2017-10-03 — — US disclosed
WO-2017165558-A1 COMBINATION FOR TREATING PAIN REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2017-09-28 — — WO disclosed
EP-2010539-B1 STEREOSELECTIVE REDUCTION OF A MORPHINONE NEKTAR THERAPEUTICS (US) 2017-06-14 — — EP disclosed
US-9309257-B2 Preparation of oxycodone base form 14-hydroxycodeinone sulfate CODY LABORATORIES, INC. (US) 2016-04-12 — — US disclosed
US-20160032308-A1 Papaver Somniferum Strain with High Concentration of Thebaine TASMANIAN ALKALOIDS PTY LTD (AU) 2016-02-04 — — US disclosed
US-7875719-B2 Oxidizing thebaine to produce 14-hydroxycodeinone, hydrogenating to produce oxycodone, mixing with n-butanol, basification with sodium hydroxide, isolating purified oxycodone NORAMCO, LLC (FORMERLY KNOWN AS NORAMCO, INC.) 2011-01-25 — — US disclosed
US-20100284960-A1 Dosage Forms and Co-Administration of Opioid Agonist and Opioid Antagonist NEKTAR THERAPEUTICS AL, CORPORATION (US) 2010-11-11 — — US disclosed
US-20100286186-A1 NOVEL DICARBOXYLIC ACID LINKED AMINO ACID AND PEPTIDE PRODRUGS OF OPIOIDS AND USES THEREOF SHIRE LLC (US) 2010-11-11 — — US disclosed
WO-2010112942-A1 NOVEL DICARBOXYLIC ACID LINKED AMINO ACID AND PEPTIDE PRODRUGS OF OPIOIDS AND USES THEREOF SHIRE LLC (US) 2010-10-07 — — WO disclosed
US-20090239892-A1 PYRIDOMORPHINANS, PYRIDAZINOMORPHINANS AND USE THEREOF SOUTHERN RESEARCH INSTITUTE (US) 2009-09-24 — — US disclosed
US-7541364-B2 Pyridomorphinans, pyridazinomorphinans and use thereof SOUTHERN RESEARCH INSTITUTE (US) 2009-06-02 — — US disclosed
US-20090005563-A1 CONVERSION OF THEBAINE TO MORPHINE DERIVATIVES BROCK UNIVERSITY 2009-01-01 — — US disclosed
US-20090005563-A1 CONVERSION OF THEBAINE TO MORPHINE DERIVATIVES BROCK UNIVERSITY 2009-01-01 — — US disclosed
US-20080194568-A1 Pyridomorphinans, Pyridazinomorphinans and Use Thereof SOUTHERN RESEARCH INSTITUTE (US) 2008-08-14 — — US disclosed
US-20080132703-A1 Oxidizing thebaine to produce 14-hydroxycodeinone, hydrogenating to produce oxycodone, mixing with n-butanol, basification with sodium hydroxide, isolating purified oxycodone NORAMCO, LLC (FORMERLY KNOWN AS NORAMCO, INC.) 2008-06-05 — — US 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 (11 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-10227354-B2 Conversion of oxycodone base to oxycodone hydrochloride OPRD1, OPRK1, OPRM1 OPRM1 3/4885OPRD1 1/4885OPRK1 2/4885
US-20100286186-A1 NOVEL DICARBOXYLIC ACID LINKED AMINO ACID AND PEPTIDE PRODRUGS OF OPIOIDS AND USES THEREOF VIP, OPRL1, OPRK1 OPRM1 4/4885OPRD1 6/4885OPRK1 3/4885
US-10760090-B2 Papaver somniferum strain with high concentration of thebaine OPRM1, POF1B, OPRK1 OPRM1 1/4885OPRD1 16/4885OPRK1 3/4885
US-20090005563-A1 CONVERSION OF THEBAINE TO MORPHINE DERIVATIVES OPRK1, OPRM1, OPRD1 OPRM1 2/4885OPRD1 3/4885OPRK1 1/4885
US-20100284960-A1 Dosage Forms and Co-Administration of Opioid Agonist and Opioid Antagonist OPRM1, OPRL1, OPRK1 OPRM1 1/4885OPRD1 5/4885OPRK1 3/4885
US-20080194568-A1 Pyridomorphinans, Pyridazinomorphinans and Use Thereof OPRK1, OPRL1, OPRM1 OPRM1 3/4885OPRD1 4/4885OPRK1 1/4885
US-20090239892-A1 PYRIDOMORPHINANS, PYRIDAZINOMORPHINANS AND USE THEREOF OPRM1, OPRK1, OPRL1 OPRM1 1/4885OPRD1 4/4885OPRK1 2/4885
US-20080132703-A1 Oxidizing thebaine to produce 14-hydroxycodeinone, hydrogenating to produce oxycodone, mixing with n-butanol, basification with sodium hydroxide, isolating purified oxycodone CYP11B1, CYP11B2, DBH OPRM1 31/4885OPRD1 5/4885OPRK1 25/4885
US-20200289489-A1 COMBINATION FOR TREATING PAIN OPRL1, ACHE, OPRK1 OPRM1 12/4885OPRD1 6/4885OPRK1 3/4885
US-20160032308-A1 Papaver Somniferum Strain with High Concentration of Thebaine OPRM1, POF1B, OPRK1 OPRM1 1/4885OPRD1 16/4885OPRK1 3/4885
US-11529340-B2 Combination for treating pain OPRL1, ACHE, OPRK1 OPRM1 12/4885OPRD1 6/4885OPRK1 3/4885

“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.

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