Hydrocodone

Hydrocodone

SCHEMBL10440385

COc1ccc2c3c1O[C@H]1C(=O)CCC4[C@@H](C2)N(C)CC[C@@]341

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRD1OPRK1OPRM1

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

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
OPRD1 known ✓ P41143 12/20 1.00
OPRM1 known ✓ P35372 11/20 1.00
OPRK1 known ✓ P41145 8/20 1.00
LMNA P02545 1/20 1.00
PDE4D Q08499 1/20 1.00
MRGPRX2 Q96LB1 1/20 1.00
GAA P10253 1/20 0.56

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
Hydrocodone SCHEMBL12638883 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL2987 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL17523150 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL101731 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL12013631 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL6744988 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL12402839 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL277572 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL21335350 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D
Hydrocodone SCHEMBL12369421 1.00 OPRD1 (1.00) OPRD1OPRM1OPRK1LMNAPDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11173209-B2 Compositions for drug administration AEGIS THERAPEUTICS, LLC (US) 2021-11-16 US disclosed
US-10758478-B2 Active agent loaded uniform, rigid, spherical, nanoporous calcium phosphate particles and methods of making and using the same LABORATORY SKIN CARE, INC. (US) 2020-09-01 US disclosed
US-20200138956-A1 COMPOSITIONS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC 2020-05-07 US disclosed
US-10576156-B2 Compositions for drug administration AEGIS THERAPEUTICS, LLC (US) 2020-03-03 US disclosed
US-10406153-B2 Process for the preparation of benzhydrocodone hydrochloride NORAMCO, INC. (US) 2019-09-10 US disclosed
US-20190209551-A1 ORAL DOSAGE FORMS FOR OXYGEN-CONTAINING ACTIVE AGENTS AND OXYL-CONTAINING POLYMER SPRIASO LLC (US) 2019-07-11 US disclosed
US-10208054-B2 Method of preparing buprenorphine JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2019-02-19 US disclosed
US-20190046523-A1 OLIGOMER-OPIOID AGONIST CONJUGATES NEKTAR THERAPEUTICS 2019-02-14 US disclosed
US-20180169247-A1 COMPOSITIONS FOR DRUG ADMINISTRATION AEGIS THERAPEUTICS, LLC 2018-06-21 US disclosed
US-9981978-B2 Preparation of saturated ketone morphinan compounds by catalytic isomerisation CAMBREX CHARLES CITY, INC. (US) 2018-05-29 US disclosed
US-8575196-B2 Oligomer-opioid agonist conjugates NEKTAR THERAPEUTICS (US) 2013-11-05 US disclosed
EP-2628489-A1 PEG oligomer-fentanyl conjugates Nektar Therapeutics (US) 2013-08-21 EP disclosed
US-8383815-B2 Heterogeneous ruthenium metal catalyst for the production of hydrocodone, hydromorphone or a derivative thereof MALLINCKRODT LLC (US) 2013-02-26 US disclosed
US-20120184581-A1 Oligomer-Opioid Agonist Conjugates NEKTAR THERAPEUTICS (US) 2012-07-19 US disclosed
US-7999104-B2 Methods for one-pot N-demethylation/N-acylation of morphine and tropane alkaloids BROCK UNIVERSITY (CA) 2011-08-16 US disclosed
US-20110071016-A1 Heterogeneous Ruthenium Metal Catalyst for the Production of Hydrocodone, Hydromorphone or a Derivative Thereof MALLINCKRODT INC. (US) 2011-03-24 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
WO-2010039560-A2 ACTIVE AGENT LOADED UNIFORM, RIGID, SPHERICAL, NANOPOROUS CALCIUM PHOSPHATE PARTICLES AND METHODS OF MAKING AND USING THE SAME LABORATORY SKIN CARE, INC. (US) 2010-04-08 WO disclosed
US-20090005565-A1 METHODS FOR ONE-POT N-DEMETHYLATION/N-ACYLATION OF MORPHINE AND TROPANE ALKALOIDS BROCK UNIVERSITY 2009-01-01 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 (13 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-11173209-B2 Compositions for drug administration SLC10A1, ABCB11, CSGALNACT1 OPRD1 3158/4885OPRM1 2050/4885OPRK1 2869/4885
US-20100286186-A1 NOVEL DICARBOXYLIC ACID LINKED AMINO ACID AND PEPTIDE PRODRUGS OF OPIOIDS AND USES THEREOF VIP, OPRL1, OPRK1 OPRD1 6/4885OPRM1 4/4885OPRK1 3/4885
US-20180169247-A1 COMPOSITIONS FOR DRUG ADMINISTRATION SLC10A1, ABCB11, CSGALNACT1 OPRD1 3158/4885OPRM1 2050/4885OPRK1 2869/4885
US-20190046523-A1 OLIGOMER-OPIOID AGONIST CONJUGATES OPRM1, OPRL1, OPRK1 OPRD1 5/4885OPRM1 1/4885OPRK1 3/4885
US-20110071016-A1 Heterogeneous Ruthenium Metal Catalyst for the Production of Hydrocodone, Hydromorphone or a Derivative Thereof OPRK1, OPRM1, OPRD1 OPRD1 3/4885OPRM1 2/4885OPRK1 1/4885
US-20190209551-A1 ORAL DOSAGE FORMS FOR OXYGEN-CONTAINING ACTIVE AGENTS AND OXYL-CONTAINING POLYMER OGFR, OPRL1, OGFRL1 OPRD1 6/4885OPRM1 4/4885OPRK1 5/4885
US-10758478-B2 Active agent loaded uniform, rigid, spherical, nanoporous calcium phosphate particles and methods of making and using the same CHERP, ORAI1, CA2 OPRD1 4265/4885OPRM1 4536/4885OPRK1 4306/4885
US-20200138956-A1 COMPOSITIONS FOR DRUG ADMINISTRATION SLC10A1, ABCB11, CSGALNACT1 OPRD1 3158/4885OPRM1 2050/4885OPRK1 2869/4885
US-10406153-B2 Process for the preparation of benzhydrocodone hydrochloride DBH, DHPS, PAH OPRD1 27/4885OPRM1 74/4885OPRK1 34/4885
US-20120184581-A1 Oligomer-Opioid Agonist Conjugates OPRM1, OPRL1, OPRK1 OPRD1 5/4885OPRM1 1/4885OPRK1 3/4885
US-20090005565-A1 METHODS FOR ONE-POT N-DEMETHYLATION/N-ACYLATION OF MORPHINE AND TROPANE ALKALOIDS HNMT, PNMT, NNMT OPRD1 18/4885OPRM1 6/4885OPRK1 12/4885
US-10576156-B2 Compositions for drug administration SLC10A1, ABCB11, CSGALNACT1 OPRD1 3158/4885OPRM1 2050/4885OPRK1 2869/4885
US-10208054-B2 Method of preparing buprenorphine OPRK1, OPRM1, OPRD1 OPRD1 3/4885OPRM1 2/4885OPRK1 1/4885

“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.