Dihydrocodeine

Dihydrocodeine

SCHEMBL10440393

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

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 12/20 0.77
OPRD1 P41143 12/20 0.77
OPRK1 P41145 9/20 0.74
MRGPRX2 Q96LB1 3/20 0.66
PDE4D Q08499 2/20 0.66
ADRB1 P08588 1/20 0.66
PDE3A Q14432 1/20 0.66
LMNA P02545 1/20 0.65

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
Dihydrocodeine SCHEMBL12402838 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL13380391 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL18569649 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL12960899 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL159237 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL12402837 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL6064584 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL6123622 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL19615457 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D
Dihydrocodeine SCHEMBL14516219 1.00 OPRM1 (0.77) OPRM1OPRD1OPRK1MRGPRX2PDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190046523-A1 OLIGOMER-OPIOID AGONIST CONJUGATES NEKTAR THERAPEUTICS 2019-02-14 US disclosed
US-9827239-B2 Oligomer-opioid agonist conjugates NEKTAR THERAPEUTICS (US) 2017-11-28 US disclosed
US-20170112826-A1 OLIGOMER-OPIOID AGONIST CONJUGATES NEKTAR THERAPEUTICS 2017-04-27 US disclosed
EP-2628489-B1 PEG oligomer-fentanyl conjugates NEKTAR THERAPEUTICS (US) 2017-03-01 EP disclosed
US-9512135-B2 Oligomer-opioid agonist conjugates NEKTAR THERAPEUTICS (US) 2016-12-06 US disclosed
US-9233168-B2 Oligomer-opioid agonist conjugates NEKTAR THERAPEUTICS (US) 2016-01-12 US disclosed
US-20150112069-A1 OLIGOMER-OPIOID AGONIST CONJUGATES NEKTAR THERAPEUTICS 2015-04-23 US disclosed
US-8952032-B2 Oligomer-opioid agonist conjugates NEKTAR THERAPEUTICS (US) 2015-02-10 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
EP-2189460-A1 IMPROVED PROCESS FOR THE PREPARATION OF 6-ALPHA-HYDROXY-N-ALKYLATED OPIATES Mallinckrodt Inc. (US) 2010-05-26 EP disclosed
US-20100113788-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates MALLINCKRODT INC. (US) 2010-05-06 US disclosed
US-20100113788-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates MALLINCKRODT INC. (US) 2010-05-06 US disclosed
EP-2180000-A1 Improved process for the preparation of 6-alpha-hydroxy-n-alkylated opiates Mallinckrodt Inc. (US) 2010-04-28 EP disclosed
US-20100041888-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates MALLINCKRODT ENTERPRISES LLC 2010-02-18 US disclosed
US-20100041888-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates MALLINCKRODT ENTERPRISES LLC 2010-02-18 US disclosed
WO-2008137672-A1 IMPROVED PROCESS FOR THE PREPARATION OF 6-ALPHA-HYDROXY-N-ALKYLATED OPIATES MALLINCKRODT INC. (US) 2008-11-13 WO disclosed
EP-1810973-A1 6-monoacetylmorphine derivatives useful in immunoassay Roche Diagnostics GmbH (DE) 2007-07-25 EP disclosed
US-7238791-B1 6-monoacetylmorphine derivatives useful in immunoassay ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2007-07-03 US disclosed
US-20070142628-A1 6-Monoacetylmorphine derivatives useful in immunoassay ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2007-06-21 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 (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-20170112826-A1 OLIGOMER-OPIOID AGONIST CONJUGATES OPRM1, OPRL1, OPRK1 OPRM1 1/4885OPRD1 5/4885OPRK1 3/4885
US-20100113788-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates OPRK1, OPRM1, CYP2D6 OPRM1 2/4885OPRD1 5/4885OPRK1 1/4885
US-20190046523-A1 OLIGOMER-OPIOID AGONIST CONJUGATES OPRM1, OPRL1, OPRK1 OPRM1 1/4885OPRD1 5/4885OPRK1 3/4885
US-20070142628-A1 6-Monoacetylmorphine derivatives useful in immunoassay OPRM1, MAG, IL6ST OPRM1 1/4885OPRD1 67/4885OPRK1 24/4885
US-20150112069-A1 OLIGOMER-OPIOID AGONIST CONJUGATES OPRM1, OPRL1, OPRK1 OPRM1 1/4885OPRD1 5/4885OPRK1 3/4885
US-20100041888-A1 Process for the Preparation of 6-Alpha-Hydroxy-N-Alkylated Opiates OPRM1, OPRK1, OPRD1 OPRM1 1/4885OPRD1 3/4885OPRK1 2/4885

“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.