Morphine

Morphine

SCHEMBL3477436

CN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1C5.O=C(O)c1ccccc1O

nearest known ligand 0.79

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

The experimentally established mechanism targets of Morphine. 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
▸ OPRM1 known ✓ P35372 7/20 0.79
▸ OPRD1 P41143 9/20 0.79
▸ OPRK1 P41145 6/20 0.79
▸ MRGPRX2 Q96LB1 2/20 0.79
▸ SLC22A1 O15245 1/20 0.79
▸ ADRA2A P08913 1/20 0.79
▸ ARRB1 P49407 1/20 0.79

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
Morphine SCHEMBL3476851 0.96 OPRD1 (0.82) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL11045706 0.96 OPRD1 (0.81) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6120656 0.92 OPRD1 (0.74) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6459790 0.91 OPRD1 (0.82) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6433223 0.91 OPRD1 (0.82) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL27446433 0.91 OPRD1 (0.66) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Codeine SCHEMBL3476298 0.91 OPRM1 (0.78) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL27547724 0.91 OPRD1 (0.96) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6266392 0.91 OPRD1 (0.75) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL15055206 0.90 OPRD1 (0.90) OPRD1OPRM1OPRK1MRGPRX2SLC22A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050203115-A1 Narcotic-NSAID ion pairs WELLS FARGO BANK, N.A. 2005-09-15 — — US claimed
US-20150133664-A1 CHEMICAL TRANSFORMATIONS OF (-)-CODEINE TO AFFORD DERIVATIVES OF CODEINE AND MORPHINE THEREOF UNIV TEXAS (US) 2015-05-14 — — US disclosed
WO-2013184902-A1 CHEMICAL TRANSFORMATIONS OF (-)-CODEINE TO AFFORD DERIVATIVES OF CODEINE AND MORPHINE THEREOF BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2013-12-12 — — WO disclosed
US-8450365-B2 Efficient synthesis of galanthamine BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2013-05-28 — — US disclosed
US-8362283-B2 Cross-conjugated 2,5-cyclohexadienone and related synthesis methods BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2013-01-29 — — US disclosed
US-8293927-B2 Efficient synthesis of morphine and codeine BOARD OF REGENTS THE UNIVERSITY OF TEXAS SYSTEM (US) 2012-10-23 — — US disclosed
CN-1376146-B Solid-state form of celecoxil having enhanced bioavailability PHARMACIA CORP 2011-04-06 — — CN disclosed
US-20100292489-A1 Cross-conjugated 2,5-cyclohexadienone and related synthesis methods BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM 2010-11-18 — — US disclosed
US-20100292475-A1 Efficient Synthesis Of Morphine And Codeine BOARD OF REGENTS THE UNIVERSITY OF TEXAS SYSTEM 2010-11-18 — — US disclosed
US-20100292466-A1 Efficient Synthesis Of Galanthamine BOARD OF REGENTS THE UNIVERSITY OF TEXAS SYSTEM 2010-11-18 — — US disclosed
CN-1203852-C Victorcy composition PHARMACIA CORP (US) 2005-06-01 — — CN disclosed
CN-1602187-A Orally disintegrating valdecoxib compositions prepared by spray drying PHARMACIA CORP (US) 2005-03-30 — — CN disclosed
CN-1549704-A Stable oral suspension formulations — 2004-11-24 — — CN disclosed
CN-1516581-A Amino-sulfonyl-containing active compound (COX-2 inhibitors), polyethylene glycol and removing free radical antioxidate and liquid — 2004-07-28 — — CN disclosed
CN-1516601-A Orally deliverable pharmaceutical composition comprising drug of low water solubility (cox-2 inhibitor), solvent, fatty acid and organic amine — 2004-07-28 — — CN disclosed
CN-1434713-A Sustained-release formulation of a cyclooxygenase-2 inhibitor PHARMACIA CORP (US) 2003-08-06 — — CN disclosed
CN-1433309-A Dual-release compositions of cyclooxygenase-2-inhibitor PHARMNACIA CORP (US) 2003-07-30 — — CN disclosed
CN-1433308-A Cyclooxygenase-2 inhibitor compositions having rapid on set therapeutic effect PHARMACIA CORP (US) 2003-07-30 — — CN disclosed
CN-1379669-A Victorcy composition PHARMACIA CORP (US) 2002-11-13 — — CN disclosed
CN-1376146-A Solid-state form of celecoxil having enhanced bioavailability FHAMACIA CORP (US) 2002-10-23 — — CN 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 (4 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-20100292466-A1 Efficient Synthesis Of Galanthamine GALR2, GALR1, OPRK1 OPRM1 4/4885OPRD1 21/4885OPRK1 3/4885
US-20100292489-A1 Cross-conjugated 2,5-cyclohexadienone and related synthesis methods OPRK1, GALR2, OPRM1 OPRM1 3/4885OPRD1 5/4885OPRK1 1/4885
US-20100292475-A1 Efficient Synthesis Of Morphine And Codeine OPRK1, OPRM1, OPRL1 OPRM1 2/4885OPRD1 5/4885OPRK1 1/4885
US-20150133664-A1 CHEMICAL TRANSFORMATIONS OF (-)-CODEINE TO AFFORD DERIVATIVES OF CODEINE AND MORPHINE THEREOF OPRK1, OPRM1, OPRD1 OPRM1 2/4885OPRD1 3/4885OPRK1 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.

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