Morphine

Morphine

SCHEMBL547919

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

nearest known ligand 0.78

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 6/20 0.78
▸ OPRD1 P41143 8/20 0.78
▸ OPRK1 P41145 5/20 0.78
▸ MRGPRX2 Q96LB1 2/20 0.78
▸ SLC22A1 O15245 1/20 0.78
▸ ADRA2A P08913 1/20 0.78
▸ ARRB1 P49407 1/20 0.78

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 SCHEMBL28246596 0.97 OPRD1 (0.81) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL3476234 0.97 OPRD1 (0.75) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL22234325 0.97 OPRD1 (0.75) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL30301300 0.94 OPRD1 (0.85) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6650502 0.92 OPRD1 (0.69) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL6650507 0.92 OPRD1 (0.69) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL16635671 0.92 OPRD1 (0.85) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL29223948 0.91 OPRD1 (0.79) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL15055206 0.89 OPRD1 (0.90) OPRD1OPRM1OPRK1MRGPRX2SLC22A1
Morphine SCHEMBL149700 0.89 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 78 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250281680-A1 DRUG-ELUTING SURGICAL ARTICLES AND RELATED METHODS BIOSAPIEN INC (US) 2025-09-11 — — US disclosed
US-20250177290-A1 DRUG-ELUTING SURGICAL ARTICLES AND METHODS OF USE THEREOF BioSapien Inc. 2025-06-05 — — US disclosed
EP-4522238-A2 DRUG-ELUTING SURGICAL ARTICLES AND METHODS OF USE THEREOF Biosapien Inc. (US) 2025-03-19 — — EP disclosed
CN-119546355-A Drug eluting surgical article and method of use 生物智慧公司 2025-02-28 — — CN disclosed
EP-3899995-B1 DRUG-ELUTING SURGICAL ARTICLES AND RELATED METHODS BIOSAPIEN INC (US) 2024-09-04 — — EP disclosed
US-11969527-B2 Drug-eluting biomaterials and related methods BioSapien Inc. (US) 2024-04-30 — — US disclosed
EP-3597262-B1 FORMULATION FOR INTRACUTANEOUS INJECTION XERIS PHARMACEUTICALS INC (US) 2023-12-27 — — EP disclosed
WO-2023220400-A2 DRUG-ELUTING SURGICAL ARTICLES AND METHODS OF USE THEREOF BioSapien Inc. (US) 2023-11-16 — — WO disclosed
CN-114588124-B Delayed release pharmaceutical composition 江苏恒瑞医药股份有限公司 2023-10-20 — — CN disclosed
CN-113632188-B Drug eluting surgical articles and related methods 生物智慧公司 2023-08-08 — — CN disclosed
US-20050112201-A1 Delayed release dosage forms PENWEST PHARMACEUTICALS CO. (US) 2005-05-26 — — US disclosed
WO-2005027843-A2 CHRONOTHERAPEUTIC DOSAGE FORMS PENWEST PHARMACEUTICALS CO. (US) 2005-03-31 — — WO disclosed
WO-2005027878-A1 DELAYED RELEASED DOSAGE FORMS PENWEST PHARMACEUTICALS CO. (US) 2005-03-31 — — WO disclosed
WO-2004093850-A1 TABLET WITH COLOURED CORE JAGOTEC AG (CH) 2004-11-04 — — WO disclosed
WO-2004093843-A1 DELAYED RELEASE TABLET WITH DEFINED CORE GEOMETRY JAGOTEC AG (CH) 2004-11-04 — — WO disclosed
CN-1499960-A Chornotherapeutic dosage forms ����˹��ҩ�﹫˾ 2004-05-26 — — CN disclosed
US-20030082230-A1 Chronotherapeutic dosage forms and methods of treatment using chronotherapy PENWEST PHARMACEUTICALS COMPANY 2003-05-01 — — US disclosed
US-5378474-A Pellet having a core including at least one highly soluble active ingredient and a coating partially soluble at high acidity; opiod drugs F. H. FAULDING & CO. LIMITED (AU) 1995-01-03 — — US disclosed
US-5330766-A Water soluble active ingredient core coated with matrix and enteric polymers; high speed, uniform release F. H. FAULDING & CO. LIMITED (AU) 1994-07-19 — — US disclosed
US-5202128-A Oral administering F. H. FAULDING & CO. LIMITED (AU) 1993-04-13 — — US disclosed
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