Baclofen

Baclofen

SCHEMBL656539

Cl.NCC(CC(=O)O)c1ccc(Cl)cc1

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GABBR1GABBR2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABBR2 known ✓ O75899 8/20 0.96
GABBR1 known ✓ Q9UBS5 8/20 0.96
LMNA P02545 3/20 0.96
CYP2C9 P11712 3/20 0.96
CYP1A2 P05177 2/20 0.96
THRB P10828 2/20 0.96
CYP2D6 P10635 2/20 0.96
CYP2C19 P33261 2/20 0.96
MEN1 O00255 2/20 0.96
KMT2A Q03164 2/20 0.96
CYP3A4 P08684 1/20 0.96
ADORA3 P0DMS8 1/20 0.96
NFKB1 P19838 1/20 0.96
DRD3 P35462 1/20 0.96
BLM P54132 1/20 0.96
TSHR P16473 1/20 0.96
MAPT P10636 1/20 0.56
PMP22 Q01453 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
NPSR1 Q6W5P4 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
Arbaclofen SCHEMBL1417519 1.00 GABBR2 (0.96) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL19334 0.98 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Arbaclofen SCHEMBL351220 0.98 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL19333 0.98 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL5556250 0.98 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL4915007 0.96 GABBR2 (0.96) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL20815463 0.95 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Arbaclofen SCHEMBL2996117 0.95 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL3004536 0.95 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL22352888 0.92 GABBR2 (0.87) GABBR2GABBR1LMNACYP2C9CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119776295-A Olefin reductase, coding gene, vector, engineering bacteria and application thereof 浙江工业大学 2025-04-08 CN claimed
US-20220016061-A1 Preparation Stabilized by Means of Nonaqueous Solvent MEDRX CO., LTD. (JP) 2022-01-20 US claimed
EP-3861993-A1 PREPARATION STABILIZED BY MEANS OF NONAQUEOUS SOLVENT MEDRx Co., Ltd. (JP) 2021-08-11 EP claimed
CN-113164423-A Formulations stabilized with non-aqueous solvents 美德阿利克斯株式会社 2021-07-23 CN claimed
WO-2020071546-A1 PREPARATION STABILIZED BY MEANS OF NONAQUEOUS SOLVENT 株式会社 メドレックス 2020-04-09 WO claimed
US-20140037718-A1 TRANSDERMAL PAIN GEL LUTZ GEORGE W (US) 2014-02-06 US claimed
US-20100226972-A1 TRANSDERMAL PAIN GEL LUTZ GEORGE W 2010-09-09 US claimed
EP-4313014-B1 A METHOD FOR THE PRODUCTION OF GASTRORETENTIVE COMPACT MATRICES FOR THE CONTROLLED RELEASE OF ACTIVE SUBSTANCES AND COMPACT MATRICES THUS OBTAINED UNIV DEGLI STUDI GENOVA (IT) 2026-01-28 EP disclosed
CN-119776295-A Olefin reductase, coding gene, vector, engineering bacteria and application thereof 浙江工业大学 2025-04-08 CN disclosed
US-20240299304-A1 A METHOD FOR THE PRODUCTION OF GASTRORETENTIVE COMPACT MATRICES FOR THE CONTROLLED RELEASE OF ACTIVE SUBSTANCES AND COMPACT MATRICES THUS OBTAINED UNIVERSITA DEGLI STUDI DI GENOVA (IT) 2024-09-12 US disclosed
CN-117561055-A Method for producing a gastroretentive dense matrix for the controlled release of active substances and dense matrix obtained 热那亚大学 2024-02-13 CN disclosed
EP-4313014-A1 A METHOD FOR THE PRODUCTION OF GASTRORETENTIVE COMPACT MATRICES FOR THE CONTROLLED RELEASE OF ACTIVE SUBSTANCES AND COMPACT MATRICES THUS OBTAINED Università degli Studi di Genova (IT) 2024-02-07 EP disclosed
CN-114685298-B Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2023-10-24 CN disclosed
US-7250043-B2 Catheter for modification of agent formulation DURECT CORPORATION (US) 2007-07-31 US disclosed
US-20070167932-A1 Local concentration management system DURECT CORPORATION 2007-07-19 US disclosed
US-20040068251-A1 Catheter for modification of agent formulation DURECT CORPORATION 2004-04-08 US disclosed
US-6629969-B2 Catheter for modification of agent formulation DURECT CORPORATION 2003-10-07 US disclosed
US-20030032942-A1 Local concentration management system DURECT CORPORATION 2003-02-13 US disclosed
US-20030028174-A1 Catheter for modification of agent formulation DURECT CORPORATION 2003-02-06 US disclosed
US-6320054-B1 INHIBIT BINDING OF ADHESIVE PROTEINS TO THE SURFACE OF DIFFERENT TYPES F CELL AND ACCORDINGLY INFLUENCE CELL-CELL AND CELL-MATRIX INTERACTIONS. HOFFMAN-LA ROCHE INC. 2001-11-20 US disclosed