Baclofen

Baclofen

SCHEMBL19333

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 1.00
GABBR1 known ✓ Q9UBS5 8/20 1.00
LMNA P02545 3/20 1.00
CYP2C9 P11712 3/20 1.00
CYP1A2 P05177 2/20 1.00
THRB P10828 2/20 1.00
CYP2D6 P10635 2/20 1.00
CYP2C19 P33261 2/20 1.00
MEN1 O00255 2/20 1.00
KMT2A Q03164 2/20 1.00
CYP3A4 P08684 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
NFKB1 P19838 1/20 1.00
DRD3 P35462 1/20 1.00
BLM P54132 1/20 1.00
TSHR P16473 1/20 1.00
MAPT P10636 1/20 0.57
PMP22 Q01453 1/20 0.57
SMN1; SMN2 Q16637 1/20 0.57
NPSR1 Q6W5P4 1/20 0.57

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
Baclofen SCHEMBL19334 1.00 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Arbaclofen SCHEMBL351220 1.00 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL5556250 1.00 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL656539 0.98 GABBR2 (0.96) GABBR2GABBR1LMNACYP2C9CYP1A2
Arbaclofen SCHEMBL1417519 0.98 GABBR2 (0.96) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL4915007 0.98 GABBR2 (0.96) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL3004536 0.96 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL20815463 0.96 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Arbaclofen SCHEMBL2996117 0.96 GABBR2 (0.93) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL22352888 0.93 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

Appears in 28692 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026106917-A1 EDIBLE TRANSMUCOSAL DRUG DELIVERY METHOD USING AN INTERMEDIATE CAPSULE AS A TEMPORARY VESSEL BioPhysics Pharma, Inc. (US) 2026-05-21 WO claimed
CN-114008013-B Treatment of CNS disorders with sleep disorders 哥本哈根大学 2026-05-15 CN claimed
EP-4736841-A1 A MUCOADHESIVE LAYER FOR BUCCAL ADMINISTRATION OF AN ACTIVE PHARMACEUTICAL INGREDIENT IQ medical GmbH (DE) 2026-05-06 EP claimed
US-20260115375-A1 MULTI-FLUID DELIVERY METHOD AND SYSTEM MCNEER RICHARD (US) 2026-04-30 US claimed
US-20260115161-A1 2-HYDROXY-OCTADECENE-9-CIS-OATE FOR USE IN THE TREATMENT OF ONCOLOGICAL PATHOLOGIES AND NEUROPATHIC PAIN LAMINAR PHARMACEUTICALS S A (ES) 2026-04-30 US claimed
US-20260115140-A1 COMPOSITIONS FOR ENHANCED MUCOSAL PENETRATION SHIN NIPPON BIOMEDICAL LABORATORIES LTD (JP) 2026-04-30 US claimed
US-12605345-B2 Transdermal drug delivery system BioPhysics Pharma, Inc. (US) 2026-04-21 US claimed
EP-4725506-A2 THE PEPTIDOMIMETIC COMPOUND (R)-2-AMINO-N-((S)-L-(((S)-5-AMINO-L-(3-BENZYL-1,2,4-OXADIAZOL-5-YL)PENTYL)AMINO)-3-(4-HYDROXY-2,6-DIMETHYLPHENYL)-1-OXOPROPAN-2-YL)-5-GUANIDINOPENTANAMIDE FOR USE IN THE TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS Stealth BioTherapeutics Inc. (US) 2026-04-15 EP claimed
EP-4719476-A1 COMPOSITIONS FOR ENHANCED MUCOSAL PENETRATION Shin Nippon Biomedical Laboratories, Ltd. (JP) 2026-04-08 EP claimed
US-12594388-B2 Device to deliver a predetermined amount of a substance to a natural orifice of the body APTARGROUP, INC. (US) 2026-04-07 US claimed
US-4780463-A CONTAINING PROPIONIC ACID COMPOUNDS ANALGESIC ASSOCIATES (US) 1988-10-25 US claimed
EP-0205492-A1 ANALGESIC, ANTI-INFLAMMATORY AND SKELETAL MUSCLE RELAXANT COMPOSITIONS SUNSHINE, Abraham (US) 1986-12-30 EP claimed
WO-1986003681-A1 ANALGESIC, ANTI-INFLAMMATORY AND SKELETAL MUSCLE RELAXANT COMPOSITIONS SUNSHINE ABRAHAM 1986-07-03 WO claimed
EP-0179583-A1 A system for enhancing the water dissolution rate and solubility of poorly soluble drugs MERCK & CO. INC. (US) 1986-04-30 EP claimed
EP-0147780-A2 Drug delivery device MERCK & CO. INC. (US) 1985-07-10 EP claimed
US-4508715-A DOPAMINE ANTAGONISTS;OVERDOSE TREATMENT UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 1985-04-02 US claimed
EP-0105361-A1 ANTAGONISM OF CENTRAL NERVOUS SYSTEM DRUGS BY THE ADMINISTRATION OF 4-AMINOPYRIDINE ALONE OR IN COMBINATION WITH OTHER DRUGS THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 1984-04-18 EP claimed
WO-1983003541-A1 ANTAGONISM OF CENTRAL NERVOUS SYSTEM DRUGS BY THE ADMINISTRATION OF 4-AMINOPYRIDINE ALONE OR IN COMBINATION WITH OTHER DRUGS UNIV GEORGIA RES FOUND (US) 1983-10-27 WO claimed
US-4126684-A 4-AMINO-3-P-HALOPHENYLBUTYRIC ACIDS AND THEIR DERIVATIVES USED IN THE CONTROL OF NARCOTIC ABUSE CIBA-GEIGY CORPORATION (US) 1978-11-21 US claimed
US-3947579-A HALOGENATED AMINO ACID NELSON RESEARCH & DEVELOPMENT COMPANY (US) 1976-03-30 US claimed