Arbaclofen

Arbaclofen

SCHEMBL351220

NC[C@H](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 Arbaclofen. 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
Baclofen SCHEMBL5556250 1.00 GABBR2 (1.00) GABBR2GABBR1LMNACYP2C9CYP1A2
Baclofen SCHEMBL19333 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

Claimed or disclosed in 334 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12605367-B2 Methods of treatment and/or prevention of disorders and symptoms related to BKCa and/or SK channelophathies Universite de Bordeaux (FR) 2026-04-21 US claimed
US-20250381138-A1 Non-opioid analgesic formulations of nanoemulsions DUQUESNE UNIVERSITY OF THE HOLY SPIRIT (US) 2025-12-18 US claimed
US-20250288548-A1 INTRANASAL BACLOFEN THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2025-09-18 US claimed
WO-2025111482-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS BEXSON BIOMEDICAL, INC. (US) 2025-05-30 WO claimed
US-20250163379-A1 METHOD FOR DIFFERENTIATING HEMATOPOIETIC STEM/PROGENITOR CELLS INTO NK CELLS HEMACELL BIOTECHNOLOGY INC. (CN) 2025-05-22 US claimed
US-20240408042-A1 ORALLY DISINTEGRATING BACLOFEN COMPOSITIONS AND METHODS OF MAKING SAME CLINICAL RES ASSOCIATES LLC (US) 2024-12-12 US claimed
US-20240390364-A1 Novel Pyridine Compositions and their use in methods for preventing or treating diseases, disorders and conditions REID CHRISTOPHER BRIAN (US) 2024-11-28 US claimed
CN-118786209-A Method for differentiating hematopoietic stem/progenitor cells into NK cells 苏州血霁生物科技有限公司 2024-10-15 CN claimed
US-20240285637-A1 PHOSPHODIESTERASE INHIBITORS FOR THE MITIGATION OF FRAGILE X SYNDROME SYMPTOMS The Royal Institution of the Advancement of Learning/McGill University (CA) 2024-08-29 US claimed
EP-4366739-A1 PHOSPHODIESTERASE INHIBITORS FOR THE MITIGATION OF FRAGILE X SYNDROME SYMPTOMS The Royal Institution for the Advancement of Learning / McGill University (CA) 2024-05-15 EP claimed
US-8669395-B2 Optically active 4-amino-3-(4-chlorophenyl)butanoic acid SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2014-03-11 US claimed
EP-2345634-B1 Optically active 4-amino-3-(4-chlorophenyl) butanoic acid SUMITOMO CHEMICAL CO (JP) 2013-03-06 EP claimed
US-8299291-B2 Methods of synthesizing 1-(acyloxy)-alkyl carbamate prodrugs XENOPORT, INC. (US) 2012-10-30 US claimed
EP-2345634-A1 Optically active 4-amino-3-(4-chlorophenyl) butanoic acid Sumitomo Chemical Company, Limited (JP) 2011-07-20 EP claimed
US-20110152572-A1 OPTICALLY ACTIVE 4-AMINO-3-(4-CHLOROPHENYL)BUTANOIC ACID SUMITOMO CHEMICAL COMPANY, LIMITED 2011-06-23 US claimed
CN-102056891-A Method of producing purified optically active 4-amino-3-(substituted phenyl)butanoic acid compound SUMITOMO CHEMICAL CO 2011-05-11 CN claimed
US-20110087049-A1 METHOD OF PRODUCING PURIFIED OPTICALLY ACITVE 4-AMINO-3-(SUBSTITUTED PHENYL)BUTANOIC ACID COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED 2011-04-14 US claimed
EP-2298730-A1 METHOD OF PRODUCING PURIFIED OPTICALLY ACTIVE 4-AMINO-3-(SUBSTITUTED PHENYL)BUTANOIC ACID COMPOUND Sumitomo Chemical Company, Limited (JP) 2011-03-23 EP claimed
US-20100087667-A1 METHODS OF SYNTHESIZING 1-(ACYLOXY)-ALKYL CARBAMATE PRODRUGS XENOPORT, INC. (US) 2010-04-08 US claimed
WO-2010017504-A1 METHODS OF SYNTHESIZING 1-(ACYLOXY)-ALKYL CARBAMATE PRODRUGS XENOPORT, INC. (US) 2010-02-11 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20100087667-A1 METHODS OF SYNTHESIZING 1-(ACYLOXY)-ALKYL CARBAMATE PRODRUGS CPS1, ASNS, NAAA GABBR2 1092/4885GABBR1 961/4885LMNA 3051/4885
US-20250288548-A1 INTRANASAL BACLOFEN SLC6A13, GABBR1, GABRB2 GABBR2 5/4885GABBR1 2/4885LMNA 4131/4885
US-20240408042-A1 ORALLY DISINTEGRATING BACLOFEN COMPOSITIONS AND METHODS OF MAKING SAME GABBR2, GABBR1, GABRB2 GABBR2 1/4885GABBR1 2/4885LMNA 3376/4885
US-12605367-B2 Methods of treatment and/or prevention of disorders and symptoms related to BKCa and/or SK channelophathies KCNN3, KCNN1, KCNN2 GABBR2 149/4885GABBR1 96/4885LMNA 766/4885
US-20110087049-A1 METHOD OF PRODUCING PURIFIED OPTICALLY ACITVE 4-AMINO-3-(SUBSTITUTED PHENYL)BUTANOIC ACID COMPOUND ALAD, OR10J3, ACMSD GABBR2 44/4885GABBR1 41/4885LMNA 3798/4885

“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.