Lesinurad

Lesinurad

SCHEMBL29353441

O=C(O)CSc1nnc(Br)n1-c1ccc(C2CC2)c2ccccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC22A12

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SLC22A12 known ✓ Q96S37 19/20 1.00
CYP2C9 P11712 2/20 1.00
CYP2C19 P33261 2/20 1.00
CYP1A2 P05177 1/20 1.00
CYP3A4 P08684 1/20 1.00
CYP2D6 P10635 1/20 1.00
SLC22A11 Q9NSA0 1/20 1.00
SLC2A9 Q9NRM0 3/20 0.69
ALDH1A1 P00352 1/20 0.54
ALOX15 P16050 1/20 0.54
HTT P42858 1/20 0.54
HSD17B10 Q99714 1/20 0.54

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
Lesinurad SCHEMBL842962 1.00 SLC22A12 (1.00) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
Lesinurad SCHEMBL2265513 0.99 SLC22A12 (0.98) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL11915750 0.96 SLC22A12 (0.92) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL16500465 0.90 SLC22A12 (0.82) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL1299832 0.90 SLC22A12 (0.82) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL4735350 0.90 SLC22A12 (0.82) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
Lesinurad SCHEMBL1299308 0.89 SLC22A12 (0.81) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL1299461 0.89 SLC22A12 (0.81) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
SCHEMBL15698391 0.89 SLC22A12 (0.81) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4
Lesinurad SCHEMBL29588047 0.89 SLC22A12 (0.81) SLC22A12CYP2C9CYP2C19CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260130853-A1 METHOD OF TREATING GOUT BY TOPICAL APPLICATION OF NANO LINIMENT Zhang, Boke (US) 2026-05-14 US claimed
US-20260130854-A1 PREPARATION OF NANO LINIMENT FOR EXTERNAL TREATMENT OF GOUT Zhang, Boke (US) 2026-05-14 US claimed
EP-4731204-A2 SELECTIVE RBP4 ANTAGONIST AND C20-D3-RETINOL FOR TREATING MACULAR DEGENERATION, NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD), AND GOUTY ARTHRITIS (GOUT) The Trustees Of Columbia University In The City Of New York (US) 2026-04-29 EP claimed
US-12583860-B2 Processes for the preparation of multicomponent crystalline forms of active pharmaceutical ingredients using solvent vapour APOTEX INC. (CA) 2026-03-24 US claimed
US-12539273-B2 External nano liniment for gout and preparation method thereof Zhang, Boke (US) 2026-02-03 US claimed
EP-4680203-A1 COMPOSITIONS FOR SUSTAINED RELEASE OF POORLY SOLUBLE ACTIVE INGREDIENTS Prolevi Bio AB (SE) 2026-01-21 EP claimed
US-20260000663-A1 RBP4 ANTAGONISTS FOR TREATMENT AND PREVENTION OF NON-ALCOHOLIC FATTY LIVER DISEASE AND GOUT THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2026-01-01 US claimed
US-12440486-B2 RBP4 antagonists for treatment and prevention of non-alcoholic fatty liver disease and gout THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2025-10-14 US claimed
WO-2025101983-A1 NON-STEROIDAL ISONITRILE BINDING COMPOUNDS OF CYTOCHROME P450 SUBTYPES BRANDEIS UNIVERSITY (US) 2025-05-15 WO claimed
WO-2025026900-A1 COMPOUNDS FOR THE TREATMENT OR PREVENTION OF GOUT UNIVERSITAT DE LES ILLES BALEARS (ES) 2025-02-06 WO claimed
WO-2023131868-A1 HETEROCYCLIC INHIBITORS OF GLUT9 FOR TREATMENT OF DISEASE HORIZON THERAPEUTICS IRELAND DAC (IE) 2023-07-13 WO claimed
CN-106866560-B Lesinurad synthesis method 浙江美诺华药物化学有限公司 2023-05-30 CN claimed
CN-108947919-B Novel preparation method of anti-gout drug Lesinurad and key intermediate thereof 上海奥博生物医药股份有限公司 2023-05-02 CN claimed
US-20220347208-A1 FORMULATIONS USING LITHIUM TO TREAT GOUT ARTHROPATHY THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 2022-11-03 US claimed
US-20220288038-A1 ABCC11 INHIBITOR THE UNIVERSITY OF TOKYO (JP) 2022-09-15 US claimed
EP-4034136-A1 FORMULATIONS USING LITHIUM TO TREAT GOUT ARTHROPATHY THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS (US) 2022-08-03 EP claimed
EP-4019048-A1 ABCC11 INHIBITOR The University of Tokyo (JP) 2022-06-29 EP claimed
US-11365180-B2 Resolution method for axis chiral enantiomers of lesinurad CHINA RESOURCES SAIKE PHARMACEUTICAL CO., LTD. (CN) 2022-06-21 US claimed
CN-114341120-A ABCC11 inhibitor 国立大学法人东京大学 2022-04-12 CN claimed
US-20220024777-A1 NOVEL AMORPHOUS ACTIVE PHARMACEUTICAL INGREDIENTS COMPRISING SUBSTANTIALLY AMORPHOUS MESOPOROUS MAGNESIUM CARBONATE DISRUPTIVE PHARMA AB (SE) 2022-01-27 US 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 (8 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-20220288038-A1 ABCC11 INHIBITOR ABCC1, ABCC3, SLCO2B1 SLC22A12 35/4885CYP2C9 1335/4885CYP2C19 1984/4885
US-20260000663-A1 RBP4 ANTAGONISTS FOR TREATMENT AND PREVENTION OF NON-ALCOHOLIC FATTY LIVER DISEASE AND GOUT RBP4, RBP1, FABP1 SLC22A12 1765/4885CYP2C9 1832/4885CYP2C19 3860/4885
US-12440486-B2 RBP4 antagonists for treatment and prevention of non-alcoholic fatty liver disease and gout RBP4, RBP1, FABP1 SLC22A12 706/4885CYP2C9 2950/4885CYP2C19 4071/4885
US-12583860-B2 Processes for the preparation of multicomponent crystalline forms of active pharmaceutical ingredients using solvent vapour CFD, CFB, CALCR SLC22A12 950/4885CYP2C9 483/4885CYP2C19 395/4885
US-11365180-B2 Resolution method for axis chiral enantiomers of lesinurad CLK4, CLK1, CLK3 SLC22A12 4629/4885CYP2C9 1592/4885CYP2C19 2093/4885
US-12539273-B2 External nano liniment for gout and preparation method thereof NLRP3, NLRP1, LCT SLC22A12 1596/4885CYP2C9 535/4885CYP2C19 650/4885
US-20260130853-A1 METHOD OF TREATING GOUT BY TOPICAL APPLICATION OF NANO LINIMENT NLRP3, XDH, NLRP1 SLC22A12 503/4885CYP2C9 150/4885CYP2C19 138/4885
US-20260130854-A1 PREPARATION OF NANO LINIMENT FOR EXTERNAL TREATMENT OF GOUT LIPA, PNP, LIPC SLC22A12 546/4885CYP2C9 1086/4885CYP2C19 1303/4885

“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.