SCHEMBL405839

SCHEMBL405839

C=CB(O)O.CC(C)(O)C(C)(C)O

nearest known ligand 0.32

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
THRB P10828 1/20 0.32

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
SCHEMBL17421860 1.00 THRB (0.32) THRB
Boric Acid SCHEMBL29096575 0.80 THRB (0.32) THRB
Boric Acid SCHEMBL28861877 0.80 THRB (0.32) THRB
SCHEMBL127444 0.78
Boric Acid SCHEMBL27938813 0.74 THRB (0.38) THRB
Boric Acid SCHEMBL474845 0.73 THRB (0.43) THRB
Boric Acid SCHEMBL4976220 0.73 THRB (0.43) THRB
Boric Acid SCHEMBL28285073 0.73 THRB (0.43) THRB
Boric Acid SCHEMBL4139673 0.73 THRB (0.43) THRB
Boric Acid SCHEMBL594481 0.73 THRB (0.43) THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630564-B2 Internal cyclic sulphiamidine amide-aryl amide compound and use thereof for treating hepatitis B SHANGHAI LONGWOOD BIOPHARMACEUTICALS CO., LTD. (CN) 2026-05-19 US disclosed
WO-2026089784-A2 COMPOUNDS AND COMPOSITIONS FOR CONJUGATION TO BIOLIGANDS FOR IMAGING AND RADIOPHARMACEUTICAL APPLICATIONS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2026-04-30 WO disclosed
EP-4713020-A2 DRUG-LINKERS AND DRUG CONJUGATES Solve Therapeutics, Inc. (US) 2026-03-25 EP disclosed
US-12577239-B2 Sulfilimines or sulfoximines containing fungicidal heterocyclic compounds PI INDUSTRIES LTD. (IN) 2026-03-17 US disclosed
US-20260049071-A1 PROTEIN TYROSINE KINASE INHIBITOR AND MEDICAL USE THEREOF BEYANG THERAPEUTICS CO LTD (CN) 2026-02-19 US disclosed
US-12552796-B2 EED inhibitor, and preparation method therefor and use thereof JING MEDICINE TECHNOLOGY (SHANGHAI) LTD. (CN) 2026-02-17 US disclosed
EP-4056570-B1 EED INHIBITOR, AND PREPARATION METHOD THEREFOR AND USE THEREOF UNIV SHANGHAI TECHNOLOGY (CN) 2026-01-07 EP disclosed
US-20260001891-A1 FUSED RING COMPOUND, CONJUGATE THEREOF AND USE THEREOF KEYMED BIOSCIENCES (CHENGDU) CO., LTD. (CN) 2026-01-01 US disclosed
EP-4623936-A1 FUSED RING COMPOUND, CONJUGATE THEREOF AND USE THEREOF Keymed Biosciences (Chengdu) Co., Ltd. (CN) 2025-10-01 EP disclosed
US-20250223303-A1 TRICYCLIC BORONIC ACID DERIVATIVE, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SHANGHAI JEMINCARE PHARMACEUTICAL CO., LTD. (CN) 2025-07-10 US disclosed
US-8710060-B2 Piperazinyl methyl phenyl cyclohexane compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2014-04-29 US disclosed
WO-2014018765-A1 THERAPEUTIC COMPOUNDS UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2014-01-30 WO disclosed
US-20130289048-A1 CYCLOHEXANE DERIVATIVE COMPOUND DAIICHI SANKYO COMPANY, LIMITED (JP) 2013-10-31 US disclosed
EP-2623492-A1 CYCLOHEXANE DERIVATIVE COMPOUND DAIICHI SANKYO COMPANY, LIMITED (JP) 2013-08-07 EP disclosed
EP-2595958-A2 NOVEL PROCESSES FOR THE MANUFACTURE OF PROPANE-1-SULFONIC ACID {3-[5-(4-CHLORO-PHENYL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL]-2,4-DIFLUORO-PHENYL}-AMIDE F.HOFFMANN-LA ROCHE AG (CH) 2013-05-29 EP disclosed
US-20120022258-A1 Novel Processes for the manufacture of Propane-1-sulfonic acid -amide F. HOFFMANN-LA ROCHE AG (CH) 2012-01-26 US disclosed
WO-2012010538-A2 NOVEL PROCESSES FOR THE MANUFACTURE OF PROPANE-1-SULFONIC ACID {3-[5-(4-CHLORO-PHENYL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL]-2,4-DIFLUORO-PHENYL}-AMIDE F. HOFFMANN-LA ROCHE AG (CH) 2012-01-26 WO disclosed
US-20100274058-A1 Process for Preparation of 2-[Vinyl (Hetero) Arylsulphonyl] Ethanol Derivatives UNIVERSITY OF DURHAM (GB) 2010-10-28 US disclosed
EP-1989181-A1 PROCESS FOR THE PREPARATION OF 2-[VINYL (HETERO) ARYL SULPHONYL]ETHANOL DERIVATIVES UNIVERSITY OF DURHAM (GB) 2008-11-12 EP disclosed
WO-2007093772-A1 PROCESS FOR THE PREPARATION OF 2- [VINYL (HETERO) ARYL SULPHONYL] ETHANOL DERIVATIVES UNIVERSITY OF DURHAM (GB) 2007-08-23 WO disclosed

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

For each of this compound's patents that has machine-readable text (9 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-12552796-B2 EED inhibitor, and preparation method therefor and use thereof HSD11B1, CYP4A11, CYP8B1 THRB 1901/4885
US-20100274058-A1 Process for Preparation of 2-[Vinyl (Hetero) Arylsulphonyl] Ethanol Derivatives SMARCC2, SMARCC1, PYM1 THRB 1101/4885
US-20250223303-A1 TRICYCLIC BORONIC ACID DERIVATIVE, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF CYP51A1, SLC10A2, BCAT2 THRB 712/4885
US-12630564-B2 Internal cyclic sulphiamidine amide-aryl amide compound and use thereof for treating hepatitis B HCCS, SLC10A1, NR1H4 THRB 372/4885
US-20260049071-A1 PROTEIN TYROSINE KINASE INHIBITOR AND MEDICAL USE THEREOF KDR, FLT1, ERBB2 THRB 394/4885
US-20120022258-A1 Novel Processes for the manufacture of Propane-1-sulfonic acid -amide SULT1A1, FASN, COASY THRB 4078/4885
US-20260001891-A1 FUSED RING COMPOUND, CONJUGATE THEREOF AND USE THEREOF HCCS, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CBR1 THRB 236/4885
US-20130289048-A1 CYCLOHEXANE DERIVATIVE COMPOUND HRH2, CBR1, HRH4 THRB 1988/4885
US-12577239-B2 Sulfilimines or sulfoximines containing fungicidal heterocyclic compounds SULT1E1, CBR1, SULT1A1 THRB 2612/4885

“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.