SCHEMBL2321634

SCHEMBL2321634

O=C(O)c1ccc(C2CC2)cc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.57
TP53 P04637 1/20 0.57
HDAC8 Q9BY41 2/20 0.52
HDAC6 Q9UBN7 2/20 0.52
HDAC1 Q13547 1/20 0.52
SRD5A2 P31213 2/20 0.50
HDAC3 O15379 1/20 0.50
HDAC11 Q96DB2 1/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
MRGPRX4 Q96LA9 1/20 0.49
HAO1 Q9UJM8 1/20 0.49
KMO O15229 1/20 0.48
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48
CA12 O43570 1/20 0.48
CA3 P07451 1/20 0.48
TYR P14679 1/20 0.48
DRD1 P21728 1/20 0.48
CA4 P22748 1/20 0.48

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
SCHEMBL901207 1.00 TSHR (0.57) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL901209 1.00 TSHR (0.57) TSHRTP53HDAC8HDAC6HDAC1
Hydrochloric Acid SCHEMBL4290507 0.98 TSHR (0.55) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL24087489 0.94 HDAC8 (0.56) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL28005910 0.92 ESR2 (0.59) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL9472162 0.91 TSHR (0.52) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL3495930 0.91 HDAC8 (0.63) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL13266972 0.91 HDAC8 (0.58) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL13186036 0.90 ESR2 (0.60) TSHRTP53HDAC8HDAC6HDAC1
SCHEMBL6686098 0.90 NPC1 (0.66) TSHRTP53HDAC8HDAC6HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117658749-B Method for preparing aryl carboxylic acid by reacting copper compound catalyzed aryl sulfonium salt with carbon dioxide NANKAI UNIVERSITY (CN) 2026-05-26 CN disclosed
EP-4739682-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS Janssen Pharmaceutica NV (BE) 2026-05-13 EP disclosed
US-20250388604-A1 Compounds and Their Use as PDE4 Activators MIRONID LIMITED (GB) 2025-12-25 US disclosed
EP-4572762-A1 COMPOUNDS AND THEIR USE AS PDE4 ACTIVATORS Mironid Limited (GB) 2025-06-25 EP disclosed
US-12281108-B2 Pyrrolidinone derivatives as formyl peptide 2 receptor agonists BRISTOL-MYERS SQUIBB COMPANY (US) 2025-04-22 US disclosed
US-20250122223-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS ALMAC DISCOVERY LIMITED (GB) 2025-04-17 US disclosed
WO-2025008058-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS JANSSEN PHARMACEUTICA NV (BE) 2025-01-09 WO disclosed
EP-4466072-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS Almac Discovery Limited (GB) 2024-11-27 EP disclosed
CN-118946566-A Heterocyclic compounds as ubiquitin-specific protease 7 inhibitors 阿尔麦克探索有限公司 2024-11-12 CN disclosed
CN-118652243-A Peroxisome proliferator-activated receptor (PPARs) agonist, preparation method and application thereof 中国医学科学院医药生物技术研究所 2024-09-17 CN disclosed
US-20090170921-A1 Benzimidazole derivatives NOVARTIS AG (CH) 2009-07-02 US disclosed
WO-2009074487-A1 INHIBITORS OF STEAROYL-COA DESATURASE F. HOFFMANN-LA ROCHE AG (CH) 2009-06-18 WO disclosed
US-20090156572-A1 Nitrogen-containing heterocyclic compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED 2009-06-18 US disclosed
WO-2009072643-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-06-11 WO disclosed
US-20090149466-A1 INHIBITORS OF STEAROYL-COA DESATURASE GILLESPIE PAUL 2009-06-11 US disclosed
US-20080300243-A1 Amide Derivatives as Ion-Channel Ligands and Pharmaceutical Compositions and Methods of Using the Same RENOVIS, INC. 2008-12-04 US disclosed
CN-1930133-A Benzimidazole derivatives NOVARTIS AG (CH) 2007-03-14 CN disclosed
EP-1709006-A1 BENZIMIDAZOLE DERIVATIVES Novartis AG (CH) 2006-10-11 EP disclosed
WO-2005068433-A9 BENZIMIDAZOLE DERIVATIVES NOVARTIS AG (CH) 2005-09-15 WO disclosed
WO-2005068433-A1 BENZIMIDAZOLE DERIVATIVES NOVARTIS AG (CH) 2005-07-28 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 (7 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-20090170921-A1 Benzimidazole derivatives CYP3A7, UGT2B7, CYP2B6 TSHR 575/4885TP53 991/4885HDAC8 22/4885
US-12281108-B2 Pyrrolidinone derivatives as formyl peptide 2 receptor agonists FPR1, FPR2, FPR3 TSHR 747/4885TP53 4367/4885HDAC8 3772/4885
US-20090149466-A1 INHIBITORS OF STEAROYL-COA DESATURASE SCD, SCD5, FADS2 TSHR 3235/4885TP53 4864/4885HDAC8 584/4885
US-20250122223-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS USP7, UBA7, SENP7 TSHR 4655/4885TP53 298/4885HDAC8 274/4885
US-20250388604-A1 Compounds and Their Use as PDE4 Activators PDE4A, PDE7A, PDE4B TSHR 1206/4885TP53 4753/4885HDAC8 614/4885
US-20080300243-A1 Amide Derivatives as Ion-Channel Ligands and Pharmaceutical Compositions and Methods of Using the Same TRPV1, TRPA1, TRPV2 TSHR 2775/4885TP53 4006/4885HDAC8 796/4885
US-20090156572-A1 Nitrogen-containing heterocyclic compound and use thereof NTSR2, NTSR1, HNMT TSHR 396/4885TP53 4801/4885HDAC8 805/4885

“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.