SCHEMBL9128317

SCHEMBL9128317

CC(C)(C)[Si](OCC1CCC(=O)O1)(c1ccccc1)c1ccccc1

nearest known ligand 0.47

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SMYD2 Q9NRG4 3/20 0.41
CYP1A2 P05177 2/20 0.35
TOP2A P11388 1/20 0.35
CYP3A4 P08684 2/20 0.35
HTT P42858 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
PSEN1 P49768 1/20 0.33
PSEN2 P49810 1/20 0.33
APH1B Q8WW43 1/20 0.33
NCSTN Q92542 1/20 0.33
APH1A Q96BI3 1/20 0.33
PSENEN Q9NZ42 1/20 0.33
CA2 P00918 1/20 0.33
GRM5 P41594 2/20 0.33
GRM1 Q13255 1/20 0.33
BACE1 P56817 1/20 0.32
GRM2 Q14416 1/20 0.31
CA1 P00915 1/20 0.30
CA9 Q16790 1/20 0.30

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
SCHEMBL1740050 1.00 SMYD2 (0.41) SMYD2CYP1A2TOP2ACYP3A4HTT
SCHEMBL1739798 1.00 SMYD2 (0.41) SMYD2CYP1A2TOP2ACYP3A4HTT
SCHEMBL1117861 0.92 SMYD2 (0.40) SMYD2TOP2ACYP3A4HTTSMN1; SMN2
SCHEMBL52552 0.82 SMYD2 (0.40) SMYD2CYP3A4HTTSMN1; SMN2PSEN1
SCHEMBL29946810 0.82 SMYD2 (0.40) SMYD2CYP3A4HTTSMN1; SMN2PSEN1
SCHEMBL18026905 0.82 SMYD2 (0.40) SMYD2CYP3A4HTTSMN1; SMN2PSEN1
SCHEMBL9274167 0.81 TOP2A (0.40) SMYD2TOP2A
SCHEMBL9266676 0.81 TOP2A (0.40) SMYD2TOP2A
SCHEMBL28346561 0.79 SMYD2 (0.40) SMYD2CYP3A4HTTSMN1; SMN2PSEN1
SCHEMBL6412838 0.79 SMYD2 (0.41) SMYD2TOP2ACYP3A4HTTSMN1; SMN2

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4747245-A1 PHARMACEUTICAL COMPOUNDS Almac Discovery Limited (GB) 2026-05-27 EP disclosed
US-20250122223-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS ALMAC DISCOVERY LIMITED (GB) 2025-04-17 US disclosed
EP-4466072-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS Almac Discovery Limited (GB) 2024-11-27 EP disclosed
WO-2023139241-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS ALMAC DISCOVERY LIMITED (GB) 2023-07-27 WO disclosed
EP-2994469-B1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES INC (US) 2018-12-19 EP disclosed
US-20180282316-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES, INC. 2018-10-04 US disclosed
US-10017501-B2 Benzimidazole derivatives as bromodomain inhibitors GILEAD SCIENCES, INC. (US) 2018-07-10 US disclosed
US-20160376261-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES, INC. 2016-12-29 US disclosed
US-9458145-B2 Benzimidazole derivatives as bromodomain inhibitors GILEAD SCIENCES, INC. (US) 2016-10-04 US disclosed
US-20160075695-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES, INC. (US) 2016-03-17 US disclosed
EP-2994469-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS Gilead Sciences, Inc. (US) 2016-03-16 EP disclosed
US-20140336190-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES, INC. (US) 2014-11-13 US disclosed
WO-2014182929-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS GILEAD SCIENCES, INC. (US) 2014-11-13 WO disclosed
EP-0544010-B1 PROCESS FOR PRODUCING 2',3'-DIDEOXY-BETA-NUCLEOSIDE JAPAN TOBACCO INC (JP) 1995-12-13 EP disclosed
US-5416204-A Method for preparing 2'-3'-dideoxy-β-nucleosides using 2,2-dideoxy-di(organothio)-pentofuranose intermediates JAPAN TOBACCO, INCORPORATED (JP) 1995-05-16 US disclosed
EP-0544010-A1 PROCESS FOR PRODUCING 2',3'-DIDEOXY-BETA-NUCLEOSIDE JAPAN TOBACCO INC. (JP) 1993-06-02 EP 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 (6 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-20180282316-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRD1 SMYD2 1518/4885CYP1A2 3097/4885TOP2A 1315/4885
US-20250122223-A1 HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS USP7, UBA7, SENP7 SMYD2 3468/4885CYP1A2 1425/4885TOP2A 2421/4885
US-10017501-B2 Benzimidazole derivatives as bromodomain inhibitors BRD4, BRD3, BRD1 SMYD2 1518/4885CYP1A2 3097/4885TOP2A 1315/4885
US-20160075695-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRD1 SMYD2 1450/4885CYP1A2 3113/4885TOP2A 1318/4885
US-20160376261-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRD1 SMYD2 1518/4885CYP1A2 3097/4885TOP2A 1315/4885
US-20140336190-A1 BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS BRD4, BRD3, BRD1 SMYD2 1486/4885CYP1A2 3133/4885TOP2A 1231/4885

“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.