SCHEMBL1585076

SCHEMBL1585076

CCOC(=O)CC1CCCO1

nearest known ligand 0.51

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.51
POLB P06746 1/20 0.51
ALDH1A1 P00352 4/20 0.49
HPGD P15428 5/20 0.44
HTT P42858 2/20 0.44
CYP1A2 P05177 1/20 0.44
MAPK1 P28482 1/20 0.44
HSD17B10 Q99714 1/20 0.44
KMT2A Q03164 1/20 0.44
MAPT P10636 1/20 0.43
CYP2C9 P11712 1/20 0.43
CYP2C19 P33261 1/20 0.43
RAB9A P51151 1/20 0.43
TSHR P16473 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
KDM4E B2RXH2 1/20 0.41

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
SCHEMBL1961403 0.95 POLB (0.46) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL29878165 0.93 POLB (0.45) LMNAPOLBALDH1A1HPGDKMT2A
SCHEMBL28474394 0.91 GAA (0.43) LMNAPOLBALDH1A1KMT2ARAB9A
SCHEMBL22169204 0.87 LMNA (0.46) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL9245030 0.83 LMNA (0.57) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL22480306 0.82 LMNA (0.45) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL11535456 0.82 ALDH1A1 (0.51) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL22169130 0.82 LMNA (0.42) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL2125917 0.81 LMNA (0.50) LMNAPOLBALDH1A1HPGDHTT
SCHEMBL15058806 0.81 LMNA (0.50) LMNAPOLBALDH1A1HPGDHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025097438-A1 ORGANIC POSITIVE ELECTRODE, AND DOUBLE-ION BATTERY AND PREPARATION METHOD THEREFOR AND USE THEREOF 深圳先进技术研究院 2025-05-15 WO claimed
CN-115304564-A Preparation method of S-tetrahydrofuran formic acid 成都融创亿恒生物医药科技有限公司 2022-11-08 CN claimed
CN-112851623-B Method for preparing epsilon-caprolactone, 6-hydroxycaproic acid and ester thereof by using tetrahydrofurfuryl acetic acid and ester thereof 中国科学院兰州化学物理研究所 2022-04-08 CN claimed
EP-2701164-B1 Electromagnet device OMRON TATEISI ELECTRONICS CO (JP) 2018-09-12 EP claimed
CN-206299895-U Counting, energy-saving high-vacuum electromagnetic valve 上海巨良电磁阀制造有限公司 2017-07-04 CN claimed
CN-106594385-A Energy-saving high-vacuum electromagnetic valve with counting function 上海巨良电磁阀制造有限公司 2017-04-26 CN claimed
CN-105646634-A Preparation method of impurities of obeticholic acid 中国药科大学 2016-06-08 CN claimed
EP-2701164-A2 Electromagnet device Omron Corporation (JP) 2014-02-26 EP claimed
US-12551490-B2 Heterocyclic modulators of lipid synthesis SAGIMET BIOSCIENCES INC. (US) 2026-02-17 US disclosed
WO-2025097438-A1 ORGANIC POSITIVE ELECTRODE, AND DOUBLE-ION BATTERY AND PREPARATION METHOD THEREFOR AND USE THEREOF 深圳先进技术研究院 2025-05-15 WO disclosed
CN-119768473-A Polymer composition and single layer phase difference material 日产化学株式会社 2025-04-04 CN disclosed
US-20240400552-A1 HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS SAGIMET BIOSCIENCES INC. 2024-12-05 US disclosed
CN-117327284-B Preparation method of sulfur-containing onium ion organic silicon resin with marine antifouling function 山东海曦新材料有限公司 2024-02-27 CN disclosed
WO-2024038887-A1 POLYMER COMPOSITION AND SINGLE-LAYER RETARDATION MATERIAL 日産化学株式会社 2024-02-22 WO disclosed
EP-0827406-A4 1998-03-11 EP disclosed
WO-1996027379-A9 CARBOPEPTOIDS AND CARBONUCLEOTOIDS 1996-11-28 WO disclosed
WO-1996027379-A1 CARBOPEPTOIDS AND CARBONUCLEOTOIDS THE SCRIPPS RESEARCH INSTITUTE (US) 1996-09-12 WO disclosed
US-5461175-A Method for separating enantiomers of aryloxipropanolamine derivatives, and chiral solid-phase chromatography material for use in the method FISCHER LUTZ (DE) 1995-10-24 US disclosed
EP-0632794-A1 METHOD FOR SEPARATING ENANTIOMERS OF ARYLOXIPROPANOLAMINE DERIVATIVES, AND CHIRAL SOLID-PHASE CHROMATOGRAPHY MATERIAL FOR USE IN THE METHOD FISCHER, Lutz (DE) 1995-01-11 EP disclosed
WO-1993009075-A1 METHOD FOR SEPARATING ENANTIOMERS OF ARYLOXIPROPANOLAMINE DERIVATIVES, AND CHIRAL SOLID-PHASE CHROMATOGRAPHY MATERIAL FOR USE IN THE METHOD FISCHER LUTZ (DE) 1993-05-13 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 (2 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-20240400552-A1 HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS FASN, FADS1, FADS2 LMNA 3576/4885POLB 2667/4885ALDH1A1 651/4885
US-12551490-B2 Heterocyclic modulators of lipid synthesis FASN, FADS1, FADS2 LMNA 2876/4885POLB 3427/4885ALDH1A1 540/4885

“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.