SCHEMBL850694

SCHEMBL850694

C=CCOCCOS(C)(=O)=O

nearest known ligand 0.46

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
USP2 O75604 2/20 0.46
TSHR P16473 2/20 0.46
KDM4E B2RXH2 1/20 0.46
ALDH1A1 P00352 1/20 0.46
LMNA P02545 1/20 0.46
MMP9 P14780 1/20 0.46
ALOX15 P16050 1/20 0.46
MEN1 O00255 1/20 0.41
POLB P06746 1/20 0.41
KMT2A Q03164 1/20 0.41
CA2 P00918 1/20 0.34
CA9 Q16790 1/20 0.34
TDP1 Q9NUW8 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
SCHEMBL2555600 0.98 TSHR (0.44) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL30711 0.79
SCHEMBL176333 0.78 MEN1 (0.36) TSHRALDH1A1MEN1POLBKMT2A
SCHEMBL4143916 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL4149480 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL4154180 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL1627440 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL4140372 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL267542 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL4148516 0.78 USP2 (0.63) USP2TSHRKDM4EALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116813513-A Quantum dot surface organic ligand composition and preparation method thereof 苏州威迈芯材半导体有限公司 2023-09-29 CN claimed
US-20240246992-A1 MACROCYCLIC LRRK2 KINASE INHIBITORS SERVIER LAB (FR) 2024-07-25 US disclosed
EP-4308570-A1 MACROCYCLIC LRRK2 KINASE INHIBITORS Les Laboratoires Servier (FR) 2024-01-24 EP disclosed
CN-117425661-A Macrocyclic LRRK2 kinase inhibitors 法国施维雅药厂 2024-01-19 CN disclosed
CN-116813513-A Quantum dot surface organic ligand composition and preparation method thereof 苏州威迈芯材半导体有限公司 2023-09-29 CN disclosed
WO-2022194976-A1 MACROCYCLIC LRRK2 KINASE INHIBITORS LES LABORATOIRES SERVIER (FR) 2022-09-22 WO disclosed
US-10351591-B2 Polypeptides, peptides, and proteins functionalized by alkylation of thioether groups via ring-opening reactions THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-07-16 US disclosed
US-20190169161-A1 CURABLE COMPOSITION, CURED PRODUCT, OPTICAL MEMBER, LENS, AND COMPOUND FUJIFILM CORPORATION (JP) 2019-06-06 US disclosed
US-20180105553-A1 POLYPEPTIDES, PEPTIDES, AND PROTEINS FUNCTIONALIZED BY ALKYLATION OF THIOETHER GROUPS VIA RING-OPENING REACTIONS NATIONAL SCIENCE FOUNDATION 2018-04-19 US disclosed
US-9487517-B2 Spiroimidazolone derivative CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-11-08 US disclosed
US-9023583-B2 Monolayer or multilayer forming composition NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2015-05-05 US disclosed
EP-2433940-B1 SPIROIMIDAZOLONE DERIVATIVE CHUGAI PHARMACEUTICAL CO LTD (JP) 2014-09-24 EP disclosed
US-20130216956-A1 MONOLAYER OR MULTILAYER FORMING COMPOSITION NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2013-08-22 US disclosed
US-20120270838-A1 SPIROIMIDAZOLONE DERIVATIVE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2012-10-25 US disclosed
US-20120270838-A1 SPIROIMIDAZOLONE DERIVATIVE CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2012-10-25 US disclosed
EP-2433940-A1 SPIROIMIDAZOLONE DERIVATIVE Chugai Seiyaku Kabushiki Kaisha (JP) 2012-03-28 EP disclosed
EP-2433940-A1 SPIROIMIDAZOLONE DERIVATIVE Chugai Seiyaku Kabushiki Kaisha (JP) 2012-03-28 EP disclosed
WO-2010126030-A1 SPIROIMIDAZOLONE DERIVATIVE 中外製薬株式会社 (JP) 2010-11-04 WO disclosed
EP-0634895-A1 HERBICIDES ZENECA LIMITED (GB) 1995-01-25 EP disclosed
WO-1993019599-A1 HERBICIDES ZENECA LIMITED (GB) 1993-10-14 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 (5 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-20120270838-A1 SPIROIMIDAZOLONE DERIVATIVE WNK3, REN, SGK3 USP2 4813/4885TSHR 914/4885KDM4E 2949/4885
US-20180105553-A1 POLYPEPTIDES, PEPTIDES, AND PROTEINS FUNCTIONALIZED BY ALKYLATION OF THIOETHER GROUPS VIA RING-OPENING REACTIONS PTMS, TMT1A, PTMA USP2 931/4885TSHR 1100/4885KDM4E 2339/4885
US-20190169161-A1 CURABLE COMPOSITION, CURED PRODUCT, OPTICAL MEMBER, LENS, AND COMPOUND CRYAA, CRYZ, CRYAB USP2 764/4885TSHR 4227/4885KDM4E 1152/4885
US-20240246992-A1 MACROCYCLIC LRRK2 KINASE INHIBITORS LRRK2, PARK7, PINK1 USP2 3359/4885TSHR 3780/4885KDM4E 3087/4885
US-10351591-B2 Polypeptides, peptides, and proteins functionalized by alkylation of thioether groups via ring-opening reactions PTMS, TMT1A, PTMA USP2 931/4885TSHR 1100/4885KDM4E 2339/4885

“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.