SCHEMBL10151471

SCHEMBL10151471

CC(C)(C)OC(=O)N1CCNCCN1C(=O)OC(C)(C)C

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTSK P43235 1/20 0.51
USP2 O75604 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
MAPK1 P28482 1/20 0.39
NR1H2 P55055 1/20 0.39
CHRM2 P08172 1/20 0.38
CHRM1 P11229 1/20 0.38
CHRM3 P20309 1/20 0.38
HPGD P15428 1/20 0.38
RECQL P46063 1/20 0.36
EPHX1 P07099 1/20 0.36
MAPT P10636 2/20 0.36
KDM4E B2RXH2 1/20 0.36
THRB P10828 1/20 0.36
SIGMAR1 Q99720 1/20 0.35
MEN1 O00255 1/20 0.35
ALDH1A1 P00352 1/20 0.35
KMT2A Q03164 1/20 0.35
PARP1 P09874 1/20 0.34
CA12 O43570 1/20 0.34

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
SCHEMBL13101490 0.89 CTSK (0.42) CTSKUSP2SMN1; SMN2MAPK1NR1H2
SCHEMBL1225127 0.83 USP2 (0.58) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL587550 0.83 USP2 (0.58) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL12005408 0.83 USP2 (0.58) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL8286 0.83 USP2 (0.58) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL13101497 0.82 CTSK (0.41) CTSKUSP2SMN1; SMN2MAPK1NR1H2
Hydrochloric Acid SCHEMBL4141237 0.82 USP2 (0.56) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL14653343 0.82 USP2 (0.56) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL132585 0.82 USP2 (0.56) USP2SMN1; SMN2MAPK1NR1H2HPGD
SCHEMBL2220355 0.82 USP2 (0.56) USP2SMN1; SMN2MAPK1NR1H2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118272016-B Aldehyde-free adhesive for artificial boards and preparation method 大洼县兰田化工有限公司 2024-11-19 CN claimed
CN-118420812-B Preparation method of porous adsorption resin for treating high-salt high-ammonia-nitrogen wastewater and metal wastewater 辽宁科技学院 2024-10-29 CN claimed
CN-118420812-A Preparation method of porous adsorption resin for treating high-salt high-ammonia-nitrogen wastewater and metal wastewater 辽宁科技学院 2024-08-02 CN claimed
CN-118272016-A Aldehyde-free adhesive for artificial boards and preparation method 大洼县兰田化工有限公司 2024-07-02 CN claimed
EP-4653419-A1 LINKER FOR ANTIBODY-DRUG CONJUGATES, AND ANTIBODY-DRUG CONJUGATE Otsuka Pharmaceutical Co., Ltd. (JP) 2025-11-26 EP disclosed
CN-119683891-B Anti-cracking admixture for mass concrete and application thereof 中交四航局第一工程有限公司 2025-05-09 CN disclosed
CN-119683891-A Anti-cracking admixture for mass concrete and application thereof 中交四航局第一工程有限公司 2025-03-25 CN disclosed
CN-118272016-B Aldehyde-free adhesive for artificial boards and preparation method 大洼县兰田化工有限公司 2024-11-19 CN disclosed
CN-118420812-B Preparation method of porous adsorption resin for treating high-salt high-ammonia-nitrogen wastewater and metal wastewater 辽宁科技学院 2024-10-29 CN disclosed
CN-118420812-A Preparation method of porous adsorption resin for treating high-salt high-ammonia-nitrogen wastewater and metal wastewater 辽宁科技学院 2024-08-02 CN disclosed
WO-2024154763-A1 LINKER FOR ANTIBODY-DRUG CONJUGATES, AND ANTIBODY-DRUG CONJUGATE 大塚製薬株式会社 2024-07-25 WO disclosed
CN-118272016-A Aldehyde-free adhesive for artificial boards and preparation method 大洼县兰田化工有限公司 2024-07-02 CN disclosed
US-8148362-B2 Compound having heterocyclic ring RESEARCH FOUNDATION ITSUU LABORATORY (JP) 2012-04-03 US disclosed
US-8148362-B2 Compound having heterocyclic ring RESEARCH FOUNDATION ITSUU LABORATORY (JP) 2012-04-03 US disclosed
US-20100256355-A1 OXAZOLIDINONE DERIVATIVE HAVING 7-MEMBERED HETERO RING Research Foundation ITSUU Laboratory and Shionogi & Co., Ltd. 2010-10-07 US disclosed
US-20100256355-A1 OXAZOLIDINONE DERIVATIVE HAVING 7-MEMBERED HETERO RING Research Foundation ITSUU Laboratory and Shionogi & Co., Ltd. 2010-10-07 US disclosed
EP-2233484-A2 Oxazolidinone derivatives having a 7-membered heterocyclic ring Research Foundation Itsuu Laboratory (JP) 2010-09-29 EP disclosed
EP-2208729-A1 OXAZOLIDINONE DERIVATIVE HAVING 7-MEMBERED HETERO RING Research Foundation Itsuu Laboratory (JP) 2010-07-21 EP disclosed
US-20090299059-A1 Novel Compound Having Heterocyclic Ring RESEARCH FOUNDATION ITSUU LABORATORY (JP) 2009-12-03 US disclosed
US-20090299059-A1 Novel Compound Having Heterocyclic Ring RESEARCH FOUNDATION ITSUU LABORATORY (JP) 2009-12-03 US 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-20090299059-A1 Novel Compound Having Heterocyclic Ring NR0B2, NR2C2, NR0B1 CTSK 4737/4885USP2 3707/4885SMN1; SMN2 2514/4885
US-20100256355-A1 OXAZOLIDINONE DERIVATIVE HAVING 7-MEMBERED HETERO RING NR0B2, NR0B1, NR2C2 CTSK 4655/4885USP2 3934/4885SMN1; SMN2 2032/4885

“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.