SCHEMBL6275487

SCHEMBL6275487

O=C1c2cccc3cccc(c23)C(=O)N1CCN1CCOCC1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 10/20 0.69
▸ RXFP1 Q9HBX9 2/20 0.69
▸ ALDH1A1 P00352 5/20 0.67
▸ RAB9A P51151 3/20 0.67
▸ SMN1; SMN2 Q16637 1/20 0.67
▸ MEN1 O00255 3/20 0.67
▸ KMT2A Q03164 3/20 0.67
▸ RAD52 P43351 2/20 0.65
▸ GAA P10253 2/20 0.63
▸ HPGD P15428 3/20 0.62
▸ TDP1 Q9NUW8 1/20 0.62
▸ POLB P06746 2/20 0.61
▸ MAPT P10636 3/20 0.60
▸ AHR P35869 1/20 0.60
▸ RECQL P46063 1/20 0.60
▸ NPSR1 Q6W5P4 1/20 0.60
▸ HEXA P06865 3/20 0.58
▸ HEXB P07686 3/20 0.58
▸ LMNA P02545 5/20 0.57
▸ TP53 P04637 1/20 0.57

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
SCHEMBL6275178 0.93 KDM4E (0.69) KDM4ERXFP1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL6272682 0.86 MAPT (0.73) KDM4ERXFP1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL8556230 0.85 GRM5 (0.66) KDM4EALDH1A1RAB9ASMN1; SMN2MEN1
Hydrochloric Acid SCHEMBL27657032 0.84 GRM5 (0.64) KDM4EALDH1A1RAB9ASMN1; SMN2MEN1
SCHEMBL2619579 0.84 KDM4E (0.64) KDM4ERXFP1ALDH1A1RAB9AMEN1
SCHEMBL11623083 0.84 HEXA (0.74) KDM4ERXFP1ALDH1A1RAB9AMEN1
SCHEMBL11441512 0.83 MEN1 (0.83) KDM4ERXFP1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL11632287 0.83 HTR7 (0.70) KDM4ERXFP1ALDH1A1MEN1KMT2A
SCHEMBL11690758 0.81 RAD52 (0.64) KDM4ERXFP1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL12133960 0.81 CYP1B1 (0.60) KDM4ERXFP1ALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110041202-B Preparation method of 1, 8-disubstituted naphthalene mononitration derivative 长江大学 2022-04-19 — — CN claimed
CN-110041203-A A kind of 1,8- bis- replaces the preparation method of naphthalene system condensed-nuclei aromatics mono-nitration derivative 长江大学 2019-07-23 — — CN claimed
CN-107325095-B A kind of lysosome hypochlorous acid fluorescence probe and its preparation method and application 济南大学 2019-03-15 — — CN claimed
CN-106008342-B A kind of fluorescence probe and preparation method thereof detecting formaldehyde in cytase body 济南大学 2018-08-21 — — CN claimed
CN-106008342-A Fluorescent probe for detecting formaldehyde in cytolysosome and preparation method thereof 济南大学 2016-10-12 — — CN claimed
CN-112939935-B Lysosome targeted fluorescent probe, synthetic method thereof and cell imaging application 中国科学院大连化学物理研究所 2022-11-15 — — CN disclosed
CN-110041202-B Preparation method of 1, 8-disubstituted naphthalene mononitration derivative 长江大学 2022-04-19 — — CN disclosed
CN-110041202-A A kind of 1,8- bis- replaces the preparation method of naphthalene mono-nitration derivative 长江大学 2019-07-23 — — CN disclosed
CN-110041203-A A kind of 1,8- bis- replaces the preparation method of naphthalene system condensed-nuclei aromatics mono-nitration derivative 长江大学 2019-07-23 — — CN disclosed
CN-106008342-B A kind of fluorescence probe and preparation method thereof detecting formaldehyde in cytase body 济南大学 2018-08-21 — — CN disclosed
CN-106008342-B A kind of fluorescence probe and preparation method thereof detecting formaldehyde in cytase body 济南大学 2018-08-21 — — CN disclosed
US-9518964-B2 Method for identifying electrophiles and nucleophiles in a sample EICHEN YOAV (IL) 2016-12-13 — — US disclosed
US-20110281742-A1 METHOD FOR IDENTIFYING ELECTROPHILES AND NUCLEOPHILES IN A SAMPLE EICHEN YOAV (IL) 2011-11-17 — — US disclosed
US-20110281742-A1 METHOD FOR IDENTIFYING ELECTROPHILES AND NUCLEOPHILES IN A SAMPLE EICHEN YOAV (IL) 2011-11-17 — — US disclosed
US-20090258430-A1 Method for identifying electrophiles and nucleophiles in a sample TECHNION RESEARCH & DEVELOPMENT FOUNDATION LTD. (IL) 2009-10-15 — — US disclosed
US-20090258430-A1 Method for identifying electrophiles and nucleophiles in a sample TECHNION RESEARCH & DEVELOPMENT FOUNDATION LTD. (IL) 2009-10-15 — — US disclosed
EP-2085766-A2 Method for identifying electrophiles and nucleophiles in a sample Technion Research and Development Foundation, Ltd. (IL) 2009-08-05 — — EP disclosed
US-20050239833-A1 Compositions and methods for modulating interaction between polypeptides MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2005-10-27 — — US disclosed
WO-2005087217-A1 COMPOSITIONS AND METHODS FOR MODULATING INTERACTION BETWEEN POLYPEPTIDES THE GENERAL HOSPITAL CORPORATION (US) 2005-09-22 — — WO disclosed
WO-2005053663-A2 NOREPINEPHRINE REUPTAKE INHIBITORS USEFUL FOR TREATMENT OF COGNITIVE FAILURE ELI LILLY AND COMPANY (US) 2005-06-16 — — 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 (1 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-20050239833-A1 Compositions and methods for modulating interaction between polypeptides IAPP, SERPINA6, SERPINA2 KDM4E 4859/4885RXFP1 1823/4885ALDH1A1 4852/4885

“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.

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