SCHEMBL583934

SCHEMBL583934

CC(=O)c1cccc2c1CCO2

nearest known ligand 0.45

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
MTNR1B P49286 13/20 0.45
MTNR1A P48039 11/20 0.45
DRD2 P14416 1/20 0.44
SLC9A1 P19634 2/20 0.43
SLC9A5 Q14940 1/20 0.43
SLC9A2 Q9UBY0 1/20 0.43
GAA P10253 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
PARP1 P09874 1/20 0.41
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
SCHEMBL29226728 0.90 MTNR1A (0.45) MTNR1BMTNR1ADRD2GAASMN1; SMN2
SCHEMBL496918 0.84 SLC9A1 (0.43) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2
SCHEMBL4104704 0.83 DRD2 (0.37) MTNR1BMTNR1ADRD2GAASMN1; SMN2
SCHEMBL10005787 0.82 MTNR1B (0.39) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2
SCHEMBL30184316 0.82 PARP1 (0.57) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2
SCHEMBL7122066 0.82 PARP1 (0.57) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2
SCHEMBL30884588 0.81 ALDH1A1 (0.46) MTNR1BMTNR1ASMN1; SMN2KDM4E
SCHEMBL28775369 0.81 ALDH1A1 (0.46) MTNR1BMTNR1ASMN1; SMN2KDM4E
SCHEMBL29133954 0.81 MTNR1B (0.46) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2
SCHEMBL30184412 0.81 MTNR1B (0.46) MTNR1BMTNR1ASLC9A1SLC9A5SLC9A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2011528012-A 2011-11-10 JP claimed
EP-2328882-A1 SYNTHESIS OF 6,7-DIHYDRO-1H-INDENO[5,4-B]FURAN-8(2H)-ONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK Pharmaceuticals d.d. (SI) 2011-06-08 EP claimed
WO-2010007022-A1 SYNTHESIS OF 6,7-DIHYDRO-1H-INDENO[5,4-B]FURAN-8(2H)-ONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-01-21 WO claimed
CN-113402490-B Preparation method of 1,2,6, 7-tetrahydro-8H-indeno [5,4-b ] furan-8-one 白银京宇新药业有限公司 2023-01-03 CN disclosed
EP-2927218-B1 TETRAZOLINONE COMPOUND AND USE THEREOF SUMITOMO CHEMICAL CO (JP) 2018-07-04 EP disclosed
US-9725423-B2 Tetrazolinone compound and applications thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-08-08 US disclosed
US-9725423-B2 Tetrazolinone compound and applications thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-08-08 US disclosed
US-9725423-B2 Tetrazolinone compound and applications thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-08-08 US disclosed
US-20150299146-A1 TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-22 US disclosed
US-20150299146-A1 TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-22 US disclosed
US-20150299146-A1 TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-10-22 US disclosed
EP-2243775-A1 Synthesis of 1-(2,3-Dihydrobenzofuran-4-YL)ethanone as intermediate in the preparation of ramelteon LEK Pharmaceuticals d.d. (SI) 2010-10-27 EP disclosed
EP-2243775-A1 Synthesis of 1-(2,3-Dihydrobenzofuran-4-YL)ethanone as intermediate in the preparation of ramelteon LEK Pharmaceuticals d.d. (SI) 2010-10-27 EP disclosed
WO-2010115897-A2 SYNTHESIS OF 1-(2,3-DIHYDROBENZOFURAN-4-YL)ETHANONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-10-14 WO disclosed
WO-2010115897-A2 SYNTHESIS OF 1-(2,3-DIHYDROBENZOFURAN-4-YL)ETHANONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-10-14 WO disclosed
WO-2010115897-A2 SYNTHESIS OF 1-(2,3-DIHYDROBENZOFURAN-4-YL)ETHANONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-10-14 WO disclosed
WO-2010115897-A2 SYNTHESIS OF 1-(2,3-DIHYDROBENZOFURAN-4-YL)ETHANONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-10-14 WO disclosed
WO-2010092107-A1 SYNTHESIS OF (S)-N-[2-(1,6,7,8-TETRAHYDRO-2H-INDENO-[5,4-B]FURAN-8-YL)ETHYL]PROPIONAMIDE LEK PHARMACEUTICALS D.D. (SI) 2010-08-19 WO disclosed
WO-2010007022-A1 SYNTHESIS OF 6,7-DIHYDRO-1H-INDENO[5,4-B]FURAN-8(2H)-ONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-01-21 WO disclosed
WO-2010007022-A1 SYNTHESIS OF 6,7-DIHYDRO-1H-INDENO[5,4-B]FURAN-8(2H)-ONE AS INTERMEDIATE IN THE PREPARATION OF RAMELTEON LEK PHARMACEUTICALS D.D. (SI) 2010-01-21 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-20150299146-A1 TETRAZOLINONE COMPOUND AND APPLICATIONS THEREOF RTN3, CYCS, ATL3 MTNR1B 2199/4885MTNR1A 2367/4885DRD2 1692/4885

“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.