SCHEMBL2383142

SCHEMBL2383142

[c]1ccc(C2CCOCC2)cc1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 2/20 0.37
HRH3 Q9Y5N1 1/20 0.37
POLB P06746 1/20 0.37
ESR2 Q92731 4/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
DAO P14920 1/20 0.33
PRKAB2 O43741 4/20 0.33
PRKAG1 P54619 4/20 0.33
PRKAA2 P54646 4/20 0.33
PRKAA1 Q13131 4/20 0.33
PRKAG3 Q9UGI9 4/20 0.33
PRKAG2 Q9UGJ0 4/20 0.33
PRKAB1 Q9Y478 4/20 0.33
SERPINE1 P05121 1/20 0.33
HTR1D P28221 1/20 0.32
OPRL1 P41146 1/20 0.32
ESR1 P03372 1/20 0.31
CYP3A4 P08684 1/20 0.31
CYP2C9 P11712 1/20 0.31
SLC18A3 Q16572 1/20 0.31

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
SCHEMBL23118049 0.92 SMN1; SMN2 (0.37) KCNH2HRH3POLBESR2SMN1; SMN2
SCHEMBL23700102 0.87 PRMT5 (0.35) POLBPRKAB2PRKAG1PRKAA2PRKAA1
SCHEMBL21590236 0.87 PRMT5 (0.35) POLBPRKAB2PRKAG1PRKAA2PRKAA1
SCHEMBL6578876 0.85 POLB (0.46) POLBESR2ESR1CYP3A4CYP2C9
SCHEMBL22929 0.85
SCHEMBL2466664 0.79 HRH3 (0.50) HRH3SMN1; SMN2OPRL1CYP3A4CYP2C9
SCHEMBL43455 0.78 ESR2 (0.47) POLBESR2ESR1CYP3A4CYP2C9
SCHEMBL21538 0.78 ESR2 (0.42) POLBESR2ESR1CYP3A4CYP2C9
SCHEMBL27814735 0.77
SCHEMBL5543159 0.76 CYP11B2 (0.42) POLBESR2SMN1; SMN2ESR1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220389009-A1 SUBSTITUTED 1,6-NAPHTHYRIDINE INHIBITORS OF CDK5 GFB (ABC), LLC 2022-12-08 US claimed
CN-114761000-A Substituted 1, 6-naphthyridine inhibitors of CDK5 金翅雀生物公司 2022-07-15 CN claimed
CN-108699052-B Anthelmintic depsipeptide compounds 勃林格殷格翰动物保健美国公司 2022-04-29 CN claimed
WO-2022011274-A1 SUBSTITUTED 1,6-NAPHTHYRIDINE INHIBITORS OF CDK5 GOLDFINCH BIO, INC. (US) 2022-01-13 WO claimed
WO-2021067569-A1 SUBSTITUTED 1, 6-NAPHTHYRIDINE INHIBITORS OF CDK5 GOLDFINCH BIO, INC. (US) 2021-04-08 WO claimed
US-20180265467-A1 PYRAZOLIDINE DERIVATIVES AND RELATED COMPOUNDS SELVITA S.A. (PL) 2018-09-20 US claimed
EP-3356331-A1 PYRAZOLIDINE DERIVATIVES AND RELATED COMPOUNDS Selvita S.A. (PL) 2018-08-08 EP claimed
US-10040759-B2 Substituted azetidinyl compounds as GlyT1 inhibitors DART NEUROSCIENCE (CAYMAN) LTD. (KY) 2018-08-07 US claimed
US-20170334846-A1 SUBSTITUTED AZETIDINYL COMPOUNDS AS GLYT1 INHIBITORS DART NEUROSCIENCE (CAYMAN) LTD. (KY) 2017-11-23 US claimed
EP-3215500-A1 SUBSTITUTED AZETIDINYL COMPOUNDS AS GLYT1 INHIBITORS Dart NeuroScience (Cayman) Ltd. (KY) 2017-09-13 EP claimed
WO-2016073420-A1 SUBSTITUTED AZETIDINYL COMPOUNDS AS GLYT1 INHIBITORS DART NEUROSCIENCE, LLC (US) 2016-05-12 WO claimed
US-11845758-B2 Pharmaceutically effective compounds inhibiting selectively the myosin 2 isoforms PRINTNET KERESKEDELMI ÉS SZOLGÁLTATÓ KFT. (HU) 2023-12-19 US disclosed
US-20230339959-A1 PHARMACEUTICALLY EFFECTIVE COMPOUNDS INHIBITING SELECTIVELY THE MYOSIN 2 ISOFORMS EÖTVÖS LORÁND TUDOMÁNYEGYETEM (HU) 2023-10-26 US disclosed
US-11746112-B2 Pharmaceutically effective compounds inhibiting selectively the myosin 2 isoforms EÖTVÖS LORÁND TUDOMÁNYEGYETEM (HU) 2023-09-05 US disclosed
US-20220389009-A1 SUBSTITUTED 1,6-NAPHTHYRIDINE INHIBITORS OF CDK5 GFB (ABC), LLC 2022-12-08 US disclosed
US-20120237475-A1 Novel Inhibitors PROBIODRUG AG (DE) 2012-09-20 US disclosed
WO-2012123563-A1 BENZ IMIDAZOLE DERIVATIVES AS INHIBITORS OF GLUTAMINYL CYCLASE PROBIODRUG AG (DE) 2012-09-20 WO disclosed
US-8269019-B2 Inhibitors PROBIODRUG AG (DE) 2012-09-18 US disclosed
WO-2011110613-A1 HETEROCYCLIC INHIBITORS OF GLUTAMINYL CYCLASE (QC, EC 2.3.2.5) PROBIODRUG AG (DE) 2011-09-15 WO disclosed
US-20110224254-A1 NOVEL INHIBITORS PROBIODRUG AG (DE) 2011-09-15 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 (9 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-11845758-B2 Pharmaceutically effective compounds inhibiting selectively the myosin 2 isoforms MYH2, MYLK2, MYO1B KCNH2 2021/4885HRH3 3226/4885POLB 1490/4885
US-20110224254-A1 NOVEL INHIBITORS GLUL, QPCT, GLS KCNH2 943/4885HRH3 3060/4885POLB 1231/4885
US-20180265467-A1 PYRAZOLIDINE DERIVATIVES AND RELATED COMPOUNDS LDHB, LDHA, PDK1 KCNH2 1382/4885HRH3 1173/4885POLB 440/4885
US-20220389009-A1 SUBSTITUTED 1,6-NAPHTHYRIDINE INHIBITORS OF CDK5 CDK5, CDK5R1, PKD1 KCNH2 3142/4885HRH3 4071/4885POLB 527/4885
US-10040759-B2 Substituted azetidinyl compounds as GlyT1 inhibitors GLRA1, AGXT, B4GALT1 KCNH2 796/4885HRH3 594/4885POLB 4264/4885
US-11746112-B2 Pharmaceutically effective compounds inhibiting selectively the myosin 2 isoforms MYH2, MYLK2, MYO1B KCNH2 2021/4885HRH3 3226/4885POLB 1490/4885
US-20230339959-A1 PHARMACEUTICALLY EFFECTIVE COMPOUNDS INHIBITING SELECTIVELY THE MYOSIN 2 ISOFORMS MYH2, MYLK2, MYO1B KCNH2 2021/4885HRH3 3226/4885POLB 1490/4885
US-20120237475-A1 Novel Inhibitors GLS, NQO2, GLS2 KCNH2 1876/4885HRH3 2879/4885POLB 2072/4885
US-20170334846-A1 SUBSTITUTED AZETIDINYL COMPOUNDS AS GLYT1 INHIBITORS GLRA1, AGXT, B4GALT1 KCNH2 796/4885HRH3 594/4885POLB 4264/4885

“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.