SCHEMBL22064100

SCHEMBL22064100

COC(=O)CC(=O)CCOC/C=C/c1cccc2ccccc12

nearest known ligand 0.44

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MTNR1A P48039 1/20 0.44
MTNR1B P49286 1/20 0.44
SMPD2 O60906 2/20 0.44
HDAC8 Q9BY41 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
CYP1A2 P05177 1/20 0.41
CYP2C19 P33261 1/20 0.41
BACE1 P56817 1/20 0.41
GRIK1 P39086 1/20 0.40
GRIK2 Q13002 1/20 0.40
NPC1 O15118 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
CNR1 P21554 1/20 0.38
CNR2 P34972 1/20 0.38
PLK1 P53350 1/20 0.38

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
SCHEMBL22064157 0.84 AKT1 (0.35) NPC1SMN1; SMN2
SCHEMBL22064188 0.83 MAOB (0.40) HDAC8HDAC6GRIK1GRIK2NPC1
SCHEMBL22063579 0.83 NFE2L2 (0.51) GRIK1GRIK2NPC1SMN1; SMN2
SCHEMBL22064154 0.81 ALDH1A1 (0.45) CYP1A2CYP2C19BACE1NPC1SMN1; SMN2
SCHEMBL22063783 0.80 IDO1 (0.45) NPC1
SCHEMBL22064190 0.79 HDAC1 (0.46) HDAC8GRIK1GRIK2CNR2
SCHEMBL28655523 0.76 RXRA (0.47) MTNR1AMTNR1BSMPD2HDAC8HDAC6
SCHEMBL28708757 0.76 SMPD2 (0.56) MTNR1AMTNR1BSMPD2HDAC8HDAC6
SCHEMBL22063766 0.75 CYP4F2 (0.43) SMN1; SMN2
SCHEMBL22064197 0.74 HDAC3 (0.39) HDAC8HDAC6NPC1SMN1; SMN2

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11691958-B2 Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions NORTHWESTERN UNIVERSITY (US) 2023-07-04 US disclosed
US-11691958-B2 Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions NORTHWESTERN UNIVERSITY (US) 2023-07-04 US disclosed
US-11174238-B2 Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions NORTHWESTERN UNIVERSITY (US) 2021-11-16 US disclosed
US-20200181106-A1 ENANTIOSELECTIVE CROSS DEHYDROGENATIVE COUPLING REACTIONS AND COMPOUNDS SYNTHESIZED BY THE REACTIONS NORTHWESTERN UNIVERSITY (US) 2020-06-11 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 (3 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-11691958-B2 Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions DUOX1, DUOX2, ALDH3A1 MTNR1A 2669/4885MTNR1B 2050/4885SMPD2 4427/4885
US-20200181106-A1 ENANTIOSELECTIVE CROSS DEHYDROGENATIVE COUPLING REACTIONS AND COMPOUNDS SYNTHESIZED BY THE REACTIONS DUOX1, DUOX2, ALDH3A1 MTNR1A 2669/4885MTNR1B 2050/4885SMPD2 4427/4885
US-11174238-B2 Enantioselective cross dehydrogenative coupling reactions and compounds synthesized by the reactions DUOX1, DUOX2, ALDH3A1 MTNR1A 2669/4885MTNR1B 2050/4885SMPD2 4427/4885

“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.