SCHEMBL1171873

SCHEMBL1171873

Cc1nnc(C(O)c2cccc(-c3cccc(OCc4ccccc4)c3)c2)o1

nearest known ligand 0.71

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 2/20 0.71
▸ HPGD P15428 2/20 0.71
▸ HTT P42858 2/20 0.71
▸ ALOX15 P16050 1/20 0.71
▸ TSHR P16473 1/20 0.71
▸ MAPK1 P28482 1/20 0.71
▸ SMN1; SMN2 Q16637 1/20 0.71
▸ GAA P10253 1/20 0.56
▸ CASP3 P42574 1/20 0.56
▸ SENP8 Q96LD8 1/20 0.56
▸ SENP7 Q9BQF6 1/20 0.56
▸ SENP6 Q9GZR1 1/20 0.56
▸ CTSA P10619 11/20 0.52
▸ ALOX5 P09917 1/20 0.51
▸ PTGER4 P35408 1/20 0.44
▸ MEN1 O00255 1/20 0.43
▸ KMT2A Q03164 1/20 0.43
▸ MRGPRX4 Q96LA9 1/20 0.43

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
SCHEMBL12746075 1.00 LMNA (0.71) LMNAHPGDHTTALOX15TSHR
SCHEMBL2775162 1.00 LMNA (0.71) LMNAHPGDHTTALOX15TSHR
SCHEMBL13183083 0.83 SMN1; SMN2 (0.49) LMNAHPGDHTTALOX15TSHR
SCHEMBL12863942 0.76 POLB (0.50) LMNAHPGDHTTALOX15TSHR
SCHEMBL1172432 0.75 CTSA (0.51) LMNAHPGDHTTALOX15TSHR
SCHEMBL12746073 0.75 CTSA (0.51) LMNAHPGDHTTALOX15TSHR
SCHEMBL1172003 0.74 MRGPRX4 (0.54) SMN1; SMN2PTGER4MRGPRX4
SCHEMBL477599 0.73 SMN1; SMN2 (0.62) LMNAHPGDHTTALOX15TSHR
SCHEMBL379281 0.72 MAOB (0.67) ALOX5MRGPRX4
SCHEMBL2137838 0.71 MRGPRX4 (0.69) ALOX5MRGPRX4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9102622-B2 Fatty acid amide hydrolase inhibitors UNIVERSITY OF CONNECTICUT (US) 2015-08-11 — — US disclosed
US-20110071178-A1 Methods and Compounds for Modulating Cannabinoid Activity NORTHEASTERN UNIVERSITY (US) 2011-03-24 — — US disclosed
US-20110039874-A1 MONOACYLGLYCEROL LIPASE INHIBITORS FOR MODULATION OF CANNABINOID ACTIVITY NORTHEASTERN UNIVERSITY (US) 2011-02-17 — — US disclosed
US-20100234379-A1 Dual modulation of endocannabinoid transport and fatty-acid amide hydrolase for treatment of excitotoxicity CONNECTICUT, UNIVERSITY OF 2010-09-16 — — US disclosed
US-20090306016-A1 FATTY ACID AMIDE HYDROLASE INHIBITORS UNIVERSITY OF CONNECTICUT 2009-12-10 — — 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 (4 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-20110039874-A1 MONOACYLGLYCEROL LIPASE INHIBITORS FOR MODULATION OF CANNABINOID ACTIVITY MGLL, FAAH, FAAH2 LMNA 2518/4885HPGD 952/4885HTT 4123/4885
US-20090306016-A1 FATTY ACID AMIDE HYDROLASE INHIBITORS FAAH, FAAH2, CNR2 LMNA 4375/4885HPGD 524/4885HTT 4397/4885
US-20100234379-A1 Dual modulation of endocannabinoid transport and fatty-acid amide hydrolase for treatment of excitotoxicity FAAH, FAAH2, CNR2 LMNA 3975/4885HPGD 1848/4885HTT 1680/4885
US-20110071178-A1 Methods and Compounds for Modulating Cannabinoid Activity FAAH, FAAH2, CNR2 LMNA 2779/4885HPGD 833/4885HTT 3707/4885

“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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