SCHEMBL2736787

SCHEMBL2736787

CCCCn1cc(-c2cc3ccccc3o2)cc(C(=O)NCc2ccc(F)cc2)c1=O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 1/20 0.45
CNR1 P21554 7/20 0.44
CNR2 P34972 6/20 0.44
TDP1 Q9NUW8 2/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
KMT2A Q03164 3/20 0.44
KDM4E B2RXH2 1/20 0.44
ATM Q13315 1/20 0.43
MEN1 O00255 1/20 0.43
RAB9A P51151 1/20 0.43
SMN1; SMN2 Q16637 2/20 0.42
POLB P06746 1/20 0.42
TP53 P04637 1/20 0.42
MAPT P10636 1/20 0.42
HTT P42858 1/20 0.42
PDE10A Q9Y233 1/20 0.42
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA4 P22748 1/20 0.42

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
SCHEMBL2736785 0.93 MAOB (0.53) MAOBCNR1CNR2TDP1L3MBTL1
SCHEMBL2736786 0.84 L3MBTL1 (0.54) MAOBCNR1CNR2L3MBTL1KMT2A
SCHEMBL2736816 0.84 SMN1; SMN2 (0.48) CNR1CNR2KMT2ASMN1; SMN2POLB
SCHEMBL2736820 0.83 CNR1 (0.50) CNR1CNR2KMT2ASMN1; SMN2POLB
SCHEMBL2736810 0.82 CNR2 (0.56) CNR1CNR2L3MBTL1KMT2APOLB
SCHEMBL2736844 0.81 CNR2 (0.52) CNR1CNR2KMT2ASMN1; SMN2POLB
SCHEMBL2736792 0.81 CNR2 (0.44) CNR1CNR2KMT2ASMN1; SMN2POLB
SCHEMBL2736808 0.81 CNR1 (0.48) CNR1CNR2KMT2ASMN1; SMN2POLB
SCHEMBL2736854 0.80 CNR1 (0.48) CNR1CNR2KMT2AKDM4EMEN1
SCHEMBL2736824 0.80 PDE10A (0.55) CNR1CNR2KDM4ESMN1; SMN2TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8088924-B2 Pyridone derivatives having a binding activity to the cannabinoid type 2 receptor SHIONOGI & CO., LTD. (JP) 2012-01-03 US disclosed
US-8088924-B2 Pyridone derivatives having a binding activity to the cannabinoid type 2 receptor SHIONOGI & CO., LTD. (JP) 2012-01-03 US disclosed
US-20100081686-A1 Pyridone derivatives having a binding activity to the cannabinoid type 2 recepter TADA YUKIO 2010-04-01 US disclosed
US-20100081686-A1 Pyridone derivatives having a binding activity to the cannabinoid type 2 recepter TADA YUKIO 2010-04-01 US disclosed
US-7652141-B2 Immunosuppressants, analgesics, antiinflammatory agents SHIONOGI & CO., LTD. (JP) 2010-01-26 US disclosed
US-7652141-B2 Immunosuppressants, analgesics, antiinflammatory agents SHIONOGI & CO., LTD. (JP) 2010-01-26 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 (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-20100081686-A1 Pyridone derivatives having a binding activity to the cannabinoid type 2 recepter CNR2, CNR1, NPY2R MAOB 928/4885CNR1 2/4885CNR2 1/4885

“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.