SCHEMBL3266308

SCHEMBL3266308

CCCCCOc1cccnc1C(N)=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.60
MEN1 O00255 1/20 0.60
NR1I2 O75469 1/20 0.60
CHRM2 P08172 1/20 0.60
CYP3A4 P08684 1/20 0.60
ADRA2A P08913 1/20 0.60
MAPT P10636 1/20 0.60
OPRK1 P41145 1/20 0.60
HTR2B P41595 1/20 0.60
SLC6A3 Q01959 1/20 0.60
KMT2A Q03164 1/20 0.60
HDAC6 Q9UBN7 1/20 0.60
PTPN1 P18031 1/20 0.53
MCHR1 Q99705 2/20 0.43
CYSLTR2 Q9NS75 2/20 0.43
CYSLTR1 Q9Y271 2/20 0.43
PDE5A O76074 2/20 0.43
PDE4A P27815 2/20 0.43
PDE4B Q07343 2/20 0.43
PDE4C Q08493 2/20 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
SCHEMBL353286 0.91 MAPT (0.48) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL27466976 0.88 LMNA (0.46) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL27480442 0.86 PTPN1 (0.60) LMNAMEN1NR1I2CHRM2CYP3A4
Zinc Ion SCHEMBL9440333 0.85 PTPN1 (0.54) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL8882025 0.85 PTPN1 (0.62) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL29941277 0.84 MKNK1 (0.48) LMNAMEN1KMT2AKDM4EALDH1A1
SCHEMBL6305012 0.84 MKNK1 (0.48) LMNAMEN1KMT2AKDM4EALDH1A1
SCHEMBL2271444 0.84 PTPN1 (0.61) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL28287263 0.83 IKBKB (0.47) LMNAMEN1NR1I2CHRM2CYP3A4
SCHEMBL6290060 0.83 TBXAS1 (0.39) LMNAMEN1NR1I2CHRM2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7692020-B2 Process for the preparation of pyridylcarboxylic amides and esters BASF SE (DE) 2010-04-06 US claimed
EP-1948609-B1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2010-03-10 EP claimed
US-20080249313-A1 Process for the Preparation of Pyridylcarboxylic Amides and Esters BASF SE (DE) 2008-10-09 US claimed
EP-1948609-A1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2008-07-30 EP claimed
WO-2007051759-A1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2007-05-10 WO claimed
US-7692020-B2 Process for the preparation of pyridylcarboxylic amides and esters BASF SE (DE) 2010-04-06 US disclosed
EP-1948609-B1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2010-03-10 EP disclosed
US-20080249313-A1 Process for the Preparation of Pyridylcarboxylic Amides and Esters BASF SE (DE) 2008-10-09 US disclosed
EP-1948609-A1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2008-07-30 EP disclosed
WO-2007051759-A1 PROCESS FOR THE PREPARATION OF PYRIDYLCARBOXYLIC AMIDES AND ESTERS BASF SE (DE) 2007-05-10 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-20080249313-A1 Process for the Preparation of Pyridylcarboxylic Amides and Esters ADH1C, ADH1A, CBR1 LMNA 2011/4885MEN1 3927/4885NR1I2 1171/4885

“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.