2-Picolinic Acid

2-Picolinic Acid

SCHEMBL593292

O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C(O)c1cc(O)ccn1.O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.O=C([O-])c1ccccn1.[Eu+3]

nearest known ligand 0.56

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.56
NAPRT Q6XQN6 1/20 0.56
P4HTM Q9NXG6 1/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
KDM4E B2RXH2 6/20 0.45
ALDH1A1 P00352 5/20 0.45
KDM5A P29375 2/20 0.45
KDM6B O15054 2/20 0.45
KDM4A O75164 2/20 0.45
KDM5C P41229 2/20 0.45
KDM4C Q9H3R0 2/20 0.45
KDM2A Q9Y2K7 2/20 0.45
KDM3A Q9Y4C1 2/20 0.45
MAPT P10636 2/20 0.45
TET3 O43151 1/20 0.45
BBOX1 O75936 1/20 0.45
ASPH Q12797 1/20 0.45
KDM4D Q6B0I6 1/20 0.45
TET2 Q6N021 1/20 0.45
ALKBH5 Q6P6C2 1/20 0.45

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
2-Picolinic Acid SCHEMBL593739 0.97 LMNA (0.56) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL593180 0.94 LMNA (0.61) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL12076591 0.91 LMNA (0.61) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL594569 0.91 LMNA (0.61) LMNANAPRTP4HTML3MBTL1KDM4E
SCHEMBL2362971 0.89 KDM4E (0.52) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL595042 0.87 LMNA (0.69) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL593726 0.87 LMNA (0.69) LMNANAPRTP4HTML3MBTL1KDM4E
SCHEMBL65841 0.82 KDM4E (0.63) LMNANAPRTP4HTML3MBTL1KDM4E
SCHEMBL29951101 0.82 KDM4E (0.63) LMNANAPRTP4HTML3MBTL1KDM4E
2-Picolinic Acid SCHEMBL28737738 0.82 CES2 (0.64) LMNANAPRTP4HTML3MBTL1KDM4E

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
EP-2294159-B1 DISTANCE-CONTROLLED ENERGY TRANSFER DYE COMPLEXES INBIO PROF JUERGEN BUEDDEFELD DR PETER KLAUTH PROF MANFRED RIETZ GBR (DE) 2012-09-05 EP claimed
US-20110189781-A1 DISTANCE-CONTROLLED ENERGY TRANSFER DYE COMPLEXES BÜDDEFELD, JÜRGEN, PROF (DE) 2011-08-04 US claimed
EP-2294159-B1 DISTANCE-CONTROLLED ENERGY TRANSFER DYE COMPLEXES INBIO PROF JUERGEN BUEDDEFELD DR PETER KLAUTH PROF MANFRED RIETZ GBR (DE) 2012-09-05 EP disclosed
EP-2417216-A2 MODIFICATION OF LAYERED SILICATES FOR LUMINESCENCE ACTIVATION Inbio Prof. Jürgen Büddefeld Dr. Peter Klauth Prof. Manfred Rietz Gbr (DE) 2012-02-15 EP disclosed
US-20110189781-A1 DISTANCE-CONTROLLED ENERGY TRANSFER DYE COMPLEXES BÜDDEFELD, JÜRGEN, PROF (DE) 2011-08-04 US disclosed
WO-2010115503-A2 MODIFICATION OF LAYERED SILICATES FOR LUMINESCENCE ACTIVATION INBIO PROF. JÜRGEN BÜDDEFELD DR. PETER KLAUTH PROF. MANFRED RIETZ GBR (DE) 2010-10-14 WO disclosed