Pyridine

Pyridine

SCHEMBL1875987

C=Cc1ccc2ccccc2c1.c1ccncc1

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RELA Q04206 1/20 0.50
ALDH1A1 P00352 4/20 0.47
L3MBTL1 Q9Y468 2/20 0.47
KDM4E B2RXH2 1/20 0.47
CYP1A1 P04798 2/20 0.43
CYP1A2 P05177 2/20 0.43
CYP1B1 Q16678 2/20 0.43
CYP3A4 P08684 1/20 0.43
CYP2D6 P10635 1/20 0.43
TSHR P16473 1/20 0.41
GRIN2D O15399 2/20 0.41
GRIN3B O60391 2/20 0.41
GRIN1 Q05586 2/20 0.41
GRIN2A Q12879 2/20 0.41
GRIN2B Q13224 2/20 0.41
GRIN2C Q14957 2/20 0.41
GRIN3A Q8TCU5 2/20 0.41
MAPT P10636 2/20 0.41
LMNA P02545 2/20 0.41
MEN1 O00255 2/20 0.41

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
SCHEMBL2997515 0.86 RELA (0.58) RELAALDH1A1L3MBTL1KDM4ECYP3A4
SCHEMBL29357489 0.86 RELA (0.58) RELAALDH1A1L3MBTL1KDM4ECYP3A4
SCHEMBL110160 0.86 RELA (0.58) RELAALDH1A1L3MBTL1KDM4ECYP3A4
Styrene SCHEMBL3214387 0.84 RELA (0.63) RELAALDH1A1L3MBTL1KDM4ECYP1B1
Hydrochloric Acid SCHEMBL5493921 0.84 RELA (0.56) RELAALDH1A1L3MBTL1KDM4ECYP3A4
Anthracene SCHEMBL28663344 0.84 RELA (0.56) RELAALDH1A1L3MBTL1KDM4ECYP3A4
Butadiene SCHEMBL23403790 0.82 RELA (0.54) RELAALDH1A1L3MBTL1KDM4ECYP3A4
SCHEMBL1264213 0.80 RELA (0.50) RELAALDH1A1L3MBTL1KDM4ECYP3A4
SCHEMBL2701546 0.80 RELA (0.50) RELAALDH1A1L3MBTL1KDM4ECYP3A4
SCHEMBL1167373 0.80 RELA (0.50) RELAALDH1A1L3MBTL1KDM4ECYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7939703-B2 Method for photocatalytic isomerization of 1,2-diphenylethylene analogues Technical Institute of Physics and Chemistry of Chinese Academy of Science (CN) 2011-05-10 US disclosed
US-20090156872-A1 METHOD FOR PHOTOCATALYTIC ISOMERIZATION OF 1,2-DIPHENYLETHYLENE ANALOGUES Technical Institute of Physics and Chemistry of the Chinese Academy of Sciences (CN) 2009-06-18 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-20090156872-A1 METHOD FOR PHOTOCATALYTIC ISOMERIZATION OF 1,2-DIPHENYLETHYLENE ANALOGUES PIN1, PPOX, DDT RELA 2309/4885ALDH1A1 732/4885L3MBTL1 3397/4885

“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.