SCHEMBL3773254

SCHEMBL3773254

O=C(O)Nc1ccc(Cc2ccccc2)cc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC1A3 P43003 1/20 0.58
SLC1A2 P43004 1/20 0.58
SLC1A1 P43005 1/20 0.58
POLB P06746 1/20 0.56
CA1 P00915 2/20 0.54
CA2 P00918 2/20 0.54
CA9 Q16790 2/20 0.54
LTA4H P09960 1/20 0.54
CA12 O43570 1/20 0.54
SAE1 Q9UBE0 3/20 0.53
UBA2 Q9UBT2 3/20 0.53
LMNA P02545 4/20 0.52
EPHX2 P34913 1/20 0.52
PLA2G10 O15496 1/20 0.52
PLA2G2A P14555 1/20 0.52
MEN1 O00255 1/20 0.52
KMT2A Q03164 1/20 0.52
CALM1 P0DP23 1/20 0.50
PTPN1 P18031 1/20 0.50
TSHR P16473 1/20 0.49

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
SCHEMBL2762349 0.94 POLB (0.62) SLC1A3SLC1A2SLC1A1POLBCA1
Phenol SCHEMBL663964 0.90 MAOA (0.53) SLC1A3SLC1A2SLC1A1POLBCA1
SCHEMBL28945385 0.84 ALDH1A1 (0.53) POLBLMNAMEN1KMT2AHTT
SCHEMBL4683087 0.84 MAPT (0.55) SLC1A3SLC1A2SLC1A1POLBCA1
SCHEMBL11244794 0.84 PTPN1 (0.70) SLC1A3SLC1A2SLC1A1POLBLMNA
SCHEMBL6436840 0.84 HDAC8 (0.56) POLBEPHX2MEN1KMT2APTPN1
SCHEMBL11788375 0.84 SLC1A3 (0.55) SLC1A3SLC1A2SLC1A1POLBCA1
SCHEMBL8859893 0.84 GAA (0.63) SLC1A3SLC1A2SLC1A1POLBCA1
SCHEMBL2891493 0.83 SMN1; SMN2 (0.71) POLBCA1CA2CA9CA12
SCHEMBL21504845 0.82 CA1 (0.57) SLC1A3SLC1A2SLC1A1POLBCA1

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
EP-2443092-B1 BICYCLIC AND TRICYCLIC COMPOUNDS AS KAT II INHIBITORS PFIZER (US) 2015-04-08 EP disclosed
US-8183238-B2 Bicyclic and tricyclic compounds as KAT II inhibitors PFIZER INC. (US) 2012-05-22 US disclosed
US-20100324043-A1 Bicyclic And Tricyclic Compounds As KAT II Inhibitors PFIZER INC 2010-12-23 US disclosed
EP-0014103-B1 IMPROVED PROCESS FOR THE MANUFACTURE OF CARBAMATES THE HALCON SD GROUP, INC. (US) 1983-05-11 EP disclosed
US-4279637-A Herbicidal N-substituted 4-imidazolin-2-ones VELSICOL CHEMICAL CORPORATION (US) 1981-07-21 US disclosed
US-4266070-A CARBONYLS OF COBALT, MOLYBDENUM, TITANIUM, RHODIUM, IRON, NICKEL AND IRIDIUM AS CATALYSTS FOR THE CARBONYLATION OF PRIMARY OR SECONDARY AMINES AND ALCOHOLS TO FORM CARBAMATES HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1981-05-05 US disclosed
US-4260781-A Process for the manufacture of carbamates HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1981-04-07 US disclosed
US-4258201-A CATALYTIC CARBONYLATION OF PRIMARY OR SECONDARY AMINES WITH CARBON MONOXIDE AND ALCOHOLS HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1981-03-24 US disclosed
US-4242520-A ONE-STEP CARBONYLATION OF AMINES IN THE PRESENCE OF A DISULFIDE HALCON RESEARCH & DEVELOPMENT CORPORATION (US) 1980-12-30 US disclosed
EP-0014103-A2 Improved process for the manufacture of carbamates THE HALCON SD GROUP, INC. (US) 1980-08-06 EP 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-20100324043-A1 Bicyclic And Tricyclic Compounds As KAT II Inhibitors KAT2A, KAT2B, KAT6B SLC1A3 1316/4885SLC1A2 312/4885SLC1A1 722/4885

“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.