SCHEMBL811388

SCHEMBL811388

C/C(CCC(=O)O)=C(/C)C(=O)O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.52
SLC15A2 Q16348 1/20 0.52
EGLN1 Q9GZT9 6/20 0.50
ALKBH5 Q6P6C2 1/20 0.50
SUCNR1 Q9BXA5 1/20 0.50
MAPK1 P28482 1/20 0.46
SLC13A3 Q8WWT9 1/20 0.46
OR51E2 Q9H255 1/20 0.46
PHF8 Q9UPP1 7/20 0.44
KDM2A Q9Y2K7 7/20 0.44
KDM5C P41229 4/20 0.44
KDM4E B2RXH2 3/20 0.44
KDM6B O15054 3/20 0.44
FFAR3 O14843 1/20 0.41
HDAC3 O15379 1/20 0.41
HDAC1 Q13547 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC8 Q9BY41 1/20 0.41
SLC22A6 Q4U2R8 1/20 0.38
ADRA1A P35348 1/20 0.38

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
SCHEMBL810926 1.00 LMNA (0.52) LMNASLC15A2EGLN1ALKBH5SUCNR1
SCHEMBL15363970 0.84 SLC22A6 (0.55) LMNAOR51E2SLC22A6TSHRNFKB1
SCHEMBL15363968 0.84 SLC22A6 (0.55) LMNAOR51E2SLC22A6TSHRNFKB1
SCHEMBL15363963 0.84 LMNA (0.55) LMNAOR51E2SLC22A6ADRA1ATSHR
Succinic Acid SCHEMBL3872448 0.84 LMNA (0.48) LMNASLC15A2EGLN1ALKBH5SUCNR1
SCHEMBL15363966 0.84 LMNA (0.55) LMNAOR51E2SLC22A6ADRA1ATSHR
SCHEMBL28726986 0.82 TSHR (0.57) LMNAOR51E2SLC22A6ADRA1ATSHR
SCHEMBL810940 0.82 TSHR (0.57) LMNAOR51E2SLC22A6ADRA1ATSHR
SCHEMBL811739 0.82 TSHR (0.57) LMNAOR51E2SLC22A6ADRA1ATSHR
SCHEMBL811493 0.82 TSHR (0.57) LMNAOR51E2SLC22A6ADRA1ATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8975267-B2 Tricyclic pyrrolo derivatives, process for their preparation and their use as kinase inhibitors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2015-03-10 US disclosed
US-20130296305-A1 TRICYCLIC PYRROLO DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2013-11-07 US disclosed
EP-2389349-A2 METHODS FOR PRODUCING DODECANEDIOIC ACID AND DERIVATIVES THEREOF Draths Corporation (US) 2011-11-30 EP disclosed
US-8041434-B2 Implantable medical electrical lead bodies providing improved electrode contact MEDTRONIC, INC. (US) 2011-10-18 US disclosed
WO-2010085712-A2 METHODS FOR PRODUCING DODECANEDIOIC ACID AND DERIVATIVES THEREOF DRATHS CORPORATION (US) 2010-07-29 WO disclosed
WO-1994023836-A1 CATALYST COMPOSITION AND PROCESS FOR THE PRODUCTION OF UNSATURATED DIESTERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1994-10-27 WO disclosed
US-4638084-A BIS (THYLENE) RHODIUM TETRAFLUOROBORATE CATALYST SHELL OIL COMPANY (US) 1987-01-20 US disclosed
US-4451665-A Process for dimerizing acrylates and methacrylates E. I. DU PONT DE NEMOURS AND COMPANY (US) 1984-05-29 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-20130296305-A1 TRICYCLIC PYRROLO DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS KINASE INHIBITORS MAP3K1, MAP3K20, MAP3K5 LMNA 2365/4885SLC15A2 4630/4885EGLN1 2502/4885

“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.