SCHEMBL2910035

SCHEMBL2910035

N#Cc1ccc(C(=O)O)o1

nearest known ligand 0.51

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CHRNA4 P43681 3/20 0.51
CHRNB2 P17787 2/20 0.51
CHRNB4 P30926 2/20 0.51
CHRNA3 P32297 2/20 0.51
TDP1 Q9NUW8 1/20 0.47
ALDH1A1 P00352 4/20 0.45
POLB P06746 2/20 0.45
HPGD P15428 1/20 0.42
CSF1R P07333 1/20 0.40
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
FAAH O00519 1/20 0.39
CES1 P23141 1/20 0.39
NCEH1 Q6PIU2 1/20 0.39
KDM4E B2RXH2 1/20 0.39
LMNA P02545 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39

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
SCHEMBL9373067 0.80 CHRNB2 (0.46) CHRNA4CHRNB2CHRNB4CHRNA3ALDH1A1
SCHEMBL16131795 0.80 CHRNB2 (0.46) CHRNA4CHRNB2CHRNB4CHRNA3ALDH1A1
SCHEMBL14634145 0.80 CHRNA4 (0.51) CHRNA4TDP1ALDH1A1POLBHPGD
Water SCHEMBL28920578 0.80 TDP1 (0.58) TDP1ALDH1A1POLBHPGDMEN1
Water SCHEMBL19857510 0.78 TDP1 (0.56) TDP1ALDH1A1POLBHPGDMEN1
SCHEMBL38726 0.77 TDP1 (0.61) TDP1ALDH1A1POLBHPGDMEN1
SCHEMBL11904537 0.77 TDP1 (0.61) TDP1ALDH1A1POLBHPGDMEN1
SCHEMBL9372891 0.77 CHRNA4 (0.44) CHRNA4CHRNB2CHRNB4CHRNA3ALDH1A1
Carbon Dioxide SCHEMBL28262228 0.75 TDP1 (0.54) TDP1ALDH1A1POLBHPGDMEN1
Cyanide SCHEMBL11195524 0.75 TDP1 (0.54) TDP1ALDH1A1POLBHPGDMEN1

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 181 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1807077-B1 INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA NV (BE) 2016-11-23 EP claimed
US-7705042-B2 Class of arylamide compounds useful as inhibitors of c-fms kinase JANSSEN PHARMACEUTICA NV (BE) 2010-04-27 US claimed
US-7662837-B2 4-cyano-1H-imidazole-2-carboxylic acid {2-cyclohex-1-enyl-4-[1-(2-dimethylamino-acetyl)-piperidin-4-yl]-phenyl}-amide; protein tyrosine kinase inhibitor; autoimmune diseases, antiinflammatory, anticarcinogenic agent JANSSEN PHARMACEUTICA N.V. (BE) 2010-02-16 US claimed
EP-1807407-B1 AROMATIC AMIDES AS INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA NV (BE) 2009-07-29 EP claimed
US-7429603-B2 Such as 5-nitro-furan-2-carboxylic acid (2-piperidin-1-yl-phenyl)-amide; diabetes, angiogenesis, psoriasis, restenosis, schizophrenia, rheumatoid arthritis, cardiovascular disease, cancer 3-DIMENSIONAL PHARMACEUTICALS, INC. (US) 2008-09-30 US claimed
EP-1951234-A2 METHOD OF INHIBITING FLT3 KINASE JANSSEN PHARMACEUTICA N.V. (BE) 2008-08-06 EP claimed
EP-1812425-A2 C-FMS KINASE INHIBITORS JANSSEN PHARMACEUTICA N.V. (BE) 2007-08-01 EP claimed
EP-1807406-A2 INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA N.V. (BE) 2007-07-18 EP claimed
EP-1807407-A1 AROMATIC AMIDES AS INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA N.V. (BE) 2007-07-18 EP claimed
EP-1807077-A2 INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA N.V. (BE) 2007-07-18 EP claimed
US-20060094081-A1 Crystal structure of the c-fms kinase domain: applications and use of heterologous substitutions of kinase insert domains for crystallization JANSSEN PHARMACEUTICA, N.V. (BE) 2006-05-04 US claimed
WO-2006047277-A2 INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA, N.V. (BE) 2006-05-04 WO claimed
WO-2006047505-A2 CRYSTAL STRUCTURE OF THE C-FMS KINASE DOMAIN JANSSEN PHARMACEUTICA, N.V. (BE) 2006-05-04 WO claimed
WO-2006047479-A2 C-FMS KINASE INHIBITORS JANSSEN PHARMACEUTICA, N.V. (BE) 2006-05-04 WO claimed
WO-2006047504-A1 AROMATIC AMIDES AS INHIBITORS OF C-FMS KINASE JANSSEN PHARMACEUTICA, N.V. (BE) 2006-05-04 WO claimed
EP-1631560-A2 C-FMS KINASE INHIBITORS 3-DIMENSIONAL PHARMACEUTICALS, INC. (US) 2006-03-08 EP claimed
US-20050131022-A1 C-fms kinase inhibitors JANSSEN PHARMACEUTICA, N.V. (BE) 2005-06-16 US claimed
US-20050113566-A1 Inhibitors of C-FMS kinase JANSSEN PHARMACEUTICA N.V. (BE) 2005-05-26 US claimed
US-20050004112-A1 C-fms kinase inhibitors 3-DIMENSIONAL PHARMACEUTICALS, INC. 2005-01-06 US claimed
WO-2004096795-A2 C-FMS KINASE INHIBITORS 3-DIMENSIONAL PHARMACEUTICALS, INC. (US) 2004-11-11 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20050131022-A1 C-fms kinase inhibitors FLT3, FES, FGR CHRNA4 4343/4885CHRNB2 4463/4885CHRNB4 4315/4885
US-20060094081-A1 Crystal structure of the c-fms kinase domain: applications and use of heterologous substitutions of kinase insert domains for crystallization FLT3, FER, FES CHRNA4 3542/4885CHRNB2 4053/4885CHRNB4 3509/4885
US-20050004112-A1 C-fms kinase inhibitors FLT3, FGR, FER CHRNA4 4296/4885CHRNB2 4308/4885CHRNB4 4219/4885
US-20050113566-A1 Inhibitors of C-FMS kinase ALK, TYRO3, PDGFRB CHRNA4 1369/4885CHRNB2 1457/4885CHRNB4 980/4885

“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.