SCHEMBL5249132

SCHEMBL5249132

CC(C(=O)CS(N)(=O)=O)c1ccc(CN2CC=CC2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FAAH O00519 3/20 0.41
ALDH1A1 P00352 1/20 0.39
HTT P42858 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
EPHX1 P07099 1/20 0.37
CA12 O43570 3/20 0.36
CA1 P00915 3/20 0.36
CA2 P00918 3/20 0.36
CA9 Q16790 3/20 0.36
CA7 P43166 1/20 0.36
CA4 P22748 2/20 0.36
CXCR1 P25024 4/20 0.35
CXCR2 P25025 4/20 0.35
PTGS1 P23219 4/20 0.35
PTGS2 P35354 4/20 0.35
LMNA P02545 2/20 0.35
CYP2C9 P11712 2/20 0.35
AKR1C3 P42330 2/20 0.35
ALB P02768 1/20 0.35
ESR1 P03372 1/20 0.35

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
SCHEMBL5213717 1.00 FAAH (0.41) FAAHALDH1A1HTTSMN1; SMN2EPHX1
SCHEMBL5214115 0.81 EPHX1 (0.57) FAAHALDH1A1HTTSMN1; SMN2EPHX1
SCHEMBL5214126 0.81 EPHX1 (0.57) FAAHALDH1A1HTTSMN1; SMN2EPHX1
SCHEMBL5218361 0.80 PTGS1 (0.56) ALDH1A1HTTSMN1; SMN2CXCR1CXCR2
SCHEMBL5248185 0.77 CXCR2 (0.63) FAAHALDH1A1HTTSMN1; SMN2CA12
SCHEMBL15285417 0.77 FAAH (0.64) FAAHEPHX1CA12CA1CA2
SCHEMBL2237283 0.77 FAAH (0.64) FAAHEPHX1CA12CA1CA2
SCHEMBL3886291 0.73 ALOX5 (0.44) FAAHSMN1; SMN2EPHX1CA2ALOX5
SCHEMBL5219685 0.73 APP (0.43) FAAHALDH1A1HTTSMN1; SMN2CXCR1
SCHEMBL5217986 0.70 TRPV1 (0.43) ALDH1A1HTTSMN1; SMN2CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1276732-B1 AMIDES OF R-2-(AMINOARYL)-PROPIONIC ACIDS FOR USE IN THEPREVENTION OF LEUCOCYTE ACTIVATION\ DOMPE PHA R MA SPA RES & MFG (IT) 2007-09-26 EP disclosed
US-7217707-B2 Amide of R-2-(aminoaryl)-propionic acid for use in the prevention of leucocyte activation DOMPE S.P.A. (IT) 2007-05-15 US disclosed
US-20040186146-A1 Amide of r-2-(aminoaryl)-propionic acid for use in theprevention of leucocyte activation DOMPÉ FARMACEUTICI S.P.A. (IT) 2004-09-23 US disclosed
EP-1276732-A1 AMIDES OF R-2-(AMINOARYL)-PROPIONIC ACIDS FOR USE IN THEPREVENTION OF LEUCOCYTE ACTIVATION\ Dompé S.P.A. (IT) 2003-01-22 EP disclosed
WO-2001079189-A2 'AMIDES OF R-2-(AMINOARYL)-PROPIONIC ACIDS FOR USE IN THEPREVENTION OF LEUCOCYTE ACTIVATION' Dompé S.p.A. (IT) 2001-10-25 WO 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-20040186146-A1 Amide of r-2-(aminoaryl)-propionic acid for use in theprevention of leucocyte activation MMP8, CXCL8, HCAR2 FAAH 330/4885ALDH1A1 391/4885HTT 2986/4885

“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.