SCHEMBL6570858

SCHEMBL6570858

COc1ccc(C(=O)N(CC(=O)O)c2ccccc2)cc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.63
HPGD P15428 1/20 0.63
TSHR P16473 1/20 0.60
NPC1 O15118 2/20 0.57
RAB9A P51151 2/20 0.57
BACE1 P56817 1/20 0.55
KMT2A Q03164 2/20 0.52
ACHE P22303 1/20 0.52
CES2 O00748 1/20 0.51
CES1 P23141 1/20 0.51
MEN1 O00255 1/20 0.49
PTGIR P43119 1/20 0.48
PTGES O14684 1/20 0.48
ALOX5 P09917 1/20 0.48
TRPM8 Q7Z2W7 1/20 0.48
HSD17B1 P14061 1/20 0.48
HSD17B2 P37059 1/20 0.48
ADRA2C P18825 1/20 0.48
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47

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
SCHEMBL3659973 0.88 TSHR (0.54) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL11311239 0.87 HPGD (0.54) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL4001480 0.84 HPGD (0.55) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL1926257 0.84 TRPM8 (0.64) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL698882 0.84 ADRA2C (0.64) HPGDTSHRNPC1RAB9AKMT2A
SCHEMBL6569544 0.83 PKM (0.56) HPGDTSHRNPC1RAB9AKMT2A
SCHEMBL6981124 0.82 KDM4E (0.60) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL4560242 0.81 NPC1 (0.60) KDM4EHPGDTSHRNPC1RAB9A
SCHEMBL9716677 0.81 ADRA2C (0.53) HPGDTSHRNPC1RAB9AKMT2A
SCHEMBL6783932 0.81 NPC1 (0.70) KDM4EHPGDTSHRNPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4757066-A Reduces renal toxicity SANKYO COMPANY LIMITED (JP) 1988-07-12 US claimed
EP-0838448-B1 Process for the separation of a mixture of enantiomers DSM IP ASSETS BV (NL) 2004-04-21 EP disclosed
US-6465684-B2 DIASTEREOMER COMPLEX OF AT LEAST THREE COMPOUNDS, AT LEAST ONE IS A RESOLVING AGENT IN OPTICALLY ACTIVE FORM, AND AT LEAST ONE IS AN ENANTIOMER IN OPTICALLY ACTIVE FORM; RAPID SEPARATION DSM N.V. (NL) 2002-10-15 US disclosed
US-20010051747-A1 Process for the separation of a mixture of enantiomers DSM N.V. 2001-12-13 US disclosed
US-6235927-B1 OPTICAL RESOLUTION OF ENANTIOMORPHS OF COMPLEXES DSM N.V. (NL) 2001-05-22 US disclosed
EP-0838448-A1 Process for the separation of a mixture of enantiomers DSM N.V. (NL) 1998-04-29 EP disclosed
EP-0178911-B1 COMPOSITION CONTAINING A PENEM OR CARBAPENEM ANTIBIOTIC SANKYO COMPANY LIMITED (JP) 1992-01-22 EP disclosed
US-4757066-A Reduces renal toxicity SANKYO COMPANY LIMITED (JP) 1988-07-12 US disclosed
EP-0178911-A2 Composition containing a penem or carbapenem antibiotic SANKYO COMPANY LIMITED (JP) 1986-04-23 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-20010051747-A1 Process for the separation of a mixture of enantiomers EPHX2, VKORC1, ALDH1A2 KDM4E 3924/4885HPGD 695/4885TSHR 4265/4885

“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.