SCHEMBL7507233

SCHEMBL7507233

CC1(C)CC(=O)NC(=O)C1.[KH]

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.52
LMNA P02545 2/20 0.52
CYP2C19 P33261 1/20 0.52
TSHR P16473 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
CRBN Q96SW2 3/20 0.42
ALDH1A1 P00352 6/20 0.41
MAPT P10636 4/20 0.40
SMN1; SMN2 Q16637 1/20 0.39
GLA P06280 1/20 0.38
GAA P10253 1/20 0.38
MAOA P21397 1/20 0.37
TOP2A P11388 1/20 0.35
TOP2B Q02880 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
POLB P06746 1/20 0.34
CTSK P43235 1/20 0.34
CYP19A1 P11511 1/20 0.34
MEN1 O00255 1/20 0.34
ALPL P05186 1/20 0.34

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
SCHEMBL1352364 0.97 KDM4E (0.55) KDM4ELMNACYP2C19TSHRNPSR1
SCHEMBL9471261 0.97 KDM4E (0.55) KDM4ELMNACYP2C19TSHRNPSR1
SCHEMBL11083062 0.94 KDM4E (0.52) KDM4ELMNACYP2C19TSHRNPSR1
Hydrochloric Acid SCHEMBL10768658 0.94 KDM4E (0.52) KDM4ELMNACYP2C19TSHRNPSR1
SCHEMBL20206752 0.78 CRBN (0.48) KDM4ELMNACYP2C19TSHRNPSR1
SCHEMBL15250760 0.73 KDM4E (0.50) KDM4ELMNACYP2C19TSHRNPSR1
SCHEMBL248285 0.71
SCHEMBL2324941 0.69
SCHEMBL2691041 0.69
SCHEMBL24372750 0.69 CRBN (0.50) KDM4ELMNACYP2C19TSHRNPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1001930-B1 N-HYDROXYFORMAMIDE DERIVATIVES AS INHIBITORS OF MATRIX METALLOPROTEINASES ABBOTT LAB (US) 2002-12-04 EP disclosed
US-20020007060-A1 Reverse hydroxamate inhibitors of matrix metalloproteinases DAVIDSEN STEVEN K (US) 2002-01-17 US disclosed
US-6294573-B1 FOR THERAPY RHEUMATOID ARTHRITIS, OSTEOARTHRITIS, OSTEOPENIAS SUCH AS OSTEOPOROSIS, PERIODONTITIS, GINGIVITIS, CORNEAL, EPIDERMAL OR GASTRIC ULCERATION, AND TUMOR GROWTH AND METASTASIS OR INVASION ABBOTT LABORATORIES 2001-09-25 US disclosed
US-6235786-B1 RHEUMATIC DISORDERS; BONE DISORDERS; ORAL DISEASES; ANTIULCER AGENTS; ANTITUMOR AGENTS ABBOTT LABORATORIES 2001-05-22 US disclosed
CN-1044474-C Improved, large-scale process for azapirone synthesis BRISTOL MYERS SQUIBB CO (US) 1999-08-04 CN disclosed
CN-1115317-A Improved, large-scale process for azapirone synthesis BRISTOL MYERS SQUIBB CO (US) 1996-01-24 CN disclosed
EP-0680961-A1 Improved, large-scale process for azapirone synthesis BRISTOL-MYERS SQUIBB COMPANY (US) 1995-11-08 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-20020007060-A1 Reverse hydroxamate inhibitors of matrix metalloproteinases MMP1, MMP9, MMP3 KDM4E 1586/4885LMNA 1058/4885CYP2C19 1997/4885

“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.