SCHEMBL4189291

SCHEMBL4189291

O=C(CCC1CCCC1)N1C(=O)OCC1Cc1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.48
MAPK1 P28482 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
NAAA Q02083 3/20 0.46
ALDH1A1 P00352 4/20 0.45
IDH1 O75874 4/20 0.42
KDM4E B2RXH2 1/20 0.41
MAPT P10636 1/20 0.41
HIF1A Q16665 1/20 0.41
USP19 O94966 1/20 0.40
DAGLA Q9Y4D2 2/20 0.39
ABHD6 Q9BV23 1/20 0.39
KLK7 P49862 1/20 0.39
PPARA Q07869 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
SCHEMBL1189230 1.00 LMNA (0.48) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL4189285 1.00 LMNA (0.48) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL3637332 0.99 LMNA (0.47) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL9743493 0.99 LMNA (0.47) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL9557087 0.99 LMNA (0.47) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL9743484 0.99 LMNA (0.47) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL3773685 0.99 LMNA (0.47) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL19814964 0.98 NAAA (0.46) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL7495438 0.98 NAAA (0.46) LMNAMAPK1SMN1; SMN2NAAAALDH1A1
SCHEMBL15443176 0.95 NAAA (0.48) LMNAMAPK1SMN1; SMN2NAAAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107032992-A A kind of synthetic method of (R) 4 (tert-butoxy) 2 (cyclopentyl-methyl) 4 ketobutyric acid 华东师范大学 2017-08-11 CN disclosed
WO-2011151434-A1 NOVEL COMPOUNDS, PHARMACEUTICAL COMPOSITION AND METHODS FOR USE IN TREATING METABOLIC DISORDERS EUROSCREEN S.A. (BE) 2011-12-08 WO disclosed
US-20090111793-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2009-04-30 US disclosed
US-20090111793-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2009-04-30 US disclosed
US-7423033-B2 Hydroxyalkanoylaminolactams and related structures as inhibitors of aβ protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-09-09 US disclosed
US-7423033-B2 Hydroxyalkanoylaminolactams and related structures as inhibitors of aβ protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-09-09 US disclosed
US-20080132482-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-06-05 US disclosed
US-20080132482-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-06-05 US disclosed
US-7342008-B2 Containing a benzodiazepine ring; 2-Cyclopentylmethyl-3(S)-hydroxyl-1-oxo-5-phenylpentyl)amino-1-methyl-5-(4-fluoro-phenyl)-2,3-dihydro-1H-1,5-benzodiazepin-2-one; Alzheimer's disease and Down's Syndrome; prevent the formation of neurological deposits of amyloid protein BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-03-11 US disclosed
US-7342008-B2 Containing a benzodiazepine ring; 2-Cyclopentylmethyl-3(S)-hydroxyl-1-oxo-5-phenylpentyl)amino-1-methyl-5-(4-fluoro-phenyl)-2,3-dihydro-1H-1,5-benzodiazepin-2-one; Alzheimer's disease and Down's Syndrome; prevent the formation of neurological deposits of amyloid protein BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2008-03-11 US disclosed
US-20030166636-A1 Hydroxyalkanoylaminolactams and related structures as inhibitors of A-beta protein production OLSON RICHARD E (US) 2003-09-04 US disclosed
EP-1052249-B1 Process for the preparation of hydroxamic acids HOFFMANN LA ROCHE (CH) 2003-08-13 EP disclosed
US-6503902-B2 Treatment of neurological disorders related to beta -amyloid production such as Alzheimer's disease and Down's Syndrome. BRISTOL-MYERS SQUIBB PHARMA COMPANY 2003-01-07 US disclosed
US-6452010-B1 HYDROXAMIC ACID DERIVATIVES OF CERTAIN CARBOXYLIC ACIDS HAVE BEEN RECOGNIZED AS INHIBITORS OF MATRIX METALLOPROTEINASES HOFFMANN-LA ROCHE INC. 2002-09-17 US disclosed
US-20020052360-A1 Hydroxyalkanoylaminolactams and related structures as inhibitors of a beta protein production BRISTOL-MYERS SQUIBB PHARMA COMPANY 2002-05-02 US disclosed
US-6316633-B1 CARTILAGE PROTECTIVE AGENTS AND USEFUL IN THE THERAPY AND PROPHYLAXIS OF DEGENERATIVE JOINT DISEASES SUCH AS ATHEROSCLEROSIS HOFFMAN-LA ROCHE INC. 2001-11-13 US disclosed
US-6197995-B1 INTERMEDIATES FOR CARTILAGE PROTECTIVE AGENTS USEFUL IN TREATMENT AND PREVENTION OF DEGENERATIVE JOINT DISEASES SUCH AS ATHEROSCLEROSIS HOFFMAN-LA ROCHE INC. 2001-03-06 US disclosed
EP-1052249-A1 Process for the preparation of hydroxamic acids F. HOFFMANN-LA ROCHE AG (CH) 2000-11-15 EP disclosed
US-5952507-A Process for manufacture of chiral succinic acid derivatives F. HOFFMANN-LA ROCHE AG (CH) 1999-09-14 US disclosed
US-5128448-A Peptide hormones HOFFMAN-LA ROCHE INC. (US) 1992-07-07 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 (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-20080132482-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION APP, BACE1, APH1A LMNA 336/4885MAPK1 696/4885SMN1; SMN2 1435/4885
US-20030166636-A1 Hydroxyalkanoylaminolactams and related structures as inhibitors of A-beta protein production APP, APH1A, APH1B LMNA 359/4885MAPK1 824/4885SMN1; SMN2 1445/4885
US-20020052360-A1 Hydroxyalkanoylaminolactams and related structures as inhibitors of a beta protein production APP, APH1A, BACE1 LMNA 373/4885MAPK1 679/4885SMN1; SMN2 1264/4885
US-20090111793-A1 HYDROXYALKANOYLAMINOLACTAMS AND RELATED STRUCTURES AS INHIBITORS OF A BETA PROTEIN PRODUCTION APP, BACE1, APH1A LMNA 336/4885MAPK1 696/4885SMN1; SMN2 1435/4885

“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.