SCHEMBL487203

SCHEMBL487203

CC(C)(C)OC(=O)C(N)Cc1cn(C(=O)OC(C)(C)C)c2ccccc12

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.63
EPHX1 P07099 1/20 0.57
ALDH1A1 P00352 1/20 0.50
MAPT P10636 1/20 0.50
RECQL P46063 1/20 0.50
ADAM17 P78536 1/20 0.48
PDE10A Q9Y233 1/20 0.45
HTR6 P50406 1/20 0.44
SCN9A Q15858 1/20 0.42
ACHE P22303 1/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41
PIM1 P11309 1/20 0.41
MARK3 P27448 1/20 0.41
MAP4K2 Q12851 1/20 0.41
CAMK2B Q13554 1/20 0.41
PIM3 Q86V86 1/20 0.41
PIM2 Q9P1W9 1/20 0.41
PTGS2 P35354 1/20 0.41
BRD4 O60885 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
SCHEMBL29918287 1.00 L3MBTL1 (0.63) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL487202 1.00 L3MBTL1 (0.63) L3MBTL1EPHX1ALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL29918249 0.99 L3MBTL1 (0.61) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL1701584 0.93 L3MBTL1 (0.60) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL31064380 0.93 L3MBTL1 (0.60) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL31404227 0.93 L3MBTL1 (0.60) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL12052756 0.93 L3MBTL1 (0.60) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL27691494 0.92 ALDH1A1 (0.54) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL27691492 0.92 ALDH1A1 (0.54) L3MBTL1EPHX1ALDH1A1MAPTRECQL
SCHEMBL25665046 0.91 L3MBTL1 (0.58) L3MBTL1EPHX1ALDH1A1MAPTRECQL

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
US-8362043-B2 Use in controlling apoptosis, as antiinflammatory agents, in treating autoimmune disease, as antiischemic agents, in treating cardiovascular disorders; for example, 3(R,S)-[2(S)-(3-Benzoylamino-2-oxo-2H-pyridin-1-yl)-3-phenyl-propionylamino]-5-fluoro-4-oxo-pentanoic acid VERTEX PHARMACEUTICALS INCORPORATED (US) 2013-01-29 US disclosed
EP-1833794-B1 3-[2-(3-ACYLAMINO-2-OXO-2H-PYRIDIN-1-YL)-ACETYLAMINO]-4-OXO-PENTANOIC ACID DERIVATIVES AND THEIR USE AS CASPASE INHIBITORS VERTEX PHARMA (US) 2012-02-01 EP disclosed
EP-1833794-A1 3-[2-(3-ACYLAMINO-2-OXO-2H-PYRIDIN-1-YL)-ACETYLAMINO]-4-OXO-PENTANOIC ACID DERIVATIVES AND THEIR USE AS CASPASE INHIBITORS Vertex Pharmceuticals Incorporated (US) 2007-09-19 EP disclosed
US-20060160862-A1 Caspase inhibitors and uses thereof VERTEX PHARMACEUTICALS INCORPORATED 2006-07-20 US disclosed
WO-2006057961-A1 3-[2-(3-ACYLAMINO-2-OXO-2H-PYRIDIN-1-YL)-ACETYLAMINO]-4-OXO-PENTANOIC ACID DERIVATIVES AND THEIR USE AS CASPASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2006-06-01 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-20060160862-A1 Caspase inhibitors and uses thereof CASP1, CASP5, CASP3 L3MBTL1 1197/4885EPHX1 976/4885ALDH1A1 1830/4885

“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.