SCHEMBL4418795

SCHEMBL4418795

CC(=O)ON=C1CCc2ccccc21

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.55
MAPT P10636 14/20 0.55
L3MBTL1 Q9Y468 4/20 0.55
KMT2A Q03164 4/20 0.55
MEN1 O00255 3/20 0.55
PLA2G1B P04054 1/20 0.55
ATG4B Q9Y4P1 1/20 0.55
SMN1; SMN2 Q16637 8/20 0.53
HTT P42858 1/20 0.53
ALDH1A1 P00352 4/20 0.52
NPC1 O15118 7/20 0.51
CASP3 P42574 1/20 0.51
SENP8 Q96LD8 1/20 0.51
SENP7 Q9BQF6 1/20 0.51
SENP6 Q9GZR1 1/20 0.51
PKM P14618 1/20 0.50
RAB9A P51151 8/20 0.49
NFKB1 P19838 1/20 0.46
NFKB2 Q00653 1/20 0.46
RELA Q04206 1/20 0.46

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
SCHEMBL12101822 1.00 LMNA (0.55) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL4418793 1.00 LMNA (0.55) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL5189232 0.90 LMNA (0.68) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL12609515 0.90 LMNA (0.68) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL12609477 0.90 LMNA (0.63) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL92004 0.81 MAPT (0.67) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL12609462 0.80 MAPT (0.46) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL12609456 0.80 MAPT (0.54) LMNAMAPTL3MBTL1KMT2AMEN1
SCHEMBL12609463 0.78 HTT (0.58) MAPTKMT2AMEN1HTTALDH1A1
SCHEMBL9411070 0.78 MAPT (0.38) LMNAMAPTL3MBTL1KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1720823-B1 NEW PROCESS FOR THE SYNTHESIS OF SUBSTITUTED ALPHA-AMINOIDAN DERIVATIVES ZACH SYSTEM (FR) 2009-08-26 EP disclosed
US-7456320-B2 Process for the synthesis of substituted alpha-aminoindan derivatives ZACH SYSTEM (FR) 2008-11-25 US disclosed
US-20070191640-A1 Process for the synthesis of substituted alpha-aminoindan derivatives PPG-SIPSY (FR) 2007-08-16 US disclosed
EP-1797030-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF INDANYLAMINE OR AMINOTETRALIN DERIVATIVES AND NOVEL INTERMEDIATES Teva Pharmaceuticals USA, Inc. (US) 2007-06-20 EP disclosed
EP-1720823-A1 NEW PROCESS FOR THE SYNTHESIS OF SUBSTITUTED ALPHA-AMINOIDAN DERIVATIVES PPG-Sipsy (FR) 2006-11-15 EP disclosed
WO-2006029135-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF INDANYLAMINE OR AMINOTETRALIN DERIVATIVES AND NOVEL INTERMEDIATES TEVA PHARMACEUTICAL USA, INC (US) 2006-03-16 WO disclosed
EP-1574498-A1 Process for the synthesis of substituted alpha-aminoindan derivatives PPG-Sipsy (FR) 2005-09-14 EP disclosed
WO-2005082838-A1 NEW PROCESS FOR THE SYNTHESIS OF SUBSTITUTED ALPHA -AMINOINDAN DERIVATIVES PPG-SIPSY (FR) 2005-09-09 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-20070191640-A1 Process for the synthesis of substituted alpha-aminoindan derivatives ALDH7A1, ALAD, ASPH LMNA 1290/4885MAPT 4049/4885L3MBTL1 4778/4885

“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.