SCHEMBL1307362

SCHEMBL1307362

COC(=O)C(=CN(c1ccccc1)c1ccccc1)NC(=O)c1ccccc1

nearest known ligand 0.57

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.57
KMT2A Q03164 2/20 0.50
MEN1 O00255 1/20 0.50
KDM4E B2RXH2 6/20 0.46
ALDH1A1 P00352 4/20 0.46
HPGD P15428 3/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
CYP1A2 P05177 2/20 0.44
CYP3A4 P08684 1/20 0.44
CYP2C9 P11712 1/20 0.43
POLB P06746 2/20 0.41
NPSR1 Q6W5P4 1/20 0.41
NPC1 O15118 2/20 0.40
RAB9A P51151 2/20 0.40
TDP1 Q9NUW8 1/20 0.40
CHIA Q9BZP6 1/20 0.40

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
SCHEMBL1307361 1.00 LMNA (0.57) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL12112857 1.00 LMNA (0.57) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL12112859 0.85 LMNA (0.59) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL1307670 0.85 LMNA (0.59) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL1307672 0.85 LMNA (0.59) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL16326401 0.81 LMNA (0.75) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL8232803 0.78 LMNA (0.81) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL7642884 0.77 LMNA (0.69) LMNAKMT2AMEN1KDM4EALDH1A1
SCHEMBL1305952 0.77 SMN1; SMN2 (0.44) LMNAKMT2AMEN1ALDH1A1HPGD
SCHEMBL12112861 0.77 SMN1; SMN2 (0.44) LMNAKMT2AMEN1ALDH1A1HPGD

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
US-8053590-B2 Method for producing enantiomeric form of 2,3-diaminopropionic acid derivatives SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2011-11-08 US disclosed
US-20090203918-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2,3-DIAMINOPROPIONIC ACID DERIVATIVES SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-08-13 US disclosed
US-7514578-B2 Method for producing enantiomeric form of 2,3-diaminopropionic acid derivatives SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-04-07 US disclosed
EP-1778627-B1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2, 3-DIAMINOPROPIONIC ACID DERIVATIVES SANOFI AVENTIS DEUTSCHLAND (DE) 2008-02-27 EP disclosed
US-20070238778-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2,3-DIAMINOPROPIONIC ACID DERIVATIVES SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-10-11 US disclosed
EP-1778627-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2, 3-DIAMINOPROPIONIC ACID DERIVATIVES Sanofi-Aventis Deutschland GmbH (DE) 2007-05-02 EP disclosed
WO-2006005436-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2, 3-DIAMINOPROPIONIC ACID DERIVATIVES SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2006-01-19 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 (2 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-20090203918-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2,3-DIAMINOPROPIONIC ACID DERIVATIVES DDC, ADM2, MTHFD2 LMNA 4330/4885KMT2A 2002/4885MEN1 715/4885
US-20070238778-A1 METHOD FOR PRODUCING ENANTIOMERIC FORM OF 2,3-DIAMINOPROPIONIC ACID DERIVATIVES DDC, DAO, ADM2 LMNA 4437/4885KMT2A 1462/4885MEN1 898/4885

“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.