SCHEMBL321810

SCHEMBL321810

COC(=O)c1cc(C(=O)c2c(C)c(O)c3ccccn23)ccc1N

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 8/20 0.44
MAPT P10636 7/20 0.44
MEN1 O00255 7/20 0.44
USP2 O75604 1/20 0.44
ALDH1A1 P00352 8/20 0.42
LMNA P02545 5/20 0.42
SMN1; SMN2 Q16637 3/20 0.42
HTT P42858 4/20 0.42
PPARG P37231 2/20 0.41
NCOR2 Q9Y618 2/20 0.41
KDM4E B2RXH2 2/20 0.41
PABPC1 P11940 1/20 0.41
NR2E3 Q9Y5X4 1/20 0.41
DAPK3 O43293 1/20 0.41
JAK2 O60674 1/20 0.41
PRKD3 O94806 1/20 0.41
MAP4K4 O95819 1/20 0.41
ABL1 P00519 1/20 0.41
CSF1R P07333 1/20 0.41
RET P07949 1/20 0.41

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
SCHEMBL4501200 0.90 MAPT (0.45) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL321101 0.88 KMT2A (0.43) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL321257 0.88 MAPT (0.43) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL1573289 0.88 HTT (0.47) KMT2AMAPTMEN1ALDH1A1LMNA
SCHEMBL13918696 0.86 MAPT (0.53) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL27737744 0.86 MAPT (0.46) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL27758529 0.84 MAPT (0.45) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL3597834 0.84 HTT (0.52) KMT2AMAPTMEN1ALDH1A1LMNA
SCHEMBL320960 0.83 MAPT (0.39) KMT2AMAPTMEN1USP2ALDH1A1
SCHEMBL320893 0.83 MAPT (0.46) KMT2AMAPTMEN1USP2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9120819-B2 FGF-receptor agonist dimeric compounds SANOFI (FR) 2015-09-01 US disclosed
EP-2590975-B1 INDOLIZINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI SA (FR) 2015-08-19 EP disclosed
US-8859544-B2 Indolizine derivatives, process for the preparation thereof and therapeutic use thereof SANOFI (FR) 2014-10-14 US disclosed
CN-101384258-B FGF Receptor Agonist Dimeric Compounds SANOFI AVENTIS 2013-06-26 CN disclosed
EP-2590975-A1 INDOLIZINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI (FR) 2013-05-15 EP disclosed
US-20130116249-A1 INDOLIZINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI (FR) 2013-05-09 US disclosed
CN-103080112-A Indolizine derivatives, process for the preparation thereof and therapeutic use thereof SANOFI SA 2013-05-01 CN disclosed
WO-2012004731-A1 INDOLIZINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI (FR) 2012-01-12 WO disclosed
US-20090069368-A1 FGF-RECEPTOR AGONIST DIMERIC COMPOUNDS SANOFI-AVENTIS (FR) 2009-03-12 US disclosed
CN-101384258-A FGF receptor agonist dimeric compounds SANOFI AVENTIS (FR) 2009-03-11 CN 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-20090069368-A1 FGF-RECEPTOR AGONIST DIMERIC COMPOUNDS FGF2, FGFR1, FGF1 KMT2A 3395/4885MAPT 3588/4885MEN1 621/4885
US-20130116249-A1 INDOLIZINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND THERAPEUTIC USE THEREOF CCNY, INMT, IDO1 KMT2A 1538/4885MAPT 961/4885MEN1 1964/4885

“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.