SCHEMBL2318167

SCHEMBL2318167

CC(C)(C)OC(=O)c1ccc(NC2CCc3cc4nc(CO)[nH]c(=O)c4cc32)cc1

nearest known ligand 0.38

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.37
ALDH1A1 P00352 2/20 0.37
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
HSD17B10 Q99714 1/20 0.37
PARP1 P09874 2/20 0.37
TNKS O95271 3/20 0.35
TNKS2 Q9H2K2 3/20 0.35
ABCG2 Q9UNQ0 1/20 0.35
PARP14 Q460N5 8/20 0.34
KDM4E B2RXH2 1/20 0.33
HTT P42858 1/20 0.33
RAB9A P51151 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33

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
SCHEMBL2318171 1.00 MAPT (0.37) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL989212 0.92 MAPT (0.38) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL989215 0.92 MAPT (0.38) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL988880 0.90 MAPT (0.37) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL988879 0.90 MAPT (0.37) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL13255695 0.89 ABCG2 (0.36) MAPTALDH1A1HSD17B10ABCG2KDM4E
SCHEMBL2319454 0.88 PARP1 (0.38) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL2319459 0.88 PARP1 (0.38) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL3674775 0.87 KDM4E (0.43) MAPTALDH1A1MEN1KMT2AHSD17B10
SCHEMBL3674777 0.87 KDM4E (0.43) MAPTALDH1A1MEN1KMT2AHSD17B10

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-2213664-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2014-04-30 EP disclosed
EP-1421069-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2011-08-10 EP disclosed
EP-2213664-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG International Limited (GB) 2010-08-04 EP disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-20040266798-A1 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2004-12-30 US disclosed
EP-1421069-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG International Limited (GB) 2004-05-26 EP disclosed
WO-2003020706-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[g]QUINAZOLINE DERIVATIVES BTG INTERNATIONAL LIMITED (GB) 2003-03-13 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-20040266798-A1 Process for the preparation of cyclopenta[g]quinazoline derivatives COX6A1, MT-ND6, CYP2D6 MAPT 3724/4885ALDH1A1 1243/4885MEN1 2322/4885

“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.