SCHEMBL1343569

SCHEMBL1343569

COCc1nc2cc3c(cc2c(=O)[nH]1)[C@@H](Nc1ccc(C(=O)O)cc1)CC3

nearest known ligand 0.43

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 4/20 0.40
KDM4E B2RXH2 2/20 0.40
RECQL P46063 1/20 0.40
ALDH1A1 P00352 3/20 0.37
MAPT P10636 2/20 0.37
MEN1 O00255 2/20 0.37
KMT2A Q03164 2/20 0.37
HSD17B10 Q99714 1/20 0.37
TSHR P16473 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
BRD4 O60885 1/20 0.36
TNKS O95271 2/20 0.36
TNKS2 Q9H2K2 2/20 0.36
PARP14 Q460N5 1/20 0.35
PDE5A O76074 1/20 0.35
HPGD P15428 1/20 0.34
TDP1 Q9NUW8 1/20 0.34

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
SCHEMBL1038155 1.00 PARP1 (0.40) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL1544255 1.00 PARP1 (0.40) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL989212 0.89 MAPT (0.38) PARP1KDM4EALDH1A1MAPTMEN1
SCHEMBL989215 0.89 MAPT (0.38) PARP1KDM4EALDH1A1MAPTMEN1
SCHEMBL987844 0.89 PARP1 (0.39) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL987842 0.89 PARP1 (0.39) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL3674775 0.89 KDM4E (0.43) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL3674777 0.89 KDM4E (0.43) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL2320352 0.88 PARP1 (0.42) PARP1KDM4ERECQLALDH1A1MAPT
SCHEMBL2320356 0.88 PARP1 (0.42) PARP1KDM4ERECQLALDH1A1MAPT

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 17 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
US-8552016-B2 Anti-cancer cyclopenta(g)quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2013-10-08 US disclosed
US-8486955-B2 Anti-cancer cyclopenta [g] quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2013-07-16 US disclosed
US-8063056-B2 Anti-cancer cyclopenta [g]quinazonline compounds BTG INTERNATIONAL LIMITED (GB) 2011-11-22 US disclosed
EP-1421069-B1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG INT LTD (GB) 2011-08-10 EP disclosed
EP-2332962-A1 Cyclopenta[g]quinazoline compounds for use in the treatment of inflammatory or allergic conditions BTG International Limited (GB) 2011-06-15 EP disclosed
EP-2311850-A1 Anti-cancer cyclopenta[g]quinazoline compounds BTG International Limited (GB) 2011-04-20 EP disclosed
US-20100273817-A1 Anti-cancer cyclopenta(g)quinazoline compounds BGT International Limited (GB) 2010-10-28 US disclosed
EP-1421105-B1 ANTI-CANCER CYCLOPENTA¬G QUINAZOLINE COMPOUNDS BTG INT LTD (GB) 2010-10-06 EP disclosed
US-20100216824-A1 Anti-cancer cyclopenta [G]quinazonline compounds BTG INTERNATIONAL LIMITED (GB) 2010-08-26 US disclosed
EP-2213664-A1 PROCESS FOR THE PREPARATION OF CYCLOPENTA[G]QUINAZOLINE DERIVATIVES BTG International Limited (GB) 2010-08-04 EP disclosed
US-7705006-B2 Anti-cancer cyclopenta[g]quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2010-04-27 US disclosed
US-20100056551-A1 Anti-cancer cyclopenta [G] quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2010-03-04 US disclosed
US-20090023760-A1 Anti-cancer cyclopenta[G]quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2009-01-22 US disclosed
US-7297701-B2 Anti-cancer cyclopenta [G]quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2007-11-20 US disclosed
US-7250511-B2 Process for the preparation of cyclopenta[g]quinazoline derivatives BTG INTERNATIONAL LIMITED (GB) 2007-07-31 US disclosed
US-20040242606-A1 Anti-cancer cyclopenta (g)quinazoline compounds BTG INTERNATIONAL LIMITED (GB) 2004-12-02 US 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 (5 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-20100056551-A1 Anti-cancer cyclopenta [G] quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, NR0B1, CNR1 PARP1 342/4885KDM4E 2730/4885RECQL 219/4885
US-20100273817-A1 Anti-cancer cyclopenta(g)quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CNR1, NR0B1 PARP1 328/4885KDM4E 2722/4885RECQL 235/4885
US-20040242606-A1 Anti-cancer cyclopenta (g)quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CBR1, NR4A1 PARP1 137/4885KDM4E 1184/4885RECQL 543/4885
US-20100216824-A1 Anti-cancer cyclopenta [G]quinazonline compounds NR0B1, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CNR1 PARP1 608/4885KDM4E 2768/4885RECQL 451/4885
US-20090023760-A1 Anti-cancer cyclopenta[G]quinazoline compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, NR0B1, CNR1 PARP1 467/4885KDM4E 2768/4885RECQL 189/4885

“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.