SCHEMBL1319932

SCHEMBL1319932

CCN(CC)CCN(C)Cc1ccc2c(c1)-c1n[nH]c(=O)c3cccc(c13)O2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 17/20 1.00
PIM1 P11309 1/20 0.64
CSNK1D P48730 1/20 0.64
NAMPT P43490 1/20 0.37
HTR6 P50406 1/20 0.36

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
SCHEMBL13613932 0.94 PARP1 (0.89) PARP1PIM1CSNK1DHTR6
SCHEMBL1321187 0.93 PARP1 (1.00) PARP1PIM1CSNK1DNAMPT
SCHEMBL61115 0.91 PARP1 (0.84) PARP1PIM1CSNK1DHTR6
SCHEMBL14336535 0.90 PARP1 (0.81) PARP1PIM1CSNK1D
SCHEMBL10035768 0.89 PARP1 (0.91) PARP1PIM1CSNK1DNAMPT
SCHEMBL2682991 0.87 PARP1 (1.00) PARP1PIM1CSNK1DNAMPT
SCHEMBL2684444 0.86 PARP1 (0.80) PARP1PIM1CSNK1DNAMPT
SCHEMBL14336601 0.86 PARP1 (0.79) PARP1PIM1CSNK1D
SCHEMBL14252328 0.85 PARP1 (0.84) PARP1PIM1CSNK1DNAMPT
SCHEMBL12658579 0.83 PARP1 (0.71) PARP1PIM1CSNK1DNAMPT

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8883787-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2014-11-11 US disclosed
US-8883787-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2014-11-11 US disclosed
US-8883787-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2014-11-11 US disclosed
US-20130345225-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP EISAI INC. (US) 2013-12-26 US disclosed
US-8470825-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2013-06-25 US disclosed
US-8470825-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2013-06-25 US disclosed
US-8470825-B2 Diazabenzo[de] anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2013-06-25 US disclosed
US-20120115873-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP EISAI INC. (US) 2012-05-10 US disclosed
US-20120115873-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP EISAI INC. (US) 2012-05-10 US disclosed
US-20120115873-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP EISAI INC. (US) 2012-05-10 US disclosed
US-20110092478-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP EISAI INC. (US) 2011-04-21 US disclosed
US-7820668-B2 Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2010-10-26 US disclosed
US-7820668-B2 Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2010-10-26 US disclosed
US-7820668-B2 Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP EISAI INC. (US) 2010-10-26 US disclosed
US-20090028815-A1 Diazabenzo[De]anthracen-3-one Compounds and Methods for Inhibiting Parp MGI GP, INC. (US) 2009-01-29 US disclosed
US-20090028815-A1 Diazabenzo[De]anthracen-3-one Compounds and Methods for Inhibiting Parp MGI GP, INC. (US) 2009-01-29 US disclosed
US-20090028815-A1 Diazabenzo[De]anthracen-3-one Compounds and Methods for Inhibiting Parp MGI GP, INC. (US) 2009-01-29 US disclosed
EP-1841771-A4 DIAZABENZO[DE]ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP MGI GP INC (US) 2008-09-24 EP disclosed
EP-1841771-A2 DIAZABENZOÝDE¨ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP MGI GP, Inc. (US) 2007-10-10 EP disclosed
WO-2006078711-A2 DIAZABENZO[DE]ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP MGI GP, INC. (US) 2006-07-27 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 (4 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-20120115873-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP PARP1, PARP2, PARP3 PARP1 1/4885PIM1 745/4885CSNK1D 3002/4885
US-20090028815-A1 Diazabenzo[De]anthracen-3-one Compounds and Methods for Inhibiting Parp PARP1, PARP2, PARP3 PARP1 1/4885PIM1 622/4885CSNK1D 3185/4885
US-20130345225-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP PARP1, PARP2, PARP3 PARP1 1/4885PIM1 622/4885CSNK1D 3185/4885
US-20110092478-A1 DIAZABENZO[DE] ANTHRACEN-3-ONE COMPOUNDS AND METHODS FOR INHIBITING PARP PARP1, PARP2, PARP3 PARP1 1/4885PIM1 622/4885CSNK1D 3185/4885

“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.