SCHEMBL5207833

SCHEMBL5207833

COC(=O)c1cccc2c1c1c(n2Cc2ccccc2)CCCC1=O

nearest known ligand 0.51

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 3/20 0.51
HDAC6 Q9UBN7 3/20 0.51
CSNK2A2 P19784 3/20 0.47
CSNK2B P67870 3/20 0.47
CSNK2A1 P68400 3/20 0.47
ABCG2 Q9UNQ0 3/20 0.47
FABP4 P15090 6/20 0.44
BRD4 O60885 1/20 0.42
FABP3 P05413 1/20 0.42
MAPK8 P45983 1/20 0.41
AR P10275 1/20 0.41
KMT2A Q03164 2/20 0.40
MEN1 O00255 1/20 0.40
KDM4E B2RXH2 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39

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
SCHEMBL6780169 0.92 HDAC1 (0.44) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6775629 0.92 HDAC1 (0.44) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6693631 0.91 HDAC1 (0.45) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6688522 0.91 HDAC1 (0.43) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6692851 0.91 FABP4 (0.45) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6694057 0.90 MAPT (0.45) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6782203 0.89 HDAC1 (0.45) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6691868 0.89 HDAC1 (0.47) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6693334 0.89 HDAC1 (0.43) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1
SCHEMBL6773523 0.89 HDAC1 (0.47) HDAC1HDAC6CSNK2A2CSNK2BCSNK2A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1395554-B1 SUBSTITUTED CARBAZOLES AS INHIBITORS OF SPLA2 LILLY CO ELI (US) 2007-02-14 EP disclosed
US-6933313-B2 Substituted carbazoles as inhibitors of sPLA2 ELI LILLY AND COMPANY (US) 2005-08-23 US disclosed
EP-0950657-B1 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitors LILLY CO ELI (US) 2004-07-14 EP disclosed
EP-0952149-B1 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitiors LILLY CO ELI (US) 2004-06-09 EP disclosed
US-20040087796-A1 Substituted carbazoles as inhibitors of spla2 HARPER RICHARD WALTZ (US) 2004-05-06 US disclosed
US-6713645-B1 INHIBITING SPLA2 MEDIATED RELEASE OF FATTY ACIDS FOR TREATMENT OF CONDITIONS SUCH AS SEPTIC SHOCK ELI LILLY AND COMPANY 2004-03-30 US disclosed
EP-1395554-A1 SUBSTITUTED CARBAZOLES AS INHIBITORS OF SPLA2 ELI LILLY AND COMPANY (US) 2004-03-10 EP disclosed
WO-2002079154-A1 SUBSTITUTED CARBAZOLES AS INHIBITORS OF SPLA2 ELI LILLY AND COMPANY (US) 2002-10-10 WO disclosed
US-6177440-B1 THERAPY FOR SEPSIS SHOCK; PHOSPHOLIPASE INHBITOR ELI LILLY AND COMPANY 2001-01-23 US disclosed
EP-0952149-A2 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitiors ELI LILLY AND COMPANY (US) 1999-10-27 EP disclosed
EP-0950657-A2 Substituted carbazoles, process for their preparation and their use as sPLA2 inhibitors ELI LILLY AND COMPANY (US) 1999-10-20 EP 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-20040087796-A1 Substituted carbazoles as inhibitors of spla2 HCAR2, ALOX12, SPTLC2 HDAC1 503/4885HDAC6 2420/4885CSNK2A2 700/4885

“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.