SCHEMBL3907931

SCHEMBL3907931

O=c1[nH]n(Cc2ccccc2Cl)c2cc(Cl)c(NS(=O)(=O)c3cc(Cl)ccc3F)cc12

nearest known ligand 0.43

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ACLY P53396 4/20 0.43
PTK2B Q14289 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
MCL1 Q07820 4/20 0.40
HPGD P15428 1/20 0.38
TSHR P16473 1/20 0.38
EPHX2 P34913 1/20 0.38
ALPL P05186 2/20 0.38
LMNA P02545 1/20 0.38
TP53 P04637 1/20 0.38
MAPT P10636 1/20 0.38
CCR2 P41597 3/20 0.37
SGK1 O00141 2/20 0.36
SLC40A1 Q9NP59 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
SCHEMBL3906458 0.90 ACLY (0.47) ACLYPTK2BSMN1; SMN2MCL1HPGD
SCHEMBL3908352 0.86 MAPT (0.43) TP53MAPTCCR2
SCHEMBL1813077 0.85 PTGES2 (0.45) ACLY
SCHEMBL1812324 0.83 CCR2 (0.41) ACLYPTK2BSMN1; SMN2CCR2
SCHEMBL3902067 0.83 ACLY (0.53) ACLYPTK2BSMN1; SMN2ALPLCCR2
SCHEMBL3904617 0.83 CCR2 (0.46) MAPTCCR2
SCHEMBL1811314 0.80 TRPV4 (0.45) MCL1HPGDTSHRLMNAMAPT
SCHEMBL3917122 0.79 NR1I2 (0.45) MCL1SGK1SLC40A1
SCHEMBL1811117 0.78 ACLY (0.47) ACLYMCL1CCR2SLC40A1
SCHEMBL3906066 0.78 ACLY (0.43) ACLYCCR2SLC40A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7528158-B2 Indazolone derivatives useful as 11b-HSD1 inhibitors HOFFMANN-LA ROCHE INC. (US) 2009-05-05 US claimed
EP-1797042-B1 INDOZOLONE DERIVATIVES AS 11B-HSD1 INHIBITORS HOFFMANN LA ROCHE (CH) 2009-01-07 EP claimed
US-20060069269-A1 Novel indazolone derivatives useful as 11b-HSD1 inhibitors F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2006-03-30 US claimed
US-7528158-B2 Indazolone derivatives useful as 11b-HSD1 inhibitors HOFFMANN-LA ROCHE INC. (US) 2009-05-05 US disclosed
EP-1797042-B1 INDOZOLONE DERIVATIVES AS 11B-HSD1 INHIBITORS HOFFMANN LA ROCHE (CH) 2009-01-07 EP disclosed
US-20060069269-A1 Novel indazolone derivatives useful as 11b-HSD1 inhibitors F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2006-03-30 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 (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-20060069269-A1 Novel indazolone derivatives useful as 11b-HSD1 inhibitors HSD17B1, HSD11B1, HSD17B7 ACLY 2238/4885PTK2B 2774/4885SMN1; SMN2 3704/4885

“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.