SCHEMBL4675409

SCHEMBL4675409

CC(=O)c1ccc(Cc2csc(CC(=O)C(=O)c3nc[nH]n3)n2)cc1

nearest known ligand 0.37

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.37
TSHR P16473 1/20 0.35
LMNA P02545 2/20 0.34
AOC3 Q16853 3/20 0.32
BCHE P06276 2/20 0.32
HDAC1 Q13547 2/20 0.31
HDAC6 Q9UBN7 2/20 0.31
PKM P14618 1/20 0.31
MAOB P27338 5/20 0.31
RAB9A P51151 1/20 0.30
MAOA P21397 1/20 0.30

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
SCHEMBL4677685 0.92 KMT2A (0.37) KMT2ATSHRLMNAAOC3HDAC1
SCHEMBL4671165 0.89 BCHE (0.39) KMT2ABCHERAB9A
SCHEMBL5899379 0.88 HDAC1 (0.43) KMT2ALMNAHDAC1HDAC6RAB9A
SCHEMBL4675488 0.87 HDAC1 (0.39) AOC3HDAC1HDAC6MAOB
SCHEMBL4672336 0.87 HDAC6 (0.39) KMT2ALMNABCHEHDAC1HDAC6
SCHEMBL4676893 0.87 HDAC1 (0.42) KMT2ALMNAHDAC1HDAC6RAB9A
SCHEMBL5899406 0.86 HDAC1 (0.32) KMT2ALMNABCHEHDAC1HDAC6
SCHEMBL4680267 0.83 XDH (0.38) KMT2ATSHRLMNAAOC3HDAC1
SCHEMBL4671892 0.81 BCHE (0.37) KMT2ALMNABCHEHDAC1HDAC6
SCHEMBL4671419 0.80 KMT2A (0.40) KMT2ATSHRLMNAMAOBMAOA

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
EP-1142872-B1 AROMATIC HETEROCYCLE COMPOUNDS HAVING HIV INTEGRASE INHIBITING ACTIVITIES SHIONOGI & CO (JP) 2008-10-15 EP disclosed
US-7098201-B2 Heteroaromatic derivatives having an inhibitory activity against HIV integrase SHIONOGI & CO., LTD. (JP) 2006-08-29 US disclosed
US-20040002485-A1 Heteroaromatic derivatives having an inhibitory activity against HIV integrase FUJISHITA TOSHIO (JP) 2004-01-01 US disclosed
US-6645956-B1 1-(5-(4-fluorobenzyl)furan-2-yl)-3-hydroxy-3-(1H-1,2,4-triazol-3 -yl)-propenone; viricides; AIDS treatment SHIONOGI & CO., LTD. (JP) 2003-11-11 US disclosed
US-6620841-B1 Furan or benzofuran derivatives substituted with triazole; acquired immunodeficiency syndrome (AIDS) SHIONOGI & CO., LTD. (JP) 2003-09-16 US disclosed
EP-1142872-A1 AROMATIC HETEROCYCLE COMPOUNDS HAVING HIV INTEGRASE INHIBITING ACTIVITIES SHIONOGI & CO., LTD. (JP) 2001-10-10 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-20040002485-A1 Heteroaromatic derivatives having an inhibitory activity against HIV integrase RCOR1, BCOR, CYP8B1 KMT2A 597/4885TSHR 1614/4885LMNA 659/4885

“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.