SCHEMBL4672686

SCHEMBL4672686

O=C(O)C(O)=CC(=O)c1cscc1Cc1cccc(F)c1

nearest known ligand 0.40

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 2/20 0.40
PTGER4 P35408 1/20 0.39
PTGER2 P43116 1/20 0.39
CYP2C9 P11712 1/20 0.36
GPR52 Q9Y2T5 1/20 0.36
SLC1A1 P43005 2/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
NR4A2 P43354 1/20 0.35
PTPN1 P18031 1/20 0.35

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
SCHEMBL4672682 1.00 HCAR2 (0.40) HCAR2PTGER4PTGER2CYP2C9GPR52
SCHEMBL4677257 0.87 CYP2C9 (0.41) PTGER4PTGER2CYP2C9PTPN1
SCHEMBL4677260 0.87 CYP2C9 (0.41) PTGER4PTGER2CYP2C9PTPN1
SCHEMBL4671187 0.86 CYP2C9 (0.36) PTGER4PTGER2CYP2C9KMT2A
SCHEMBL4671185 0.86 CYP2C9 (0.36) PTGER4PTGER2CYP2C9KMT2A
SCHEMBL4674192 0.81 HCAR2 (0.42) HCAR2GPR52SLC1A1NR4A2
SCHEMBL4674196 0.81 HCAR2 (0.42) HCAR2GPR52SLC1A1NR4A2
SCHEMBL4672985 0.80 HCAR2 (0.39) HCAR2GPR52SLC1A1NR4A2PTPN1
SCHEMBL4672983 0.80 HCAR2 (0.39) HCAR2GPR52SLC1A1NR4A2PTPN1
SCHEMBL4678288 0.80 PTPN1 (0.39) CYP2C9GPR52MEN1KMT2APTPN1

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 7 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
CN-1335834-A Aromatic heterocyclic compounds having HIV integrase inhibitory activity SHIONOGI & CO (JP) 2002-02-13 CN 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 HCAR2 276/4885PTGER4 4235/4885PTGER2 4764/4885

“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.