SCHEMBL4675172

SCHEMBL4675172

O=C(Cc1csc(S(=O)(=O)c2ccc(F)cc2)c1)C(=O)c1nn[nH]n1

nearest known ligand 0.34

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CXCR3 P49682 1/20 0.34
CFTR P13569 4/20 0.33
RORC P51449 3/20 0.33
TDP1 Q9NUW8 1/20 0.33
KEAP1 Q14145 1/20 0.33
NFE2L2 Q16236 1/20 0.33
HTR2A P28223 1/20 0.32
KCNH2 Q12809 1/20 0.32
PTGDR2 Q9Y5Y4 5/20 0.32
CYP2C8 P10632 2/20 0.32
CYP2C19 P33261 2/20 0.32
CYP2C9 P11712 1/20 0.32
MEN1 O00255 1/20 0.31
KMT2A Q03164 1/20 0.31
EGFR P00533 1/20 0.31
ERBB2 P04626 1/20 0.31
AKR1B1 P15121 1/20 0.31

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
SCHEMBL4679653 0.90 CES1 (0.37) KEAP1PTGDR2CYP2C8CYP2C19CYP2C9
SCHEMBL4675060 0.89 CXCR3 (0.36) CXCR3CYP2C19KMT2AEGFRERBB2
SCHEMBL4674440 0.83 HTR2A (0.34) CFTRHTR2AKCNH2MEN1KMT2A
SCHEMBL4680059 0.82 RORC (0.33) CXCR3CFTRRORCTDP1KEAP1
SCHEMBL4676297 0.81 LOX (0.39) CFTRTDP1
SCHEMBL4674444 0.81 TDP1 (0.34) CXCR3TDP1PTGDR2KMT2A
SCHEMBL4673275 0.80 RORC (0.35) CXCR3RORCTDP1KEAP1NFE2L2
SCHEMBL4676317 0.79 LOXL2 (0.36) CXCR3RORCTDP1HTR2AKCNH2
SCHEMBL4678124 0.79 CXCR3 (0.34) CXCR3RORCTDP1KEAP1NFE2L2
SCHEMBL4672470 0.79 KMT2A (0.39) CXCR3RORCTDP1HTR2AKCNH2

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 CXCR3 1130/4885CFTR 3324/4885RORC 230/4885

“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.