SCHEMBL4674484

SCHEMBL4674484

O=C(Cc1cc(S(=O)(=O)c2ccc(F)cc2)co1)C(=O)c1nc[nH]n1

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAMPT P43490 6/20 0.35
HTR2A P28223 4/20 0.32
KCNH2 Q12809 4/20 0.32
HTR2C P28335 2/20 0.32
AKR1B1 P15121 1/20 0.32
ALDH1A1 P00352 1/20 0.32
DAO P14920 1/20 0.31
CA2 P00918 1/20 0.31
CFTR P13569 2/20 0.31
MMP1 P03956 1/20 0.31
MMP2 P08253 1/20 0.31
MMP3 P08254 1/20 0.31
MMP9 P14780 1/20 0.31
MMP12 P39900 1/20 0.31
MMP13 P45452 1/20 0.31
MMP14 P50281 1/20 0.31
HTR2B P41595 1/20 0.30
KDM4E B2RXH2 1/20 0.30
LMNA P02545 1/20 0.30
HTT P42858 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
SCHEMBL4671865 0.90 ALDH1A1 (0.35) NAMPTALDH1A1CA2KDM4ELMNA
SCHEMBL4677188 0.89 NAMPT (0.35) NAMPTAKR1B1ALDH1A1DAOCA2
SCHEMBL4675035 0.83 DAO (0.33) ALDH1A1DAOLMNA
SCHEMBL4671572 0.83 NAMPT (0.35) NAMPTHTR2AKCNH2HTR2CAKR1B1
SCHEMBL4671208 0.82 HTR2A (0.32) NAMPTHTR2AKCNH2HTR2CAKR1B1
SCHEMBL4671019 0.81 POLB (0.34) NAMPTHTR2AKCNH2HTR2CAKR1B1
SCHEMBL4673439 0.81 L3MBTL1 (0.34) DAOLMNA
SCHEMBL4674792 0.80 LOX (0.33) NAMPTHTR2AKCNH2HTR2CAKR1B1
SCHEMBL4673364 0.79 SMN1; SMN2 (0.35) NAMPTHTR2AKCNH2HTR2CAKR1B1
SCHEMBL4677764 0.79 LOX (0.39) HTR2AKCNH2HTR2CCFTRSMN1; SMN2

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 NAMPT 2333/4885HTR2A 441/4885KCNH2 3174/4885

“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.