SCHEMBL3147682

SCHEMBL3147682

CC(C(=O)O)(C(=O)c1ccccc1O)c1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 7/20 0.48
KDM4E B2RXH2 7/20 0.48
ALDH1A1 P00352 4/20 0.48
SMN1; SMN2 Q16637 3/20 0.48
CA12 O43570 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
HMGB1 P09429 1/20 0.48
CA4 P22748 1/20 0.48
CA6 P23280 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
NAPRT Q6XQN6 1/20 0.48
CA14 Q9ULX7 1/20 0.48
LMNA P02545 3/20 0.43
TSHR P16473 2/20 0.43
HSD17B10 Q99714 4/20 0.42
MAPT P10636 4/20 0.42
KMT2A Q03164 2/20 0.41
ALOX15 P16050 1/20 0.41

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
SCHEMBL12083366 0.81 KDM4E (0.54) HPGDKDM4EALDH1A1SMN1; SMN2CA12
SCHEMBL1560417 0.78 MAPT (0.54) KDM4EALDH1A1TSHRMAPTKMT2A
SCHEMBL7553464 0.77 HPGD (0.56) HPGDKDM4EALDH1A1SMN1; SMN2CA12
SCHEMBL6445601 0.77 CES1 (0.53) ALDH1A1NAPRTLMNATSHRHSD17B10
Benzene SCHEMBL28249468 0.77 HPGD (0.56) HPGDKDM4EALDH1A1SMN1; SMN2CA12
SCHEMBL3349740 0.76 HPGD (0.50) HPGDKDM4EALDH1A1SMN1; SMN2CA12
SCHEMBL21269860 0.76 MAPT (0.52) KDM4EALDH1A1TSHRMAPTKMT2A
SCHEMBL21269958 0.76 MAPT (0.52) KDM4EALDH1A1TSHRMAPTKMT2A
SCHEMBL21269891 0.76 MAPT (0.52) KDM4EALDH1A1TSHRMAPTKMT2A
SCHEMBL28315718 0.76 MAPT (0.52) KDM4EALDH1A1TSHRMAPTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7705050-B2 Amides, useful in the inhibition of IL-8-induced chemotaxis of neutrophils DOMPÉ FARMACEUTICI S.P.A. (IT) 2010-04-27 US disclosed
EP-1255726-B1 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8 INDUCED CHEMIOTAXIS OF NEUTROPHILS DOMPE PHA R MA SPA RES & MFG (IT) 2009-11-11 EP disclosed
US-20040181073-A1 Amides, useful in the inhibition of il-8-induced chemotaxis of neutrophils DOMPÉ FARMACEUTICI S.P.A. (IT) 2004-09-16 US disclosed
EP-1255726-A2 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8 INDUCED CHEMIOTAXIS OF NEUTROPHILS Dompé S.P.A. (IT) 2002-11-13 EP disclosed
WO-2001058852-A2 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8-INDUCED CHEMIOTAXIS OF NEUTROPHILS Dompé S.p.A. (IT) 2001-08-16 WO 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-20040181073-A1 Amides, useful in the inhibition of il-8-induced chemotaxis of neutrophils CXCL8, MMP8, CCR8 HPGD 152/4885KDM4E 4469/4885ALDH1A1 582/4885

“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.