SCHEMBL13536741

SCHEMBL13536741

COC(=O)C(Cc1cccc(O)c1)NC(=O)OCc1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.61
ALOX15 P16050 1/20 0.61
KYNU Q16719 1/20 0.57
NLRP3 Q96P20 1/20 0.56
CTSL P07711 2/20 0.56
CTSB P07858 2/20 0.56
CTSS P25774 2/20 0.56
CTSK P43235 1/20 0.56
CYP3A4 P08684 3/20 0.54
TSHR P16473 3/20 0.54
TACR1 P25103 2/20 0.54
TYR P14679 1/20 0.54
MEN1 O00255 1/20 0.53
MAPT P10636 1/20 0.53
KMT2A Q03164 1/20 0.53

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
SCHEMBL14623159 1.00 ALDH1A1 (0.61) ALDH1A1ALOX15KYNUNLRP3CTSL
SCHEMBL9825830 0.90 TYR (0.58) ALDH1A1ALOX15CTSLCTSBCTSS
SCHEMBL5288135 0.90 TYR (0.58) ALDH1A1ALOX15CTSLCTSBCTSS
SCHEMBL7151822 0.89 ALDH1A1 (0.74) ALDH1A1ALOX15KYNUCTSLCTSB
SCHEMBL329686 0.89 ALDH1A1 (0.74) ALDH1A1ALOX15KYNUCTSLCTSB
SCHEMBL13536740 0.89 POLB (0.63) ALDH1A1ALOX15KYNUCTSLCTSB
Hydrochloric Acid SCHEMBL7928050 0.88 ALDH1A1 (0.72) ALDH1A1ALOX15KYNUCTSLCTSB
SCHEMBL9001871 0.88 TACR1 (0.52) ALDH1A1ALOX15CTSLCTSBCTSS
SCHEMBL16224709 0.88 ALDH1A1 (0.59) ALDH1A1ALOX15KYNUCTSLCTSB
SCHEMBL5122829 0.88 ALDH1A1 (0.59) ALDH1A1ALOX15KYNUCTSLCTSB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7649015-B2 Cellular accumulation of phosphonate analogs of HIV protease inhibitor compounds GILEAD SCIENCES, INC. (US) 2010-01-19 US disclosed
US-7371853-B2 Macrocyclic β-secretase inhibitors for the treatment of Alzheimer's disease MERCK & CO., INC. (US) 2008-05-13 US disclosed
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds GILEAD SCIENCES, INC. 2007-01-11 US disclosed
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds GILEAD SCIENCES, INC. 2007-01-11 US 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-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds PPA1, PNP, PPME1 ALDH1A1 3337/4885ALOX15 3167/4885KYNU 3479/4885

“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.