SCHEMBL5046100

SCHEMBL5046100

CO[C@](C)(C(=O)O)c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNN4 O15554 1/20 0.50
CES1 P23141 1/20 0.50
KMT2A Q03164 2/20 0.47
MAPT P10636 1/20 0.47
PPARG P37231 1/20 0.45
PPARA Q07869 1/20 0.45
CYP2C19 P33261 1/20 0.45
HIF1A Q16665 1/20 0.45
ALDH1A1 P00352 3/20 0.45
CYP1A2 P05177 2/20 0.45
ALOX15 P16050 1/20 0.45
HDAC3 O15379 1/20 0.44
HDAC4 P56524 1/20 0.44
HDAC1 Q13547 1/20 0.44
HDAC7 Q8WUI4 1/20 0.44
HDAC2 Q92769 1/20 0.44
HDAC10 Q969S8 1/20 0.44
HDAC11 Q96DB2 1/20 0.44
HDAC8 Q9BY41 1/20 0.44
HDAC6 Q9UBN7 1/20 0.44

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
SCHEMBL22722985 1.00 KCNN4 (0.50) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL2517938 1.00 KCNN4 (0.50) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL10710486 0.85 CES1 (0.48) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL15120026 0.83 CES1 (0.47) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL10837067 0.83 KCNN4 (0.62) KCNN4CES1KMT2AMAPTCYP2C19
SCHEMBL19275896 0.83 CES1 (0.47) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL5806173 0.83 ESR1 (0.52) ALDH1A1ESR1ESR2CYP3A4TSHR
SCHEMBL4554194 0.83 MAPT (0.59) KCNN4CES1KMT2AMAPTCYP2C19
SCHEMBL420635 0.83 KCNN4 (0.47) KCNN4CES1KMT2AMAPTPPARG
SCHEMBL31512970 0.83 CES1 (0.47) KCNN4CES1KMT2AMAPTPPARG

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
US-10857517-B2 Porous chiral materials and uses thereof NANKAI UNIVERSITY (CN) 2020-12-08 US disclosed
EP-1930441-A1 METHOD FOR PRODUCTION OF OPTICALLY ACTIVE -HYDROXYCARBOXYLIC ACID Daiichi Fine Chemical Co., Ltd. (JP) 2008-06-11 EP disclosed
EP-1567498-B1 MANDELIC ACID DERIVATIVES HOFFMANN LA ROCHE (CH) 2008-01-23 EP disclosed
US-7129238-B2 Mandelic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2006-10-31 US disclosed
EP-1567498-A2 MANDELIC ACID DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2005-08-31 EP disclosed
US-20040122057-A1 Novel mandelic acid derivatives HOFFMANN-LA ROCHE INC. 2004-06-24 US disclosed
WO-2004048335-A2 MANDELIC ACID DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2004-06-10 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 (2 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-20040122057-A1 Novel mandelic acid derivatives F7, F11, F9 KCNN4 4725/4885CES1 720/4885KMT2A 1963/4885
US-10857517-B2 Porous chiral materials and uses thereof ANXA7, XDH, OPRM1 KCNN4 2631/4885CES1 3864/4885KMT2A 3099/4885

“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.