SCHEMBL490866

SCHEMBL490866

COC(OC)(c1ccccc1)C(C(=O)O)C(=O)O

nearest known ligand 0.47

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.47
KCNN4 O15554 1/20 0.47
CYP1A2 P05177 1/20 0.44
CYP2D6 P10635 1/20 0.44
EDNRB P24530 8/20 0.41
EDNRA P25101 8/20 0.41
NR1I2 O75469 1/20 0.41
KCNE1 P15382 1/20 0.41
KCNQ1 P51787 1/20 0.41
POLB P06746 1/20 0.41
KMT2A Q03164 3/20 0.39
MAPT P10636 1/20 0.39
KIF11 P52732 3/20 0.39
CYP2C19 P33261 1/20 0.38
HIF1A Q16665 1/20 0.38
TSHR P16473 1/20 0.38

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
SCHEMBL4603935 0.80 PIN1 (0.46) CES1KCNN4POLBKMT2AMAPT
SCHEMBL28724250 0.80 EDNRB (0.51) CES1KCNN4CYP1A2CYP2D6EDNRB
SCHEMBL7691954 0.78 CES1 (0.44) CES1KCNN4CYP1A2CYP2D6EDNRB
SCHEMBL10800116 0.77 CES1 (0.42) CES1KCNN4CYP1A2CYP2D6CYP2C19
SCHEMBL27315793 0.76 ATM (0.44) CES1KCNN4CYP1A2CYP2D6EDNRB
SCHEMBL28721298 0.74 EDNRB (0.47) CES1KCNN4CYP1A2CYP2D6EDNRB
SCHEMBL10512565 0.73 CES1 (0.40) CES1KCNN4CYP1A2CYP2D6EDNRB
SCHEMBL1507630 0.73 CYP2D6 (0.42) CES1KCNN4CYP1A2CYP2D6KMT2A
SCHEMBL10884190 0.73 KCNN4 (0.44) CES1KCNN4CYP1A2CYP2D6KMT2A
SCHEMBL7288198 0.72 CYP1A2 (0.48) CES1KCNN4CYP1A2CYP2D6KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180207080-A1 COMPOSITIONS OF FLUORINATED SURFACTANTS AND ANTIOXIDANTS MERCK PATENT GMBH (DE) 2018-07-26 US disclosed
US-8598228-B2 Cinnamic acid ascorbates MERCK PATENT GMBH (DE) 2013-12-03 US disclosed
US-8268293-B2 Using compounds which do not themselves exhibit significant UV absorption in the UV-A or UV-B region, but are reactive under use conditions, such as 4-hydroxyphenylpropionic acid, or 2-ethylhexyl 4-hydroxy-3,5-dimethoxycinnamate, or polysiloxanes which contain benzylidenemalonic acid derivatives MERCK PATENT GMBH (DE) 2012-09-18 US disclosed
US-20120052028-A1 CINNAMIC ACID ASCORBATES MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 2012-03-01 US disclosed
US-8106233-B2 Applying di-2-ethylhexyl 4-hydroxy-3,5-dimethoxy-benzylmalonate; protective action against UV rays, oxidative stress on body cells, counters skin ageing MERCK PATENT GMBH (DE) 2012-01-31 US disclosed
US-7906684-B2 Antioxidants MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 2011-03-15 US disclosed
US-20090246158-A1 ANTIOXIDANTS MERCK PATENT GESELLSCHAFT (DE) 2009-10-01 US disclosed
US-20090098072-A1 ANTIOXIDANTS MERCK PATENT GESELLSCHAFT (DE) 2009-04-16 US disclosed
US-20080171004-A1 Using compounds which do not themselves exhibit significant UV absorption in the UV-A or UV-B region, but are reactive under use conditions, such as 4-hydroxyphenylpropionic acid, or 2-ethylhexyl 4-hydroxy-3,5-dimethoxycinnamate, or polysiloxanes which contain benzylidenemalonic acid derivatives MERCK PATENT GMBH (DE) 2008-07-17 US disclosed
US-20080152603-A1 Antioxidants SUSONITY Commercial GmbH (DE) 2008-06-26 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 (6 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-20080152603-A1 Antioxidants GPX4, GPX1, CAT CES1 1034/4885KCNN4 2854/4885CYP1A2 250/4885
US-20090246158-A1 ANTIOXIDANTS LPO, GPX1, GPX4 CES1 1806/4885KCNN4 2936/4885CYP1A2 939/4885
US-20090098072-A1 ANTIOXIDANTS GPX1, PRDX3, XDH CES1 757/4885KCNN4 3046/4885CYP1A2 293/4885
US-20080171004-A1 Using compounds which do not themselves exhibit significant UV absorption in the UV-A or UV-B region, but are reactive under use conditions, such as 4-hydroxyphenylpropionic acid, or 2-ethylhexyl 4-hydroxy-3,5-dimethoxycinnamate, or polysiloxanes which contain benzylidenemalonic acid derivatives HPD, HAAO, UGT1A6 CES1 2253/4885KCNN4 4033/4885CYP1A2 325/4885
US-20180207080-A1 COMPOSITIONS OF FLUORINATED SURFACTANTS AND ANTIOXIDANTS LPO, CAT, GPX4 CES1 993/4885KCNN4 4606/4885CYP1A2 1758/4885
US-20120052028-A1 CINNAMIC ACID ASCORBATES PROC, C1S, NISCH CES1 330/4885KCNN4 4735/4885CYP1A2 232/4885

“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.