SCHEMBL1743778

SCHEMBL1743778

CC(C)(C)OC(=O)[C@H](COC(=O)C(C)(C)C)[C@H](CO)c1ccc(C(F)(F)F)cc1

nearest known ligand 0.43

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PRKCA P17252 2/20 0.38
ALDH1A1 P00352 2/20 0.38
PRKCD Q05655 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
CES2 O00748 1/20 0.36
CES1 P23141 1/20 0.36
PPARG P37231 1/20 0.35
PPARA Q07869 1/20 0.35
GSK3B P49841 1/20 0.35
FFAR1 O14842 3/20 0.34
CYP26A1 O43174 1/20 0.33
LDHA P00338 1/20 0.33
LDHB P07195 1/20 0.33
PDPK1 O15530 1/20 0.33
MAPT P10636 1/20 0.33
AAK1 Q2M2I8 1/20 0.33
NOD2 Q9HC29 1/20 0.33
NOD1 Q9Y239 1/20 0.33

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
SCHEMBL1743781 1.00 PRKCA (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1743782 1.00 PRKCA (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1595147 0.91 PRKCA (0.41) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1595149 0.91 PRKCA (0.41) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1743817 0.89 ALDH1A1 (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1743820 0.89 ALDH1A1 (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1743821 0.89 ALDH1A1 (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1744162 0.88 PPARG (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1744160 0.88 PPARG (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2
SCHEMBL1744164 0.88 PPARG (0.38) PRKCAALDH1A1PRKCDL3MBTL1CES2

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
EP-1981884-B1 THIAZOLE COMPOUNDS AS PROTEIN KINASE B (PKB) INHIBITORS AMGEN INC (US) 2012-06-13 EP disclosed
US-8084479-B2 Thiazole compounds and methods of use AMGEN INC. (US) 2011-12-27 US disclosed
EP-2387570-A1 FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE Amgen, Inc (US) 2011-11-23 EP disclosed
US-20110263647-A1 FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2011-10-27 US disclosed
WO-2010083246-A1 FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2010-07-22 WO disclosed
US-20090270445-A1 Thiazole compounds and methods of use AMGEN INC. (US) 2009-10-29 US disclosed
US-7514566-B2 Thiazole compounds and methods of use AMGEN, INC. (US) 2009-04-07 US disclosed
EP-1981884-A2 THIAZOLE COMPOUNDS AS PROTEIN KINASE B (PKB) INHIBITORS Amgen, Inc (US) 2008-10-22 EP disclosed
WO-2007084391-A2 THIAZOLE COMPOUNDS AS PROTEIN KINASE B ( PKB) INHIBITORS AMGEN INC. (US) 2007-07-26 WO disclosed
US-20070173506-A1 Thiazole compounds and methods of use AMGEN INC. (US) 2007-07-26 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 (3 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-20110263647-A1 FLUOROISOQUINOLINE SUBSTITUTED THIAZOLE COMPOUNDS AND METHODS OF USE TFEB, PCK2, JAK2 PRKCA 152/4885ALDH1A1 2488/4885PRKCD 655/4885
US-20090270445-A1 Thiazole compounds and methods of use MTOR, JAK2, TK2 PRKCA 95/4885ALDH1A1 2019/4885PRKCD 403/4885
US-20070173506-A1 Thiazole compounds and methods of use MTOR, JAK2, PCK2 PRKCA 206/4885ALDH1A1 2061/4885PRKCD 764/4885

“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.