SCHEMBL2353009

SCHEMBL2353009

CCCC(=O)Oc1ccc(-c2ccc3c(c2C(O)c2cc(F)ccc2C)C(C)=CC(C)(C)N3)c(OC)c1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.42
LMNA P02545 5/20 0.42
ALDH1A1 P00352 5/20 0.42
NPSR1 Q6W5P4 3/20 0.42
HTT P42858 4/20 0.41
KDM4E B2RXH2 4/20 0.41
HSD17B10 Q99714 2/20 0.41
G6PD P11413 2/20 0.41
TP53 P04637 1/20 0.41
GFER P55789 1/20 0.41
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
HPGD P15428 2/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
IL6 P05231 2/20 0.39
PGR P06401 8/20 0.39
NR3C1 P04150 9/20 0.38
AR P10275 4/20 0.38
ALOX15 P16050 2/20 0.38
ALOX12 P18054 2/20 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
Hydrochloric Acid SCHEMBL1781572 0.91 MAPT (0.41) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL4427343 0.88 PGR (0.41) MAPTLMNANPSR1HTTTP53
SCHEMBL14837209 0.86 MAPT (0.46) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL2396439 0.83 PGR (0.45) PGRNR3C1ARNR3C2ESR1
SCHEMBL1314102 0.82 IL6 (0.51) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL1316521 0.79 IL6 (0.49) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL1313997 0.77 MAPT (0.46) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL2394873 0.76 PGR (0.45) PGRNR3C1ARNR3C2ESR1
SCHEMBL2544665 0.76 MAPT (0.40) MAPTLMNAALDH1A1NPSR1HTT
SCHEMBL1315486 0.76 ALDH1A1 (0.40) MAPTLMNAALDH1A1NPSR1HTT

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
EP-2085387-B1 NOVEL 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING SUBSTITUTED PHENYLCHALCOGENO LOWER ALKYL GROUP AND ESTER-INTRODUCED PHENYL GROUP AS SUBSTITUENTS SANTEN PHARMACEUTICAL CO LTD (JP) 2013-04-10 EP disclosed
US-8008496-B2 1,2-dihydroquinoline derivative having substituted phenylchalcogeno lower alkyl group and ester-introduced phenyl group as substituents SANTEN PHARMACEUTICAL CO., LTD. (JP) 2011-08-30 US disclosed
US-20100056504-A1 NOVEL 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING SUBSTITUTED PHENYLCHALCOGENO LOWER ALKYL GROUP AND ESTER- INTRODUCED PHENYL GROUP AS SUBSTITUENTS AYUMI PHARMACEUTICAL CORPORATION (JP) 2010-03-04 US disclosed
EP-2085387-A1 NOVEL 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING SUBSTITUTED PHENYLCHALCOGENO LOWER ALKYL GROUP AND ESTER-INTRODUCED PHENYL GROUP AS SUBSTITUENTS Santen Pharmaceutical Co., Ltd (JP) 2009-08-05 EP 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-20100056504-A1 NOVEL 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING SUBSTITUTED PHENYLCHALCOGENO LOWER ALKYL GROUP AND ESTER- INTRODUCED PHENYL GROUP AS SUBSTITUENTS NR3C1, NR3C2, NR5A1 MAPT 4857/4885LMNA 4440/4885ALDH1A1 3364/4885

“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.