SCHEMBL6542942

SCHEMBL6542942

COC(=O)CCC1(C)CCCCC1=O

nearest known ligand 0.43

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.38
FNTA P49354 1/20 0.33
FNTB P49356 1/20 0.33
LMNA P02545 2/20 0.33
HSD17B10 Q99714 2/20 0.33
MAPT P10636 2/20 0.33
ALDH1A1 P00352 1/20 0.33
HTT P42858 1/20 0.33
KMT2A Q03164 1/20 0.33
CYP3A4 P08684 2/20 0.32
NOTUM Q6P988 1/20 0.32
KDM4E B2RXH2 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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
SCHEMBL11638039 0.95 TSHR (0.39) TSHRFNTAFNTBLMNAHSD17B10
SCHEMBL26135862 0.91 TSHR (0.41) TSHRLMNAALDH1A1KMT2A
SCHEMBL11285445 0.83 TP53 (0.40) TSHRHSD17B10MAPTKMT2ACYP3A4
SCHEMBL11640427 0.82 TP53 (0.39) TSHRLMNAHSD17B10MAPTALDH1A1
SCHEMBL7495347 0.81 MME (0.39) FNTAFNTBHSD17B10ALDH1A1KDM4E
SCHEMBL7495343 0.81 MME (0.39) FNTAFNTBHSD17B10ALDH1A1KDM4E
SCHEMBL21002272 0.79 GRIN2D (0.31) TSHRLMNA
SCHEMBL21002274 0.79 GRIN2D (0.31) TSHRLMNA
SCHEMBL10727487 0.78 TSHR (0.35) TSHRLMNAHSD17B10MAPTALDH1A1
SCHEMBL10727481 0.78 TSHR (0.35) TSHRLMNAHSD17B10MAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6730242-B2 EFFICIENCY THE UNIVERSITY OF ROCHESTER 2004-05-04 US disclosed
US-20030164473-A1 Glass-forming liquid crystalline compositions and optical devices formed therefrom NATIONAL SCIENCE FOUNDATION 2003-09-04 US disclosed
US-6558572-B2 Optical device UNIVERSITY OF ROCHESTER 2003-05-06 US disclosed
US-20010036517-A1 Glass-forming liquid crystalline compositions and optical devices formed therefrom NATIONAL SCIENCE FOUNDATION 2001-11-01 US disclosed
EP-0729498-B1 CHIRAL NEMATIC LIQUID CRYSTALLINE COMPOSITIONS UNIV ROCHESTER (US) 2001-07-25 EP disclosed
EP-0729498-A1 CHIRAL NEMATIC LIQUID CRYSTALLINE COMPOSITIONS THE UNIVERSITY OF ROCHESTER (US) 1996-09-04 EP disclosed
EP-0729498-A4 CHIRAL NEMATIC LIQUID CRYSTALLINE COMPOSITIONS UNIV ROCHESTER (US) 1996-07-16 EP disclosed
US-5514296-A Glassy low molar mass chiral nematic liquid crystalline compositions and optical articles formed therefrom THE UNIVERSITY OF ROCHESTER (US) 1996-05-07 US disclosed
WO-1995014067-A1 CHIRAL NEMATIC LIQUID CRYSTALLINE COMPOSITIONS UNIVERSITY OF ROCHESTER (US) 1995-05-26 WO disclosed
US-5378393-A That produce reflected light in visible and infrared regions; thermotropic compounds that include a cycloaliphatic radical THE UNIVERSITY OF ROCHESTER (US) 1995-01-03 US disclosed
US-4959293-A Deep UV photoresist with alkyl 2-diazo-1-ones as solubility modification agents J. T. BAKER, INC. (US) 1990-09-25 US disclosed
US-4291170-A A,B-UNSATURATED ESTER, KETONE, PRIMARY AMINE OR SCHIFF BASE, ACID STAMICARBON, B.V. (NL) 1981-09-22 US disclosed
US-4128560-A Tricyclic alkylamine derivatives AYERST MCKENNA & HARRISON LTD. (CA) 1978-12-05 US disclosed
US-4057559-A ANTIINFLAMMATORY AGENTS AMERICAN HOME PRODUCTS CORPORATION (US) 1977-11-08 US disclosed