SCHEMBL2278796

SCHEMBL2278796

C1CCCCC(C2CCCCCCC2)CCC1

nearest known ligand 0.89

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.89
HSD17B10 Q99714 1/20 0.40
SLC18A3 Q16572 1/20 0.39
THRB P10828 1/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
TSHR P16473 1/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
HSD11B1 P28845 1/20 0.35
MAPT P10636 1/20 0.33
EPHX1 P07099 1/20 0.33
HIF1A Q16665 1/20 0.33
NOS1 P29475 1/20 0.33
NOS2 P35228 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
SCHEMBL11359726 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL48866 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
Biphenyl SCHEMBL2997707 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL7738712 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL2999797 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL7739675 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL7741464 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL22284064 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL22284066 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1
SCHEMBL231054 1.00 ALDH1A1 (0.89) ALDH1A1HSD17B10SLC18A3THRBMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7994311-B2 Metal binding, electron donating dipyrrin functionality linked to electron withdrawing functionality, base to which chemosensor can be fixedly attached; for quantitative and qualitative sensing of +2 transition metals using ratiometric fluorescence capable of forming stable transition metal complex STC. UNM (US) 2011-08-09 US disclosed