Styrene

Styrene

SCHEMBL7627581

C1=CCC=C1.C1=CCC=C1.C=Cc1ccccc1.Oc1cccc(O)c1

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.48
TSHR P16473 2/20 0.48
LCK P06239 2/20 0.43
CYP3A4 P08684 2/20 0.41
CA12 O43570 1/20 0.41
CA2 P00918 1/20 0.41
LMNA P02545 1/20 0.41
CA5A P35218 1/20 0.41
CA9 Q16790 1/20 0.41
HSD17B10 Q99714 1/20 0.41
CA14 Q9ULX7 1/20 0.41
CA5B Q9Y2D0 1/20 0.41
MGAM O43451 1/20 0.39
GAA P10253 1/20 0.39
SI P14410 1/20 0.39
MGAM2 Q2M2H8 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
TP53 P04637 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
CCNB2 O95067 1/20 0.36

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
Styrene SCHEMBL27677421 0.91 ALDH1A1 (0.54) ALDH1A1TSHRCYP3A4CA12CA2
Styrene SCHEMBL16828347 0.87 ALDH1A1 (0.64) ALDH1A1TSHRLCKCYP3A4CA12
Styrene SCHEMBL6930140 0.85 ALDH1A1 (0.67) ALDH1A1TSHRLMNATP53TDP1
Styrene SCHEMBL27598723 0.85 ALDH1A1 (0.67) ALDH1A1TSHRLMNATP53TDP1
Styrene SCHEMBL21496228 0.85 ALDH1A1 (0.67) ALDH1A1TSHRLMNATP53TDP1
Styrene SCHEMBL25407202 0.83 ALDH1A1 (0.58) ALDH1A1TSHRLCKCYP3A4CA12
Styrene SCHEMBL28874819 0.83 TSHR (0.45) ALDH1A1TSHRCA12CA2LMNA
Styrene SCHEMBL26644759 0.83 ALDH1A1 (0.64) ALDH1A1TSHRLMNATP53TDP1
Styrene SCHEMBL10771405 0.81 ALDH1A1 (0.61) ALDH1A1TSHRLMNATP53TDP1
Styrene SCHEMBL27764303 0.81 ALDH1A1 (0.61) ALDH1A1TSHRLMNATP53TDP1

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-6472457-B1 METHODS FOR PREPARING FORMALDEHYDE-FREE RESORCINOL RESINS ARE DISCLOSED. THE METHODS GENERALLY COMPRISE REACTING RESORCINOL FIRST WITH DICYCLOPENTADIENE AND THEN REACTING THAT MIXTURE WITH AN OLEFINIC COMPOUND. INDSPEC CHEMICAL CORPORATION 2002-10-29 US disclosed