SCHEMBL3967693

SCHEMBL3967693

CC(CC(C)(c1ccccc1O)c1ccccc1O)(c1ccccc1O)c1ccccc1O

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.62
TSHR P16473 5/20 0.62
TDP1 Q9NUW8 2/20 0.62
ALOX15 P16050 4/20 0.41
CA2 P00918 3/20 0.41
LMNA P02545 2/20 0.41
HSD17B10 Q99714 2/20 0.41
KDM4E B2RXH2 2/20 0.41
MAPT P10636 2/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
HIF1A Q16665 2/20 0.41
NPC1 O15118 1/20 0.41
CA12 O43570 1/20 0.41
GMNN O75496 1/20 0.41
EGFR P00533 1/20 0.41
FYN P06241 1/20 0.41
POLB P06746 1/20 0.41
CA3 P07451 1/20 0.41
CYP3A4 P08684 1/20 0.41
MMP9 P14780 1/20 0.41

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
SCHEMBL29381738 0.84 TSHR (0.60) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL3152876 0.84 TSHR (0.60) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL3963329 0.82 ALDH1A1 (0.48) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL9330085 0.80 ALDH1A1 (0.56) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL1581665 0.80 ALDH1A1 (0.56) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL15459418 0.80 ALDH1A1 (0.56) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL2979378 0.79 TSHR (0.54) ALDH1A1TSHRTDP1CA2HSD17B10
SCHEMBL5503676 0.79 ALDH1A1 (0.54) ALDH1A1TSHRTDP1ALOX15CA2
SCHEMBL29779511 0.79 TSHR (0.54) ALDH1A1TSHRTDP1CA2HSD17B10
SCHEMBL324566 0.77 ALDH1A1 (0.58) ALDH1A1TSHRTDP1ALOX15CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1572611-B1 PROCESS FOR THE SYNTHESIS OF BISPHENOL SABIC INNOVATIVE PLASTICS IP (NL) 2009-07-22 EP disclosed
US-7132575-B2 Process for the synthesis of bisphenol GENERAL ELECTRIC COMPANY (US) 2006-11-07 US disclosed
US-7112702-B2 Process for the synthesis of bisphenol GENERAL ELECTRIC COMPANY (US) 2006-09-26 US disclosed
WO-2005005358-A1 PROCESS FOR THE SYNTHESIS OF BISPHENOL GENERAL ELECTRIC COMPANY (US) 2005-01-20 WO disclosed
US-20050004406-A1 Process for the synthesis of bisphenol SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2005-01-06 US disclosed
US-20040116751-A1 PROCESS FOR THE SYNTHESIS OF BISPHENOL SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2004-06-17 US disclosed
US-6133190-A SUPPORTED MERCAPTOAKYL-SUBSTITUTED POLYSTYRENESULFONATE IS USED AS A CATALYST FOR CONDENSATION OF ALDEHYDE OR KETONE WITH PHENOL TO FORM DIHYDROXY COMPOUND THE DOW CHEMICAL COMPANY (US) 2000-10-17 US disclosed
US-6051658-A A POLYSTYRENE HAVING MERCAPTOSULFONIC ACID RESIDUE, USEFUL AS CATALYST THE DOW CHEMICAL COMPANY (US) 2000-04-18 US disclosed
US-5939494-A CATALYST USEFUL FOR THE CONDENSATION OF AN ALDEHYDE OR KETONE STARTING MATERIAL WITH A PHENOL IS AN INSOLUBLE MERCAPTOSULFONIC ACID COMPOUND THE DOW CHEMICAL COMPANY (US) 1999-08-17 US disclosed
EP-0848693-A4 ISOMERIZATION OF BISPHENOLS DOW CHEMICAL CO (US) 1999-03-17 EP disclosed
CN-1200105-A Isomerization of bisphenols DOW CHEMICAL CO (US) 1998-11-25 CN disclosed
EP-0848693-A1 ISOMERIZATION OF BISPHENOLS THE DOW CHEMICAL COMPANY (US) 1998-06-24 EP disclosed
WO-1997008122-A1 ISOMERIZATION OF BISPHENOLS THE DOW CHEMICAL COMPANY (US) 1997-03-06 WO disclosed
EP-0725771-A1 PROCESS FOR MAKING POLYPHENOLS FROM KETONES OR ALDEHYDES AND PHENOLS THE DOW CHEMICAL COMPANY (US) 1996-08-14 EP disclosed
WO-1996006819-A1 PROCESS FOR MAKING POLYPHENOLS FROM KETONES OR ALDEHYDES AND PHENOLS THE DOW CHEMICAL COMPANY (US) 1996-03-07 WO disclosed
US-5463140-A Condensing aldehyde or ketone with phenol in presence of soluble or insoluble mercaptosulfonic acid compound to form geminal bisphenol moiety at each aldehyde or ketone moiety THE DOW CHEMICAL COMPANY (US) 1995-10-31 US disclosed